Compositions and methods for acetylcholine receptor chimeric autoantibody receptor cells

Abstract

The present invention includes chimeric autoantibody receptors (CAARs) specific for anti-acetylcholine receptor (AChR) B cell receptors (BCRs), compositions comprising the CAARs, polynucleotides encoding the CAARs, vectors comprising polynucleotides encoding the CAARs, and recombinant cells, e.g., T cells, comprising the CAARs.

Description

[Technical field]

[0001] CROSS-REFERENCE TO RELATED APPLICATIONS This application claims priority under 35 U.S.C. § 119(e) to U.S. Provisional Application No. 62 / 847,121, filed May 13, 2019, which is incorporated by reference in its entirety. [Background technology]

[0002] 2. Background of the Invention Myasthenia gravis (MG) is one of the most common autoantibody-mediated diseases in humans, affecting a total of 25,000–50,000 patients with an incidence of 3,000 new cases per year in the United States; nearly one million patients in the United States, Europe, and Asia are estimated to have myasthenia gravis. Antibody attack of proteins expressed at the neuromuscular junction (NMJ) leads to muscle weakness, which manifests as droopy eyes, double vision, unsteady gait, slurred speech, and difficulty swallowing and breathing. Autoantibodies produced by MG patients destroy the NMJ by fixing complement or spoofing acetylcholine receptor (AChR) clusters. Formation of AChR clusters, which is essential for signaling through AChR, depends on activation of muscle-specific kinase (MuSK), a transmembrane protein. Most MG patients exhibit either anti-AChR antibodies (85%) or anti-MuSK antibodies (4%). Eleven percent of patients are classified as "seronegative," due to low titer antibodies against AChR, MuSK, or other NMJ proteins, such as LRP4.Myasthenic crisis, defined as the need for mechanical ventilation due to life-threatening weakness of the muscles that control breathing, occurs in 10-20% of patients with MG; the overall mortality rate from myasthenic crisis is 4.5%.

[0003] Currently, mild MG is treated with acetylcholinesterase inhibitors to block the breakdown of acetylcholine. Moderate to severe MG is treated with antiproliferative agents such as prednisone, mycophenolate or azathioprine, complement inhibitors, and in more advanced disease, rituximab, a strategy that may be associated with infections and other side effects due to immunosuppression.

[0004] There is an urgent need in the art to achieve more specific and effective treatments for myasthenia gravis. The present invention addresses this need. Summary of the Invention

[0005] Provided is a polynucleotide encoding a chimeric autoantibody receptor (CAAR), wherein the CAAR comprises an extracellular domain comprising an acetylcholine receptor (AChR) autoantigen or a fragment thereof, and optionally a transmembrane domain, an intracellular domain of a costimulatory molecule, and / or a signal transduction domain.In some embodiments, the AChR autoantigen or a fragment thereof is derived from the α subunit of AChR.In some embodiments, the AChR autoantigen or a fragment thereof is encoded by a nucleic acid sequence comprising the nucleic acid sequence selected from the group consisting of SEQ ID NO: 3, 5, 7, 22, 23, 29, 33, and 42. In some other embodiments, the AChR autoantigen or fragment thereof is encoded by a nucleic acid sequence comprising a nucleic acid sequence having at least 60%, at least 65%, at least 70%, at least 75%, at least 80%, at least 81%, at least 82%, at least 83%, at least 84%, at least 85%, at least 86%, at least 87%, at least 88%, at least 89%, at least 90%, at least 91%, at least 92%, at least 93%, at least 94%, at least 95%, at least 96%, at least 97%, at least 98%, or at least 99% sequence identity to a nucleic acid sequence selected from the group consisting of SEQ ID NOs: 3, 5, 7, 22, 23, 29, 33, and 42. In some embodiments, the AChR autoantigen or fragment thereof comprises an amino acid sequence selected from the group consisting of SEQ ID NOs: 13, 15, 17, 26, 27, 31, 35, and 44.In yet other embodiments, the AChR autoantigen or fragment thereof comprises an amino acid sequence having at least 60%, at least 65%, at least 70%, at least 75%, at least 80%, at least 81%, at least 82%, at least 83%, at least 84%, at least 85%, at least 86%, at least 87%, at least 88%, at least 89%, at least 90%, at least 91%, at least 92%, at least 93%, at least 94%, at least 95%, at least 96%, at least 97%, at least 98%, or at least 99% sequence identity to an amino acid sequence selected from the group consisting of SEQ ID NOs: 13, 15, 17, 26, 27, 31, 35, and 44.

[0006] In some embodiments, the transmembrane domain comprises a CD8α transmembrane domain. In some embodiments, the CD8α transmembrane domain is encoded by a nucleic acid sequence comprising SEQ ID NO: 9. In some other embodiments, the CD8α transmembrane domain comprises the amino acid sequence of SEQ ID NO: 19.

[0007] In some embodiments, the intracellular domain of the costimulatory molecule comprises a 4-1BB intracellular domain. In some embodiments, the 4-1BB intracellular domain is encoded by a nucleic acid sequence comprising SEQ ID NO: 10 or 16. In some embodiments, the 4-1BB intracellular domain comprises the amino acid sequence of SEQ ID NO: 20. In some other embodiments, the signaling domain comprises a CD3 zeta signaling domain. In some embodiments, the CD3 zeta signaling domain is encoded by a nucleic acid sequence comprising SEQ ID NO: 24 or SEQ ID NO: 53. In still other embodiments, the CD3 zeta signaling domain comprises the amino acid sequence of SEQ ID NO: 38.

[0008] In some embodiments, the CAAR is encoded by a nucleic acid sequence comprising a nucleic acid sequence selected from the group consisting of SEQ ID NO: 1, 6, 21, 28, 32, 36, 41, 45, 47, 48, 49, 50, 51, and 52. In some other embodiments, the CAAR comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 11, 25, 30, 34, 39, 43, and 46. In some embodiments, the CAAR further comprises a hinge. In some embodiments, the hinge is encoded by a nucleic acid sequence comprising SEQ ID NO: 8. In still other embodiments, the hinge comprises the amino acid sequence of SEQ ID NO: 18.

[0009] In some embodiments, the CAAR comprises an acetylcholine receptor (AChR) autoantigen or a fragment thereof, a killer immunoglobulin-like receptor (KIR) transmembrane domain, and a KIR cytoplasmic domain.

[0010] Provided is a vector, comprising any one of the polynucleotides of the previous aspect.In some embodiments, the vector is a lentivirus vector.In some other embodiments, the vector is an RNA vector.In some embodiments, the vector comprises an inducible promoter operably linked to the polynucleotide encoding CAAR.

[0011] Provided is a chimeric autoantibody receptor (CAAR), comprising an extracellular domain comprising an acetylcholine receptor (AChR) autoantigen or a fragment thereof, and optionally a transmembrane domain, an intracellular domain of a costimulatory molecule, and / or a signal transduction domain. In some embodiments, the AChR autoantigen or a fragment thereof is derived from the α subunit of AChR. In some other embodiments, the AChR autoantigen or a fragment thereof is encoded by a nucleic acid sequence selected from the group consisting of SEQ ID NO: 3, 5, 7, 22, 23, 29, 33, and 42. In still other embodiments, the AChR autoantigen or fragment thereof is encoded by a nucleic acid sequence having at least 60%, at least 65%, at least 70%, at least 75%, at least 80%, at least 81%, at least 82%, at least 83%, at least 84%, at least 85%, at least 86%, at least 87%, at least 88%, at least 89%, at least 90%, at least 91%, at least 92%, at least 93%, at least 94%, at least 95%, at least 96%, at least 97%, at least 98%, or at least 99% sequence identity to a nucleic acid sequence selected from the group consisting of SEQ ID NOs: 3, 5, 7, 22, 23, 29, 33, and 42. In some embodiments, the AChR autoantigen or fragment thereof comprises an amino acid sequence selected from the group consisting of SEQ ID NOs: 13, 15, 17, 26, 27, 31, 35, and 44. In some embodiments, the AChR autoantigen or fragment thereof comprises an amino acid sequence having at least 60%, at least 65%, at least 70%, at least 75%, at least 80%, at least 81%, at least 82%, at least 83%, at least 84%, at least 85%, at least 86%, at least 87%, at least 88%, at least 89%, at least 90%, at least 91%, at least 92%, at least 93%, at least 94%, at least 95%, at least 96%, at least 97%, at least 98%, or at least 99% sequence identity to an amino acid sequence selected from the group consisting of SEQ ID NOs: 13, 15, 17, 26, 27, 31, 35, and 44.

[0012] In some embodiments, the transmembrane domain comprises a CD8α transmembrane domain. In some other embodiments, the CD8α transmembrane domain is encoded by a nucleic acid sequence comprising SEQ ID NO: 9. In some embodiments, the CD8α transmembrane domain comprises the amino acid sequence of SEQ ID NO: 19. In some embodiments, the intracellular domain of the costimulatory molecule comprises a 4-1BB intracellular domain. In some other embodiments, the 4-1BB intracellular domain is encoded by a nucleic acid sequence comprising SEQ ID NO: 10 or 16. In still other embodiments, the 4-1BB intracellular domain comprises the amino acid sequence of SEQ ID NO: 20. In some embodiments, the signaling domain comprises a CD3ζ signaling domain. In some embodiments, the CD3ζ signaling domain is encoded by a nucleic acid sequence comprising SEQ ID NO: 24 or SEQ ID NO: 53. In some other embodiments, the CD3ζ signaling domain comprises the amino acid sequence of SEQ ID NO: 38.

[0013] In some embodiments, the CAAR is encoded by a nucleic acid sequence selected from the group consisting of SEQ ID NOs: 1, 6, 21, 28, 32, 36, 41, 45, 47, 48, 49, 50, 51, and 52. In still other embodiments, the CAAR comprises an amino acid sequence selected from the group consisting of SEQ ID NOs: 11, 25, 30, 34, 39, 43, and 46. In some embodiments, the CAAR comprises an extracellular domain comprising an acetylcholine receptor (AChR) autoantigen or a fragment thereof, a killer immunoglobulin-like receptor (KIR) transmembrane domain, and a KIR cytoplasmic domain.

[0014] Provided is a genetically modified cell comprising any one of the CAARs of the above-mentioned embodiments. In some embodiments, the cell expresses CAAR and has high affinity for autoantibody-based BCR on B cells. In some other embodiments, the cell expresses CAAR and induces the death of B cells that express autoantibodies or B cells that can mature into antibody-secreting cells. In some embodiments, the cell expresses CAAR and has limited toxicity to healthy cells. In some embodiments, the cell is selected from the group consisting of helper T cells, cytotoxic T cells, memory T cells, regulatory T cells, γδ T cells, natural killer cells, cytokine-induced killer cells, cell lines thereof, T memory stem cells, T cells derived from pluripotent stem cells, and other effector cells.

[0015] A genetically modified cell is provided, comprising: (a) a chimeric autoantibody receptor of any one of the preceding aspects; and (b) DAP12. In some embodiments, the cell comprises a polynucleotide encoding CAAR operably linked to an inducible promoter.

[0016] A pharmaceutical composition is provided comprising the polynucleotide of any one of the previous aspects, the CAAR of any one of the previous aspects, or the cell of any one of the previous aspects, and a pharma- ceutically acceptable excipient.

[0017] A method is provided for treating an autoantibody-mediated neuromuscular junction (NMJ) disease in a subject, the method comprising administering to the subject an effective amount of a genetically modified cell comprising a polynucleotide encoding a chimeric autoantibody receptor (CAAR), the polynucleotide encoding an extracellular domain comprising an AChR autoantigen or a fragment thereof, and optionally a transmembrane domain, an intracellular domain of a costimulatory molecule, and / or a signaling domain, thereby treating the autoantibody-mediated NMJ disease in the subject.

[0018] Methods are provided for preventing or reducing NMJ damage in a subject at risk for or suffering from an autoantibody-mediated neuromuscular junction (NMJ) disease, the method comprising administering to the subject an effective amount of a genetically modified cell comprising a polynucleotide encoding a chimeric autoantibody receptor (CAAR), the polynucleotide encoding an extracellular domain comprising an AChR autoantigen or a fragment thereof, and optionally a transmembrane domain, an intracellular domain of a costimulatory molecule, and / or a signaling domain, thereby preventing or reducing NMJ damage in the subject.

[0019] A method for treating an autoantibody-mediated neuromuscular junction (NMJ) disease in a subject is provided, the method comprising administering to the subject an effective amount of a genetically modified cell comprising: (a) a polynucleotide encoding a chimeric autoantibody receptor (CAAR), the polynucleotide encoding an extracellular domain comprising an AChR autoantigen or a fragment thereof, a killer immunoglobulin-like receptor (KIR) transmembrane domain, and a KIR cytoplasmic domain; and (b) a polynucleotide encoding DAP12, thereby treating the autoantibody-mediated NMJ disease in the subject.

[0020] Provided is a method for preventing or reducing NMJ damage in a subject at risk for or suffering from an autoantibody-mediated neuromuscular junction (NMJ) disease, the method comprising administering to the subject an effective amount of a genetically modified cell comprising: (a) a polynucleotide encoding a chimeric autoantibody receptor (CAAR), the polynucleotide encoding an extracellular domain comprising an AChR autoantigen or a fragment thereof, a killer immunoglobulin-like receptor (KIR) transmembrane domain, and a KIR cytoplasmic domain; and (b) a polynucleotide encoding DAP12, thereby treating the autoantibody-mediated NMJ disease in the subject.

[0021] In some embodiments, the polynucleotide is a polynucleotide of any one of the preceding embodiments. In some embodiments, the CAAR is a CAAR of any one of the preceding embodiments. In some embodiments, the autoantibody-mediated NMJ disease is myasthenia gravis (MG). In some other embodiments, the subject is a human. In some embodiments, the genetically modified cell is a T cell. In some embodiments, the modified cell targets a B cell. [The present invention 1001] A polynucleotide encoding a chimeric autoantibody receptor (CAAR), the CAAR comprising an extracellular domain comprising an acetylcholine receptor (AChR) autoantigen or a fragment thereof, and optionally a transmembrane domain, an intracellular domain of a costimulatory molecule, and / or a signaling domain. [The present invention 1002] 1001. The polynucleotide of the present invention, wherein said AChR autoantigen or a fragment thereof is derived from the alpha subunit of AChR. [The present invention 1003] The polynucleotide of the present invention 1001, wherein the AChR autoantigen or a fragment thereof is encoded by a nucleic acid sequence comprising a nucleic acid sequence selected from the group consisting of SEQ ID NO: 3, 5, 7, 22, 23, 29, 33, and 42. [The present invention 1004] The polynucleotide of the present invention 1001, wherein the AChR autoantigen or a fragment thereof is encoded by a nucleic acid sequence comprising a nucleic acid sequence having at least 60%, at least 65%, at least 70%, at least 75%, at least 80%, at least 81%, at least 82%, at least 83%, at least 84%, at least 85%, at least 86%, at least 87%, at least 88%, at least 89%, at least 90%, at least 91%, at least 92%, at least 93%, at least 94%, at least 95%, at least 96%, at least 97%, at least 98%, or at least 99% sequence identity to a nucleic acid sequence selected from the group consisting of SEQ ID NOs: 3, 5, 7, 22, 23, 29, 33, and 42. [The present invention 1005] The polynucleotide of the present invention, wherein the AChR autoantigen or a fragment thereof comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 13, 15, 17, 26, 27, 31, 35, and 44. [The present invention 1006] The polynucleotide of the present invention 1001, wherein the AChR autoantigen or a fragment thereof comprises an amino acid sequence having at least 60%, at least 65%, at least 70%, at least 75%, at least 80%, at least 81%, at least 82%, at least 83%, at least 84%, at least 85%, at least 86%, at least 87%, at least 88%, at least 89%, at least 90%, at least 91%, at least 92%, at least 93%, at least 94%, at least 95%, at least 96%, at least 97%, at least 98%, or at least 99% sequence identity to an amino acid sequence selected from the group consisting of SEQ ID NOs: 13, 15, 17, 26, 27, 31, 35, and 44. [The present invention 1007] The polynucleotide of any one of 1001 to 1006, wherein the transmembrane domain comprises a CD8α transmembrane domain. [The present invention 1008] The polynucleotide of the present invention 1007, wherein the CD8α transmembrane domain is encoded by a nucleic acid sequence comprising SEQ ID NO:9. [The present invention 1009] The polynucleotide of the present invention, wherein the CD8α transmembrane domain comprises the amino acid sequence of SEQ ID NO:19. [The present invention 1010] The polynucleotide of any of claims 1001 to 1009, wherein the intracellular domain of the costimulatory molecule comprises a 4-1BB intracellular domain. [The present invention 1011] The polynucleotide of the present invention 1010, wherein the 4-1BB intracellular domain is encoded by a nucleic acid sequence comprising SEQ ID NO: 10 or 16. [The present invention 1012] The polynucleotide of the present invention, wherein the 4-1BB intracellular domain comprises the amino acid sequence of SEQ ID NO:20. [The present invention 1013] The polynucleotide of any one of 1001 to 1012, wherein the signaling domain comprises a CD3ζ signaling domain. [The present invention 1014] The polynucleotide of the present invention, wherein the CD3 zeta signaling domain is encoded by a nucleic acid sequence comprising SEQ ID NO: 24 or SEQ ID NO: 53. [The present invention 1015] The polynucleotide of the present invention, wherein the CD3 zeta signaling domain comprises the amino acid sequence of SEQ ID NO:38. [The present invention 1016] Any of the polynucleotides of 1001 to 1015, wherein the CAAR is encoded by a nucleic acid sequence comprising a nucleic acid sequence selected from the group consisting of SEQ ID NOs: 1, 6, 21, 28, 32, 36, 41, 45, 47, 48, 49, 50, 51, and 52. [The present invention 1017] The polynucleotide of any one of claims 1001 to 1015, wherein the CAAR comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 11, 25, 30, 34, 39, 43, and 46. [The present invention 1018] The polynucleotide of any one of 1001 to 1017, wherein the CAAR further comprises a hinge. [The present invention 1019] The polynucleotide of the present invention, wherein the hinge is encoded by a nucleic acid sequence comprising SEQ ID NO:8. [The present invention 1020] The polynucleotide of the present invention, wherein the hinge comprises the amino acid sequence of SEQ ID NO:18. [The present invention 1021] The polynucleotide of any of claims 1001 to 1006, wherein the CAAR comprises an acetylcholine receptor (AChR) autoantigen or a fragment thereof, a killer immunoglobulin-like receptor (KIR) transmembrane domain, and a KIR cytoplasmic domain. [The present invention 1022] A vector comprising any one of the polynucleotides of the present inventions 1001 to 1020. [The present invention 1023] The vector of the present invention, which is a lentiviral vector. [The present invention 1024] The vector of the present invention 1023 which is an RNA vector. [The present invention 1025] The vector of any of claims 1022 to 1024, comprising an inducible promoter operably linked to a polynucleotide encoding CAAR. [The present invention 1026] A chimeric autoantibody receptor (CAAR) comprising an extracellular domain that contains an acetylcholine receptor (AChR) autoantigen or a fragment thereof. [The present invention 1027] A chimeric autoantibody receptor (CAAR) comprising an extracellular domain comprising an acetylcholine receptor (AChR) autoantigen or a fragment thereof, and optionally a transmembrane domain, an intracellular domain of a costimulatory molecule, and / or a signaling domain. [The present invention 1028] The CAAR of claim 1026 or 1027, wherein the AChR autoantigen or a fragment thereof is derived from the α subunit of AChR. [The present invention 1029] The CAAR of claim 1026 or 1027, wherein the AChR autoantigen or a fragment thereof is encoded by a nucleic acid sequence selected from the group consisting of SEQ ID NOs: 3, 5, 7, 22, 23, 29, 33, and 42. [The present invention 1030] The CAAR of invention 1026 or invention 1027, wherein the AChR autoantigen or a fragment thereof is encoded by a nucleic acid sequence having at least 60%, at least 65%, at least 70%, at least 75%, at least 80%, at least 81%, at least 82%, at least 83%, at least 84%, at least 85%, at least 86%, at least 87%, at least 88%, at least 89%, at least 90%, at least 91%, at least 92%, at least 93%, at least 94%, at least 95%, at least 96%, at least 97%, at least 98%, or at least 99% sequence identity to a nucleic acid sequence selected from the group consisting of SEQ ID NOs: 3, 5, 7, 22, 23, 29, 33, and 42. [The present invention 1031] The CAAR of claim 1026 or claim 1027, wherein the AChR autoantigen or a fragment thereof comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 13, 15, 17, 26, 27, 31, 35, and 44. [The present invention 1032] The CAAR of invention 1026 or invention 1027, wherein the AChR autoantigen or a fragment thereof comprises an amino acid sequence having at least 60%, at least 65%, at least 70%, at least 75%, at least 80%, at least 81%, at least 82%, at least 83%, at least 84%, at least 85%, at least 86%, at least 87%, at least 88%, at least 89%, at least 90%, at least 91%, at least 92%, at least 93%, at least 94%, at least 95%, at least 96%, at least 97%, at least 98%, or at least 99% sequence identity to an amino acid sequence selected from the group consisting of SEQ ID NOs: 13, 15, 17, 26, 27, 31, 35, and 44. [The present invention 1033] The CAAR of any one of 1027 to 1032, wherein the transmembrane domain comprises a CD8α transmembrane domain. [The present invention 1034] The CAAR of the present invention, wherein the CD8α transmembrane domain is encoded by a nucleic acid sequence comprising SEQ ID NO: 9. [The present invention 1035] The CAAR of the present invention, wherein the CD8α transmembrane domain comprises the amino acid sequence of SEQ ID NO: 19. [The present invention 1036] The CAAR of any of claims 1027 to 1035, wherein the intracellular domain of the costimulatory molecule includes a 4-1BB intracellular domain. [The present invention 1037] The CAAR of the present invention, wherein the 4-1BB intracellular domain is encoded by a nucleic acid sequence comprising SEQ ID NO: 10 or 16. [The present invention 1038] The CAAR of the present invention, wherein the 4-1BB intracellular domain comprises the amino acid sequence of SEQ ID NO: 20. [The present invention 1039] A CAAR of any of claims 1027 to 1038, wherein the signaling domain comprises a CD3ζ signaling domain. [The present invention 1040] The CAAR of the present invention 1039, wherein the CD3 zeta signaling domain is encoded by a nucleic acid sequence comprising SEQ ID NO: 24 or SEQ ID NO: 53. [The present invention 1041] The CAAR of the present invention, wherein the CD3ζ signaling domain comprises the amino acid sequence of SEQ ID NO: 38. [The present invention 1042] Any of the CAARs of the present invention 1026 to 1041, encoded by a nucleic acid sequence selected from the group consisting of SEQ ID NOs: 1, 6, 21, 28, 32, 36, 41, 45, 47, 48, 49, 50, 51, and 52. [The present invention 1043] A CAAR of any of claims 1026 to 1042, comprising an amino acid sequence selected from the group consisting of SEQ ID NOs: 11, 25, 30, 34, 39, 43, and 46. [The present invention 1044] The CAAR of any of claims 1026 to 1032, comprising an extracellular domain comprising an acetylcholine receptor (AChR) autoantigen or a fragment thereof, a killer immunoglobulin-like receptor (KIR) transmembrane domain, and a KIR cytoplasmic domain. [The present invention 1045] A genetically modified cell comprising any one of CAARs 1026 to 1044 of the present invention. [The present invention 1046] The cells of the present invention 1045 express CAAR and have high affinity for autoantibody-based BCR on B cells. [The present invention 1047] expressing CAAR, and B cells expressing autoantibodies, or B cells that can mature into antibody-secreting cells The cell of the present invention 1045 or 1046, which induces the death of [The present invention 1048] The cell of any of claims 1045 to 1047, which expresses CAAR and has limited toxicity to healthy cells. [The present invention 1049] The cell of any one of 1045 to 1048 of the present invention, selected from the group consisting of helper T cells, cytotoxic T cells, memory T cells, regulatory T cells, γδ T cells, natural killer cells, cytokine-induced killer cells, cell lines thereof, T memory stem cells, T cells derived from pluripotent stem cells, and other effector cells. [The present invention 1050] A genetically modified cell comprising: (a) a chimeric autoantibody receptor of the present invention 1044; and (b) DAP12. [The present invention 1051] The cell of any of claims 1045 to 1050, comprising a polynucleotide encoding CAAR operably linked to an inducible promoter. [The present invention 1052] A pharmaceutical composition comprising any one of the polynucleotides of the present inventions 1001 to 1021, any one of the CAARs of the present inventions 1026 to 1044, or any one of the cells of the present inventions 1045 to 1051, and a pharma- ceutically acceptable excipient. [The present invention 1053] 1. A method for treating an autoantibody-mediated neuromuscular junction (NMJ) disease in a subject, the method comprising: A polynucleotide encoding a chimeric autoantibody receptor (CAAR), the polynucleotide encoding an extracellular domain comprising an AChR autoantigen or a fragment thereof, and optionally a transmembrane domain, an intracellular domain of a costimulatory molecule, and / or a signaling domain. administering to the subject an effective amount of genetically modified cells comprising: [The present invention 1054] 1. A method for preventing or reducing neuromuscular junction (NMJ) damage in a subject at risk for or suffering from an autoantibody-mediated NMJ disease, the method comprising: A polynucleotide encoding a chimeric autoantibody receptor (CAAR), the polynucleotide encoding an extracellular domain comprising an AChR autoantigen or a fragment thereof, and optionally a transmembrane domain, an intracellular domain of a costimulatory molecule, and / or a signaling domain. administering to the subject an effective amount of genetically modified cells comprising: [The present invention 1055] 1. A method for treating an autoantibody-mediated neuromuscular junction (NMJ) disease in a subject, the method comprising: (a) a polynucleotide encoding a chimeric autoantibody receptor (CAAR), the polynucleotide encoding an extracellular domain comprising an AChR autoantigen or a fragment thereof, a killer immunoglobulin-like receptor (KIR) transmembrane domain, and a KIR cytoplasmic domain; (b) a polynucleotide encoding DAP12; administering to the subject an effective amount of genetically modified cells comprising: [The present invention 1056] 1. A method for preventing or reducing neuromuscular junction (NMJ) damage in a subject at risk for or suffering from an autoantibody-mediated NMJ disease, the method comprising: (a) a polynucleotide encoding a chimeric autoantibody receptor (CAAR), the polynucleotide encoding an extracellular domain comprising an AChR autoantigen or a fragment thereof, a killer immunoglobulin-like receptor (KIR) transmembrane domain, and a KIR cytoplasmic domain; (b) a polynucleotide encoding DAP12; administering to the subject an effective amount of genetically modified cells comprising: [The present invention 1057] The method according to any one of claims 1053 to 1056, wherein the polynucleotide is any one of claims 1001 to 1020. [The present invention 1058] The method according to any one of claims 1053 to 1057, wherein the CAAR is any one of claims 1025 to 1042. [The present invention 1059] The method of any of claims 1053 to 1058, wherein said autoantibody mediated NMJ disease is myasthenia gravis (MG). [The present invention 1060] The method of any one of claims 1053 to 1059, wherein the subject is a human. [The present invention 1061] The method of any one of claims 1053 to 1060, wherein the genetically modified cell is a T cell. [The present invention 1062] The method according to any one of claims 1053 to 1061, wherein the modified cells target B cells. [Brief description of the drawings]

[0022] The following detailed description of the preferred embodiments of the invention will be better understood when read in conjunction with the accompanying drawings. For the purpose of illustrating the invention, there are shown in the drawings embodiments which are presently preferred. It should be understood, however, that the invention is not limited to the precise arrangements and instrumentalities of the embodiments shown in the drawings.

[0023] [Figure 1] Schematic diagram of α39P and α65P AChR CAARs, whose extracellular domains (ECDs) contain a segment mimic of the major immunogenic region (MIR) of the α subunit of AChR, the primary target of autoantibodies in MG, followed by a spacer (CD8 hinge domain), CD8 transmembrane domain, and tandem cytoplasmic signaling domains, 4-1BB and CD3ζ (BBz). α65P incorporates an additional EC1 domain sequence compared to α39P; numbers refer to amino acid positions in the AChR protein after signal sequence cleavage. [Diagram 2] 2A-2B are a series of graphs showing that α39P AChR CAAR and α65P AChR CAAR are expressed on the surface of Jurkat cells and primary human T cells as shown by staining with anti-AChR α subunit monoclonal antibody 210 (mAb 210). Jurkat cells and CD3+ T cells were transduced with lentivirus. Flow cytometry analysis was performed on day 3 (Jurkat cells) or day 5 (primary human CD3+ T cells) post-transduction. NTD: non-transduced cells. [Diagram 3]Figures 3A-3B show that α39P CAAR Jurkat NFAT-GFP cells and α65P CAAR Jurkat NFAT-GFP cells activate CAAR signaling after co-culture with TIB-175 (ATCC, mAb 35 hybridoma cells, https: / / www.atcc.org / Products / All / TIB-175.aspx), which express surface anti-AChR B cell receptors and secrete myasthenogenic antibodies in animal models. "TIB-175" and "mAb35 hybridoma cells" are used interchangeably herein to refer to TIB-175 cells. NTD: non-transduced. Flow cytometry analysis was performed 12 hours after co-culture with mAb 35 hybridoma cells. Jurkat NFAT-GFP cells induce GFP expression upon TCR signal transduction. [Figure 4] We show that α39P AChR CAAR Jurkat NFAT-GFP cells activate CAAR signaling after co-culture with Nalm6 195, but not Nalm6 192, a human B cell line engineered to express an anti-AChR B cell receptor targeting a different epitope. Flow cytometry analysis was performed 12 hours after co-culture with Nalm6 control, Nalm6 192, or Nalm6 195 cells. Jurkat cells were stained with anti-CD3-AF647 antibody to distinguish them from the Nalm6 cell population (GFP+CD3-). Nalm6 cells constitutively express click beetle green luciferase and GFP. Plots of CD3+ Jurkat cells are shown in the lower panel. Jurkat NFAT-GFP cells induce GFP expression upon TCR signaling. [Diagram 5]We show that α65P AChR CAAR Jurkat NFAT-GFP cells activate CAAR signaling after co-culture with either Nalm6 192 or Nalm6 195, which shows broader epitope specificity compared to α39P AChR CAAR Jurkat NFAT-GFP cells. Flow cytometry analysis was performed 12 hours after co-culture with either Nalm6 192 or Nalm6 195 cells. Jurkat cells were stained with anti-CD3-AF647 antibody to distinguish them from Nalm6 cell populations. Nalm6 cells constitutively express click beetle green luciferase and GFP. Plots of CD3+ Jurkat cells are shown in the lower panel. Jurkat NFAT-GFP cells induce GFP expression upon TCR signal transduction. [Figure 6] In vitro cytolytic activity of α39P AChR-CAART cells and α65P AChR-CAART cells against the indicated anti-AChR target cells: TIB-175 cells, Nalm6 192 cells, and Nalm6 195 cells. Luciferase activity was measured 15-24 hours after co-culture with the indicated target cells at an effector to target cell ratio of 10:1. mAb 35 hybridoma cells and Nalm6 cells constitutively express click beetle green luciferase. % of specific lysis is calculated using the following equation: % of specific lysis = [(test cell death - spontaneous cell death) / (maximum cell death - spontaneous cell death)]*100, where spontaneous cell death is cell death in medium alone without T cells and maximum cell death is cell death after treatment with 10% SDS at a 1:1 ratio before detection. NTD: non-transduced, and as determined by unpaired Student's t test, *<0.05, **<0.005, ***<0.0005. [Figure 7]Schematic diagram of α208, α210, and α211 AChR CAARs expressing different amino acid lengths of the AChR extracellular domain EC1 followed by either a CD8 hinge or a glycine-serine (GS) linker, the CD8 transmembrane domain (TMD), and the tandem cytoplasmic signaling domains 4-1BB and CD3ζ (BBz). [Figure 8] Figure 1 shows that α208.GS.BBz CAAR incorporating a glycine-serine (GS) linker is not expressed on the surface of 293T cells, whereas α210.GS.BBz CAAR and α211.GS.BBz CAAR incorporating a GS linker are expressed on the cell surface. 293T cells were transiently transfected with lentiviral plasmids without packaging DNA plasmids. Two days after transfection, surface expression of AChR CAAR was detected using mAb 210. Numbers indicate the percentage of AChR CAAR surface positive 293T cells. [Figure 9] Figures 9A-9C show that αAChR CAAR Jurkat NFAT-GFP cells do not activate CAAR signaling after co-culture with Nalm6 3-28, which expresses anti-MuSK B cell receptor as a negative control, but do activate CAAR signaling after co-culture with Nalm6 192, Nalm6 195 (Figure 9A), Nalm6 637 (Figure 9B), or mAb 35 hybridoma (Figure 9C), which express surface anti-AChR B cell receptor. α208.GS.BBz CAAR serves as a negative control, as it is not expressed on the Jurkat cell surface. Flow cytometry analysis was performed 12 hours after co-culture with target cells. GFP expression in Jurkat cells after gating on CD3+ cells is shown. Jurkat NFAT-GFP cells induce GFP expression upon TCR signal transduction. Numbers indicate the percentage of GFP+ AChR CAAR Jurkat cells. [Figure 10]Expression of α208.GS.BBz CAAR, α210.GS.BBz CAAR, and α211.GS.BBz CAAR on the surface of primary human T cells after lentiviral transduction as demonstrated by staining with anti-AChR α subunit monoclonal antibody 210. Flow cytometry analysis was performed 5 days after transduction. NTD: non-transduced. [Figure 11] In vitro cytolytic activity of α210.GS.BBz CAART cells (light grey bars) and α211.GS.BBz CAART cells (dark grey bars) against the indicated target cells: Nalm6 wild-type control, Nalm6 192, Nalm6 195, and mAb 35 hybridoma cells. Luciferase activity was measured 21 hours after co-culture with the indicated target cells at an effector to target cell ratio of 30:1. mAb 35 hybridoma cells and Nalm6 cells constitutively express click beetle green luciferase. % specific lysis is calculated using the following equation: % specific lysis = [(test cell death - spontaneous cell death) / (maximum cell death - spontaneous cell death)] * 100, where spontaneous cell death is cell death in medium alone without T cells, and maximum cell death is cell death after treatment with 10% SDS at a 1:1 ratio before detection. NTD: non-transduced. [Figure 12] Figure 12 shows human interferon-γ (hIFNγ) concentrations in the supernatants of the co-cultures shown in Figure 11. Bar graphs (Nalm6 control - black bars; Nalm6 192 - medium grey bars; Nalm6 195 - light grey bars; TIB-175 - dark grey bars) show the average of samples tested in duplicate. [Figure 13A]Figures 13A-13B show the in vitro cytolytic activity of α210.GS.BBz CAART cells against either Nalm6 control (Figure 13A) or Nalm6 637 (Figure 13B) anti-AChR cells. Luciferase activity was measured after 24 hours of co-culture at the indicated effector to target (E / T) cell ratios. Nalm6 cells constitutively express click beetle green luciferase. Specific lysis [%] is calculated using the following equation: Specific lysis [%] = [(Test cell death - Spontaneous cell death) / (Maximum cell death - Spontaneous cell death)] * 100, where Spontaneous cell death is cell death in medium alone without T cells and Maximum cell death is cell death after treatment with 10% SDS at a 1:1 ratio before detection. NTD: Non-transduced. [Figure 13B] See legend to Figure 13A. [Figure 14] Human interferon-γ (hIFNγ) concentrations in the supernatants of the co-cultures shown in Figure 13 are shown. NTD: non-transduced. [Figure 15] 15A-15B show the in vivo efficacy of α39P.CD8H.BBz CAART cells and α210.GS.BBz CAART cells against either Nalm6 192 (A) or Nalm6 195 (B) target cells. Either 0.3×106 Nalm6 192 or Nalm6 195 cells were injected intravenously into NSG mice after 2 days of pretreatment with intravenous immunoglobulin (IVIG, Privigen). Four days after target cell injection, 3×106 CAART cells or non-transduced (NTD) T cells were injected intravenously. At the indicated time points, bioluminescence was quantified with an IVIS Lumina. At the same time, 600 mg / kg IVIG was also administered intraperitoneally every 2 days. Total flux was quantified using Living Image 4.5 software (PerkinElmer). Images were taken continuously at 1 min intervals, and the highest flux value was selected for analysis. Figure 15A: 5 mice per group. Target cells: Nalm6 192. Figure 15B: 5 mice per group. Target cells: Nalm6 195. [Figure 16]Figure 1 shows the in vivo efficacy of α210.GS.BBz CAART cells and α211.GS.BBz CAART cells against a mixture of Nalm6 192 / 195 cells (1:1 ratio). A total of 0.3x106 Nalm6 192 / 195 cells were injected intravenously into NSG mice after 2 days of pretreatment with intravenous immunoglobulin (IVIG, Privigen). Four days after injection, 3x106 CAART cells or non-transduced (NTD) T cells were injected intravenously. Bioluminescence was quantified with IVIS Lumina on the indicated days. At the same time, 600 mg / kg IVIG was also administered intraperitoneally every 2 days. Total flux was quantified using Living Image 4.5 software (PerkinElmer). Images were captured continuously at 1 min intervals and the highest flux value was selected for analysis. Two mice per group; symbols indicate mean bioluminescence flux. Target cells: Nalm6 192 / 195 1:1 mixture. [Figure 17] In vivo efficacy of α210.GS.BBz CAART cells against Nalm6 637 target cells is shown. 0.2×106 Nalm6 637 (84.3% sIgG+) cells were injected intraperitoneally into NSG mice after 2 days of pretreatment with intravenous immunoglobulin (IVIG, Privigen). Five days after target cell injection, 6×106 α210.GS.BBz CAART cells or NTD T cells were injected intraperitoneally. Bioluminescence was quantified with IVIS Lumina on the indicated days. At the same time, 600 mg / kg IVIG was also administered intraperitoneally every 2 days until day 13. Total flux was quantified using Living Image 4.5 software (PerkinElmer). Images were taken consecutively at 1 min intervals and the highest flux value was selected for analysis. 5 mice per group. Target cells: Nalm6 637. [Figure 18]Figure 18A illustrates the natural killer immunoglobulin-like receptor, two Ig domains and short cytoplasmic tail 2 (KIR2DS2), and the DAP12 multichain complex on the left, and the AChR extracellular domain 1 (EC1) KIR-CAAR (shown here with a glycine-serine (GS) linker connecting the AChR EC1 domain with the KIR2DS2 transmembrane (TM) and cytoplasmic domains). Figure 18B shows a schematic of a lentivector construct consisting of a DAP12 sequence connected to the KIR-CAAR sequence by a ribosomal skipping site such as T2A, flanked by long terminal repeats (LTRs), a partial gag sequence, and the human EF1α promoter, and a woodchuck hepatitis virus posttranscriptional regulatory element (WHV PRE). DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

[0024] Detailed Description The present invention includes a chimeric autoantibody receptor (CAAR) specific for an anti-acetylcholine receptor (AChR) B cell receptor (BCR), a composition comprising the CAAR, a polynucleotide encoding the CAAR, a vector comprising a polynucleotide encoding the CAAR, and a recombinant cell, e.g., a T cell, comprising the CAAR.

[0025] The present invention also includes a method for producing genetically modified cells, such as genetically modified T cells, that express AChR-CAAR, where the expressed CAAR comprises AChR extracellular domain.In some embodiments, the AChR extracellular domain is derived from the α subunit of AChR nicotinic receptor.

[0026] The present invention also generally relates to the use of cells, e.g., T cells, engineered to express CAAR to treat neuromuscular junction (NMJ) diseases (e.g., myasthenia gravis (MG)) associated with targeting of self-antigens (e.g., AChR). In one embodiment, cells, e.g., T cells, expressing the CAAR of the present invention specifically bind to and kill anti-AChR BCR-expressing cells, but do not bind to and kill healthy B cells, i.e., B cells that do not express an autoantibody-based BCR.

[0027] definition Unless otherwise defined, all technical and scientific terms used herein have the same meaning as commonly understood by one of ordinary skill in the art to which this invention belongs. Although any methods and materials similar or equivalent to those described herein can be used in the practice of and / or for the testing of the present invention, the preferred materials and methods are described herein. In describing and claiming the present invention, the following terminology will be used in accordance with how and where its definitions are provided.

[0028] It is also to be understood that the terminology used herein is for the purpose of describing particular aspects only, and is not intended to be limiting.

[0029] The articles "a" and "an" are used herein to refer to one or to more than one (i.e., to at least one) of the grammatical object of the article. By way of example, "an element" means one element or more than one element.

[0030] As used herein, "about" when referring to a measurable value, such as an amount, duration, or the like, is intended to encompass variations of ±20% or ±10%, in some cases ±5%, in some cases ±1%, and in some cases ±0.1% from the specified value, as such variations are reasonable in practicing the disclosed methods.

[0031] The term "antibody" refers to an immunoglobulin molecule that binds to an antigen. An antibody may be an intact immunoglobulin from a natural or recombinant source, or may be an immune-responsive portion of an intact immunoglobulin. An antibody is typically a tetramer of an immunoglobulin molecule. Antibodies may exist in a variety of forms in which the antibody is expressed as part of a continuous polypeptide chain, including, for example, single domain antibody fragments (sdAbs), single chain antibodies (scFvs), and humanized antibodies (Harlow et al., 1999, In: Using Antibodies: A Laboratory Manual, Cold Spring Harbor Laboratory Press, NY; Harlow et al., 1989, In: Antibodies: A Laboratory Manual, Cold Spring Harbor, New York; Houston et al., 1988, Proc. Natl. Acad. Sci. USA 85:5879-5883; Bird et al., 1988, Science 242:423-426).

[0032] The term "high affinity" as used herein refers to the high specificity of binding molecule binding or interaction or attraction to target molecule.For example, in some embodiments, binding molecule can have affinity to target molecule stronger than 100nM, 50nM, 20nM, 15nM, 10nM, 9nM, 8nM, 7nM, 6nM, 5nM, 4nM, 3nM, 2nM or 1nM, for example, when measured by surface plasmon resonance.

[0033] The term "antigen" or "Ag" as used herein is defined as a molecule that elicits an immune response. This immune response may include either or both antibody production or activation of specific immunocompetent cells. Those skilled in the art will understand that virtually any macromolecule, including any protein or peptide, can serve as an antigen. Moreover, the antigen may be derived from recombinant or genomic DNA. Those skilled in the art will understand that any DNA that includes a nucleotide sequence or partial nucleotide sequence that encodes a protein that elicits an immune response therefore encodes an "antigen" as that term is used herein. Moreover, those skilled in the art will also understand that an antigen need not be encoded solely by the full-length nucleotide sequence of a gene. It is readily apparent that the present invention includes, but is not limited to, the use of partial nucleotide sequences of multiple genes, and that these nucleotide sequences are arranged in various combinations to encode a polypeptide that elicits a desired immune response. Moreover, those skilled in the art will also understand that an antigen need not be encoded by a "gene" at all. It is readily apparent that an antigen can be synthetically produced or obtained from a biological sample. Such biological samples may include, but are not limited to, a tissue sample, a tumor sample, a cell, or a biological fluid.

[0034] "Autoantigen" refers to an endogenous antigen that stimulates the production of an autoimmune response, such as the production of an autoantibody. Autoantigens also include self-antigens or antigens derived from normal tissues that are targets of cell-mediated or antibody-mediated immune responses that can result in the development of autoimmune diseases. Examples of autoantigens include, but are not limited to, AChR and fragments thereof.

[0035] As used herein, the term "limited toxicity" refers to peptides, polynucleotides, cells, and / or antibodies of the invention that exhibit a substantial lack of negative biological effects or substantial negative physiological symptoms on healthy, non-diseased, non-target cells, or populations of such cells, either in vitro or in vivo.

[0036] "Autoantibody" refers to an antibody that is specific for a self-antigen.

[0037] As used herein, the term "autoimmune disease" is defined as a disorder or condition resulting from an antibody-mediated autoimmune response to a self-antigen. An autoimmune disease results in the production of inappropriately and / or excessively produced autoantibodies against a self-antigen or autoantigen.

[0038] As used herein, the term "autologous" is intended to refer to any material derived from the same individual that is subsequently reintroduced into that individual.

[0039] "Allogeneic" refers to any material derived from different animals of the same species.

[0040] "Xenogeneic" refers to any material derived from an animal of a different species.

[0041] "Chimeric autoantibody receptor" or "CAAR" refers to an engineered receptor that is expressed on cells, such as T cells or any other effector cell type, such as effector cell type that is capable of cell-mediated cytotoxicity. In some embodiments, CAAR is expressed on Treg cells. CAAR comprises an antigen or fragment thereof that is specific for BCR and / or autoantibody, such as pathogenic BCR and / or autoantibody. CAAR also optionally comprises a transmembrane domain, an intracellular domain, and / or a signaling domain.

[0042] As used herein, the term "conservative sequence modification" is intended to refer to an amino acid modification that does not significantly affect or change the binding properties of the antibody containing the amino acid sequence. Such conservative modifications include amino acid substitutions, additions, and deletions. Modifications can be introduced into the antibody of the present invention by standard techniques known in the art, such as site-directed mutagenesis and PCR-mediated mutagenesis. Conservative amino acid substitutions are those in which an amino acid residue is replaced by an amino acid residue that has a similar side chain. Families of amino acid residues that have similar side chains have been clearly defined in the art. These families include amino acids with basic side chains (e.g., lysine, arginine, histidine), amino acids with acidic side chains (e.g., aspartic acid, glutamic acid), amino acids with uncharged polar side chains (e.g., glycine, asparagine, glutamine, serine, threonine, tyrosine, cysteine, tryptophan), amino acids with non-polar side chains (e.g., alanine, valine, leucine, isoleucine, proline, phenylalanine, methionine), amino acids with β-branched side chains (e.g., threonine, valine, isoleucine), and amino acids with aromatic side chains (e.g., tyrosine, phenylalanine, tryptophan, histidine). Thus, for example, one or more amino acid residues in the extracellular region of the CAAR of the present invention can be replaced by other amino acid residues with similar side chains or charges, and the altered CAAR can be tested for its ability to bind to autoantibodies using the functional assays described herein.

[0043] "Costimulatory ligand," as that term is used herein, includes a molecule on an antigen-presenting cell (e.g., aAPC, dendritic cell, B cell, etc.) that can specifically bind to a cognate costimulatory molecule on a T cell, thereby providing signals that mediate T cell responses, including, but not limited to, proliferation, activation, differentiation, etc., in addition to the primary signal provided by binding of, e.g., a peptide-loaded MHC molecule to the TCR / CD3 complex.

[0044] "Costimulatory molecule" refers to the cognate binding partner on a T cell that specifically binds to a costimulatory ligand, thereby mediating a costimulatory response by the T cell, such as, but not limited to, proliferation. Costimulatory molecules include, but are not limited to, MHC class I molecules, BTLA, and Toll ligand receptors.

[0045] The term "CRISPR / CAS", "clustered regularly interspaced short palindromic repeats system", or "CRISPR" refers to DNA loci that contain short repeats of a base sequence. Each repeat is followed by a short segment of spacer DNA from a previous exposure to a virus. Bacteria and archaea have evolved an adaptive immune defense called the CRISPR-CRISPR associated (Cas) system that uses short RNAs to direct the degradation of foreign nucleic acids. In bacteria, the CRISPR system provides adaptive immunity against invading foreign DNA via RNA-guided DNA cleavage.

[0046] In type II CRISPR / Cas systems, short segments of foreign DNA, called "spacers," are integrated into the CRISPR genomic locus and transcribed and processed into short CRISPR RNAs (crRNAs). These crRNAs anneal to transactivating crRNAs (tracrRNAs) and direct sequence-specific cleavage and silencing of pathogenic DNA by Cas proteins. Recent studies have shown that target recognition by Cas9 proteins requires a "seed" sequence in the crRNA and a protospacer adjacent motif (PAM) sequence that contains a conserved dinucleotide upstream of the crRNA binding region. To direct Cas9 to cleave the sequence of interest, a crRNA-tracrRNA fusion transcript, hereafter referred to as "guide RNA" or "gRNA," can be designed from the human U6 polymerase III promoter.

[0047] The term "CRISPRi" refers to the CRISPR system for sequence-specific gene silencing or inhibition of gene expression at the transcriptional level.

[0048] "Encoding" refers to the inherent property of a particular nucleotide sequence in a polynucleotide, such as a gene, cDNA, or mRNA, to serve as a template for the synthesis of other polymers and macromolecules in biological processes, either with a predetermined nucleotide sequence (i.e., rRNA, tRNA, and mRNA) or with a predetermined amino acid sequence, and the biological properties resulting therefrom. That is, a gene encodes a protein when the protein is produced in a cell or other biological system by transcription and translation of the mRNA corresponding to that gene. Both the coding strand, which has a nucleotide sequence identical to the mRNA sequence and is usually presented as a sequence listing, and the non-coding strand, which is used as a template for transcription of a gene or cDNA, can be referred to as encoding a protein or other product of that gene or cDNA.

[0049] "Effective amount" or "therapeutically effective amount" are used interchangeably herein and refer to an amount of a compound, formulation, material, or composition described herein that is effective to achieve a particular biological result. Such result may include, but is not limited to, inhibition of viral infection, as determined by any means suitable in the art.

[0050] The term "effector function" refers to a specialized function of a cell.

[0051] As used herein, "endogenous" refers to any material that originates from or is produced within an organism, cell, tissue or system.

[0052] As used herein, the term "exogenous" refers to any material that is introduced into, or produced outside, an organism, cell, tissue or system.

[0053] As used herein, the term "expression" is defined as the transcription and / or translation of a particular nucleotide sequence driven by a promoter.

[0054] "Expression vector" refers to a vector that contains a recombinant polynucleotide that includes an expression control sequence operably linked to a nucleotide sequence to be expressed. An expression vector contains sufficient cis-acting elements for expression; other elements for expression can be supplied by the host cell or in an in vitro expression system. Expression vectors include all those known in the art, such as cosmids incorporating recombinant polynucleotides, plasmids (e.g., naked or contained in liposomes), retrotransposons (e.g., piggyback, sleeping beauty), and viruses (e.g., lentiviruses, retroviruses, adenoviruses and adeno-associated viruses).

[0055] "Homologous" as used herein refers to the subunit sequence identity between two polymer molecules, for example, between two nucleic acid molecules, such as two DNA molecules or two RNA molecules, or between two polypeptide molecules. If a subunit position in both of the two molecules is occupied by the same monomeric subunit; for example, if a position in each of the two DNA molecules is occupied by adenine, they are homologous at that position. The homology between two sequences is a direct function of the number of positions that match or are homologous; for example, if half of the positions in the two sequences (e.g., 5 positions in a polymer that is 10 subunits long) are homologous, the two sequences are 50% homologous; if 90% of the positions (e.g., 9 out of 10) are matched or homologous, the two sequences are 90% homologous.

[0056] "Identity" as used herein refers to the subunit sequence identity between two amino acid molecules, such as between two polymer molecules, particularly between two polypeptide molecules. If two amino acid sequences have the same residue at the same position; for example, if a position is occupied by arginine in each of the two polypeptide molecules, they are identical at that position. The identity or the degree to which two amino acid sequences have the same residue at the same position in an alignment is often expressed as a percentage. The identity between two amino acid sequences is a direct function of the number of positions that match or are identical; for example, if half of the positions in the two sequences (e.g., 5 positions in a polymer that is 10 amino acids in length) are identical, the two sequences are 50% identical; if 90% of the positions (e.g., 9 out of 10) are identical or matched, the two amino acid sequences are 90% identical.

[0057] As used herein, "instructional material" includes publications, records, diagrams, or any other medium of expression that can be used to communicate the utility of the compositions and methods of the invention. The instructional material of the kits of the invention may, for example, be affixed to a container which contains the nucleic acids, peptides, and / or compositions of the invention or may be shipped together with a container which contains the nucleic acids, peptides, and / or compositions. Alternatively, the instructional material may be shipped separately from the container, with the intention that the instructional material and the compounds be used together by the recipient.

[0058] "Intracellular domain" refers to a portion or region of a molecule that is present inside a cell.

[0059] The term "intracellular signaling domain" is meant to include any full-length or truncated portion of the intracellular domain sufficient to transduce an effector function signal.

[0060] "Isolated" means altered or removed from the natural state. For example, a nucleic acid or peptide that is naturally present in a living animal is not "isolated," but the same nucleic acid or peptide that is partially or completely separated from the coexisting materials in its natural state is "isolated." An isolated nucleic acid or protein can exist in a substantially purified form, or can exist in a non-native environment, such as, for example, a host cell.

[0061] In the context of the present invention, the following abbreviations are used for commonly occurring nucleobases: "A" refers to adenosine, "C" refers to cytosine, "G" refers to guanosine, "T" refers to thymidine and "U" refers to uridine.

[0062] Unless otherwise specified, a "nucleotide sequence encoding an amino acid sequence" includes all nucleotides that are degenerate versions of each other and that encode the same amino acid sequence. The phrase nucleotide sequence encoding a protein or RNA can also include introns, to the extent that nucleotide sequences encoding proteins may contain introns in some forms.

[0063] As used herein, "lentivirus" refers to a genus of the Retroviridae family. Lentiviruses are unique among retroviruses in that they can infect non-dividing cells; they can deliver a significant amount of genetic information into the DNA of host cells, making them one of the most efficient methods of gene delivery vectors. HIV, SIV and FIV are all examples of lentiviruses. Lentivirus-derived vectors provide a means to achieve a fairly high level of gene transfer in vivo.

[0064] The term "operably linked" refers to a functional link between a regulatory sequence and a heterologous nucleic acid sequence that results in the expression of the latter. For example, a first nucleic acid sequence is operably linked to a second nucleic acid sequence if the first nucleic acid sequence is placed in a functional relationship with the second nucleic acid sequence. For example, a promoter is operably linked to a coding sequence if it affects the transcription or expression of the coding sequence. Generally, operably linked DNA sequences are contiguous and, where necessary to connect two protein coding regions, are in the same reading frame.

[0065] "Parenteral" administration of the immunogenic compositions includes, for example, subcutaneous (sc), intravenous (iv), intramuscular (im) or intrasternal injection or infusion.

[0066] As used herein, "plasma cell" refers to a type of white blood cell that can produce and secrete antibodies. Plasma cells are also called plasmocytes, plasmacytes, or effector B cells.

[0067] The term "polynucleotide" as used herein is defined as a chain of nucleotides. Moreover, a nucleic acid is a polymer of nucleotides. Thus, as used herein, nucleic acid and polynucleotide are interchangeable. Those skilled in the art have the general knowledge that nucleic acids are polynucleotides, which can be hydrolyzed into monomeric "nucleotides". Monomeric nucleotides can be hydrolyzed into nucleosides. As used herein, polynucleotide includes, but is not limited to, all nucleic acid sequences obtained by any means available in the art, including, but not limited to, recombinant means, i.e., cloning a nucleic acid sequence from a recombinant library or a cellular genome using conventional cloning techniques and PCR™, and synthetic means. In some embodiments, a nucleic acid sequence is considered to have at least 95%, 96%, 97%, 98%, or 99% identity or homology to any of the nucleic acid sequences disclosed herein.

[0068] As used herein, the terms "peptide", "polypeptide" and "protein" are used interchangeably and refer to compounds composed of amino acid residues covalently linked by peptide bonds. A protein or peptide must contain at least two amino acids, and there is no limit to the maximum number of amino acids that may make up a protein or peptide sequence. A polypeptide includes any peptide or protein that contains two or more amino acids linked together by peptide bonds. As used herein, the term refers to both short chains, also commonly referred to in the art as peptides, oligopeptides and oligomers, and longer chains, commonly referred to in the art as proteins, of which there are many varieties. "Polypeptides" include, for example, biologically active fragments, substantially homologous polypeptides, oligopeptides, homodimers, heterodimers, variants of polypeptides, modified polypeptides, derivatives, analogs, and fusion proteins, to name a few. A polypeptide includes natural peptides, recombinant peptides, synthetic peptides, or combinations thereof. In some embodiments, an amino acid sequence is deemed to have 95%, 96%, 97%, 98%, or 99% identity or homology to any of the amino acid sequences described herein.

[0069] The term "proinflammatory cytokine" refers to a cytokine or factor that promotes inflammation or an inflammatory response. Examples of proinflammatory cytokines include, but are not limited to, chemokines (CCL, CXCL, CX3CL, XCL), interleukins (e.g., IL-1, IL-2, IL-3, IL-5, IL-6, IL-7, IL-9, IL-10, and IL-15), interferons (IFNγ), and tumor necrosis factors (TNFα and TNFβ).

[0070] The term "promoter" as used herein is defined as a DNA sequence recognized by the synthetic machinery of the cell, or introduced synthetic machinery, necessary to initiate the specific transcription of a polynucleotide sequence.

[0071] As used herein, the term "promoter / regulatory sequence" refers to a nucleic acid sequence required for expression of a gene product operably linked to the promoter / regulatory sequence. In some cases, this sequence may be a core promoter sequence, and in other cases, this sequence may also include enhancer sequences and other control elements required for expression of the gene product. The promoter / regulatory sequence may, for example, be one that causes the gene product to be expressed in a tissue-specific manner.

[0072] A "constitutive" promoter is a nucleotide sequence that, when operably linked to a polynucleotide encoding or specifying a gene product, causes that gene product to be produced in a cell under most or all physiological conditions of the cell.

[0073] An "inducible" promoter is a nucleotide sequence that, when operably linked to a polynucleotide encoding or specifying a gene product, causes that gene product to be produced in a cell substantially only when an inducer corresponding to that promoter is present in the cell.

[0074] A "tissue-specific" promoter is a nucleotide sequence that, when operably linked to a polynucleotide that encodes or specifies a gene product, causes that gene product to be produced in a cell substantially only if the cell is a cell of the tissue type corresponding to the promoter.

[0075] A "signal transduction pathway" refers to the biochemical relationships between various signaling molecules that play a role in transmitting a signal from one part of a cell to another part of the cell. The phrase "cell surface receptor" includes molecules and complexes of molecules that can receive and transmit a signal across the membrane of a cell.

[0076] "Signaling domain" refers to a portion or region of a molecule that recruits and interacts with specific proteins in response to an activating signal.

[0077] The term "subject" is intended to include living organisms (eg, mammals) in which an immune response can be elicited.

[0078] As used herein, a "substantially purified" cell is one that is essentially free of other cell types. A substantially purified cell also refers to a cell that is separated from other cell types that are naturally associated with it in its natural state. In some cases, a population of substantially purified cells refers to a homogenous cell population. In other cases, the term simply refers to a cell that is separated from the cells that are naturally associated with it in its natural state. In some embodiments, the cells are cultured in vitro. In other embodiments, the cells are not cultured in vitro.

[0079] As used herein, the term "therapeutic" refers to treatment and / or prophylaxis. A therapeutic effect is achieved by suppressing, ameliorating, or eradicating the disease state.

[0080] As used herein, the terms "transfected" or "transformed" or "transduced" refer to the process by which exogenous nucleic acid is transferred or introduced into a host cell. A "transfected" or "transformed" or "transduced" cell is one that has been transfected, transformed by, or transduced with an exogenous nucleic acid. This cell includes the primary subject cell and its progeny.

[0081] "Transmembrane domain" refers to the portion or region of a molecule that spans the lipid bilayer.

[0082] As used herein, the phrase "under transcriptional control" or "operably linked" means that the promoter is in the correct position and orientation to control the initiation of transcription by RNA polymerase and expression of the polynucleotide.

[0083] A "vector" refers to a composition that contains an isolated nucleic acid and can be used to deliver the isolated nucleic acid to the inside of a cell. Numerous vectors are known in the art, including but not limited to linear polynucleotides, polynucleotides associated with ionic or amphiphilic compounds, plasmids and viruses. Thus, the term "vector" includes autonomously replicating plasmids or viruses. This term should also be construed to include non-plasmid and non-viral compounds that facilitate the transfer of nucleic acid into cells, such as polylysine compounds, liposomes, etc. Examples of viral vectors include but are not limited to adenoviral vectors, adeno-associated viral vectors, retroviral vectors, lentiviral vectors, etc.

[0084] As used herein, the term "specifically binds" refers to an antibody or ligand that recognizes and binds to a cognate binding partner (e.g., a stimulatory and / or costimulatory molecule present on a T cell) protein present in a sample, but does not substantially recognize or bind to other molecules in the sample.

[0085] The term "stimulation" refers to a primary response induced by the binding of a stimulatory molecule (e.g., the TCR / CD3 complex) to its cognate ligand, thereby mediating a signaling event, such as, but not limited to, signaling through the TCR / CD3 complex. Stimulation may mediate altered expression of certain molecules, such as downregulation of TGF-β and / or remodeling of cytoskeletal structures.

[0086] By "stimulatory molecule," as that term is used herein, is meant a molecule on a T cell that specifically binds to a cognate stimulatory ligand present on an antigen-presenting cell.

[0087] "Stimulatory ligand," as used herein, means a ligand that, when present on an antigen-presenting cell (e.g., aAPC, dendritic cell, B cell, etc.), can specifically bind to a cognate binding partner (referred to herein as a "stimulatory molecule") on a T cell, thereby mediating a primary response by the T cell, including, but not limited to, activation, initiation of an immune response, proliferation, etc. Stimulatory ligands are well known in the art and include, among others, peptide-loaded MHC class I molecules, anti-CD3 antibodies, superagonist anti-CD28 antibodies, and superagonist anti-CD2 antibodies.

[0088] Ranges: Throughout this disclosure, various aspects of the invention can be presented in a range format. It should be understood that the description in range format is merely for convenience and brevity and should not be considered as an inflexible limitation on the scope of the invention. Thus, the description of a range should be considered to have specifically disclosed all possible subranges within that range, as well as each individual number. For example, the description of a range such as 1-6 should be considered to have specifically disclosed each individual number within that range, e.g., 1, 2, 2.7, 3, 4, 5, 5.3, and 6, as well as subranges such as 1-3, 1-4, 1-5, 2-4, 2-6, 3-6, etc. This applies regardless of the broadness of the range.

[0089] As used herein, a "fragment" of a polynucleotide, protein, or receptor refers to a fragment of a polynucleotide, protein, or receptor that retains, for example, at least 10%, at least 20%, at least 30%, at least 40%, at least 50%, at least 60%, at least 70%, at least 80%, at least 90%, or 100% of the biological activity of the corresponding full-length polynucleotide, protein, or receptor. For example, a "functional fragment" of an acetylcholine receptor (AChR) autoantigen refers to a fragment of a full-length acetylcholine receptor (AChR) autoantigen that retains, for example, at least 10%, at least 20%, at least 30%, at least 40%, at least 50%, at least 60%, at least 70%, at least 80%, at least 90%, or 100% of the binding activity of the corresponding full-length acetylcholine receptor (AChR) autoantigen to BCR or autoantibody.

[0090] Throughout the description where a polynucleotide, protein, receptor, cell, or composition is described as having, including, or comprising particular components, or where processes and methods are described as having, including, or comprising particular steps, it is additionally envisaged that there are polynucleotides, proteins, receptors, cells, or compositions of the invention that consist essentially of, or consist of, the recited components, and that there are processes and methods according to the invention that consist essentially of, or consist of, the recited processing steps.

[0091] explanation Chimeric Autoantibody Receptor (CAAR) The present invention is based in part on the discovery that chimeric autoantibody receptors can be used to target B cells expressing autoantibody-based B cell receptors, which can cause autoantibody-mediated neuromuscular junction (NMJ) diseases (e.g., myasthenia gravis (MG)) after activation and autoantibody secretion.The present invention includes chimeric autoantibody receptors (CAARs) specific to anti-acetylcholine receptor (AChR) B cell receptors (BCRs), compositions comprising the CAARs, polynucleotides encoding the CAARs, vectors comprising polynucleotides encoding the CAARs, and recombinant cells, such as T cells, comprising the CAARs.The present invention also includes a method for producing genetically modified cells, such as genetically modified T cells, that express AChR CAARs, where the expressed CAARs comprise AChR extracellular domains.

[0092] The present invention includes techniques for treating autoantibody-mediated NMJ diseases. In particular, techniques that target B cells that ultimately produce and present autoantibodies on their cell surface categorize these B cells as disease-specific targets for therapeutic intervention. Thus, the present invention includes methods for efficiently targeting and killing pathogenic B cells in autoantibody-mediated diseases by targeting disease-causing B cells with antigen-specific (e.g., AChR) chimeric autoantibody receptors (i.e., CAARs). In one embodiment of the present invention, only specific anti-AChR BCR-expressing B cells are killed, leaving beneficial B cells and antibodies that protect against infection intact.

[0093] In one aspect, the present invention comprises a chimeric autoantibody receptor (CAAR) comprising an extracellular domain comprising an acetylcholine receptor (AChR) autoantigen or a fragment thereof. In some embodiments, the AChR autoantigen comprises the α subunit of AChR or a fragment thereof. In some embodiments, the AChR autoantigen is the α subunit of AChR.

[0094] In one aspect, the present invention includes a chimeric polypeptide comprising an AChR autoantigen or a fragment thereof, wherein the AChR autoantigen or a fragment thereof is linked to a transmembrane domain of a chimeric autoantibody receptor (CAAR).

[0095] In one aspect, the present invention includes a polynucleotide encoding a chimeric autoantibody receptor (CAAR), the polynucleotide encoding an AChR autoantigen or a fragment thereof. In some embodiments, the polynucleotide also encodes a transmembrane domain, an intracellular domain of a costimulatory molecule, and / or a signal transduction domain.

[0096] In some embodiments, the AChR CAAR comprises an amino acid sequence selected from the group consisting of SEQ ID NOs: 11, 25, 30, 34, 39, 43, and 46. In one embodiment, the AChR CAAR is encoded by a nucleic acid sequence selected from the group consisting of SEQ ID NOs: 1, 6, 21, 28, 32, 36, 41, 45, 47, 48, 49, 50, 51, and 52.

[0097] In some embodiments, the AChR CAAR comprises an amino acid sequence having 85%, 86%, 87%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, or 99% sequence identity to an amino acid sequence selected from the group consisting of SEQ ID NOs: 11, 25, 30, 34, 39, 43, and 46. In other embodiments, the AChR CAAR is encoded by a nucleic acid sequence having 85%, 86%, 87%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, or 99% sequence identity to a nucleic acid sequence selected from the group consisting of SEQ ID NOs: 1, 6, 21, 28, 32, 36, 41, 45, 47, 48, 49, 50, 51, and 52.

[0098] autoantigen part In one embodiment, the CAAR of the present invention comprises an autoantibody binding domain, which is otherwise called autoantigen or its fragment.The selection of the autoantigen for use in the present invention depends on the type of autoantibody or BCR (e.g., anti-AChR) that is targeted.For example, the autoantigen may be selected to recognize the BCR or autoantibody on target cells, such as BCR-expressing B cells, that are associated with a certain autoantibody-mediated disease state, for example, myasthenia gravis (MG).

[0099] In some cases, it is beneficial that the autoantibody binding domain is derived from the same species in which the CAAR will ultimately be used. For example, for use in humans, it may be beneficial that the autoantibody binding domain of the CAAR comprises a human autoantigen (or a fragment thereof) that binds to a human BCR or autoantibody.

[0100] In one exemplary embodiment, the engineered chimeric autoantibody receptor comprises an AChR or a fragment thereof that binds to an anti-AChR BCR, eg, an anti-AChR BCR on a B cell in a subject.

[0101] In one embodiment, the CAAR comprises an AChR autoantigen or a fragment thereof. In some embodiments, the AChR autoantigen or a fragment thereof is encoded by a nucleic acid sequence selected from the group consisting of SEQ ID NOs: 3, 5, 7, 22, 23, 29, 33, and 42. Acceptable variations of the autoantigen or a fragment thereof will be known to those of skill in the art. For example, in some embodiments, the AChR autoantigen or fragment thereof is encoded by a nucleic acid sequence having at least 60%, at least 65%, at least 70%, at least 75%, at least 80%, at least 81%, at least 82%, at least 83%, at least 84%, at least 85%, at least 86%, at least 87%, at least 88%, at least 89%, at least 90%, at least 91%, at least 92%, at least 93%, at least 94%, at least 95%, at least 96%, at least 97%, at least 98%, or at least 99% sequence identity to a nucleic acid sequence selected from the group consisting of SEQ ID NOs: 3, 5, 7, 22, 23, 29, 33, and 42. In some embodiments, the AChR autoantigen or fragment thereof is encoded by a nucleic acid sequence comprising one or more (e.g., one, two, three, four, or five) nucleic acid sequences selected from the group consisting of SEQ ID NOs: 3, 5, 7, 22, and 23. In certain embodiments, the AChR autoantigen or fragment thereof is encoded by a nucleic acid sequence comprising one or more (e.g., one, two, three, four, or five) nucleic acid sequences having at least 60%, at least 65%, at least 70%, at least 75%, at least 80%, at least 81%, at least 82%, at least 83%, at least 84%, at least 85%, at least 86%, at least 87%, at least 88%, at least 89%, at least 90%, at least 91%, at least 92%, at least 93%, at least 94%, at least 95%, at least 96%, at least 97%, at least 98%, or at least 99% sequence identity to a nucleic acid sequence selected from the group consisting of SEQ ID NOs: 3, 5, 7, 22, and 23.

[0102] In other embodiments, the AChR autoantigen or fragment thereof comprises an amino acid sequence selected from the group consisting of SEQ ID NOs: 13, 15, 17, 26, 27, 31, 35, and 44. In yet other embodiments, the AChR autoantigen or fragment thereof comprises an amino acid sequence having at least 60%, at least 65%, at least 70%, at least 75%, at least 80%, at least 81%, at least 82%, at least 83%, at least 84%, at least 85%, at least 86%, at least 87%, at least 88%, at least 89%, at least 90%, at least 91%, at least 92%, at least 93%, at least 94%, at least 95%, at least 96%, at least 97%, at least 98%, or at least 99% sequence identity to an amino acid sequence selected from the group consisting of SEQ ID NOs: 13, 15, 17, 26, 27, 31, 35, and 44. In certain embodiments, the AChR autoantigen or fragment thereof comprises one or more (eg, one, two, three, four, or five) amino acid sequences selected from the group consisting of SEQ ID NOs: 13, 15, 17, 26, and 27. In certain embodiments, the AChR autoantigen or fragment thereof comprises one or more (e.g., one, two, three, four, or five) amino acid sequences having at least 60%, at least 65%, at least 70%, at least 75%, at least 80%, at least 81%, at least 82%, at least 83%, at least 84%, at least 85%, at least 86%, at least 87%, at least 88%, at least 89%, at least 90%, at least 91%, at least 92%, at least 93%, at least 94%, at least 95%, at least 96%, at least 97%, at least 98%, or at least 99% sequence identity to an amino acid sequence selected from the group consisting of SEQ ID NOs: 13, 15, 17, 26, and 27.

[0103] Transmembrane domain In some embodiments, AChRCAAR comprises a transmembrane domain that is fused to the extracellular domain of AChR CAAR.In one embodiment, AChR CAAR comprises a transmembrane domain that naturally associates with one of the domains in AChR CAAR.In some cases, the transmembrane domain is selected or modified by amino acid substitution to avoid binding to the transmembrane domain of the same or different surface membrane protein, so as to minimize interaction with other members of the receptor complex.

[0104] The transmembrane domain may be derived from either natural or synthetic sources. If the source is natural, the domain may be derived from any membrane-bound or transmembrane protein. In one embodiment, the transmembrane domain may be synthetic, in which case it will primarily comprise hydrophobic residues such as leucine and valine. In one aspect, triplets of phenylalanine, tryptophan, and valine will be found at each end of the synthetic transmembrane domain. Optionally, a short oligopeptide or polypeptide linker, 2-10 amino acids in length, may form the link between the transmembrane domain and the cytoplasmic signaling domain of the AChR CAAR. A glycine-serine (GS) doublet provides a particularly suitable linker.

[0105] Optionally, various spacer domains before the transmembrane domain can be used as well, including CD8 or human Ig (immunoglobulin) hinges, or glycine-serine linkers.

[0106] Examples of hinge and / or transmembrane domains include those of the α, β, or ζ chains of the T cell receptor, CD28, CD3ε, CD45, CD4, CD5, CD8, CD9, CD16, CD22, CD33, CD37, CD64, CD80, CD86, CD134, CD137, CD154, KIR, OX40, CD2, CD27, LFA-1 (CD11a, CD18), ICOS (CD27 8), 4-1BB (CD137), GITR, CD40, BAFFR, HVEM (LIGHTR), SLAMF7, NKp80 (KLRF1), CD160, CD19, IL2Rβ, IL2 Rγ, IL7Rα, ITGA1, VLA1, CD49a, ITGA4, IA4, CD49D, ITGA6, VLA-6, CD49f, ITGAD, CD11d, ITGAE, CD103, I TGAL, CD11a, LFA-1, ITGAM, CD11b, ITGAX, CD11c, ITGB1, CD29, ITGB2, CD18, LFA-1, ITGB7, TNFR2, DNA M1 (CD226), SLAMF4 (CD244, 2B4), CD84, CD96 (Tactile), CEACAM1, CRTAM, Ly9 (CD229), CD160 (BY55), P Non-limiting examples include the hinge and / or transmembrane domains of SGL1, CD100 (SEMA4D), SLAMF6 (NTB-A, Ly108), SLAM (SLAMF1, CD150, IPO-3), BLAME (SLAMF8), SELPLG (CD162), LTBR, ​​PAG / Cbp, NKp44, NKp30, NKp46, NKG2D, and / or NKG2C.

[0107] In one embodiment, the AChR CAAR comprises, but is not limited to, the CD8α transmembrane domain: TIFF0007649755000001.tif5128 (This is TIFF0007649755000002.tif12151).

[0108] In some embodiments, the CD8 alpha transmembrane domain comprises an amino acid sequence having at least 60%, at least 65%, at least 70%, at least 75%, at least 80%, at least 81%, at least 82%, at least 83%, at least 84%, at least 85%, at least 86%, at least 87%, at least 88%, at least 89%, at least 90%, at least 91%, at least 92%, at least 93%, at least 94%, at least 95%, at least 96%, at least 97%, at least 98%, or at least 99% sequence identity to the amino acid sequence of SEQ ID NO:19. In further embodiments, the CD8 alpha transmembrane domain is encoded by a nucleic acid sequence having at least 60%, at least 65%, at least 70%, at least 75%, at least 80%, at least 81%, at least 82%, at least 83%, at least 84%, at least 85%, at least 86%, at least 87%, at least 88%, at least 89%, at least 90%, at least 91%, at least 92%, at least 93%, at least 94%, at least 95%, at least 96%, at least 97%, at least 98%, or at least 99% sequence identity to the nucleic acid sequence of SEQ ID NO:9.

[0109] In another embodiment, the AChR CAAR is TIFF0007649755000003.tif4128 (This is TIFF0007649755000004.tif4128).

[0110] In some embodiments, the AChR CAAR comprises the CD8α hinge region: TIFF0007649755000005.tif12139 (This is TIFF0007649755000006.tif26152).

[0111] In some embodiments, the hinge region comprises an amino acid sequence having at least 60%, at least 65%, at least 70%, at least 75%, at least 80%, at least 81%, at least 82%, at least 83%, at least 84%, at least 85%, at least 86%, at least 87%, at least 88%, at least 89%, at least 90%, at least 91%, at least 92%, at least 93%, at least 94%, at least 95%, at least 96%, at least 97%, at least 98%, or at least 99% sequence identity to the amino acid sequence of SEQ ID NO: 18, or a sequence identical to that of SEQ ID NO: 8, and is encoded by a nucleic acid sequence having at least 60%, at least 65%, at least 70%, at least 75%, at least 80%, at least 81%, at least 82%, at least 83%, at least 84%, at least 85%, at least 86%, at least 87%, at least 88%, at least 89%, at least 90%, at least 91%, at least 92%, at least 93%, at least 94%, at least 95%, at least 96%, at least 97%, at least 98%, or at least 99% sequence identity to 8.

[0112] Intracellular domains of costimulatory molecules In some embodiments, the AChR CAAR comprises the intracellular domain of a costimulatory molecule.The intracellular domain of the AChR CAAR of the present invention is the cytoplasmic domain that is responsible for activating at least one of the normal effector functions of the immune cell in which the AChR CAAR is located.

[0113] The effector function of T cells can be, for example, cytolytic activity or helper activity, including secretion of cytokines. Thus, the term "intracellular domain of a costimulatory molecule" refers to a portion of a protein that transmits effector function signals to direct cells to perform specialized functions. The entire intracellular domain of a costimulatory molecule can be used, but in many cases it is not necessary to use the entire domain. To the extent that a truncated portion of the intracellular domain of a costimulatory molecule is used, such a truncated portion may be used in place of the intact domain, so long as it transmits effector function signals.

[0114] The intracellular domain of a costimulatory molecule refers to a portion of CAAR that contains the intracellular domain of a costimulatory molecule. A costimulatory molecule is a cell surface molecule other than an antigen receptor or its ligand that is required for an efficient response of lymphocytes to antigens. Examples of such molecules include CD27, CD28, 4-1BB (CD137), OX40, CD30, CD40, PD-1, ICOS, lymphocyte function-associated antigen-1 (LFA-1), CD2, CD7, LIGHT, NKG2C, B7-H3, and CD83 specific binding ligand, CDS, ICAM-1, GITR, BAFFR, HVEM (LIGHTR), SLAMF7, NKp80 (KLRF1), CD 127, CD160, CD19, CD4, CD8α, CD8β, IL2Rβ, IL2Rγ, IL7Rα, ITGA4, VLA1, CD49a, ITGA4, IA4, CD49D, ITGA6, VLA- 6, CD49f, ITGAD, CD11d, ITGAE, CD103, ITGAL, CD11a, LFA-1, ITGAM, CD11b, ITGAX, CD11c, ITGB1, CD29, ITGB2 , CD18, LFA-1, ITGB7, TNFR2, TRANCE / RANKL, DNAM1 (CD226), SLAMF4 (CD244, 2B4), CD84, CD96 (Tactile), CEACAM1, CRTAM, Ly9 (CD229), CD160 (BY55), PSGL1, CD100 (SEMA4D), CD69, SLAMF6 (NTB-A, Ly108), SLAM (SLAMF1, CD150, IPO-3), BLAME (SLAMF8), SELPLG (CD162), LTBR, ​​LAT, GADS, SLP-76, PAG / Cbp, NKp44, NKp30, NKp46, NKG2D, other costimulatory molecules described herein, any derivative, variant, or fragment thereof, any synthetic sequence of a costimulatory molecule having the same functional capability, as well as any combination thereof. Thus, although the present invention is exemplified primarily with 4-1BB (CD137) as the costimulatory signaling domain, other costimulatory domains are within the scope of the present invention.

[0115] In one embodiment, the nucleic acid sequence of the intracellular domain of a costimulatory molecule comprises the amino acid sequence of the costimulatory molecule 4-1BB (also known and referred to as the CD137 intracellular domain): Encode TIFF0007649755000007.tif4147.

[0116] In some embodiments, the intracellular domain of the costimulatory molecule comprises an amino acid sequence having at least 60%, at least 65%, at least 70%, at least 75%, at least 80%, at least 81%, at least 82%, at least 83%, at least 84%, at least 85%, at least 86%, at least 87%, at least 88%, at least 89%, at least 90%, at least 91%, at least 92%, at least 93%, at least 94%, at least 95%, at least 96%, at least 97%, at least 98%, or at least 99% sequence identity to SEQ ID NO: 20. In yet another embodiment, the nucleic acid sequence encoding the 4-1BB intracellular domain is Includes TIFF0007649755000008.tif19151 (codon optimized).

[0117] In some embodiments, the nucleic acid sequence encoding the 4-1BB intracellular domain is Contains TIFF0007649755000009.tif19153.

[0118] In some embodiments, the 4-1BB intracellular domain comprises an amino acid sequence having at least 60%, at least 65%, at least 70%, at least 75%, at least 80%, at least 81%, at least 82%, at least 83%, at least 84%, at least 85%, at least 86%, at least 87%, at least 88%, at least 89%, at least 90%, at least 91%, at least 92%, at least 93%, at least 94%, at least 95%, at least 96%, at least 97%, at least 98%, or at least 99% sequence identity to an amino acid sequence selected from the group consisting of SEQ ID NO:20. In other embodiments, the 4-1BB intracellular domain is encoded by a nucleic acid sequence having at least 60%, at least 65%, at least 70%, at least 75%, at least 80%, at least 81%, at least 82%, at least 83%, at least 84%, at least 85%, at least 86%, at least 87%, at least 88%, at least 89%, at least 90%, at least 91%, at least 92%, at least 93%, at least 94%, at least 95%, at least 96%, at least 97%, at least 98%, or at least 99% sequence identity to a nucleic acid sequence selected from the group consisting of SEQ ID NO: 10 or 16.

[0119] The human intracellular 4-1BB domain provides costimulatory intracellular signaling upon binding to extracellular self-antigens, such as AChR, or fragments thereof, without the requirement of the original ligand.

[0120] It is well recognized that signals generated through the TCR alone are insufficient for full activation of T cells, and that secondary or costimulatory signals are also required. Thus, T cell activation can be said to be mediated by two distinct classes of cytoplasmic signaling sequences: those that initiate antigen-dependent primary activation through the TCR (primary cytoplasmic signaling sequences), and those that act in an antigen-independent manner to provide secondary or costimulatory signals (secondary cytoplasmic signaling sequences).

[0121] Signaling domains In some embodiments, AChR CAAR comprises signal transduction domain.The primary cytoplasmic signal transduction sequence regulates the primary activation of TCR complex in either stimulatory or inhibitory manner.The primary cytoplasmic signal transduction sequence that acts in stimulatory manner can contain signal transduction motif, known as immunoreceptor tyrosine-based activation motif or ITAM.

[0122] Examples of primary signaling sequences containing ITAMs that are particularly useful in the present invention include those derived from TCRzeta, FcRgamma, FcRbeta, CD3gamma, CD3delta, CD3epsilon, CD5, CD22, CD79a, CD79b, and CD66d. It is particularly preferred that the signaling molecule in the CAAR of the present invention comprises a signaling domain derived from CD3zeta.

[0123] In one embodiment, the signaling domain of CAAR can be designed to include a CD3 zeta signaling domain alone or in combination with any other desired cytoplasmic domain useful in the context of the CAAR of the present invention.For example, the signaling domain of CAAR can include a CD3 zeta chain portion and a costimulatory signaling domain.

[0124] In some embodiments, AChR CAAR comprises CD3ζ signaling domain alone or in combination with any other desired cytoplasmic domain useful in the context of AChR CAAR of the present invention.For example, AChR CAAR can comprise CD3ζ chain portion and intracellular domain of costimulatory molecule.In some embodiments, CD3ζ chain portion is human T cell surface glycoprotein CD3ζ chain isoform 3 intracellular domain (human CD247).Human intracellular CD3ζ domain provides stimulatory intracellular signaling without HLA restriction when binding to extracellular self-antigen such as AChR or its fragment.

[0125] In one embodiment, the nucleic acid sequence of the signaling domain comprises a nucleic acid sequence encoding a CD3 zeta signaling domain. In another embodiment, the nucleic acid sequence of the CD3 zeta signaling domain is Encoding the amino acid sequence containing TIFF0007649755000010.tif19153.

[0126] In another embodiment, the nucleic acid sequence encoding the CD3 zeta signaling domain is Contains TIFF0007649755000011.tif48153.

[0127] In another embodiment, the nucleic acid sequence encoding the CD3 zeta signaling domain is Contains TIFF0007649755000012.tif48152.

[0128] In some embodiments, the signaling domain comprises an amino acid sequence having at least 60%, at least 65%, at least 70%, at least 75%, at least 80%, at least 81%, at least 82%, at least 83%, at least 84%, at least 85%, at least 86%, at least 87%, at least 88%, at least 89%, at least 90%, at least 91%, at least 92%, at least 93%, at least 94%, at least 95%, at least 96%, at least 97%, at least 98%, or at least 99% sequence identity to SEQ ID NO:38, or to SEQ ID NO:24 or SEQ ID NO: 53.

[0129] Other domains In some embodiments, the AChR CAAR and the polynucleotide encoding the AChR CAAR comprise a human T cell surface glycoprotein CD8 alpha chain signal peptide. The human CD8 alpha signal peptide is responsible for translocation of the receptor to the T cell surface.

[0130] In other embodiments, the AChR CAAR and the polynucleotide encoding the AChR CAAR comprise an IgG signal peptide. In some embodiments, the IgG signal peptide is In another embodiment, the IgG signal peptide is encoded by a nucleic acid sequence comprising: TIFF0007649755000014.tif4128. In some embodiments, the IgG signal peptide is encoded by a nucleic acid sequence having at least 60%, at least 65%, at least 70%, at least 75%, at least 80%, at least 81%, at least 82%, at least 83%, at least 84%, at least 85%, at least 86%, at least 87%, at least 88%, at least 89%, at least 90%, at least 91%, at least 92%, at least 93%, at least 94%, at least 95%, at least 96%, at least 97%, at least 98%, or at least 99% sequence identity to the nucleic acid sequence of SEQ ID NO:2. In some embodiments, the IgG signal peptide comprises an amino acid sequence having at least 60%, at least 65%, at least 70%, at least 75%, at least 80%, at least 81%, at least 82%, at least 83%, at least 84%, at least 85%, at least 86%, at least 87%, at least 88%, at least 89%, at least 90%, at least 91%, at least 92%, at least 93%, at least 94%, at least 95%, at least 96%, at least 97%, at least 98%, or at least 99% sequence identity to the amino acid sequence of SEQ ID NO:12.

[0131] In one embodiment, the polynucleotide encoding the AChR CAAR comprises a peptide linker nucleic acid sequence. In another embodiment, the AChR CAAR comprises a peptide linker. In yet another embodiment, the cytoplasmic signaling sequences within the intracellular signaling domain of the AChR CAAR can be linked together in a random order or a specified order. Optionally, a short oligopeptide or polypeptide linker, for example, 2-10 amino acids in length, can form the linkage. A glycine-serine (GS) doublet is a particularly suitable linker.

[0132] In some embodiments, CAAR comprises a transmembrane domain and / or a cytoplasmic (intracellular) domain from a killer immunoglobulin-like receptor (KIR) family protein (Figures 18A-18B). The KIR gene family has at least 15 loci (KIR2DL1, KIR2DL2 / L3, KIR2DL4, KIR2DL5A, KIR2DL5B, KIR2DS1, KIR2DS2, KIR2DS3, KIR2DS4, KIR2DS5, KIR3DL1 / S1, KIR3DL2, KIR3DL3) and two pseudogenes (KIR2DP1 and KIR3DP1) encoded within the 100-200 Kb region of the Leukocyte Receptor Complex (LRC) located on chromosome 19 (19q13.4). The LRC constitutes a large 1 Mb dense cluster of rapidly evolving immune genes that contains genes encoding other cell surface molecules with characteristic Ig-like extracellular domains. In addition, the expanded LRC contains genes encoding transmembrane adaptor molecules DAP10 and DAP12. Thus, cells containing the CAAR of the present invention that contains KIR transmembrane and / or cytoplasmic domains may also contain polynucleotides encoding DAP10 or DAP12 (Figures 18A-18B). In some embodiments, the KIR is KIRS2 or KIR2DS2.

[0133] Vector containing AChR CAAR In one aspect, the present invention includes a vector comprising a polynucleotide encoding a chimeric autoantibody receptor (CAAR), the polynucleotide comprising an extracellular domain comprising a human AChR autoantigen or a fragment thereof, and optionally a transmembrane domain, and / or an intracellular signaling domain. In one embodiment, the vector comprises any of the nucleic acid sequences encoding CAAR as described herein.

[0134] The vector can be introduced into cells, such as T cells, in vivo or ex vivo. In some embodiments, cells are transduced in vivo or ex vivo. In some embodiments, cells are transduced in vivo. In some embodiments, a vector containing a nucleic acid encoding the CAAR of the present invention is administered to a subject to transduce cells (e.g., T cells, NK cells) in the subject in vivo, thereby generating CAAR cells in the subject in vivo. Examples of in vivo transduction of cells and methods of in vivo transduction of cells include those described in Pfeiffer et al., EMBO Mol Med. 2018 Nov; 10(11): e9158; and Agarwal et al. (2019) OncoImmunology, 8:12, DOI: 10.1080 / 2162402X.2019.1671761.

[0135] In another embodiment, the vector includes a plasmid vector, a viral vector, a retrotransposon (e.g., piggyback, sleeping beauty), a site-specific insertion vector (e.g., CRISPR, zinc finger nuclease, TALEN), or a suicide expression vector, or other vectors known in the art. Examples of the use of CRISPR, Zn finger nuclease, and TALEN gene editing systems to genetically modify cells that may be used therapeutically include those described in Hoban et al., Blood 2015 Apr 23; 125(17): 2597-2604; Pino-Barrio et al., Sci. Rep., 2020 Apr 24; 10(1):6997. doi: 10.1038 / s41598-020-63971-z; DeWitt et al., Methods, 2017 May 15; 121-122: 9-15; and Rui et al., Trends Biotechnol. 2019 Mar; 37(3): 281-293.

[0136] In some embodiments, the third generation self-inactivating lentiviral vector plasmid can be used, in which the expression of CAR is regulated by the human elongation factor 1 alpha promoter.This results in the stable (permanent) expression of CAR in host cells, such as host T cells.As an alternative approach, coding mRNA can be electroporated into host cells, which will achieve the same therapeutic effect as the host cell transduced with virus, but it is not considered to be permanent because mRNA is diluted with cell division.

[0137] All constructs disclosed herein can be used with the third generation lentiviral vector plasmid, other viral vectors, or RNA approved for use in human cells.In one embodiment, vector is a viral vector, such as lentiviral vector.In another embodiment, vector is an RNA vector.

[0138] The expression of AChR CAAR can be verified by sequencing. The expression of full-length CAAR protein can be verified by immunoblotting, immunohistochemistry, flow cytometry or other techniques known and available in the art.

[0139] The present invention also provides a vector into which the DNA encoding the CAAR of the present invention is inserted.Vector, including those derived from retroviruses such as lentiviruses, are suitable tools for achieving long-term gene transfer, because they allow the long-term and stable integration of transgenes and their propagation in daughter cells.Lentivirus vectors have the additional advantage over vectors derived from oncoretroviruses such as mouse leukemia virus, in that they can transduce non-proliferating cells such as hepatocytes.They also have the additional advantage of resulting in low immunogenicity in the subjects into which they are introduced.

[0140] In brief summary, expression of natural or synthetic polynucleotides encoding CAAR is typically achieved by functionally linking the nucleic acid encoding CAAR polypeptide or a portion thereof to a promoter (e.g., EF1α promoter) and incorporating the construct into an expression vector.Vector is generally capable of replicating in mammalian cells and / or being integrated into mammalian cell genome.Typical vectors contain transcription and translation terminators, initiation sequences, and promoters useful for regulating the expression of desired nucleic acid sequences.

[0141] Nucleic acid can be cloned into any number of different kinds of vectors.For example, nucleic acid can be cloned into vectors including, but not limited to, plasmids, phagemids, phage derivatives, animal viruses, and cosmids.Vectors of particular interest include expression vectors, replication vectors, probe generation vectors, and sequencing vectors.

[0142] Expression vector may be provided to cell in the form of viral vector.Viral vector technology is well known in the art and described, for example, in Sambrook et al., 2012, MOLECULAR CLONING: A LABORATORY MANUAL, volumes 1-4, Cold Spring Harbor Press, NY, and other manuals of virology and molecular biology.Viruses that are useful as vectors include, but are not limited to, retroviruses, adenoviruses, adeno-associated viruses, herpes viruses, and lentiviruses.Generally, suitable vectors contain a replication origin that functions in at least one organism, a promoter sequence, a convenient restriction endonuclease site, and one or more selectable markers (e.g., WO 01 / 96584; WO 01 / 29058; and U.S. Patent No. 6,326,193).

[0143] In some embodiments, the vector is a transposon-based expression vector. A "transposon" or "transposable element" is a DNA sequence that can change its position in a genome. There are two distinct types of transposons: class II transposons, which contain DNA that moves from place to place directly; and class I transposons, which are retrotransposons that first transcribe DNA into RNA and then use reverse transcriptase to make a DNA copy of the RNA and insert it into a new location. In a transposon system, the transcription unit that contains the nucleic acid sequence that codes for, for example, CAAR is flanked by the terminal repeats of the transposon. The transposon typically interacts with a transposase that recognizes the terminal repeats and mediates the movement of the transposon. The transposase can be co-delivered, for example, as a protein, can be encoded on the same vector as CAAR, or can be encoded on a separate vector. Non-limiting examples of transposon / transposase systems include Sleeping Beauty, Piggybac, Frog Prince, and Prince Charming.Examples of transposon systems include Ivics et al., Cell 1997 Nov 14;91(4):501-10;Ding et al., Cell. 2005 Aug 12;122(3):473-83.;Li et al., Proc Natl Acad Sci US A. 2013 Feb 5;110(6):E478-87. doi: 10.1073 / pnas.1121543109;Hudecek et al., Curr Opin Genet Dev. 2018 Oct;52:100-108. doi: 10.1016 / j.gde.2018.06.003;Tipanee et al., Biosci Rep. 2017 Dec 5;37(6). pii: BSR20160614. doi: 10.1042 / BSR20160614; and VandenDriessche et al., Blood. 2009 Aug 20;114(8):1461-8. doi: 10.1182 / blood-2009-04-210427.

[0144] Other promoter elements, such as enhancers, regulate the frequency of transcription initiation. Typically, these are located in the region 30-110 bp upstream of the start site, but many promoters have recently been shown to contain functional elements downstream of the start site as well. In many cases, the spacing between promoter elements is flexible, so that promoter function is preserved even if elements are inverted or moved relative to one another. In the thymidine kinase (tk) promoter, promoter elements can be spaced up to 50 bp apart without loss of responsiveness. In some promoters, individual elements appear to be able to activate transcription either cooperatively or independently.

[0145] An example of a promoter is the cytomegalovirus (CMV) immediate early promoter sequence. This promoter sequence is a strong constitutive promoter sequence capable of driving high levels of expression of any polynucleotide sequence operably linked to it. However, other constitutive promoter sequences can also be used, including but not limited to the Simian Virus 40 (SV40) early promoter, mouse mammary tumor virus (MMTV), human immunodeficiency virus (HIV) long terminal repeat (LTR) promoter, MoMuLV promoter, avian leukosis virus promoter, Epstein-Barr virus immediate early promoter, Rous sarcoma virus promoter, elongation factor-1α promoter, and human gene promoters such as, but not limited to, actin promoter, myosin promoter, hemoglobin promoter, and creatine kinase promoter. Furthermore, the present invention should not be limited to the use of constitutive promoters. Inducible promoters are also contemplated as part of the present invention. The use of an inducible promoter provides a molecular switch that can enable expression of a polynucleotide sequence operably linked to it when such expression is desired and disable expression when expression is not desired. Examples of inducible promoters include, but are not limited to, metallothionine promoter, glucocorticoid promoter, progesterone promoter and tetracycline promoter.In some embodiments, inducible promoter is activated in response to extracellular ligand.For example, in some embodiments, inducible promoter is activated (and CAAR expression is regulated) by extracellular ligand that binds to synthetic receptor.For example, in some embodiments, synthetic receptor, for example, synthetic Notch receptor (i.e., "synNotch"), can be used as binding-triggered transcription switch, which activates the promoter that CAAR coding nucleic acid sequence is functionally linked to when it binds to its ligand.Thus, as a non-limiting example, such a system may require the presence of a ligand (e.g., synNotch binds) for immune cells to be responsive to BCR (e.g., CAAR binds) or autoantibodies. Requiring a specific combination to generate a signaling output in a molecular circuit results in a logic gate. See, e.g., Roybal et al., 2016 Cell 164(4):770-9.

[0146] Other examples of systems for expressing or regulating the expression of chimeric receptors include Wu et al. (2015) Science 350: aab4077;Fedorov et al. (2014) Cancer Journal 20:160-165;Kloss et al. (2013) Nature Biotechnology 31: 71-75;Sakemura et al. (2016) Cancer Immunol. Res. 4:658-668;Hill et al. (2018) Nature Chemical Biology 14:112-117;Di Stasi et al. (2011) N. Engl. J. Med. 365:1673-1683;Budde et al. (2013) PLoS One 8: e82742;Wei et al. (2012) Nature 488: 384-388;Ma et al. (2016) Proc. Natl. Acad. Sci. USA 113: E450-458; Rodgers et al. (2016) Proc. Natl. Acad. Sci. USA 113: E459-468; Kudo et al. (2014) Cancer Res. 74: 93-103, and Chen et al. (2010) Proc. Natl. Acad. Sci. USA 107, 8531-8536.

[0147] In order to evaluate the expression of CAAR polypeptide or its part, the expression vector introduced into cell can also contain a selection marker gene or a reporter gene or both, so as to facilitate the identification and selection of expressing cells from the group of cells to be transfected or infected by viral vector.In other aspects, the selection marker can also be carried on a separate piece of DNA and used in co-transfection procedures.Both the selection marker gene and the reporter gene can be flanked by appropriate regulatory sequences to allow expression in host cell.Useful selection markers include, for example, antibiotic resistance genes, such as neo.

[0148] Reporter genes are used to identify potentially transfected cells and to evaluate the functionality of regulatory sequences. In general, a reporter gene is a gene that is not present in or expressed by the recipient organism or tissue and encodes a polypeptide whose expression is manifested by some easily detectable property, such as enzymatic activity. Expression of the reporter gene is evaluated at a suitable time after the DNA is introduced into the recipient cells. Suitable reporter genes may include genes encoding luciferase, β-galactosidase, chloramphenicol acetyltransferase, secreted alkaline phosphatase, or green fluorescent protein (e.g., Ui-Tei et al., 2000 FEBS Letters 479:79-82). Suitable expression systems are well known and can be prepared using known techniques or obtained commercially. In general, the construct with the minimal 5' flanking region that exhibits the highest level of expression of the reporter gene is identified as the promoter. Such promoter regions can be linked to reporter genes and used to assess the ability of agents to modulate transcription driven by the promoter.

[0149] Methods for introducing and expressing genes into cells are known in the art.In relation to expression vectors, the vectors can be easily introduced into host cells, such as mammalian cells, bacterial cells, yeast cells or insect cells, by any method in the art.For example, the expression vectors can be introduced into host cells by physical, chemical or biological means.

[0150] The physical method for introducing polynucleotide into host cell includes calcium phosphate precipitation, lipofection, particle bombardment, microinjection, electroporation, etc. The method for preparing cells containing vector and / or exogenous nucleic acid is well known in the art. For example, see Sambrook et al., 2012, MOLECULAR CLONING: A LABORATORY MANUAL, volumes 1-4, Cold Spring Harbor Press, NY. One of the preferred methods for introducing polynucleotide into host cell is calcium phosphate transfection.

[0151] Biological methods for introducing polynucleotide of interest into host cells include the use of DNA vectors and RNA vectors. RNA vectors include vectors with RNA promoters and / or other related domains for the production of RNA transcripts. Viral vectors, especially retroviral vectors, have become the most widely used method for inserting genes into mammalian cells, such as human cells. Other viral vectors can be derived from lentiviruses, poxviruses, herpes simplex viruses, adenoviruses and adeno-associated viruses, etc. See, for example, U.S. Patent Nos. 5,350,674 and 5,585,362.

[0152] Chemical means for introducing polynucleotides into host cells include colloidal dispersion systems, such as macromolecular complexes, nanocapsules, microspheres, beads, and the like, as well as lipid-based systems, including oil-in-water emulsions, micelles, mixed micelles, and liposomes. One exemplary colloidal system for use as a delivery vehicle in vitro and in vivo is a liposome (e.g., an artificial membrane vesicle).

[0153] When a non-viral delivery system is utilized, one exemplary delivery vehicle is a liposome. The use of lipid formulations is envisaged for the introduction of nucleic acid into host cells (in vitro, ex vivo or in vivo). In another aspect, the nucleic acid may be associated with lipid. The nucleic acid associated with lipid may be encapsulated in the aqueous interior of liposome, located within the lipid bilayer of liposome, attached to liposome via a linking molecule that binds both liposome and oligonucleotide, encapsulated within liposome, complexed with liposome, dispersed in a solution containing lipid, mixed with lipid, combined with lipid, contained in suspension in lipid, contained or complexed in micelle, or otherwise associated with lipid. The composition to which lipid, lipid / DNA or lipid / expression vector is associated is not limited to any particular structure in solution. For example, they may exist in a bilayer structure, as micelles, or as a "disintegrated" structure. They may also simply be scattered in the solution and may form aggregates that are not uniform in size or shape. Lipids are fatty substances that may be natural or synthetic. For example, lipids include the lipid droplets that occur naturally in the cytoplasm, as well as the class of compounds that contain long-chain aliphatic hydrocarbons and their derivatives, such as fatty acids, alcohols, amines, aminoalcohols, and aldehydes.

[0154] Lipids suitable for use can be obtained from commercial sources. For example, dimyristyl phosphatidylcholine ("DMPC") can be obtained from Sigma, St. Louis, MO; diacetyl phosphate ("DCP") can be obtained from K & K Laboratories (Plainview, NY); cholesterol ("Choi") can be obtained from Calbiochem-Behring; dimyristyl phosphatidylglycerol ("DMPG") and other lipids can be obtained from Avanti Polar Lipids, Inc. (Birmingham, AL). Stock solutions of lipids in chloroform or chloroform / methanol can be stored at about -20°C. Chloroform evaporates more readily than methanol, so it is preferred to use it as the only solvent. "Liposome" is a generic term that encompasses a variety of unilamellar and multilamellar lipid vehicles formed by the formation of closed lipid bilayers or aggregates. Liposomes can be characterized as having a vesicular structure with a phospholipid bilayer membrane and an internal aqueous medium. Multilamellar liposomes have multiple lipid layers separated by aqueous medium. They form spontaneously when phospholipids are suspended in an excess of aqueous solution. The lipid components undergo self-rearrangement followed by the formation of closed structures, trapping water and dissolved solutes between the lipid bilayers (Ghosh et al., 1991 Glycobiology 5:505-10). However, compositions with structures in solution that differ from the normal vesicular structure are also encompassed. For example, lipids may adopt a micellar structure or simply exist as heterogeneous aggregates of lipid molecules. Lipofectamine-nucleic acid complexes are also contemplated.

[0155] Any domain and / or fragment of CAAR, vectors, and promoters may be synthetic gene fragments amplified by PCR or any other means known in the art.

[0156] Cells containing CAAR In another aspect, the present invention includes genetically modified cells comprising the AChR chimeric autoantibody receptors (CAARs) disclosed herein.

[0157] In another embodiment, the genetically modified cell expresses AChR CAAR.In this embodiment, the cell has high affinity for AChR autoantibody-based B cell receptor (BCR) on B cells or on B cells that have differentiated into plasma cells that have not yet downregulated their BCR.As a result, the genetically modified cell can induce the direct killing of anti-AChR B cells or the indirect killing of plasma cells that express AChR autoantibody.In yet another embodiment, the genetically modified cell has low affinity for antibodies that bind to Fc receptors.

[0158] In one embodiment, the genetically modified cell is an immune cell, such as a T cell, a monocyte, a natural killer (NK) cell, or a cytokine-induced killer cell. In one embodiment, the genetically modified cell is a T cell, such as a helper T cell, a cytotoxic T cell, a memory T cell, a regulatory T cell, a γδ T cell, a cell line thereof, a T memory stem cell, or other T effector cell.

[0159] It is also useful that genetically modified cells, such as T cells, have limited toxicity to healthy cells and specificity to cells expressing autoantibodies.Such specificity prevents or reduces the off-target toxicity that prevails in current therapies that are not specific to autoantibodies.In one embodiment, genetically modified cells, such as T cells, have limited toxicity to healthy cells.In one embodiment, genetically modified cells, such as T cells, are autologous cells.In another embodiment, genetically modified cells, such as T cells, are allogeneic cells.

[0160] In some embodiments, the present invention includes genetically modified immune cells derived from in vitro differentiated pluripotent stem cells. Examples of pluripotent stem cells include induced pluripotent stem cells (IPSCs) and embryonic stem (ES) cells. In some other embodiments, the genetically modified immune cells are derived from multipotent stem cells, such as hematopoietic stem cells (HSCs). In some embodiments, the genetically modified immune cells are derived from induced pluripotent stem cells (IPSCs). In some embodiments, the genetically modified immune cells are derived from hematopoietic stem cells (HSCs) or hematopoietic stem and progenitor cells (HSPCs). Examples of immune cells, e.g., T cells and NK cells, derived from pluripotent stem cells such as IPSCs or derived from multipotent stem cells such as HSCs include Hermanson et al., Stem Cells, 2016 Jan;34(1):93-101. doi: 10.1002 / stem.2230;Zeng at al., Stem Cell Reports. 2017 Dec 12;9(6):1796-1812. doi: 10.1016 / j.stemcr.2017.10.020;Equizabal et al., Front Immunol. 2014 Sep 15;5:439. doi: 10.3389 / fimmu.2014.00439;Seet et al., Nat Methods. 2017 May;14(5):521-530. doi: 10.1038 / nmeth.4237; Nianias et al., Curr Hematol Malig Rep. 2019; 14(4): 261-268. In some embodiments, the genetically modified immune cells are T cells or NK cells derived from pluripotent stem cells. In some embodiments, the genetically modified immune cells are T cells or NK cells derived from multipotent stem cells. In some embodiments, the pluripotent stem cells are induced pluripotent stem cells (IPSCs). In some embodiments, the multipotent stem cells are hematopoietic stem cells (HSCs). In other embodiments, the invention includes T cells, such as primary cells, expanded T cells derived from primary T cells, T cells derived from in vitro differentiated stem cells, T cell lines such as Jurkat cells, T cells from other sources, combinations thereof, and other effector cells.For example, Jurkat cell lines transduced with NFAT response elements followed by GFP can be used to detect and isolate AChR-specific B cells and to clone AChR-specific antibody repertoires in a comprehensive and unbiased manner. Interacting B and Jurkat cells can be detected as GFP-positive doublets or multimers and sorted by flow cytometry. Expression cloning of genes encoding B cell receptors will provide further information about autoimmunity and autoantibodies in autoantibody-mediated neuromuscular junction (NMJ) diseases such as myasthenia gravis (MG).

[0161] In some embodiments, the present invention includes cells genetically modified in vivo, e.g., CAAR cells generated in vivo by delivery of a vector containing a nucleic acid encoding CAAR to a target cell (e.g., a T cell or NK cell) in a subject.

[0162] The functional ability of CAAR to bind autoantibodies and serum, including but not limited to MG serum, can be evaluated in Jurkat reporter cell line, which depends on the activation of CAAR by binding to plate-bound autoantibodies (in response, activated cells emit green fluorescence due to the NFAT-GFP reporter construct contained therein). Such a method is a useful and reliable qualitative measurement of functional binding ability. Proper processing of autoantigens on the cell surface is also important and can be measured using monoclonal antibodies. In addition, truncations or mutations of AChR based on major disease epitopes are also useful and are included herein. Versions with various lengths of hinge regions or GS linkers are also useful. With regard to safety, it is preferable to prevent or reduce possible homophilic and heterophilic interactions and activation (e.g., AChR-AChR) between transduced cells or to neuromuscular junctions.

[0163] Further evaluation of the efficacy and safety of CAAR can be performed, for example, as follows.

[0164] The constructs can be transiently transfected into human cells such as 293T / 17. Surface expression can be detected with monoclonal antibodies (either IgG or ScFv) specific for the above-mentioned extracellular domains, interdomain linkers, or other structures contained in CAAR. Binding can be verified with specific secondary antibodies and quantified by flow cytometry.

[0165] The construction of membrane-expressed constructs of human anti-AChR antibodies of any isotype can serve as target cells for testing various AChR-CAARs. Additional target cell lines can be created as required by expressing human monoclonal antibodies on the surface of cell lines (e.g., Nalm6 cells or K562 cells).

[0166] autoimmune disease The present invention also provides a method for preventing, treating, and / or managing disorders or autoimmune diseases associated with autoantibody-expressing cells in the context of autoantibody-mediated neuromuscular junction (NMJ) disease. The method includes administering genetically modified cells, such as T cells, that contain the CAAR of the present invention that binds to autoantibody-expressing cells to a subject in need thereof. In one aspect, the subject is a human. Non-limiting examples of autoantibody-mediated NMJ disease include, but are not limited to, myasthenia gravis (MG).

[0167] The cells of the present invention administered can be autologous, allogeneic, or xenogeneic to the subject to be treated.In the method of treatment, cells, such as T cells, isolated from a subject can be modified to express appropriate CAAR, expanded ex vivo, and then reinfused into the same subject (e.g., T cells are autologous T cells).In some embodiments, cells, such as T cells, are reinfused into a subject different from the donor of the original T cells (e.g., T cells are allogeneic T cells).Modified cells, such as T cells, recognize target cells, such as B cells or plasma cells that produce AChR autoantibodies, and are activated, resulting in the death of autoimmune target cells.

[0168] In patients with autoimmune diseases, such as MG patients, relapses may also occur. In patients treated with drugs (e.g., prednisone or rituximab), relapses may be mediated by the persistence of the same autoantibody B cell clones, whereas remission is associated with the disappearance of these clones. By infusing AChR CAAR cells, e.g., T cells, autoimmune cells are depleted, inducing long-term remission, and / or autoantigen-reactive clones do not reappear, likely due to the long life span of AChR CAAR cells, e.g., T cells.

[0169] In order to monitor AChR CAAR expressing cell in vitro, in situ or in vivo, AChR CAAR cell can further express detectable marker.When AChR CAAR binds to target, detectable marker is activated and expressed, which can be detected by assays known in the art, such as flow cytometry.In one embodiment, AChR CAAR comprises NFAT response element and detectable marker, such as green fluorescent protein (GFP), in order to detect and quantify AChR CAAR expressing cell.

[0170] Source of T cells In some embodiments, cells, e.g., T cells, are transduced ex vivo. Prior to expansion and genetic modification, T cells (e.g., autologous or allogeneic T cells) are obtained from a subject. Examples of subjects include humans, dogs, cats, mice, rats, and transgenic species thereof. T cells can be obtained from a number of sources, including skin, peripheral blood mononuclear cells, bone marrow, lymph node tissue, umbilical cord blood, thymus tissue, tissue from an infection site, ascites, pleural effusion, spleen tissue, and tumors. In some embodiments of the invention, any of a variety of T cell lines available in the art can be used. In some embodiments of the invention, T cells are obtained from a blood unit collected from a subject using any of a variety of techniques known to those skilled in the art, such as Ficoll™ separation. In a preferred embodiment, cells from an individual's shed blood are obtained by apheresis. Apheresis products typically include lymphocytes, including T cells, monocytes, granulocytes, B cells, other nucleated white blood cells, red blood cells, and platelets. In one embodiment, the cells collected by apheresis can be washed to remove the plasma fraction, and the cells can be placed in a suitable buffer or medium for the subsequent processing steps. In one embodiment of the present invention, the cells are washed with phosphate buffered saline (PBS). In an alternative embodiment, the washing solution is calcium-free and magnesium-free or many, but not all, divalent cations. Surprisingly, an initial activation step in the absence of calcium also results in enhanced activation. As the skilled artisan will readily appreciate, the washing step can be accomplished by methods known in the art, such as by using a semi-automated "flow-through" centrifuge (such as, for example, the Cobe 2991 cell processor, Baxter CytoMate, or Haemonetics Cell Saver 5) according to the manufacturer's instructions. After washing, the cells can be resuspended in a variety of biocompatible buffers, such as, for example, Ca-free, Mg-free PBS, PlasmaLyte A, or other saline solutions with or without buffering agents.Alternatively, the undesirable components of the apheresis sample may be removed and the cells resuspended directly in culture medium.

[0171] In another embodiment, T cells are isolated from peripheral blood lymphocytes by lysing red blood cells and depleting monocytes, for example, by centrifugation on a PERCOLL™ gradient or by counterflow centrifugal elutriation. + , CD28 + , CD4 + , CD8 + , CD45RA + , and CD45RO +A particular subpopulation of T cells, such as T cells, can be further isolated by positive or negative selection methods. For example, in one preferred embodiment, T cells are isolated by incubation with anti-CD3 / anti-CD28 (i.e., 3x28)-conjugated beads, such as DYNABEADS® M-450 CD3 / CD28 T, for a period sufficient for positive selection of the desired T cells. In one embodiment, this period is about 30 minutes. In one further embodiment, this period ranges from 30 minutes to 36 hours or more, and all integer values ​​therebetween. In one further embodiment, this period is at least 1 hour, 2 hours, 3 hours, 4 hours, 5 hours, or 6 hours. In yet another preferred embodiment, this period is 10 to 24 hours. In one preferred embodiment, the incubation period is 24 hours. For some patients, a longer incubation period, such as 24 hours, can be used to increase cell yield. In any situation where there are few T cells compared to other cell types, such as in immunocompromised individuals, longer incubation times can be used to isolate T cells. Furthermore, the use of longer incubation times can also increase the efficiency of capture of CD8+ T cells. Thus, by simply shortening or extending this time, T cells can bind to the CD3 / CD28 beads, and / or by increasing or decreasing the ratio of beads to T cells (as further described herein), subpopulations of T cells can be preferentially selected for or excluded at the beginning of culture or at other times during the process. Additionally, by increasing or decreasing the ratio of anti-CD3 and / or anti-CD28 antibodies on the beads or other surface, subpopulations of T cells can be preferentially selected for or against at the beginning of culture or at other desired times. Those skilled in the art will recognize that multiple rounds of selection can be used in the context of the present invention. In some embodiments, it may be desirable to perform this selection procedure and use "unselected" cells in the activation and expansion process. The "unselected" cells can also be subjected to further selection.

[0172] Enrichment of a T cell population by negative selection can be performed by a combination of antibodies against unique surface markers on the negatively selected cells. One method is cell sorting and / or selection by negative magnetic immunoadhesion or flow cytometry using a cocktail of monoclonal antibodies against cell surface markers present on the negatively selected cells. For example, negative selection can be used to enrich for CD4 + Monoclonal antibody cocktails for enriching cells typically include antibodies against CD14, CD20, CD11b, CD16, HLA-DR, and CD8. In some embodiments, typically CD4 + , CD25 + , CD62L + , G.I.T.R. + , and FoxP3 + It may be desirable to enrich or positively select regulatory T cells expressing CD25. Alternatively, in some embodiments, regulatory T cells are depleted by anti-CD25-bound beads or other similar selection methods. In other embodiments, subpopulations of T cells can be isolated by positive or negative selection techniques, including, but not limited to, cells positive for or expressing high levels of one or more surface markers, such as CD28+, CD8+, CCR7+, CD27+, CD127+, CD45RA+, and / or CD45RO+ T cells.

[0173] To isolate the desired cell population by positive or negative selection, the concentration of cells and surfaces (e.g., particles such as beads) can be varied. In some embodiments, it may be desirable to significantly reduce the volume in which the beads and cells are mixed together (i.e., increase the concentration of cells) to ensure maximum contact between the cells and beads. For example, in one embodiment, a concentration of 2 billion cells / ml is used. In one embodiment, a concentration of 1 billion cells / ml is used. In further embodiments, greater than 100 million cells / ml is used. In further embodiments, a cell concentration of 10 million cells / ml, 15 million cells / ml, 20 million cells / ml, 25 million cells / ml, 30 million cells / ml, 35 million cells / ml, 40 million cells / ml, 45 million cells / ml, or 50 million cells / ml is used. In yet another embodiment, a cell concentration from 75 million / ml, 80 million / ml, 85 million / ml, 90 million / ml, 95 million / ml, or 100 million / ml is used. In a further embodiment, a concentration of 125 million / ml or 150 million / ml can be used. The use of a high concentration can result in increased cell yield, cell activation, and cell expansion. Furthermore, the use of a high cell concentration can increase the efficiency of capture of cells that weakly express the target antigen of interest, such as CD28-negative T cells, or from samples where many tumor cells are present (i.e., leukemic blood, tumor tissue, etc.). Such cell populations are therapeutically valuable and desirable to obtain. For example, the use of a high concentration of cells can increase the efficiency of capture of cells that weakly express the target antigen of interest, such as CD28-negative T cells, or from samples where many tumor cells are present (i.e., leukemic blood, tumor tissue, etc.). + This allows for more efficient selection of T cells.

[0174] In a related embodiment, it may be desirable to use a lower concentration of cells. High dilution of the mixture of T cells and surfaces (e.g., particles such as beads) minimizes interactions between the particles and the cells. This selects for cells that express large amounts of the desired antigen that binds to these particles. For example, CD4 + T cells express higher levels of CD28 and CD8 at dilute concentrations. +In one embodiment, the cell concentration used is 5×10 6 In another embodiment, the concentration used is about 1×10 5 pieces / ml~1×10 6 pieces / ml, and any integer in between.

[0175] In other embodiments, the cells can be incubated on a rotator for various times at various speeds at either 2-10° C. or at room temperature.

[0176] Also, the T cells for stimulation can be frozen after the washing step. Without wishing to be bound by theory, the freezing step and the subsequent thawing step provide a more homogenous preparation by removing granulocytes and to some extent monocytes in the cell population. After the washing step that removes plasma and platelets, the cells can be suspended in a freezing solution. While many freezing solutions and parameters are known in the art and useful in this context, one method involves the use of PBS containing 20% ​​DMSO and 8% human serum albumin, or 10% dextran 40 and 5% dextrose, 20% human serum albumin and 7.5% DMSO, or 31.25% Plasmalyte-A, 31.25% dextrose 5%, 0.45% NaCl, 10% dextran 40 and 5% dextrose, 20% human serum albumin and 7.5% DMSO, or other suitable cell freezing medium containing, for example, Hespan and PlasmaLyte A, and then the cells are frozen to -80°C at a rate of once per minute and stored in the vapor phase in a liquid nitrogen storage tank. In addition to other controlled freezing methods, immediate -20°C or uncontrolled freezing in liquid nitrogen may also be used.

[0177] In one embodiment, cryopreserved cells are thawed and washed as described herein and allowed to sit at room temperature for 1 hour prior to activation using the methods of the invention.

[0178] The present invention also contemplates collection of blood samples or apheresis products from subjects at a time before expanded cells as described herein are required. To this end, the source of cells to be expanded can be collected at any time required, and the desired cells, such as T cells, can be isolated and frozen for later use in T cell therapy for any of a variety of diseases or conditions that may benefit from T cell therapy, such as those described herein. In one embodiment, blood samples or apheresis are taken from generally healthy subjects. In one embodiment, blood samples or apheresis are taken from generally healthy subjects who are at risk of developing disease, but have not yet developed the disease, and the cells of interest are isolated and frozen for later use. In one embodiment, T cells are expanded, frozen, and used at a later time. In one embodiment, samples are collected from patients shortly after diagnosis of a particular disease as described herein, but before any treatment has been administered. In a further embodiment, the cells are isolated from a blood sample or apheresis from a subject prior to any of a variety of appropriate therapeutic modalities, including but not limited to treatment with agents such as rituximab or other anti-CD20 or anti-CD19 agents, anti-FcRn agents, Btk inhibitors, plasma exchange, corticosteroids, mycophenolate, azathioprine, methotrexate, cyclosporine, cyclophosphamide, and the like. These drugs can, for example, inhibit the calcium-dependent phosphatase calcineurin (cyclosporine and FK506) or inhibit p70S6 kinase (rapamycin), which is important for growth factor-induced signal transduction (Liu et al., Cell, 66:807-815,1991; Henderson et al., Immun., 73:316-321,1991; Bierer et al., Curr. Opin. Immun., 5:763-773,1993). In another embodiment, the cells can be pre-isolated and frozen for later use in treatment, for example, following B cell depletion therapy with Rituxan.In a further embodiment, the cells are isolated from the patient and frozen for later use in patients who are concurrently undergoing treatment aimed at inhibiting the complement pathway.

[0179] In a further embodiment of the present invention, T cells are obtained directly from the patient after treatment. In this regard, it has been observed that following the cessation of certain immunosuppressive treatments, particularly with drugs that impair the immune system, the quality of the T cells obtained may be optimal or improved in their ability to expand ex vivo immediately after treatment during the period when the patient would normally be considered to be recovering from the treatment. Similarly, after ex vivo manipulation using the methods described herein, these cells may be in a favorable state for enhanced engraftment and in vivo expansion. Thus, in the context of the present invention, it is envisioned to collect blood cells, including T cells, dendritic cells, or other cells of the hematopoietic lineage, during this recovery phase. Furthermore, in certain embodiments, mobilization (e.g., mobilization with GM-CSF) and conditioning regimens can be used to create conditions in the subject that favor the repopulation, recirculation, regeneration, and / or expansion of certain cell types, particularly during certain defined time frames after treatment. Exemplary cell types include T cells, B cells, dendritic cells, and other cells of the immune system.

[0180] T cell activation and expansion T cells are activated and expanded generally using methods described, for example, in U.S. Patent Nos. 6,352,694; 6,534,055; 6,905,680; 6,692,964; 5,858,358; 6,887,466; 6,905,681; 7,144,575; 7,067,318; 7,172,869; 7,232,566; 7,175,843; 5,883,223; 6,905,874; 6,797,514; 6,867,041; and U.S. Patent Application Publication No. 20060121005.

[0181] In general, the T cells of the present invention are expanded by contact with a surface to which is attached an agent that stimulates CD3 / TCR complex-associated signals and a ligand that stimulates costimulatory molecules on the surface of the T cells. In particular, the T cell population may be stimulated, for example, by contact with an anti-CD3 antibody or its antigen-binding fragment or an anti-CD2 antibody immobilized on a surface, as described herein, or by contact with a protein kinase C activator (e.g., bryostatin) with a calcium ionophore. For costimulation of accessory molecules on the surface of the T cells, a ligand that binds to the accessory molecule is used. For example, the T cell population can be contacted with an anti-CD3 antibody and an anti-CD28 antibody under conditions suitable for stimulating the proliferation of the T cells. CD4 + T cells or CD8 + To stimulate the proliferation of any of T cells, anti-CD3 antibody and anti-CD28 antibody. Examples of anti-CD28 antibody include 9.3, B-T3, XR-CD28 (Diaclone, Besancon, France), and can be used as well as other methods generally known in the art (Berg et al., Transplant Proc. 30(8):3975-3977, 1998;Haanen et al., J. Exp. Med. 190(9):13191328, 1999;Garland et al., J. Immunol Meth. 227(1-2):53-63, 1999).

[0182] In some embodiments, the primary and costimulatory signals for T cells can be provided by various protocols. For example, the agents providing each signal can be in solution or bound to a surface. If bound to a surface, the agents can be bound to the same surface (i.e., in a "cis" formation) or to separate surfaces (i.e., in a "trans" formation). Alternatively, one agent can be bound to a surface and the other agent can be in solution. In one embodiment, the agent providing the costimulatory signal is bound to a cell surface and the agent providing the primary activation signal is in solution or bound to a surface. In some embodiments, both agents can be in solution. In another embodiment, the agents can be in soluble form and then crosslinked to a surface, such as a cell expressing an Fc receptor or an antibody or other binding agent that binds to the agent. In this regard, see, for example, US Patent Application Publication Nos. 20040101519 and 20060034810 regarding artificial antigen presenting cells (aAPCs) contemplated for use in the present invention in activating and expanding T cells.

[0183] In some embodiments, T cell activation and expansion is performed using a non-bead-based method. In some embodiments, the method is based on co-stimulation through T cell receptor signaling and costimulation. In some embodiments, the method uses a dissolvable matrix that induces cross-linking. Examples of non-bead-based methods for T cell activation and expansion include T Cell TransAct™ (Miltenyi Biotec) (https: / / www.miltenyibiotec.com / upload / assets / IM0020239.PDF); Cloudz™ Cell Activation (https: / / www.rndsystems.com / products / cloudz-cell-selection-kits); and soluble antibodies such as those described in Li et al., Journal of Translational Medicine volume 8, Article number: 104 (2010).

[0184] In one embodiment, the two agents are immobilized on beads, either on the same bead, i.e., "cis," or on separate beads, i.e., "trans." As an example, the agent providing the primary activation signal is an anti-CD3 antibody or an antigen-binding fragment thereof, and the agent providing the costimulatory signal is an anti-CD28 antibody or an antigen-binding fragment thereof; and both agents are co-immobilized in equimolar amounts on the same bead. In one embodiment, the CD8 + A 1:1 ratio of each antibody bound to the beads for T cell expansion and T cell proliferation is used. +A 1:1 ratio of each antibody is used for binding to beads for T cell expansion and T cell proliferation. In one aspect of the invention, a ratio of anti-CD3:CD28 antibodies is used for binding to beads such that an increase in T cell expansion is observed compared to the increase observed using a 1:1 ratio. In one particular embodiment, an increase of about 1 to about 3 fold is observed compared to the increase observed using a 1:1 ratio. In one embodiment, the ratio of CD3:CD28 antibodies bound to beads ranges from 100:1 to 1:100 and all integers therebetween. In one aspect of the invention, more anti-CD28 antibodies are bound to the particles than anti-CD3 antibodies, i.e., the ratio of CD3:CD28 is less than 1. In one embodiment of the invention, the ratio of anti-CD28 antibodies to anti-CD3 antibodies bound to beads is greater than 2:1. In one particular embodiment, a 1:100 CD3:CD28 ratio is used for antibodies bound to beads. In another embodiment, a CD3:CD28 ratio of 1:75 is used for the antibody bound to the beads. In a further embodiment, a CD3:CD28 ratio of 1:50 is used for the antibody bound to the beads. In another embodiment, a CD3:CD28 ratio of 1:30 is used for the antibody bound to the beads. In a preferred embodiment, a CD3:CD28 ratio of 1:10 is used for the antibody bound to the beads. In another embodiment, a CD3:CD28 ratio of 1:3 is used for the antibody bound to the beads. In yet another embodiment, a CD3:CD28 ratio of 3:1 is used for the antibody bound to the beads.

[0185] To stimulate T cells or other cellular targets, particle to cell ratios of 1:500 to 500:1 and any integer value therebetween can be used. As one of skill in the art will readily appreciate, the particle to cell ratio can depend on the particle size relative to the target cells. For example, small sized beads may only bind a few cells, while larger beads may bind many. In some embodiments, the cell to particle ratio ranges from 1:100 to 100:1 and any integer value therebetween, and in further embodiments, the ratio includes 1:9 to 9:1 and any integer value therebetween, which can also be used to stimulate T cells. The ratio of anti-CD3-conjugated particles and anti-CD28-conjugated particles to T cells that results in T cell stimulation can vary as described above, but some preferred values ​​include 1:100, 1:50, 1:40, 1:30, 1:20, 1:10, 1:9, 1:8, 1:7, 1:6, 1:5, 1:4, 1:3, 1:2, 1:1, 2:1, 3:1, 4:1, 5:1, 6:1, 7:1, 8:1, 9:1, 10:1 and 15:1, where at least 1:1 particles per T cell is one preferred ratio. In one embodiment, a particle to cell ratio of 1:1 or less is used. In one particular embodiment, the preferred particle:cell ratio is 1:5. In further embodiments, the particle to cell ratio can vary depending on the day of stimulation. For example, in one embodiment, the ratio of particles to cells is 1:1 to 10:1 on day 1, and then additional particles are added to the cells every day or every other day for up to 10 days to a final ratio of 1:1 to 1:10 (based on the number of cells on the day of addition). In one particular embodiment, the ratio of particles to cells is 1:1 on day 1 of stimulation, and adjusted to 1:5 on days 3 and 5 of stimulation. In another embodiment, particles are added every day or every other day, and the final ratio is 1:1 on day 1, and 1:5 on days 3 and 5 of stimulation. In another embodiment, the ratio of particles to cells is 2:1 on day 1 of stimulation, and adjusted to 1:10 on days 3 and 5 of stimulation. In another embodiment, particles are added every day or every other day, and the final ratio is 1:1 on day 1, and 1:10 on days 3 and 5 of stimulation.Those of skill in the art will appreciate that a variety of other ratios are suitable for use in the present invention, particularly as the ratios will vary depending on particle size and cell size and type.

[0186] In a further embodiment of the present invention, cells such as T cells are combined with beads coated with an agent, and then the beads and cells are separated, and then the cells are cultured.In an alternative embodiment, the beads coated with an agent and the cells are not separated before culturing, but are cultured together.In a further embodiment, the beads and cells are first concentrated by applying a force, such as a magnetic force, to increase the ligation of cell surface markers, thereby inducing cell stimulation.

[0187] As an example, cell surface proteins can be ligated by contacting the T cells with paramagnetic beads (3x28 beads) that have anti-CD3 and anti-CD28 attached. In one embodiment, cells (e.g., 10 4 ~10 9T cells) and beads (e.g., DYNABEADS® M-450 CD3 / CD28 T paramagnetic beads, 1:1 ratio) are combined in a buffer, e.g., PBS (without divalent cations such as calcium and magnesium). Again, one skilled in the art will readily appreciate that any cell concentration may be used. For example, the target cells may be very rare in the sample, constituting only 0.01% of the sample, or the entire sample (i.e., 100%) may be composed of the target cells of interest. Thus, any cell number is within the context of the present invention. In some embodiments, it may be desirable to significantly reduce the volume in which the particles and cells are mixed together (i.e., to increase the concentration of cells) to ensure maximum cell-particle contact. For example, in one embodiment, a concentration of about 2 billion cells / ml is used. In another embodiment, more than 100 million cells / ml is used. In a further embodiment, a cell concentration of 10, 15, 20, 25, 30, 35, 40, 45, or 50 million / ml is used. In yet another embodiment, a cell concentration of 75, 80, 85, 90, 95, or 100 million / ml is used. In a further embodiment, a concentration of 125 or 150 million cells / ml can be used. Using a high concentration can result in increased cell yield, cell activation, and cell expansion. Furthermore, using a high cell concentration allows more efficient capture of cells that weakly express target antigens of interest, such as CD28 negative T cells. In some embodiments, such cell populations may have therapeutic value and are desirable to obtain. For example, using a high concentration of cells allows for more efficient selection of CD8+ T cells, which normally have weaker CD28 expression.

[0188] In one embodiment of the invention, the mixture may be cultured for a period of time ranging from a few hours (about 3 hours) to about 14 days, or any integer value in between. In another embodiment, the mixture may be cultured for 21 days. In one embodiment of the invention, the beads and T cells are cultured together for about 8 days. In another embodiment, the beads and T cells are cultured together for 2-3 days. Several stimulation cycles may be desirable, resulting in a culture time of 60 days or longer for the T cells. Suitable conditions for culturing T cells include a suitable medium (e.g., Minimum Essential Medium or RPMI Medium 1640 or X-vivo 15 (Lonza)) that may contain factors necessary for growth and survival, including serum (e.g., fetal bovine serum or human serum), interleukin-2 (IL-2), insulin, IFN-γ, IL-4, IL-7, GM-CSF, IL-10, IL-12, IL-15, TGFβ and TNF-α, or other additives for cell growth known to those of skill in the art. Other additives for cell growth include, but are not limited to, detergents, plasmanate, and reducing agents such as N-acetyl-cysteine ​​and 2-mercaptoethanol. Media may include RPMI 1640, AIM-V, DMEM, MEM, α-MEM, F-12, X-Vivo 15, and X-Vivo 20, supplemented with amino acids, sodium pyruvate, and vitamins, serum-free or supplemented with an appropriate amount of serum (or plasma) or a defined set of hormones and / or a fixed amount of cytokines sufficient for T cell growth and expansion. Antibiotics such as penicillin and streptomycin are included only in experimental cultures, not in cultures of cells to be infused into subjects. Target cells are grown under the necessary conditions to support growth, such as an appropriate temperature (e.g., 37° C.) and atmosphere (e.g., air+5% CO ). 2 ) will be maintained under

[0189] T cells exposed to various stimulation times can exhibit different characteristics. For example, a typical blood or apheresis peripheral blood mononuclear cell product contains a population of helper T cells (T H , CD4 +) into cytotoxic or suppressor T cell populations (T C , CD8 + ) than T cells. Ex vivo expansion of T cells by stimulation of CD3 and CD28 receptors results in predominantly T cells before about day 8-9. H After about 8-9 days, the T cell population becomes T C Thus, depending on the therapeutic goal, the treatment may consist primarily of T C Cells or T H It may be advantageous to infuse a subject with a T cell population consisting of T C If an antigen-specific subset of cells has been isolated, it may be beneficial to enrich this subset to a higher extent.

[0190] Furthermore, in addition to CD4 and CD8 markers, other phenotypic markers also vary significantly, but largely reproducibly, during cell expansion, allowing for the tailoring of activated T cell preparations.

[0191] Therapeutic Applications In one aspect, the present invention comprises a method for treating autoantibody-mediated NMJ disease in a subject.The method comprises administering to a subject an effective amount of genetically modified cells, such as T cells, comprising a polynucleotide encoding chimeric autoantibody receptor (CAAR), the polynucleotide encoding an acetylcholine receptor (AChR) autoantigen or a fragment thereof, and optionally a transmembrane domain, an intracellular domain of a costimulatory molecule, and / or a signal transduction domain, thereby treating autoantibody-mediated NMJ disease in the subject.In some embodiments, the polynucleotide further encodes a KIR element.

[0192] In another aspect, the present invention comprises a method for preventing or reducing NMJ damage in a subject at risk of or suffering from autoantibody-mediated NMJ disease.The method comprises administering to a subject an effective amount of genetically modified cells, such as T cells, comprising a polynucleotide that codes CAAR, and that codes AChR autoantigen or its fragment, and optionally a transmembrane domain, an intracellular domain of costimulatory molecule, and / or a signal transduction domain, thereby preventing or reducing NMJ damage in the subject.In some embodiments, the polynucleotide further codes KIR element.

[0193] In one embodiment, the autoantibody-mediated NMJ disease is myasthenia gravis (MG). In another embodiment, the subject is a human.

[0194] Without wishing to be bound by any particular theory, the anti-autoantibody immune response induced by CAAR modified cells, such as T cells, can be active or passive immune response.In yet another embodiment, modified cells, such as T cells, target B cells.For example, autoantibody-expressing B cells may be susceptible to indirect destruction by CAAR re-inducing cells, such as T cells, that have previously reacted to nearby autoantibody-expressing cells.

[0195] In one embodiment, the genetically modified cell of the present invention, such as T cell, is modified by fully human CAAR.In one embodiment, the fully human CAAR genetically modified cell, such as T cell, can be a kind of vaccine for ex vivo immunization and / or in vivo therapy in mammal.In one embodiment, the mammal is human.

[0196] For ex vivo immunization, prior to administering the cells to a mammal, at least one of the following is performed in vitro: i) expanding the cells, ii) introducing a polynucleotide encoding CAAR into the cells, iii) cryopreserving the cells.

[0197] Ex vivo procedures are well known in the art and will be discussed in more detail below. Briefly, cells are isolated from a mammal (e.g., human) and genetically modified (i.e., transduced or transfected in vitro) with a nucleic acid (e.g., vector) expressing the CAAR disclosed herein. The CAAR-modified cells can be administered to a mammalian recipient to provide therapeutic benefits. The mammalian recipient can be a human, and the CAAR-modified cells can be autologous to the recipient. Alternatively, the cells can be allogeneic, syngeneic, or xenogeneic to the recipient.

[0198] The procedure for ex vivo expansion of hematopoietic stem and progenitor cells is described in U.S. Patent No. 5,199,942, which is incorporated herein by reference, and can be applied to the cells of the present invention. Other suitable methods are known in the art, and thus the present invention is not limited to any particular method of ex vivo expansion of cells. Briefly, the ex vivo culture and expansion of T cells includes: (1) collecting mammalian CD34+ hematopoietic stem and progenitor cells from peripheral blood collection or bone marrow explant; and (2) expanding such cells ex vivo. In addition to the cell growth factors described in U.S. Patent No. 5,199,942, other factors such as flt3-L, IL-1, IL-3, and c-kit ligand can be used for cell culture and expansion.

[0199] In addition to using cell-based vaccines for ex vivo immunization, the present invention also includes compositions and methods for in vivo immunization to elicit an immune response against an antigen in a patient.

[0200] Generally, the cells activated and expanded as described herein may be used for the treatment and prevention of diseases occurring in individuals with reduced immune function.In particular, the AChR CAAR modified cells of the present invention, such as T cells, are used in the treatment of diseases, disorders, and conditions associated with the expression of autoantibodies.In some embodiments, the cells of the present invention are used in the treatment of patients at risk of developing autoimmune NMJ diseases, disorders, and conditions associated with the expression of autoantibodies.Therefore, the present invention provides a method for the treatment or prevention of autoimmune NMJ diseases, disorders, and conditions associated with the expression of autoantibodies (anti-AChR), comprising administering a therapeutically effective amount of the CAAR modified cells of the present invention, such as T cells, to a subject in need thereof.

[0201] The CAAR modified cells of the present invention, such as T cells, may be administered either alone or as a pharmaceutical composition in combination with diluents and / or other components such as IL-2 or other cytokines or cell populations. Briefly, the pharmaceutical composition of the present invention may comprise a target cell population as described herein in combination with one or more pharma- ceutical or physiologically acceptable carriers, diluents, or excipients. Such compositions may comprise buffers such as neutral buffered saline, phosphate buffered saline, etc.; carbohydrates such as glucose, mannose, sucrose, or dextran, mannitol; proteins; polypeptides, or amino acids such as glycine; antioxidants; chelating agents such as EDTA or glutathione; adjuvants (e.g., aluminum hydroxide); and preservatives. The compositions of the present invention are in one aspect formulated for intravenous administration.

[0202] The pharmaceutical composition of the present invention can be administered in a manner appropriate to the disease to be treated (or prevented). The appropriate dosage can be determined by clinical trials, but the amount and frequency of administration will be determined by factors such as the condition of the patient and the type and severity of the patient's disease.

[0203] When an "immunologically effective amount", "anti-autoantibody effective amount", "anti-BCR effective amount", "autoimmune disease-inhibiting effective amount", or "therapeutic amount" is indicated, the exact amount of the composition of the present invention to be administered can be determined by a physician, taking into account individual differences in the age, weight, and condition of the patient (subject). Pharmaceutical compositions comprising the cells, e.g., T cells, described herein can be administered in the form of a 10-mL dose of the cells. 4 ~10 9 / kg body weight, in some cases 10 cells 5 ~10 6 It is generally stated that the cells may be administered at a dosage of 1000 cells / kg body weight, including all integer values ​​within these ranges. The cells, for example, T cell compositions, may also be administered multiple times at these dosages. The cells may be administered by using infusion techniques that are generally known in immunotherapy (see, for example, Rosenberg et al., New Eng. J. of Med. 319:1676, 1988). The optimal dosage and treatment regimen for a particular patient can be easily determined by those skilled in the art of medicine by monitoring the patient for symptoms of disease and adjusting the treatment accordingly.

[0204] In some embodiments, activated cells, e.g., T cells, are administered to a subject. Following administration, blood is again drawn or apheresed, and cells, e.g., T cells, are activated and expanded therefrom using the methods described herein, and then reinfused back into the patient. This process can be performed multiple times, every 2-3 weeks. In some embodiments, cells, e.g., T cells, can be activated from a blood draw of 10cc to 400cc. In some embodiments, cells, e.g., T cells, are activated from a blood draw of 20cc, 30cc, 40cc, 50cc, 60cc, 70cc, 80cc, 90cc, or 100cc. Without being bound by theory, this multiple blood draw / multiple reinfusion protocol can be used to select certain populations of cells, e.g., T cells.

[0205] The cells of the invention that are administered may be autologous, allogeneic, or xenogeneic to the subject being treated.

[0206] Administration of the cells of the invention may be performed by any convenient means, including aerosol inhalation, injection, oral ingestion, infusion, implantation, or transplantation. The compositions described herein may be administered to a patient intraarterially, subcutaneously, intradermally, intranodally, intramedullary, intramuscularly, intravenously (iv) or intraperitoneally. In one embodiment, the cells, e.g., T cell compositions, of the invention are administered to a patient by intradermal or subcutaneous injection. In another embodiment, the cells, e.g., T cell compositions, of the invention are administered by iv injection. The cells, e.g., T cell compositions, may be directly injected into lymph nodes or other sites of pathophysiological activity.

[0207] In some embodiments of the invention, cells activated and expanded using the methods described herein or other methods known in the art to expand cells, e.g., T cells, to therapeutic levels are administered to patients along with (e.g., before, simultaneously with, or after) any number of relevant treatment modalities, including but not limited to treatment with antiviral therapy, interleukin-2, rituximab (or any other generalized B cell depleting agent, such as Btk inhibitors or other anti-CD20 / CD19 or B cell targeting agents), and / or agents such as Soliris® (eculizumab, terminal complement inhibitor). In further embodiments, the cells, e.g., T cells, of the invention may be used in combination with anti-FcRn antibodies, IVIg, or plasma exchange to reduce anti-AChR antibody concentrations prior to treatment. In yet other embodiments, mild lymphodepleting regimens (e.g., low-dose fludarabine or Cytoxan) may precede treatment with the cells, e.g., T cells, of the invention.

[0208] The dosages of the above treatments administered to a patient will vary depending on the exact nature of the condition being treated and the recipient of the treatment. Dosages for administration to humans can be increased or decreased according to accepted practices in the art. For example, doses of CAMPATH generally range from 1 to about 100 mg for an adult patient, and are usually administered daily for a period of 1 to 30 days. A preferred daily dose is 1 to 10 mg / day, although lower or higher doses up to 40 mg / day can be used in some cases (as described in U.S. Patent No. 6,120,766). EXAMPLES

[0209] Experimental Example The invention will now be described with reference to the following experimental examples, which are provided for illustrative purposes only and the invention should in no way be considered as being limited to these examples, but should also be considered to encompass any and all variations that become evident as a result of the teachings provided herein.

[0210] Without further description, one of ordinary skill in the art can, using the preceding description and the following illustrative examples, make and utilize the compounds of the present invention and practice the claimed methods. The following examples, therefore, specifically point out preferred embodiments of the present invention, and are not to be construed as limiting in any way the remainder of the disclosure.

[0211] The materials and methods used in carrying out the experiments disclosed herein are now described.

[0212] -AChR CAAR construct (as shown in Figure 1) #1 pTRPE.α39P AChR.CD8H.BBz CAAR (nucleic acid sequence, SEQ ID NO: 1) TIFF0007649755000015.tif146153 pTRPE.α39P AChR.CD8H.BBz CAAR: 1-879 (SEQ ID NO: 47) without a stop codon #1 pTRPE.α39P AChR.CD8H.BBz CAAR (amino acid sequence, SEQ ID NO: 11) TIFF0007649755000016.tif85152 #2 pTRPE.α65P AChR.CD8H.BBz CAAR (nucleic acid sequence, SEQ ID NO: 21) TIFF0007649755000017.tif149153 pTRPE.α65P AChR.CD8H.BBz CAAR: 1-957 (SEQ ID NO: 48) without a stop codon #2 pTRPE.α65P AChR.CD8H.BBz CAAR (amino acid sequence, SEQ ID NO: 25) TIFF0007649755000018.tif90152 #3 pTRPE.α208 AChR.CD8H.BBz CAAR (nucleic acid sequence, SEQ ID NO: 28) TIFF0007649755000019.tif177153 pTRPE.α208 AChR.CD8H.BBz CAAR: 1-1386 (SEQ ID NO: 49) without the stop codon #3 pTRPE.α208 AChR.CD8H.BBz CAAR (amino acid sequence, SEQ ID NO: 30) TIFF0007649755000020.tif77152 #4 pTRPE.α210 AChR.CD8H.BBz CAAR (nucleic acid sequence, SEQ ID NO: 32) TIFF0007649755000021.tif177153 pTRPE.α210 AChR.CD8H.BBz CAAR: 1-1392 (SEQ ID NO: 50) without the stop codon #4 pTRPE.α210 AChR.CD8H.BBz CAAR (amino acid sequence, SEQ ID NO: 34) TIFF0007649755000022.tif80153 #5 pTRPE.α210 AChR.gs.BBz CAAR (nucleic acid sequence, SEQ ID NO: 36) TIFF0007649755000023.tif165153 pTRPE.α210 AChR.gs.BBz CAAR: 1-1263 (SEQ ID NO: 51) without a stop codon #5 pTRPE.α210 AChR.gs.BBz CAAR (amino acid sequence, SEQ ID NO: 39) TIFF0007649755000024.tif80153 #6 pTRPE.α211 AChR.CD8H.BBz CAAR (nucleic acid sequence, SEQ ID NO: 41) TIFF0007649755000025.tif177153 pTRPE.α211 AChR.CD8H.BBz CAAR: 1-1395 (SEQ ID NO: 52) without the stop codon #6 pTRPE.α211 AChR.CD8H.BBz CAAR (amino acid sequence, SEQ ID NO: 43) TIFF0007649755000026.tif80153 #7 pTRPE.α211 AChR.gs.BBz CAAR (nucleic acid sequence, SEQ ID NO: 45) TIFF0007649755000027.tif168153 pTRPE.α211 AChR.gs.BBz CAAR: 1-1266 (SEQ ID NO: 6) without a stop codon #7 pTRPE.α211 AChR.gs.BBz CAAR (amino acid sequence, SEQ ID NO: 46) TIFF0007649755000028.tif80152

[0213] Table 1. Description of anti-AChR antibodies (expressed in target cells as membrane-bound B cell receptor + / - secreted antibodies) TIFF0007649755000029.tif1401631. Tzartos et al, 1981. JBC, 256:8635-8645. 2. Tzartos et al, 1983. FEBS Letters, 157:116-118. 3. Luo et al, 2009. J Neurosci, 29:13898-13908. 4. Kontou et al, 1996. FEBS Letters, 389:195-198 5. Papanastasiou et al, J Neuroimmunol,104:124-32. 6. Graus et al, 1997. Immunol Lett. 57:59-62. 7. Van der Neut Kolfschoten et al, 2007. Science, 317:1554-1557.

[0214] Hybridoma mAb35, isolated as a hybridoma from rats after immunization with the muscle-type nicotinic AChR of electric eel electric organ, binds to the major immunogenic region (MIR) of the α subunit of the AChR and cross-reacts with chicken, rat, mouse, and human AChRs. It binds to native but not denatured AChRs and has a K of 2.06 nM for the α1 AChR subunit. D It causes myasthenia in passively transferred experimental autoimmune myasthenia gravis (EAMG) models in both rat and mouse hosts.

[0215] mAb 192 and mAb 195 were isolated as hybridomas from rats after immunization with purified human muscle extract. mAb 192 binds to the native but not denatured AChR and has a K of 0.007 nM for the α1 AChR subunit. D mAb 195 has a K of 0.01 nM for the α1 AChR subunit. Dand induces myasthenia in a rat passive transfer model.

[0216] mAb 637 was isolated from the thymus of a patient with MG by phage display of isolated lymphocytes. It has a K of 0.005 nM for the α1 AChR subunit. D mAb 637 passively transfers MG to monkeys.

[0217] The results of the experiment are described below.

[0218] The present invention relates to compositions and methods for treating MG.

[0219] Example 1: α39P AChR CAART Cells and α65P AChR CAART Cells It is known in the art that autoantibodies from MG patients destroy AChR clusters and NMJs. Anti-AChR antibodies interfere with AChR clusters. AChR is a multi-subunit structure. Pathogenic autoantibodies primarily target a defined region in the amino-terminal domain of the α subunit, called the major immunogenic region (MIR).

[0220] Figure 1 is a schematic diagram of some of the CAARs of the present invention, whose extracellular domains (ECDs) contain a segment mimic of the major immunogenic region (MIR) of the α subunit of the AChR, the primary target of autoantibodies in MG, followed by the CD8 hinge domain, the CD8 transmembrane domain (TMD), and the tandem cytoplasmic signaling domains 4-1BB and CD3ζ (BBZ). α65P incorporates an additional EC1 domain sequence compared to α39P.

[0221] As shown in Figures 2A-2B, α39P AChR CAAR and α65P AChR CAAR were expressed on the surface of Jurkat cells and T cells as shown by staining with anti-AChR α subunit monoclonal antibody 210 (mAb 210). Jurkat cells and CD3+ T cells were transduced with lentivirus. Flow cytometry analysis was performed on day 3 (Jurkat cells) or day 5 (primary human CD3+ T cells) post-transduction. NTD: non-transduced cells.

[0222] As shown in Figures 3A-3B, α39P AChR CAAR Jurkat NFAT-GFP cells and α65P AChR CAAR Jurkat NFAT-GFP cells expressed surface anti-AChR IgG and recognized TIB-175 (ATCC, mAb 35 hybridoma cells, https: / / www.atcc.org / Products / All / TIB-175.aspx), which secretes antibodies that cause myasthenia in animal models. "TIB-175" and "mAb35 hybridoma cells" are used interchangeably herein to refer to TIB-175 cells. Flow cytometry analysis was performed 12 hours after co-culture with mAb 35 hybridoma cells. Jurkat NFAT-GFP cells induce GFP expression when TCR signals are transduced.

[0223] As shown in Figure 4, α39P AChR CAAR Jurkat NFAT-GFP cells recognized Nalm6 195, but not Nalm6 192, a human B cell line engineered to express an anti-AChR antibody targeting a different epitope. Flow cytometry analysis was performed 12 hours after co-culture with Nalm6, Nalm6 192, or Nalm6 195 cells. Jurkat cells were stained with anti-CD3-AF647 antibody to distinguish them from the Nalm6 cell population. Nalm6 cells constitutively express CBG (click beetle green luciferase, whose emission spectrum overlaps with the GFP channel) and GFP. CD3 +Plots gated on (Jurkat cells) are shown in the lower panel. Jurkat NFAT-GFP cells induce GFP expression upon TCR signaling.

[0224] As shown in Figure 5, α65P AChR CAAR Jurkat NFAT-GFP cells recognized both Nalm6 195 and Nalm6 192. Flow cytometry analysis was performed 12 hours after co-culture with either Nalm6 192 or Nalm6 195 cells. Jurkat cells were stained with anti-CD3-AF647 antibody to distinguish them from Nalm6 cell populations. Nalm6 cells constitutively express CBG (click beetle green luciferase, whose emission spectrum overlaps with the GFP channel) and GFP. CD3 + FACS plots gated on (Jurkat cells) are shown in the lower panel. Jurkat NFAT-GFP cells induce GFP expression upon TCR signaling.

[0225] Example 2: Killing assays of α39P AChR CAART and α65P AChR CAART As shown in Figure 6, in the luciferase-based killing assay, α39P AChR-CAART cells and α65P AChR-CAART cells killed mAb 35 hybridoma cells and Nalm6 195 cells, but only α65P AChR-CAART cells could kill Nalm6 192 cells. The luciferase-based killing assay was performed as follows: T cells (NTD, α39P, and α65P) were co-incubated with each target cell (mAb 35 hybridoma cells, Nalm6 192, and Nalm6 195) at an E:T ratio of 10:1 for 15-24 hours. % of specific lysis = [(test cell death - spontaneous cell death) / (maximum cell death - spontaneous cell death)]*100. Spontaneous cell death: only medium without T cells. Maximum cell death: treated with 10% SDS at a 1:1 ratio before detection.

[0226] Example 3: α208 AChR CAART Cells, α210 AChR CAART Cells, and α211 AChR CAART Cells Schematics of the α208, α210, and α211 AChR CAARs are shown in Figure 7. The α208, α210, and α211 AChR CAARs express different amino acid lengths of the AChR extracellular domain EC1, followed by either a CD8 hinge or a glycine-serine (GS) linker, the CD8 transmembrane domain (TMD), and tandem cytoplasmic signaling domains, 4-1BB and CD3ζ (BBZ).

[0227] As shown in Figure 8, α208.GS.BBz AChR CAAR incorporating a GS linker was not expressed on the surface of 293T cells, whereas α210.GS.BBz AChR CAAR and α211.GS.BBz AChR CAAR incorporating a GS linker were expressed on the cell surface. 293T cells were transiently transfected with lentiviral plasmids without packaging DNA. Two days after transfection, surface expression of AChR ECD was detected using mAb 210.

[0228] αAChR CAAR Jurkat NFAT-GFP cells do not activate CAAR signaling after co-culture with Nalm6 3-28, which expresses the anti-MuSK B cell receptor as a negative control, but do activate CAAR signaling after co-culture with Nalm6 192, Nalm6 195 (Figure 9A), Nalm6 637 (Figure 9B), or mAb 35 hybridoma (Figure 9C), which express surface anti-AChR B cell receptors. α208.GS.BBz CAAR serves as a negative control, as it is not expressed on the Jurkat cell surface.

[0229] FIG. 10 shows that α210.GS.BBz CAAR and α211.GS.BBz CAAR are expressed on the surface of primary human T cells following lentiviral transduction, as shown by staining with anti-AChR α subunit monoclonal antibody 210.

[0230] Example 4: Killing and Cytokine Secretion Assays of α210 AChR CAART and α211 AChR CAART As shown in Figure 11, α210.GS.BBz CAART cells and α211.GS.BBz AChR CAART cells kill mAb 35 hybridoma cells, Nalm6 192, and Nalm6 195 target cells in luciferase-based killing assays (after 21 hours of co-culture). Supernatants from co-cultures of α210.GS.BBz CAART cells and α211.GS.BBz AChR CAART cells with mAb 35 hybridoma cells, Nalm6 192, and Nalm6 195 target cells have increased hIFNγ concentrations compared to media only, NTD, or Nalm6 WT controls (Figure 12). Luciferase-based killing assays were performed as follows. T cells (NTD, α210, and α211) were co-incubated with target cells (Nalm6 control, Nalm6 192, Nalm6 195, and mAb 35 hybridoma cells) at an E:T ratio of 30:1 for 21 hours. % of specific lysis = [(test cell death - spontaneous cell death) / (maximum cell death - spontaneous cell death)]*100. Spontaneous cell death: medium only without T cells. Maximum cell death: treated with 10% SDS at a 1:1 ratio before detection.

[0231] As shown in Figures 13A-13B, α210.GS.BBz CAART cells kill Nalm6 637 anti-AChR cells. Supernatants of co-cultures of α210.GS.BBz CAART cells with Nalm6 637 anti-AChR cells have increased hIFNγ concentrations compared to NTD controls (Figure 14). Luciferase activity was measured 24 hours after co-culture at the indicated effector to target (E / T) cell ratios. Nalm6 cells constitutively express click beetle green luciferase. Specific lysis [%] is calculated using the following equation: Specific lysis [%] = [(Test cell death - Spontaneous cell death) / (Maximum cell death - Spontaneous cell death)] * 100. Spontaneous cell death: medium only without T cells. Maximum cell death: treatment with 10% SDS at a 1:1 ratio before detection.

[0232] Example 5: In vivo potency of α210 AChR CAART cells and α211 AChR CAART cells Figures 15A-15B show the in vivo potency of α39P.CD8H.BBz CAART cells and α210.GS.BBz CAART cells against either Nalm6 192 (Figure 15A) or Nalm6 195 (Figure 15B) target cells. Figure 16 shows the in vivo potency of α210.GS.BBz CAART cells and α211.GS.BBz CAART cells against a mixture of Nalm6 192 / 195 cells (1:1 ratio). The in vivo potency of α210.GS.BBz CAART cells against Nalm6 637 target cells is shown in Figure 17.

[0233] Other Aspects The disclosures of each and every patent, patent application, and publication cited herein are incorporated herein by reference in their entirety. Although the present invention has been disclosed with respect to specific embodiments, it is apparent that other embodiments and variations of the present invention may be devised by those skilled in the art without departing from the true spirit and scope of the present invention. It is intended that the appended claims be construed to include all such embodiments and equivalent variations.

Claims

1. A polynucleotide encoding a chimeric autoantibody receptor (CAAR), the CAAR comprising: The polynucleotide comprising an extracellular domain comprising an acetylcholine receptor (AChR) autoantigen or a fragment thereof, wherein the AChR autoantigen or a fragment thereof comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 35 and 44, and optionally a transmembrane domain, an intracellular domain of a costimulatory molecule, and / or a signaling domain.

2. The polynucleotide of claim 1, wherein the transmembrane domain comprises a CD8α transmembrane domain.

3. The polynucleotide of claim 2, wherein the CD8α transmembrane domain comprises the amino acid sequence of SEQ ID NO:

19.

4. The polynucleotide of any one of claims 1 to 3, wherein the intracellular domain of the costimulatory molecule comprises a 4-1BB intracellular domain.

5. The polynucleotide of claim 4, wherein the 4-1BB intracellular domain comprises the amino acid sequence of SEQ ID NO:

20.

6. The polynucleotide of any one of claims 1 to 5, wherein the signaling domain comprises a CD3 zeta signaling domain.

7. The polynucleotide of claim 6, wherein the CD3ζ signaling domain comprises the amino acid sequence of SEQ ID NO:

38.

8. The polynucleotide of any one of claims 1 to 7, wherein the CAAR comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 34, 39, 43, and 46.

9. The polynucleotide of claim 1, wherein the CAAR comprises a killer immunoglobulin-like receptor (KIR) transmembrane domain and a KIR cytoplasmic domain.

10. The polynucleotide of claim 1, wherein the transmembrane domain comprises a CD28 transmembrane domain.

11. A vector comprising the polynucleotide according to any one of claims 1 to 10.

12. The vector of claim 11, which is a lentiviral vector or an RNA vector.

13. A chimeric autoantibody receptor (CAAR) comprising an extracellular domain comprising an acetylcholine receptor (AChR) autoantigen or a fragment thereof, wherein the AChR autoantigen or a fragment thereof comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 35 and 44.

14. The CAAR of claim 13, further comprising a transmembrane domain, an intracellular domain of a costimulatory molecule, and / or a signal transduction domain.

15. The CAAR of claim 14, wherein the transmembrane domain comprises a CD8α transmembrane domain.

16. The CAAR of claim 15, wherein the CD8α transmembrane domain comprises the amino acid sequence of SEQ ID NO:

19.

17. The CAAR according to any one of claims 14 to 16, wherein the intracellular domain of the costimulatory molecule comprises a 4-1BB intracellular domain.

18. The CAAR of claim 17, wherein the 4-1BB intracellular domain comprises the amino acid sequence of SEQ ID NO:

20.

19. The CAAR of any one of claims 14 to 18, wherein the signaling domain comprises a CD3ζ signaling domain.

20. The CAAR of claim 19, wherein the CD3ζ signaling domain comprises the amino acid sequence of SEQ ID NO:

38.

21. The CAAR of any one of claims 13 to 20, comprising an amino acid sequence selected from the group consisting of SEQ ID NO: 34, 39, 43, and 46.

22. A CAAR described in claim 13 or 14, comprising a killer immunoglobulin-like receptor (KIR) transmembrane domain and a KIR cytoplasmic domain.

23. The CAAR described in claim 14, wherein the transmembrane domain includes a CD28 transmembrane domain.

24. A genetically modified cell comprising the CAAR of any one of claims 13 to 23.

25. expressing CAAR, and (i) have high affinity for the autoantibody-based BCR on B cells; (ii) induces the death of B cells that express autoantibodies or that can mature into antibody-secreting cells; and / or (iii) have limited toxicity to healthy cells; The cell of claim 24.

26. 26. The cell of claim 24 or 25, selected from the group consisting of helper T cells, cytotoxic T cells, memory T cells, regulatory T cells, γδ T cells, natural killer cells, cytokine-induced killer cells, cell lines thereof, T memory stem cells, T cells derived from pluripotent stem cells, and other effector cells.

27. ​​A cell described in any one of claims 24 to 26, which is a cytotoxic T cell.

28. 23. A genetically modified cell comprising: (a) the chimeric autoantibody receptor of claim 22; and (b) DAP12.

29. A pharmaceutical composition comprising a polynucleotide according to any one of claims 1 to 10, a CAAR according to any one of claims 13 to 23, or a cell according to any one of claims 24 to 28, and a pharma- ceutically acceptable excipient.

30. A therapeutic composition comprising a therapeutically effective amount of a genetically modified cell according to any one of claims 24 to 28.

31. 31. The therapeutic composition of claim 30, wherein the treatment comprises treating an autoantibody-mediated neuromuscular junction (NMJ) disease in a subject or preventing or reducing NMJ damage in a subject at risk for or suffering from an autoantibody-mediated neuromuscular junction (NMJ) disease.

32. (a) CAAR comprises a killer immunoglobulin-like receptor (KIR) transmembrane domain and a KIR cytoplasmic domain; (b) the cell further contains DAP12; 32. The therapeutic composition of claim 31.

33. The therapeutic composition of claim 31, wherein the autoantibody-mediated NMJ disease is myasthenia gravis (MG).

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