Methods and compositions for non-myeloablative bone marrow reconstitution

Abstract

To provide a pharmaceutical composition for use in a method that performs a bone marrow transplant in a patient.SOLUTION: The present invention provides a pharmaceutical composition comprising cyclophosphamide. The patient is administered a pharmaceutical composition containing at least one non-myeloablative dose of cyclophosphamide and a population of cyclophosphamide-resistant modified bone marrow cells, wherein the population of cyclophosphamide-resistant modified bone marrow cells includes a heterologous gene encoding aldehyde dehydrogenase 1 (ALDH1). The non-myeloablative dose of cyclophosphamide is about 0.16 mg / kg / day to less than 2.5 mg / kg / day.SELECTED DRAWING: None

Description

[Technical field]

[0001] CROSS-REFERENCE TO RELATED APPLICATIONS This application claims priority to U.S. Provisional Patent Application No. 62 / 586,813, filed November 15, 2017, which is incorporated by reference in its entirety.

[0002] Technical Field The present disclosure provides methods and compositions for non-myeloablative bone marrow transplantation, including during the treatment of various diseases such as HIV, cancer (e.g., hematological cancer), and the like. In some embodiments, modified stem cells are provided herein that are grafted into a patient's bone marrow and allow for bone marrow reconstitution without the negative side effects experienced during conventional bone marrow transplantation. The cells can also be used to express proteins of interest that may be therapeutic in nature. [Background technology]

[0003] Bone marrow transplantation (BMT) is a procedure in which damaged or destroyed bone marrow is replaced with healthy bone marrow stem cells isolated from either the patient (autologous) or another person (allogeneic). BMT is used to treat not only leukemia, but many other diseases, including severe aplastic anemia, lymphoma, multiple myeloma, immune deficiency disorders, and some solid tumor cancers. Summary of the Invention [Problem to be solved by the invention]

[0004] Myeloablative BMT involves first treating the patient to kill cells in the bone marrow (both normal and abnormal cells) and then infusing healthy bone marrow cells. In the first step, high doses of chemotherapy and / or radiation are required to kill the cells, after which allogeneic or autologous cells are introduced. This process of eradicating the patient's bone marrow is called myeloablative. Because this process kills not only unhealthy cells but also healthy immune and stem cells, the patient is highly susceptible to infection and often needs to be administered multiple antibiotics and remain in a sterile environment. Until the bone marrow is reconstituted, the patient remains at high risk for infection and the recovery period can last up to six months. During this period, the patient is recommended to remain near the hospital or clinic where the procedure is being performed in cases where complications arise. In addition to acute toxicity, myeloablative chemotherapy is associated with many other side effects, including cataracts, growth retardation, cardiac toxicity, and endocrine and reproductive problems. Younger patients are particularly susceptible to these effects. Thus, there is a need for novel compositions and methods for performing BMT. This disclosure fulfills these needs and more. [Means for solving the problem]

[0005] [Once the claims are finalized, everything will be written] [Brief description of the drawings]

[0006] [Figure 1]Figure 4 shows the percentage of live GFP (green fluorescent protein) positive (GFP+) granulocytes in the peripheral blood of mice receiving bone marrow cells transduced with lentiviral vector expressing EGFP ("control vector") or lentiviral vector expressing EGFP+ALDH1A1 ("test vector", SEQ ID NO: 2, Figure 4) and treated with the indicated concentrations of intraperitoneal (ip) cyclophosphamide (CTX) once a day. On days 23, 35, and 42 of the study (corresponding to days 16, 28, and 35 of CTX administration, respectively), blood was collected by retro-orbital bleeding and the percentage of live GFP+ granulocytes in the peripheral blood was assessed by flow cytometry. n=3 in each of the groups without post-transplant CTX treatment, and n=6 in all other groups. [Figure 2A] Figure 2 shows the percentage of GFP+ cells in bone marrow assessed by flow cytometry for mice receiving bone marrow cells transduced with control vector or bone marrow cells transduced with test vector and subjected to a once-daily regimen of CTX at the indicated concentrations. n=3 for each group without post-transplant CTX treatment, n=6 for all other groups. Figure 2A shows the % of total (dead and live) GFP+ cells. [Figure 2B] Figure 2B shows the percentage of GFP+ cells in bone marrow assessed by flow cytometry for mice receiving bone marrow cells transduced with control vector or test vector and subjected to a once-daily regimen of CTX at the indicated concentrations. n=3 for each group without post-transplant CTX treatment, n=6 for all other groups. Figure 2B shows the % of live GFP+ granulocytes. [Diagram 3]Figure 1 shows white blood cell (WBC) counts for mice receiving bone marrow cells transduced with control vector or bone marrow cells transduced with test vector and subjected to a once-daily regimen of CTX at the indicated concentrations, n=3 for each in the group without post-transplant CTX treatment and n=5 for all other groups. [Figure 4] FIG. 1 shows a non-limiting schematic diagram of a lentiviral vector according to one embodiment of the present disclosure. [Diagram 5] FIG. 1 shows a non-limiting schematic diagram of a lentiviral vector according to one embodiment of the present disclosure. [Figure 6] FIG. 1 shows a non-limiting schematic diagram of a lentiviral vector according to one embodiment of the present disclosure. [Figure 7] FIG. 1 shows a non-limiting schematic of the study design for dose ranging and efficacy studies of lentiviral vectors. [Figure 8] FIG. 1 shows a non-limiting schematic of the study design for lentiviral vector expression and efficacy of shRNA knockdown studies. [Figure 9] FIG. 1 shows a non-limiting schematic diagram of a study design for transplanting cells with HIV multi-resistance and chemo-resistance to CTX into HIV+ patients according to one embodiment of the present disclosure. [Figure 10] Figure 1 shows a non-limiting schematic diagram of the study design in which HIV+ patients are treated with CTX once a day after transplanting cells with HIV multi-resistance and CTX chemotherapy resistance into the patient.It is contemplated that the same study design can be performed on HIV- subjects to prevent HIV. [Figure 11] FIG. 1 shows a non-limiting schematic diagram of a lentiviral vector according to one embodiment of the present disclosure. [Figure 12] FIG. 1 shows a non-limiting schematic diagram of a lentiviral vector according to one embodiment of the present disclosure. DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

[0007] It is understood, although not always explicitly stated, that all numerical designations are preceded by the term "about." As used herein, the term "about" means that the numerical values ​​are approximations and that small variations do not significantly affect the practice of the disclosed embodiments.

[0008] As used in this specification and the appended claims, the singular forms "a," "an," and "the" should be understood to include plural referents unless the context clearly indicates otherwise. Thus, for example, reference to a "cell" includes a plurality of cells.

[0009] definition As used herein, the following terms have the following meanings.

[0010] The term "about" when used before numerical designations, e.g., temperature, time, amounts, concentrations, and the like, including ranges, indicates approximations that may vary by (+) or (-) 20%, 10%, 5%, or 1%.

[0011] Similarly, as used herein, "and / or" refers to and includes any and all possible combinations of one or more of the associated listed items, as well as the lack of combinations when interpreted by alternatives ("or").

[0012] The terms "administering", "administering" and the like refer to the introduction of an agent (e.g., cells) into a subject. Typically, an effective amount is administered, which is determined by the treating physician and the like. Any route of administration can be used, such as topical, subcutaneous, peritoneal, intravenous, intra-arterial, inhalation, vaginal, rectal, nasal, oral, buccal, introduction into the cerebrospinal fluid, or infusion into a body compartment. The terms and phrases "administering" and "administration of" when used in connection with compositions (and grammatical equivalents) refer to both direct administration, which can be administration to a patient by a medical professional or by self-administration by the patient, and / or indirect administration, which can be the act of prescribing a drug. For example, a physician who instructs a patient to self-administer an agent (e.g., cells) and / or provides a prescription for a drug to a patient is administering the agent to the patient. "Intermittent administration" or "regular administration" refers to multiple treatments on a daily, weekly, or monthly basis. Intermittent administration can also refer to administration of an agent once, twice, three times, or more per day.

[0013] As used herein, the terms "comprising" (and any form of comprising, e.g., "comprise," "comprises," and "comprised"), "having" (and any form of having, e.g., "have" and "has"), "including" (and any form of including, e.g., "includes" and "include"), or "containing" (and any form of containing, e.g., "contains" and "contain") are inclusive or open-ended and do not exclude additional, unrecited elements or method steps. Any process or composition using the transitional phrase "comprising" or "comprising" can also be said to be described with the transitional phrase "consisting of" or "consists of."

[0014] An "effective amount" is an amount of an agent or compound (e.g., a cell or cell population) sufficient to produce a beneficial or desired result. An effective amount can be in one or more administrations, applications, or doses. The determination of these parameters is well within the skill of the art. These considerations, as well as effective formulations and administration procedures, are well known in the art and are described in standard texts.

[0015] As used herein, the term "contacting" refers to bringing two elements together in an in vitro system or in an in vivo system. For example, the contacting of a virus with a cell. "Contacting" a virus with an individual, patient, or cell includes administering a virus to an individual, such as a human, or patient, as well as introducing a compound into a sample containing, for example, a cell preparation or purified preparation containing the cell of interest.

[0016] The term "heterologous" when referring to a nucleic acid molecule, a protein, a vector, or an expression cassette refers to a nucleic acid molecule, a protein, a vector, or an expression cassette that is expressed in a cell through user manipulation and is not native.For example, a heterologous gene refers to a gene that is expressed by a vector or other vehicle that is introduced into a cell, or a gene that is in a genome that is modified through gene editing methods such as CRISPR or other recombinant techniques to replace a gene in a cell.Those skilled in the art will understand that the term "heterologous" does not refer to a natural gene in the genome of a cell that is not modified."Heterologous" can also be referred to as "exogenous".

[0017] The term "isolated" as used herein with respect to nucleic acids such as DNA or RNA refers to a molecule that is separated from other DNA or RNA present in the natural source of the macromolecule, respectively. The term "isolated" as used herein also refers to a nucleic acid or peptide that is substantially free of cellular material, viral material, or culture medium when produced by recombinant DNA technology, or chemical precursors or other chemicals when chemically synthesized. Furthermore, "isolated nucleic acid" includes nucleic acid fragments that do not naturally occur as fragments and are not found in the natural state. An "isolated cell", for example an isolated bone marrow cell, is a cell that is substantially free of other cellular material, tissue, and medium of the environment in which it is naturally found.

[0018] The term "myeloablative" refers to a treatment that produces long-lasting (usually irreversible) pancytopenia, kills cells in the bone marrow within 1 to 3 weeks of administration, and does not allow autologous hematological recovery. Bacigalupo et al., Biol Blood Marrow Transplant. 2009, 15(12):1628-1633. Examples of myeloablative doses of cyclophosphamide include, but are not limited to, 2.5 mg / kg / day CTX or more over a period of time that results in cumulative toxicity (McKinley et al., Clin J Am Soc Nephrol. 2009, 4:1754-1760).

[0019] The term "non-myeloablative" refers to treatment that produces no, minimal, or reversible cytopenias and is associated with little toxicity. A non-myeloablative regimen is immunoablation. Examples of non-myeloablative doses include, but are not limited to, approximately 1.3 mg / kg / day for a period of time that does not produce cumulative toxicity, or 1.0 to 1.5 mg / kg / day for 2 to 4 months (McKinley et al., Clin J Am Soc Nephrol. 2009, 4:1754-1760). Other non-myeloablative doses are described throughout and are included in the definition of non-myeloablative doses. An agent or dose of an agent that produces "accumulated toxicity" refers to a dose that produces toxicity in a patient over time. For example, cyclophosphamide, when administered to humans at a dose of 2.5 mg / kg / day for several weeks, produces cumulative toxicity.

[0020] A "subject," "individual," or "patient" is used interchangeably herein to refer to a vertebrate, such as a primate, a mammal, or preferably a human. Mammals include, but are not limited to, horses, dogs, cows, sheep, mice, rats, monkeys, and humans.

[0021] The term "sequence identity" with respect to a protein or amino acid sequence (or DNA or RNA sequence) refers to the percentage of a specific protein or amino acid sequence in a candidate sequence after aligning the sequences and introducing gaps, if necessary, to obtain the maximum percent sequence identity, and without considering any conservative substitutions as part of the sequence identity. Alignment refers to the percentage of amino acid residues (or nucleotide residues) that are identical to the amino acid residues (or nucleotide residues in a specific DNA or RNA sequence) in a sequence. Alignment can be performed by any method known to those of skill in the art, for example, by using publicly available programs such as BLAST and EMBOSS. Those of skill in the art can determine appropriate parameters for measuring alignment, including any algorithms required to achieve maximum alignment over the full length of the sequences being compared, although in some embodiments, default parameters are used. Programs can be accessed, for example, at the National Center for Biotechnology Information.

[0022] The term "variant" as used herein refers to a nucleic acid or protein that differs from a reference nucleic acid or protein (i.e., calmodulin or a fragment thereof) but retains essential properties (i.e., biological activity). A typical variant of a polynucleotide differs in nucleotide sequence from another reference polynucleotide. A change in nucleotide sequence may or may not alter the amino acid sequence of a polypeptide encoded by a reference polynucleotide. A change in nucleotide sequence may result in an amino acid substitution, addition, deletion, fusion, and / or truncation in the polypeptide encoded by the reference sequence.

[0023] The term "vector" is used herein to refer to a nucleic acid molecule that can transfer or carry another nucleic acid molecule. The transferred nucleic acid is generally linked to, for example, the nucleic acid molecule of the vector. The vector can include sequences that direct autonomous replication in a cell, or can include sequences sufficient to allow integration into cellular DNA. Vectors include, for example, plasmids (e.g., DNA or RNA plasmids), transposons, cosmids, bacterial or yeast artificial chromosomes, and viral vectors. Useful viral vectors include, for example, adenoviruses, retroviruses, particularly replication-deficient retroviruses, and lentiviruses. In some embodiments, the vector has the nucleotide sequence of SEQ ID NO:2 or SEQ ID NO:4. In some embodiments, the vector includes the nucleotide sequence of SEQ ID NO:1, SEQ ID NO:3, SEQ ID NO:6, SEQ ID NO:7, SEQ ID NO:8, SEQ ID NO:9, or any combination thereof.

[0024] The expression "pharmacologically acceptable" is used herein to refer to compounds, materials, compositions, and / or dosage forms that are within the scope of sound medical judgment and suitable for use in contact with the tissues of human beings and animals without excessive toxicity, irritation, allergic response, or other problem or complication, commensurate with a reasonable benefit / risk ratio.

[0025] Methods for performing bone marrow transplants Provided herein is a method for performing bone marrow transplantation in a patient in need thereof.Also provided is a method for replacing a subject's bone marrow cells with a population of cells expressing a heterologous nucleic acid molecule expression cassette or a plurality of heterologous expression cassettes, or with genome-edited cells that are different from the subject's genome.In some embodiments, these methods include administering one or more chemotherapy-resistant modified cells to a patient, and administering at least one dose of a chemotherapeutic agent.In certain embodiments, the dose is a non-myeloablative dose of the chemotherapeutic agent.In some embodiments, the amount of cells is a therapeutically effective amount.

[0026] In some embodiments of the methods provided herein, the patient has HIV.

[0027] The modified chemotherapy-resistant cells for use in the disclosed methods can be any suitable cells known to those skilled in the art. For example, the cells can be stem cells or immune cells. Non-limiting examples of stem cells include umbilical cord blood cells, fetal stem cells, embryonic stem cells (ESCs), and the like. , hematopoietic stem cells (HSCs), hematopoietic progenitor cells, pluripotent stem cells (PSCs), induced PSCs (iPSCs), or cells derived therefrom. In some embodiments, the immune cells are T cells. In some embodiments, the cells are CD34+ and / or CD4+. In some embodiments, the cells are mesenchymal stem cells, stromal stem cells, hematopoietic stem / progenitor cells from umbilical cord blood, stem / progenitor cells from umbilical cord tissue, iPSCs, HESCs, stem cells from fetal tissue, CD4+ cells, and the like. In some embodiments, the stem cells are CD34+.

[0028] Chemotherapy resistance The chemotherapy-resistant cells for use in the method can be generated using any method known in the art for conferring chemotherapy resistance.In certain embodiments, the bone marrow transplantation method provided herein comprises modifying one or more cells to be chemotherapy-resistant.For example, in certain embodiments, a method is provided for performing bone marrow transplantation in a patient in need thereof, comprising generating chemotherapy-resistant modified cells, administering an effective amount of chemotherapy-resistant modified cells to the patient, and administering at least one dose of chemotherapy.In certain embodiments, the dose is a non-myeloablative dose of chemotherapy.In some embodiments, the chemotherapy-resistant cells are resistant to cyclophosphamide.In some embodiments, the chemotherapy-resistant cells are resistant to non-myeloablative amounts of cyclophosphamide.

[0029] In some embodiments, the cells can be modified to express an exogenous chemotherapy resistance gene (i.e., a transduced gene), for example, the exogenous chemotherapy resistance gene can be a nucleic acid sequence encoding a cyclophosphamide resistance gene, its variant, or a portion thereof. In some embodiments, the cyclophosphamide resistance gene is aldehyde dehydrogenase 1 (ALDH1). In some embodiments, ALDH1 is a nucleic acid molecule comprising the sequence shown in SEQ ID NO:1 or a variant thereof. In some embodiments, ALDH1 is expressed in a lentiviral vector comprising the sequence shown in SEQ ID NO:2 or SEQ ID NO:4 or a variant thereof. Cells modified with ALDH1 but resistant to cyclophosphamide can remain sensitive to other non-cyclophosphamide chemotherapy drugs (i.e., the cells do not become multi-drug resistant).

[0030] Any modification method known to those skilled in the art can be used to express the exogenous chemotherapy resistance gene, including viral vectors (e.g., adenoviruses, retroviruses such as replication-defective retroviruses, and lentiviruses), non-viral vectors (e.g., episomal plasmids), or transposon systems (e.g., Sleeping Beauty or PiggyBac). In some embodiments, the vector has the nucleotide sequence of SEQ ID NO: 2 or SEQ ID NO: 4. In some embodiments, the chemotherapy resistance gene is a synthetic messenger RNA (mRNA). Synthetic mRNA provides the genetic information to make a protein of interest and can be chemically modified to avoid eliciting an immune response. Zangi et al. (2013) Nature Biotech 31:898-907. Because mRNA is not integrated into the host cell genome, the synthetic RNA acts for a period of time and then disappears when the cell divides. In some embodiments, the synthetic mRNA is modified, for example with pseudouridine and / or 5-methyl-cytidine, to reduce the inherent antiviral response to single-stranded RNA. In some embodiments, the synthetic RNA encodes ALDH (e.g., ALDH1) and / or its respective equivalent.

[0031] In some embodiments, chemotherapy resistance, e.g., cyclophosphamide resistance, is transiently expressed by the modified cells. The sufamide is expressed by the modified cells for a period of about 1 week, about 2 weeks, about 3 weeks, about 1 month, about 2 months, about 3 months, about 6 months, about 1 year, about 2 years, or about 3 years. Transient expression refers to the persistence of expression of the gene or protein that confers resistance. Transient means that the resistance is not permanent.

[0032] In some embodiments, exogenous chemotherapy resistance gene, for example cyclophosphamide resistance gene, is introduced into cell by any one of various well-known techniques, such as non-viral-based transfection of cell.The introduction into cell can be carried out by any non-viral-based transfection method known in the art, for example, but not limited to, electroporation, calcium phosphate-mediated transfection, nucleofection, sonoporation, heat shock, magnetofection, liposome-mediated transfection, microinjection, particle gun-mediated transfection (nanoparticles), cationic polymer-mediated transfection (DEAE-dextran, polyethyleneimine, polyethylene glycol (PEG), and the like), or cell fusion.Other methods of transfection include transfection reagents such as Lipofectamine™, Dojindo Highlymax™, Fugene™, jetPEI™, Effectene™, and DreamFect™.

[0033] Cell isolation and / or purification The chemoresistant modified cells for use in the method can be the patient's cells (i.e., autologous cells), donor's cells (i.e., allogeneic cells), or any combination thereof, which are modified to confer chemoresistant. In certain embodiments, the method provided herein further comprises isolating and / or purifying cells from the patient or donor. In certain of these embodiments, the method further comprises modifying cells to be chemoresistant. For example, in certain embodiments, a method is provided for performing bone marrow transplantation in a patient in need thereof, comprising isolating and / or purifying one or more cells from a patient or subject, modifying one or more cells to be chemoresistant as described herein, administering an effective amount of one or more chemoresistant modified cells to the patient, and administering at least one dose of a chemotherapeutic agent.

[0034] The cells can be isolated by any method known to one of skill in the art, for example, based on expression / lack of expression of certain markers, proliferation rate, and differentiation potential. In some embodiments, the cells are isolated by any method known to one of skill in the art, for example, based on expression / lack of expression of certain markers, proliferation rate, and differentiation potential. In some embodiments, the cells are isolated by any method known to one of skill in the art, for example, based on expression / lack of expression of certain markers, proliferation rate, and differentiation potential. low , CD45RA, CD123, ILT-7, MHC class II, MHC class II low , TLR7, and / or TRL9). In some embodiments, cells are isolated based on the presence of a particular marker or combination of markers, including CD3, CD14, CD19, CD56, and / or CD66b. In other embodiments, negative selection is performed, for example, for T cell, B cell, granulocyte, and / or myelomonocytic markers. In some embodiments, cells are isolated based on the presence of Thy-1, alone or in combination with any other marker. In some embodiments, HSCs are isolated based on the presence of Lin - Thy1 + Sca-1 + In some embodiments, mouse HSCs are isolated based on the expression profile CD34 - , Sca1 + , c-kit + In some embodiments, human HSCs can be isolated based on expression of CD34.

[0035] Chemotherapeutic agents In some embodiments, the methods provided herein include administering to the patient one or more doses of a chemotherapeutic agent. In some embodiments, the dose is a non-myeloablative dose of the chemotherapeutic agent. The chemotherapeutic agent can be any suitable chemotherapeutic agent known to those of skill in the art. Non-limiting examples of chemotherapeutic agents include actinomycin, all-trans retinoic acid, azacitidine, azathioprine, bleomycin, bortezomib, busulfan, capecitabine, carboplatin, carmustine (BCNU), cisplatin, chlorambucil, cyclophosphamide, cytarabine, daunorubicin, docetaxel, doxifluridine, doxorubicin, epirubicin, epothilone, etoposide, fluorouracil, gemcitabine, hydroxychloroquine, hydroxypropyl 1,1-dihydropyridine, 1,2 ... These include: ciurea, idarubicin, imatinib, irinotecan, lomustine (CCNU), mechlorethamine, melphalan, mercaptopurine, methotrexate, mitoxantrone, nimustine (ACNU), oxaliplatin, paclitaxel, pemetrexed, temezolamide, teniposide, thiotepa, thioguanine, topotecan, treosulfan, valrubicin, vemurafenib, vinblastine, vincristine, vindesine, and vinorelbine.

[0036] Disease-specific modification In certain embodiments of the methods provided herein, the modified chemo-resistant cells may include one or more additional modifications that are not related to chemo-resistance. For example, in certain embodiments, the cells are further modified to express additional HIV / disease-specific modifications. Thus, in certain embodiments, the bone marrow transplantation methods provided herein further include incorporating one or more additional modifications, including one or more HIV / disease-specific modifications. For example, in certain embodiments, a method is provided for performing bone marrow transplantation in a patient in need thereof, comprising isolating and / or purifying one or more cells from a patient or subject, modifying one or more cells to be chemo-resistant as described herein, incorporating one or more additional modifications into the one or more cells, administering an effective amount of one or more modified chemo-resistant cells to the patient, and administering at least one dose of a chemotherapeutic agent. In some embodiments, the dose is a non-myeloablative dose of the chemotherapeutic agent.

[0037] In some embodiments, the modified cells are further modified to be HIV-resistant. For example, the modified cells can be further modified to express at least one mutant HIV coreceptor that confers resistance to HIV infection, one or more mutations in at least one HIV coreceptor, expression of at least one HIV fusion inhibitor, or any combination thereof. In some embodiments, the cells are modified to express a molecule that inhibits or reduces expression of an HIV coreceptor. In some embodiments, the molecule is an antisense molecule. In some embodiments, the cells are modified to express shCCR5, shCXCR4, GP-41 fusion inhibitor, C46 fusion inhibitor, C34 fusion inhibitor, any other C-peptide fusion inhibitor, or any combination thereof. In some embodiments, the CCR5 mutation is a CCR5-delta32 mutation. In some embodiments, both copies of the CCR5 gene in the cell are replaced with a CCR5-delta32 mutation. In some embodiments, one copy of the CCR5 gene is replaced with a CCR5-delta32 mutation.

[0038] The present disclosure provides cells that have been modified to have chemotherapy resistance, e.g., cyclophosphamide resistance, and HIV resistance. In some embodiments, the cells can be modified to have cyclophosphamide resistance and HIV resistance. HIV resistance can be achieved by reducing the expression of at least one HIV co-receptor, inhibiting one of the at least one HIV co-receptor. The HIV resistance is conferred by a natural mutation or mutations, expression of at least one HIV fusion inhibitor, or any combination thereof. The HIV resistance is conferred by reduced expression of the CCR5 HIV coreceptor, reduced expression of the CXCR4 coreceptor, expression of a C-peptide fusion inhibitor (e.g., a C46 fusion inhibitor or a C34 fusion inhibitor), or any combination thereof.

[0039] The cells can also be modified to express any molecule of interest, as determined by the user or by the needs of a particular patient.

[0040] Patient Administration In some embodiments, the method provided herein comprises administering to a subject an effective amount of chemotherapy-resistant modified cells and a non-myeloablative dose of a chemotherapeutic agent.The modified cells and chemotherapeutic agent can be administered by any suitable route that will be apparent to those skilled in the art, depending on the disease or condition to be treated.Exemplary administration routes include intravenous, intraarterial, intramuscular, subcutaneous, intracranial, intranasal, intradermal, oral, or intraperitoneal.

[0041] In some embodiments, the subject's body surface area of ​​1 m 2 Approximately 1 x 10 8 From about 1×10 11 Cells can be administered to an individual on an absolute cell number basis, for example, the individual can be administered from about 1000 cells / injection up to about 10 billion cells / injection, for example, about, at least about, or up to about 1 x 10 cells per injection. 8 , 1×10 7 , 5×10 7 , 1×10 6 , 5×10 6 , 1×10 5 , 5×10 5 , 1×10 4 , 5×10 4 , 1×10 3 , 5×10 3 (and so on) cells, or any range between any two of these values, inclusive, can be administered. In some embodiments, about 5×10 cells 6 From pcs / kg to about 10 x 10 6 1 / kg will be used for HSC transplantation.

[0042] In another embodiment, the subject is administered about 1000 cells / injection / ml 2up to approximately 10 billion cells / injection / m 2 can be administered, for example, about, at least about, or up to about 1×10 per injection. 8 pieces / m 2 , 1×10 7 pieces / m 2 , 5×10 7 pieces / m 2 , 1×10 6 pieces / m 2 , 5×10 6 pieces / m 2 , 1×10 5 pieces / m 2 , 5×10 5 pieces / m 2 , 1×10 4 pieces / m 2 , 5×10 4 pieces / m 2 , 1×10 3 pieces / m 2 , 5×10 3 pieces / m 2 (etc.) of cells, or any range between any two of these values, inclusive, can be administered.

[0043] In other embodiments, cells can be administered to such individuals on a relative number basis of cells, e.g., the individual can be administered from about 1000 cells per kilogram of the individual up to about 10 billion cells, e.g., about, at least about, or at most about 1×10 cells per kilogram of the individual. 8 pieces, 5×10 7 pieces, 1×10 7 pieces, 5×10 6 pieces, 1×10 6 pieces, 5×10 5 pieces, 1×10 5 pieces, 5×10 4 pieces, 1×10 4 pieces, 5×10 3 pieces, 1×10 3 (etc.) cells, or any range between any two of these values, inclusive, can be administered.

[0044] In some embodiments, at least one dose of a non-myeloablative chemotherapeutic agent is administered to the patient. The administration of the chemotherapeutic agent can be performed simultaneously or sequentially with the administration of the modified cells. In some embodiments, at least one dose of a non-myeloablative chemotherapeutic agent is administered after the administration of the modified cells. In some embodiments, a preconditioning step (also referred to herein as a "pretreatment step") is performed before the administration of the cells, in which at least one dose of a chemotherapeutic agent, such as fludarabine or cyclophosphamide, is administered to the patient before the administration of the modified cells. In some embodiments, the preconditioning step (also referred to herein as a "pretreatment step") is performed before the administration of the cells, in which at least one dose of a chemotherapeutic agent, such as fludarabine or cyclophosphamide, is administered to the patient before the administration of the modified cells. The conditioning step is a preconditioning step with a non-myeloablative chemotherapy drug. In some embodiments, a preconditioning step is not performed before administering the cells. Even if a preconditioning step (e.g., fludarabine) is not performed before administering the cells, it is believed that the cells of the present disclosure will still be efficiently engrafted into the patient's bone marrow.

[0045] In some embodiments, at least one non-myeloablative dose of a chemotherapeutic agent for a human subject or patient is a non-myeloablative dose of cyclophosphamide. In some embodiments, the non-myeloablative dose of cyclophosphamide is from about 0.15 mg / kg / day to less than 2.5 mg / kg / day, from about 0.4 mg / kg / day to about 1.7 mg / kg / day, or from about 0.8 mg / kg / day to about 1.5 mg / kg / day. In some embodiments, the non-myeloablative dose of cyclophosphamide is about 0.15 mg / kg / day, about 0.2 mg / kg / day, about 0.25 mg / kg / day, about 0.3 mg / kg / day, about 0.35 mg / kg / day, about 0.4 mg / kg / day, about 0.45 mg / kg / day, about 0.5 mg / kg / day, about 0.55 mg / kg / day, about 0.6 mg / kg / day, about 0.65 mg / kg / day, about 0.7 mg / kg / day, about 0.75 mg / kg / day, about 0.8 mg / kg / day, about 0.85 mg / kg / day, about 0.95 mg / kg / day, about 100 mg / kg / day, about 15 ... In some embodiments, the non-myeloablative dose of cyclophosphamide is about 1.3 mg / kg / day, about 0.9 mg / kg / day, about 0.95 mg / kg / day, about 1.0 mg / kg / day, about 1.1 mg / kg / day, about 1.2 mg / kg / day, about 1.3 mg / kg / day, about 1.4 mg / kg / day, about 1.5 mg / kg / day, about 1.6 mg / kg / day, about 1.7 mg / kg / day, about 1.8 mg / kg / day, about 1.9 mg / kg / day, about 2.0 mg / kg / day, about 2.1 mg / kg / day, about 2.2 mg / kg / day, about 2.3 mg / kg / day, or about 2.4 mg / kg / day. In some embodiments, the non-myeloablative dose of cyclophosphamide is about 1.3 mg / kg / day. In some embodiments, the non-myeloablative dose of cyclophosphamide is about 0.8 mg / kg / day to about 1.6 mg / kg / day, about 0.8 mg / kg / day, about 0.98 mg / kg / day, about 1.3 mg / kg / day, about 1.5 mg / kg / day, or about 1.6 mg / kg / day. In some embodiments, the non-myeloablative dose of cyclophosphamide is about 0.5 to about 2 mg / kg / day.

[0046] In some embodiments, a non-myeloablative dose of a chemotherapeutic agent is administered daily for at least about 1 day, at least about 2 days, at least about 3 days, at least about 4 days, at least about 5 days, at least about 6 days, at least about 1 week, at least about 2 weeks, at least about 3 weeks, at least about 1 month, at least about 2 months, at least about 3 months, at least about 4 months, at least about 5 months, at least about 6 months, at least about 1 year, or more.

[0047] In some embodiments, the non-myeloablative dose is provided over a period of time that does not result in cumulative toxicity, such as a period of less than about 1 year, less than about 6 months, less than about 3 months, less than about 2 months, less than about 1 month, less than about 3 weeks, less than about 2 weeks, less than about 1 week, less than about 6 days, less than about 5 days, less than about 4 days, less than about 3 days, or less than about 2 days.

[0048] In some embodiments, there is at least one interruption between administration of cyclophosphamide-resistant modified cells and administration of at least one dose of non-myeloablative chemotherapy.For example, the interruption can be about 2 days, about 3 days, about 4 days, about 5 days, about 6 days, about 1 week, about 2 weeks, about 3 weeks, about 1 month, about 2 months, about 3 months, about 6 months, about 1 year, or more.In some embodiments, the interruption is about 3 days, about 7 days, about 10 days, and about 14 days.

[0049] In some embodiments, greater than about 60%, greater than about 70%, greater than about 80%, greater than about 90%, greater than about 95%, or 100% of the patient's bone marrow is replaced with modified cells. In some embodiments, more than about 60%, more than about 70%, more than about 80%, more than about 90%, more than about 95%, or 100% of the patient's bone marrow is replaced with modified cells within about one year. In some embodiments, more than about 60%, more than about 70%, more than about 80%, more than about 90%, more than about 95%, or 100% of the patient's bone marrow is replaced with modified cells within about six months. In some embodiments, more than about 60%, more than about 70%, more than about 80%, more than about 90%, more than about 95%, or 100% of the patient's bone marrow is replaced with modified cells within about five months. In some embodiments, more than about 60%, more than about 70%, more than about 80%, more than about 90%, more than about 95%, or 100% of the patient's bone marrow is replaced with modified cells within about four months. In some embodiments, more than about 60%, more than about 70%, more than about 80%, more than about 90%, more than about 95%, or 100% of the patient's bone marrow is replaced with modified cells within about 3 months. In some embodiments, more than about 60%, more than about 70%, more than about 80%, more than about 90%, more than about 95%, or 100% of the patient's bone marrow is replaced with modified cells within about 2 months. In some embodiments, more than about 60%, more than about 70%, more than about 80%, more than about 90%, more than about 95%, or 100% of the patient's bone marrow is replaced with modified cells within about 1 month. In some embodiments, more than about 60%, more than about 70%, more than about 80%, more than about 90%, more than about 95%, or 100% of the patient's bone marrow is replaced with modified cells within about 2 weeks. In some embodiments, greater than about 60%, greater than about 70%, greater than about 80%, greater than about 90%, greater than about 95%, or 100% of the patient's bone marrow is replaced with modified cells within about one week.

[0050] In some embodiments, the patient is not myeloablated and / or immunocompromised during the method, hi some embodiments, the patient does not experience clinically relevant anemia, neutropenia, thrombocytopenia, pancytopenia, low platelets, low white blood cells, low red blood cells, or any combination thereof, or associated symptoms.

[0051] In another embodiment, upon treatment with the cells and chemotherapeutic agents of the present disclosure, a subject or group of subjects may exhibit one or more of the following outcomes: (i) an increase in white blood cells of at least about 5%, at least about 10%, at least about 15%, at least about 20%, at least about 25%, at least about 30%, at least about 35%, at least about 40%, at least about 45%, at least about 50%, at least about 55%, at least about 60%, at least about 65%, at least about 70%, at least about 75%, at least 80%, at least 85%, at least 90%, at least 95%, or at least 99% (actual % change, or median % change) compared to a control; (ii) an increase in granulocytes of at least about 5%, at least about 10%, at least about 15%, at least about 20%, at least about 25%, at least about 30%, at least about 35%, at least about 40%, at least about 45%, at least about 50%, at least about 55%, at least about 60%, at least about 65%, at least about 70%, at least about 75%, at least 80%, at least 85%, at least 90%, at least 95%, or at least 99% (actual % change, or median % change) compared to a control; (iii) an increase in neutrophils of at least about 5%, at least about 10%, at least about 15%, at least about 20%, at least about 25%, at least about 30%, at least about 35%, at least about 40%, at least about 45%, at least about 50%, at least about 55%, at least 60%, at least 65%, at least 70%, at least about 75%, at least 80%, at least 85%, at least 90%, at least 95%, or at least 99% (actual % change, or median % change) compared to a control; (iv) at least about 5%, at least about 10%, at least about 15%, at least about 20%, at least about 25%, at least about 30%, at least about 35%, at least about 40%, at least about 45%, at least about 50%, at least about 55%, at least 60%, at least 65%, at least 70%, at least about 75%, at least 80%, at least 85%, at least 90%, at least 95%, and is at least 99% (actual % change or median % change) lymphocyte expansion; (v) an increase in eosinophils of at least about 5%, at least about 10%, at least about 15%, at least about 20%, at least about 25%, at least about 30%, at least about 35%, at least about 40%, at least about 45%, at least about 50%, at least about 55%, at least 60%, at least 65%, at least 70%, at least about 75%, at least 80%, at least 85%, at least 90%, at least 95%, or at least 99% (actual % change, or median % change) compared to a control; (vi) an increase in monocytes of at least about 5%, at least about 10%, at least about 15%, at least about 20%, at least about 25%, at least about 30%, at least about 35%, at least about 40%, at least about 45%, at least about 50%, at least about 55%, at least about 60%, at least about 65%, at least about 70%, at least about 75%, at least 80%, at least 85%, at least 90%, at least 95%, or at least 99% (actual % change, or median % change) compared to a control; (vii) an increase in basophils of at least about 5%, at least about 10%, at least about 15%, at least about 20%, at least about 25%, at least about 30%, at least about 35%, at least about 40%, at least about 45%, at least about 50%, at least about 55%, at least about 60%, at least about 65%, at least about 70%, at least about 75%, at least 80%, at least 85%, at least 90%, at least 95%, or at least 99% (actual % change, or median % change) compared to a control; (viii) an increase in red blood cells of at least about 5%, at least about 10%, at least about 15%, at least about 20%, at least about 25%, at least about 30%, at least about 35%, at least about 40%, at least about 45%, at least about 50%, at least about 55%, at least about 60%, at least about 65%, at least about 70%, at least about 75%, at least 80%, at least 85%, at least 90%, at least 95%, or at least 99% (actual % change, or median % change) compared to a control; (ix) an increase in all three blood cellular components (red blood cells, white blood cells, and platelets) of at least about 5%, at least about 10%, at least about 15%, at least about 20%, at least about 25%, at least about 30%, at least about 35%, at least about 40%, at least about 45%, at least about 50%, at least about 55%, at least about 60%, at least about 65%, at least about 70%, at least about 75%, at least 80%, at least 85%, at least 90%, at least 95%, or at least 99% (actual % change, or median % change) compared to a control; (x) being free of recurrence for at least about 6 months, about 1 year, about 2 years, about 3 years, about 4 years, about 5 years, about 6 years, about 7 years, about 8 years, about 9 years, about 10 years, about 15 years, about 20 years, about 25 years, about 30 years, about 35 years, about 40 years, about 45 years, about 50 years, about 55 years, about 60 years, or more; (xi) an increase in recurrence-free survival of the patient for at least about 1 year, about 2 years, about 3 years, about 4 years, about 5 years, about 6 years, about 7 years, about 8 years, about 9 years, about 10 years, about 15 years, about 20 years, about 25 years, about 30 years, about 35 years, about 40 years, about 45 years, about 50 years, about 55 years, about 60 years, or more, compared to a control; (xii) an increase in patient survival relative to a control for at least about 1 year, about 2 years, about 3 years, about 4 years, about 5 years, about 6 years, about 7 years, about 8 years, about 9 years, about 10 years, about 15 years, about 20 years, about 25 years, about 30 years, about 35 years, about 40 years, about 45 years, about 50 years, about 55 years, about 60 years, or more; (xiii) an increase in the intracellular lifespan of HIV of at least about 5%, at least about 10%, at least about 15%, at least about 20%, at least about 25%, at least about 30%, at least about 35%, at least about 40%, at least about 45%, at least about 50%, at least about 55%, at least about 60%, at least about 65%, at least about 70%, at least about 75%, at least 80%, at least 85%, at least 90%, at least 95%, or at least 99% (actual % change, or median % change) compared to a control. Shortening; (xiv) a reduction in HIV reservoir host count of at least about 5%, at least about 10%, at least about 15%, at least about 20%, at least about 25%, at least about 30%, at least about 35%, at least about 40%, at least about 45%, at least about 50%, at least about 55%, at least about 60%, at least about 65%, at least about 70%, at least about 75%, at least 80%, at least 85%, at least 90%, at least 95%, or at least 99% (actual % change, or median % change) compared to a control; and (xv) depletion of viral DNA by at least about 5%, at least about 10%, at least about 15%, at least about 20%, at least about 25%, at least about 30%, at least about 35%, at least about 40%, at least about 45%, at least about 50%, at least about 55%, at least 60%, at least 65%, at least 70%, at least about 75%, at least 80%, at least 85%, at least 90%, at least 95%, or at least 99% (actual % change, or median % change) compared to a control.

[0052] In some embodiments, the control can be a subject treated with a placebo, a baseline control, or a subject treated with unmodified cells.

[0053] In some embodiments, the modified cells are administered to a subject for a period of time effective to reduce at least one symptom of HIV by at least about 2%, at least about 3%, at least about 4%, at least about 5%, at least about 6%, at least about 7%, at least about 8%, at least about 9%, at least about 10%, at least about 11%, at least about 12%, at least about 13%, at least about 14%, at least about 15%, at least about 20%, at least about 25%, at least about 30%, at least about 35%, at least about 40%, at least about 45%, at least about 50%, at least about 55%, at least about 60%, at least about 65%, at least about 70%, at least about 75%, at least about 80%, at least about 85%, at least about 90%, at least about 95%, at least about 97%, at least about 98%, at least about 99%, or 100% compared to a control. Controls can be subjects treated with a placebo, a baseline control, or subjects treated with unmodified cells.

[0054] Non-limiting symptoms include fever, headache, lack of energy, skin rash, skin pain, enlarged glands, infection (e.g., pneumonia, tuberculosis, Hepatitis C), night sweats, diarrhea, nausea and vomiting, weight loss, severe headache, joint pain, muscle pain, and chronic cough.

[0055] In some embodiments, the modified cells are administered with at least one other HIV therapy. Suitable other HIV therapies include any HIV therapy known to one of skill in the art. Non-limiting examples of other HIV therapies include combination drugs (e.g., efavirenz / emtricitabine / tenofovir disoproxil fumarate (Atripla®), emtricitabine / rilpivirine / tenofovir disoproxil fumarate (Complera®), elvitegravir / cobicistat / emtricitabine / tenofovir disoproxil fumarate (Stribild®), and abacavir / dolutegravir / lamivudine (Triumeq®)), nucleoside / nucleotide reverse transcriptase inhibitors (NRTs), and combination HIV therapies (e.g., abacavir / dolutegravir / lamivudine (Triumeq®)), and combination HIV therapies (e.g., abacavir / dolutegravir / lamivudine (Triumeq®)). I) (e.g., abacavir (Ziagen®), efavirenz / emtricitabine / tenofovir disoproxil fumarate (Atripla®), lamivudine / zidovudine (Combivir®), emtricitabine / rilpivirine / tenofovir disoproxil fumarate (Complera®), emtricitabine (Emtriva®), lamivudine (Epivir®), abacavir / lamivudine (Epzicom®), zidovudine (Retrovir®), abacavir / lamivudine Other examples of antiviral drugs include rifavir / zidovudine (Trizivir), emtricitabine / tenofovir disoproxil fumarate (Truvada®), didanosine (Videx®), didanosine extended-release (Videx EC®), tenofovir disoproxil fumarate (Viread®), and stavudine (Zerit®)), non-nucleoside reverse transcriptase inhibitors (NNRTIs), protease inhibitors (e.g., tipranavir (Aptivus®), indinavir (Crixivan®), atazanavir / cobicistat (Evotaz®), saquinavir (Invirase®), lopinavir / ritonavir (Kaletra®), fosamprenavir (Lexiva®), ritonavir (Norvir®), darunavir / cobicistat (Prezcobix®), darunavir (Prezista®), atazanavir (Reyataz®), nelfinavir (Viracept®), entry inhibitors (e.g., enfuvirtide (Fuzeon®)), integrase inhibitors (e.g., raltegravir (Isentress®), doxorubicin (Delta®), ribavirin (Renvir ... These include tegravir (Tivicay®), and elvitegravir (Vitekta®), chemokine co-receptor antagonists (CCR5 antagonists) (e.g., maraviroc (Selzentry®) or vicriviroc), cytochrome P4503A inhibitors, and immune-based therapies (e.g., hydroxychloroquine sulfate (Plaquenil). In some embodiments, the modified cells and at least one other HIV therapy are administered simultaneously. In other embodiments, the modified cells and at least one other HIV therapy are administered sequentially. In some embodiments, administration of at least one of the above other HIV therapies is specifically excluded, for example, in some embodiments, NRTIs are specifically excluded. In some embodiments, no other HIV therapy is administered other than the modified cells disclosed herein and at least one dose of a non-myeloablative chemotherapeutic agent (e.g., cyclophosphamide).

[0056] The cells, chemotherapeutic agents, and optionally other HIV therapies can be administered once to a patient with HIV, or multiple times during the course of therapy, for example, once every hour, every 2 hours, every 3 hours, every 4 hours, every 5 hours, every 6 hours, every 7 hours, every 8 hours, every 9 hours, every 10 hours, every 11 hours, every 12 hours, every 13 hours, every 14 hours, every 15 hours, every 16 hours, every 17 hours, every 18 hours, every 19 hours, every 20 hours, every 21 hours, every 22 hours, or every 23 hours, or once every 1 day, 2 days, 3 days, 4 days, 5 days, 6 days, or 7 days, or once every 1 week, 2 weeks, 3 weeks, 4 weeks, 5 weeks, 6 weeks, 7 weeks, 8 weeks, 9 weeks, 10 weeks, or more weeks, or any range between any two of these values, inclusive of the endpoints.

[0057] In some embodiments, a method of treating a patient with HIV is provided. In some embodiments, the method comprises: + This involves mobilizing stem cells from the bone marrow to the periphery. In some embodiments, the cells are mobilized by administering G-CSF (granulocyte colony stimulating factor). G-CSF can be administered, for example, as a 1-day, 2-day, 3-day, 4-day, or 5-day regimen. In some embodiments, G-CSF is administered for 3-5 days. The mobilized cells can be captured using methodologies such as apheresis. In some embodiments, isolation of cells, for example by apheresis, is accomplished by isolating the cells using CD34 + The cell count is 10.0 to 20.0 × 10 cells per kg of body weight. 6 In some embodiments, the cell count is between 5.0 and 25.0 x 10 cells / kg body weight or greater. 6 Cd34+ cells are used as a marker to capture cells for transduction, although other cell markers, such as those described herein, can also be used. For example, specific markers or markers can be used to capture cells for transduction. Cells that can be used are isolated based on the presence of a combination of markers, such as CD34, CD4, Sca-1, CD38, CD123, CD90, CD45, CD133, antigen presenting cell markers (CD8, CD8 alpha, CD11b, CD11c, CD103, CD205, CD24, CD115, CD117, CD135, CD11c low , CD45RA, CD123, ILT-7, MHC class II, MHC class II low , TLR7, and / or TRL9). In some embodiments, cells are isolated based on the absence of certain markers, e.g., CD3, CD14, CD19, CD56, and / or CD66b. In other embodiments, negative selection is performed, e.g., for T cell, B cell, granulocyte, and / or myelomonocytic markers. In some embodiments, cells are isolated based on the presence of Thy-1, alone or in combination with any other marker. In some embodiments, HSCs are isolated based on the presence of Lin - Thy1 + Sca-1 + In some embodiments, mouse HSCs are isolated based on the expression profile CD34 - , Sca1 + , c-kit + In some embodiments, human HSCs can be isolated based on expression of CD34. In some embodiments, the isolated cells are CD34+ or CD4+, or any combination thereof.

[0058] In some embodiments, the method includes centrifuging the cell harvest. This is done, for example, to develop a cell-enriched pellet. The cells are then resuspended in a cryopreservation solution and frozen. In some embodiments, the cryopreservation solution includes a solution of heparinized Plasmalyte and 10% DMSO (dimethyl sulfoxide). In some embodiments, the cells are first stored at -4°C, and then the sample is frozen down to a target temperature of -156°C (if stored in vapor phase) to -196°C (if stored in liquid phase).

[0059] In some embodiments, the method includes transducing isolated cells to render them resistant to chemotherapeutic agents such as cyclophosphamide. As described herein, chemotherapy resistance is achieved by expression of ALDH1. ALDH1 can be introduced into selected cells through the use of a vector (described throughout the present specification), such as the use of a lentiviral vector. ALDH1 can be operably linked to a promoter, which can be cell-specific. In some embodiments, the promoter is a CD34 promoter. In some embodiments, the promoter is a hCD34 promoter. In some embodiments, the promoter has a sequence of SEQ ID NO: 12. In some embodiments, the promoter is a hCD4 promoter, such as provided in SEQ ID NO: 8. In some embodiments, the sequence of ALDH1 is expressed as a protein provided in SEQ ID NO: 10. In some embodiments, ALDH1 is encoded by a nucleic acid molecule comprising the sequence of SEQ ID NO: 1. Due to the degenerate nature of the genetic code, the sequence of SEQ ID NO: 1 is provided as a non-limiting example, and other nucleic acid molecules are also used to encode the expression of a protein comprising SEQ ID NO: 10. In some embodiments, ALDH1 comprises 1-10 conservative substitutions that do not alter the function of ALDH1. In some embodiments, the expressed ALDH1 is at least 95% homologous or identical to SEQ ID NO:10.

[0060] The expression of ALDH1 in the vector is also driven by an enhancer element.For example, the enhancer element can be a CD3E enhancer.In some embodiments, the CD3E enhancer comprises the sequence of SEQ ID NO:9.

[0061] In some embodiments, CD34 + Cells can be isolated by magnetic bead separation. + Transduction of cells can be achieved by, for example, the expression of cytokines such as stem cell factor (SCF), Fms-related tyrosine kinase 3 ligand (FLT3L), and the like. The pre-stimulation may include a 24 hour pre-stimulation of the cells in medium supplemented with ALDH1, thrombopoietin (TPO), IL-6, IL-2, IL-3, fibronectin, or any combination thereof. In some embodiments, the cells are then contacted (infected) with a lentivirus expressing ALDH1. In some embodiments, the vector comprises the sequence of SEQ ID NO:2, SEQ ID NO:4, or SEQ ID NO:5. The contacting ... -1 ) The cells may then be optionally frozen or not. In some embodiments, the cells are not contacted with an AAV or AV vector.

[0062] In some embodiments, the method includes injecting the transduced cells into a subject. In some embodiments, the subject has HIV. In some embodiments, the subject does not have HIV but is at high risk of contracting HIV and therefore desires to become HIV resistant.

[0063] In some embodiments, after infusion of the modified cells, a non-myeloablative dose of chemotherapy, such as cyclophosphamide, is administered. In some embodiments, the dosage is between 50 and 200 mg, administered once per day. In some embodiments, the non-myeloablative dose of cyclophosphamide is from about 0.15 mg / kg / day to less than 2.5 mg / kg / day, from about 0.4 mg / kg / day to about 1.7 mg / kg / day, or from about 0.8 mg / kg / day to about 1.5 mg / kg / day. In some embodiments, the non-myeloablative dose of cyclophosphamide is about 0.15 mg / kg / day, about 0.2 mg / kg / day, about 0.25 mg / kg / day, about 0.3 mg / kg / day, about 0.35 mg / kg / day, about 0.4 mg / kg / day, about 0.45 mg / kg / day, about 0.5 mg / kg / day, about 0.55 mg / kg / day, about 0.6 mg / kg / day, about 0.65 mg / kg / day, about 0.7 mg / kg / day, about 0.75 mg / kg / day, about 0.8 mg / kg / day, about 0.85 mg / kg / day, about 0.95 mg / kg / day, about 100 mg / kg / day, about 15 ... In some embodiments, the non-myeloablative dose of cyclophosphamide is about 1.3 mg / kg / day, about 0.9 mg / kg / day, about 0.95 mg / kg / day, about 1.0 mg / kg / day, about 1.1 mg / kg / day, about 1.2 mg / kg / day, about 1.3 mg / kg / day, about 1.4 mg / kg / day, about 1.5 mg / kg / day, about 1.6 mg / kg / day, about 1.7 mg / kg / day, about 1.8 mg / kg / day, about 1.9 mg / kg / day, about 2.0 mg / kg / day, about 2.1 mg / kg / day, about 2.2 mg / kg / day, about 2.3 mg / kg / day, or about 2.4 mg / kg / day. In some embodiments, the non-myeloablative dose of cyclophosphamide is about 1.3 mg / kg / day. In some embodiments, the non-myeloablative dose of cyclophosphamide is about 0.8 mg / kg / day to about 1.6 mg / kg / day, about 0.8 mg / kg / day, about 0.98 mg / kg / day, about 1.3 mg / kg / day, about 1.5 mg / kg / day, or about 1.6 mg / kg / day. In some embodiments, the non-myeloablative dose of cyclophosphamide is about 0.5 to about 2 mg / kg / day. Doses can be administered as indicated herein. Without being bound to any particular theory, oral cyclophosphamide once a day to facilitate grafting expands the genetically modified bone marrow cells. Modified CD34 +The patient was HIV positive at the time the cells were infused. + In this case, the cells may function to treat and / or cure HIV, or may be modified CD34 + The patient was HIV positive at the time the cells were infused. - It is possible that, in this case, the cells are functioning to prevent future HIV infection. + A non-limiting schematic diagram of patient treatment is shown in Figures 9 and 10, where the patient is HIV - But it is understood that this is possible.

[0064] In some embodiments, subjects are also treated with fludarabine prior to infusion of the modified cells. In some embodiments, on day 2 after harvest (or day pre-transplant -5), patients are administered fludarabine (15 mg / m 2 In some embodiments, instead of fludarabine, patients are treated with 4 In some embodiments, patients are treated with a single dose of 1000mg / m2 cyclophosphamide on day -2 prior to transplantation. However, after injecting the cells, subjects are treated with a non-myeloablative dose of cyclophosphamide as indicated herein.

[0065] As described herein, the vector may also include other expression cassettes, including those expressing shCCR5 or fusion inhibitors, such as C44, C46, ​​or others described herein. The fusion inhibitor may be a fusion of a GPI anchor and an HIV fusion inhibitor. In some embodiments, the fusion inhibitor is encoded by the nucleic acid sequence of SEQ ID NO:3. In some embodiments, the fusion inhibitor is a protein comprising the amino acid sequence of SEQ ID NO:11. In some embodiments, the fusion inhibitor is encoded by the nucleic acid sequence of SEQ ID NO:14. In some embodiments, the fusion inhibitor is a protein comprising the amino acid sequence of SEQ ID NO:15. In some embodiments, the fusion inhibitor is membrane anchored by a GPI anchor. In some embodiments, the anchor is encoded by a nucleic acid molecule comprising the sequence of SEQ ID NO:16. In some embodiments, the anchor comprises the sequence of SEQ ID NO:17. In some embodiments, the fusion-anchor protein comprises an IgG hinge region. In some embodiments, the IgG hinge region is IgG3. In some embodiments, the fusion inhibitor protein comprises the sequence of SEQ ID NO:19. In some embodiments, the fusion inhibitor protein is encoded by a nucleic acid molecule comprising the sequence of SEQ ID NO:18. In some embodiments, the anchor is GP41.

[0066] In some embodiments, the fusion inhibitor is under the control of a promoter different from that of the ALDH1 promoter.In some embodiments, the promoter is an EFS promoter.In some embodiments, the promoter is a CD4 promoter, for example, the CD4 promoter described herein.

[0067] In some embodiments, the vector transduced into cells as provided herein expresses an antisense molecule that reduces or inhibits the expression of CCR5. In some embodiments, the vector encodes a shCCR5 inhibitor molecule. In some embodiments, the lentiviral vector encodes the sense sequence of hCCR5 shRNA of SEQ ID NO: 6, or its complement, and / or the antisense sequence of hCCR5 shRNA of SEQ ID NO: 7, or its complement. In some embodiments, the sequence can also be in the reverse direction. In some embodiments, the vector comprises a mir30 expression cassette. In some embodiments, the mir30 expression cassette encodes hCCR5 shRNA. In some embodiments, the mir30 construct comprises the sequence of SEQ ID NO: 13. The antisense molecules that can be used to inhibit the expression of CCR5 are non-limiting examples, and other antisense molecules that target CCR5 can also be used.

[0068] Thus, in some embodiments, a nucleic acid molecule is provided that comprises the sequence of SEQ ID NO:6, SEQ ID NO:7, and / or SEQ ID NO:13.

[0069] In some embodiments, the disclosure provides a protein comprising SEQ ID NO:10, SEQ ID NO:11, SEQ ID NO:14, SEQ ID NO:17, SEQ ID NO:18, and / or SEQ ID NO:19.

[0070] In some embodiments, a nucleic acid molecule is provided that comprises SEQ ID NO:1 or a variant thereof, SEQ ID NO:3 or a variant thereof, SEQ ID NO:6 or a variant thereof, SEQ ID NO:7 or a variant thereof, SEQ ID NO:13 or a variant thereof, SEQ ID NO:14 or a variant thereof, SEQ ID NO:16 or a variant thereof, SEQ ID NO:18 or a variant thereof, or any combination thereof. In some embodiments, the nucleic acid molecule comprises SEQ ID NO:1 or a variant thereof, SEQ ID NO:6 or a variant thereof, SEQ ID NO:7 or a variant thereof, as well as SEQ ID NO:3, SEQ ID NO: SEQ ID NO:14, and one or more of SEQ ID NO:18. In some embodiments, nucleic acid molecules are provided that encode proteins comprising SEQ ID NO:2, and one or more of SEQ ID NO:11, SEQ ID NO:15, and SEQ ID NO:19.

[0071] In some embodiments, the disclosure provides nucleic acid molecules encoding ALDH1 or a mutant thereof, shCCR5 molecules or mutants thereof, and / or fusion inhibitors, including immobilized fusion inhibitors.

[0072] In some embodiments, a single nucleic acid molecule, such as a single vector, is used to encode or express each of the nucleic acid molecules or proteins provided herein. In some embodiments, a single lentivirus comprises the nucleic acid sequence provided herein. In some embodiments, a lentivirus is provided that comprises a single expression construct that encodes each of ALDH1 or its variants, shCCR5 molecules or its variants, and / or fusion inhibitors. Non-limiting examples of vectors that comprise various elements described herein are shown in Figure 4, Figure 5, Figure 6, Figure 11, and Figure 12. The promoters and response elements that operably connect the nucleic acid molecules that encode ALDH1, shCCR5, and fusion inhibitors (including fixed fusion inhibitors) are non-limiting, and other promoters and response elements can also be used. It will be understood by those skilled in the art that the different promoters described are interchangeable with each other.

[0073] Non-limiting examples of nucleic acid sequences that can be used as viral vectors or as a basis for forming lentiviruses include, for example, nucleic acid sequences comprising SEQ ID NO:2, SEQ ID NO:4, and SEQ ID NO:5.

[0074] In some embodiments, the nucleic acid molecule comprises 5'LTR and 3'LTR flanking the nucleic acid molecule encoding ALDH1, shCCR5, and / or fusion inhibitor protein. For the avoidance of doubt, the shCCR5 sequence and the fusion inhibitor sequence can be replaced with other sequences of interest that are used to be co-expressed with ALDH1. Thus, in some embodiments, the nucleic acid molecule comprises a sequence encoding ALDH1 and a sequence of interest that can be, for example, any other protein, antisense, miRNA, or other nucleic acid molecule that is desired to be expressed in bone marrow or cell types provided herein.

[0075] Thus, in some embodiments, a method is provided that includes administering to an individual cells that express ALDH1 and a molecule of interest, and administering a non-myeloablative dose of a chemotherapeutic agent (e.g., cyclophosphamide) to the subject.

[0076] In some embodiments, a method of treating HIV in a subject is provided, comprising administering to the subject a population of cells heterologously expressing ALDH1 and one of i) heterologous nucleotide molecules encoding at least one HIV coreceptor mutant, at least one HIV coreceptor mutation or mutations, at least one HIV fusion inhibitor, a molecule that reduces the expression of an HIV coreceptor, or any combination thereof. In some embodiments, the method comprises administering at least one dose of a non-myeloablative chemotherapeutic agent. In some embodiments, the cells are autologous to the subject. In some embodiments, the cells are allogeneic to the subject. In some embodiments, the cells express shCCR5, shCXCR4, and / or a C-peptide fusion inhibitor. In some embodiments, the cells comprise a nucleic acid molecule comprising a sequence of 1, 3, 6, 7, 8, 9, 12, 13, 14, 16, 18, or any combination thereof. In some embodiments, the cells comprise a nucleic acid molecule encoding a sequence of SEQ ID NO: 10, 11, 6, 7, 13, 15, 17, 19, or any combination thereof. In some embodiments, the cells are CD34+ and / or CD4+ or are any of the CD4+ and CD5+ cells described herein. Others are provided.

[0077] In some embodiments, a method is provided for expressing a molecule of interest in a subject, comprising administering to the subject a cell that heterologously expresses ALDH1 and the molecule of interest; and administering a non-myeloablative dose of cyclophosphamide.In some embodiments, the cell is CD34+ and / or CD4+, or other as provided herein.In some embodiments, the molecule of interest is a molecule that reduces the expression of CCR5; a molecule that reduces the expression of CXCR4; a molecule that encodes the expression of a C-peptide fusion inhibitor; or any combination thereof.In some embodiments, the molecule of interest that reduces the expression of CCR5 is shCCR5.In some embodiments, the molecule comprises a nucleic acid molecule that comprises or encodes SEQ ID NO:6 and / or SEQ ID NO:7.In some embodiments, the C-peptide fusion inhibitor comprises the sequence of SEQ ID NO:11, the sequence of SEQ ID NO:15, the sequence of SEQ ID NO:19, or any combination thereof.

[0078] It is understood that various sequences are provided herein. In addition to exact sequences, sequences that are variants of the disclosed sequences are also provided. In some embodiments, sequences are provided that have at least, about, or exactly 70, 71, 72, 73, 74, 75, 76, 77, 78, 79, 80, 81, 82, 83, 84, 85, 86, 87, 88, 89, 90, 91, 92, 93, 94, 95, 96, 97, 98, or 99 percent homology or identity to the sequence mentioned. Those skilled in the art will easily understand how to determine the homology of two proteins or nucleic acids. For example, the homology can be calculated after aligning the two sequences so that the homology is at its highest level. In some embodiments, the homology calculation can be performed by a published algorithm. Optimal alignment of sequences for comparison can be performed by the local homology algorithm of Smith and Waterman Adv. Appl. Math. 2:482 (1981), by the homology alignment algorithm of Needleman and Wunsch, J. MoL Biol. 48:443 (1970), by the search for similarity method of Pearson and Lipman, Proc. Natl. Acad. Sci. USA 85:2444 (1988), by computerized implementations of these algorithms (GAP, BESTFIT, FASTA, and TFASTA in the Wisconsin Genetics Software Package, Genetics Computer Group, 575 Science Dr., Madison, Wis.), or by inspection. The same type of homology can be obtained for nucleic acids by algorithms disclosed in, for example, Zuker, M. Science 244:48-52, 1989; Jaeger et al., Proc. Natl. Acad. Sci. USA 86:7706-7710, 1989; Jaeger et al., Methods Enzymol. 183:281-306, 1989, which are incorporated by reference herein for at least their material on nucleic acid alignment.For example, Blastn or BlastP using default settings can be used to align two sequences using the website maintained by the National Center for Biotechnology Information.

[0079] For example, as used herein, a sequence that is said to have a certain homology percentage to another sequence refers to a sequence that has the said homology when calculated by any one or more of the above calculation methods.For example, if a first sequence is calculated to have 80% homology to a second sequence using the Zuker calculation method, the first sequence has 80% homology to the second sequence as defined herein, even if the first sequence does not have 80% homology to the second sequence when calculated by any other calculation method.As another example, using both the Zuker calculation method and the Pearson and Lipman calculation method, If a first sequence is calculated to have 80 percent homology to a second sequence, the first sequence has 80 percent homology to the second sequence, as defined herein, even if the first sequence does not have 80 percent homology to the second sequence when calculated by either the Smith and Waterman calculation method, the Needleman and Wunsch calculation method, the Jaeger calculation method, or other calculation method. As yet another example, if a first sequence is calculated to have 80 percent homology to a second sequence using each of the calculation methods, the first sequence has 80 percent homology to the second sequence, as defined herein (although in practice, different calculation methods often result in different calculations of homology percentages).

[0080] Cells and compositions In certain embodiments, the above-mentioned chemotherapy-resistant modified cells related to the disclosed method and the use of these cells in the disclosed method are provided herein.Also provided is the method of generating these cells by incorporating one or more modifications that confer chemotherapy resistance into suitable cells, and optionally by incorporating one or more additional modifications that are not related to chemotherapy resistance, such as additional HIV / disease-specific modifications.

[0081] Also provided herein is a composition, which in certain embodiments comprises at least one of the chemotherapy-resistant modified cells provided herein, and is used in the method provided herein.In some embodiments, the composition further comprises a pharmaceutically acceptable excipient, diluent, carrier, or any combination thereof.

[0082] The composition may include pharma- ceutically acceptable excipients, pharma-ceutically acceptable salts, diluents, carriers, vehicles, and other such inactive agents well known to those skilled in the art. Vehicles and excipients commonly utilized in pharmaceutical preparations include, for example, talc, gum arabic, lactose, starch, magnesium stearate, cocoa butter, aqueous or non-aqueous solvents, oils, paraffin derivatives, glycols, and the like. Solutions can be prepared using water or physiologically compatible organic solvents, such as ethanol, 1,2-propylene glycol, polyglycols, dimethyl sulfoxide, aliphatic alcohols, triglycerides, partial esters of glycerin, and the like. The composition can be prepared using conventional techniques, including sterile isotonic saline, water, 1,3-butanediol, ethanol, 1,2-propylene glycol, polyglycols mixed with water, Ringer's solution, and the like. In one embodiment, a coloring agent is added to facilitate identifying the location of the composition and placing it accurately at the intended treatment site.

[0083] The composition may contain a preservative and / or stabilizer.Non-limiting examples of preservatives include methylparaben, ethylparaben, propylparaben, sodium benzoate, benzoic acid, sorbic acid, potassium sorbate, propionic acid, benzalkonium chloride, benzyl alcohol, thimerosal, phenylmercury salts, chlorhexidine, phenol, 3-cresol, quaternary ammonium compounds (QACs), chlorbutanol, 2-ethoxyethanol, and imidurea.

[0084] To adjust tonicity, the composition may contain physiological salts such as sodium salts. Sodium chloride (NaCl) is preferred, which may be present at between 1 and 20 mg / ml. Other salts that may be present include potassium chloride, potassium dihydrogen phosphate, disodium phosphate dihydrate, magnesium chloride, and calcium chloride.

[0085] The composition may include one or more buffers. Typical buffers include: phosphate buffer; Tris buffer; borate buffer; succinate buffer; histidine buffer; or citrate buffer. Buffers are typically included at concentrations ranging from 5 to 20 mM. The pH of the composition is generally between 5 and 8, more typically between 6 and 8, for example between 6.5 and 7.5, or between 7.0 and 7.8.

[0086] In some embodiments, the composition may include a cryoprotectant, non-limiting examples of which include glycols (e.g., ethylene glycol, propylene glycol, and glycerin), dimethyl sulfoxide (DMSO), formamide, sucrose, trehalose, dextrose, and any combination thereof.

[0087] In one embodiment, the cells are part of a population of cultured cells (i.e., in vitro). In another embodiment, the cells are part of a population of cells of a subject (i.e., in vivo). For example, the modified cells and / or non-myeloablative doses of chemotherapeutic agents are delivered to cells in vivo, or to a population of cells in vivo that form a tissue or organ in a subject, for the purpose of treating or preventing HIV or a disease of interest. Alternatively, the modified cells and / or non-myeloablative doses of chemotherapeutic agents are delivered to cultured cells or a population of cultured cells for the purpose of conducting experiments to study their effect on a particular type of cell.

[0088] The composition can be included in an implantable device.Suitable implantable devices contemplated by the present invention include intravascular stents (e.g., self-expanding stents, balloon-expanding stents, and stent-grafts), scaffolds, grafts, and the like.Such implantable devices can be coated on at least one side with a composition that can treat or prevent HIV or other diseases, or can be impregnated with a composition that can treat or prevent HIV or other diseases.

[0089] References to sequences herein refer to sequences in the following tables or equivalents:

[0090] [Table 1] [Table 2] [Table 3] [Table 4] [Table 5] [Table 6] [Table 7] [Table 8] [Table 9] [Table 10] [Table 11] [Table 12] [Table 13]

[0091] The composition can be administered to the subject by any suitable manner and route. Non-limiting examples include internal, pulmonary, rectal, nasal, vaginal, lingual, intravenous, intraarterial, intramuscular, intraperitoneal, intradermal, and subcutaneous routes. The composition is also suitable for transdermal delivery as part of a cream, gel, or patch. Other dosage forms include tablets; capsules; pills; powders; aerosols; suppositories; parenteral drugs; and oral liquids, including suspensions, solutions, and emulsions. Sustained release dosage forms can also be used. Non-myeloablative doses of chemotherapy can be administered orally or by other methods provided herein.

[0092] In some embodiments, the embodiments provided herein also include, but are not limited to, the following:

[0093] 1. A method for performing a bone marrow transplant in a patient, comprising modifying cyclophosphamide resistance administering to the patient a population of selected cells and at least one dose of non-myeloablative cyclophosphamide.

[0094] 2. The method of embodiment 1, wherein the population of cyclophosphamide-resistant modified cells comprises a heterologous gene encoding aldehyde dehydrogenase 1 (ALDH1).

[0095] 3. The method of embodiment 1, wherein the population of cyclophosphamide-resistant modified cells expresses ALDH1.

[0096] 4. The method of embodiment 1, wherein the cyclophosphamide resistance of the cyclophosphamide-resistant modified cells is conferred by expression of aldehyde dehydrogenase 1 (ALDH1).

[0097] 5. The method of any one of embodiments 1-4, wherein more than 50% of the patient's bone marrow is replaced with cyclophosphamide-resistant modified cells or cells derived therefrom within 6 months.

[0098] 6. The method of any one of embodiments 1-5, wherein the patient has HIV.

[0099] 7. The method of any one of embodiments 1-6, wherein the cyclophosphamide resistance of the modified cells is transient.

[0100] 8. The method of any one of embodiments 1 to 7, wherein the cell is a stem cell or an immune cell.

[0101] 9. The method of embodiment 8, wherein the stem cells are fetal stem cells, stem cells derived from umbilical cord blood, hematopoietic stem cells (HSC), pluripotent stem cells (PSC), induced PSC (iPSC), embryonic stem cells (ESC), or cells derived therefrom, such as CD34+ cells, CD90+ cells, CD45+ cells, CD17+ cells, CD45RA- cells, CD38- cells, or any combination thereof.

[0102] 10. The method of embodiment 8, wherein the immune cell is a T cell.

[0103] 11. The method of any one of embodiments 1-10, wherein the modified cells are autologous to the patient, allogeneic to the patient, or a combination thereof.

[0104] 12. The method of any one of embodiments 1-11, further comprising contacting the unmodified cells with an expression vector encoding expression of ALDH1 to produce modified cells that are cyclophosphamide resistant.

[0105] 13. The method of embodiment 12, wherein the expression vector is a viral vector or a non-viral vector.

[0106] 14. The method of embodiment 13, wherein the viral vector is a lentiviral vector or an adenoviral vector.

[0107] 15. The method of embodiment 12, wherein the expression vector is a retrovirus, a transposon, an episomal expression vector, modified RNA, a plasmid, or any combination thereof.

[0108] 16. At least one dose of a non-myeloablative chemotherapy agent is administered after administration of the modified cells. The method of any one of embodiments 1-15, wherein the patient is administered

[0109] 17. The method of any one of embodiments 1-16, wherein at least one non-myeloablative dose of the chemotherapeutic agent is a non-myeloablative dose of cyclophosphamide.

[0110] 18. The method of embodiment 17, wherein the non-myeloablative dose of cyclophosphamide is from about 0.16 mg / kg / day to less than 2.5 mg / kg / day.

[0111] 19. The method of embodiment 17, wherein the non-myeloablative dose of cyclophosphamide is about 0.41 mg / kg / day to about 1.63 mg / kg / day.

[0112] 20. The method of embodiment 17, wherein the non-myeloablative dose of cyclophosphamide is about 0.81 mg / kg / day to about 1.46 mg / kg / day.

[0113] 21. The method of embodiment 17, wherein the non-myeloablative dose of cyclophosphamide is about 1.3 mg / kg / day.

[0114] 22. The patient received 100 mg / m 2 The method of any one of embodiments 17-21, wherein the / day dose of cyclophosphamide is not administered for 1 to 14 consecutive days.

[0115] 23. Patients should be on a diet of 5-7g / m 2 The method of any one of embodiments 17-22, wherein the dose of cyclophosphamide is not administered for 12 to 24 hours.

[0116] 24. The method according to any one of embodiments 1-23, wherein the non-myeloablative chemotherapy agent is administered daily for at least 1 week, at least 2 weeks, at least 3 weeks, at least 1 month, at least 2 months, at least 3 months, at least 4 months, at least 5 months, or at least 6 months.

[0117] 25. The method according to any one of embodiments 1 to 24, further comprising not administering a non-myeloablative dose of a chemotherapeutic agent for a period of time between administration of the cyclophosphamide-resistant modified cells and administration of at least one dose of a non-myeloablative chemotherapeutic agent.

[0118] 26. The method of embodiment 25, wherein the period of time is selected from the group consisting of about 3 days, about 7 days, about 10 days, and about 14 days.

[0119] 27. The method of any one of embodiments 1-26, wherein more than about 60%, more than about 70%, more than about 80%, more than about 90%, more than about 95%, or 100% of the patient's bone marrow is replaced with modified cells.

[0120] 28. The method of any one of embodiments 1-27, wherein the patient is not myeloablative and / or immunocompromised as a result of administration of at least one dose of a non-myeloablative chemotherapy agent.

[0121] 29. The method of any one of embodiments 1-28, wherein the patient does not experience clinically relevant anemia, neutropenia, thrombocytopenia, pancytopenia, low platelets, low white blood cells, or any combination thereof or related symptoms.

[0122] 30. The method according to any one of embodiments 1 to 29, wherein the preconditioning step is carried out before administering the cells.

[0123] 31. The method of embodiment 30, wherein the preconditioning step is a non-myeloablative chemotherapy preconditioning step.

[0124] 32. The method according to any one of embodiments 1 to 31, wherein the modified cells are resistant to HIV infection.

[0125] 33. The method of embodiment 32, wherein the modified cells heterologously express at least one HIV coreceptor mutation resistant to HIV infection, one or more mutations in at least one HIV coreceptor, at least one HIV fusion inhibitor, a molecule that reduces expression of an HIV coreceptor, or any combination thereof.

[0126] 34. The method of embodiment 32, wherein the modified cells heterologously express shCCR5, shCXCR4, a C-peptide fusion inhibitor, or any combination thereof.

[0127] 35. The method of embodiment 32, wherein the modified cells do not express an HIV co-receptor.

[0128] 36. The method of embodiment 32, wherein the modified cells do not express CCR5, CXCR4, or express CCR5-Δ32, or a combination thereof.

[0129] 37. ALDH1, and i) a heterologous nucleotide molecule encoding at least one HIV coreceptor mutant, at least one HIV coreceptor mutation or mutations, at least one HIV fusion inhibitor, a molecule that reduces expression of an HIV coreceptor, or any combination thereof; and / or ii) an endogenous HIV coreceptor mutation or deletion. A cell comprising a heterologous nucleotide molecule encoding expression of.

[0130] 38. The cell of embodiment 37, wherein the cell comprises a heterologous nucleotide sequence that: i. encodes a molecule that reduces expression of CCR5; ii. encodes a molecule that reduces expression of CXCR4; iii. encodes expression of a C-peptide fusion inhibitor; iv. comprises a sequence of 1, 3, 6, 7, 8, 9, 12, 13, 14, 16, 18, or any combination thereof; v. encodes a sequence of SEQ ID NO: 10, 11, 6, 7, 13, 15, 17, 19, or any combination thereof; or any combination thereof.

[0131] 39. The cell of embodiment 37 or 38, expressing shCCR5, shCXCR4, and / or a C-peptide fusion inhibitor such as C44.

[0132] 40. The cell of embodiment 37, which has been modified to express a heterologous nucleotide sequence using a non-viral gene transfer system.

[0133] 41. The cell of embodiment 40, wherein the non-viral gene transfer system is a transposon gene transfer system.

[0134] 42. The cell of embodiment 37, wherein the transposon gene transfer system is a Sleeping Beauty gene transfer system or a PiggyBac transposon gene transfer system.

[0135] 43. The cell of any one of embodiments 37 to 42, comprising a heterologous nucleic acid sequence of SEQ ID NO: 4.

[0136] 44. A composition comprising one or more cells of any one of embodiments 37-43.

[0137] 45. ALDH1, and i) one of the heterologous nucleotide molecules encoding at least one HIV coreceptor mutant, at least one mutation or mutations of at least one HIV coreceptor, at least one HIV fusion inhibitor, a molecule that reduces expression of an HIV coreceptor, or any combination thereof; A nucleic acid molecule encoding

[0138] 46. ​​The nucleic acid molecule of embodiment 45, wherein the heterologous nucleotide sequence encodes a molecule that: i. reduces expression of CCR5; ii. reduces expression of CXCR4; encodes expression of a C-peptide fusion inhibitor; or any combination thereof.

[0139] 47. The nucleic acid molecule of embodiment 45 or 46, wherein the nucleic acid molecule codes for expression of shCCR5, shCXCR4, and / or a C-peptide fusion inhibitor.

[0140] 48. The nucleic acid molecule of embodiment 45, wherein the molecule comprises a sequence of 1, 3, 6, 7, 8, 9, 12, 13, 14, 16, 18, or any combination thereof.

[0141] 49. The nucleic acid molecule of embodiment 45, wherein the molecule comprises a nucleic acid molecule encoding the sequence of SEQ ID NO: 10, 11, 6, 7, 13, 15, 17, 19, or any combination thereof.

[0142] 50. A vector comprising the nucleic acid molecule of any one of embodiments 45 to 49.

[0143] 51. The vector of embodiment 50, which is a vector that can be used to produce a lentivirus.

[0144] 52. The vector of embodiment 50, which is a lentiviral vector.

[0145] 53. The vector of embodiment 50, comprising the sequence of SEQ ID NO: 1, 3, 6, 7, 8, 9, 12, 13, 14, 16, 18, or any combination thereof.

[0146] 54. The vector of embodiment 50, comprising a nucleic acid molecule encoding the sequence of SEQ ID NO: 10, 11, 6, 7, 13, 15, 17, 19, or any combination thereof.

[0147] 55.ALDH1, and i) one of the heterologous nucleotide molecules encoding at least one HIV coreceptor mutant, at least one mutation or mutations of at least one HIV coreceptor, at least one HIV fusion inhibitor, a molecule that reduces expression of an HIV coreceptor, or any combination thereof; A population of cells heterologously expressing At least one nonmyeloablative dose of chemotherapy 46. ​​A method of treating HIV in a subject comprising administering to the subject.

[0148] 56. The method of embodiment 55, wherein the cells express shCCR5, shCXCR4, and / or a C-peptide fusion inhibitor.

[0149] 57. The method of embodiment 55, wherein the cell comprises a nucleic acid molecule comprising a sequence of 1, 3, 6, 7, 8, 9, 12, 13, 14, 16, 18, or any combination thereof.

[0150] 58. The method of embodiment 55, wherein the cell comprises a nucleic acid molecule encoding the sequence of SEQ ID NO: 10, 11, 6, 7, 13, 15, 17, 19, or any combination thereof.

[0151] 59. A method for expressing a molecule of interest in a subject, comprising administering to the subject cells that heterologously express ALDH1 and the molecule of interest; and administering a non-myeloablative dose of cyclophosphamide.

[0152] 60. The method of embodiment 59, wherein the cells are CD34+ and / or CD4+, or others provided herein.

[0153] 61. The method of embodiment 59, wherein the molecule of interest reduces expression of CCR5; reduces expression of CXCR4; encodes expression of a C-peptide fusion inhibitor; or any combination thereof.

[0154] 62. The method of embodiment 61, wherein the molecule of interest for reducing the expression of CCR5 is shCCR5.

[0155] 63. The method of embodiment 62, wherein the molecule comprises a nucleic acid molecule comprising or encoding SEQ ID NO:6 and / or SEQ ID NO:7.

[0156] 64. The method of embodiment 61, wherein the C-peptide fusion inhibitor comprises the sequence of SEQ ID NO: 11, 15, 19, or any combination thereof.

[0157] The following examples are illustrative, but not limiting, of the compounds, compositions, and methods described herein. Other suitable modifications and adaptations known to those skilled in the art are within the scope of the following embodiments. EXAMPLES

[0158] Engraftment efficiency in autologous bone marrow transplantation in mice method Bone marrow isolation. Bone marrow was flushed from femurs and tibias of 8- to 16-week-old syngeneic donor mice using Iscove's modified Dulbecco's medium (IMDM) containing 0.5 mM EDTA, 2% fetal bovine serum (FBS), and antibiotics. Cells were washed with a buffer (phosphate-buffered saline [PBS]) containing 5 mM EDTA and bovine serum albumin.

[0159] Bone marrow transduction. Mouse bone marrow cells were transduced with a lentiviral vector expressing EGPF only (i.e., pLV-Puro-EF1A-EGFP ("control vector")) or a lentiviral vector expressing EGFP and human ALDH1A (i.e., pLV-Puro-EF1A-EGFP-hALDH1A, FIG. 4, SEQ ID NO: 2 ("test vector")) at an MOI of 10. 48 hours after transduction, the efficiency of transduction was determined. The cells were then transplanted into irradiated mice as described below.

[0160] Transplantation. Syngeneic recipient mice (Balb / c) were pretreated with 0.5 mg / kg fludarabine on days -5 and -4, cyclophosphamide on day -2, and busulfan on day -1. On the day of transplantation (day 0), mice were anesthetized and 4 x 10 6 cells / mouse in 100 μl IMDM were injected. 6 Bone marrow cells were transplanted by tail vein injection, and hematopoietic recovery of the transplants was monitored by FACS analysis of GFP.

[0161] Treatment with cyclophosphamide. Seven days after implantation, mice were treated with different doses of CTX: 0 mg / kg ("0 mg / kg post-implant CTX"), 16 mg / kg ("16 mg / kg post-implant CTX"). In the study, mice were given 5 weeks of CTX, 1 week of no CTX, followed by 1 week of CTX treatment, i.e., 6 weeks of CTX treatment in total.

[0162] GFP analysis of peripheral blood. Fifty microliters of peripheral blood from each mouse was collected from the retro-orbital or tail vein and mixed with 1 ml of PBS containing 0.5 mM EDTA. Cells were lysed with red blood cells, washed in PBS, and then further diluted in 400 ul of PBS. Live GFP + The percentage of granulocytes was analyzed using a flow cytometer.

[0163] Terminal analysis of bone marrow. Six weeks after CTX treatment, animals were sacrificed and GFP in the bone marrow was detected. + The percentage of cells was evaluated by flow cytometry. Granulocytes / neutrophils were identified using conventional forward scatter vs. side scatter variance, in which cells were plotted according to light reflection, size and internal complexity (granularity), respectively. Each group without CTX treatment after transplantation had n=3, and all other groups had n=6. After 6 weeks, the number of white blood cells in the blood was determined for each mouse. The results showed the presence of outliers in each of the CTX-treated groups, and these data were removed in the statistical analysis. Thus, each group without CTX treatment after transplantation had n=3, and all other groups had n=5.

[0164] Results and Discussion When observing bone marrow repopulation after transplantation, peripheral blood can provide an indication of transplant success, but it is necessary to understand the cellular complexity of immune cells before transplantation is performed, since bone marrow gives rise to a variety of immune cells with different life spans. For example, lymphocytes can have a life span of as long as 180 days, whereas neutrophils have a life span of only 5-7 days. Furthermore, monocytes can only live for a few days in the periphery, whereas monocytes can become tissue resident and extend their life span up to several months. Thus, when attempting to analyze lymphocyte populations for donor bone marrow reconstitution, an accurate reflection will not be obtained until all of the donor's pre-transplant lymphocytes have died, i.e., 6 months after the procedure. To provide a more "real-time" readout of the recipient's cellular bone marrow graft, the granulocyte population provides the best indicator. Since all of the donor's pre-transplant neutrophils die within 7 days, at 2 weeks post-transplant, these cells are the most direct reflection of the bone marrow environment and recipient engraftment success, which can also be measured by identifying the percentage of transduced neutrophils, which reflects the graft rate.

[0165] According to the method described above, blood was collected by retro-orbital bleeding on days 23, 35, and 42 of the study (days 16, 28, and 35 of CTX administration, respectively), and GFP in the peripheral blood of each mouse was measured. + The percentage of granulocytes was assessed by flow cytometry.

[0166] The results showed that all mouse groups had live GFP + Furthermore, on day 42 of the study, bone marrow cells transduced with the test vector (i.e., EGFP-positive bone marrow cells) were shown to contain granulocytes (Figure 1). + Mice receiving bone marrow cells transduced with the test vector and treated with 16 mg / kg / day of CTX had significantly more viable GFP-positive mice than mice receiving bone marrow cells transduced with the test vector and treated with 30 mg / kg / day of CTX. + A similar percentage of granulocytes was shown (compare FIG. 1, "Test Vector, 16 mg / kg Post-Transplant CTX" and "Test Vector, 30 mg / kg Post-Transplant CTX").

[0167] After 6 weeks, the results were: total GFP + The presence of live and dead cells was demonstrated (Figure 2A). The grafts expressed live GFP + The percentage of granulocyte / neutrophil population was shown (Figure 2B). Surprisingly, the bone marrow cells transduced with the test vector (i.e. Both mice receiving test vector-transduced bone marrow cells (i.e., expressing EGFP+ALDH1A1) and treated with non-myeloablative 16 mg / kg / day CTX and mice receiving test vector-transduced bone marrow cells and treated with myeloablative 30 mg / kg / day CTX demonstrated similar grafts of over 40% (Figure 2B, compare "Test Vector, 16 mg / kg pt post-transplant CTX" with "Test Vector, 30 mg / kg pt post-transplant CTX"). Furthermore, mice receiving test vector-transduced bone marrow cells and treated with 16 mg / kg / day CTX had a significantly higher graft percentage compared to mice receiving control vector-transduced bone marrow cells and treated with the same dose of CTX (i.e., 16 mg / kg / day CTX) (Figure 2B, compare "Test Vector, 16 mg / kg pt post-transplant CTX" with "Control Vector, 16 mg / kg pt post-transplant CTX").

[0168] White blood cells (WBC) help fight infections caused by attacks of foreign agents that invade the body. WBC counts can be useful for detecting hidden infections and / or susceptibility to infection. WBC counts in peripheral blood were determined for each study group after 6 weeks of CTX treatment. As shown in Figure 3, mice that received bone marrow cells transduced with either control vector or test vector and did not receive CTX treatment had WBC counts within the normal range. There was one outlier in each CTX treatment group, which was removed in the statistical analysis. The ranges of high, normal, and low WBC are in accordance with the ranges known in the art, provided for male mice in Charles River Research Models (BALB / C Mouse Hematology, North American Colonies, January 2008-December 2012), http: / / www.criver.com / files / pdfs / rms / balbc / rm_rm_r_balb-c_mouse_clinical_pathology_data.aspx. Notably, mice receiving test vector-transduced bone marrow cells and treated with 16 mg / kg / day CTX had significantly higher numbers of WBCs compared to mice receiving test vector-transduced bone marrow cells and treated with 30 mg / kg / day CTX (Figure 3, compare "Test Vector, 16 mg / kg pt Post-Transplant CTX" with "Test Vector, 30 mg / kg pt Post-Transplant CTX"). EXAMPLES

[0169] In vivo humanized mouse study #1 Stem cell purification. Human PBMCs were collected from healthy donors treated with 5 mcg / kg / day granulocyte colony-stimulating factor (G-CSF) (Amgen, Thousand Oaks, CA) for 5 days, followed by leukapheresis on days 5 and 6. Patients were placed on a regimen of 10 μg / kg filgrastim or G-CSF to enhance CD34 + Stem cells were mobilized from bone marrow to the periphery for isolation. +The cell count is 10.0 to 20.0 × 10 cells per kg of body weight. 6 When the number exceeded 10, apheresis was performed. + were purified using positive selection enrichment followed by magnetic bead isolation. Samples were washed in PBS containing 2% FBS, centrifuged, and resuspended in PBS. CD34+ cells were then tested for purity by FACS analysis by staining for CD34, and viability was assessed by trypan blue staining. Cells were then immediately transplanted into mice. Appropriate written informed consent in accordance with the Declaration of Helsinki protocols was obtained from donors prior to collection.

[0170] Transplantation of human HSCs into NOG mice. Adult mice were 10-12 week old NOG mice. For neonatal mice, mice were used 1-2 days after birth. Mice were irradiated 1 day prior to cell transfer under SPF conditions with 2-2.5 Gy for adult mice and 1 Gy for neonatal mice. Mice weighing less than 18 g may die from this dose of radiation. For adult mice, 0.25 mL of cell suspension (1–0.5 × 10 4 ) were injected into mice via the tail vein using a 1 mL syringe with a 27 G needle or a microinjector syringe with a 29 G needle while slightly anesthetized with isoflurane.

[0171] Transduction of stem cells. CD34 from the same donor + Cells were cultured at 1 × 10 in fibronectin-coated tubes in X-Vivo 10 medium (Lonza) supplemented with stem cell factor (SCF) 100 ng / ml, thrombopoietin (TPO), and Fms-like tyrosine kinase 3 ligand (Flt-3L) (CellGenix, Freiberg, Germany), and optionally with IL-2, IL-3, IL-6, or any combination thereof, for 16 h at 37°C and 5% CO. 6 The priming medium was then removed and the cells were cultured at 1.35 × 10 cells / ml, corresponding to a multiplicity of infection (MOI) between MOI 2 and MOI 50. 8Fresh culture medium was added, containing 100 tu / ml of vector ("control vector" = pLV-Puro-EF1A-EGFP, or "test vector" = SEQ ID NO: 4, FIG. 5), and 4 mg / ml of protamine sulfate (Sigma, Saint Louis, MO). The transduction mixture was returned to the incubator for 12 to 48 hours. Transduced cells were detached with trypsin (Lonza, Walkersville, MD), washed, resuspended in PBS, and immediately transplanted into mice (as above, without irradiation).

[0172] GFP analysis of peripheral blood and terminal analysis of spleen, blood, and bone marrow were performed as described above. A schematic of the study is shown in Figure 8, however, this depiction is for illustrative purposes only and other study designs can be used. EXAMPLES

[0173] In vivo humanized mouse study #2 Stem cell purification. Human PBMCs were collected from healthy donors treated with granulocyte colony-stimulating factor (G-CSF) (Amgen, Thousand Oaks, CA) 5 mcg / kg / day for 5 days, followed by leukapheresis on days 5 and 6. CD34 + were purified by positive selection using immunomagnetic beads. Samples were washed in PBS containing 0.5% HSA, centrifuged, and resuspended in PBS. CD34 + The cells were then tested for purity by flow cytometry analysis by staining for CD34 and staining for viability. The cells were then immediately transplanted into mice. Appropriate written informed consent in accordance with the Helsinki Declaration protocol was obtained from the donors prior to collection.

[0174] Transplantation of human HSCs into NOG mice. For adult mice, 10-12 week old NOG mice were used. For neonatal mice, mice were used 1-2 days after birth. Mice were irradiated 1 day before cell transfer under SPF conditions with 2-2.5 Gy for adult mice and 1 Gy for neonatal mice. Mice weighing less than 18 g may die from this dose of radiation. For adult mice, 0.25 mL of cell suspension (1-0.5 × 10 4 ) was injected into mice via the tail vein using a 1 mL syringe with 27 G.

[0175] Transduction of stem cells. CD34 from the same donor + Cells were cultured at 1 × 10 in fibronectin-coated tubes in X-Vivo 10 medium (Lonza) supplemented with stem cell factor (SCF) 100 ng / ml, thrombopoietin (TPO), and Fms-like tyrosine kinase 3 ligand (Flt-3L) (CellGenix, Freiberg, Germany), and optionally IL-3 and IL-6, for 16 h at 37°C and 5% CO. 6 The priming medium was then removed and the cells were cultured at 1.35 × 10 cells / ml, corresponding to a multiplicity of infection (MOI) between MOI 2 and MOI 50. 8 ul / ml of vector ("control vector" = pLV-Puro-EF1A-EGFP Fresh culture medium was added, further containing a "test vector" (or "test vector"). Suitable "test vectors" included any one or combination of the following:

[0176] [Table 14]

[0177] The transduction mixture was returned to the incubator for 12 to 48 hours. The transduced cells were harvested, washed, resuspended in PBS, and immediately implanted into mice (as above, but without irradiation).

[0178] GFP analysis of peripheral blood and terminal analysis of spleen, blood, and bone marrow were performed as described above. A schematic of the study is shown in Figure 8, however, this depiction is for illustrative purposes only and other study designs can be used. EXAMPLES

[0179] Lentiviral proof of concept research Lentiviral vector expression of human CD34 + Cells were transduced with lentivirus (LV) vectors containing four expression cassettes. The expression levels of ALDH and C-peptide, shRNA-mediated CCR5 knockdown, and in some cases, shRNA-mediated CXCR4 knockdown were evaluated in transduced cells. The expression of cellular C-peptide was then correlated with the knockdown of CCR5.

[0180] Briefly, mobilized CSF, cryopreserved human CD34+ cells were thawed at 37°C until the contents of the vial were completely in liquid phase. The cells were transferred to a sterile 15 mL conical tube (Corning, Tewksbury, MA). Pre-warmed medium X-Vivo 10 serum-free medium (Lonza, Basel, Switzerland) was added dropwise and with gentle agitation to 15 mL. The cells were then centrifuged at 200-300 × g for 5 min. After aspirating the supernatant, the pellet was resuspended in 10 mL of medium and a small aliquot was retained for counting and viability determination. The cells were then centrifuged, the supernatant was aspirated, and 1.0 × 2.0 × 10 6 Resuspend to a density of 10 cells / m and place in a T75cm 3 The cells were then transferred to tissue culture flasks (Corning, Tewksbury, MA).

[0181] The cells were prestimulated by adding 100 ng / mL each of stem cell factor (SCF), thrombopoietin (TPO), and flt3 / flk2 ligand (Flt3L) (R&D Systems, Minneapolis, MN) to the culture medium and cultured for 24 hours at 37°C in a 5% CO2 incubator. The cells were then removed from the incubator and centrifuged. The cells were cultured at 1.0 × 10 in X-Vivo 10 medium supplemented with 100 ng / mL of both SCF and Flt3L, 10 ng / mL of TPO, and 60 ng / mL of IL-3. 6 The cells were resuspended at a density of 10 cells / mL in 12 wells of tissue culture untreated Retronectin (5 μg / cm 2 ) Covering plate (Takaraby (Osaka Co., Ltd., Shiga, Japan) per well. 6 The cells were then plated.

[0182] Lentiviral particles were thawed at 37° C. (CCR5.C peptide.LV or CCR5.C peptide.ALDH.LV) and mixed gently upon thawing. Each of the particles was added to the culture at an MOI of about 2 to 50, e.g., 9, and mixed by gently swirling the plate. The cells were then returned to a 37° C., 5% CO2 incubator and cultured for 24 to 48 hours. Samples were then retained for evaluation of cell number, viability, and transduction efficiency by flow cytometry and qRTPCR evaluation.

[0183] The remaining cells were centrifuged, the supernatant gently aspirated, and 1 mL / well of fresh X Vivo 10 medium was added to each well. The plates were returned to the incubator. The cells were allowed to grow for up to 3 days post-transduction.

[0184] Flow cytometry staining and analysis proceeded immediately. If the LV construct contained a fluorescent marker, acquisition was performed on a MacsQuant FACS Analyzer. If a fluorescent marker was not contained in the vector, the target protein or HIV-1 A staining procedure for transcriptional activation of the LTR was performed.

[0185] The cells can be used for further characterization. If further characterization is not required, immediately after transduction (or expansion after transduction), the cells can be cultured at 5 × 10 in a solution consisting of 50% IMEM (Thermo Fisher Scientific, Carlsbad, CA), 45% human serum albumin (HAS) (Sigma-Aldrich, St. Louis, MO), and 5% 0.2 μm filtered DMSO in a control rate freezer. 6 The cells were then cryopreserved at a density of 100 cells / mL. The cells can then be immediately transferred to liquid nitrogen or shipped on dry ice.

[0186] Chemical protection. Human CD34 transduced with LV vector (e.g., SEQ ID NO: 2 or SEQ ID NO: 5) exhibits expression of ALDH. + The cells were treated with various doses of cyclophosphamide to demonstrate resistance to chemotherapy drugs. Experiments can also be performed by treating mixed cultures of transduced and non-transduced cells with various doses of cyclophosphamide. The survival of both transduced and non-transduced cells was measured after treatment with each dose of cyclophosphamide.

[0187] Briefly, lyophilized mafosfamide was resuspended in sterile water to a working stock solution of 1 mg / mL. The transduced cells were then washed once with regular medium (RPMI+10% FBS) and the transduced cells (both the test vector (e.g., SEQ ID NO: 4) and the control vector (e.g., SEQ ID NO: 5)) were cultured at 0.5×10 in MethoCult 3330 medium (StemCell Technologies, Vancouver, BC, Canada). 6The cells were resuspended to a density of 100 cells / mL. The final solution consisted of 0.8% methylcellulose in alpha medium supplemented with FBS, erythropoietin (1 U / ml), IL-3 (200 U / ml), IL-6 (200 U / ml), SCF (100 ng / ml), IL-1β (200 ng / ml), and 100 ng / ml granulocyte colony-stimulating factor (StemCell Technologies).

[0188] To each set of dishes (control and test dishes), mafosfamide was added to the following final concentrations: 0.15, 2.5, 5, 10, 15, 20 μM. The plates were then incubated at 37°C, 5% CO2 for 14 days. After 14 days, colonies were scored in each plate using an inverted light microscope. A Mann-Whitney U test was then performed to determine the differences in colonies formed by cells expressing the test vector and cells expressing the control vector. It was determined whether there were any significant statistical differences in the number of colonies formed. EXAMPLES

[0189] Fusion inhibition studies T cells isolated from the spleen and thymus of humanized mice were co-cultured with HIV strains as described above. The expression level of C44 was evaluated using anti-Gp41 antibody that recognizes C-peptide, detected by flow cytometry. The expression level of C-peptide (positive percentage and median fluorescence intensity) was then correlated with the degree of HIV fusion blockade.

[0190] Materials and Reagents. 293T cells (ATCC); pAdVAntage (Promega Corporation); pCMV4-BlaM-Vpr (Addgene); pNL4-3 proviral DNA (NIH AIDS Reagent Program) or TN6-GFP encoding the primary Env; DMEM (Mediatech, Cellgro®); RPMI 1640 (Mediatech, Cellgro®); 1× phosphate-buffered saline (PBS); fetal bovine serum (FBS); 100 U / ml penicillin and 100 U / ml streptomycin (Thermo Fisher Scientific, Gibco®); 2 M CaCl2; Alliance HIV-I p24 ELISA kit (PerkinElmer) or FlaQ assay reagent (Hayden et al., 2003); peripheral blood lymphocytes (PBL); CCF2-AM substrate and loading solution (Thermo Fisher Scientific); CO2-independent medium (Thermo Fisher Scientific, Gibco®); probenecid (Sigma-Aldrich); mouse anti-human CD3 conjugated to APC-Cy7 and mouse anti-human CD4 conjugated to PE-Cy7 (BD Biosciences); BD CompBeads (BD Biosciences); 16% paraformaldehyde (Electron Microscopy Sciences); HBSS (see recipe); Dulbecco's Modified Eagle's Medium (DMEM) culture medium (see recipe); Roswell Park Memorial Institute (RPMI) culture medium (see recipe); CCF2 loading solution (see recipe); stock solution of probenecid (250 mM) prepared in 250 mM NaOH (see recipe); growth medium (see recipe).

[0191] Vector: pLV[Exp]-H1>hCCR5[shRNA] EF1A>hALDH1A1[NM_000689.4](ns):T2A:{C peptide} (e.g., SEQ ID NO:4)

[0192] Preparation: HBSS (280 mM NaCl; 10 mM KCl; 1.5 mM Na2HPO4; 12 mM dextrose; 50 mM N-(2-hydroxyethylpiperazine)-N'-(2-ethanesulfonic acid) (HEPES) (pH 7.05); store at -20°C.

[0193] Flow cytometry staining buffer (1× phosphate buffered saline (PBS) without Ca++ and Mg++; 0.5% HSA; store at 4°C).

[0194] Dulbecco's modified Eagle's medium (DMEM) culture medium (DMEM; 10% heat-inactivated fetal bovine serum; penicillin 100 U / ml; streptomycin 100 μg / ml).

[0195] RPMI culture medium (RPMI 1640; 10% heat-inactivated fetal bovine serum; penicillin 100 U / ml; streptomycin 100 μg / ml).

[0196] CCF2 loading solution: CCF2-AM in dimethyl sulfoxide (CCF2 kit Resuspended in 1000 mM NaOH (solution A) to obtain a stock solution (1 mM CCF2-AM). Aliquot and stored at -80°C in the dark. 1 μl of 1 mM CCF2-AM was mixed with 9 μl of a solution containing Pluronic-F127 100 mg / ml and 0.1% acetic acid (solution B from the CCF2 kit) by vortex mixing. 1 ml of CO2-independent medium was added and vortexed again. Stock solution of probenecid (250 mM) prepared in 250 mM NaOH. Aliquot and stored at -20°C.

[0197] Growth medium (2.5 mM probenecid; 10% fetal bovine serum in CO2-independent medium).

[0198] Equipment: T175 cm2 culture flask; 96-well V-bottom plates (Corning Incorporated); 5 ml, 10 ml, 25 ml pipettes; 50 ml Falcon tubes; 0.22 μm pore size Steriflip (EMD Millipore); 2 ml Nalgene tubes (Thermo Fisher Scientific); clear ultracentrifuge tubes (BD); 37°C, 5% CO2 incubator; ultracentrifugation equipment with SW28 rotor; flow cytometer. The fusion assay alone required a flow cytometer with violet laser excitation (405 nm) and two measurement parameters. A photomultiplier tube (PMT) with a 450 / 50 nm bandpass filter, commonly used for Pacific Blue detection, was used for detection of the cleaved CCF2 substrate. Another PMT with a 515 / 20 nm bandpass filter, commonly used for Amcyan detection, was used for detection of the uncleaved CCF2 substrate. Additional PMTs were required for the measurement of fluorochromes associated with the CD3 and CD4 antibodies. APC-Cy7 was excited by a 633 nm red laser and detected with a PMT with a 755 long-pass filter. PE-Cy7 was excited by a 531 nm yellow-green laser and detected with a PMT with a 755 long-pass filter.

[0199] Software. FlowJoX software (Tree Star) or other FACS analysis software.

[0200] Fusion inhibition assay: 1.5×10 7 293T cells were cultured in a T175cm plate with 20 ml of DMEM culture medium. 2The 293T cells were seeded into 100 ml tissue culture flasks and cultured overnight in a humidified incubator at 37°C with 5% CO2. 1.75 ml of H2O was prepared containing 60 μg of TN6-GFP proviral DNA, 20 μg of pCMV-BlaM-Vpr, and 10 μg of pAdVAntage vector. 2 ml of 2×HBSS was then added slowly and mixed gently by pipetting up and down. 250 μl of 2M CaCl2 was added dropwise. DNA was precipitated by incubating at room temperature for 10 minutes. The 293T cell culture medium was replaced with 40 ml of fresh DMEM culture medium pre-warmed to 37°C. 4 ml of DNA precipitate was then added and incubated at 37°C for 16 hours. The medium was then replaced with 40 ml of fresh DMEM culture medium pre-warmed to 37°C and incubated at 37°C for 24 hours.

[0201] The supernatant of transfected 293T cells was collected in a 50 ml Falcon tube and centrifuged at room temperature for 10 min to remove cell debris. The clarified supernatant was then filtered through a Steriflip. 36 ml of virion-containing supernatant was transferred to an Ultraclear centrifuge tube. The tube was placed in the bucket of an SW28 rotor, balanced with DMEM culture medium as required, and ultracentrifuged at 4°C without brake (72000 x g, 90 min). The supernatant was removed and the virus pellet was resuspended in 1 ml DMEM, divided into 100 μl aliquots and stored at -80°C.

[0202] p24 in viral preparations Gag The content was quantified by enzyme-linked immunosorbent assay or FlaQ assay ( Maiti et al., 2014 ).

[0203] The PBLs were washed with RPMI culture medium, the PBLs were counted, and 2×10 7 The cell suspension was then distributed in a V-bottom 96-well plate in 100 μl (2 × 10 6The cells were divided into aliquots of 100 x 100 cells (100 x 100 cells). Two additional cell aliquots were distributed into two wells to serve as compensation controls. One well was loaded with CCF2 substrate, while the other was left unloaded. These two control wells were not stained with anti-CD3-APC-Cy7 and anti-CD4-PE-Cy7 antibodies.

[0204] 400ng p24 Gag An amount of HIV-1 virions containing BlaM-Vpr equivalent to 10 ...

[0205] The cells were then harvested by centrifugation at room temperature for 5 minutes, washed once with 200 μl of CO2-independent medium and centrifuged for 5 minutes at room temperature. The pellet was resuspended in 100 μl of CCF2-AM loading solution and incubated for 1 hour at room temperature in the dark, with one well being ensured to remain unstained by resuspending in CO2-independent medium only. The cells were harvested by centrifugation at 365×g for 5 minutes at room temperature. The harvested cells were then washed with 200 μl of growth medium, centrifuged for 5 minutes at room temperature, and the pellet was resuspended in 200 μl of growth medium and the cells were incubated for 16 hours at room temperature in the dark.

[0206] To two empty wells, each of the BD compensation bead vials (negative control and anti-mouse IgK) was added dropwise. The cells and beads were then collected by centrifugation for 5 minutes at 4°C. The cells and beads were then washed once by adding 200 μl of FACS staining buffer, collected by centrifugation for 5 minutes at 4°C, and the pellet was resuspended in 100 μl of immunostaining solution (in flow cytometry staining buffer) containing anti-CD3-APC-Cy7 at 1 / 100 dilution and anti-CD4-PE-Cy7 at 1 / 50 dilution. Neither the two compensation controls nor the compensation beads were stained. The CompBeads were stained with flow cytometry staining buffer containing either anti-CD3-APC-Cy7 at 1 / 100 dilution or anti-CD4-PE-Cy7 at 1 / 50 dilution. The samples were incubated for 30 minutes at 4°C.

[0207] After 30 min incubation at 4° C., the cells and beads were collected by centrifugation for 5 min at 4° C. The cells and beads were then washed with 200 μl of flow cytometry staining buffer. The cells were fixed for 24 h at 4° C. using flow cytometry staining buffer supplemented with 1.2% paraformaldehyde.

[0208] Samples were acquired using a flow cytometer-MACSQuant instrument. Sample sets included: unloaded unstained cells, unstained cells loaded with CCF2, beads stained with CD3-APC-Cy7, beads stained with CD4-PE-Cy7, uninfected controls loaded with CCF2 and immunostained, and infected samples loaded with CCF2 and immunostained. Data were analyzed using FlowJo. EXAMPLES

[0209] HIV challenge: human CD4 transduced by lentiviral vectors + T cells GFP reporter CD4 transduced by LV containing CCR5shRNA / c-peptide / ALDH + T cells, or T cells transduced with LV containing an empty control vector, were cultured with R5, X4, or both experimental HIV strains. HIV infectivity was analyzed by reporter marker (when using a T cell reporter system) or by p24 ELISA. EXAMPLES

[0210] Dose ranging and lentiviral vector efficacy studies Sca1 transduced with lentivirus containing CCR5shRNA / C-peptide / ALDH expression vector or control empty vector + / c-kit - Stem and progenitor cells were transplanted into pre-conditioned C57BL / 6 syngeneic mice.

[0211] Briefly, after 7 days, all mice were started on a daily regimen of cyclophosphamide (CTX) treatment. Both groups of mice were treated with various dosages of CTX (6 mice per group per dose): 0, 10, 13, 16, 19, and 40 mg / kg. One week after CTX treatment was started, mice were bled on a weekly basis. A complete blood count (CBC) panel was performed to monitor for any cytotoxic effects of chemotherapy (engraft efficacy: ALDH conferring CTX resistance (conference)), while flow cytometry analysis measured the expression of lineage-specific markers in these cells as well as C-peptide and CCR5 expression (expression efficiency: efficacy of shRNA to knock down target genes). The study continued for at least 10 weeks of CTX treatment or until complete engraftment of bone marrow had occurred. A schematic of the study is shown in Figure 7 and a more detailed protocol is provided below.

[0212] Materials and Reagents: EasySep™ Mouse Hematopoietic Progenitor Cell Isolation Kit (StemCell Technologies); Falcon 15 mL conical tubes (Corning); 5 mL (12 × 75 mm) polystyrene round-bottom tubes (Corning); StemSpan serum-free medium (StemCell Technologies); Mouse Hematopoietic Stem Cell Expansion Kit Cytokine Panel (R&D); RetroNectin recombinant human fibronectin fragment (Clontec); RPMI-1640 (Thermo Fisher Scientific); Petri dishes (Thermo Fisher Scientific); HBSS (Thermo Fisher Scientific); 27G × 1 / 2 needle (BD); Centrifuge (Thermo Fisher Scientific); Sorvall ST 40R Countess II automated cell counter (Thermo Fisher Scientific); Trypan blue (Thermo Fisher Scientific); lineage cocktail (mCD3, mGr-1, mCD11b, mB220, mTer119) (including isotype controls) (Biolegend); Ly-6A / E (Sca-1) (Thermo Fisher Scientific); CD117 (c-kit) (Thermo Fisher Scientific); viability dye eFluor 506 (Thermo Fisher Scientific); anti-mouse CD16 / 32 FC Block (Biolegend); cell staining buffer (Biolegend); Balb / c female mice (Charles River).

[0213] Vector: pLV[Exp]-H1>hCCR5[shRNA]- EF1A>hALDH1A1[NM_000689.4](ns):T2A:{C peptide} (e.g., SEQ ID NO:4)

[0214] Isolation of progenitor cells from bone marrow (number of progenitor cells required). From the table below, the number of (donor) mice required to obtain the required number of cells for transduction was calculated.

[0215] [Table 15]

[0216] Isolation of mouse bone marrow. BALB / c mice (female, 20-25 g, 8-10 weeks old) were euthanized by CO2 asphyxiation. Subsequent experimental steps were performed in a laminar airflow biosafety cabinet (BSC). Bone marrow cells were harvested from femurs. Briefly, the contents of the bone marrow were flushed with 2 ml of HBSS using a 1 ml insulin syringe with a 27G × 1 / 2 needle. The contents were collected in a sterile 50 ml centrifuge tube. The BM cell suspension harvested above was then diluted with RPMI-1640 to a final volume of 7.5 ml. Any clusters in the bone marrow suspension were broken apart by vigorous pipetting. The cells were then centrifuged, washed, and centrifuged again. The cell pellet from each femur was gently resuspended in 7.5 ml of RPMI-1640 to prepare a homogenous suspension. An aliquot of the cell suspension was removed for total cell count and viability using an NC-200 automated cell counter.

[0217] Isolation of progenitor cells. Transfer isolated cells to a new tube, spin down, and resuspend in EasySep buffer (PBS + 2% FBS + 1 mM EDTA) in a volume range of 0.5-2 mL to a concentration of 1 × 10 8 The concentration was 1000 cells / mL. Rat serum was then added to the samples at 50 μL / mL and the samples were transferred to 5 mL (12×75 mm) polystyrene round-bottom tubes. EasySep Mouse Hematopoietic Progenitor Cell Isolation Cocktail was then added to the samples at 50 μL per mL of sample. Samples were mixed and incubated at 4° C. for 15 minutes. Rapid spheres was vortexed for 30 seconds and then added to the samples at 75 μL / mL. Samples were mixed and incubated at 4° C. for 10 minutes and the total volume was brought up to 2.5 mL using EasySep buffer. Progenitor cells were isolated using magnetic sorting.

[0218] Evaluation of isolated progenitor cells by flow cytometer. Cells were transferred to a new 96-well plate, spun down, and resuspended in 50 μL FACS buffer (PBS + 2% FBS + 1 mM EDTA). 3 μL FC Block (anti-CD16 / 32) was added to each sample and incubated for 15 minutes at 4° C. The following panels and amounts were used:

[0219] [Table 16]

[0220] Controls included: Fluorescence Minus One (FMO) control for CD117, Ly6A / E, and lineage cocktail isotype controls.

[0221] Each well was brought up to a total volume of 100 μL and incubated at 4° C. in the dark for 30 minutes. Cells were then washed with 200 μL of flow cytometer buffer and resuspended in a volume. Flow cytometer was acquired on a MACS QuantCytometer. Purity was calculated by summing the % of Sca1- / c-kit+, Sca1+ / c-kit-, Sca1+ / c-kit+ and multiplying by the percentage of live lineage cocktail negative events.

[0222] Lentiviral transduction and proliferation of progenitor cells. On day 0, 12- or 24-well plates were coated with 0.3 ml of Retronectin (100 ng / ml) and incubated at room temperature for at least 2 hours. The coating medium was then aspirated from the plates and the plates were blocked with 2% BSA in 1×PBS for at least 30 minutes at room temperature and then washed three times with 1×PBS. The plates were now ready to use. It should be noted that the plates were not allowed to dry out.

[0223] Freshly isolated bone marrow progenitor cells were cultured at approximately 0.2–0.4 × 10 per ml of bone marrow progenitor cell culture medium. 6The cells were seeded with lentivirus at MOI=3 for 24 hours.

[0224] On day 1, the cells were spun down, the lentivirus-containing medium was removed, and fresh bone marrow progenitor culture medium was added.

[0225] On day 2, after lentiviral transduction, puromycin (1 μg / ml) was added to the bone marrow progenitor cell culture medium to select lentiviral-infected cells. Cells were treated for 4 days.

[0226] On day 4, fresh medium with puromycin was added.

[0227] On day 6, the cells were spun down and fed with fresh medium without puromycin.

[0228] On day 7, cells were harvested for cell counting and GFP flow was performed to determine transduction efficiency. Fresh bone marrow progenitor cell culture medium was fed to the remaining cells.

[0229] The bone marrow progenitor cells were cultured for an additional 3 days until day 10, at which point the medium was changed.

[0230] On day 10, cells were harvested for counting and flow cytometry analysis was performed to determine transduction efficiency.

[0231] [Table 17]

[0232] Bone marrow progenitor cell transplantation and treatment - Preconditioning: Prior to transplantation, mice were administered two doses of Fludarabine (5mg / Kg for 2 days). On day 0 (2 days after treatment with Fludarabine), 36 mice were transplanted via IV with stem and progenitor cells transduced with the control vector, and 36 mice were transplanted with stem and progenitor cells transduced with the test vector. After transplantation, animals were checked once a day for morbidity and mortality. At regular monitoring times, animals were checked for any effect of treatment on normal behavior such as motility, dull eyes / coat, and any other abnormal effects, as well as visual estimation of food and water consumption, weight gain / loss (weight was measured twice a week). Mortality and observed clinical signs were recorded in detail for each animal in the comments section of the data sheet.

[0233] CTX treatment. Seven days after bone marrow transplantation, CTX (cyclophosphamide) treatment was started at the following doses: 0, 10, 13, 16, 19, and 40 mg / kg, IP administered once daily for 12 weeks, and the treatment was not discontinued unless there was a weight loss >15%. The experimental groups and treatment details are shown in the table below.

[0234] [Table 18]

[0235] Sample collection. Seven days after the first CTX dose, blood was collected by tail vein puncture. 100 μL of blood was collected for immunophenotyping panels corresponding to LV vector expression and shRNA knockdown efficacy (see table below). Samples were analyzed by FACS. An additional 20 μL of blood was collected for complete CBC analysis. Collections were taken every 7 days from each animal until the end of the study. Bone marrow was collected at the end of the study to assess complete engraftment.

[0236] [Table 19]

[0237] Termination. Animals were humanely euthanized if there was unacceptable toxicity and / or severe weight loss (>20%) or if they showed continued deterioration before reaching coma. Animals showing obvious signs of severe distress and / or pain were humanely euthanized by CO2 followed by cervical dislocation. The study was terminated when complete grafting (>90%) was observed in one group of animals. EXAMPLES

[0238] Human studies Stem cell mobilization and harvest. Three days prior to harvest, patients were transfected with CD34 + To mobilize stem cells, a 3- to 5-day G-CSF regimen was started. + The number of cells is 10.0 to 20.0 × 10 per kg of body weight. 6 When the number of cells exceeded 100, apheresis was performed. + For stem cell isolation and transduction, the cells were transported in a controlled transport at 2-8 °C to a GMP facility. The target concentration was 3.0 to 4.0 × 10 6 CD34 + Cells / kg, 2 to 3 x 10 6 On day 2 after harvest (or day -5 pre-transplant), patients were re-infused with 15 mg / m 2 Patients were then treated with 1000 mg / m2 fludarabine for 5 days (until pre-transplant day -1). Alternatively, on pre-transplant day -1, patients were treated with 4 mg / kg busulfan. Patients were then treated with a single dose of 1000 mg / m2 fludarabine on pre-transplant day -2. 2 The patient was treated with cyclophosphamide.

[0239] Cryopreservation of stem cells. Patient-derived cells (containing hematopoietic stem cells) were optionally centrifuged to obtain a cell-rich pellet. A solution consisting of heparinized Plasmalyte solution and 10% DMSO (dimethyl sulfoxide) was added to the plasma supernatant in which the pelleted cells were resuspended. Cells were initially stored at -4°C, and then samples were frozen down to a target temperature of -156°C (if stored in vapor phase) to -196°C (if stored in liquid phase). Cells were optionally shipped according to standard procedures.

[0240] CD34 + Lentiviral transduction of cells. Upon arrival at the GMP facility, CD34 + Cells were isolated by magnetic bead separation. 4 + Transduction of cells involves pre-stimulation of cells for 24 hours in medium supplemented with the cytokines stem cell factor (SCF), Fms-related tyrosine kinase 3 ligand (FLT3L), thrombopoietin (TPO), IL-6, IL-2, IL-3, fibronectin, or any combination thereof, followed by exposure to vector (e.g., SEQ ID NO: 2 or SEQ ID NO: 4) for 24 hours, both of which are supplemented with the cytokines SCF, FLT3L, and TPO (100 ng ml each) in serum-free X-Vivo 10 medium. -1 The cells were then cryopreserved and shipped to the clinical site.

[0241] Modified CD34 + Re-infusion of cells. Modified CD34 +After thawing the cells, the current standard washing protocol according to the New York Blood Center protocol was used. This involved two-step dilution of the thawed stem cell units with 2.5% human serum albumin and 5% dextran 40, followed by centrifugation at 10°C for 10 minutes. The supernatant was then removed and HSA and dextran solution was added again twice to a final DMSO concentration of less than 1.7%. The washed solution was infused into the patient as soon as possible. After a period of time after the cells were infused, for example 7-45 days, the patient was started on a low dose (50-200 mg or a non-myeloablative dose as described herein) of oral cyclophosphamide once a day to facilitate the expansion of the graft of the genetically modified bone marrow cells. The modified CD34 + The patient was HIV positive at the time the cells were infused. + In this case, the cells may function to treat and / or cure HIV, or may be modified CD34 + The patient was HIV positive at the time the cells were infused. - It is possible that, in this case, the cells are functioning to prevent future HIV infection. + A schematic diagram of the treatment of a patient is shown in Figures 9 and 10, where the patient is HIV - But it is understood that this is possible.

[0242] The above detailed description of the embodiments of the present technology is not intended to be exhaustive or to limit the present technology to the exact form disclosed above. Specific embodiments of the present technology and examples of the present technology are described above for illustrative purposes, but as will be recognized by those skilled in the art, various equivalent modifications are possible within the scope of the present technology. The various embodiments described herein can also be combined to provide further embodiments.

[0243] From the foregoing description, it will be understood that, although specific embodiments of the present technology are described herein for illustrative purposes, well-known structures and functions have not been shown or described in detail in order to avoid unnecessarily obscuring the description of the embodiments of the present technology. Where the context permits, singular or plural terms may also include the respective plural or singular terms.

[0244] Although specific embodiments are described herein for illustrative purposes, it is understood that various modifications can be made without departing from the technology. Furthermore, while advantages associated with certain embodiments of the technology are described in the context of these embodiments, other embodiments may also exhibit such advantages, and not all embodiments necessarily must exhibit such advantages in order to fall within the scope of the technology. Thus, the disclosure and related technology may encompass other embodiments not expressly shown or described herein.

Claims

1. 1. A method for performing a bone marrow transplant in a patient, comprising: administering to the patient a population of cyclophosphamide-resistant modified cells and at least one dose of a non-myeloablative chemotherapy agent. The method comprising:

2. 2. The method of claim 1, wherein the population of cyclophosphamide-resistant modified cells comprises a heterologous gene encoding aldehyde dehydrogenase 1 (ALDH1).

3. The method of claim 1 , wherein the population of cyclophosphamide-resistant modified cells expresses ALDH1.

4. 2. The method of claim 1, wherein cyclophosphamide resistance of the cyclophosphamide-resistant modified cells is conferred by expression of aldehyde dehydrogenase 1 (ALDH1).

5. 10. The method of claim 1, wherein greater than 50% of the patient's bone marrow is replaced with the cyclophosphamide-resistant modified cells or cells derived therefrom within six months.

6. The method of claim 1 , wherein the patient has HIV.

7. The method of claim 1 , wherein the cyclophosphamide resistance of the modified cells is transient.

8. The method of claim 1 , wherein the cell is a stem cell or an immune cell.

9. 9. The method of claim 8, wherein the stem cells are fetal stem cells, stem cells derived from umbilical cord blood, hematopoietic stem cells (HSCs), pluripotent stem cells (PSCs), induced PSCs (iPSCs), embryonic stem cells (ESCs), or cells derived therefrom, such as CD34+ cells, CD90+ cells, CD45+ cells, CD17+ cells, CD45RA- cells, CD38- cells, or any combination thereof.

10. The method of claim 8 , wherein the immune cell is a T cell.

11. 10. The method of claim 1, wherein the modified cells are autologous to the patient, allogeneic to the patient, or a combination thereof.

12. 2. The method of claim 1, further comprising contacting the unmodified cells with an expression vector encoding expression of ALDH1 to produce modified cells that are cyclophosphamide resistant.

13. The method of claim 12, wherein the expression vector is a viral vector or a non-viral vector.

14. The method of claim 13, wherein the viral vector is a lentiviral vector or an adenoviral vector.

15. 13. The method of claim 12, wherein the expression vector is a retrovirus, a transposon, an episomal expression vector, modified RNA, a plasmid, or any combination thereof.

16. At least one dose of a non-myeloablative chemotherapeutic agent is administered following administration of the modified cells. The method of claim 1 .

17. 2. The method of claim 1, wherein at least one non-myeloablative dose of a chemotherapeutic agent is a non-myeloablative dose of cyclophosphamide.

18. 18. The method of claim 17, wherein the non-myeloablative dose of cyclophosphamide is about 0.16 mg / kg / day to less than 2.5 mg / kg / day.

19. 18. The method of claim 17, wherein the non-myeloablative dose of cyclophosphamide is about 0.41 mg / kg / day to about 1.63 mg / kg / day.

20. 18. The method of claim 17, wherein the non-myeloablative dose of cyclophosphamide is about 0.81 mg / kg / day to about 1.46 mg / kg / day.

21. 18. The method of claim 17, wherein the non-myeloablative dose of cyclophosphamide is about 1.3 mg / kg / day.

22. Patients received 100 mg / m ２ 18. The method of claim 17, wherein no more than one daily dose of cyclophosphamide is administered for 1 to 14 consecutive days.

23. Patients should be given 5-7 g / m ２ 18. The method of claim 17, wherein the dose of cyclophosphamide is not administered for 12 to 24 hours.

24. 10. The method of claim 1, wherein the non-myeloablative chemotherapeutic agent is administered daily for at least 1 week, at least 2 weeks, at least 3 weeks, at least 1 month, at least 2 months, at least 3 months, at least 4 months, at least 5 months, or at least 6 months.

25. 10. The method of claim 1, further comprising not administering a non-myeloablative dose of a chemotherapeutic agent for a period of time between administration of the cyclophosphamide-resistant modified cells and administration of the at least one dose of a non-myeloablative chemotherapeutic agent.

26. 26. The method of claim 25, wherein the period of time is selected from the group consisting of about 3 days, about 7 days, about 10 days, and about 14 days.

27. 10. The method of claim 1, wherein greater than about 60%, greater than about 70%, greater than about 80%, greater than about 90%, greater than about 95%, or 100% of the patient's bone marrow is replaced with the modified cells.

28. 10. The method of claim 1, wherein the patient is not myeloablative and / or immunocompromised as a result of administration of at least one dose of a non-myeloablative chemotherapy agent.

29. 10. The method of claim 1, wherein the patient does not experience clinically relevant anemia, neutropenia, thrombocytopenia, pancytopenia, low platelets, low white blood cells, or any combination thereof or related symptoms.

30. The method of claim 1 , wherein the preconditioning step is performed prior to administering the cells.

31. 31. The method of claim 30, wherein the preconditioning step is a non-myeloablative chemotherapy preconditioning step.

32. The method of claim 1 , wherein the modified cells are resistant to HIV infection.

33. 33. The method of claim 32, wherein the modified cell heterologously expresses at least one HIV coreceptor mutation resistant to HIV infection, at least one HIV coreceptor mutation or mutations, at least one HIV fusion inhibitor, a molecule that reduces expression of an HIV coreceptor, or any combination thereof.

34. 33. The method of claim 32, wherein the modified cells heterologously express shCCR5, shCXCR4, a C-peptide fusion inhibitor, or any combination thereof.

35. 33. The method of claim 32, wherein the modified cells do not express an HIV co-receptor.

36. 33. The method of claim 32, wherein the modified cells do not express CCR5, CXCR4, or express CCR5-Δ32, or a combination thereof.

37. ALDH1, and i) a heterologous nucleotide molecule encoding at least one HIV coreceptor mutant, at least one HIV coreceptor mutation or mutations, at least one HIV fusion inhibitor, a molecule that reduces expression of an HIV coreceptor, or any combination thereof; and / or ii) an endogenous HIV coreceptor mutation or deletion. A cell comprising a heterologous nucleotide molecule encoding expression of.

38. The cells are i. encodes a molecule that reduces the expression of CCR5; ii. encodes a molecule that reduces the expression of CXCR4; iii. Encoding expression of a C-peptide fusion inhibitor; iv. containing a sequence of 1, 3, 6, 7, 8, 9, 12, 13, 14, 16, 18, or any combination thereof; v. encoding the sequence of SEQ ID NO: 10, 11, 6, 7, 13, 15, 17, 19, or any combination thereof; or any combination of these 38. The cell of claim 37, comprising a heterologous nucleotide sequence.

39. 38. The cell of claim 37, which expresses a C-peptide fusion inhibitor, such as shCCR5, shCXCR4, and / or C44.

40. 38. The cell of claim 37, which has been modified to express a heterologous nucleotide sequence using a non-viral gene transfer system.

41. 41. The cell of claim 40, wherein the non-viral gene transfer system is a transposon gene transfer system.

42. 38. The cell of claim 37, wherein the transposon gene transfer system is the Sleeping Beauty gene transfer system or the PiggyBac transposon gene transfer system.

43. The cell of claim 37, comprising the heterologous nucleic acid sequence of SEQ ID NO:

4.

44. 38. A composition comprising one or more cells according to claim 37.

45. ALDH1, and i) one of a heterologous nucleotide molecule encoding at least one HIV coreceptor mutant, at least one HIV coreceptor mutation or mutations, at least one HIV fusion inhibitor, a molecule that reduces expression of an HIV coreceptor, or any combination thereof; A nucleic acid molecule encoding

46. The heterologous nucleotide sequence may be i. reducing the expression of CCR5; ii. reduce the expression of CXCR4; iii. Encoding expression of a C-peptide fusion inhibitor; or any combination of these 46. ​​A nucleic acid molecule according to claim 45 which encodes the molecule.

47. The nucleic acid molecule of claim 45, wherein the nucleic acid molecule encodes expression of shCCR5, shCXCR4, and / or a C-peptide fusion inhibitor.

48. 46. ​​The nucleic acid molecule of claim 45, wherein the molecule comprises a sequence of 1, 3, 6, 7, 8, 9, 12, 13, 14, 16, 18, or any combination thereof.

49. 46. ​​The nucleic acid molecule of claim 45, wherein the molecule comprises a nucleic acid molecule encoding the sequence of SEQ ID NO: 10, 11, 6, 7, 13, 15, 17, 19, or any combination thereof.

50. A vector comprising the nucleic acid molecule of claim 45.

51. 51. The vector of claim 50, which is a vector that can be used to produce a lentivirus.

52. 51. The vector of claim 50 which is a lentiviral vector.

53. 51. The vector of claim 50, comprising the sequence of SEQ ID NO: 1, 3, 6, 7, 8, 9, 12, 13, 14, 16, 18, or any combination thereof.

54. 51. The vector of claim 50, comprising a nucleic acid molecule encoding the sequence of SEQ ID NO: 10, 11, 6, 7, 13, 15, 17, 19, or any combination thereof.

55. ALDH1, and i) one of a heterologous nucleotide molecule encoding at least one HIV coreceptor mutant, at least one HIV coreceptor mutation or mutations, at least one HIV fusion inhibitor, a molecule that reduces expression of an HIV coreceptor, or any combination thereof; A population of cells heterologously expressing At least one dose of a non-myeloablative chemotherapy agent 46. ​​A method of treating HIV in a subject comprising administering to the subject.

56. 56. The method of claim 55, wherein the cell expresses shCCR5, shCXCR4, and / or a C-peptide fusion inhibitor.

57. 56. The method of claim 55, wherein the cell comprises a nucleic acid molecule comprising a sequence of 1, 3, 6, 7, 8, 9, 12, 13, 14, 16, 18, or any combination thereof.

58. 56. The method of claim 55, wherein the cell comprises a nucleic acid molecule encoding the sequence of SEQ ID NO: 10, 11, 6, 7, 13, 15, 17, 19, or any combination thereof.

59. A method of expressing a molecule of interest in a subject, comprising administering to the subject cells that heterologously express ALDH1 and the molecule of interest; and administering a non-myeloablative dose of cyclophosphamide.

60. 60. The method of claim 59, wherein the cells are CD34+ and / or CD4+, or others provided herein.

61. 60. The method of claim 59, wherein the molecule of interest reduces expression of CCR5; reduces expression of CXCR4; encodes expression of a C-peptide fusion inhibitor; or any combination thereof.

62. 62. The method of claim 61, wherein the molecule of interest for reducing expression of CCR5 is shCCR5.

63. 63. The method of claim 62, wherein the molecule comprises a nucleic acid molecule comprising or encoding SEQ ID NO:6 and / or SEQ ID NO:

7.

64. 62. The method of claim 61, wherein the C-peptide fusion inhibitor comprises the sequence of SEQ ID NO: 11, 15, 19, or any combination thereof.

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