Compositions and methods for treating lupus

Abstract

The present invention relates to compositions and methods for the treatment of lupus, particularly systemic lupus erythematosus. The invention involves, inter alia, binding proteins comprising a T-cell receptor (TCR) α chain variable (Vα or V alpha) domain and a TCR β chain variable (Vβ or V beta) domain, which are capable of binding to a complex of a fragment of Smith protein and an HLA-DR15 molecule or an HLA-DR3 molecule.

Description

[Technical Field]

[0001] The present invention relates to compositions and methods for treating lupus, particularly systemic lupus erythematosus.

[0002] Related applications This application claims priority to Australian Provisional Patent Application No. 2020900864, ​​the contents of which are incorporated herein by reference. [Background technology]

[0003] Systemic lupus erythematosus (SLE) is a chronic, inflammatory autoimmune disease characterized by the production of autoantibodies with broad specificity against autoantigens. SLE autoantibodies mediate organ damage by forming immune complexes that directly bind to host tissues, deposit in vascular tissue, and activate immune cells. Targeted organs in SLE include the skin, kidneys, vascular system, joints, mucous membranes and serosa, various blood elements, and the central nervous system (CNS). Disease severity, the spectrum of clinical interventions, and responses to treatment vary significantly among patients. This clinical heterogeneity makes the diagnosis and management of lupus challenging.

[0004] Due to the great clinical diversity and idiopathic nature of SLE, the management of idiopathic SLE depends on its specific symptoms and severity. Therefore, the medications suggested for treating SLE are generally not effective for treating all symptoms of SLE and their resulting complications, such as lupus nephritis (LN). LN typically develops early in the disease course, within 5 years of diagnosis. The pathogenesis of LN is thought to be due to the deposition of immune complexes in the renal glomeruli, which trigger an inflammatory response. An estimated 30-50% of patients with SLE develop nephritis requiring medical assessment and treatment. LN is a progressive disease that follows a course of clinical exacerbations and clinical remissions.

[0005] Despite important research on SLE, there is a lack of effective targeting therapies in SLE. Current treatments, such as corticosteroids, methotrexate, hydroxychloroquine, other immunosuppressive agents (e.g., to name a few, cyclosporine, leflunomide, azathioprine), and non-steroidal anti-inflammatory drugs, do not precisely inhibit the specific autoimmunity associated with the disorder but rather non-specifically inhibit the activation of the immune system.

[0006] Many patients do not respond to or only have a partial response to the standard medical treatments listed above. On the other hand, the long-term use of high-dose corticosteroids and cytotoxic therapies can lead to serious side effects, such as bone marrow suppression, an increased risk of infections by opportunistic bacteria, irreversible ovarian failure, hair loss, and an increased risk of malignancies. Infectious complications that occur simultaneously with active SLE and its treatment with immunosuppressive medications are one of the most common causes of death in patients with SLE.

Summary of the Invention

Problems to be Solved by the Invention

[0007] Therefore, new or improved treatments for SLE are needed.

Means for Solving the Problems

[0008] Any reference to prior art in this specification is not an admission or suggestion that this prior art forms part of the common general knowledge in any legal jurisdiction, or that this prior art would be understood and considered relevant by a person skilled in the art, and / or that it would be reasonably foreseeable that this prior art would be combined with other fragments of the prior art.

[0009] (Summary of the Invention) In one embodiment, the present invention provides a binding protein comprising a T cell receptor (TCR) α chain variable (Vα or V-alpha) domain and a TCR β chain variable (Vβ or V-beta) domain, which is capable of binding to a complex of a Smith protein fragment with an HLA-DR15 molecule or an HLA-DR3 molecule. Preferably, the HLA-DR15 molecule is HLA-DR3. * 01:01 molecule and HLA-DRB1 * 15:01 molecule. Preferably, HLA-DR3 is HLA-DRA * 01:01 molecule and HLA-DRB1 * 03:01 is a molecule.

[0010] For example, the binding protein of the present invention can bind to a peptide consisting of 4, 5, 6, 7, 8, 9, 10 or more consecutive amino acid residues, as specified in any one of SEQ ID NOs: 1, 2, 3, 4, 258, or 259.

[0011] In any embodiment, a fragment of Smith protein capable of forming a complex with an HLA-DR15 molecule comprises or consists of the amino acid sequence of residues 6-14 or 62-70 of the SmB / B' protein or an equivalent amino acid sequence, preferably the SmB' protein comprising the sequence of SEQ ID NO: 5. In one embodiment, the fragment of SmB / B' protein comprises or consists of the amino acid sequence of SEQ ID NO: 3 or 4.

[0012] In any embodiment, a fragment of Smith protein capable of forming a complex with an HLA-DR15 molecule comprises or consists of the amino acid sequence of residues 1-15 of the SmB / B' protein or an equivalent amino acid sequence, preferably the SmB' protein comprising the sequence of SEQ ID NO: 5. In one embodiment, the fragment of SmB / B' protein comprises or consists of the amino acid sequence of SEQ ID NO: 1.

[0013] In any embodiment, a fragment of Smith protein capable of forming a complex with an HLA-DR15 molecule comprises or consists of the amino acid sequence of residues 58-72 of the SmB / B' protein or an equivalent amino acid sequence, preferably the SmB' protein comprising the sequence of SEQ ID NO: 5. In one embodiment, the SmB / B' protein comprises the amino acid sequence of SEQ ID NO: 2.

[0014] In any embodiment, a fragment of Smith protein capable of forming a complex with an HLA-DR3 molecule comprises or consists of the amino acid sequence of residues 78-92 of the SmD1 protein or an equivalent amino acid sequence, preferably the SmD1 protein comprising the sequence of SEQ ID NO: 260. In one embodiment, the fragment of SmD1 protein comprises or consists of the amino acid sequence of SEQ ID NO: 258.

[0015] In any embodiment, a fragment of Smith protein capable of forming a complex with an HLA-DR3 molecule comprises or consists of the amino acid sequence of residues 7-21 of the SmB / B' protein or an equivalent amino acid sequence, preferably the SmB' protein comprising the sequence of SEQ ID NO: 5. In one embodiment, the fragment of SmB / B' protein comprises or consists of the amino acid sequence of SEQ ID NO: 259.

[0016] In any embodiment, a fragment of Smith protein capable of forming a complex with the HLA-DR15 molecule contains or comprises any one or more amino acid sequences from SEQ ID NOs: 1-4.

[0017] In any embodiment, a fragment of Smith protein capable of forming a complex with an HLA-DR3 molecule comprises or comprises the amino acid sequence of SEQ ID NO: 258 or 259.

[0018] In another embodiment, the present invention also provides a binding protein comprising a T cell receptor (TCR) α chain variable (Vα or V-alpha) domain and a TCR β chain variable (Vβ or V-beta) domain, wherein the Vα domain comprises an amino acid sequence (TRA) of any "CDR alpha" or any Vα domain as defined in any one of Tables 1 to 4 herein, and / or the Vβ domain comprises an amino acid sequence (TRB) of any "CDR beta" or any Vβ domain as defined in any one of Tables 1 to 4 herein.

[0019] In another embodiment, the present invention also relates to a binding protein comprising a T cell receptor (TCR) α chain variable (Vα or V-alpha) domain and a TCR β chain variable (Vβ or V-beta) domain, The Vα domain contains a CDR3 comprising an amino acid sequence that is at least approximately 80%, at least 85%, at least 90%, at least 92%, at least 95%, at least 97%, or at least 99% identical to any one of the sequences among SEQ ID NOs: 8, 20, 32, 44, 56, 68, 80, 92, 104, 107, 122, 134, 146, 158, 170, 182, 194, 197, 212, 224, 236, and 248; and / or The Vβ domain contains a CDR3 containing an amino acid sequence that is at least approximately 80%, at least 85%, at least 90%, at least 92%, at least 95%, at least 97%, or at least 99% identical to any one of the sequences among sequence numbers 11, 23, 35, 47, 59, 71, 83, 95, 110, 125, 137, 149, 161, 173, 185, 200, 215, 227, 239, and 251, The binding protein can bind to a complex of a Smith protein fragment and the HLA-DR15 molecule. It also provides binding proteins.

[0020] In another embodiment, the present invention also relates to a binding protein comprising a T cell receptor (TCR) α chain variable (Vα or V-alpha) domain and a TCR β chain variable (Vβ or V-beta) domain, The Vα domain contains a CDR3 comprising an amino acid sequence that is at least approximately 80%, at least 85%, at least 90%, at least 92%, at least 95%, at least 97%, or at least 99% identical to any one of the sequences among SEQ ID NOs: 263, 275, 287, 299, 311, 323, 335, 347, 359, 371, 383, 395, 407, 419, 431, 443, 455, 467, 479, and 491; and / or The Vβ domain contains a CDR3 containing an amino acid sequence that is at least approximately 80%, at least 85%, at least 90%, at least 92%, at least 95%, at least 97%, or at least 99% identical to any one of the sequences among sequence numbers 266, 278, 290, 302, 314, 326, 338, 350, 362, 374, 386, 398, 410, 422, 434, 446, 458, 470, 482, and 494, The binding protein can bind to a complex of Smith protein fragments and the HLA-DR3 molecule. It also provides binding proteins.

[0021] In another embodiment, the present invention also relates to a binding protein comprising a T cell receptor (TCR) α chain variable (Vα or V-alpha) domain and a TCR β chain variable (Vβ or V-beta) domain, The Vα domain contains a CDR3 having one of the amino acid sequences among SEQ ID NOs: 8, 20, 32, 44, 56, 68, 80, 92, 104, 107, 122, 134, 146, 158, 170, 182, 194, 197, 212, 224, 236, and 248; and / or The Vβ domain contains a CDR3 having one of the amino acid sequences among SEQ ID NOs: 11, 23, 35, 47, 59, 71, 83, 95, 110, 125, 137, 149, 161, 173, 185, 200, 215, 227, 239, and 251. The binding protein can bind to a complex of a Smith protein fragment and the HLA-DR15 molecule. It also provides binding proteins.

[0022] In a particularly preferred embodiment, the Vα domain comprises a CDR3 containing any one of the amino acid sequences of SEQ ID NOs: 8, 20, or 32, and the Vβ domain comprises a CDR3 containing any one of the amino acid sequences of SEQ ID NOs: 11, 23, or 35.

[0023] In another embodiment, the present invention also relates to a binding protein comprising a T cell receptor (TCR) α chain variable (Vα or V-alpha) domain and a TCR β chain variable (Vβ or V-beta) domain, The Vα domain contains a CDR3 having one of the amino acid sequences among SEQ ID NOs: 263, 275, 287, 299, 311, 323, 335, 347, 359, 371, 383, 395, 407, 419, 431, 443, 455, 467, 479, and 491; and / or The Vβ domain contains a CDR3 containing one of the amino acid sequences among SEQ ID NOs: 266, 278, 290, 302, 314, 326, 338, 350, 362, 374, 386, 398, 410, 422, 434, 446, 458, 470, 482, and 494. The binding protein can bind to a complex of Smith protein fragments and the HLA-DR3 molecule. It also provides binding proteins.

[0024] In a particularly preferred embodiment, the Vα domain comprises a CDR3 containing the amino acid sequence of SEQ ID NO: 263, and the Vβ domain comprises a CDR3 containing the amino acid sequence of SEQ ID NO: 266.

[0025] In another embodiment, the present invention also relates to a binding protein comprising a T cell receptor (TCR) α chain variable (Vα or V-alpha) domain and a TCR β chain variable (Vβ or V-beta) domain, The variable (Vα or V-alpha) domain of the T cell receptor (TCR) α chain is (i) Complementarity Determination Region (CDR) 1, which is at least approximately 80%, at least 85%, at least 90%, at least 92%, at least 95%, at least 97%, and at least 99% identical to the sequence specified in SEQ ID NOs: 6, 18, 30, 42, 54, 66, 78, 90, 102, 105, 120, 132, 144, 156, 168, 180, 192, 195, 210, 222, 234, or 246; SEQ ID NOs: 7, 19, 31, 43, 55, 67, 79, 91, 103, 106, 121, 133, 145, 157, 169, 181, 193, 196, 211, 223, 235, or 247 CDR2 containing a sequence that is at least approximately 80%, at least 85%, at least 90%, at least 92%, at least 95%, at least 97%, and at least 99% identical to the sequence explicitly stated in; and CDR3 containing a sequence that is at least approximately 80%, at least 85%, at least 90%, at least 92%, at least 95%, at least 97%, and at least 99% identical to the sequence explicitly stated in sequence numbers 8, 20, 32, 44, 56, 68, 80, 92, 104, 107, 122, 134, 146, 158, 170, 182, 194, 197, 212, 224, 236, or 248; or (ii) CDR1 containing the sequences specified in SEQ ID NOs: 6, 18, 30, 42, 54, 66, 78, 90, 102, 105, 120, 132, 144, 156, 168, 180, 192, 195, 210, 222, 234 or 246; SEQ ID NOs: 7, 19, 31, 43, 55, 67, 79, 91, 103, 106, 121, 133, 145, 15 CDR2 containing the sequences specified in sequence numbers 7, 169, 181, 193, 196, 211, 223, 235, or 247; and CDR3 containing the sequences specified in sequence numbers 8, 20, 32, 44, 56, 68, 80, 92, 104, 107, 122, 134, 146, 158, 170, 182, 194, 197, 212, 224, 236, or 248. Includes, The TCRβ chain variable (Vβ or Vbeta) domain (i) CDR1 containing sequences that are at least approximately 80%, at least 85%, at least 90%, at least 92%, at least 95%, at least 97%, and at least 99% identical to the sequences explicitly stated in SEQ ID NOs: 9, 21, 33, 45, 57, 69, 81, 93, 108, 123, 135, 147, 159, 171, 183, 198, 213, 225, 237, or 249; and sequences explicitly stated in SEQ ID NOs: 10, 22, 34, 46, 58, 70, 82, 94, 109, 124, 136, 148, 160, 172, 184, 199, 214, 226, 238, or 250 CDR2 containing a sequence that is at least approximately 80%, at least 85%, at least 90%, at least 92%, at least 95%, at least 97%, and at least 99% identical to the sequence; and CDR3 containing a sequence that is at least approximately 80%, at least 85%, at least 90%, at least 92%, at least 95%, at least 97%, and at least 99% identical to the sequence specified in SEQ ID NOs. 11, 23, 35, 47, 59, 71, 83, 95, 110, 125, 137, 149, 161, 173, 185, 200, 215, 227, 239, or 251; or (ii) CDR1 containing the sequence specified in SEQ ID NOs: 9, 21, 33, 45, 57, 69, 81, 93, 108, 123, 135, 147, 159, 171, 183, 198, 213, 225, 237, or 249; CDR2 containing the sequence specified in SEQ ID NOs: 10, 22, 34, 46, 58, 70, 82, 94, 109, 124, 136, 148, 160, 172, 184, 199, 214, 226, 238, or 250; and CDR3 containing the sequence specified in SEQ ID NOs: 11, 23, 35, 47, 59, 71, 83, 95, 110, 125, 137, 149, 161, 173, 185, 200, 215, 227, 239, or 251. including It also provides binding proteins.

[0026] In another embodiment, the present invention also relates to a binding protein comprising a T cell receptor (TCR) α chain variable (Vα or V-alpha) domain and a TCR β chain variable (Vβ or V-beta) domain, The variable (Vα or V-alpha) domain of the T cell receptor (TCR) α chain is (i) Complementarity Determination Region (CDR) 1 which is at least approximately 80%, at least 85%, at least 90%, at least 92%, at least 95%, at least 97%, or at least 99% identical to the sequence specified in SEQ ID NOs: 262, 274, 286, 298, 310, 322, 334, 346, 358, 370, 382, ​​394, 406, 418, 430, 442, 454, 466, 478, or 490 CDR2 containing a sequence that is at least approximately 80%, at least 85%, at least 90%, at least 92%, at least 95%, at least 97%, and at least 99% identical to the sequence explicitly stated in; and CDR3 containing a sequence that is at least approximately 80%, at least 85%, at least 90%, at least 92%, at least 95%, at least 97%, and at least 99% identical to the sequences explicitly stated in SEQ ID NOs. 263, 275, 287, 299, 311, 323, 335, 347, 359, 371, 383, 395, 407, 419, 431, 443, 455, 467, 479, and 491; or (ii) CDR1 containing sequences specified in SEQ ID NOs: 261, 273, 285, 297, 309, 321, 333, 345, 357, 369, 381, 393, 405, 417, 429, 441, 453, 465, 477 or 489; SEQ ID NOs: 262, 274, 286, 298, 310, 322, 334, 346, 358, 370, 382, ​​3 CDR2 containing the sequences specified in 94, 406, 418, 430, 442, 454, 466, 478 or 490; and CDR3 containing the sequences specified in SEQ ID NOs. 263, 275, 287, 299, 311, 323, 335, 347, 359, 371, 383, 395, 407, 419, 431, 443, 455, 467, 479 and 491. Includes, The TCRβ chain variable (Vβ or Vbeta) domain (i) CDR1 containing sequences that are at least approximately 80%, at least 85%, at least 90%, at least 92%, at least 95%, at least 97%, and at least 99% identical to the sequences explicitly shown in SEQ ID NOs: 265, 277, 289, 301, 313, 325, 337, 349, 361, 373, 385, 397, 409, 421, 433, 445, 457, 469, 481, or 493 CDR2 containing a sequence that is at least approximately 80%, at least 85%, at least 90%, at least 92%, at least 95%, at least 97%, and at least 99% identical to the sequence explicitly stated in; and CDR3 containing a sequence that is at least approximately 80%, at least 85%, at least 90%, at least 92%, at least 95%, at least 97%, and at least 99% identical to the sequences explicitly stated in SEQ ID NOs. 266, 278, 290, 302, 314, 326, 338, 350, 362, 374, 386, 398, 410, 422, 434, 446, 458, 470, 482, and 494; or (ii) CDR1 containing sequences specified in SEQ ID NOs: 264, 276, 288, 300, 312, 324, 336, 348, 360, 372, 384, 396, 408, 420, 432, 444, 456, 468, 480 or 492; SEQ ID NOs: 265, 277, 289, 301, 313, 325, 337, 349, 361, 373, 385, CDR2 containing the sequences specified in SEQ ID NOs: 397, 409, 421, 433, 445, 457, 469, 481, or 493; and CDR3 containing the sequences specified in SEQ ID NOs: 266, 278, 290, 302, 314, 326, 338, 350, 362, 374, 386, 398, 410, 422, 434, 446, 458, 470, 482, and 494. including It also provides binding proteins.

[0027] In another embodiment, the present invention also relates to a binding protein comprising a T cell receptor (TCR) α chain variable (Vα or V-alpha) domain and a TCR β chain variable (Vβ or V-beta) domain, CDR1 containing one amino acid sequence from among SEQ ID NOs: 6, 18, 30, 42, 54, 66, 78, 90, 102, 105, 120, 132, 144, 156, 168, 180, 192, 195, 210, 222, 234, and 246; SEQ ID NOs: 7, 19, 31, 43, 55, 67, 79, 91, 103, 106, 121, 133, 145, 157, 169 , CDR2 containing any one amino acid sequence of 181, 193, 196, 211, 223, 235 and 247; CDR3 containing any one amino acid sequence of SEQ ID NOs: 8, 20, 32, 44, 56, 68, 80, 92, 104, 107, 122, 134, 146, 158, 170, 182, 194, 197, 212, 224, 236 and 248; and / or CDR1 containing one amino acid sequence from among SEQ ID NOs: 9, 21, 33, 45, 57, 69, 81, 93, 108, 123, 135, 147, 159, 171, 183, 198, 213, 225, 237, and 249; SEQ ID NOs: 10, 22, 34, 46, 58, 70, 82, 94, 109, 124, 136, 148, 160, CDR2 containing any one amino acid sequence among 172, 184, 199, 214, 226, 238 and 250; CDR3 containing any one amino acid sequence among SEQ ID NOs: 11, 23, 35, 47, 59, 71, 83, 95, 110, 125, 137, 149, 161, 173, 185, 200, 215, 227, 239 and 251, The binding protein can bind to a complex of a Smith protein fragment and the HLA-DR15 molecule. It also provides binding proteins.

[0028] In another embodiment, the present invention also relates to a binding protein comprising a T cell receptor (TCR) α chain variable (Vα or V-alpha) domain and a TCR β chain variable (Vβ or V-beta) domain, CDR1 whose Vα domain contains one of the amino acid sequences among SEQ ID NOs: 261, 273, 285, 297, 309, 321, 333, 345, 357, 369, 381, 393, 405, 417, 429, 441, 453, 465, 477, or 489; SEQ ID NOs: 262, 274, 286, 298, 310, 322, 334, 346, 358, 370, 382, ​​394, 40 CDR2 containing any one amino acid sequence of 6, 418, 430, 442, 454, 466, 478 or 490; CDR3 containing any one amino acid sequence of SEQ ID NOs: 263, 275, 287, 299, 311, 323, 335, 347, 359, 371, 383, 395, 407, 419, 431, 443, 455, 467, 479 and 491; and / or CDR1 containing one amino acid sequence from among SEQ ID NOs: 264, 276, 288, 300, 312, 324, 336, 348, 360, 372, 384, 396, 408, 420, 432, 444, 456, 468, 480, or 492; SEQ ID NOs: 265, 277, 289, 301, 313, 325, 337, 349, 361, 373, 385, 397, CDR2 containing any one amino acid sequence among 409, 421, 433, 445, 457, 469, 481, or 493; CDR3 containing any one amino acid sequence among SEQ ID NOs: 266, 278, 290, 302, 314, 326, 338, 350, 362, 374, 386, 398, 410, 422, 434, 446, 458, 470, 482, and 494; The binding protein can bind to a complex of Smith protein fragments and the HLA-DR3 molecule. It also provides binding proteins.

[0029] In another embodiment, the present invention also relates to a binding protein comprising a T cell receptor (TCR) α chain variable (Vα or V-alpha) domain and a TCR β chain variable (Vβ or V-beta) domain, The T cell receptor (TCR) α chain variable (Vα or V-alpha) domain includes CDR1, 2, and 3 as shown in Table 1 or 2; and / or The T cell receptor (TCR) β-chain variable (Vβ or V-beta) domain includes CDR1, 2, and 3 as shown in Table 1 or 2. It also provides binding proteins.

[0030] Preferably, the binding protein contains the sequence of TCR1, 2, or 3 as shown in Table 1, or the sequence of TCR1 as shown in Table 2.

[0031] In any embodiment, the binding protein has a TCRα chain comprising or derived from the amino acid sequence expressed in any one of SEQ ID NOs: 501, 503, 505, 507, 509, 511, 513, 515, 517, 518, 520, 522, 524, 526, 528, 530, 532, 533, 535, 537, 539, and 541; and / or a TCRβ chain comprising or derived from the amino acid sequence expressed in any one of SEQ ID NOs: 502, 504, 506, 508, 510, 512, 514, 516, 519, 521, 523, 525, 527, 529, 531, 534, 536, 538, 540, and 542 or any combination thereof.

[0032] In any embodiment, the binding protein has a TCRα chain comprising or derived from the amino acid sequence expressed in any one of SEQ ID NOs: 585, 587, 589, 591, 593, 595, 597, 599, 601, 603, 605, 607, 609, 611, 613, 615, 617, 619, 621, and 623; and / or a TCRβ chain comprising or derived from the amino acid sequence expressed in any one of SEQ ID NOs: 586, 588, 590, 592, 594, 596, 598, 600, 602, 604, 606, 608, 610, 612, 614, 616, 618, 620, 622, and 624 or any combination thereof.

[0033] In any embodiment of the present invention, the binding protein comprises a TCRα chain containing a Vα domain and a TCRβ chain containing a Vβ domain. Preferably, the TCRα chain and the TCRβ chain are modified to include cysteine ​​residues that enable the formation of further interchain disulfide bonds. The cysteine ​​introduced into each of the TCRα and TCRβ chains enables preferential pairing of the TCRα chain and the TCRβ chain when expressed in cells expressing endogenous TCRα and endogenous TCRβ chains. Preferably, the residue at Thr48 or an equivalent residue on the TCRα chain and the residue at Ser57 or an equivalent residue on the TCRβ chain are replaced with cysteine ​​to facilitate the creation of further disulfide bonds between the constant regions of the TCR.

[0034] In another embodiment, the present invention provides a peptide comprising, or derived from, the amino acid sequence of residues 1-15 or 58-72 of the SmB / B' protein or an equivalent amino acid sequence. In one embodiment, the SmB' protein comprises the amino acid sequence of SEQ ID NO: 5. In one embodiment, the peptide comprises, or derived from, the amino acid sequence expressed in any one of SEQ ID NOs: 1, 2, 3, and 4, preferably the amino acid sequence expressed in SEQ ID NO: 3 or 4.

[0035] In any embodiment, the peptide of the present invention can bind to or form a complex with the HLA-DR15 molecule, preferably the HLA-DR15 molecule is HLA-DR15. * 01:01 molecule and HLA-DRB1 * It is a 15:01 molecule.

[0036] In another embodiment, the present invention provides a peptide comprising, essentially, or derived from, the amino acid sequence of residues 7-21 of the SmB / B' protein or an equivalent amino acid sequence. In one embodiment, the SmB' protein comprises the amino acid sequence of SEQ ID NO: 5. In one embodiment, the peptide comprises, or derived from, the amino acid sequence explicitly shown in SEQ ID NO: 259.

[0037] In another embodiment, the present invention provides a peptide comprising, or derived from, the amino acid sequence of residues 78-92 of the SmD1 protein or an equivalent amino acid sequence. In one embodiment, the SmB / B' protein comprises the amino acid sequence of SEQ ID NO: 260. In one embodiment, the peptide comprises, or derived from, the amino acid sequence explicitly shown in SEQ ID NO: 258.

[0038] In any embodiment, the peptide of the present invention can bind to or form a complex with an HLA-DR3 molecule, preferably the HLA-DR3 molecule is HLA-DRA * 01:01 molecule and HLA-DRB1 * 03:01 is a molecule.

[0039] In another embodiment, the present invention provides nucleic acids comprising, essentially derived from, a nucleotide sequence encoding a binding protein or peptide of the present invention.

[0040] In another embodiment, the present invention provides a vector comprising a nucleotide sequence encoding a binding protein or peptide of the present invention. Typically, the vector results in the presentation of a binding protein on the cell surface as a result of enabling the expression of the nucleotide sequence within the cell. The vector may be a retroviral vector, preferably a lentiviral vector. Typically, the vector enables the expression of the nucleotide sequence within a T cell, preferably a helper T cell, for example, a CD4+ T cell. The CD4+ T cell may be a CD4+CD25high T cell.

[0041] In one embodiment, the vector comprises the nucleic acid of the present invention, operably linked to a promoter.

[0042] In embodiments of the present invention that target binding proteins with a single polypeptide chain, the expression construct may include a promoter linked to the nucleic acid encoding the polypeptide chain.

[0043] In embodiments of the present invention, which target multiple polypeptide chains that form a binding protein, the vector includes, for example, a nucleic acid encoding a polypeptide containing Vα operably linked to a promoter, and for example, a nucleic acid encoding a polypeptide containing Vβ operably linked to a promoter.

[0044] In another example, the expression construct consists of the following components, operably linked in the order of 5' to 3': (i) promoter (ii) Nucleic acid encoding the first polypeptide; (iii) Internal ribosome entry sites; and (iv) comprising a nucleic acid encoding a second polypeptide, The first polypeptide is a bicistronic expression construct containing Vα and the second polypeptide containing Vβ, or vice versa. Preferably, the vector allows translation of the nucleotide sequence encoding Vβ before translation of the nucleotide sequence encoding Vα.

[0045] In any embodiment, the vector of the present invention is as follows: (i) EF1α (alpha) promoter; (ii) 2A ribosome skipping sequence; (iii) Woodchuck hepatitis virus post-transcriptional regulatory element (WPRE); (iv) A configuration in which the TCRβ chain variable (Vβ or V-beta) domain is translated before the (TCR)α chain variable (Vα or V-alpha) domain; or (v) Arrangement that translates the TCRβ chain variable (Vβ or V-beta) chain before the (TCR)α chain variable (Vα or V-alpha) chain. It may include one or more, or all, of the following.

[0046] Preferably, the vector is a lentiviral vector. More preferably, the lentiviral vector has one or more or all of the features shown in Figure 4.

[0047] In another embodiment, the present invention also envisions separate vectors, one of which encodes a first polypeptide comprising Vα, and the other of which encodes a second polypeptide comprising Vβ. For example, the present invention also envisions, (i) A first expression construct comprising a nucleic acid encoding a polypeptide containing Vα operably linked to a promoter; and (ii) A second expression construct comprising a nucleic acid encoding a polypeptide containing Vβ operably linked to a promoter. We also provide compositions containing the above.

[0048] In another embodiment, the present invention provides cells comprising a vector or nucleic acid as described herein. Preferably, the cells are isolated, substantially purified, or recombinant. In one example, the cells comprise the vector or nucleic acid of the present invention. (i) A first expression construct comprising a nucleic acid encoding a polypeptide containing Vα operably linked to a promoter; and (ii) A second expression construct comprising a nucleic acid encoding a polypeptide containing Vβ operably linked to a promoter. Includes, In this case, the first polypeptide and the second polypeptide associate to form the binding protein of the present invention. Preferably, the cell is a T cell, more preferably a helper T cell, such as a CD4+ T cell. The CD4+ T cell may be a CD4+ CD25high T cell.

[0049] In another embodiment, the present invention provides cells that express the binding protein of the present invention on their surface. Preferably, the cells are T cells, more preferably CD4+ T cells. The CD4+ T cells may be CD4+ CD25high T cells.

[0050] In another embodiment, the present invention relates to a method for preparing a population of regulatory T cells for use in the treatment of SLE, Steps to prepare a population of regulatory T cells; A step of introducing the nucleic acid or vector of the present invention into a population of regulatory T cells; A step that provides conditions that enable the expression of binding proteins on the surface of regulatory T cells. This invention provides a method for preparing a population of regulatory T cells for use in the treatment of SLE.

[0051] In another embodiment, the present invention is a method for treating SLE in a subject, The procedure involves administering an effective amount of regulatory T cells to a subject, which express a binding protein on their surface that contains a T cell receptor (TCR) α-chain variable (Vα or V-alpha) domain and a TCR β-chain variable (Vβ or V-beta) domain, and which is capable of binding to a complex of Smith protein fragments with an HLA-DR15 molecule or an HLA-DR3 molecule, thereby treating SLE in the subject. The present invention provides a method comprising the following: Preferably, the binding protein is any binding protein of the present invention as described herein.

[0052] In another embodiment, the present invention relates to a method for preparing, ex vivo, a population of regulatory T cells exhibiting at least one characteristic of Smith protein-specific T cells, A step of preparing a population of T cells that exhibit at least one characteristic of regulatory T cells; A step of introducing the nucleic acid or vector of the present invention into a population of T cells, wherein the nucleic acid or vector encodes a binding protein of the present invention; A step that provides conditions that enable the expression of binding proteins on the surface of T cells. The present invention relates to a method for preparing, ex vivo, a population of Smith protein-specific T cells exhibiting at least one characteristic of regulatory T cells. Preferably, the T cells exhibiting at least one characteristic of regulatory T cells are derived from a biological sample from a subject having SLE.

[0053] The regulatory T cells used in the method or use of the present invention, which exhibit at least one characteristic, may be selected from subjects diagnosed with SLE or from healthy subjects. The T cells may be isolated from histocompatible donors.

[0054] In an alternative embodiment, the present invention relates to a method for preparing ex vivo a population of Smith protein-specific regulatory T cells exhibiting at least one characteristic of regulatory T cells, A step of preparing a population of T cells that exhibit at least one characteristic of normal T cells, wherein the T cell population is optionally a mixed T cell population; A step of introducing the nucleic acid or vector of the present invention into a population of T cells, wherein the nucleic acid or vector encodes a binding protein of the present invention; A step that creates conditions on the surface of T cells that enable the expression of binding proteins; A step that provides the conditions necessary for the conversion of a T cell population into regulatory T cells. The present invention provides a method for preparing, ex vivo, a population of Smith protein-specific T cells exhibiting at least one characteristic of regulatory T cells. Preferably, the T cell population exhibiting at least one characteristic of conventional T cells or a mixed T cell population is derived from a biological sample from a subject with SLE. Alternatively, the T cells may be derived from a histocompatibility donor.

[0055] The present invention also relates to a composition of regulatory T cells in which more than 20% of the cells express the binding protein of the present invention. Preferably, the composition contains more than 30%, 40%, 50%, 60%, 70%, 80%, 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, or 99% of the cells expressing the binding protein of the present invention.

[0056] In another embodiment, the present invention relates to a method for preparing a population of regulatory T cells for use in the treatment of SLE, A step of culturing a population of regulatory T cells in the presence of the peptide of the present invention, under conditions that allow for the expansion of subpopulations activated by the peptide, for a sufficient amount of time. This invention provides a method for preparing a population of regulatory T cells for use in the treatment of SLE.

[0057] Furthermore, the present invention relates to a method for preparing a population of regulatory T cells for use in the treatment of SLE, A step of culturing a mixed T cell population or a T cell population exhibiting the characteristics of at least one normal T cell in the presence of the peptide of the present invention, under conditions that allow for the expansion of subpopulations activated by the peptide, for a sufficient amount of time; A step of culturing T cells under conditions that enable the conversion of T cells into regulatory T cells. This invention provides a method for preparing a population of regulatory T cells for use in the treatment of SLE.

[0058] In any embodiment, the conditions for enabling the conversion of a normal T cell population or a mixed T cell population into regulatory T cells may include contacting the normal T cell population or the mixed T cell population with one or more agents or increasing the expression of one or more factors suitable for the conversion of normal T cells into regulatory T cells. The one or more agents or factors may include TGF-β, Foxp3, or agents for increasing their expression.

[0059] In another aspect, the present invention is a method of immunotherapy with adoptive cells, comprising: extracting a mixed T cell population from a subject diagnosed with a condition associated with an abnormal, unwanted, or otherwise inappropriate immune response to a Smith protein; isolating, from the population, a subpopulation comprising CD4 + CD25 + T cells (Treg cells) by negative and positive immunoselection and cell sorting; expanding the Treg cells among the subpopulation by contacting the subpopulation with an effective amount of a peptide of the present invention; and introducing the Treg cells expanded ex vivo into the subject and providing an immunotherapy comprising the same.

[0060] In another aspect, the present invention provides a composition comprising a binding protein, peptide, cell or vector of the present invention and a pharmaceutically acceptable carrier, diluent or excipient.

[0061] In another aspect, the present invention is a method of treating or preventing a condition associated with an abnormal, unwanted, or otherwise inappropriate immune response to a Smith protein in a subject, comprising administering to the subject a binding protein, peptide, cell, nucleic acid or composition of the present invention, thereby treating or preventing the condition in the subject.

[0062] In another aspect, the present invention is a method of treating or preventing a condition associated with an abnormal, unwanted, or otherwise inappropriate immune response to a Smith protein in a subject, comprising: providing a T cell population exhibiting at least one characteristic of regulatory T cells; introducing a nucleic acid or vector of the present invention into the population of T cells, wherein the nucleic acid or vector encodes a binding protein of the present invention; providing conditions that allow for expression of the binding protein on the surface of the T cells; The step of administering T cells that express binding proteins on their surfaces. The present invention provides a method for treating or preventing a condition in a subject, which includes the following: Preferably, the regulatory T cells exhibiting at least one characteristic are derived from a biological sample from a subject having SLE.

[0063] In another embodiment, the present invention provides a use of the binding proteins, peptides, cells, nucleic acids, or compositions of the present invention in the manufacture of a pharmaceutical for treating or preventing a condition in a subject, wherein the condition is related to an abnormal, undesirable, or otherwise inappropriate immune response to Smith protein.

[0064] In another embodiment, the present invention provides binding proteins, peptides, cells, nucleic acids, or compositions for use in treating or preventing conditions associated with abnormal, undesirable, or otherwise inappropriate immune responses to Smith protein in a subject.

[0065] In any embodiment, a condition associated with an abnormal, undesirable, or otherwise inadequate immune response to the Smith protein is systemic lupus erythematosus (SLE). Alternatively, a condition associated with an abnormal, undesirable, or otherwise inadequate immune response to the Smith protein is lupus nephritis (LN). Consequently, the subjects requiring this are those diagnosed with SLE or LN.

[0066] Preferably, the subject with SLE is the HLA-DR15 allele or the HLA-DR3 allele, more preferably the HLA-DRA * 01:01 molecule and HLA-DRB1 * 15:01 molecule or HLA-DRA * 01:01 molecule and HLA-DRB1 * It is identified as possessing the 03:01 molecule.

[0067] Preferably, the peptides for use in the treatment or prevention of SLE are SmB / B':1-15 or peptides SmB / B':58-72 or fragments thereof as described herein. Preferably, the peptides consist of, or are essentially derived from, the sequence expressed in any one of SEQ ID NOs: 1-4.

[0068] Unless the context requires otherwise, the term "containing," as used herein, and its variations such as "containing," "containing," and "included," are not intended to exclude further additives, ingredients, integers, or steps.

[0069] Further aspects of the present invention and further embodiments of the aspects described in the preceding paragraphs will become apparent from the following description, which is given for illustrative purposes with reference to the accompanying drawings. [Brief explanation of the drawing]

[0070] [Figure 1A] This figure shows the identification of Sm-derived peptides that bind to HLA-DR15. Using the MHC class II Proimmune REVEAL assay, Sm-derived peptides (12 amino acids, 15-mer duplication) that bind to HLA-DR15 were identified. The assay results are presented as binding percentages compared to the positive control at 0 hours (blue bars) and 24 hours (red bars). Based on these scores, a stability index (red bars) was derived for each peptide. The positive control score was 100% at 0 hours and 6.4% at 24 hours, resulting in a stability index of 6.0. [Figure 1B] This figure shows the identification of Sm-derived peptides that bind to HLA-DR15. The binding scores and stability indices for SmB / B'-derived peptides, SmD1-derived peptides, and SmD3-derived peptides are shown. [Figure 1C-D]This figure shows the identification of Sm-derived peptides that bind to HLA-DR15. The binding scores and stability indices for SmB / B'-derived peptides, SmD1-derived peptides, and SmD3-derived peptides are shown. [Figure 2A] This figure shows the human T cell reactivity to the top three HLA-DR15-restricted Sm peptides. To determine whether HLA-DR15-restricted Sm peptides can induce T cell reactivity, three highly binding peptides—SmB / B':1-15, SmB / B':58-72, or SmD3:43-57—were cultured with human CD4+ T cells and monocyte-derived dendritic cells from HLA-DRB1*15:01 homozygous donors, respectively. T cell reactivity was determined by a cell proliferation assay using Cell Trace Violet (CTV). [Figure 2B] This figure shows the human T cell response to the top three HLA-DR15-restricted Sm peptides. It is a representative FACS plot showing the percentage of CTVlo CD4+ T cells. CD4+ T cells cultured with SmB / B':1-15 and SmB / B':58-72 showed a stronger proliferation response compared to CD4+ T cells cultured without the peptides and with SmD3:43-57. [Figure 3A] This figure shows the reactivity of human T cells to HLA-DR3-restricted Sm peptides. To determine whether human T cell reactivity to HLA-DR3-restricted Sm peptides can be measured, the inventors investigated the SmD1:78-92 peptides already identified by Deshmukh US et al., 2011. The top peptides in the computer (IEDB (Immune Epitope Database)) predicted binding to the SmB / B' and SmB / B':7-21 peptides. These peptides were cultured individually with CD4+ T cells in a co-culture cell proliferation assay, and their reactivity was evaluated using the Cell Trace Violet (CTV) dilution method. [Figure 3B]This figure shows the human T cell response to the HLA-DR3-restricted Sm peptide. It is a representative FACS plot showing the percentage of CTVlo CD4+ T cells. A strong proliferative response was observed only in CD4+ T cells cultured with SmD1:78-92. [Figure 4] This figure shows a map of the modified lentiviral construct used to transduce the TCR into human regulatory T cells. It shows the relative positions of the alpha and beta chains, P2A, T2A, as well as the introduced mouse mutations and cysteine. [Figure 5A] This figure shows the transduction of TCR into human Treg cells. It is a time series of the TCR transduction protocol. First, human Treg cells (CD4+ CD25hi CD127lo) were isolated by flow cytometry, then stimulated with anti-CD3 and anti-CD28 beads, followed by transduction with the lentiviral construct shown in Figure 4 on day 2. After two rounds of restimulation (days 9 and 26), Treg cells were collected and the expression of TCR and the stability of the Treg phenotype were analyzed. [Figure 5B] This figure shows the transduction of TCR into human Tregs. Analysis of TCR expression in human Tregs at day 20 shows that more than 90% of the transductioned Tregs express the GFP tag. [Figure 5C] This figure shows the transduction of TCR into human Treg cells. Intracellular cytokine staining for the pro-inflammatory cytokine IFN-γ indicates that the transduced Treg cells did not switch to pro-inflammatory cells (staining for IL-17A was also negative). [Figure 5D]This figure shows the transduction of a TCR into human Treg cells. The transductioned TCR is functional. To determine whether this protocol results in a functional TCR, the inventors transduced the TCR into a Jurkat T cell line and stimulated the transductioned Jurkat T cells with an antigen-presenting cell line (HLA-DR15+ B-LCL) pulsed with a TCR cognitive peptide. This demonstrated an upregulation of CD69, an early activation marker, after stimulation, supporting the idea that the TCR transduced using this protocol results in a functional TCR on the surface of T cells. [Figure 6A] This figure shows that Sm-TCR transducible Tregs are more potent inhibitors of Sm-specific Tconv cell responsiveness compared to polyclonal Tregs. This is an in vitro T cell proliferation assay. HLA-DR15+ PBMCs isolated from SLE patients were stimulated with the dominant Sm peptide SmB / B':58-72 and co-cultured with polyclonal Tregs (left FACS plot) or Sm-TCR transducible Tregs (right plot). Proliferation of pro-inflammatory conventional T cells (Tconv) was evaluated by Cell Trace Violet (CTV) dilution. Sm-TCR transducible Tregs more potently inhibited Tconv cell proliferation, at 12.1% compared to 22.4%. [Figure 6B] This figure shows that Sm-TCR transducible Tregs are more potent inhibitors of Sm-specific Tconv cell responsiveness compared to polyclonal Tregs. The count of proliferating cells showed that more Sm-specific Tconv cells were observed in the polyclonal group compared to the Sm-TCR group (8659 compared to 2053). [Figure 6C]This figure shows that Sm-TCR transducible Tregs are stronger inhibitors of Sm-specific Tconv cell responsiveness compared to polyclonal Tregs. The mean fluorescence intensity (MFI) of Sm-responsive Tconv cells reflects the number of cell divisions. Tconv cells undergo more divisions the lower their MFI. The MFI of Sm-responsive Tconv cells in the polyclonal Treg group was lower than that in the Sm-TCR Treg group (89.1 compared to 271). Error bars are SEM. ***P<0.001 by t-test. [Figure 7] This figure shows the expansion of regulatory T cells (Tregs) after stimulation with peptide SmB / B':1-15 or peptide SmB / B':58-72. The ratio of Tregs to total CD4+ T cells was determined after stimulation with SmB / B':1-15 or SmB / B':58-72, either in the absence of peptide stimulation or in vitro. The use of SmB / B':1-15 or SmB / B':58-72 was found to selectively enhance Treg expansion, supported by a significant increase in the ratio of Tregs after peptide stimulation. The data shown are mean ± SD for two independent experiments. ***P<0.001 compared to the no-peptide group by one-way ANOVA with Tukey's post-hoc test. [Figure 8] This figure shows that dominant HLA-DR15-restricted Sm-TCRs bind to HLA-DR15 Dextramers that exhibit high affinity and SmB / B': 58-72. The TCR-binding affinity of Sm-specific TCRs derived by the inventors was determined using a Dextramer-based flow cytometry binding assay. The inventors cloned the top three TCRs (i.e., TCR1, TCR2, and TCR3, identified in Table 1) into the Jurkat T cell line. The inventors measured mean fluorescence intensity (MFI) by flow cytometry and represented the data using scatchard plots. Relative Bmax and dissociation constant (Kd) are shown for each plot. [Figure 9A]This figure shows that HLA-DR15-restricted Sm-TCR Tregs suppress the anti-Sm specific pro-inflammatory response and restore tolerance. PBMCs derived from HLA-DR15+ / anti-Sm+ SLE patients with lupus nephritis were co-cultured with dominant HLA-DR15-restricted Sm peptide (SmB / B': 58-72) and Treg-less, polyclonal Tregs (pTregs), or Tregs transduced with HLA-DR15-restricted Sm-specific TCR1 (Sm-Tregs). In the presence of Sm-Tregs, the number of Sm-specific Tregs was significantly increased relative to the number of Tconv cells. [Figure 9B] This figure shows that HLA-DR15-restricted Sm-TCR Tregs suppress anti-Sm-specific pro-inflammatory responses and restore tolerance. PBMCs derived from HLA-DR15+ / anti-Sm+ SLE patients with lupus nephritis were co-cultured with dominant HLA-DR15-restricted Sm peptide (SmB / B': 58-72) and Treg-less, polyclonal Treg (pTreg), or transduced Treg (Sm-Treg) with HLA-DR15-restricted Sm-specific TCR1. In the presence of Sm-Tregs, the anti-inflammatory response, i.e., high IL-10 and low IFN-gamma / IL-17A, was dominant (similar to healthy individuals), whereas in the absence of Tregs or in the presence of pTregs alone, the pro-inflammatory response was dominant, i.e., low IL-10 and high IFN-gamma / IL-17A (predicted in patients with autoimmune diseases). These data support the ability of Sm-Treg to correct abnormal immune responses and restore tolerance to targeted autoepitopes. Results are expressed as mean ± SEM, *P<0.05, **P<0.01, compared to the no-Treg group and the pTreg group, using samples from four SLE patients. [Figure 9C]This figure shows that HLA-DR15-restricted Sm-TCR Tregs suppress anti-Sm-specific pro-inflammatory responses and restore tolerance. PBMCs derived from HLA-DR15+ / anti-Sm+ SLE patients with lupus nephritis were co-cultured with dominant HLA-DR15-restricted Sm peptide (SmB / B': 58-72) and Treg-less, polyclonal Treg (pTreg), or transduced Treg (Sm-Treg) with HLA-DR15-restricted Sm-specific TCR1. In the presence of Sm-Tregs, the anti-inflammatory response, i.e., high IL-10 and low IFN-gamma / IL-17A, was dominant (similar to healthy individuals), whereas in the absence of Tregs or in the presence of pTregs alone, the pro-inflammatory response was dominant, i.e., low IL-10 and high IFN-gamma / IL-17A (predicted in patients with autoimmune diseases). These data support the ability of Sm-Treg to correct abnormal immune responses and restore tolerance to targeted autoepitopes. Results are expressed as mean ± SEM, *P<0.05, **P<0.01, compared to the no-Treg group and the pTreg group, using samples from four SLE patients. [Figure 9D]This figure shows that HLA-DR15-restricted Sm-TCR Tregs suppress anti-Sm-specific pro-inflammatory responses and restore tolerance. PBMCs derived from HLA-DR15+ / anti-Sm+ SLE patients with lupus nephritis were co-cultured with dominant HLA-DR15-restricted Sm peptide (SmB / B': 58-72) and Treg-less, polyclonal Treg (pTreg), or transduced Treg (Sm-Treg) with HLA-DR15-restricted Sm-specific TCR1. In the presence of Sm-Tregs, the anti-inflammatory response, i.e., high IL-10 and low IFN-gamma / IL-17A, was dominant (similar to healthy individuals), whereas in the absence of Tregs or in the presence of pTregs alone, the pro-inflammatory response was dominant, i.e., low IL-10 and high IFN-gamma / IL-17A (predicted in patients with autoimmune diseases). These data support the ability of Sm-Treg to correct abnormal immune responses and restore tolerance to targeted autoepitopes. Results are expressed as mean ± SEM, *P<0.05, **P<0.01, compared to the no-Treg group and the pTreg group, using samples from four SLE patients. [Figure 10A] This figure shows that HLA-DR15-restricted Sm-Tregs halt the progression of nephritis. NSGMHCnull mice were inoculated with PBMCs derived from SLE patients with lupus nephritis who were positive for anti-Sm antibodies and HLA-DR15+. At week 3, the onset of functional kidney injury (measured by increased proteinuria), the mice were administered either no Treg, polyclonal Tregs (pTregs), or HLA-DR15-restricted Sm-Tregs (transduced to HLA-DR15 TCR1). [Figure 10B-C]This figure shows that HLA-DR15-restricted Sm-Tregs halt the progression of nephritis. Mice that were not treated with Tregs or those treated with pTregs progressed to severe nephritis (i.e., high levels of proteinuria and necrosis of >50% of glomeruli), but mice treated with Sm-Tregs did not progress. Results are expressed as mean ± SEM of 5 SLE patient samples. ***P<0.001 compared to the no-Treg group and the pTreg group. [Figure 11A-C] This figure shows that HLA-DR3-restricted Sm-Tregs suppress the anti-Sm pro-inflammatory cytokine response and halt the progression of lupus nephritis. PBMCs derived from HLA-DR3+ / anti-Sm+ SLE patients with lupus nephritis were co-cultured with dominant HLA-DR3-restricted T cell epitopes (SmD1:78-92) and transduced Tregs (Sm-Tregs) that were either Treg-less, polyclonal Tregs (pTregs), or HLA-DR3-restricted TCRs (HLA-DR3 TCR1, identified in Table 2). Cytokine responses were measured on day 8. [Figure 11D-E] This figure shows that HLA-DR3-restricted Sm-Tregs suppress the anti-Sm pro-inflammatory cytokine response and halt the progression of lupus nephritis. NSGMHCnull mice were inoculated with PBMCs derived from SLE patients with lupus nephritis who were positive for anti-Sm antibodies and HLA-DR3+. At week 3, the onset of functional kidney injury (measured by increased proteinuria), the mice were administered either no Treg, polyclonal Tregs (pTregs), or HLA-DR3-restricted Sm-Tregs (transduced to HLA-DR3 TCR1). [Modes for carrying out the invention]

[0071] The present invention as disclosed and defined herein is understood to extend to all alternative combinations of two or more individual features mentioned or evident from the text or drawings. All of these different combinations constitute diverse alternative embodiments of the present invention.

[0072] Further aspects of the present invention and further embodiments of the aspects described in the preceding paragraphs will become apparent from the following description, which is given for illustrative purposes with reference to the accompanying drawings.

[0073] Herein, a detailed reference is made to certain embodiments of the present invention. While the present invention is described in conjunction with its embodiments, it should be understood that the intent is not to limit the invention to these embodiments. Conversely, the present invention is intended to cover all alternative methods, modifications, and equivalents that may fall within the scope of the present invention as defined by the claims.

[0074] The inventors identified peptides derived from Smith protein that bind to DR15 and DR3, which are frequently found HLA molecules in individuals with SLE. When bound to HLA molecules, these peptides result in the proliferation of CD4+ helper T cells, enabling the identification of Smith protein-specific T cell receptors. Therefore, the present invention relates to the use of peptide immunotherapy or adoptive cell therapy with regulatory T cells engineered to express Smith protein-specific TCRs to treat SLE.

[0075] An advantage of the embodiments of the present invention is that both the identified peptides and TCRs are involved in interactions with HLA-DR subtypes common to lupus patients. Furthermore, antigen-specific modulated T cell therapy typically exerts a more potent immunosuppressive effect than polyclonal modulated T cell therapy. Finally, antigen-specific modulated T cell therapy typically exerts a more limited immunosuppressive effect on protective T cell immunity, such as that used to respond to viral infections and / or cancer.

[0076] General Throughout this specification, unless otherwise explicitly stated or the context requires, references to a single step, composition, group of steps, or group of compositions shall be understood to encompass one and more (i.e., one or more) of those steps, compositions, group of steps, or group of compositions. Accordingly, as used herein, the singular forms "a," "an," and "that" include multiple aspects unless the context explicitly indicates otherwise. For example, a reference to "a" includes one and more; a reference to "an" includes one and more; a reference to "that" includes one and more, and so on.

[0077] Those skilled in the art will understand that the present invention is subject to variations and modifications other than those described in detail. It will be understood that the present invention includes all such variations and modifications. The present invention also includes, individually or collectively, all of the steps, features, compositions and compounds mentioned or indicated herein, including any combination and all of the combinations or any two or more of the steps or features.

[0078] Those skilled in the art will recognize many methods and materials similar to or equivalent to those described herein and that can be used in carrying out the present invention. The present invention is not limited in any way to the methods and materials described herein.

[0079] All patents and publications referenced herein are incorporated in their entirety by reference.

[0080] The present invention is intended to be illustrative only and is not limited to the detailed examples described herein. Functionally equivalent products, compositions, and methods are clearly within the scope of the present invention.

[0081] Unless otherwise explicitly stated, any example or embodiment of the Invention herein is understood to be applicable to any other example or embodiment of the Invention, with modifications as necessary.

[0082] Unless otherwise specified, technical and scientific terms used herein shall be understood to have the same meaning as those commonly understood by those skilled in the art (e.g., those skilled in cell culture, molecular genetics, immunology, immunohistochemistry, protein chemistry, and biochemistry).

[0083] Unless otherwise indicated, the recombinant protein methods, cell culture methods and immunological methods used in this disclosure are standard procedures well known to those skilled in the art. Regarding such techniques, see J. Perbal, "A Practical Guide to Molecular Cloning," John Wiley and Sons (1984); J. Sambrook et al., "Molecular Cloning: A Laboratory Manual," Cold Spring Harbor Laboratory Press (1989); TA Brown (ed.), "Essential Molecular Biology: A Practical Approach," Volumes 1 and 2, IRL Press (1991); DMGlover and B.D. Hames (eds.), "DNA Cloning: A Practical Approach," Volumes 1-4, IRL Press (1995 and 1996); and FMAusubel et al. (eds.), "Current Protocols in Molecular Biology," Greene Pub. Associates and Wiley-Interscience (1988; including all revisions to date); Ed Harlow and David Lane (eds.), "Antibodies: A Laboratory Manual," Cold Spring Harbor Laboratory (1988); and JEColigan et al. (eds.), "Current Protocols in This is described and explained throughout the literature in sources such as "Immunology" by John Wiley & Sons (including all revisions to date).

[0084] The descriptions and definitions of variable regions and their portions, T cell receptors and their fragments in this specification can be further clarified by the discussions in Kabat, "Sequences of Proteins of Immunological Interest," National Institutes of Health, Bethesda, Md., 1987 and 1991; Bork et al., J Mol. Biol., 242, 309-320, 1994; Chothia and Lesk, J. Mol Biol., 196:901-917, 1987; Chothia et al., Nature 342, 877-883, 1989 and / or Al-Lazikani et al., J Mol Biol, 273, 927-948, 1997.

[0085] The terms "and / or," for example, "X and / or Y," shall be understood to mean "X and Y" or "X or Y," and shall be understood to provide explicit support for both meanings or one of them.

[0086] As used herein, the term “derived from ~” shall be understood to mean that a specified integer may not necessarily originate directly from this source, but can be obtained from a particular source.

[0087] References to, for example, a range of residues in this specification are understood to be inclusive. For example, a reference to “the region containing amino acids 1-15” is understood to be inclusive, i.e., the region includes the sequence of amino acids numbered 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14 and 15 within the given sequence.

[0088] The term "essentially derived from" limits the scope of the claims to materials or steps that do not materially affect the specified materials or steps or the essential features of the claimed invention. For example, a protein domain, region, or module (e.g., a binding domain, hinge region, linker module) or protein (which may have one or more domains, regions, or modules) "essentially consists of" a particular amino acid sequence if, in combination, the amino acid sequence of the domain, region, module, or protein contributes 20% or less (e.g., 15%, 10%, 8%, 6%, 5%, 4%, 3%, 2%, or 1%) of the length of the domain, region, module, or protein and does not substantially affect the activity of the domain(s), region(s), module(s), or protein (e.g., the target binding affinity of a binding protein) (i.e., the activity reduction does not exceed 50%, such as 40%, 30%, 25%, 20%, 15%, 10%, 5%, or 1%), includes elongation, deletion, mutation, or a combination thereof (e.g., amino acids at the amino terminus, carboxy terminus, or between domains).

[0089] As used herein, “nucleic acid” or “nucleic acid molecule” refers to any of the following: deoxyribonucleic acid (DNA), ribonucleic acid (RNA), oligonucleotides, for example, fragments produced by polymerase chain reaction (PCR) or translation in vitro, and fragments produced by any of ligation, cleavage, endonuclease action or exonuclease action. In certain embodiments, the nucleic acids of this disclosure are produced by PCR. Nucleic acids may consist of monomers that are naturally occurring nucleotides (such as deoxyribonucleotides and ribonucleotides), analogs of naturally occurring nucleotides (for example, α-optical isomers of naturally occurring nucleotides), or combinations of both. Modified nucleotides may have modifications or substitutions of sugar moieties, pyrimidine base moieties, or purine base moieties. Nucleic acid monomers may be linked by phosphodiester bonds or analogs of such linkages. Phosphodiester linkage analogues include phosphorothioates, phosphorodithioates, phosphoroselenoates, phosphorodiselenoates, phosphoranilothioates, phosphoranilideates, and phosphoramidates. Nucleic acid molecules can be single-stranded or double-stranded.

[0090] The term "isolated" means that the material has been removed from its original environment (for example, the natural environment if the material is naturally occurring). For example, naturally occurring nucleic acids or polypeptides present in living animals are not isolated, but the same nucleic acids or polypeptides separated from some or all of the material coexisting in a natural system are isolated. Such nucleic acids may be part of a vector, and / or such nucleic acids or polypeptides may be part of a composition (for example, a cell lysate), but such vectors or compositions may also be isolated from the nucleic acids or polypeptides in the sense that they are not part of the natural environment. The term "gene" means a segment of DNA involved in the production of a polypeptide chain, and includes the "leader and trailer," which are the regions preceding and succeeding the coding region, as well as the sequences (introns) interposed between individual coding segments (exons).

[0091] As used herein, the term “recombinant” refers to cells, microorganisms, nucleic acid molecules, or vectors that have been genetically modified by artificial intervention (i.e., modified by the introduction of exogenous or heterologous nucleic acid molecules), or to cells or microorganisms whose expression of endogenous nucleic acid molecules or endogenous genes has been altered to be controlled, deregulated, or constitutive. Artificially produced genetic modifications may include, for example, modifications that introduce nucleic acid molecules encoding one or more proteins or enzymes (which may include expression regulatory elements such as promoters), or modifications that add, delete, or substitute other nucleic acid molecules, or other functional disruption or addition to the genetic material of a cell. Exemplary modifications include modifications within the coding region or functional fragment thereof of heterologous or homologous polypeptides derived from a reference molecule or parent molecule.

[0092] In the art, a “conservative substitution” is recognized as the substitution of one amino acid with another amino acid having similar properties. Exemplary conservative substitutions are well known in the art (see, for example, WO97 / 09433, p. 10; Lehninger, “Biochemistry,” 2nd edition, Worth Publishers, Inc., NY, NY, pp. 71-77, 1975; Lewin, “Genes IV,” Oxford University Press, NY and Cell Press, Cambridge, MA, p. 8, 1990).

[0093] Binding proteins As used herein, “binding protein” refers to a proteinaceous molecule or part thereof (e.g., peptide, oligopeptide, polypeptide, protein) that has the ability to specifically and non-covalently associate with, integrate with, or combine with a target (e.g., Smith protein or a fragment thereof, Smith protein fragment: MHC complex). Binding proteins may be purified, substantially purified, synthesized, or recombinant. Exemplary binding proteins include single-chain immunoglobulin variable regions (e.g., scTCR, scFv).

[0094] In certain embodiments, any of the binding proteins of the present invention are T cell receptors (TCRs), chimeric antigen receptors, or antigen-binding fragments of TCRs, any of which may be chimeric TCRs, humanized TCRs, or human TCRs. In further embodiments, the antigen-binding fragment of a TCR includes a single-chain TCR (scTCR) or a chimeric antigen receptor (CAR). In certain embodiments, the binding protein is a TCR.

[0095] A "T cell receptor" (TCR) refers to an immunoglobulin superfamily member (having a variable binding domain, a constant domain, a transmembrane region, and a short cytoplasmic tail) that is capable of specifically binding to an antigen peptide bound to an MHC receptor. See, for example, Janeway et al., "Immunobiology: The Immune System in Health and Disease," 3rd edition, Current Biology Publications, pp. 4-33, 1997. TCRs may be found on the cell surface or in a soluble form, and are generally composed of heterodimers having α (alpha) and β (beta) chains (also known as TCRα and TCRβ, respectively) or γ and δ chains (also known as TCRγ and TCRδ, respectively). Similar to immunoglobulins, the extracellular portion of the TCR chain (e.g., α-chain, β-chain) contains two immunoglobulin domains: a variable domain at the N-terminus (e.g., α-chain variable domain or Vα, β-chain variable domain or Vβ; typically amino acids 1-116 based on Kabat numbering; Kabat et al., "Sequences of Proteins of Immunological Interest," US Dept. Health and Human Services, Public Health Service, National Institutes of Health, 1991, 5th edition) and one constant domain adjacent to the cell membrane (e.g., α-chain constant domain or Cα, typically amino acids 117-259 based on Kabat, β-chain constant domain or Cβ, typically amino acids 117-295 based on Kabat). Similar to immunoglobulins, the variable domain also contains a complementarity-determining region (CDR) separated by a framework region (FR) (see, for example, Jores et al., Proc. Nat'l Acad. Sci. USA, 57:9138, 1990; Chothia et al., EMBO J., 7:3745, 1988; and Lefranc et al., Dev. Comp. Immunol., 27:55, 2003).In certain embodiments, the TCR is found on the surface of a T cell (or T lymphocyte) and associates with the CD3 complex. The sources of the TCRs used in this disclosure may originate from a variety of animal species, such as humans, mice, rats, rabbits, or other mammals.

[0096] In any of the embodiments described above, the disclosure comprises an alpha chain (α chain) and a beta chain (β chain), wherein the TCR is bound to a complex of a Smith protein fragment and an HLA-DR15 molecule, and preferably the HLA-DR15 molecule is HLA-DRA * 01:01 molecule and HLA-DRB1 *The 15:01 molecule presents a high-affinity manipulated T cell receptor (TCR). In certain embodiments, the V beta chain contains or is derived from alleles of TRBV3, TRBV4, TRBV5, TRBV6, TRBV7, TRBV11, TRBV19, TRBV20, TRBV24, or TRBV28. In further embodiments, the V alpha chain contains or is derived from alleles of TRAV1, TRAV2, TRAV3, TRAV4, TRAV8, TRAV9, TRAV12, TRAV14, TRAV17, TRAV21, TRAV23, TRAV25, TRAV26, TRAV27, TRAV29, TRAV38, TRAV39, or TRAV40.In certain embodiments, the binding protein of the present invention comprises (a) a V beta chain containing or derived from the TRBV11 allele (preferably TRBV11-2) and a V alpha chain containing or derived from the TRAV9 allele (preferably TRAV9-2); (b) a V beta chain containing or derived from the TRBV6 allele (preferably TRBV6-1) and a V alpha chain containing or derived from the TRAV25 allele; (c) a V beta chain containing or derived from the TRBV7 allele (preferably TRBV7-9). (d) containing the V beta chain and TRAV29 allele derived therefrom, or the V alpha chain derived therefrom; (e) containing the TRBV28 allele, or containing the V beta chain and TRAV23 allele derived therefrom, or the V alpha chain derived therefrom; (f) containing the TRBV7 allele (preferably TRBV7-9), or containing the V beta chain and TRAV26 allele (preferably TRAV26-1), or the V alpha chain derived therefrom; (f) containing the TRBV7 allele (preferably TRBV7-3), or (i) (i) (i) (i) (i) (i) (i) (i) (i) (i) (i) (i) (i) (i) (i) (i) (i) (i) (i) (i) (i) (i) (i) (i) (i) (i) (i) (i) (i) (i) (i) (i) (i) (i) (i) (i) (i) (i) (i) (i) (i) (i) (j) A V beta chain and a TRAV17 allele, or a V alpha chain, derived therefrom, comprising the TRBV4 allele (preferably TRBV4-2); (k) A V beta chain and a TRAV27 allele, or a V alpha chain, derived therefrom, comprising the TRBV4 allele (preferably TRBV4-2); (k) A V beta chain and a TRAV2 allele, or a V alpha chain, derived therefrom, comprising the TRBV6 allele (preferably TRBV6-5); or a V beta chain and a TRAV2 allele, or a V alpha chain, derived therefrom.

[0097] In further embodiments, the binding protein of the present invention comprises: (a) a V-beta chain containing or derived from the TRBV20 allele (preferably TRBV20-1) and a V-alpha chain containing or derived from the TRAV38 allele (preferably TRAV38-1); (b) a V-beta chain containing or derived from the TRBV6 allele (preferably TRBV6-4) and a V-alpha chain containing or derived from the TRAV1 allele (preferably TRAV1-2); (c) a V-beta chain containing or derived from the TRBV6 allele (preferably TRBV6-4) and a V-alpha chain containing or derived from the TRAV4 allele; and (d) a TRBV4 allele. (e) A V beta chain and TRAV17 allele derived from (preferably TRBV4-1), or a V alpha chain derived therefrom; (f) A V beta chain and TRAV21 allele derived therefrom, or a V alpha chain derived therefrom; (g) A V beta chain and TRAV27 allele derived from TRBV28, or a V alpha chain derived therefrom, or a V beta chain derived therefrom; (g) A V beta chain and TRAV1 allele derived from TRBV24, or TRBV24-1, or a V beta chain derived therefrom, or a V alpha chain derived therefrom.

[0098] In any aspect or embodiment, the binding protein of the present invention comprises (a) a V-beta chain containing or derived from the TRBJ2 allele (preferably TRBJ2-7) and a V-alpha chain containing or derived from the TRAJ47 allele; (b) a V-beta chain containing or derived from the TRBJ2 allele (preferably TRBJ2-3) and a V-alpha chain containing or derived from the TRAJ54 allele; (c) a V-alpha chain containing or derived from the TRBJ1 allele (preferably TRBJ1-1). (d) A V-alpha chain containing the V-beta chain and TRAJ48 allele derived therefrom; (e) A V-beta chain and TRAJ44 allele derived therefrom, or a V-alpha chain derived therefrom, containing the TRBJ2 allele (preferably TRBJ2-1), or a V-beta chain and TRAJ44 allele derived therefrom; (f) A TRBJ2 allele (preferably TRBJ2 (i) A V beta chain containing or derived therefrom, and a V alpha chain containing or derived therefrom; (g) A V beta chain containing or derived therefrom, and a V beta chain containing or derived therefrom, and a V alpha chain containing or derived therefrom, and a TRBJ2 allele (preferably TRBJ2-7); (h) A V beta chain containing or derived therefrom, and a V alpha chain containing or derived therefrom, and derived therefrom, and a TRBJ1 allele (preferably TRBJ1-1); (i) A TRBJ2 allele (i) A V beta chain and TRAJ45 allele, or a V alpha chain, that include (preferably TRBJ2-3) or derived therefrom; (j) A V beta chain and TRAJ49 allele, or a V alpha chain, that include the TRBJ2 allele (preferably TRBJ2-3) or derived therefrom; (k) A V beta chain and TRAJ7 allele, or a V alpha chain, that include the TRBJ1 allele (preferably TRBJ1-2) or derived therefrom.

[0099] In any aspect or embodiment, the binding protein of the present invention comprises (a) a V-beta chain containing or derived from the TRBJ1 allele (preferably TRBJ1-4) and a V-alpha chain containing or derived from the TRAJ48 allele; (b) a V-beta chain containing or derived from the TRBJ1 allele (preferably TRBJ1-5) and a V-alpha chain containing or derived from the TRAJ48 allele; (c) a V-alpha chain containing or derived from the TRBJ2 allele (preferably TRBJ2-1). (d) A V-alpha chain derived from or containing the V-beta chain and TRAJ48 allele; (e) A V-beta chain derived from or containing the TRBJ2 allele (preferably TRBJ2-7) and TRAJ48 allele; (f) A V-alpha chain derived from or containing the TRBJ1 allele (preferably TRBJ1-1) and TRAJ88 allele; (g) A V-alpha chain derived from or containing the TRBJ1 allele (preferably TRBJ (1-2) containing or derived from the V beta chain and the TRAJ12 allele, or derived from the V alpha chain; (g) containing the TRBJ1 allele (preferably TRBJ1-2), or derived from the V beta chain and the TRAJ3 allele, or derived from the V alpha chain; (h) containing the TRBJ1 allele (preferably TRBJ1-3), or derived from the V beta chain and the TRAJ9 allele, or derived from the V alpha chain; (i) TRBJ2 allele (i) A V beta chain and TRAJ28 allele, or a V alpha chain, that include (preferably TRBJ2-1) or derived therefrom; (j) A V beta chain and TRAJ41 allele, or a V alpha chain, that include the TRBJ1 allele (preferably TRBJ1-2) or derived therefrom; (k) A V beta chain and TRAJ9 allele, or a V alpha chain, that include the TRBJ2 allele (preferably TRBJ2-1) or derived therefrom.

[0100] In any embodiment or configuration, the binding protein of the present invention comprises or includes a V-beta chain derived from the TRBD1 or TRBD2 allele.

[0101] In any embodiment or configuration, the binding protein of the present invention comprises or includes a V-beta chain derived from the TRC1 or TRBC2 allele and a TRAC allele or a V-alpha chain derived from the TRAC allele.

[0102] In any of the embodiments described above, the disclosure includes an alpha chain (α chain) and a beta chain (β chain), wherein the TCR is bound to a complex of a Smith protein fragment and an HLA-DR3 molecule, and preferably the HLA-DR3 molecule is HLA-DRA * 01:01 molecule and HLA-DRB1 * 03:01 presents a high-affinity manipulated T cell receptor (TCR), which is a molecule. In certain embodiments, the V beta chain comprises or is derived from alleles of TRB2, TRBV4, TRBV5, TRB6, TRB7, TRBV9, TRB10, TRBV11, TRB12, TRBV20, TRBV24, TRB27, or TRBV29. In further embodiments, the V alpha chain comprises or is derived from alleles of TRAV1, TRAV2, TRAV8, TRAV9, TRAV10, TRAV12, TRAV20, TRAV26, TRAV30, or TRAV36.

[0103] In certain embodiments, the binding protein of the present invention comprises (a) a V beta chain containing or derived from the TRBV5 allele (preferably TRBV5-1) and a V alpha chain containing or derived from the TRAV20 allele; (b) a V beta chain containing or derived from the TRBV29 allele (preferably TRBV29-1) and a V alpha chain containing or derived from the TRAV12 allele (preferably TRAV12-1); and (c) a V alpha chain containing the TRBV4 allele (preferably TRBV4-1). (d) A V-alpha chain derived therefrom, comprising a V-beta chain and an allele of TRAV26 (preferably TRAV26-2), or a V-alpha chain derived therefrom; (e) A V-alpha chain derived therefrom, comprising a TRBV4 allele (preferably TRBV4-1), comprising a V-beta chain derived therefrom, and an allele of TRAV30, or a V-alpha chain derived therefrom; (c) A V-alpha chain derived therefrom, comprising a TRBV4 allele (preferably TRBV4-1), comprising a V-beta chain derived therefrom, and an allele of TRAV36 (preferably TRAV36DV7), or a V-alpha chain derived therefrom (f) A chain containing the allele of TRBV24 (preferably TRBV24-1), or derived therefrom, and a V beta chain containing the allele of TRAV12 (preferably TRAV12-1), or derived therefrom, and a V alpha chain; (g) A chain containing the allele of TRBV11 (preferably TRBV11-2), or derived therefrom, and a V beta chain containing the allele of TRAV12 (preferably TRAV12-3), or derived therefrom, and a V alpha chain; (h) A chain containing the allele of TRBV20 (preferably TRBV20-1), or derived therefrom (i) a V beta chain derived from and an allele of TRAV9 (preferably TRAV9-2), or a V alpha chain derived therefrom; (j) a V beta chain derived from and an allele of TRBV9 (preferably TRAV9-2), or a V alpha chain derived therefrom; (j) a V beta chain derived from and an allele of TRBV20 (preferably TRBV20-1), or a V beta chain derived therefrom and an allele of TRAV12 (preferably TRAV12-1), or a V alpha chain derived therefrom.

[0104] In further embodiments, the binding protein of the present invention comprises: (a) a V-beta chain containing or derived from the TRBV27 allele and a TRAV12 allele (preferably TRAV12-1) or derived from the TRBV12 allele and a V-alpha chain; (b) a V-beta chain containing or derived from the TRBV6 allele (preferably TRBV6-1) and a TRAV1 allele (preferably TRAV1-2) or derived from the TRAV1 allele and a V-alpha chain; (c) a V-beta chain containing or derived from the TRBV7 allele (preferably TRBV7-9) and a TRAV12 allele (preferably TRAV12-2) or derived from the TRBV7 allele and a V-alpha chain; (d) a V-beta chain containing or derived from the TRBV2 allele and a TRAV8 allele (TRAV8-3) or derived from the TRBV8 allele and a V-alpha chain; (e) a TRBV8 allele (preferably TRB (f) A V beta chain containing or derived from V8-3) and a TRAV5 allele (preferably TRAV5-1) or a V alpha chain derived therefrom; (g) A V beta chain containing or derived from TRBV7 allele (preferably TRBV7-9) and a TRAV10 allele or a V alpha chain derived therefrom; (h) A V beta chain containing or derived from TRBV7 allele (preferably TRBV7-9) and a TRAV19 allele or a V alpha chain derived therefrom; (i) A V beta chain containing or derived from TRBV12 allele (preferably TRBV12-4) and a TRAV20 allele or a V alpha chain derived therefrom.

[0105] In certain embodiments, the V beta chain comprises or is derived from the alleles TRBJ1 or TRBJ2. In further embodiments, the V alpha chain comprises or is derived from the alleles TRAJ3, TRAJ6, TRAJ9, TRAJ13, TRAJ17, TRAJ23, TRAJ27, TRAJ28, TRAJ31, TRAJ33, TRAJ37, TRAJ42, TRAJ45, TRAJ47, TRAJ48, TRAV49, or TRAV54.

[0106] In certain embodiments, the binding protein of the present invention comprises: (a) a V-beta chain containing or derived from the TRBJ1 allele (preferably TRBJ1-1) and a V-alpha chain containing or derived from the TRAJ6 allele; (b) a V-beta chain containing or derived from the TRBJ1 allele (preferably TRBJ1-5) and a V-alpha chain containing or derived from the TRAJ45 allele; (c) a V-beta chain containing or derived from the TRBJ2 allele (preferably TRBJ2-2) and a V-alpha chain containing or derived from the TRAJ54 allele; (d) a V-beta chain containing or derived from the TRBJ2 allele (preferably TRBJ2-1) and a V-alpha chain containing or derived from the TRAJ28 allele; (e) a V-beta chain containing or derived from the TRBJ2 allele (preferably TRBJ2-1) and a V-alpha chain containing or derived from the TRAJ49 allele. (f) A V-alpha chain derived from; (g) A V-alpha chain derived from; (h) A V-alpha chain derived from; (i) A V-alpha chain derived from; (i) A V-alpha chain derived from; (j) A V-alpha chain derived from; (ii) A V-alpha chain derived from; (iii) A V-alpha chain derived from; (iii) A V-alpha chain derived from; (iv

[0107] In certain embodiments, the binding protein of the present invention comprises: (a) a V-beta chain and a TRAJ9 allele derived from or containing a TRBJ1 allele (preferably TRBJ1-2) and a V-alpha chain derived therefrom; (b) a TRBJ2 allele (preferably TRBJ2-7) and a V-beta chain and a TRAJ33 allele derived therefrom, and a V-alpha chain derived therefrom; (c) a TRBJ2 allele (preferably TRBJ2-1) and a V-beta chain and a TRAJ49 allele derived therefrom, and a V-alpha chain derived therefrom; (d) a TRBJ2 allele (preferably TRBJ2-6) and a V-beta chain and a TRAJ13 allele derived therefrom, and a V-alpha chain derived therefrom; (e) a TRBJ1 allele (preferably TRBJ1-1) and a V-beta chain and a TRAJ23 allele derived therefrom, and (f) A V-alpha chain derived from; (g) A V-alpha chain derived from; (h) A V-alpha chain derived from; (i) A V-alpha chain derived from; (i) A V-alpha chain derived from; (j) A V-alpha chain derived from; (g) A V-alpha chain derived from; (h) A V-alpha chain derived from; (i) A V-alpha chain derived from; (j) A V-alpha chain derived from; (ii) A V-alpha chain derived from; (iii) A V-alpha chain derived from; (iii) A V-alpha chain derived from; (iv

[0108] In any embodiment or configuration, the binding protein of the present invention comprises or includes a V-beta chain derived from the TRBD1 or TRBD2 allele.

[0109] In any embodiment or configuration, the binding protein of the present invention comprises or includes a V-beta chain derived from the TRC1 or TRBC2 allele and a TRAC allele or a V-alpha chain derived from the TRAC allele.

[0110] In any embodiment of the present invention, the binding protein comprises a Vα chain containing a Vα domain and a Vβ chain containing a Vβ domain. Preferably, the Vα and Vβ chains are modified to include cysteine ​​residues that enable the formation of further interchain disulfide bonds. The cysteine ​​introduced into each of the Vα and Vβ chains enables preferential pairing of the Vα and Vβ chains, which, when expressed intracellularly, leads to the expression of endogenous TCR Vα and endogenous TCR Vβ chains. Preferably, the residue at Thr48 or an equivalent residue on the TCRα chain and the residue at Ser57 or an equivalent residue on the TCRβ chain are replaced with cysteine ​​to facilitate the creation of further disulfide bonds between the constant regions of the TCR. This modification enables preferential pairing of the introduced TCR and reduces mispairing with the endogenous TCR. This is particularly beneficial in adoptive cell therapy in which regulatory T cells are modified to express exogenous TCRs.

[0111] For example, a useful method for separating and purifying recombinant soluble TCRs may include obtaining a supernatant from a suitable host cell / vector system that secretes recombinant soluble TCRs into culture medium, and then concentrating the medium using a commercially available filter. After concentration, the concentrate may be applied to a single suitable purification matrix or a series of suitable matrices, such as an affinity matrix or ion exchange resin. One or more reverse-phase HPLC steps may be used to further purify the recombinant polypeptide. These purification methods may also be used to separate immunogens from their natural environment. Methods for the large-scale preparation of one or more of the isolated / recombinant soluble TCRs described herein include batch cell culture methods that are monitored and controlled to maintain suitable culture conditions. Purification of soluble TCRs may be carried out according to methods described herein and known in the art.

[0112] The SmB / B'-specific binding proteins or SmB / B'-specific binding domains described herein (e.g., SEQ ID NOs: 6-257 and their variants) may be functionally characterized according to any of the numerous methods accepted in the Art for assaying T cell activity, which include determining T cell binding, activation, or induction, and also determining antigen-specific T cell responses. Examples include T cell proliferation, T cell cytokine release, antigen-specific T cell stimulation, MHC-restricted T cell stimulation, CTL activity (e.g., by detecting Cr release from preloaded target cells), changes in T cell phenotypic marker expression, and determination of other measures of T cell function. Procedures for performing these assays and similar assays can be found, for example, in Lefkovits' "Immunology Methods Manual: Comprehensive Sourcebook of Techniques," 1998. See also "Current Protocols in Immunology"; Weir, "Handbook of Experimental Immunology," Blackwell Scientific, Boston, MA (1986); Mishell and Shigii (eds.), "Selected Methods in Cellular Immunology," Freeman Publishing, San Francisco, CA (1979); Green and Reed, Science, 281:1309 (1998), and the references cited therein.

[0113] As used herein, SmB / B' refers to the ribonucleoprotein known as "Smith protein" or "small nuclear ribonucleoprotein associated protein B and B'" in humans, which is encoded by the SNRPB gene. SmB / B' may also be referred to by other names: COD, SNRPB1, snRNP-B, CCMS, and small nuclear ribonucleoprotein polypeptides B and B1.

[0114] The protein encoded by the SNRPB gene is one of several nuclear proteins commonly found among the small ribonucleoprotein particles (snRNPs) U1, U2, U4 / U6, and U5. These snRNPs are involved in premRNA splicing, and the encoded protein may also play a role in premRNA splicing or in the structure of snRNPs. Two transcript variants encoding different isoforms (B and B') have been identified for this gene.

[0115] Sm antigens and nuclear ribonucleoprotein (RNP) antigens are particulate complexes composed of small nuclear RNA (U-RNA) and proteins. These complexes are also called ENAs (extractable nuclear antigens) because they are soluble in physiological saline. Autoantibodies against these antigens are produced in systemic lupus erythematosus and mixed connective tissue disease.

[0116] Sm (Smith) protein and related nuclear ribonucleoproteins (nRNPs) are targets for autoantibodies in SLE. These antigens reside within intracellular organelles called spliceosomes, which are composed of peptides containing small RNA molecules. Anti-Sm antibodies are present in 15–30% of patients with SLE, but are highly specific to SLE. Sm proteins are most frequently produced (60%) in young Black women with SLE. Sm proteins are almost never produced in healthy individuals or patients with other diseases. Anti-Sm antibodies should not be confused with anti-smooth muscle antibodies detected in autoimmune liver diseases.

[0117] Systemic lupus erythematosus (SLE) is characterized by the presence of diverse autoantibodies directed against numerous intracellular antigens. Among the different candidate autoantigens recognized by autoantibodies in SLE, the Sm antigen of the small nuclear ribonucleoprotein U-1 complex is considered a pathological feature of SLE. Antibodies against these autoantigens are discriminative enough to be part of the American College of Rheumatology (ACR) classification criteria for SLE.

[0118] Adoptive cell therapy The present invention provides a method for preparing cells for adoptive cell therapy, a method for treating a subject with these cells, and the cells themselves.

[0119] In a particular embodiment, a nucleic acid molecule encoding the binding protein of the present invention is used to transfect / transduce host cells (e.g., Treg cells) for use in adoptive transfer therapy.

[0120] In an alternative embodiment, one or more peptides of the present invention are used to activate and / or expand a population of T cells in order to produce T cells (e.g., Treg cells) that have specificity for the peptide.

[0121] Advances in TCR sequencing have been described (e.g., Robins et al., Blood, 114:4099, 2009; Robins et al., Sci. Translat. Med., 2:47~64, 2010; Robins et al. (September 10), J. Imm. Meth., Epub Rapid Edition, 2011; Warren et al., Genome Res., 2, 1:790, 2011) and may be utilized in the process of implementing embodiments of this disclosure. Similarly, regarding methods for transfecting T cells with a desired nucleic acid / transduction of a desired nucleic acid into T cells, adoptive transfer procedures using T cells with desired antigen specificity are described (e.g., Schmitt et al., Hum. Gen., 20:1240, 2009; Dossett et al., Mol. Ther., 77:742, 2009; Till et al., Blood, 772:2261, 2008; Wang et al., Hum. Gene As described in Ther., 75:712, 2007; Kuball et al., Blood, 709:2331, 2007; US2011 / 0243972; US2011 / 0189141; Leen et al., Ann. Rev. Immunol., 25:243, 2007 (for example, U.S. Patent Application Publication No. US2004 / 0087025), the application of these methods to the embodiments disclosed herein is therefore assumed based on the teachings herein, including the teachings relating to the binding proteins of the present invention.

[0122] Cell populations containing regulatory T (Treg) cells can originate from any source where Treg cells are present, such as peripheral blood, thymus, lymph nodes, spleen, and bone marrow.

[0123] Cell populations containing Treg cells may also originate from mixed T cell populations or conventional T cell populations. As described herein, mixed populations or conventional T cells may be contacted with the peptides of the present invention to enrich Sm antigen specificity within the T cells. Alternatively, nucleic acids encoding the binding proteins of the present invention may be transduced into mixed populations or conventional T cells. The T cells may then be converted into Treg cells using standard techniques known to those skilled in the art for the production of Treg cells. In certain embodiments, mixed T cell populations or conventional T cells are cultured under conditions that allow for increased expression of TGF-beta and Foxp3. This includes culturing cells with anti-CD3 / anti-CD28 antibodies, and inhibition of CDK8 / 19 with high doses of IL-2, TGF-beta, and rapamycin. In further embodiments, the converted or enriched Treg cell population is stabilized (e.g., by contacting the cells with vitamin C or other agents for stabilizing Tregs).

[0124] The Treg cells used for injection (or, in fact, the Tconv or mixed T cell population used to create Tregs) may be isolated from an allogeneic donor, preferably an HLA-matched donor, or from a subject diagnosed with a condition associated with an abnormal, undesirable, or otherwise inappropriate immune response to Smith protein. Preferably, the condition is SLE.

[0125] T cells can also be produced from induced pluripotent stem cells (iPSCs) or embryonic stem cells, preferably from the differentiation of embryonic stem cell lines. Those skilled in the art are familiar with standard techniques for producing Treg cells from stem cells, including iPSCs. Examples of these techniques are described in Hague et al. (2012), J.Immunol., 189:2338~36; and Hague et al. (2019) JCI Insight, 4:pii 126471.

[0126] Furthermore, in the context of mixed T cell populations, those skilled in the art are familiar with standard techniques for isolating subpopulations of T cells that are CD4+ CD25+ T cells (Treg cells). For example, CD4+ CD25+ T cells (Treg cells) can be obtained from biological samples derived from a subject by negative and positive immunoselection and cell sorting.

[0127] In any method of the present invention, Treg cells cultured in the presence of nucleic acids or vectors may be transferred to the same object from which the cells were obtained. In other words, the cells used in the methods of the present invention may be autologous cells, i.e., they may be obtained from an object in which a medical condition is being treated or prevented. Alternatively, the cells may be homotransferred to another object. Preferably, the cells are autologous cells to the object in the method of treating or preventing a medical condition in the object.

[0128] As used herein, the terms “exvivo” or “exvivo therapy” refer to a modified therapy in which cells are obtained from a patient or a suitable alternative source, such as a suitable allogeneic donor, and the modified cells can be used to treat a disease that is improved by the therapeutic benefits provided by the modified cells. The treatment includes the administration or reintroduction of modified cells to a patient. The benefit of exvivo therapy is the ability to provide the patient with the benefits of the treatment without exposing the patient to unwanted side effects derived from the treatment.

[0129] The term "administered" means the administration of a therapeutically effective dose of the aforementioned composition, including each cell, to an individual. "Therapeutic dose" means the dose that produces the intended effect of the administered dose. The exact dose depends on the purpose of the treatment and can be determined by those skilled in the art using known techniques. Corrections may be necessary for systemic delivery compared to local delivery, age, weight, general health status, sex, diet, number of doses, drug interactions, and severity of condition, as are known in the art and described above, and can be determined by those skilled in the art with the appropriate experiments.

[0130] An "enriched" or "purified" cell population is defined as an increase in the ratio of specific cells to other cells, for example, the ratio compared to cells found in the subject's body or the ratio compared to the ratio before exposure to the peptide, nucleic acid, or vector of the present invention. In some embodiments, within the enriched or purified cell population, specific cells comprise at least 20%, 30%, 40%, 50%, 60%, 70%, 75%, 80%, 90%, 95%, or 99% of the total cell population. The cell population may be defined by one or more cell surface markers and / or characteristics.

[0131] Treg cells expressing the binding protein of the present invention may be administered to a subject by any method, including, for example, injection, infusion, deposition, implantation, oral ingestion, topical administration, or any combination thereof. Injection may be, for example, intravenous, intramuscular, intradermal, subcutaneous, or intraperitoneal injection, preferably intravenous. Single or multiple doses may be administered over a given time, depending on the condition, its severity, and the overall health of the subject, as can be determined by those skilled in the art without unnecessary experimentation. Injection may be performed at multiple locations.

[0132] Treg cell administration may be performed alone or in combination with other therapeutic agents. Each dose corresponds to approximately 10 × 10 CD8+ T cells. 3 pieces, cells 20×10 3 pieces, cells 50×10 3 pieces, cells 100×10 3 pieces, cells 200×10 3 pieces, cells 500×10 3 pieces, cells 1×10 6 pieces, cells 2×10 6 pieces, cells 20×10 6 pieces, cells 50×10 6 pieces, cells 100×10 6 pieces, cells 200×10 6 pieces, cells 500×10 6 pieces, cells 1×10 9 pieces, cells 2×10 9 pieces, cells 5×109 pieces, cells 10×10 9 This may include individual cells, etc. The frequency of administration may be, for example, once a week, twice a week, once every two weeks, once every three weeks, once every four weeks, once a month, once every two months, once every three months, once every four months, once every five months, once every six months, etc. The total number of days over which administration is performed may be one day, two days, or three, four, five, six, seven, eight, nine, ten, eleven, twelve, thirteen, fifteen, sixteen, seventeen, eighteen, nineteen, or twenty days, etc. Any administration performed may involve two or more infusions on the same day. Of the Treg cells administered for administration, at least 20%, at least 30%, at least 40%, at least 50%, at least 60%, at least 70%, at least 80%, at least 90%, at least 95%, and at least 99% will exhibit at least one characteristic of Treg cells.

[0133] peptide This invention relates to Smith protein, specifically HLA-DR15, and more particularly, HLA-DRA * 01:01 molecule and HLA-DRB1 * The present invention provides peptides that can bind to the 15:01 molecule and induce the proliferation of CD4+ T cells. These peptides are particularly applicable in immunotherapies treating conditions associated with abnormal, undesirable, or otherwise inadequate immune responses to Smith protein. Preferably, the condition is SLE.

[0134] In another embodiment, the present invention provides a peptide comprising, or derived from, the amino acid sequence of residues 1-15 or 58-72 of the SmB / B' protein or an equivalent amino acid sequence. In one embodiment, the SmB' protein comprises the amino acid sequence of SEQ ID NO: 5. In a further embodiment, the peptide comprises, or derived from, or derived from the amino acid sequence expressed in any one of SEQ ID NOs: 1, 2, 3, or 4.

[0135] In any embodiment, the peptide of the present invention can bind to or form a complex with the HLA-DR15 molecule, preferably the HLA-DR15 molecule is HLA-DR15. * 01:01 molecule and HLA-DRB1 * It is a 15:01 molecule.

[0136] Furthermore, the present invention is derived from Smith protein, HLA-DR3, and more specifically, HLA-DR3. * 01:01 molecule and HLA-DRB1 * The 03:01 molecule provides peptides that can bind to the molecule and induce the proliferation of CD4+ T cells. These peptides are particularly applicable in immunotherapies that treat conditions associated with abnormal, undesirable, or otherwise inappropriate immune responses to Smith protein. Preferably, the condition is SLE.

[0137] In another embodiment, the present invention provides a peptide comprising, or essentially comprising, the amino acid sequence of residues 7-21 of the SmB / B' protein or an equivalent amino acid sequence, or a peptide comprising, or essentially comprising, the amino acid sequence of residues 78-92 of the SmD1 protein or an equivalent amino acid sequence. In one embodiment, the SmB' protein comprises the amino acid sequence of SEQ ID NO: 5, in which case, preferably, the peptide comprises, or is essentially comprising, the amino acid sequence expressed in SEQ ID NO: 259. In one embodiment, the SmD1 protein comprises the amino acid sequence of SEQ ID NO: 260, in which case, preferably, the peptide comprises, or is essentially comprising, the amino acid sequence expressed in SEQ ID NO: 258.

[0138] In any embodiment, the peptide of the present invention can bind to or form a complex with an HLA-DR3 molecule, preferably the HLA-DR3 molecule is HLA-DRA * 01:01 molecule and HLA-DRB1 * 03:01 is a molecule.

[0139] References to “peptides” include references to peptides, polypeptides, or proteins, or parts thereof. Peptides may be glycosylated or unglycosylated and / or may contain a range of other molecules fused, linked, conjugated, or otherwise associated with proteins such as amino acids, lipids, carbohydrates, or other peptides, polypeptides, or proteins. References to “peptides” as used herein include peptides comprising amino acid sequences, as well as peptides associated with other molecules such as amino acids, lipids, carbohydrates, or other peptides, polypeptides, or proteins.

[0140] "Derivatives" include fragments, parts, portions, and variants derived from natural, synthetic, or recombinant sources, including fusion proteins. Parts or fragments include, for example, the active region of the target peptide. Derivatives may be derived from amino acid insertions, deletions, or substitutions. Amino acid insertion derivatives include amino-terminal and / or carboxyl-terminal fusions of one or more amino acids, as well as intrasequence insertions. Amino acid sequence insertion variants are insertion variants in which one or more amino acid residues are introduced into a predetermined site in the protein, although random insertions are also possible by appropriate screening of the resulting product. Deletion variants are characterized by the removal of one or more amino acids from the sequence.

[0141] An amino acid substitution variant is a variant in which at least one residue in a sequence is removed and a different residue is inserted in its place. An example of an amino acid substitution variant is a conserved amino acid substitution. Conserved amino acid substitutions typically include substitutions within the following groups: glycine and alanine; valine, isoleucine and leucine; aspartic acid and glutamic acid; asparagine and glutamine; serine and threonine; lysine and arginine; and phenylalanine and tyrosine. Additions to amino acid sequences include fusions with other peptides, polypeptides, or proteins. In one embodiment, a cysteine ​​residue is substituted with serine, as illustrated herein.

[0142] Chemical and functional equivalents of the target peptides are understood to be molecules that exhibit one or more of the functional activities of these molecules, and may originate from any source, such as chemically synthesized sources or sources identified through screening processes such as screening of natural products.

[0143] The analogues envisioned herein include, but are not limited to, modifications to side chains, the incorporation of unnatural amino acids and / or their derivatives during peptide synthesis, polypeptide synthesis, or protein synthesis, the use of crosslinking agents, and the use of other methods to impart conformational constraints to proteinaceous molecules or their analogues.

[0144] Examples of side-chain modifications envisioned by the present invention include reduction with NaBH4 following reductive alkylation by a reaction involving an aldehyde; amidation with methylacetoimidate; acylation with acetic anhydride; carbamylation of the amino group with cyanate; trinitrobenzylation of the amino group with 2,4,6-trinitrobenzenesulfonic acid (TNBS); acylation of the amino group with succinic anhydride and tetrahydrophthalic anhydride; and reduction with NaBH4 following pyrodosylation of lysine with pyrodoxal-5'-phosphate, among other modifications of the amino group.

[0145] The guanidine group of the arginine residue can be modified by the formation of heterocyclic condensation products with reagents such as 2,3-butanedione, phenylglyoxal, and glyoxal. The carboxyl group can be modified by carbodiimide activation, which follows the formation of O-acyl isourea and subsequent derivatization to the corresponding amide, for example. The sulfhydryl group can be modified by carboxymethylation with iodoacetic acid or iodoacetamide; pergoxidation to cysteic acid; formation of disulfides mixed with other thiol compounds; reactions with maleimide, maleic anhydride, or other substituted maleimides; formation of mercury derivatives using 4-chloromerclybenzoate, 4-chloromerclyphenylsulfonic acid, phenylmercury chloride, 2-chloromerclyc-4-nitrophenol, and other mercury agents; and carbamoylation with cyanates at alkaline pH. The tryptophan residue can be modified, for example, by oxidation with N-bromosuccinimide, or by alkylation of the indole ring with 2-hydroxy-5-nitrobenzyl bromide or halogenated sulfenyl. On the other hand, the tyrosine residue can be modified by nitration with tetranitromethane to form a 3-nitrotyrosine derivative.

[0146] Modification of the imidazole ring of a histidine residue can be achieved by alkylation with an iodoacetic acid derivative or N-carbonethoxylation with diethyl pyrocarbonate.

[0147] Examples of the incorporation of non-natural amino acids and derivatives during protein synthesis include, but are not limited to, norleucine, 4-aminobutyric acid, 4-amino-3-hydroxy-5-phenylpentanoic acid, 6-aminohexanoic acid, t-butylglycine, norvaline, phenylglycine, ornithine, sarcosine, 4-amino-3-hydroxy-6-methylheptanoic acid, 2-thienylalanine, and / or D-isomers of amino acids.

[0148] The crosslinking agent is, for example, (CH2) n=1 to n=6. nThree-dimensional conformations can be stabilized using homobifunctional crosslinking agents such as bifunctional imide esters having spacer groups, glutaraldehyde, N-hydroxysuccinimide esters, and heterobifunctional reagents that typically contain an amino-reactive moiety such as N-hydroxysuccinimide and another group-specific reactive moiety.

[0149] The structure of peptides according to the present invention can be modified for a variety of purposes, such as increasing solubility, enhancing therapeutic or prophylactic efficacy, increasing stability, or increasing resistance to proteolysis. Modified peptides can be prepared by altering the amino acid sequence through amino acid substitution, deletion, or addition to modify immunogenicity. Similarly, components may be added to the peptides of the present invention to produce the same results.

[0150] For example, a peptide may be modified to exhibit the ability to induce T cell anergy. In this case, the most important binding residues to the T cell receptor can be determined using known techniques (e.g., substitution of each residue and determination of the presence or absence of T cell reactivity). In one example, a residue shown to be essential for interacting with the T cell receptor may be modified by replacing the essential amino acid with another, preferably similar, amino acid residue whose presence has been shown to alter T cell reactivity or T cell function (conservative substitution). In addition, amino acid residues not essential for interacting with the T cell receptor may be modified by replacing them with other amino acids, in which case the incorporation may alter T cell reactivity or T cell function, but not, for example, eliminate binding to the target MHC protein.

[0151] Exemplary conservative substitutions are detailed below and include the following:

[0152] [Table 1]

[0153] Such modifications result in the creation of molecules that fall within the range of “mutants” of the target peptide as defined herein. A “mutant” is understood as a reference to a peptide that exhibits one or more structural features or functional activities that are significantly different from those exhibited by the unmutated peptide counterpart.

[0154] The peptides of the present invention may also be modified to incorporate one or more polymorphisms arising from natural allele variants, and the peptides may be substituted with D-amino acids, unnatural amino acids, or amino acid analogs to result in modified peptides that fall within the scope of the present invention. The peptides may also be modified by known techniques via conjugation with polyethylene glycol (PEG). Reporter groups may also be added to facilitate the purification of peptides according to the present invention and to potentially increase their solubility. Other well-known types of modifications, including the insertion of specific endoprotease cleavage sites, the addition of functional groups, or the replacement of hydrophobic residues with less hydrophobic residues, and site-directed mutagenesis of the DNA encoding the peptides of the present invention, may also be used to introduce modifications that may be useful for a wide range of purposes. The various modifications to peptides according to the present invention mentioned above are mentioned for illustrative purposes only and are intended only to illustrate the breadth of possible modifications.

[0155] The peptides of the present invention may be prepared by recombinant means or by chemical synthesis. In a preferred embodiment of the present invention, recombinant peptides or mutants thereof are provided, which are expressed by T cells derived from an individual exhibiting autoreactivity to Smith protein and by host cells that are preferentially immunoreactive and transformed with a vector encoding the peptide sequence of the present invention. The peptides may be fused with other peptides, polypeptides, or proteins. Alternatively, the peptides may be prepared by chemical synthesis methods such as the Merrifield solid-phase synthesis procedure. Furthermore, while the synthetic peptides of the sequences presented above represent a preferred embodiment, the present invention is also extended to biologically pure preparations of naturally occurring peptides or fragments thereof. "Biologically pure" means a preparation containing at least about 60%, preferably at least about 70%, or preferably at least about 80%, and more preferably at least about 90% or more, as determined by weight, activity, or other suitable means.

[0156] Nucleic acids and vectors In another embodiment, the present invention provides nucleic acid molecular compositions comprising one or more nucleic acid molecules that encode, or are complementary to, sequences encoding the binding proteins and peptides of the present invention or derivatives, homologs, or analogs thereof. The nucleic acid molecules of the present invention may be used to produce the binding proteins or peptides of the present invention, or they may be used for cell therapies to treat the diseases or conditions described herein.

[0157] The term "construct" refers to any polynucleotide containing recombinant nucleic acid molecules. Constructs may reside within a vector (e.g., a bacterial vector, a viral vector) or be incorporated into a genome. A "vector" is a nucleic acid molecule capable of carrying another nucleic acid. Vectors can be linear or circular DNA or RNA molecules, and may include plasmids, cosmids, viruses, RNA vectors, or chromosomal nucleic acids, non-chromosomal nucleic acids, semi-synthetic nucleic acids, or synthetic nucleic acids. Exemplary vectors are self-replicating vectors (episome vectors) or vectors capable of expressing nucleic acid molecules linked together (expression vectors).

[0158] Viral vectors include negative-strand RNA viruses such as retroviruses, adenoviruses, parvoviruses (e.g., adeno-associated viruses), coronaviruses, orthomyxoviruses (e.g., influenza virus), rhabdoviruses (e.g., rabies virus and varicella stomatitis virus), and paramyxoviruses (e.g., measles virus and Sendai virus), positive-strand RNA viruses such as picornaviruses and alphaviruses, and double-stranded DNA viruses including adenoviruses, herpesviruses (e.g., herpes simplex virus type 1 and herpes simplex virus type 2, Epstein-Barr virus, and cytomegalovirus), as well as poxviruses (e.g., vaccinia virus, fowlpox virus, and canarypox virus). Other viruses include, for example, Norwalk virus, togavirus, flavivirus, reovirus, papovavirus, hepadnavirus, and hepatitis virus. Examples of retroviruses include avian leukemia sarcoma virus, mammalian type C retrovirus, mammalian type B retrovirus, mammalian type D retrovirus, HTLV-BLV group retrovirus, lentivirus, and spumavirus (Coffin, JM, "Retroviridae: The viruses and their replication," "Fundamental Virology," 3rd edition, edited by BNFields et al., Lippincott-Raven Publishers, Philadelphia, 1996).

[0159] As used herein, “lentiviral vector” refers to an HIV-based lentiviral vector for gene delivery that may be embedded or non-embedded, may have a relatively large packaging capacity, and is capable of transducing into a range of different cell types. Lentiviral vectors are typically produced after transient transfection of three or more plasmids (packaging plasmid, envelope plasmid, and transfer plasmid) into producing cells. Similar to HIV, lentiviral vectors enter target cells via the interaction of glycoproteins on the viral surface with receptors on the cell surface. Once inside, the viral RNA undergoes reverse transcription, mediated by the viral reverse transcriptase complex. The product of reverse transcription is double-stranded linear viral DNA, which serves as a substrate for the integration of the virus into the DNA of the infected cell.

[0160] In any embodiment, the vector of the present invention is as follows: (i) EF1α (alpha) promoter; (ii) 2A ribosome skipping sequence; (iii) Woodchuck hepatitis virus post-transcriptional regulatory element (WPRE); (iv) A configuration in which the TCRβ chain variable (Vβ or V-beta) domain is translated before the (TCR)α chain variable (Vα or V-alpha) domain; or (v) Arrangement that translates the TCRβ chain variable (Vβ or V-beta) chain before the (TCR)α chain variable (Vα or V-alpha) chain. It may include one or more, or all, of the following.

[0161] Preferably, the vector is a lentiviral vector. More preferably, the lentiviral vector has one or more or all of the features shown in Figure 4.

[0162] The term "operatably linked" refers to the association of two or more nucleic acid molecules on a single nucleic acid fragment such that the function of one is influenced by the other. For example, a promoter is operatably linked to a coding sequence if it can influence the expression of that coding sequence (i.e., the coding sequence is under the transcriptional control of the promoter). "Not linked" means that the associated gene elements are not closely related to each other, and the function of one does not affect the other.

[0163] As used herein, “expression vector” refers to a DNA construct containing a nucleic acid molecule operably ligated to a suitable regulatory sequence capable of producing expression of the nucleic acid molecule in a suitable host. Such regulatory sequences include a promoter that produces transcription, an optional operator sequence that controls such transcription, a sequence encoding a ribosome-binding site for a suitable mRNA, and sequences that control the termination of transcription and translation. A vector can be a plasmid, a phage particle, a virus, or simply a potential genome insert. Once a suitable host is transformed, the vector may replicate and function independently of the host genome, or, in some cases, be integrated into the genome itself. In this specification, “plasmid,” “expression plasmid,” “virus,” and “vector” are often used interchangeably.

[0164] As used herein, the term “expression” refers to the process by which polypeptides are produced based on the coding sequence of nucleic acid molecules, such as genes. The process may include transcription, post-transcriptional regulation, post-transcriptional modification, translation, post-translational regulation, post-translational modification, or any combination thereof.

[0165] In the context of inserting nucleic acid molecules into cells, the term “introduced” means “transfection,” “transformation,” or “transduction,” and includes reference to the integration of nucleic acid molecules into eukaryotic or prokaryotic cells, in which case the nucleic acid molecule may be integrated into the cell’s genome (e.g., chromosomal DNA, plasmid DNA, plastid DNA, or mitochondrial DNA), converted into an autonomous replicon, or transiently expressed (e.g., transfected mRNA).

[0166] As used herein, “heterogeneous” nucleic acid molecules, “heterogeneous” constructs or “heterogeneous” sequences, or “exogenous” nucleic acid molecules, “exogenous” constructs or “exogenous” sequences, refer to nucleic acid molecules or portions of nucleic acid molecules that are not native to a host cell, but may be homologous to nucleic acid molecules or portions of nucleic acid molecules derived from a host cell. The source of heterogeneous nucleic acid molecules, heterogeneous constructs or heterogeneous sequences, or exogenous nucleic acid molecules, exogenous constructs or exogenous sequences, may originate from different genera or species. In certain embodiments, heterogeneous or exogenous nucleic acid molecules are added to a host cell or host genome (i.e., not endogenous or native) by means of, for example, conjugation, transformation, transfection, electroporation, etc., in which case the added molecule may be incorporated into the host genome, exist as extrachromosomal genetic material (e.g., as a plasmid or other form of self-replicating vector), and may exist in multiple copies. In addition, "heterogeneous" refers to non-natural enzymes, proteins, or other activities encoded by exogenous nucleic acid molecules introduced into host cells, even if the host cell encodes homologous proteins or activities.

[0167] As described herein, one or more heterologous nucleic acid molecules or exogenous nucleic acid molecules may be introduced into a host cell as separate nucleic acid molecules, as multiple individually controlled genes, as polycistronic nucleic acid molecules, as a single nucleic acid molecule encoding a fusion protein, or as any combination thereof. For example, as disclosed herein, a host cell may be modified to express two or more heterologous nucleic acid molecules or exogenous nucleic acid molecules encoding desired TCRs (e.g., TCRα and TCRβ) specific to the WT-1 antigen peptide. When two or more exogenous nucleic acid molecules are introduced into a host cell, they may be introduced as a single nucleic acid molecule (e.g., on a single vector), on separate vectors, integrated into the host chromosome at one or more sites, or in any combination thereof. The number of activities of the heterologous nucleic acid molecules or heterologous proteins mentioned refers to the number of encoding nucleic acid molecules or protein activities, and not to the number of separate nucleic acid molecules introduced into the host cell.

[0168] As used herein, the terms “endogenous” or “native” refer to genes, proteins, or activities that are normally present in a host cell. Furthermore, genes, proteins, or activities that are mutated, overexpressed, shuffled, duplicated, or otherwise modified compared to the parent gene, protein, or activity are also considered endogenous or native in that particular host cell. For example, an endogenous regulatory sequence derived from a first gene (e.g., a promoter, a translational repression sequence) may be used to alter or regulate the expression of a second native gene or nucleic acid molecule, in which case the expression or regulation of the second native gene or nucleic acid molecule will differ from the normal expression or regulation in the parent cell.

[0169] The terms "homologous" or "homologous" refer to molecules or activities found in or derived from host cells, host species, or host strains. For example, heterologous or exogenous nucleic acid molecules may be homologous to native host cell genes, may have altered expression levels, different sequences, altered activities, or any combination thereof.

[0170] As used herein, “sequence identity” refers to the percentage of amino acid residues in one sequence that are identical to amino acid residues in another reference polypeptide sequence, after the sequences have been aligned to achieve the maximum possible sequence identity percentage, gaps have been introduced where necessary, and conservative substitutions have not been considered part of the sequence identity. The percentage values ​​of sequence identity can be generated using NCBI BLAST2.0 software with parameters set to their default values, as defined by Altschul et al. (1997), “Gapped BLAST and PSI-BLAST: a new generation of protein database search programs,” Nucleic Acids Res., 25:3389~3402.

[0171] As used herein, the term “host” refers to a cell (e.g., a Treg cell) or microorganism targeted for genetic modification with a heterologous or exogenous nucleic acid molecule to produce a polypeptide of interest (e.g., an anti-WT-1 TCR with high affinity or enhanced affinity). In certain embodiments, the host cell may optionally already possess, or be modified to include, other genetic modifications that confer desired characteristics (e.g., incorporation of a detection marker; deletion, alteration, or cleavage of an endogenous TCR; increased expression of a costimulatory factor), whether or not they are associated with the biosynthesis of a heterologous or exogenous protein. In some embodiments, the host cell is genetically modified to express a protein or fusion protein (e.g., immunomodulatory fusion protein of WO2016 / 141357, for example, immunomodulatory fusion proteins incorporated herein by reference in their entirety) that modulates immune signaling in the host cell to promote, for example, the viability and / or growth advantages of the modified cell.

[0172] Nucleic acid molecules can be ligated into expression vectors that can be expressed in prokaryotic cells (e.g., E. coli) or eukaryotic cells (e.g., yeast cells, fungal cells, insect cells, mammalian cells, or plant cells). Nucleic acid molecules may also be ligated, fused, or otherwise associated with other nucleic acid molecules encoding other entities, such as signal peptides. Nucleic acid molecules may also include further nucleotide sequence information fused, linked, or otherwise associated with them at either the 3' or 5' terminus, or both. Nucleic acid molecules may also be part of a vector, such as an expression vector. The latter embodiment facilitates the preparation of recombinant forms of the binding protein or peptide of the present invention.

[0173] Such nucleic acids may be useful for the recombinant production of the binding proteins or peptides of the present invention, or proteins containing them, by insertion into a suitable vector and transfection into a suitable cell line. Such expression vectors and host cell lines also constitute embodiments of the present invention.

[0174] In the preparation of peptides by recombinant methods, host cells transformed with nucleic acids or functional equivalents of nucleic acid sequences having sequences encoding binding proteins or peptides according to the present invention are cultured in a medium suitable for the specific target cells. Subsequently, the binding proteins or peptides can be purified from the cell culture medium, host cells, or both using techniques well known in the art, such as ion exchange chromatography, gel filtration chromatography, ultrafiltration, electrophoresis, or immunopurification with antibodies specific to the binding proteins or peptides.

[0175] The nucleic acids encoding the binding proteins or peptides of the present invention can be expressed in bacterial cells such as E. colly, insect cells, yeast cells, or mammalian cells such as Chinese hamster ovary cells (CHO). Suitable expression vectors, promoters, enhancers, and other expression regulatory elements are mentioned in Sambruck et al. (1989). Other suitable expression vectors, promoters, enhancers, and other expression elements are well known to those skilled in the art. Examples of suitable expression vectors in yeast include Yep Sec 1 (Balderi et al., 1987, Embo J., 6:229~234); pMFa (Kurjan and Herskowitz., 1982, Cell., 30:933~943); JRY88 (Schultz et al., 1987, Gene., 54:113~123) and pYES2 (Invitrogen Corporation, San Diego, CA). These vectors, as well as baculovirus and mammalian expression systems, are available without restriction. For example, baculoviruses are commercially available for expression in insect cells (ParMingen, San Diego, CA), while pMsg vectors are commercially available for expression in mammalian cells (Pharmacia, Piscataway, NJ).

[0176] Expression vectors suitable for expression within E. kohlii include, in particular, pTrc (Amann et al., 1998, Gene., 69:301~315); pGex (Amrad Corporation, Melbourne, Australia); pMal (NEBiolabs, Beverley, MA); pRit5 (Pharmacia, Piscataway, NJ); pEt-11d (Novagen, Maddison, WI) (Jameel et al., 1990, J. Virol., 64:3963~3966) and pSem (Knapp et al., 1990, Bio Techniques., 8:280~281). The use of pTRC and pEt-11d results in, for example, the expression of non-fusion proteins. The use of pMal, pRit5, pSem, and pGex results in the expression of proteins or peptides fused to maltose E-binding protein (pMal), protein A (pRit5), cleavage-type galactosidase (PSEM), or glutathione S-transferase (pGex). When the binding protein or peptide is expressed as a fusion protein, it is particularly advantageous to introduce an enzymatic cleavage site at the fusion site between the carrier protein and the target peptide. The binding protein or peptide of the present invention can then be recovered from the fusion protein via enzymatic cleavage at the enzymatic site and biochemical purification using standard techniques for protein and peptide purification. Different vectors also have different promoter regions that enable constitutive expression, inducible expression, or temperature-induced expression. In addition, it may be appropriate to express recombinant peptides in different E. collie hosts in which the ability to degrade recombinantly expressed proteins is altered. Alternatively, it may be advantageous to modify the nucleic acid sequence to use codons preferred by E. kohlii, and such nucleic acid modifications do not affect the amino acid sequence of the expressed protein.

[0177] Host cells can be transformed to express the nucleic acids of the present invention using conventional techniques such as calcium phosphate or calcium chloride coprecipitation, DEAE-dextran-mediated transfection, or electroporation. Suitable methods for transforming host cells can be found in Sambruck et al. (1989) and other experimental textbooks. The nucleic acid sequences of the present invention may also be chemically synthesized using standard techniques.

[0178] In addition to preparation by recombinant peptide according to the present invention, nucleic acids can also be used as probes for experimental or purification purposes.

[0179] The state to be treated Hereinafter, the identification and synthesis of the binding proteins, peptides, cells, nucleic acids, vectors, and compositions of the present invention disclosed herein facilitates the development of prophylactic and therapeutic treatment protocols, spanning a range of uses related to immune conditions associated with Smith's protein. It also facilitates the development of reagents for use in these protocols. Therefore, it should be understood that the present invention extends to the use of peptides or their functional derivatives, homologs, or analogs in the therapeutic and / or prophylactic treatment of patients. Such treatment methods include, but are not limited to, the following:

[0180] Administration to a patient of cells expressing the target peptide or the binding protein of the present invention as a means of desensitization or induction of immunological tolerance. This can be achieved, for example, by inducing Th2 anergy or apoptosis directed to Smith protein. Treatment protocols based on the administration of a given cell or peptide expressing the binding protein at a specific concentration, according to a specific regimen for inducing tolerance, can be utilized. Such methods can eliminate hypersensitivity to Smith protein or reduce the severity of hypersensitivity or susceptibility to Smith protein.

[0181] Preferably, such treatment regimens can modify the T cell response or both the B cell and T cell responses of the individual under study. Modification of the autoimmune response used herein may be defined as the induction of non-responsiveness or reduction of immunity to Smith protein or other autoantigens, as determined by standard clinical procedures. In particular, since immunosuppressive cells (e.g., Tregs and myeloid-derived suppressor cells) mobilized as a result of Sm-specific Treg therapy exhibit non-antigen-specific immunosuppressive ability, creating a tolerance environment for multiple autoantigens, it is predicted that the use of Sm-specific Tregs may induce immune tolerance to autoantigens beyond Smith protein.

[0182] Exposure of an individual to the binding proteins, peptides, cells, nucleic acids, vectors, and compositions of the present invention may induce tolerance or anergy in appropriate T cell subpopulations so that they become unresponsive to Smith protein and other autoantigens and do not participate in stimulating the immune response at such exposure.

[0183] In one embodiment, the method desensitizes to or induces immunological tolerance to the Smith protein.

[0184] In another embodiment, the desensitization or tolerance is achieved by inducing T cell anergy or apoptosis.

[0185] In yet another embodiment, the desensitization or tolerance is achieved by inducing Smith-specific Treg cells.

[0186] The term "therapeutic dose" generally refers to the amount of cells expressing the binding protein or peptide of the present invention that (i) treat a particular disease, condition, or disorder; (ii) alleviate, improve, or eliminate one or more symptoms of a particular disease, condition, or disorder; or (iii) delay the onset of one or more symptoms of a particular disease, condition, or disorder as described herein.

[0187] As used herein, “preventing” or “prevention” is intended to mean at least reducing the likelihood or risk (or susceptibility) to developing a disease or disorder (i.e., preventing the development of at least one of the clinical symptoms of a disease in individuals who may be exposed to the disease and may be predisposed to it, but who have not yet gone through or presented symptoms of the disease). Biological and physiological parameters for identifying such patients are presented herein and are well known to physicians.

[0188] In a particularly preferred embodiment, the method of the present invention may prevent, reduce the severity of, or inhibit or minimize the progression, relapse, or symptoms of any disease or condition described herein. Thus, the method of the present invention has not only therapeutic utility but also preventative utility.

[0189] The terms “treatment” or “treatment of” the subject include any objective action to delay, slow, stabilize, cure, heal, alleviate, reduce, modify, restore, reduce exacerbations, improve, or influence the disease or condition, the symptoms of the disease or condition, or the risk (or susceptibility to them). The terms “treatment of” refer to any indicator of success of treatment or improvement of SLE and related conditions described herein, including any objective or subjective parameters such as sedation; remission; reduced rate of exacerbation; reduced severity of condition; stabilization, reduction or increased tolerability of the condition for the individual; slowing the rate of degeneration or debilitation; suppression of the debilitating phase of the final degeneration; or improvement of the subject’s physical or mental well-being.

[0190] It is also understood that the methods described herein may be used in combination with existing standard treatments / therapies for SLE. Those skilled in the art are familiar with existing standard treatments for SLE, including but not limited to the use of steroids, antimalarial agents (hydroxychloroquine, chloroquine), immunosuppressants (azathioprine, methotrexate, mycophenolate mofetil, mycophenolic acid, tacrolimus, voclosporine, cyclosporine), kinase inhibitors (baricitinib, tofacitinib, upadacitinib), and biological agents (belimumab, rituximab, aniflorumab, ustekinumab, obinotuzumab). The present invention includes combinations of existing standard treatments with the specific methods of the present invention.

[0191] In this specification, “subject” preferably refers to a human subject. Although the present invention is applicable to humans, it is also useful for veterinary purposes. The present invention is useful for livestock or farm animals such as cattle, sheep, horses and poultry; companion animals such as cats and dogs; and zoo animals. The terms “subject” and “individual” are understood to refer to an individual requiring treatment according to the present invention.

[0192] Systemic lupus erythematosus (SLE) is a multisystem autoimmune disease. At least 5 million people worldwide have SLE, 90% of those diagnosed are women, and most develop SLE between the ages of 15 and 44. In Australia, SLE is diagnosed in approximately 1 in 1,000 people, and is more frequent and severe in African Australians and Asian Australians. SLE patients suffer from chronic immune-mediated inflammatory damage in the brain, kidneys, heart, lungs, joints, skin, and other organs, resulting in a marked reduction in life expectancy, exemplified by a standardized mortality rate greater than 3. In a UK cohort, the mean age at death for patients who died during the follow-up period (14% of patients) was only 52 years. The clinical course is often characterized by intermittent relapses associated with increasing irreversible organ damage and subsequent death.

[0193] Other forms of lupus include discoid lupus, drug-induced lupus, and neonatal lupus. Of these, systemic lupus erythematosus (also known as SLE) is the most common and severe form. A more complete classification of lupus includes the following types: acute cutaneous lupus erythematosus, subacute cutaneous lupus erythematosus, discoid lupus erythematosus (chronic cutaneous), childhood discoid lupus erythematosus, generalized discoid lupus erythematosus, focal discoid lupus erythematosus, frostbite-lichen planus syndrome, lupus panniculitis (deep lupus erythematosus), pyogenic lupus erythematosus, verrucous lupus erythematosus (hypertrophic lupus erythematosus), cutaneous lupus mucin deposition, complement deficiency syndrome, drug-induced lupus erythematosus, neonatal lupus erythematosus, and systemic lupus erythematosus.

[0194] Cutaneous lupus erythematosus (CLE) is present in the majority of SLE cases and is often observed in sun-exposed skin, manifesting as various severe skin erythemas and, in some cases, disfiguring skin erythema. Lupus can also manifest as a purely cutaneous form, also known as incomplete lupus erythematosus. While not all factors contributing to the onset and intermittent relapse patterns of SLE are known, it is clear that sun exposure is important not only for the exacerbation of systemic disease but also for the exacerbation of skin disease.

[0195] Among the common symptoms in patients diagnosed with lupus, almost all patients have joint pain and / or joint swelling (i.e., arthritis). The most frequently affected joints are the fingers, palms, wrists, and knees. Other common symptoms include pleuritic chest pain, oral and nasal ulcers, fatigue, fever without other cause, general discomfort, anxiety or feeling unwell (malaise), hair loss, photosensitivity, and erythema ("butterfly" rash) in about half of SLE sufferers, as well as scarring "discoid" lesions and lymph node swelling. Those skilled in the art are familiar with a variety of other important symptoms of lupus, including but not limited to nephritis, CNS lesions, hematological lesions, gastrointestinal lesions, and vasculitis.

[0196] As used herein, photosensitivity or abnormal photosensitivity in individuals with CLE or SLE includes erythema resulting from an unusual reaction to sunlight. Exposure to sunlight may, beyond the onset of erythema, lead to increased disease activity in lupus co-habitants, accompanied by symptoms such as joint pain, weakness, fatigue, and fever. Two-thirds of lupus sufferers have increased sensitivity to ultraviolet (UV) light from sunlight, UV light from artificial indoor lighting such as fluorescent lights, or both.

[0197] composition The administration of the composition of the present invention (as referred to herein as the “agent”) in the form of a pharmaceutical composition may be carried out by any convenient means. In certain embodiments, the agent is a peptide comprising or essentially comprising the peptide described herein, preferably the sequence expressed in any one of SEQ ID NOs: 1 to 4. The agent of the pharmaceutical composition is expected to exhibit therapeutic activity when administered in a dose that depends on the specific case. Variation depends, for example, on the human or animal and the selected agent. A wide range of doses may be applicable. Considering the patient, for example, about 0.01 μg to about 1 mg of the agent may be administered per dose. The dosage regimen may be adjusted to produce an optimal therapeutic response. For example, several divided doses may be administered daily, weekly, monthly or at other appropriate time intervals, and the dose may be proportionally reduced as indicated by the requirements of the situation. In another example, the composition is first administered to induce tolerance, and then, if necessary, additional doses of the composition are administered to maintain tolerance. These additional doses may be administered, for example, monthly, or over any period of time, including the patient's lifetime.

[0198] The drug may be administered by convenient means such as orally, intravenously (if water-soluble), intraperitoneally, intramuscularly, subcutaneously, intradermally (with or without the use of conventional injection needles or other transdermal delivery devices), transdermally, intranasally, sublingually, or via suppository routes or implantation (e.g., using sustained-release molecules). Preferably, the composition is administered intradermally. The drug may be administered in the form of pharmaceutically acceptable non-toxic salts, such as acid addition salts or metal complexes, e.g., zinc, iron (considered to be the salts for which this application is intended). Examples of such acid addition salts include hydrochloride, hydrobromide, sulfate, phosphate, maleate, acetate, citrate, benzoate, succinate, malate, ascorbate, and tartrate. When the active ingredient is administered in tablet form, the tablet may contain a binder such as tragacanth, corn starch, or gelatin; a disintegrant such as alginate; and a lubricant such as magnesium stearate. In the context of peptides for administration, compositions containing such peptides may be in the form of liposomes or conjugated into nanoparticles. Those skilled in the art are familiar with standard methods for formulating peptides for administration to subjects requiring them.

[0199] Suitable pharmaceutical forms for use by injection may include sterile aqueous solutions (if soluble in water) or sterile aqueous dispersions, and sterile powders for the immediate preparation of sterile injection solutions or sterile injection dispersions, or they may be in the form of creams or other forms suitable for topical application. Pharmaceutical forms must be stable under manufacturing and storage conditions and protected from contamination by microorganisms such as bacteria and fungi. Carriers may be solvents containing, for example, water, ethanol, polyols (e.g., glycerol, propylene glycol, and liquid polyethylene glycol), suitable mixtures thereof, and vegetable oils, or they may be dispersion media. Appropriate fluidity can be maintained, for example, by using coatings such as lecithin, by maintaining the required particle size in the case of dispersions, and by using surfactants. Prevention of microbial activity can be achieved by various antimicrobial and antifungal agents, such as parabens, chlorobutanol, phenol, sorbic acid, and thimerosal. In many cases, it is preferable for the composition to contain isotonic agents, such as sugars, polyalcohols like mannitol and sorbitol, and sodium chloride. Osmotic regulators are useful in keeping the preparation isotonic with human plasma, thereby avoiding tissue damage. Commonly used isotonic agents include dextrose, trehalose, glycerin, and mannitol. Glycerol and sodium chloride are other options, but are not commonly used. In many cases, it is preferable to include isotonic agents, such as sugars or sodium chloride. Delayed absorption of the injectable composition can be achieved by using absorption-delaying agents in the composition, such as aluminum monostearate and gelatin.

[0200] Sterile injectable solutions can be prepared by incorporating the active compound, along with various other components listed above as required, in the required amounts in a suitable solvent, followed by sterilization by filtration. Generally, dispersions are prepared by incorporating various sterilizing active ingredients into a sterilizing medium containing other required components derived from a basic dispersion medium and the other components listed above. In the case of sterilizing powders for preparing sterilizing injectable solutions, preferred preparation methods are vacuum drying and freeze-drying, which yield a powder from an already sterilized filtered solution of the active ingredient with any further desired components added.

[0201] The active ingredient, when protected in an appropriate form, may be administered orally, for example, with an inert diluent or an assimilated edible carrier; encapsulated in a hard-shell or soft-shell gelatin capsule; compressed into a tablet; or directly incorporated into a diet. For oral therapeutic administration, the active compound may be incorporated with excipients and used in the form of edible tablets, oral tablets, lozenges, capsules, elixirs, suspensions, syrups, wafers, etc. Such compositions and preparations shall contain at least 1% by weight of the active compound. The percentage of the composition and preparation may, of course, vary, and is preferably between about 5% and about 80% of the unit weight. The amount of the active compound in such therapeutically useful compositions is such that an appropriate dose is obtained. Preferred compositions or preparations according to the present invention are prepared so that the oral unit dosage form contains between about 0.1 μg and 1000 μg of the active compound.

[0202] Tablets, lozenges, pills, capsules, etc., may also contain ingredients listed later in this specification: binders such as gum, acacia, corn starch, or gelatin; excipients such as calcium diphosphate; disintegrants such as corn starch, potato starch, or alginic acid; lubricants such as magnesium stearate; and sweeteners such as sucrose, lactose, or saccharin, or flavorings such as peppermint, wintergreen oil, or cherry flavorings. In the case of capsules, the unit dosage form may also contain a liquid load in addition to the above types of materials. Other diverse materials may be present as coatings, or to modify the physical unit dosage form in other ways. For example, tablets, pills, or capsules may be coated with shellac, coated with sugar, or coated with both. Syrups or elixirs may contain active compounds, sucrose as a sweetener, methylparaben and propylparaben as preservatives, dyes, and flavorings such as cherry or orange flavorings. Naturally, any materials used in the preparation of any unit dosage form shall be pharmaceutically pure and substantially non-toxic in the amount used. In addition, the active compound(s) may be incorporated into sustained-release preparations and sustained-release formulations.

[0203] The pharmaceutical composition may also include a vector capable of transfecting target cells, and may contain a genetic molecule such as a vector containing a nucleic acid molecule encoding a regulatory drug. The vector may be, for example, a viral vector.

[0204] The routes of administration include, but are not limited to, respiratory routes (e.g., via aerosol, intranasal route, or oral route), endotracheal route, nasopharyngeal route, intravenous route, intraperitoneal route, subcutaneous route, intracranial route, intradermal route, percutaneous route, intramuscular route, intraocular route, intrathecal route, intracerebral route, intranasal route, infusion, oral, rectal, IV drip patch route, implantation route, and sublingual route. Preferably, the route of administration is intravenous, subcutaneous, intradermal, percutaneous, or intranasal route, and more preferably intravenous route.

[0205] A further aspect of the present invention relates to the compositions specified herein as used in any method of the present invention.

[0206] [Table 2] TIFF0007851611000003.tif229165TIFF0007851611000004.tif230165TIFF0007851611000005.tif227168TIFF000 7851611000006.tif228165TIFF0007851611000007.tif229167TIFF0007851611000008.tif229166TIFF00078516110 00009.tif229167TIFF0007851611000010.tif227165TIFF0007851611000011.tif227165TIFF0007851611000012.t if226167TIFF0007851611000013.tif226166TIFF0007851611000014.tif228169TIFF0007851611000015.tif170166

[0207] [Table 3] TIFF0007851611000017.tif228166TIFF0007851611000018.tif220166TIFF0007851611000019.tif226166TIFF0007851611000020.tif227169TIFF0007851611000021.tif228168TIFF0007851611000022.tif226168TIFF0007851611000023.tif228168TIFF0007851611000024.tif226166TIFF0007851611000025.tif225168TIFF0007851611000026.tif228166TIFF0007851611000027.tif227167TIFF0007851611000028.tif226168TIFF0007851611000029.tif98165

[0208]

Table 4

[0209]

Table 5

[0210] [Example 1] Epitope Mapping To identify Sm-derived peptides that bind to HLA-DR15, the inventors utilized the REVEAL MHC-peptide Binding Assay from ProImmune. Briefly, 149 peptides (12 amino acids, 15-mer duplications) were synthesized across three known immunogenic Sm proteins (SmB / B', SmD1, and SmD3 (Migliorini, 2005, Autoimmunity, 38:47~54)). * 01:01+HLA-DRB1 * The relative affinity of each peptide to 15:01) was measured against a known positive control. Peptides that bind with high affinity emit a strong signal by forming a tertiary complex that can be detected by the antibody.

[0211] HLA Typing Healthy human whole donor blood was HLA-typed at high resolution by Victorian Transplant and Immunogenetics Service, Red Cross, and Melbourne. Common and well-documented alleles (CWD) typing was performed using the IMGT / HLA reference database and SSO / SSP method, or using next-generation sequencing (NGS) or sequence-based typing (SBT) (Mack et al., 2013, Tissue Antigens, 81:194-203).

[0212] Isolation of primary human cells Completely HLA typed freshly drawn human whole blood was collected, and PBMCs were isolated using Lymphoprep density gradient medium in Sepmate-50 tubes according to the manufacturer's (Stemcell) instructions. Monocytes were purified from PBMCs using the EasySep magnet and Human Monocyte Isolation Kit according to the manufacturer's (Stemcell) instructions. Monocytes were differentiated into mature dendritic cells over 7 days using the ImmunoCult Dendritic Cell Culture Kit (Stemcell).

[0213] CD4+ cells were directly purified from whole blood using the RosetteSep Human CD4+ T Cell Enrichment Cocktail according to the manufacturer's (Stemcell) instructions.

[0214] First, CD4+ cells were enriched using the RosetteSep Human CD4+ T Cell Enrichment Cocktail, and then naive regulatory T cells were purified by sorting CD4+ cells, CD25high cells, CD127low cells, CD45RA+ cells, and PI− cells on a FACS Aria Fusion flow cytometer (BD) using the following antibodies: anti-human CD4 Pacific Blue (Biolegend), anti-human CD25 APC (Biolegend), anti-human CD127 PE (Biolegend), anti-human CD45RA PE Cy7 (BD).

[0215] Co-culture in vitro 200,000 freshly isolated CD4+ enriched cells were stained with 5 μM Cell Trace Violet (CTV) cell proliferation dye (Invitrogen) and placed in one well of a 96-well flat-bottom tissue culture plate (Corning) in RPMI 1640 medium (Gibco) supplemented with 10% human AB serum, 2 mM L-glutamine (Gibco), 1% penicillin / streptomycin (Gibco), and 100 μg / mL of the peptide SmD1 78-92 (HLA-DRB1:0301), SmB / B’ 7-21 (HLA-DRB1:0301), SmB / B’ 1-15 (HLA-DRB1:1501) or SmB / B’ 58-72 (HLA-DRB1:1501)(Mimotopes) and co-cultured with 100,000 HLA-matched mature dendritic cells. To determine the efficacy of Sm-TCR-transduced Tregs, 10 5 PBMCs were cultured with 10 3 Sm-TCR-transduced Tregs or 10 4 control polyclonal Tregs. Replicate wells were seeded and co-cultured for 5 days in a 5% CO2, 37 °C incubator.

[0216] <0,000907>Flow cytometry After 5 days of co-culture, cells were harvested and stained with a custom dCODE Dextramer-PE according to the manufacturer's (Immudex) instructions. Cells were further stained with anti-human CD4 APC (eBioscience), anti-human CD8 Alexa Fluor 488 (Biolegend), and propidium iodide (PI) (Sigma). CD8− cells, PI− cells, CD4+ cells, and CTVlow cells were sorted using a FACS Aria Fusion flow cytometer (BD), counted by trypan blue staining on a hemocytometer, and immediately sent for 10× sequencing.

[0217] 10× sequencing For V(D)J / Dextramer enrichment, FACS-prepared cells were resuspended at a concentration of 700–1200 cells per 1 μL to create a cDNA library for single-cell whole-transcriptome sequencing. These cells were then loaded into a Chromium Controller (10× Genomics) according to the manufacturer's protocol for the Chromium Single Cell Reagent Kit, which included the Chromium V(D)J human T cell enrichment kit and the Chromium Single Cell Feature Barcode Library Kit (all 10× Genomics). The target cell yield was set at 10,000 cells. The single-cell cDNA library was sequenced on an Illumina NextSeq Sequencer using 150 bp paired-end (V(D)J library) or single-end (transcriptome) reads. Whole-transcriptome data, along with the V(D)J paired reads, were processed using Cell Ranger Version 3.1 (10× Genomics) and the Seurat R Package. After data processing, the data was visualized using Loupe Cell Browser and Loupe VDJ Browser (10× Genomics), and cloned TCR sequences were selected for further analysis.

[0218] Plasmid design A lentiviral plasmid backbone (Creative Biolabs) was used, containing the EF1 alpha promoter at the 5' end of the EcoRI restriction site and the woodchuck hepatitis virus post-transcriptional regulatory element (WPRE) at the 3' end of the XbaI restriction site. These elements were flanked by a 5'LTR (long terminal repeat) sequence and a 3'LTR sequence, respectively. The TCR transgene sequence was designed using SnapGene (GSL Biotech LLC) to contain the 5'EcoRI restriction site, followed by the TCR beta chain, spaced by a P2A ribosome skipping sequence, followed by the TCR alpha chain, spaced by a T2A ribosome skipping sequence, followed by an enhanced green fluorescent protein (eGFP) sequence, and finally the 3'XbaI restriction site. Using the GeneOptimiser tool (Invitrogen), the TCR alpha and beta chains were subjected to minimal mouse-like transformation (Sommermeyer, J Immunol, 2010), cysteine ​​transformation (Cohen, Cancer Res, 2007), and codon and gene optimization for human (Homo sapiens). A TCR trans-gene cassette was synthesized using GeneArt (Invitrogen) and ligated to the lentiviral scaffold at the EcoRI and XbaI restriction sites.

[0219] Virus creation Lentiviral particles encoding the TCR were prepared by transient transfection of HEK 293T cells using Lipofectamine 3000 reagent, according to the manufacturer's (Life Technologies) instructions. The lentiviral vector pLenti-TCR, containing an alpha-beta TCR insert, eGFP, and the LentiArt viral packaging plasmids pHelp1, pHelp2, and pHelp3 (Creative Biolabs), was mixed in a 3:1:1:1 ratio (pLenti-TCR:pHelp1:pHelp2:pHelp3) and transfected at a rate of 25.9 μg per 55 cm² Petri dish. The supernatant was collected 24 and 52 hours after transfection, filtered through a 0.45 μm PVDF Millex-HV filter, and concentrated with Lenti-X Concentrator reagent, according to the manufacturer's (Clontech) instructions. The virus particles were resuspended in PBS and frozen in aliquots at -80°C until use. The HIV-1 Gag p24 antigen concentration was measured using the HIV-1 p24 Antigen ELISA kit (Abcam).

[0220] Virus-induced transduction To transduce primary human naive regulatory T cells (Tregs), the isolated Tregs were placed in RPMI-1640 (Gibco) refilled with 10% human type AB serum, 2 mM L-glutamine (Gibco), and 50 μM 2-mercaptoethanol, and incubated with T Cell Activator aCD2, aCD3, aCD28 Microbeads (Miltenyi Biotech) in a 1:2 bead-to-cell ratio and 300 IU of IL-2 (Stemcell) per mL for 48 hours. Lentiviral particles (400 ng of HIV-1 p24 Gag per cell) were administered at 32°C and 1,500 × g for 2 hours at a rate of 5 ug / cm³. 2The cells were spinocured into 24-well plates coated with RetroNectin (Takara Bio Inc.). Activated Treg cells (0.25 x 10⁶ cells per well) were then added. 6 The sample was added and spinocured at 32°C and 1,500 × g for 2 hours, then placed in a 5% CO2 incubator at 37°C for 48 hours.

[0221] Expansion and phenotypic analysis of transgenic Tregs Forty-eight hours after transduction and every fourteen hours thereafter, 50% of the cell culture medium was aspirated and replaced with fresh RPMI-1640 supplemented with 10% human type AB serum, 2 mM L-glutamine, 50 μM 2-mercaptoethanol, 1% penicillin / streptomycin, and 300 IU IL-2 per mL. The cell cultures were expanded at ≥80% confluence. After two weeks of expansion, Treg cells were analyzed on an LSR Fortessa ×20 flow cytometer (BD) after staining with Live / Dead Fixable Near-IR (Invitrogen), CD4-BUV496 (BD), CD25-BUV395 (BD), CD127-PE CF594 (BD), TCRVbx-PE (where x is an antibody specific to a particular TCR clone), FoxP3-BV421 (Biolegend), Latency Associated Peptide (LAP)-APC (eBioscience), GARP-BV786 (BD), Helios-PECy7 (Biolegend), IL10-BV650 (BD), IFN-Gamma-BB700 (BD), IL17A-APCR700 (BD), and IL2-BV711 (BD) to assess phenotypic stability.

[0222] [Example 2] Identification of Sm-derived peptides that bind to HLA-DR15 The identification of Sm-derived peptides that bind to HLA-DR15 is shown in Figure 1. Specifically, in Figure 1A, the Sm-derived peptides that bind to HLA-DR15 (12 amino acids, 15-mer duplication) were identified using the MHC class II Proimmune REVEAL assay. The assay results are presented as binding percentages compared to the positive control at 0 hours (blue bars) and 24 hours (red bars). Based on these scores, a stability index (red bars) was derived for each peptide. The positive control score was 100% at 0 hours and 6.4% at 24 hours, with a stability index of 6.0. Figures 1B-D show the binding scores and stability indices for SmB / B'-derived peptides, SmD1-derived peptides, and SmD3-derived peptides.

[0223] [Example 3] Human T cell reactivity to the top 3 HLA-DR15-restricted Sm peptides The human T cell reactivity to the top three HLA-DR15-restricted Sm peptides is shown in Figure 2. More specifically, as shown in Figure 2A, to determine whether HLA-DR15-restricted Sm peptides can induce T cell reactivity, the top three highly binding peptides—SmB / B':1-15, SmB / B':58-72, or SmD3:43-57—were cultured with human CD4+ T cells. T cell reactivity was determined by a cell proliferation assay using Cell Trace Violet (CTV).

[0224] Figure 2B shows a representative FACS plot illustrating the percentage of CTVlo CD4+ T cells. CD4+ T cells cultured with SmB / B':1-15 and SmB / B':58-72 showed a stronger proliferation response compared to CD4+ T cells cultured without the peptide and with SmD3:43-57.

[0225] [Example 4] Human T cell reactivity to HLA-DR3-restricted Sm peptide The reactivity of human T cells to HLA-DR3-restricted Sm peptides is shown in Figure 3. More specifically, as shown in Figure 3A, in order to determine whether human T cell reactivity to HLA-DR3-restricted Sm peptides could be measured, the inventors investigated the SmD1:78-92 peptides already identified by Deshmukh US et al., 2011. The top peptides on computer (IEDB (Immune Epitope Database)) predicted binding to the SmB / B' and SmB / B':7-21 peptides. These peptides were cultured individually with CD4+ T cells in a co-culture cell proliferation assay, and their reactivity was evaluated using the Cell Trace Violet (CTV) dilution method.

[0226] Figure 3B shows a representative FACS plot illustrating the percentage of CTVlo CD4+ T cells. A strong proliferation response was observed only in CD4+ T cells cultured with SmD1:78-92.

[0227] [Example 5] Modified lentivirus construct Figure 4 shows a map of the modified lentiviral constructs used to transduce the TCR into human regulatory T cells. The relative positions of the alpha and beta chains, P2A, T2A, and the introduced mouse mutations and cysteine ​​are shown.

[0228] [Example 6] Transduction of TCR into human Treg Transduction of the TCR into human Tregs is shown in Figure 5. More specifically, Figure 5A shows the time series of the TCR transduction protocol. First, human Tregs (CD4+ CD25hi CD127lo) were isolated by flow cytometry, then stimulated with anti-CD3 / anti-CD28 beads, followed by TCR transduction with lentivirus on day 2. After two rounds of restimulation (days 9 and 26), Tregs were collected and analyzed for TCR expression and Treg phenotype stability.

[0229] Figure 5B shows that analysis of TCR expression in human Tregs on day 20 indicates that more than 90% of the transduced Tregs express the GFP tag.

[0230] Intracellular cytokine staining for the pro-inflammatory cytokine IFN-γ is shown in Figure 5C, which reveals that transduced Treg cells do not switch to pro-inflammatory cells (staining for IL-17A was also negative).

[0231] The results in Figure 5D demonstrate that the transduced TCR is functional. To determine whether this protocol results in a functional TCR, the inventors transduced Jurkat T cell lines and stimulated the transduced Jurkat T cells with an antigen-presenting cell line (HLA-DR15+ B-LCL) pulsed with a TCR cognitive peptide. This resulted in the inventors demonstrating upregulation of CD69, an early activation marker, after stimulation, supporting the conclusion that the transduced TCR using this protocol results in a functional TCR on the surface of T cells.

[0232] [Example 7] Transduction of Sm-TCR is a more potent inhibitor of Sm-specific Tconv cell reactivity. HLA-DR15+ PBMCs were stimulated with the dominant Sm peptide SmB / B':58-72 and co-cultured with polyclonal Tregs or Sm-TCR transduced Tregs (the Tregs were transduced using the lentiviral vector shown in Figure 4, and the TCRs corresponded to HLA-DR15 TCR#1, possessing the CDR3α sequence of CALSSYGNKLVF (SEQ ID NO: 8) and the CDR3β sequence of CASSSLSGSSYEQYF (SEQ ID NO: 11)). An in vitro T cell proliferation assay was performed. Proliferation of pro-inflammatory conventional T cells (Tconv) was evaluated by the Cell Trace Violet (CTV) dilution method. Sm-TCR transduced Tregs more strongly inhibited Tconv cell proliferation, at 12.1% compared to 22.4%.

[0233] The counting of proliferating cells showed that in the polyclonal group, more Sm-specific Tconv cells were seen compared to the Sm-TCR group (8659 compared to 2053).

[0234] The mean fluorescence intensity (MFI) of Sm-reactive Tconv cells reflects the number of cell divisions. The lower the MFI of Tconv cells, the more cell divisions they have undergone. The MFI of Sm-reactive Tconv cells within the group treated with polyclonal Treg was lower (89.1 compared to 271) than that within the Sm-TCR Treg group. The data are shown in Figure 6. Error bars are SEM. *** P < 0.001 by t-test.

[0235] These data support that Treg transduced with Sm-specific TCR more potently suppresses the autoreactive inflammation-promoting response to Sm antigen. The inventors believe that these data provide a proof of concept that Treg transduced with Sm-specific TCR is better in suppressing the autoreactive T cell response to Sm self-antigen and requires fewer Treg to bring about antigen-specific suppression. In addition, the ability to use fewer Treg reduces the risk of side effects in patients receiving Treg.

[0236] [Example 8] Stimulation with the peptide SmB / B’: 1-15 or the peptide SmB / B’: 58-72 causes the expansion of regulatory T cells CD4+ T cells derived from DR15 homozygous donors were co-cultured with autologous monocyte-derived dendritic cells pulsed with peptide SmB / B':1-15 or peptide SmB / B':58-72, or with no peptide (control). After 8 days, the CD4+ cells were subjected to single-cell sequencing using the 10× Genomics Human Immune Repertoire Single Cell Profiling Kit. Cell clusters with high expression of Foxp3 and TIGIT, as well as clusters with high expression of CD52 and LTB, were labeled as Tregs.

[0237] The results shown in Figure 7 support the conclusion that stimulation with the peptide SmB / B':1-15 or the peptide SmB / B':58-72 results in selective expansion of Tregs, as evidenced by a significant increase in the proportion of Tregs after peptide stimulation. The data shown are mean ± SD for two independent experiments. *** P<0.001 was observed when comparing the peptide-free group to the peptide-free group using a one-way ANOVA with Tukey's post-hoc test.

[0238] [Example 9] Dominant HLA-DR15-constrained Sm-TCRs bind to HLA-DR15 Dextramers that exhibit high affinity and SmB / B': 58-72. To determine the binding affinity of dominant Sm-specific TCRs, the inventors performed a Dextramer-based flow cytometry binding assay. The Dextramer contains 10 peptide-MHC complexes integrally bound to a dextran backbone. These fluorescently labeled Dextramers enable the detection of Sm-specific T cells and can be used to determine the relative affinity of Sm-specific TCRs.

[0239] First, using a custom lentiviral vector, the inventors cloned the top three TCRs obtained in Example 8 into the Jurkat T cell line. These TCRs are identified as TCR1 to TCR3 in Table 1.

[0240] Next, the inventors measured the mean fluorescence intensity (MFI) by flow cytometry and represented the data using a scatchard plot. The results are shown in Figure 8. The lower the concentration at which the MFI plateaus, the lower the dissociation constant (Kd), which indicates high affinity. The inventors found that the top-ranking Sm TCR bound with the highest affinity compared to the second and third-ranking Sm-specific TCRs. This result is important to justify this novel method of identifying high-affinity TCRs for disease treatment using high-throughput single-cell TCR sequencing.

[0241] [Example 10] Sm-TCR Treg suppresses anti-Sm specific pro-inflammatory response and restores tolerance. To determine the efficacy of Sm-Tregs in suppressing anti-Sm specific pro-inflammatory responses, the inventors created Sm-Tregs using Tregs derived from SLE patients and examined them in in vitro co-cultures. The inventors compared patient anti-Sm responses with or without Tregs or with polyclonal Tregs (pTregs).

[0242] First, the inventors used a proliferation assay to measure the effect of Sm-Tregs on the expansion of pro-inflammatory Sm-specific conventional T cells (Tconv). The results (Figure 9A) show that in the presence of Sm-Tregs, the number of Tregs significantly increases compared to the number of Sm-specific Tconv. This result means that Sm-Tregs strongly suppress the expansion of Sm-specific Tconv cells. Furthermore, the ratio of autoantigen-specific Tregs to Tconv being >10 is consistent with the inventors' other data indicating that healthy individuals have 10 times more autoantigen-specific Tregs than Tconv.

[0243] Next, the inventors measured cytokine production and found that in the presence of Sm-Tregs, an anti-inflammatory response, i.e., high IL-10 and low IFN-g / IL-17A, was dominant (similar to that in healthy individuals), whereas in the absence of Tregs or the presence of pTregs alone, a pro-inflammatory response was dominant, i.e., low IL-10 and high IFN-g / IL-17A (predicted in patients with autoimmune diseases). These data (shown in Figures 9B-9D) support the idea that Sm-Tregs have the ability to correct abnormal immune responses and restore tolerance to target autoepitopes. The results were obtained using samples from four SLE patients, comparing the Treg-free group and the pTreg group, with mean ± SEM values. * P<0.05, ** This is expressed as P < 0.01.

[0244] [Example 11] HLA-DR15-restricted Sm-Treg stops the progression of nephritis. To support the effectiveness of Sm-Treg in halting disease progression, the inventors devised a novel humanized model of lupus nephritis.

[0245] In this model, adoptive transfer of PBMCs from patients with lupus nephritis to immunocompromised NSGMHCnull mice resulted in the development of functional kidney injury (measured by increased urinary protein) and intrasegmental glomerular necrosis (measured by histological staining of kidney sections). At 3 weeks, when functional kidney injury occurred, the mice were administered either without Tregs, with polyclonal Tregs (pTregs), or with Sm-Tregs. Figure 10A shows an outline of the experimental protocol.

[0246] Mice that were not treated with Tregs or those treated with pTregs progressed to severe nephritis (i.e., high levels of proteinuria and necrosis of >50% of glomeruli), while nephritis mice treated with Sm-Tregs did not show further disease progression (see Figures 10B-10C). Results are expressed as mean ± SEM values ​​from five SLE patient samples. ***The p-value was < 0.001 when compared to the group without Treg and the group with pTreg.

[0247] [Example 12] HLA-DR3-restricted Sm-Treg stops the progression of nephritis. Similar to the method outlined in Example 11, the inventors determined whether HLA-DR3-restricted Sm-Treg also possesses therapeutic efficacy.

[0248] As shown in Figure 11, HLA-DR3-restricted Sm-Treg cells were shown to suppress the anti-Sm pro-inflammatory cytokine response and halt the progression of lupus nephritis. Briefly, PBMCs derived from HLA-DR3+ / anti-Sm+ SLE patients with lupus nephritis were co-cultured with dominant HLA-DR3-restricted T cell epitopes (SmD1:78-92) and transduced Treg cells (Sm-Treg) that were either Treg-less, polyclonal Tregs (pTreg), or HLA-DR3-restricted TCRs (HLA-DR3 TCR1, identified in Table 2). Cytokine responses were measured on day 8.

[0249] NSGMHC Null mice were inoculated with PBMCs derived from SLE patients with lupus nephritis who were positive for anti-Sm antibodies and HLA-DR3+. At week 3, the time of functional renal injury (measured by increased proteinuria), the mice were administered either no Treg, polyclonal Tregs (pTregs), or HLA-DR3-restricted Sm-Tregs (transduced to HLA-DR3 TCR1).

[0250] conclusion In summary, the results in this embodiment support the inventors' identification of highly reactive T cell receptors specific to Smith (Sm) antigen, a key target autoantigen in lupus. Furthermore, it is demonstrated that these T cell receptors can be transduced into human Treg cells that can be used to specifically suppress autoimmunity against Sm antigen.

[0251] The inventors have demonstrated that both HLA-DR15-restricted SmTCR and HLA-DR3-restricted SmTCR are therapeutically effective and can be used to halt the progression of autoimmune diseases.

[0252] Clinically, the present invention enables a novel antigen-specific regulatory cell-based treatment in which Sm antigen-specific autoregulatory T cells are adopted and transferred into lupus patients to suppress the underlying disease causes and halt disease progression.

[0253] Current treatments for lupus are nonspecific and cause toxic side effects. Current standard treatment for lupus involves the use of corticosteroids, which themselves cause serious side effects including diabetes and osteoporosis, as well as nonspecific immunosuppressants, which have adverse side effects and poor efficacy. In the last 50 years, the only newly approved add-on treatment for lupus is belimumab, an anti-BAFF antibody. However, belimumab currently exhibits limited clinical efficacy, and its contraindications include active glomerulonephritis and central nervous system symptoms. Therefore, an increased risk of irreversible organ damage over time is a common outcome associated with existing treatments, resulting in a standardized mortality rate approximately 2-3 times higher than in the healthy community. Thus, the need for better treatments for lupus remains clear and unmet.

[0254] The treatments described herein, namely the use of Sm-specific Tregs and peptides disclosed herein, are expected to enhance the potency of Tregs and induce enhanced immunosuppression while maintaining minimal suppressive effects on protective immunity. The use of Sm-specific Tregs (and peptides that activate / enhance such Tregs) is expected to induce immune tolerance to autoantigens beyond Smith proteins, as immunosuppressive cells (e.g., Tregs and myeloid-derived suppressor cells) mobilized as a result of Sm-specific Treg therapy will exhibit further non-antigen-specific immunosuppressive capabilities, thereby creating a tolerance environment for multiple autoantigens.

[0255] It is understood that the present invention, as disclosed and defined herein, extends to all alternative combinations of two or more individual features mentioned or evident from the text or drawings. All of these different combinations constitute diverse alternative embodiments of the present invention.

Claims

1. A binding protein comprising a T cell receptor (TCR) α-chain variable (Vα or V-alpha) domain and a TCR β-chain variable (Vβ or V-beta) domain, which is capable of binding to a complex of a Smith protein fragment and an HLA-DR15 molecule. A fragment of Smith protein capable of forming a complex with the HLA-DR15 molecule contains an amino acid sequence of 5, 7, 8, 9, or 10 or more consecutive amino acid residues of SEQ ID NO: 1 or SEQ ID NO: 2, (1) The TCRα chain variable (Vα or V-alpha) domain includes a complementarity-determining region (CDR) 1 containing the sequence specified in SEQ ID NO: 6; CDR 2 containing the sequence specified in SEQ ID NO: 7; and CDR 3 containing the sequence specified in SEQ ID NO: 8; and the TCRβ chain variable (Vβ or V-beta) domain includes a CDR 1 containing the sequence specified in SEQ ID NO: 9; CDR 2 containing the sequence specified in SEQ ID NO: 10; and CDR 3 containing the sequence specified in SEQ ID NO: 11; (2) The TCRα chain variable (Vα or V-alpha) domain includes CDR1 containing the sequence specified in SEQ ID NO: 18; CDR2 containing the sequence specified in SEQ ID NO: 19; and CDR3 containing the sequence specified in SEQ ID NO: 20; and the TCRβ chain variable (Vβ or V-beta) domain includes CDR1 containing the sequence specified in SEQ ID NO: 21; CDR2 containing the sequence specified in SEQ ID NO: 22; and CDR3 containing the sequence specified in SEQ ID NO: 23; or (3) The TCRα chain variable (Vα or V-alpha) domain includes CDR1 containing the sequence specified in SEQ ID NO: 30; CDR2 containing the sequence specified in SEQ ID NO: 31; and CDR3 containing the sequence specified in SEQ ID NO: 32; and the TCRβ chain variable (Vβ or V-beta) domain includes CDR1 containing the sequence specified in SEQ ID NO: 33; CDR2 containing the sequence specified in SEQ ID NO: 34; and CDR3 containing the sequence specified in SEQ ID NO: 35; Binding proteins.

2. A binding protein comprising a T cell receptor (TCR) α-chain variable (Vα or V-alpha) domain and a TCR β-chain variable (Vβ or V-beta) domain, which is capable of binding to a complex of a Smith protein fragment and an HLA-DR15 molecule. A fragment of Smith protein capable of forming a complex with the HLA-DR15 molecule contains an amino acid sequence of 5, 7, 8, 9, or 10 or more consecutive amino acid residues of SEQ ID NO: 1 or SEQ ID NO: 2, The TCRα chain variable (Vα or V-alpha) domain comprises a complementation-determining region (CDR) 1 containing the sequence specified in SEQ ID NO: 6; CDR 2 containing the sequence specified in SEQ ID NO: 7; and CDR 3 containing the sequence specified in SEQ ID NO: 8; and the TCRβ chain variable (Vβ or V-beta) domain comprises a CDR 1 containing the sequence specified in SEQ ID NO: 9; CDR 2 containing the sequence specified in SEQ ID NO: 10; and CDR 3 containing the sequence specified in SEQ ID NO: 11; and is a binding protein.

3. The HLA-DR15 molecule is HLA-DRA ＊ 01:01 molecule and HLA-DRB1 ＊ A binding protein according to claim 1 or 2, which is a 15:01 molecule.

4. A binding protein according to any one of claims 1 to 3, which binds to a peptide consisting of 5, 7, 8, or 9 consecutive amino acid residues of the sequence specified in either SEQ ID NO: 3 or 4.

5. The binding protein according to any one of claims 1 to 4, wherein the Smith protein fragment consists of the amino acid sequence of SEQ ID NO: 1 or SEQ ID NO:

2.

6. (1) The TCRα chain comprises or consists of the amino acid sequence specified in SEQ ID NO: 501; and / or the TCRβ chain comprises or consists of the amino acid sequence specified in SEQ ID NO: 502 (2) The TCRα chain contains or is derived from the amino acid sequence specified in SEQ ID NO: 503; and / or the TCRβ chain contains or is derived from the amino acid sequence specified in SEQ ID NO: 504, (3) The binding protein according to any one of claims 1 to 5, wherein the TCRα chain comprises or is derived from the amino acid sequence specified in SEQ ID NO: 505; and / or the TCRβ chain comprises or is derived from the amino acid sequence specified in SEQ ID NO:

506.

7. A binding protein comprising a T cell receptor (TCR) α chain and a TCRβ chain, wherein the TCRα chain comprises the amino acid sequence specified in SEQ ID NO: 501, and the TCRβ chain comprises the amino acid sequence specified in SEQ ID NO: 502, and the binding protein is capable of binding to a complex of a Smith protein fragment and an HLA-DR15 molecule, and the Smith protein fragment capable of forming a complex with the HLA-DR15 molecule comprises an amino acid sequence of 5, 7, 8, 9, or 10 or more consecutive amino acid residues of SEQ ID NO: 1 or SEQ ID NO:

2.

8. The binding protein according to any one of claims 1 to 7, wherein the TCRα chain and the TCRβ chain are modified to include cysteine ​​residues that enable the formation of further interchain disulfide bonds.

9. The binding protein according to claim 8, wherein the Thr residue at position 181 of the TCRα chain containing the sequence described in SEQ ID NO: 511 or an equivalent residue, and the Ser residue at position 220 of the TCRβ chain containing the sequence described in SEQ ID NO: 502 or an equivalent residue, are replaced with cysteine ​​to facilitate the creation of further disulfide bonds between the TCR constant regions.

10. A peptide consisting of the amino acid sequence specified in any one of SEQ ID NOs: 1, 2, 3, and 4.

11. A nucleic acid comprising or consisting of a nucleotide sequence encoding a binding protein according to any one of claims 1 to 9, or consisting of a nucleotide sequence encoding a peptide according to claim 10.

12. A vector comprising the nucleic acid described in claim 11.

13. (i) This enables the expression of nucleotide sequences within cells, resulting in the presentation of binding proteins on the cell surface. (ii) It is a retroviral vector, or (iii) Below: (a) EF1α (alpha) promoter; (b) 2A ribosome skipping sequence; (c) Woodchuck hepatitis virus post-transcriptional regulatory element (WPRE); (d) A configuration in which the TCRβ chain variable (Vβ or Vbeta) domain is translated before the (TCR)α chain variable (Vα or Valpha) domain; or (e) Arrangement to translate the TCRβ chain variable (Vβ or Vbeta) chain before the (TCR)α chain variable (Vα or Valpha) chain The vector according to claim 12, comprising one or more or all of the following.

14. A cell comprising the vector according to claim 12 or 13 or the nucleic acid according to claim 11.

15. A method for preparing a population of regulatory T cells for use in the treatment of systemic lupus erythematosus (SLE), wherein the regulatory T cells are obtained from a subject, and the method is: Steps to prepare a population of regulatory T cells; A step of introducing the nucleic acid according to claim 11 or the vector according to claim 12 or 13 into a population of regulatory T cells; A step that provides conditions that enable the expression of binding proteins on the surface of regulatory T cells. including, or A step of preparing a mixed T cell population or T cell population that exhibits at least one characteristic of normal T cells; A step of introducing the nucleic acid according to claim 11 or the vector according to claim 12 or 13 into a population of T cells; A step that creates conditions on the surface of T cells that enable the expression of binding proteins; The steps include isolating regulatory T cells from a mixed T cell population, or alternatively, culturing cells under conditions that promote the conversion of cells within the population into regulatory T cells; A step to selectively stabilize converted regulatory T cells. including, or A step of culturing a T cell population for a sufficient amount of time in the presence of the peptide described in claim 10, under conditions that allow for the expansion of a subpopulation of cells activated by the peptide; The step of selectively isolating regulatory T cells from a mixed cell population or converting T cells to regulatory T cells if the T cell population includes a mixed cell population or includes normal T cells. A method comprising, thereby, preparing a population of regulatory T cells for use in the treatment of SLE.

16. The method according to claim 15, wherein the T cells are derived from a biological sample derived from a subject having SLE or from an allogeneic donor not having SLE.

17. The method according to claim 15, wherein the T cells are derived from a subject requiring treatment for SLE.

18. The method according to claim 15, wherein the T cells are derived from stem cells, and optionally the stem cells are induced pluripotent stem cells (iPSCs) or embryonic stem cells.

19. A composition comprising a binding protein according to any one of claims 1 to 9, a peptide according to claim 10, a cell according to claim 14, a nucleic acid according to claim 11, or a vector according to claim 12 or 13, and a pharmaceutically acceptable carrier, diluent, or excipient.

20. A composition for use in a method of treating or preventing a lupus condition associated with an abnormal, undesirable, or otherwise inappropriate immune response to Smith protein in a subject, wherein the composition is A step of preparing a population of T cells that exhibit at least one characteristic of regulatory T cells; The steps of introducing the nucleic acid described in claim 11 or the vector described in claim 12 or 13 into a population of T cells; and A step that provides conditions on the surface of T cells that enable the expression of binding proteins. The process includes T cells that express binding proteins on their surface, obtained by a process including the following: The method comprises the step of administering T cells expressing binding proteins on their surfaces, thereby treating or preventing a lupus condition in a subject, comprising a composition.

21. Use of a binding protein according to any one of claims 1 to 9, a peptide according to claim 10, a cell according to claim 14, a nucleic acid according to claim 11, or a vector according to claim 12 or 13 in the manufacture of a pharmaceutical for treating or preventing a lupus condition in a subject, wherein the lupus condition is associated with an abnormal, undesirable, or otherwise inappropriate immune response to Smith protein.

22. A composition comprising a binding protein according to any one of claims 1 to 9, a peptide according to claim 10, a cell according to claim 14, a nucleic acid according to claim 11, or a vector according to claim 12 or 13, for use in treating or preventing a lupus condition associated with an abnormal, undesirable, or otherwise inappropriate immune response to Smith protein in a subject.

23. The composition according to claim 20 or 22, wherein the lupus condition associated with an abnormal, undesirable, or otherwise inappropriate immune response to Smith protein is systemic lupus erythematosus (SLE) or lupus nephritis (LN).

24. The use according to claim 21, wherein the lupus condition associated with an abnormal, undesirable, or otherwise inappropriate immune response to Smith protein is systemic lupus erythematosus (SLE) or lupus nephritis (LN).

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