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Definitions

• TILs Tumor Infiltrating Lymphocytes
• TILs are immune cells (e.g., T cells) found within tumors that can recognize and kill cancer cells.
• Adoptive transfer of autologous TILs have been extensively studied, but one disadvantage of TIL-based therapies is that these cells often exhibit cellular markers of extensive differentiation and aging along with loss of functionality. See, e.g., Gurusamy, et ak, 2020, Cancer Cell 37, 818-833; Jiang, et ak, 2015, Cell Death Dis 6, el792.
• TILs are largely composed of TEM or TEMRA cells and have characteristics of exhaustion. Sakuishi et ak, 2010, J Exp Med 207, 2187-2194. Additionally, preclinical evidence strongly suggests that impaired T cell function in the tumor site can drive poor clinical efficacy of T cell products.
• T cells also termed T lymphocytes
• T lymphocytes are a type of blood cell with unique properties that develop from stem cells found in bone marrow; T cells protect against infection and fight cancer.
• T cells are structurally and functionally different from other cell types such as fibroblasts and undergo a complex development that requires positive and negative selection in the thymus and involves somatic gene rearrangement at the T cell receptor gene loci (see e.g., Kurd and Robey, Immunol Rev. 2016 May; 271(1): 114-126).
• fibroblasts are also involved in the body’s immune response, fibroblasts are cells that synthesize extracellular matrix and collagen, thereby producing the structural framework for animal tissues. Fibroblasts are primarily involved in the process of wound healing.
• Tumor reactive T cells in addition to exhibiting characteristics of exhaustion and increased differentiation, are subject to the induction of cell senescence pathways. Senescence is a process of progressive loss of potency and functionality that results from aging and repeated cycles of cell divisions.
• Senescence is a process of progressive loss of potency and functionality that results from aging and repeated cycles of cell divisions.
• epigenetic changes Vodnala et ak, 2019, Cancer Cell 37, 818-833 e819
• reduced length of telomeres Rosenberg et al., 2011, Clin Cancer Res 17, 4550-4557
• the loss of functionality proliferative potential and cell viability
• TIL -based cell therapy can mediate responses in some patients, clinical evidence has demonstrated that TIL products with elevated expression of CCR7 and increased telomere length are associated with improved therapeutic outcome. Rosenberg et al., 2011, Clin Cancer Res 17, 4550-4557. Accordingly, many groups have pursued methods of cellular dedifferentiation or reprogramming as a method of reversing T cell exhaustion, differentiation and senescence.
• Cellular dedifferentiation has been accomplished in the past by utilizing iPS cell technology to revert somatic cells into pluripotent stem cells, followed by re differentiation into desired cellular lineages.
• Takahashi et al. 2007, Cell 131, 861-872.
• iPS cell technology has been shown to be able to reprogram tumor antigen specific tumor infiltrated lymphocytes into iPS cells with the ability to generate T lineage cells in vitro. Vizcardo et al., 2013, Cell Stem Cell 12, 31-36.
• Driving cells to iPS cells has the advantage of totally resetting the biological and epigenetic clock of the cell.
• the iPS cells derived from T cells often have abnormal biology — for example, immature phenotype, non MHC dependent killing, improper CD8o$ dimerization, dysregulation of gene expression and failure to produce a developmentally homogeneous population of T cells (see e.g., Vizcardo et al., 2018, Cell Rep 22, 3175-3190; Takada, K., Kondo, K., and Takahama, Y. 2017 J. Immunol. 198, 2215-2222.; Yamagata, T., et al., (2004). Nat. Immunol. 5, 597-605; Fink, P.J. (2013). Annu. Rev. Immunol.
• the present disclosure relates to methods for improving therapeutic T cell product quality and anti-tumor potential, compositions comprising such improved T cells and methods of treatment and other uses of the improved T cell compositions. Consequently, this system can be applicable to many other therapeutic processes for cancer, such as TCR and CAR transduced T cells, along with cells genetically modified with anti- exhaustion or pro-functionality genes for improved function of T cells in the tumor microenvironment.
• This system will also be amenable to new methods of T cell expansion in future iterations of media and innovations devised by artificial neoproteins.
• the rejuvenated T cells of the present disclosure can enhance the efficiency of all modalities of cellular immunotherapy by generating T cells that have enhanced capacity for expansion, improved metabolic qualities, and augmented ability to persist and eliminate established solid tumors.
• the present disclosure relates to a method of producing a rejuvenated T cell, comprising, contacting a population of T cells with at least one reprogramming factor selected from the group consisting of KLF4, OCT3/4, SOX2 and C- MYC; and optionally SV40 for at least a period of time sufficient for T cell derived adherent cells to form and wherein said T cells are not transformed into iPS or totipotent cells; and contacting the T cell derived adherent cells with at least one T cell activating agent.
• the present disclosure provides a method of producing a rejuvenated T cell, comprising contacting a T cell with (i) at least one reprogramming factor selected from the group consisting of KLF4, OCT3/4, SOX2 and C-MYC, and (ii) optionally SV40, for a period of time sufficient for a T cell derived adherent cell to form and wherein said T cell is not transformed into an iPS or totipotent cell; and contacting the T cell derived adherent cell with at least one T cell activating agent.
• the present disclosure relates to a method of producing a T cell, comprising contacting a population of T cells in a first culture medium in a culture vessel with at least one reprogramming factor selected from the group consisting of KLF4, OCT3/4, SOX2 and C-MYC; and optionally SV40 for at least a period of time sufficient for the T cells to form at least one colony attached to the culture vessel surface and wherein said T cells are not transformed into iPS cells; and contacting the at least one attached colony with at least one T cell activating agent.
• at least one reprogramming factor selected from the group consisting of KLF4, OCT3/4, SOX2 and C-MYC
• SV40 for at least a period of time sufficient for the T cells to form at least one colony attached to the culture vessel surface and wherein said T cells are not transformed into iPS cells
• the present disclosure relates to a method of producing a T cell, comprising contacting a population of isolated T cells in a first culture medium with at least one reprogramming factor selected from the group consisting of KLF4, OCT3/4, SOX2 and C-MYC; and SV40 for a period of at least about 5 days to about 10 days and wherein said T cells are not transformed into iPS cells or totipotent cells; contacting said contacted T cells with at least one T cell activating agent.
• at least one reprogramming factor selected from the group consisting of KLF4, OCT3/4, SOX2 and C-MYC
• SV40 for a period of at least about 5 days to about 10 days and wherein said T cells are not transformed into iPS cells or totipotent cells
• the present disclosure relates to a method of producing at least one T cell, comprising contacting a population of isolated T cells with at least one reprogramming factor selected from the group consisting of KLF4, OCT3/4, SOX2 and C- MYC; and SV40 for at least a period of time sufficient for the T cells to express at least one marker selected from the group consisting of SSEA4, CD9, and CD90 and wherein said T cells are not transformed into iPS cells or totipotent cells; and contacting said contacted T cells with at least one T cell activating agent.
• at least one reprogramming factor selected from the group consisting of KLF4, OCT3/4, SOX2 and C- MYC
• SV40 for at least a period of time sufficient for the T cells to express at least one marker selected from the group consisting of SSEA4, CD9, and CD90 and wherein said T cells are not transformed into iPS cells or totipotent cells
• the isolated T cells are contacted with the at least one reprogramming factor for at least a period of time sufficient for at least a portion of the T cells to express CD3 and at least one marker selected from the group consisting of SSEA4, CD9, and CD90.
• the T cells are transiently contacted with the at least one reprogramming factor for at least a period of time sufficient for at least a portion of said contacted T cells to express SSEA4 and CD3.
• the T cells are transiently contacted with the at least one reprogramming factor for at least a period of time sufficient for at least a portion of said contacted T cells to express CD3, CD9 and CD90.
• the T cells are contacted with the at least one reprogramming factor for at least a period of time sufficient for at least a portion of said contacted T cells to express CD3, SSEA4, CD9 and CD90.
• the transiently contacted T cells are contacted with IL-2 and at least one compound capable of activating said isolated T cells.
• the T cell is a TCRo$ T cell; a TCRgd T cell; a CD4+CD8o$+ double positive cell, CD4+ single positive cell (such as Thl, Th2, Thl7, Treg), a naive T cell, a central memory T cell, or effector memory T cell.
• the T cell is a TIL.
• said isolated T cells are isolated from a mammal.
• the isolated T cells are transiently contacted with KLF4, OCT3/4, SOX2 and C-MYC. In various embodiments, the isolated T cells are transiently contacted with KLF4, OCT3/4, SOX2 and C-MYC for at least about 4 to 10 days.
• the isolated T cells are contacted with KLF4, OCT3/4, SOX2 and C-MYC for at least about 4 to 7 days. In various embodiments, the isolated T cells are contacted with KLF4, OCT3/4, SOX2 and C-MYC for about 5 days.
• KLF4, OCT3/4, SOX2 and C-MYC are transiently expressed in the T cell.
• KLF4, OCT3/4, SOX2 and C-MYC are transiently expressed using a non-integrating viral vector.
• the T cells may be transduced with one or more viral vectors encoding the reprogramming factors.
• KLF4, OCT3/4, SOX2 and C-MYC are transiently expressed using a Sendai virus.
• KLF4, OCT3/4, SOX2 and C-MYC are constitutively expressed, wherein expression is later inhibited by the addition of a compound that inhibits expression of KLF4, OCT3/4, SOX2 AND C-MYC.
• said compound is a small molecule inhibitor that specifically inhibits the expression of one or more of KLF4, OCT3/4, SOX2 and C-MYC expression.
• said compound is an siRNA or shRNA molecule that specifically inhibits the expression of one or more of KLF4, OCT3/4, SOX2 and C-MYC.
• KLF4, OCT3/4, SOX2 and C-MYC are transiently expressed following delivery using a nanoparticle.
• the disclosure provides further contacting the contacted T cells (i.e., the partially reprogrammed T cells) with at least one T cell activating compound, and optionally at least one cytokine selected from the group consisting of IL-2, IL-7, IL-15, and IL-12.
• the partially reprogrammed cells are T cell derived adherent cells.
• said at least one T cell activating compound comprises an antibody that binds CD3 or an antibody that binds CD28 or both; or wherein the at least one T cell activating compound is a tumor antigen.
• the disclosure provides further engineering the T cell to express a cell surface receptor, wherein said T cell is engineered prior to contacting said T cell with said at least one reprogramming factor. In various embodiments, the disclosure provides further engineering the T cell to express a cell surface receptor, wherein said T cell is engineered after transiently contacting said T cell with said at least one reprogramming factor.
• said cell surface receptor is either a chimeric antigen receptor or an engineered T cell receptor or a hybrid receptor thereof. In various embodiments, said cell surface receptor recognizes a specific antigenic moiety on the surface of a target cell. In various embodiments, the antigenic moiety is MHC class I dependent. In various embodiments, the antigenic moiety is MHC class I independent.
• the resulting T cells comprise an incomplete set of V, D, and J segments of T cell receptor genes.
• the disclosure provides further measuring the epigenetic age of the resulting T cells.
• the epigenetic age of the resulting T cells is at least 5% younger than the population of T cells prior to reprogramming.
• the partially reprogrammed T cells are capable of expanding at least 25-fold greater than the initially isolated cells.
• the disclosure provides further contacting said isolated T cells with at least one factor selected from the group consisting of KLF4, OCT3/4, SOX2 and C-MYC; and SV40 results in a reduction in CD3 and CD8 expression.
• the present disclosure provides for a method of producing a T cell, comprising, obtaining a plurality of isolated T cells from a source; culturing said isolated T cells in a first medium comprising IL-2 and activating said isolated T cells with at least one T cell activating compound or agent and a costimulatory agent, such as an antibody specific for CD3 and/or for CD28; transiently contacting said activated T cells with KLF4, OCT3/4, SOX2 and C-MYC, for a period of about 5 days to about 10 days in a second culture medium that does not comprise IL-2, or antibody specific for CD3 or CD28; wherein said isolated T cells are not completely reprogrammed into iPS cells; replacing said second culture medium with a third culture medium comprising IL-2 and at least one antibody specific for CD3 and/or CD28; wherein said transiently contacted T cells are cultured in said third culture medium for at least about 5 days.
• a costimulatory agent such as an antibody specific for CD3 and/or for
• the disclosure provides further expanding said partially reprogrammed, reactivated T cells.
• said T cell is a TCRo$ cell; a TCRgd cell; a CD4+CD8a.p+ double positive cell, CD4+ single positive cell (Thl, Th2, Thl7,Treg), a naive T cell, a central memory T cell, or effector memory T cell.
• said T cell is a tumor infiltrating lymphocyte (TIL).
• the present disclosure provides for a population of T cells whose epigenetic age is at least 5% younger than its chronological age. In various embodiments, the present disclosure provides for a population of T cells, wherein the epigenetic age is at least 25% younger than its chronological age. In various embodiments, the present disclosure provides for a population of T cell derived adherent cells, wherein at least 70% of the cells express both CD3 and SSEA4. In various embodiments, the present disclosure provides for a population of T cell derived adherent cells, wherein at least 30% of the cells express CD9 or CD90 or both CD9 and CD90.
• the invention provides for a population of tumor infiltrating lymphocytes, wherein at least 35%, 40%, 45%, 50%, 55%, 60%, 65%, 70%, 75%, 80%, 85%, 90%, or 95% of the tumor infiltrating lymphocytes express both CCR7 and CD62L.
• the invention provides, for a population of tumor infiltrating lymphocytes, wherein at least 35%, 40%, 45%, 50%, 55%, 60%, 65%, 70%, 75%, 80%, 85%, 90%, or 95% of the tumor infiltrating lymphocytes express both CCR7 and TCF7.
• the present disclosure provides for a population of T cells produced by a method comprising transiently contacting a population of T cells with at least one reprogramming factor selected from the group consisting of KLF4, OCT3/4, SOX2 AND C-MYC; and optionally SV40 for a period of time sufficient for T cell derived adherent cells to form and wherein said isolated T cells are not transformed into iPS or totipotent cells; and contacting the T cell derived adherent cells with at least one T cell activating compound.
• the present disclosure provides for a population of T cells produced by a method comprising transiently contacting a population of isolated T cells in a first culture medium in a culture vessel with at least one reprogramming factor selected from the group consisting of KLF4, OCT3/4, SOX2 and C-MYC; and optionally SV40 for a period of time sufficient for the isolated T cells to form at least one colony attached to the culture vessel surface and wherein said isolated T cells are not transformed into iPS cells; and contacting the at least one attached colony with at least one T cell activating compound.
• the present disclosure provides for a population of T cells produced by a method comprising transiently contacting a population of isolated T cells in a first culture medium with at least one reprogramming factor selected from the group consisting of KLF4, OCT3/4, SOX2 and C-MYC; and SV40 for a period of at least about 5 days and no more than about 10 days and wherein said isolated T cells are not transformed into iPS cells; contacting said transiently contacted T cells with at least one T cell activating compound.
• the present disclosure provides for a population of T cells produced by a method comprising transiently contacting a population of isolated T cells with at least one reprogramming factor selected from the group consisting of KLF4, OCT3/4, SOX2 and C-MYC; and SV40 for a period of time sufficient for the isolated T cells to express at least one marker selected from the group consisting of SSEA4, CD9, and CD90 and wherein said isolated T cells are not transformed into iPS cells; and contacting said transiently contacted T cells with at least one T cell activating compound.
• a method comprising transiently contacting a population of isolated T cells with at least one reprogramming factor selected from the group consisting of KLF4, OCT3/4, SOX2 and C-MYC; and SV40 for a period of time sufficient for the isolated T cells to express at least one marker selected from the group consisting of SSEA4, CD9, and CD90 and wherein said isolated T cells are not transformed into iPS cells; and contacting said transiently contacted T
• the isolated T cells are transiently contacted with the at least one reprogramming factor for a period of time sufficient for at least a portion of the isolated T cells to express CD3 and at least one marker selected from the group consisting of SSEA4, CD9, and CD90.
• the isolated T cells are transiently contacted with the at least one reprogramming factor for a period of time sufficient for at least a portion of said transiently contacted T cells to express SSEA4 and CD3.
• the isolated T cells are transiently contacted with the at least one reprogramming factor for a period of time sufficient for at least a portion of said transiently contacted T cells to express CD3, CD9 and CD90.
• the isolated T cells are transiently contacted with the at least one reprogramming factor for a period of time sufficient for at least a portion of said transiently contacted T cells to express CD3, SSEA4, CD9 and CD90.
• said transiently contacted T cells prior to contacting said isolated T cells with the at least one reprogramming factor, are contacted with IL-2 and at least one compound capable of activating said isolated T cells.
• the T cell is a TCRo$ cell; a TCRyo cell; a CD4+CD8o$+ double positive cell, CD4+ single positive cell (such as Thl, Th2, Thl7, Treg), a naive T cell, a central memory T cell, or effector memory T cell.
• the T cell is a TIL.
• said isolated T cells are isolated from a mammal.
• the isolated T cells are transiently contacted with KLF4, OCT3/4, SOX2 and C- MYC.
• the isolated T cells are transiently contacted with KLF4, OCT3/4, SOX2 and C-MYC for at least about 4 to 10 days. In various embodiments, the isolated T cells are transiently contacted with KLF4, OCT3/4, SOX2 and C-MYC for at least about 4 to 7 days.
• the isolated T cells are transiently contacted with KLF4, OCT3/4, SOX2 and C-MYC for about 5 days.
• KLF4, OCT3/4, SOX2 and C-MYC are transiently expressed in the T cell.
• KLF4, OCT3/4, SOX2 and C-MYC are transiently expressed using a non-integrating viral vector.
• KLF4, OCT3/4, SOX2 and C-MYC are transiently expressed using a Sendai virus.
• KLF4, OCT3/4, SOX2 and C-MYC are constitutively expressed, wherein expression is later inhibited by the addition of a compound that inhibits expression of KLF4, OCT3/4, SOX2 AND C-MYC.
• said compound is a small molecule inhibitor that specifically inhibits the expression of one or more of KLF4, OCT3/4, SOX2 and C-MYC expression.
• said compound is an siRNA or shRNA molecule that specifically inhibits the expression of one or more of KLF4, OCT3/4, SOX2 and C-MYC.
• KLF4, OCT3/4, SOX2 and C-MYC are transiently expressed using a nanoparticle.
• the present disclosure provides for further contacting the transiently contacted T cells (e.g., the partially reprogrammed T cells) with at least one cytokine selected from the group consisting of IL-2, IL-7, IL-15, and IL-12; and/or with at least one T cell activating agent and/or at least one T cell costimulatory agent (e.g., anti-CD3 and/or anti-CD28 antibodies).
• at least one T cell activating compound comprises an antibody that binds CD3 or an antibody that binds CD28 or both; or wherein the at least one T cell activating compound is a tumor antigen.
• the present disclosure provides for further engineering the T cell to express a cell surface receptor, wherein said T cell is engineered prior to transiently contacting said T cell with said at least one reprogramming factor. In various embodiments, the present disclosure provides for further engineering the T cell to express a cell surface receptor, wherein said T cell is engineered after transiently contacting said T cell with said at least one reprogramming factor.
• said cell surface receptor is either a chimeric antigen receptor or a T cell receptor or a hybrid receptor thereof.
• said cell surface receptor recognizes a specific antigenic moiety on the surface of a target cell.
• the antigenic moiety is MHC class I dependent.
• the antigenic moiety is MHC class I independent.
• the resulting T cells comprise an incomplete set of V, D, and J segments of T cell receptor genes.
• the present disclosure provides for further measuring the epigenetic age of the resulting T cells.
• the epigenetic age of the resulting T cells is at least 5% younger than the population of T cells prior to reprogramming.
• the partially reprogrammed T cells are capable of expanding at least 25 -fold greater than the initially isolated cells.
• the present disclosure provides for further contacting said isolated T cells with at least one factor selected from the group consisting of KLF4, OCT3/4, SOX2 and C-MYC; and SV40 results in a reduction in CD3 and CD8 expression.
• the present disclosure relates to a population of T cells produced by a method comprising obtaining a plurality of isolated T cells from a source; culturing said isolated T cells in a first medium comprising IL-2 and activating said isolated T cells with at least one antibody specific for CD3 and/or for CD28; transiently contacting said activated T cells with KLF4, OCT3/4, SOX2 and C-MYC, for a period of about 5 days to about 10 days in a second culture medium that does not comprise IL-2, or antibody specific for CD3 and/or CD28; wherein said isolated T cells are not completely reprogrammed into iPS cells; replacing said second culture medium with a third culture medium comprising IL-2 and at least one antibody specific for CD3 and/or CD28; wherein said transiently contacted T cells are cultured in said third culture medium for at least about 5 days.
• the present disclosure relates to further expanding said transiently contacted T cells.
• said T cell is a TOIab cell; a TCRyo cell; a CD4+CD8o$+ double positive cell, CD4+ single positive cell (Thl, Th2, Thl7,Treg), a naive T cell, a central memory T cell, or effector memory T cell.
• said T cell is a TOIab cell; a TCRyo cell; a CD4+CD8o$+ double positive cell, CD4+ single positive cell (Thl, Th2, Thl7,Treg), a naive T cell, a central memory T cell, or effector memory T cell.
• said T cell is a TOIab cell; a TCRyo cell; a CD4+CD8o$+ double positive cell, CD4+ single positive cell (Thl, Th2, Thl7,Treg), a naive T cell, a central memory T cell, or effector memory T cell.
• T cell is a tumor infiltrating lymphocyte (TIL).
• TIL tumor infiltrating lymphocyte
• the present disclosure relates to a method of treating a patient in need thereof with a population of T cells produced by a method disclosed herein or by the population of T cells disclosed herein.
• the method of treatment is a method for treating a cancer, a viral condition or an automimmune disorder.
• the cancer is acute lymphocytic cancer, acute myeloid leukemia, alveolar rhabdomyosarcoma, bone cancer, brain cancer, breast cancer, cancer of the anus, anal canal, or anorectum, cancer of the eye, cancer of the intrahepatic bile duct, cancer of the joints, cancer of the neck, gallbladder, or pleura, head and neck cancers (e.g., cancer of the nose, nasal cavity, or middle ear, cancer of the oral cavity), cancer of the vulva, chronic lymphocytic leukemia, chronic myeloid cancer, colon cancer, esophageal cancer, cervical cancer, gastrointestinal carcinoid tumor, Hodgkin lymphoma, hypopharynx cancer, kidney cancer, larynx cancer, liver cancer, lung cancer, malignant mesothelioma, melanoma, multiple myeloma, nasopharynx cancer, non-Hodgkin lymphom
• the invention relates to a method of producing at least one rejuvenated T cell, comprising: a. isolating a T cell from a tumor, wherein the T cell is a tumor infiltrating lymphocyte; wherein the tumor infiltrating lymphocyte expresses CD 137; b. activating said tumor infiltrating lymphocyte with at least one T cell activating compound, wherein the T cell activating compound is a tumor antigen; c.
• the invention relates to a method of producing at least one rejuvenated tumor infiltrating lymphocyte (TIL), the method comprising (a)isolating a TIL from a tumor, wherein the TIL expresses CD 137, (b) activating said TIL with at least one first tumor antigen, and (c) transiently contacting a population of isolated TILs with (i) at least one reprogramming factor selected from the group consisting of KLF4, OCT3/4, SOX2 and C- MYC, and (ii) optionally SV40, for a period of time sufficient for TIL-derived adherent cells to form and wherein said isolated TILs are not transformed into iPS or totipotent cells.
• TIL rejuvenated tumor infiltrating lymphocyte
• the invention relates to a method of producing rejuvenated T cells, comprising contacting a population of T cells (i) at least one reprogramming factor selected from the group consisting of KLF4, OCT3/4, SOX2 and C-MYC, and (ii) optionally SV40, for at least a period of time sufficient for at least 20% of the contacted T cells to express a ⁇ b ⁇ integrin and wherein said contacted T cells are not transformed into iPS cells; isolating said at least 20% of the contacted T cells with a binding molecule that specifically binds to a ⁇ b ⁇ integrin; contacting the isolated cells of (b) with a T cell activating and/or a T cell costimulatory agent; thereby producing rejuvenated T cells.
• the invention relates to a method of producing at least one rejuvenated T cell, comprising transiently contacting the population of T cells with (i) at least one reprogramming factor selected from the group consisting of KLF4, OCT3/4, SOX2 AND C-MYC, and (ii) optionally SV40, for a period of time sufficient for T cell derived adherent cells to form; wherein said T cells are not transformed into iPS or totipotent cells; isolating a subpopulation of T cell derived adherent cells that express either a6 (CD49f) or bl (CD29) integrin or both; and contacting the isolated subpopulation with at least one T cell activating compound.
• at least one reprogramming factor selected from the group consisting of KLF4, OCT3/4, SOX2 AND C-MYC, and (ii) optionally SV40, for a period of time sufficient for T cell derived adherent cells to form; wherein said T cells are not transformed into iPS or toti
• the invention relates to a population of rejuvenated T cells produced by a method comprising contacting the population of T cells with (i) at least one reprogramming factor selected from the group consisting of KLF4, OCT3/4, SOX2 AND C- MYC, and (ii) SV40, for a period of time sufficient for T cell derived adherent cells to form; wherein said T cells are not transformed into iPS or totipotent cells; isolating a subpopulation of T cell derived adherent cells that express either a6 integrin, bl integrin or both; and contacting the subpopulation of T cell derived adherent cells with at least one T cell activating compound.
• the invention relates to a population of T cell derived adherent cells, wherein at least 70% of the cells express integrin a6 or integrin b ⁇ .
• the invention relates to a population of T cell derived adherent cells, wherein at least 50% of the cells express both integrin a6 and integrin b ⁇ .
• the invention relates to a population of T cell derived adherent cells, wherein at least 70% of the cells express both integrin a6 and integrin b ⁇ .
• FIG. 1 shows the experimental design for partial reprogramming using Sendai virus transduction. After isolation from peripheral blood mononuclear cells (PBMC), T cells were activated for three days with a CD3, CD28 activation culture media comprising IL2 (Day -2 to Day 0).
• PBMC peripheral blood mononuclear cells
• cells were either (i) left undisturbed (Group #1); (ii) placed in a stem cell culture medium without IL2 (Group #2); (iii) placed in a stem cell culture media without IL2 and transduced with two Sendai viruses — one expressing EmGFP; and one expressing SV40 (Group #3); or (iv) placed in a stem cell culture media without IL2 and transduced with four Sendai viruses — expressing KOS (KLF4, OCT3/4, SOX2), KLF4, cMyc and SV40 (Group #4). Expression continued for five days.
• FIG. 2 shows the formation of colonies in Group #4 starting at Day 4 to Day 9 after transduction with Sendai virus expressing OSKM+SV40.
• FIGs. 3A-3F show the difference in morphology of T cells cultured in different conditions as described in Example 1.
• FIG. 3 A shows the attached cells colony formation from Group #4
• FIG. 3B shows the T cells in Group #3 which do not show attachment and colony formation
• FIG. 3C shows the same panel as FIG. 3A for comparison to FIG. 3D.
• FIG. 3D shows T cells after 3 days in standard T cell culture medium with anti-CD3 antibody (100 ng/ml) and anti-CD28 antibody (2 pg/ml) stimulation
• FIG. 3E is the same panel as FIG. 3A for comparison to FIG. 3F.
• FIG. 3F shows a normal iPS cell colony.
• the attached cells shown in FIG. 3A, 3C, and 3E are referred to herein as T cell derived adherent cells.
• FIG. 4 shows CD3 expression on days 3, 4 and 5 of partial reprogramming. Notably, the reprogrammed cells in Group #4 demonstrated a loss of CD3 over the course of partial reprogramming.
• FIG. 5 shows a side scatter / forward scatter (SSC/FSC) FACS plot of the attached cells in Group #4 indicating that the attached cells are larger and have a more complex structure as compared to cells in Groups 1 and 3.
• FIG. 6 is a SSC/FSC FACS contour plot showing that day 5 attached cells become bigger with a complex structure.
• FIG. 7 shows that the attached cells in Group #4 regain CD3 and CD8 expression after T cell activation for two days followed by culture in T cell culture medium for five more days.
• T cells were activated at day 5 using one to one hundred diluted (1: 100) T cell TRANSACTTM (Miltenyi Biotec) in T cell culture medium for 2 days in a 96 well plate.
• Cells in the Group #4 condition were divided into 2 wells at day 5, floating cells and attached cells which were harvested by pipetting. All the cells were cultured in T cell culture medium for 5 more days after activation.
• FIG. 8 shows the phenotype of CD3 positive cells at day 12.
• CCR7 and CD62L are markers to detect certain T cell types, such as naive, memory stem cells, and central memory T cells. The cells regained CD3 expression at day 12 indicating a return to T cell phenotype.
• FIG. 9 is a bar graph that depicts cell expansion at Day 0, Day 5 and Day 12. Cell expansion was measured by counting beads (123count eBeads Counting beads, Thermo) using flow cytometry. Though attached cells in group #4 showed aberrant appearance and reduced CD3 expression at day 5, after activation from day 5, they responded to the activation and expanded. The fold change of day 12 versus day 5 indicated increased expansion of #4 compared to #1 especially for attached cells. This indicates that the partial rejuvenation method used herein increases T cell expansion potential especially in the attached cells.
• FIG. 10 is a FACS contour plot analysis of SSEA4 and CD3 expression in partially reprogrammed T cells.
• Sendai vims infected T cells as described in Example 2 were transferred onto iMatrix coated dishes on day 1 and were cultured in iPS cell media + 60 II I/ml IL2 for 3 days and then changed to iPS cell media without IL2 from day 4.
• FACS analysis was performed on day 8 of reprogramming. The figure shows that partially reprogrammed T cells express the hiPS cell marker SSEA4 and lose expression of the CD3 T cell marker.
• FIG. 11 is a schematic outlining the partial reprogramming of PBMC-derived CD8 T cells (See Example 4, Table 4).
• FIGs. 12A-12B show results from flow cytometry measuring CD8a, CD8b, CD3 in cells that have been partially reprogrammed for the indicated number of days prior to reactivation.
• FIG. 12A show FACS plots for expression of CD8a and CD8b days 7, 9 and 10 and
• FIG. 12B is a graph plotting the percentage of cells positive for CD8a and CD3CD8ab on days 6-10. See Example 4.
• the CD4-CD8a+ population was gated for further analysis of CD8B and CD3.
• No Sendai infection means CD8 T cells received the first and the second stimulation but were not infected by Sendai virus (no reprogramming factors).
• FIG. 13 is a schematic outlining the partial reprogramming and reactivation of NY- ESO-1+ T cells. The different phases of the full process are labeled for clarity.
• FIGs. 14A-14D are graphs showing the results from cytokine production and degranulation assays of rejuvenated NY-ESO-1 TCR transduced T cells.
• the FACS results were analyzed by FlowJo software.
• Single cells > Live cells > CD3+ > CD8+ CD4- > NY- ESO-1 tetramer+ cells were gated for NY-ESO-1 Tg T cells and Single cells > Live cells > CD3+ > CD8+ CD4- > NY-ESO-1 tetramer- cells were gated for mock control T cells.
• the frequency of IFNg + (A), TNFa + (B), IL-2 + (C), and CD107a + (D) were calculated and plotted as shown.
• FIG. 15 is a waterfall plot of the ratio of the level of cell surface marker expression in stimulated T cells versus T cell derived iPS cell (see also Table 5).
• FIG. 16 is a waterfall plot of the ratio of the level of cell surface marker expression in unstimulated T cells versus T cell derived iPS cells (see also Table 5).
• FIG. 17 shows that CD9 and CD90 are potential cell surface marker indicators of the early phase of partial reprogrammed T cells.
• the figure shows the flow cytometry analysis of the expression of CD9 and CD90 in stimulated T cells, unstimulated T cells and day 5 attached partially reprogrammed T cells (T cell derived adherent cells). Expression of the early iPS cell surface marker SSEA4 is not significantly changed at day 5 in T cell derived adherent cells, in contrast to expression of CD9 and CD90.
• FIGs. 18A-18D show that stimulation signaling is critical for partially reprogrammed T cells to reacquire expression of conventional T cell markers CD3 and CD8a, and to survive and proliferate.
• FIG. 18A is a FACS contour plot showing the percentage of partially reprogrammed cells expressing CD3 and CD8a at day 7 (day of detachment).
• FIG. 18B is a FACS contour plot showing percentage of cells expressing CD3 and CD8a at day 20 after either activation with 1:500 or 1:1000 dilution TRANSACT or in T cell culture media (TCM + IL2 60IU/ml) only.
• FIGs 18C and 18D show proliferation and viability of the different groups.
• FIGs. 19A-19B show that rejuvenated T cells exhibit dramatically enhanced and sustained proliferation in vitro. T cells were obtained from a 37-year-old Female, a 42-year-old male and a 52-year-old male donor.
• FIGs. 20A-20C show the effect of IL-2 on rejuvenated T cells.
• the rejuvenated T cells were co-cultured in TCM without IL-2.
• the FACS results were analyzed by FlowJo software. Single cells > Live cells > CD3+ cells were gated for all cell groups.
• FIG 20B and FIG. 20C cells co-cultured without IL-2 died within six days.
• FIG. 21 shows the results from cytokine production assays of rejuvenated 37yF, 42yM and 52yM T cells.
• the FACS results were analyzed by FlowJo software. Single cells > Live cells > CD3+ > CD8+ CD4- cells were gated for all cell groups. The frequency of IL2+ and IFNg + were calculated and plotted as shown.
• FIGs. 22A-22C show that rejuvenated T cells show effector phenotype after long term expansion.
• Sendai vims infected T cells were transferred onto iMatrix coated dishes on day 1 and were cultured in T cell media + 60 IU/ml IL2 or in iPS cell media + 60 II I/ml IL2 for 3 days and then changed to iPS cell media without IL2 from day 4.
• FACS analysis was performed on day 7 and day 26 after reprogramming.
• FIG. 23 is a FACS contour plot analysis of cell markers used to define differentiation state of T cells (CD3, CD45RA, CD45RO, CD62L and CCR7).
• FIG. 24 shows the fold expansion of NY-ESO-1 rejuvenated or control cells from two different donors (#3 and #4) after stimulation with TRANSACT. Rejuvenated T cells proliferated longer than control and exceed controls around 2-3 weeks of culture.
• FIG. 25 is a FACS contour plot analysis of NY-ESO-1 -CD3, CD4-CD8b, CCR7- CD62L and CD45RO-CD45RA expression in partially reprogrammed NY-ESO-1 T cells.
• FIGs. 26A-26D are graphs showing the results from cytokine production and degranulation assays of rejuvenated NY-ESO-1 TCR transduced T cells. The FACS results were analyzed by FlowJo software.
• PMA/I cells activated with PMA/Ionomycin (+ control).
• FIGs. 27A-27B show that rejuvenation of tumor infiltrating lymphocytes (TIL) augmented proliferation and resulted in more stem cell-like product.
• FIG. 27 A is a graph plotting the cell expansion and comparing the fold change of rejuvenated TIL to the control cells.
• FIG. 27B shows FACS plots for expression of CCR7-CD62L and CCR7-TCF7 and shows the rejuvenated TIL exhibited a high expression of sternness related markers.
• FIG. 28 depicts an exemplary, non-limiting scheme of the rejuvenation protocol employed in Example 12 described below.
• FIGs. 29A and 29B show phenotypic analysis conducted in connection with the rejuvenation protocol of Example 12.
• FIG. 29A shows representative FACS plots of Donor 1, showing the frequency of CD3+CD8b+ (gated on singlets, dead stain negative, and lymphocyte SSC/FSC).
• FIG. 29B is a bar graph of CD3+CD8b+ frequencies gated as in FIG. 29A; each bar shows the average of Donors 1-3. The error bar indicates +/-1SD
• FIGs. 30A-30C show the skin and blood clock results before Sev transduction, and days 7, 13, 18 after the transduction in Donors 1-3 of Example 12.
• “Before Sev transduction” indicates the sample before the activation for Sendai vims transduction.
• the error bar shows ⁇ 1SD.
• FIG. 31 illustrates the results of rejuvenation of NY-ESO-1 Tg CD4 and CD8 T cells.
• CD4 or CD8 T cells were stimulated by Transact and transduced with NY-ESO-1 TCR before reprogramming.
• FIGs. 32A and 32B illustrate the results of rejuvenation NY-ESO-1 Tg CD4 and CD8 T cells showed less differentiated phenotype.
• FIG. 33 illustrates the results of rejuvenation NY-ESO-1 Tg CD4 and CD8 T cells proliferated more than control NY-ESO-1 Tg CD4 and CD8 T cells.
• FIG. 34A and 34B are bar graphs showing eAge values from two donors: a 24-year old male (A) and a 35-year old male (B).
• the figure illustrates that rejuvenated NY-ESO-1 Tg CD4 and CD8 T cells showed younger phenotype by epigenetic age analysis than control NY- ESO-1 Tg CD4 and CD8 T cells and chronological age of the donors.
• Graphs show the mean and S.D. of the values of age analyzed from methylation status of certain CpG sites.
• FIG. 35 depicts bar graphs showing intracellular cytokine staining from rejuvenated and control NY-ESO-1 cells.
• the graph shows that rejuvenated NY-ESO-1 Tg CD4 and CD8 T cells produced more cytokines (IFNg (A), IL-2 (B) and TNFa (C)) upon co-culture with T2 cells with NY-ESO-1 peptide t-test p- value statistical significance: * ⁇ 0.05, ** ⁇ 0.005, *** ⁇ 0.0005, **** ⁇ 0.0001.
• FIG. 36 illustrates the results of rejuvenation NY-ESO-1 Tg CD8 T cells persisted and kept their cytotoxic activity longer upon repeated co-culture with NY-ESO-1 expressing target cells (A375-NLR).
• FIG. 37 describes the enhanced cytotoxicity of rejuvenated NY-ESO-1 Tg CD8 T cells resulting from addition of rejuvenated NY-ESO-1 Tg CD4 T cells.
• FIGs. 38A and 38B show the expression levels of adaptive immune related cytokines of rejuvenated cells and control cells from two different donors at the indicated time points.
• the y-axis denotes concentration of cytokine in pg/mL.
• FIGs. 39A and 39B show the expression levels of innate immune related cytokines of rejuvenated cells and control cells from two different donors at indicated times.
• the y-axis denotes concentration of cytokine in pg/mL.
• FIG. 40 describes NY-ESO-1 TCR transduction efficiency in CD8 T cells using representative FACS plots of NY-ESO-1 TCR transduced T cells: (Left) CD4 x CD8b, (Right) CD3 x NY-ESO-1 TCR TE. See Example 15.
• FIG. 41 provides a schematic representation of the procedure of Example 15.
• FIG. 42 provides bar graphs showing the fold change of the detached cell numbers collected from each condition on day 7 as compared to day 0. See Example 15.
• FIGs. 43 describes the re- stimulation of partially reprogrammed NY-ESO-1 TCR Tg T cells.
• FIG. 43 provides representative FACS plots of the day 14. Frequency of NY-ESO-1 TCR TE+ cells are provided. See Example 15.
• FIGs. 44 describes the re- stimulation of partially reprogrammed NY-ESO-1 TCR Tg T cells.
• FIG. 44 provides representative bar graphs of the day 14 frequency of NY-ESO-1 TCR TE+ cells. See Example 15.
• FIGs. 45 is a proliferation curve showing that rejuvenated NY-ESO-1 Tg T cells have higher proliferative capacity than non-rejuvenated controls (see Example 15).
• FIG. 46 illustrates the CD 19 CAR transduction efficiency in CD8 T cells. See Example 16. Cells were gated as Lymphocytes > Single cells > Live/Dead -, and plotted as CD3 x CD8a (second from right), CAR idiotype x EGFR (far right). tEGFR was expressed as a marker of successful transduction.
• FIG. 47 illustrates that rejuvenated CD 19 CAR T cells showed less differentiated phenotype.
• control and rejuvenated CD 19 CAR Tg T cells were analyzed for surface markers and Tcfl expression by FACS.
• Cells were gated as Lymphocytes > Single cells > Live/Dead - > CD19 CAR+, and plotted as CD4 x CD8a (second from left), CCR7 x CD62L (second from right) and CCR7 x Tcfl (far right)
• FIG. 48 shows that rejuvenated CD19 CAR T cells proliferated more than control CD19 CAR T cells. See Example 16. CD19 CAR Tg T cells were rejuvenated and cultured as described in section 3, and cell number was counted every 3-4 days. The Graph depicts the fold changes compared to day7 after transduction of the reprogramming factors in two healthy donors and their corresponding control cells over time.
• FIG. 49 illustrates that rejuvenated CD 19 CAR T cells produced comparable level of cytokines upon co-culture with CD19 expressing target cells. See Example 16. On day 20 control or rejuvenated CD19 CAR Tg T cells were cultured alone, or with PMA/Ionomycin, Colo205 (CD19-) or Nalm6 (CD 19+) in the presence of Golgi transporter inhibitors. After staining surface antigens, cells were fixed, permeabilized and stained by intracellular Abs. Frequency of each cytokine positive CAR+ cells were depicted.
• FIGs. 50A and 50B show that rejuvenated CD19 CAR T cells persisted and retained their cytotoxic activity longer upon repeated co-culture with CD19 expressing target cells. See Example 16.
• FIG. 50A and 50B show the results of co-culturing control or rejuvenated CD19 CAR Tg T cells with Nalm6-NLR cell line. Every 3-4 days, 25% (10% for 4th and 5th co culture) of the previous culture was transferred into a new plate with fresh targets. Growth of the target was monitored using the Incucyte® live-cell analysis system and analyzed with the Base Software Analysis Module. Graphs show the numbers of Nalm6-NLR/image of each condition of Donor #1 (FIG. 50A) and #2 (FIG. 50B).
• FIG. 51 is an exemplary, non- limiting experimental design of the rejuvenation protocol described in Example 17 for purposes of illustration.
• FIGs. 52A and 52B are the results of phenotypic analyses of cells detached on Day 11 (FIG. 52A) and the same cells (i.e., having detached on Day 11) on Day 17 (FIG. 52B) in each of the Sev and mSev groups discussed in Example 17.
• the provided FACS plots show the frequency of CD3+CD8b+ (gated on singlets, dead stain negative, and lymphocyte SSC/FSC).
• FIGs. 53A-53C are proliferation curves showing the fold change after various numbers of days following detachment (see Example 17).
• FIG. 53A shows fold change in cell count following detachment occurring on Day 7.
• FIG. 53B shows fold change in cell count following detachment occurring on Day 9.
• FIG. 53C shows fold change in cell count following detachment occurring on Day 11.
• Each dot in each of FIGS. 53A-53C indicates the average of the 2 donors. Error bars indicate ⁇ 1 SD.
• FIG. 54A shows the sternness phenotype exhibited 6 days after detachment of the reprogrammed T cells of Example 17. Bar graphs show the average TCF1+CCR7+ frequency (gated on singlets, dead stain negative, lymphocyte SSC/FSC, and CD3+CD8b+) in technical duplicates. Error bars indicate ⁇ 1SD.
• FIG. 54B shows the sternness phenotype six days after detachment of the reprogrammed T cells of Example 17. Bar graphs show the average CCR7+CD62L+ frequency (gated on singlets, dead stain negative, lymphocyte SSC/FSC, and CD3+CD8b+) in technical duplicates. Error bars indicate ⁇ 1SD
• FIG. 55 shows the epigenetic age of T cells transiently reprogrammed with either Sev or mSev and detached at Days 7, 9, and 11, as described in Example 17. Epigenetic age was measured using the Horvath skin blood clock.
• FIG. 56 shows proliferation curves for rejuvenated and control cells of Example 18.
• FIGs. 57A-57D shows the transcriptome profiling of healthy donor CD8+ T-cells from control and rejuvenated cells on Day 7 and Day 13 of Example 18.
• FIG. 57A shows single-cell RNA-seq data of CD8+ T-cells from control and rejuvenated cells from all four donors visualized by UMAP.
• FIG. 57B shows expression levels of transcripts encoding for the Yamanaka factors in the rejuvenated cells in single-cell RNA-seq data of CD8+ T-cells from control and rejuvenated cells.
• FIG. 57C shows expression levels of transcripts encoding for the Yamanaka factors in bulk RNA-seq data of CD8+ T-cells from control and rejuvenated cells.
• FIG. 57D shows the genome alignment visualization of reads that align to the endogenous cMYC gene in healthy donor CD8+ T-cells from control and rejuvenated cells on Days 7 and 13.
• FIG. 58A depicts Enrichment of metabolic gene sets in rejuvenated cells compared to control cells on Days 7 and 13 in the 3 donors of the bulk RNA-seq data of Example 18 (i.e., Donor Nos. 11347, 12254 and 26221).
• the difference in the scale of x-axis shows the adjusted p values for Days 7 and 13.
• the solid gray line shows the threshold of significance (Adjusted P value ⁇ 0.05).
• FIG. 58B shows the AddModule scores of glycolysis and oxidative phosphorylation gene sets on the same UMAP representation shown in Figure 59A (see Example 18).
• FIG. 59A is a UMAP illustrating that rejuvenated cells are enriched for naive gene sets (Gattinoni) on Day 13 as compared to control cells (see Example 18).
• FIG. 59B is a bar graph illustrating that rejuvenated cells are enriched for naive gene sets (Gattinoni) on Day 13 as compared to control cells (see Example 18).
• FIGs. 60A and 60B are graphs showing proliferation curves of Donors 1 and 2 following rejuvenation. All rejuvenated cells showed much higher fold of expansion than control group. In one donor, TransAct stimulated group showed higher expansion than CD 137+ selected group while in the other donor it is lower. This suggested a differing affinity of tumor-reactive populations to stimulation. Expansion after 33 days showed a decrease, which can be due to seeding cell density of that culture is suboptimal for the culture plate causing insufficient nutrient and oxygen supply. See Example 19.
• FIGs. 61A and 61B are graphs showing expression of CD62L and CCR7 in rejuvenated and control cells over time.
• CD62L+CCR7+ was preserved in the early stage of rejuvenation.
• Cells were harvested at indicated day and stained with fluorescent labeled antibodies, followed by analysis on flow cytometry. Results showed that rejuvenated cells were highly expressing CD62L+CCR7+ at D14 and D17 in these two donors. See Example 19.
• FIG. 62 is a graph showing proliferation curves of Donor 3 following rejuvenation.
• TILs were enriched with CD45+, and then stimulated with TransAct, followed by rejuvenation. Cells were counted at indicated days. Rejuvenated CD45+ showed a much-enhanced proliferation as compared to control cells, while CD45- group showed very limited expansion. See Example 19.
• FIG. 63 shows FACS contour plots measuring expression of markers associated with sternness in control and Donor 3 at day 15. Rejuvenated CD45+ TILs but not CD45- cells showed much higher expression of CD62L+CCR7+ and TCF7+CCR7+. See Example 19.
• FIG. 64 is a graph showing proliferation curves of controls and Donor 4 following rejuvenation. Cells were stimulated with TransAct either 1:500 (HI) or 1:2000 (LO). Rejuvenated cells (both HI and LO group) showed similar expansion rate as controls after redirection to T cells.
• FIG. 65 shows FACS contour plots measuring expression of markers associated with sternness in control cells and Donor 4 and day 21 following rejuvenation. Rejuvenated cells (both HI and LO group) showed higher expression of CD62L+CCR7+ and TCF7+CCR7+ than control cells. See Example 19.
• FIG. 66 is a graph showing epigenetic age (eAge) of control or rejuvenated cells from Donor 7 at indicated times.
• the epigenetic age of the control cells was similar to the donor chronological age, while rejuvenated cells showed a much lower age at day 15, which gradually increased with expansion time. See Example 19.
• FIG. 67 is a graph showing epigenetic age (eAge) of control or rejuvenated cells from Donor 9 at indicated times.
• the epigenetic age of the control group is similar to the chronological donor age, while rejuvenated cells showed a much lower epigenetic age at day 15, which gradually returned to control level over time of proliferation in culture. See Example 19.
• FIG. 68 is a graph showing the proliferation of control and rejuvenated cells from Donor 7 and Donor 9. Rejuvenated cells showed similar expansion rate as controls after redirection to T cells. See Example 19.
• FIG. 69A shows the phenotypic analysis of Day 11 detached cells on Days 14 and 18 from Donor 6 of Example 20.
• the FACS plots show the frequency of CD3+ (gated on singlets, dead stain negative, and CD3+ cells). Rejuvenated cells showed higher TCF7+CCR7+ on Days 14 and 18. See Example 20 and Table 10.
• FIG. 69B shows the phenotypic analysis of Day 11 detached cells on Days 14 and 18 from Donor 8 of Example 20.
• the FACS plots show the frequency of CD3+ (gated on singlets, dead stain negative, and CD3+ cells). Rejuvenated cells showed higher TCF7+CCR7+ on Days 14 and 18. See Example 20 and Table 10.
• FIG. 70 shows that attached cells (weakly attached cells, attached cells, strongly attached cells) show higher integrin a6 and integrin bl expression than activated T cell control on Day 10. Strongly attached cells show higher expression of integrin a6 and integrin bl than weakly attached cells and attached cells.
• the plots were acquired after singlet and live gating.
• FIG. 71 shows integrin a6 and integrin bl expression was reduced after T cell activation on day 10.
• the bar graph shows MFI (mean fluorescent intensity) of the plots of FIG. 70. The values were normalized by the MFI of activated T cell control of each time point. The control values were 1.
• FIG. 72 shows that attached cells lost CD3 expression on day 10 but acquired CD3 expression on Day 17.
• FIG. 73 shows high proliferation exhibited by weakly attached cells, attached cells, and strongly attached cells.
• the strongly attached cells showed late start of cell expansion.
• FIGs. 74A and 74B show that attached cells (especially strongly attached) exhibited high TCF1 and CCR7 expression on Days 10 (FIG. 74A) and 17 (FIG. 74B).
• the MFI was acquired from the data after singlet and live gating.
• FIG. 75 shows Simpson clonality distribution of single cell TCR sequences from control and rejuvenated cells at day 7 and day 13 (see Example 18).
• the present disclosure relates in part to methods of generating rejuvenated T cells by a process of partial reprogramming and reactivation to return the partially reprogrammed cells to a rejuvenated and functioning T cell.
• partial reprogramming comprises the transient expression in the T cells of reprogramming factors.
• the partial reprogramming process results in the formation of “T cell derived adherent” cells that express one or more markers of de-differentiated cells but that retain phenotypic markers of the T cell lineage.
• a T cell derived adherent cell is a partially dedifferentiated T cell that, when contacted with a T cell activating compound agent, returns to a functioning T cell.
• T cells generated by this process show characteristics of cellular rejuvenation while retaining lineage stability and retaining antigen-specificity, as described in further detail herein.
• immune cell(s) denotes any type of immune cell, including for example T cells, B cells, monocytes, macrophages, dendritic cells, and the like.
• immune cells disclosed herein are T cells.
• polynucleotide includes both single- stranded and double- stranded nucleotide polymers.
• the nucleotides comprising the polynucleotide can be ribonucleotides or deoxyribonucleotides or a modified form of either type of nucleotide.
• Said modifications include base modifications such as bromouridine and inosine derivatives, ribose modifications such as 2’, 3’-dideoxyribose, and internucleotide linkage modifications such as phosphorothioate, phosphorodithioate, phosphoroselenoate, phosphoro-diselenoate, phosphoro-anilothioate, phoshoraniladate and phosphoroamidate.
• base modifications such as bromouridine and inosine derivatives
• ribose modifications such as 2’, 3’-dideoxyribose
• internucleotide linkage modifications such as phosphorothioate, phosphorodithioate, phosphoroselenoate, phosphoro-diselenoate, phosphoro-anilothioate, phoshoraniladate and phosphoroamidate.
• oligonucleotide refers to a polynucleot
• Oligonucleotides can be single stranded or double stranded, e.g., for use in the construction of a mutant gene. Oligonucleotides can be sense or antisense oligonucleotides. An oligonucleotide can include a label, including a radiolabel, a fluorescent label, a hapten or an antigenic label, for detection assays. Oligonucleotides can be used, for example, as PCR primers, cloning primers or hybridization probes.
• control sequence refers to a polynucleotide sequence that can affect the expression and processing of coding sequences to which it is ligated. The nature of such control sequences can depend upon the host organism.
• control sequences for prokaryotes can include a promoter, a ribosomal binding site, and a transcription termination sequence.
• control sequences for eukaryotes can include promoters comprising one or a plurality of recognition sites for transcription factors, transcription enhancer sequences, and transcription termination sequence.
• Control sequences can include leader sequences (signal peptides) and/or fusion partner sequences.
• operably linked means that the components to which the term is applied are in a relationship that allows them to carry out their inherent functions under suitable conditions.
• vector means any molecule or entity (e.g., nucleic acid, plasmid, bacteriophage or virus) used to transfer protein coding information into a host cell.
• expression vector or “expression construct” refers to a vector that is suitable for transformation of a host cell and contains nucleic acid sequences that direct and/or control (in conjunction with the host cell) expression of one or more heterologous coding regions operatively linked thereto.
• An expression construct can include, but is not limited to, sequences that affect or control transcription, translation, and, if introns are present, affect RNA splicing of a coding region operably linked thereto.
• the term “host cell” refers to a cell that has been transformed, or is capable of being transformed, with a nucleic acid sequence and thereby expresses a gene of interest.
• the term includes the progeny of the parent cell, whether or not the progeny is identical in morphology or in genetic make-up to the original parent cell, so long as the gene of interest is present.
• transformation refers to a change in a cell’s genetic characteristics, and a cell has been transformed when it has been modified to contain new DNA or RNA.
• a cell is transformed where it is genetically modified from its native state by introducing new genetic material via transfection, transduction, delivery using nanoparticles (e.g., lipid nanoparticles), or other techniques.
• the transforming DNA can recombine with that of the cell by physically integrating into a chromosome of the cell, or can be maintained transiently as an episomal element without being replicated, or can replicate independently as a plasmid.
• a cell is considered to have been “stably transformed” when the transforming DNA is replicated with the division of the cell.
• the term “transfection” refers to the uptake of foreign or exogenous genetic material (DNA or RNA) by a cell.
• transduction refers to the process whereby foreign DNA or RNA is introduced into a cell via viral vector. See, e.g., Jones et ak, Genetics: Principles and Analysis, 1998, Boston: Jones & Bartlett Pubk
• polypeptide or “protein” refer to a macromolecule having the amino acid sequence of a protein, including deletions from, additions to, and/or substitutions of one or more amino acids of the native sequence.
• polypeptide and protein specifically encompass antigen-binding molecules, antibodies, or sequences that have deletions from, additions to, and/or substitutions of one or more amino acid of antigen-binding protein.
• polypeptide fragment refers to a polypeptide that has an amino-terminal deletion, a carboxyl-terminal deletion, and/or an internal deletion as compared with the full-length native protein. Such fragments can also contain modified amino acids as compared with the native protein.
• Useful polypeptide fragments include immunologically functional fragments of antigen-binding molecules.
• isolated means (i) free of at least some other proteins with which it would normally be found, (ii) is essentially free of other proteins from the same source, e.g., from the same species, (iii) separated from at least about 50 percent of polynucleotides, lipids, carbohydrates, or other materials with which it is associated in nature, (iv) operably associated (by covalent or noncovalent interaction) with a polypeptide with which it is not associated in nature, or (v) does not occur in nature.
• a “variant” of a polypeptide comprises an amino acid sequence wherein one or more amino acid residues are inserted into, deleted from and/or substituted into the amino acid sequence relative to another polypeptide sequence.
• Variants include fusion proteins.
• identity refers to a relationship between the sequences of two or more polypeptide molecules or two or more nucleic acid molecules, as determined by aligning and comparing the sequences. “Percent identity” means the percent of identical residues between the amino acids or nucleotides in the compared molecules and is calculated based on the size of the smallest of the molecules being compared. For these calculations, gaps in alignments (if any) are preferably addressed by a particular mathematical model or computer program (i.e., an “algorithm”).
• the sequences being compared are typically aligned in a way that gives the largest match between the sequences.
• One example of a computer program that can be used to determine percent identity is the GCG program package, which includes GAP (Devereux et al., Nucl. Acid Res., 1984, 12, 387; Genetics Computer Group, University of Wisconsin, Madison, Wis.).
• GAP is used to align the two polypeptides or polynucleotides for which the percent sequence identity is to be determined.
• the sequences are aligned for optimal matching of their respective amino acid or nucleotide (the “matched span”, as determined by the algorithm).
• a standard comparison matrix (see, e.g., Dayhoff et al., 1978, Atlas of Protein Sequence and Structure, 5:345-352 for the PAM 250 comparison matrix; Henikoff et al., 1992, Proc. Natl. Acad. Sci. U.S.A., 89, 10915-10919 for the BLO-SUM 62 comparison matrix) is also used by the algorithm.
• the twenty conventional (e.g., naturally occurring) amino acids and their abbreviations follow conventional usage. See, e.g., Immunology A Synthesis (2nd Edition, Golub and Green, Eds., Sinauer Assoc., Sunderland, Mass. (1991)), which is incorporated herein by reference for any purpose.
• Stereoisomers e.g., D-amino acids
• unnatural amino acids such as alpha-, alpha-disubstituted amino acids, N-alkyl amino acids, lactic acid, and other unconventional amino acids can also be suitable components for polypeptides of the present disclosure.
• Examples of unconventional amino acids include: 4-hydroxyproline, ycarboxy-glutamate, epsilon-N,N,N-trimethyllysine, e- N-acetyllysine, 0-phosphoserine, N-acetylserine, N-formylmethionine, 3-methylhistidine, 5- hydroxylysine, .sigma.-N-methylarginine, and other similar amino acids and imino acids (e.g., 4-hydroxyproline).
• the left-hand direction is the amino terminal direction and the right-hand direction is the carboxy-terminal direction, in accordance with standard usage and convention.
• Naturally occurring residues can be divided into classes based on common side chain properties: a) hydrophobic: norleucine, Met, Ala, Val, Leu, lie; b) neutral hydrophilic: Cys, Ser, Thr, Asn, Gin; c) acidic: Asp, Glu; d) basic: His, Lys, Arg; e) residues that influence chain orientation: Gly, Pro; and f) aromatic: Trp, Tyr, Phe.
• non-conservative substitutions can involve the exchange of a member of one of these classes for a member from another class.
• the hydropathic index of amino acids can be considered. Each amino acid has been assigned a hydropathic index on the basis of its hydrophobicity and charge characteristics.
• derivative refers to a molecule that includes a chemical modification other than an insertion, deletion, or substitution of amino acids (or nucleic acids).
• derivatives comprise covalent modifications, including, but not limited to, chemical bonding with polymers, lipids, or other organic or inorganic moieties.
• a chemically modified antigen-binding molecule can have a greater circulating half-life than an antigen-binding molecule that is not chemically modified.
• a derivative antigen-binding molecule is covalently modified to include one or more water soluble polymer attachments, including, but not limited to, polyethylene glycol, polyoxyethylene glycol, or polypropylene glycol.
• Peptide analogs are commonly used in the pharmaceutical industry as non-peptide drugs with properties analogous to those of the template peptide. These types of non-peptide compound are termed “peptide mimetics” or “peptidomimetics.” Fauchere, J. L., 1986, Adv. Drug Res., 1986, 15, 29; Veber, D. F. & Freidinger, R. M., 1985, Trends in Neuroscience, 8, 392-396; and Evans, B. E., et al., 1987, J. Med. Chem., 30, 1229-1239, which are incorporated herein by reference for any purpose.
• therapeutically effective amount refers to the amount of immune cells (e.g., T cells) or other therapeutic agent determined to produce a therapeutic response in a mammal. Such therapeutically effective amounts are readily ascertained by one of ordinary skill in the art.
• patient and “subject” are used interchangeably and include human and non-human animal subjects as well as those with formally diagnosed disorders, those without formally recognized disorders, those receiving medical attention, those at risk of developing the disorders, etc.
• treat and “treatment” includes therapeutic treatments, prophylactic treatments, and applications in which one reduces the risk that a subject will develop a disorder or other risk factor. Treatment does not require the complete curing of a disorder and encompasses embodiments in which one reduces symptoms or underlying risk factors.
• prevent does not require the 100% elimination of the possibility of an event. Rather, it denotes that the likelihood of the occurrence of the event has been reduced in the presence of the compound or method.
• Standard techniques can be used for recombinant DNA, oligonucleotide synthesis, and tissue culture and transformation (e.g., electroporation, lipofection).
• Enzymatic reactions and purification techniques can be performed according to manufacturer’s specifications or as commonly accomplished in the art or as described herein.
• the foregoing techniques and procedures can be generally performed according to conventional methods well known in the art and as described in various general and more specific references that are cited and discussed throughout the present specification. See, e.g., Sambrook et ak, Molecular Cloning: A Laboratory Manual (2d ed., Cold Spring Harbor Laboratory Press, Cold Spring Harbor, N.Y. (1989)), which is incorporated herein by reference for any purpose.
• the term “substantially” or “essentially” refers to a quantity, level, value, number, frequency, percentage, dimension, size, amount, weight or length that is about 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, or 99% higher compared to a reference quantity, level, value, number, frequency, percentage, dimension, size, amount, weight or length.
• the terms “essentially the same” or “substantially the same” refer to a range of quantity, level, value, number, frequency, percentage, dimension, size, amount, weight or length that is about the same as a reference quantity, level, value, number, frequency, percentage, dimension, size, amount, weight or length.
• the terms “substantially free of’ and “essentially free of’ are used interchangeably, and when used to describe a composition, such as a cell population or culture media, refer to a composition that is free of a specified substance, such as, 95% free, 96% free, 97% free, 98% free, 99% free of the specified substance, or is undetectable as measured by conventional means. Similar meaning can be applied to the term “absence of,” where referring to the absence of a particular substance or component of a composition.
• the term “appreciable” refers to a range of quantity, level, value, number, frequency, percentage, dimension, size, amount, weight or length or an event that is readily detectable by one or more standard methods.
• the terms “not- appreciable” and “not appreciable” and equivalents refer to a range of quantity, level, value, number, frequency, percentage, dimension, size, amount, weight or length or an event that is not readily detectable or undetectable by standard methods.
• an event is not appreciable if it occurs less than 5%, 4%, 3%, 2%, 1%, 0.1%, 0.001%, or less of the time.
• the term “about” or “approximately” refers to a quantity, level, value, number, frequency, percentage, dimension, size, amount, weight or length that varies by as much as 30, 25, 20, 15, 10, 9, 8, 7, 6, 5, 4, 3, 2 or 1% to a reference quantity, level, value, number, frequency, percentage, dimension, size, amount, weight or length.
• the terms “about” or “approximately” when preceding a numerical value indicates the value plus or minus a range of 15%, 10%, 5% or 1%, or any intervening ranges thereof.
• association with denotes a relationship between two events, entities and/or phenomena. Two events, entities and/or phenomena are “associated” with one another, as that term is used herein, if the presence, level and/or form of one is correlated with that of the other.
• the term "memory" T cells refers to T cells that have previously encountered and responded to their cognate antigen (e.g., in vivo, in vitro, or ex vivo) or which have been stimulated, e.g., with an anti-CD3 antibody (e.g., in vitro or ex vivo).
• Immune cells having a "memory-like" phenotype upon secondary exposure, such memory T cells can reproduce to mount a faster and stronger immune response than during the primary exposure.
• memory T cells comprise central memory T cells (TCM cells), effector memory T cells (TEM cells), tissue resident memory T cells (TRM cells), stem cell-like memory T cells (TSCM cells), or any combination thereof.
• TCM cells central memory T cells
• TEM cells effector memory T cells
• TRM cells tissue resident memory T cells
• TSCM cells stem cell-like memory T cells
• T memory stem cells refers to memory T cells that express CD95, CD45RA, CCR7, and CD62L and are endowed with the stem cell-like ability to self-renew and the multipotent capacity to reconstitute the entire spectrum of memory and effector T cell subsets.
• central memory T cells refers to memory T cells that express CD45RO, CCR7, and CD62L. Central memory T cells are generally found within the lymph nodes and in peripheral circulation.
• effector memory T cells or “TEM cells” refers to memory T cells that express CD45RO but lack expression of CCR7 and CD62L. Because effector memory T cells lack lymph node-homing receptors (e.g., CCR7 and CD62L), these cells are typically found in peripheral circulation and in non-lymphoid tissues.
• tissue resident memory T cells refers to memory T cells that do not circulate and remain resident in peripheral tissues, such as skin, lung, and gastrointestinal tract. In some aspects, tissue resident memory T cells are also effector memory T cells.
• TN cells refers to T cells that express CD45RA, CCR7, and CD62L, but which do not express CD95.
• TN cells represent the most undifferentiated cell in the T cell lineage. The interaction between a TN cell and an antigen presenting cell (APC) induces differentiation of the TN cell towards an activated TEFF cell and an immune response.
• APC antigen presenting cell
• the term “sternness,” “stem cell-like,” “stem-like,” or “less- differentiated” refers to an immune cell (e.g., a T cell or a TIL), that expresses markers consistent with a more naive phenotype.
• a less differentiated T cell can express one or more marker characteristic of a TN or a TSCM cell.
• a "less- differentiated” or “stem-like” T cell expresses CD45RA, CCR7, and CD62L.
• a “less-differentiated” or “stem-like” T cell expresses CD45RA, CCR7, CD62L, and TCF7.
• a "less-differentiated" or “stem-like” T cell does not express CD45RO or is CD45R01ow.
• the methods disclosed herein promote immune cells (e.g., T cells) having a less-differentiated phenotype.
• the methods disclosed herein block, inhibit, or limit differentiation of less-differentiated immune cells (e.g., T cells), resulting in an increased number of stem- like cells in culture. For example, it is generally thought that to effectively control tumors, adoptive transfer of less-differentiated immune cells, e.g., T cells, with a stem cell-like memory or central memory phenotype are preferred.
• Sternness is characterized by the capacity to self-renew, the multipotency, and the persistence of proliferative potential.
• sternness is characterized by a particular gene signature, e.g., a combined pattern of expression across a multitude of genes.
• the stem-like cells can be identified by a transcriptome analysis, e.g., using sternness gene signatures disclosed herein.
• the gene signature comprises one or more genes selected from ACTN1, DSC1, TSHZ2, MYB, LEF1, TIMD4, MAL, KRT73, SESN3, CDCA7L, LOC283174, TCF7, SLC16A10, LASS6, UBE2E2, IL7R, GCNT4, TAF4B, SULT1B1, SELP, KRT72, STXBP1, TCEA3, FCGBP, CXCR5, GPA33, NELL2, APBA2, SELL, VIPR1, FAM153B, PPFIBP2, FCER1G, GJB6, OCM2, GCET2, LRRN1, IL6ST, LRRC16A, IGSF9B, EFHA2, LOC129293, APP, PKIA, ZC3H12D, CHMP7, KIAA0748, SLC22A17, FLJ13197, NRCAM, C5orfl3, GIPC3, WNT7A, FAM117B, BEND5, LGM
• the gene signature comprises one or more gene selected from NOG, TIMD4, MYB, UBE2E2, FCER1G, HAVCR1, FCGBP, PPFIBP2, TPST1, ACTN1, IGF1R, KRT72, SLC16A10, GJB6, LRRN1, PRAGMIN, GIPC3, FLNB, ARRB1, SLC7A8, NUCB2, LRRC7, MY015B, MAL, AEBP1, SDK2, BZW2, GAL3ST4, PITPNM2, ZNF496, FAM117B, C16orf74, TDRD6, TSPAN32, C18orf22, C3orf44, LOC129293, ZC3H12D, MLXIP,
• nuclear cell refers to a cell found in blood that has a single, round nucleus.
• totipotent refers to the ability of a cell to give rise to any cell type found in an embryo as well as extra-embryonic (placenta) cells.
• pluripotent refers to the ability of a cell to form all lineages of the body or soma (i.e., the embryo proper but not the placenta).
• an embryonic stem cell is a type of pluripotent stem cell that is available to form cells from each of the three germ layers: the ectoderm, the mesoderm and the endoderm. Pluripotency can be determined in part, by assessing the pluripotency characteristics of the cells.
• Pluripotency characteristics may include, but are not limited to: (i) pluripotent stem cell morphology; (ii) the potential for unlimited self-renewal; (iii) ability to differentiate to all three somatic lineages (ectoderm, mesoderm and endoderm); (iv) teratoma formation consisting of the three somatic lineages; and (v) formation of embryoid bodies consisting of cells from the three somatic lineages; (vi) expression of one or more pluripotent stem cell markers including, but not limited to SSEA1 (mouse only), SSEA3/4, SSEA5, TRA1-60/81, TRA2-54 (ALP), TRA1-85, GCTM-2, TG343, TRA2-49, CD340, CD326, Podoplanin, and TG30 (CD9); (vii) expression of certain other markers associated with somatic stem cells or early differentiated cells from embryonic stem cells, including, but not limited to, integrin a ⁇ b ⁇ , CD29, CD133/promin
• multipotent refers to the ability of a cell to develop into a limited number of cell types in a particular lineage.
• non-pluripotent cell refers to any cell that does not possess full pluripotency, such as incompletely or partially pluripotent stem cells, multipotent cells, oligopotent cells, unipotent cells (e.g. progenitor cells), and terminally differentiated cells.
• introducing refers to a process that comprises contacting a cell with a polynucleotide, polypeptide, or small molecule.
• An introducing step may also comprise microinjection of polynucleotides or polypeptides into the cell, use of liposomes to deliver polynucleotides or polypeptides into the cell, or fusion of polynucleotides or polypeptides to cell permeable moieties to introduce them into a cell.
• An embodiment of the disclosure provides a method of preparing an isolated or purified population of immune cells (e.g., T cells) in vitro.
• the isolated or purified population of immune cells e.g., T cells
• “Differentiation” is the process by which a cell loses its potency and capacity for self renewal and ultimately becomes a mature and discrete cell type within a discrete lineage (see e.g., Crompton 2014, Trends in Immunol. 35:178-185).
• Dedifferentiation refers to a process by which cells become less specialized. In certain embodiments, dedifferentiation is the loss of specialization characteristics that are within the normal development path or within the same cell lineage. In certain embodiments, dedifferentiation is dedifferentiation within the same cell lineage (hierarchical dedifferentiation). However, as described herein, in another embodiment, dedifferentiation may not be within the same cell lineage.
• partial reprogramming of T cells as described herein results in cells that dedifferentiate by gaining expression of CD9 and/or CD90 and/or SSEA4, markers not usually associated with the conventional T cell lineage in humans, and which cells begin to lose expression of T cell markers CD3 and/or CD4 and/or CD8.
• dedifferentiation is not along the standard T cell hierarchical lineage.
• These cells can return to conventional T cells following stimulation with T cell activation agents.
• CD90 expression is only associated with rare populations of human T cells such as cortical thymocytes and a subset of Thl7.
• Rejuvenation is a process in which cellular function lost by cell aging is restored.
• Cell age can be described as the sum of the chronological age of the donor plus an alpha factor determined by the combination of several factors inducing stress in the cell microenvironment. These factors can be observed in vivo (e.g. heavy smoking, chronic illness including autoimmune disease, infection, obesity, metabolic problems and possibly depression) and might be artificially induced in vitro (e.g. long exposure to tumor antigens or other stimulation, high levels of cytokines, hypoxia etc.). Cells that become older due to chronological age or as a product of continual strong stress stimuli are known as senescent cells.
• Several cellular processes have been identified as compromised by cell age such as chronological age, tumor antigen specificity, killer cell properties, proliferation ability, metabolism, DNA repair system abrogation, telomere length and loss of sternness potential.
• Rejuvenated T cell refers to a T cell that has been contacted with one or more reprogramming factors for a period of time sufficient for the T cells to begin to attach to the culture vessel surface to form T cell derived adherent cells that return to a functioning T cell after stimulation with a T cell activation agent and optionally, an immunomodulatory molecule.
• the methods described herein produce rejuvenated T cells that provide any one or more of increased in vivo proliferation, survival, persistence, and/or cytotoxicity; reduced epigenetic age, increased telomere length, improved metabolism, decreased apoptosis and other markers associated with cell senescence and improved anti-tumor activity as compared to terminally differentiated T cells.
• rejuvenated T cells exhibit a polyclonal TCR repertoire and the capacity for long term in vivo engraftment.
• Rejuvenated T cells may exhibit biological and phenotypic characteristics of younger T cells in terms of epigenetic signature, telomere length, metabolic activity and functionality.
• the partial reprogramming process as described herein may cause the T cell to partially dedifferentiate, e.g., to lose certain aspects of the T cell phenotype, which are regained through T cell activation through TCR signaling and/or culturing in an appropriate media.
• the rejuvenated T cells can be used to target cancers, viruses, or autoimmune diseases.
• the partially reprogrammed T cells can be used to reconstitute the whole adaptive immune system or alleviate immunocompromised patients.
• the T cells are partially reprogrammed and rejuvenated through transient expression of reprogramming factors.
• the morphology and cell surface expression profile of the T cells begins to change.
• the cell begins to express certain cell surface markers and the expression of T cell markers decreases.
• the cell begins to express certain cell surface markers and the expression of T cell markers decreases from about day 5 of partial reprogramming, indicating that the dedifferentiation process has initiated.
• the dedifferentiated T cells are stimulated with one or more T cell activating molecules, such as anti-CD3 antibodies or other CD3 agonist, and cultured in a T cell culture condition.
• this T cell stimulation also referred to herein as “reactivation”
• the reactivated T cells have characteristics of much younger cells based on the epigenetic clock analysis, have a more stem-like phenotype and have acquired high proliferating potential.
• transient means for a period of time sufficient to achieve partial reprogramming of one or more T cells, (e.g., a period of time sufficient for T cell derived adherent cells to form, but not long enough to transform the one or more T cells into iPS cells or totipotent cells).
• “transiently contacting” with one or more reprogramming factors means contacting with one or more reprogramming factors for a period of time which is sufficient for T cell derived adherent cells to form, or for the one or more T cells to form at least one colony attached to a culture vessel surface, but not a period of time long enough to permit the one or more T cells to transform into iPS cells or totipotent cells.
• “transiently contacting” with one or more reprogramming factors means contacting with one or more reprogramming factors for a period of time which is sufficient for T cell derived adherent cells to form, or for the one or more T cells to form at least one colony attached to a culture vessel surface, but not a period of time long enough to permit the one or more T cells to transform into iPS cells or totipotent cells.
• “transiently contacting” can mean contacting for a period of time of up to 1 day, or up to 2 days, or up to 3 days, or up to 4 days, or up to 5 days, or up to 6 days, or up to 7 days, or up to 8 days, or up to 9 days, or up to 10 days, or up to 11 days, or up to 12 days, or up to 13 days, or up to 14 days.
• transiently expressing or “transient expression” or the like means expression or causing expression of one or more of the Yamanaka factors so as to achieve partial reprogramming of one or more T cells (i.e., where transformation to an iPS cell or totipotent cell is not achieved).
• epigenetic age means the age of a cell as determined using known epigenetic clocks, e.g., the Horvath Clock, the Hannum Clock or the Levine Clock (see, e.g., Horvath et ak, 2018, Aging 10, 1758-1775; Hannum et al ⁇ 2013, Mol. Cell. 49(2), 359-367; Levine et ak, 2018, Aging, 10(4):573-592).
• the eAge is the age of a cell as determined using the Horvath Clock method of measuring methylation status at 353 CpGs (Horvath and Raj, 2018 Nature Reviews Genetics, 19:371-385).
• T cells that are differentiated from iPS cells in absence of an autologous thymic education, lack true T cell function and possess abnormalities including immature phenotype, non MHC dependent killing, improper CD8o$ dimerization, dysregulation of gene expression and failure to produce a developmentally homogeneous population of T cells. Vizcardo et ak, 2018, Cell Rep 22, 3175-3190.
• the rejuvenated T cells generated using the partial reprogramming methods described herein provide unexpected and advantageous properties over T cells generated using methods known in the art.
• the present disclosure relates to a method of producing rejuvenated T cells.
• the method comprises (i) transiently contacting a population of T cells with at least one reprogramming factor for a period of time sufficient to achieve partial reprogramming and wherein said T cells are not transformed into iPS cells; and (ii) contacting the partially reprogrammed T cell with at least one T cell activating compound or agent and, optionally, one or more immunomodulating agent.
• the present disclosure relates to a method of producing rejuvenated T cells.
• the method comprises (i) transiently contacting a population of T cells with at least one reprogramming factor selected from the group consisting of KLF4, OCT3/4, SOX2, NANOG, LIN28, L-MYC and C-MYC; and optionally SV40 for a period of time sufficient to achieve partial reprogramming, wherein said T cells are not transformed into iPS cells; and (ii) contacting the partially reprogrammed T cell with at least one T cell activating compound or agent and, optionally, one or more immunomodulating agent.
• the present disclosure relates to a method of producing rejuvenated T cells.
• the method comprises (i) contacting a population of T cells with at least one reprogramming factor selected from the group consisting of KLF4, OCT3/4, SOX2, NANOG, LIN28, L-MYC and C-MYC; and optionally SV40 for a period of time sufficient for formation of T cell derived adherent cells and wherein said T cells are not transformed into iPS cells; and (ii) contacting the T cell derived adherent cells with at least one T cell activating compound or agent and/or a T cell costimulatory agent, and optionally, one or more immunomodulating agent.
• reprogramming refers to the process of erasing and/or re-establishing epigenetic modifications acquired during mammalian cell development or in cell culture.
• muscle cells can be reprogrammed to a neuron.
• Reprogramming is not intrinsically related to aging and rejuvenation (see e.g., Takahashi et al., Cell (2007) 131, 861-872)
• Complete reprogramming refers to reprogramming of a somatic cell to a pluripotent stem (iPS) cell or a totipotent stem cell.
• Partial reprogramming refers to a process of reprogramming without reaching a totipotent stem cell state or a pluripotent stem cell state (iPS cell).
• iPS cell pluripotent stem cell state
• partial preprogramming is any reprogramming that is not complete reprogramming.
• Partial or “incomplete” or “transient” reprogramming is reprogramming that is not complete reprogramming, e.g., as compared to a cell that has been completely reprogrammed to an iPS cell.
• partial reprogramming is reprogramming carried out from about 1 to about 20 days.
• partial reprogramming is reprogramming carried out for about 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, or about 25 days.
• partial T cell reprogramming is a reprogramming process carried out until T cell reactivation is initiated.
• partial T cell reprogramming is a reprogramming process that is carried out at least until the T cells begin to lose expression of one or more T cell markers and/or begin to express markers associated with a non-T cell lineage.
• partial T cell reprogramming is a process of reprogramming carried out for a period of time up to the time that the T cells can no longer be returned to a cell expressing CD3, CD4 and/or CD8 by reactivation with a T cell activation agent.
• Partially reprogrammed T cell refers to a T cell that has been reprogrammed without reaching a totipotent stem cell state or a pluripotent stem cell state (iPS cells).
• partial reprogramming of a T cell is incomplete and/or partial and/or transient reprogramming compared to an iPS cell.
• a partially reprogrammed T cell refers to a T cell that has been reprogrammed by contacting the T cells with one or more reprogramming factors for a period of time such that the T cells form T cell derived adherent cells.
• the T cell derived adherent cells are loosely attached to the culture vessel surface.
• T cell derived adherent cells as described herein retain lineage stability e.g., return to the T cell lineage after stimulation (reactivation) with a T cell activation agent and optionally an immunomodulatory molecule (e.g. cytokines).
• a T cell activation agent e.g. cytokines
• the T cell derived adherent cells are semi-adherent, loosely adherent, adherent, or strongly adherent (strongly attached).
• the cells useful in the methods of partial reprogramming described herein in some embodiments are derived from primary cells, e.g., primary human cells.
• the samples include tissue, fluid, and other samples taken directly from the subject, as well as samples resulting from one or more processing steps, such as separation, centrifugation, genetic engineering (e.g. transduction with viral vector), washing, and/or incubation.
• the biological sample can be a sample obtained directly from a biological source or a sample that is processed.
• Biological samples include, but are not limited to, body fluids, such as blood, plasma, serum, cerebrospinal fluid, synovial fluid, urine and sweat, tissue and organ samples, including processed samples derived therefrom.
• the sample from which the cells are derived or isolated is blood or a blood-derived sample, or is or is derived from an apheresis or leukapheresis product.
• Exemplary samples include whole blood, peripheral blood mononuclear cells (PBMCs), leukocytes, bone marrow, thymus, tissue biopsy, tumor, leukemia, lymphoma, lymph node, gut associated lymphoid tissue, mucosa associated lymphoid tissue, spleen, other lymphoid tissues, liver, lung, stomach, intestine, colon, kidney, pancreas, breast, bone, prostate, cervix, testes, ovaries, tonsil, or other organ, and/or cells derived therefrom.
• Samples include, in the context of cell therapy, e.g., adoptive cell therapy, samples from autologous and allogeneic sources.
• the cells for use in the partial reprogramming methods are derived from cell lines, e.g., T cell lines.
• the cells in some embodiments are obtained from a xenogeneic source, for example, from mouse, rat, non-human primate, and pig.
• the present disclosure relates to isolating T cells from a source and partially reprogramming said T cells to ameliorate aging and improving the function of the T cells.
• suitable source cells include, but are not limited to, peripheral blood mononuclear cells (PBMCs).
• T cells for use in the methods herein may include, but are not limited to, cultured T cells, e.g., primary T cells or T cells from a cultured T cell line, e.g., Jurkat, SupTl, etc., or T cells obtained from a mammal.
• the source cells can be obtained from numerous sources, including but not limited to blood, bone marrow, lymph node, tumor, thymus, spleen, or other tissues or fluids. Source cells can also be enriched for or purified.
• the T cells can be any type of T cells and can be of any developmental stage, including but not limited to CD4+CD8o$+ double positive T cells, CD4+ helper T cells, e.g., Thl and Th2 cells, CD4+ T cells, CD8+ T cells (e.g., cytotoxic T cells), peripheral blood mononuclear cells (PBMCs), peripheral blood leukocytes (PBLs), tumor infiltrating cells (TILs), memory T cells, naive T cells, and the like.
• CD4+CD8o$+ double positive T cells CD4+ helper T cells, e.g., Thl and Th2 cells
• CD4+ T cells e.g., CD4+ T cells
• CD8+ T cells e.g., cytotoxic T cells
• PBMCs peripheral blood mononuclear cells
• PBLs peripheral blood leukocytes
• TILs tumor infiltrating cells
• memory T cells naive T cells, and the like.
• the T cells are isolated from tumors, in particular the T cells for use in the partial reprogramming methods described herein are TILs.
• TILs are TILs.
• TILs tumor infiltrating lymphocytes
• TILs include, but are not limited to, CD8+ cytotoxic T cells (lymphocytes), Thl and Thl7 CD4+ T cells, natural killer cells, dendritic cells and Ml macrophages.
• TILs include both primary and secondary TILs.
• Primary TILs are those that are obtained from patient tissue samples as outlined herein (sometimes referred to as “freshly harvested”).
• TILs can be categorized by expressing one or more of the following biomarkers: CD4, CD 8, TCRo$, CD27, CD28, CD56, CCR7, CD45Ra, CD95, PD-1, and CD25.
• the source cells may have a naive T cell ((TN) phenotype, central memory T cell (TCM) phenotype, or effector memory T cell (TEM) phenotype, stem-like T cell (Tscm).
• TN naive T cell
• TCM central memory T cell
• TEM effector memory T cell
• Tscm stem-like T cell
• CCR7 and CD62L are expressed by TN and TCM cells, but are not expressed by TEM cells.
• the transcription factors LEF1, FOXP1 and KLF7 are expressed by TN and TCM cells, but are not expressed by TEM cells.
• CD45RO and KLRG1 are not expressed by TN cells, but are expressed by TEM cells.
• TN and TCM cells may be characterized by longer telomeres as compared to those of TEM cells.
• a specific subpopulation of T cells such as CD3+, CD45+, CD137+, CD25+, CD28+, CD4+, CD8+, CD45RA+, GITR+, and/or CD45RO+ T cells, can be isolated by positive or negative selection techniques (e.g., using fluorescence-based or magnetic-based cell sorting).
• T cells can be isolated by incubation with any of a variety of commercially available antibody-conjugated beads, such as Dynabeads®, CELLectionTM, DETACHaBEADTM (Thermo Fisher) or MACS® cell separation products (Miltenyi Biotec), for a time period sufficient for positive selection of the desired T cells or negative selection for removal of unwanted cells.
• antibody-conjugated beads such as Dynabeads®, CELLectionTM, DETACHaBEADTM (Thermo Fisher) or MACS® cell separation products (Miltenyi Biotec
• the T cells are cultured in an appropriate culture media.
• T cell culture conditions are known in the art.
• the media for culturing the T cells here in certain embodiments may be carried out from a starting media, referred to as a "basal" media.
• Basal media refers to any starting media that is supplemented with one or more of the additional elements disclosed herein, e.g., glucose, one of a variety of salts, one or more cytokines, such as IL-2, IL-7, IL-15, IL-21, or any combination thereof.
• the basal media can be any media for culturing immune cells, e.g., T cells.
• the basal media comprises a balanced salt solution (e.g., PBS, DPBS, HBSS, EBSS), Dulbecco's Modified Eagle's Medium (DMEM), Click’s medium, Minimal Essential Medium (MEM), Basal Medium Eagle (BME), F-10, F-12, RPMI 1640, Glasgow Minimal Essential Medium (GMEM), alpha Minimal Essential Medium (alpha MEM), Iscove's Modified Dulbecco's Medium (IMDM), M199, OPTMIZERTM Pro, OPTMIZERTM CTSTM T-Cell Expansion Basal Medium (ThermoFisher), OPTMIZERTM, OPTMIZERTM Complete, IMMUNOCULTTM XF (STEMCELLTM Technologies), AIM VTM, TEXMACSTM medium, PRIME-XV® T cell CDM, X-VIVOTM 15 (Lonza), TRANSACTTM TIL expansion medium, , or any combination thereof.
• a balanced salt solution e.g
• the basal medium is serum free.
• the basal media comprises PRIME- XV® T cell CDM.
• the basal media comprises OPTMIZERTM.
• the basal media comprises OPTMIZERTM Pro.
• the basal medium further comprises immune cell serum replacement (ICSR).
• cytokine refers to small, secreted proteins released by cells that have a specific effect on the interactions and communications between cells.
• Non-limiting examples of cytokines include interleukins (e.g., interleukin (IL)-l, IL-2, IL-4, IL-7, IL-9, IL- 13, IL-15, IL-3, IL-5, IL-6, IL-11, IL-10, IL-20, IL-14, IL-16, IL-17, IL-21 and IL-23), interferons (IFN; e.g., IFN-a, IFN-b, and IFN-g), tumor necrosis factor (TNF) family members, and transforming growth factor (TGF) family members.
• IFN interferons
• TGF tumor necrosis factor
• Some aspects of the present disclosure are directed to methods of culturing and/or expanding immune cells, e.g., T cells or one or more engineered immune cell disclosed herein, in a medium comprising a cytokine.
• the cytokine is an interleukin.
• the cytokine comprises IF-2, IF-7, IL- 15, IL-21 or any combination thereof.
• the T cells for use in the partial reprogramming methods herein are TCRo$ cells.
• the TCRo ⁇ cells may express a functional, antigen-specific T cell receptor (TCR) including both an alpha (a) chain and a beta (b) chain.
• TCR alpha and beta chains are known in the art.
• the TCR can comprise any amino acid sequence, provided that the TCR can specifically bind to and immunologically recognize an antigen.
• the TCR may have antigenic specificity for any desired antigen.
• antigen-specific and antigenic specificity mean that the TCR can specifically bind to and immunologically recognize an antigen, e.g., a condition-specific antigen, or an epitope thereof, such that biding of the TCR to an antigen, or the epitope thereof, elicits an immune response.
• an antigen e.g., a condition-specific antigen, or an epitope thereof, such that biding of the TCR to an antigen, or the epitope thereof, elicits an immune response.
• the mammal from which a T cell is isolated is immunized with an antigen of, or specific for, a condition.
• the mammal is immunized prior to obtaining the T cell from the mammal.
• the isolated T cell can include T cells induced to have specificity for the condition to be treated, or include a higher proportion of cells specific for the condition.
• a T cell comprising an endogenous antigen-specific TCR can be a T cell within a mixed population of cells isolated from a mammal.
• the mixed population can be exposed to the antigen which is recognized by the endogenous TCR while being cultured in vitro.
• the T cell which comprises the TCR that recognizes the condition- specific antigen expands or proliferates in vitro, thereby increasing the number of T cells having the endogenous antigen-specific receptor.
• the antigen-specific TCR can be an exogenous TCR, i.e., an antigen-specific TCR that is not native to (not naturally-occurring on) the T cell.
• a recombinant TCR is a TCR which has been generated through recombinant expression of one or more exogenous TCR a-, b-, g-, and/or d-chain encoding genes.
• a recombinant TCR can comprise polypeptide chains derived entirely from a single mammalian species, or the antigen- specific TCR can be a chimeric or hybrid TCR comprised of amino acid sequences derived from TCRs from two-different mammalian species.
• the antigen-specific TCR can comprise a variable region derived from a murine TCR, and a constant region of a human TCR such that the TCR is “humanized.”
• Methods of making recombinant TCRs are known in the art. See, e.g., U.S. Pat. Nos. 7,820,174; 8,785,601; 8,216,565; and U.S. Patent Application Publication No. 2013/0274203.
• a T cell comprising an endogenous antigen-specific TCR can also be transformed, e.g., transduced or transfected, with one or more nucleic acids encoding an exogenous (e.g., recombinant) TCR or other recombinant chimeric receptor.
• exogenous chimeric receptors e.g., chimeric CRs
• a T cell comprising an endogenous antigen-specific TCR can also be transformed, e.g., transduced or transfected, with one or more nucleic acids encoding a “chimeric antigen receptor” (CAR).
• CAR comprises the antigen binding domain of an antibody, e.g., a single-chain variable fragment (scFv), fused to the transmembrane and intracellular domains of a TCR; and in some embodiments, one or more costimulatory domains such as an intracellular signaling region of a T cell costimulatory molecule.
• the antigenic specificity of a TCR can be encoded by a scFv which specifically binds to the antigen, or an epitope thereof.
• Methods of making such CARs are known in the art. See, e.g., U.S. Pat. Nos. 8,465,743, 10,533,055, 10,603,380 and U.S. Patent Application Publication Nos.
• any suitable nucleic acid encoding a CAR, engineered TCR, or TCR-like protein or polypeptide can be used.
• the partial reprogramming process as discussed further below, can occur before, after or simultaneously with, genetic modification of a T cell with a CAR, engineered TCR or TCR-like protein or polypeptide.
• the CAR or engineered TCR encoded by the nucleic acids can be of any suitable form including for example, a single-chain CAR or TCR or a fusion with other proteins or polypeptides (e.g., without limitation co-stimulatory molecules).
• the antigen which is recognized by the T cells herein, whether by the endogenous antigen-specific TCR, an engineered TCR or CAR, can be any antigen which is associated with a condition.
• the antigen may be, but is not limited to, a cancer antigen (also termed a tumor antigen or a tumor- associated antigen) or an infectious condition antigen (e.g., a viral antigen.
• a cancer antigen also termed a tumor antigen or a tumor- associated antigen
• infectious condition antigen e.g., a viral antigen.
• Viral antigens are known in the art and include, for example, any viral protein, e.g., env, gag, pol, gpl20, thymidine kinase, and the like).
• the antigen is or is derived from CD19, TRAC, TCR , BCMA, CLL-1, CS1, CD38, CD19, TSHR, CD123, CD22, CD30, CD70, CD171, CD33, EGFRvIII, GD2, GD3, Tn Ag, PSMA, ROR1, ROR2, GPC1, GPC2, FLT3, FAP, TAG72, CD44v6, CEA, EPCAM, B7H3, KIT, IL- 13Ra2, mesothelin, IL-1 IRa, PSCA, PRSS21, VEGFR2, LewisY, CD24, PDGFR-beta, SSEA-4, CD20, folate receptor alpha, ERBB2 (Her2/neu), MUC1, MUC16, EGFR, NCAM, prostase, PAP, ELF2M, Ephrin B2, IGF-I receptor, CAIX, LMP2, gplOO, bcr-abl, tyros
• the CAR or engineered TCR targets AFP, CD19, TRAC, TCR , BCMA, CLL-1, CS1, CD38, CD19, TSHR, CD123, CD22, CD30, CD171, CD33, EGFRvIII, GD2, GD3, Tn Ag, PSMA, ROR1, ROR2, GPC1, GPC2, FLT3, FAP, TAG72, CD44v6, CEA, EPCAM, B7H3, KIT, IL- 13Ra2, mesothelin, IL-1 IRa, PSCA, PRSS21, VEGFR2, LewisY, CD24, PDGFR-beta, SSEA-4, CD20, folate receptor alpha, ERBB2 (Her2/neu), MUC1, MUC16, EGFR, NCAM, prostase, PAP, ELF2M, Ephrin B2, IGF-I receptor, CAIX, LMP2, gplOO, bcr-abl, tyros
• cancer antigen refers to any molecule (e.g., protein, polypeptide, peptide, lipid, carbohydrate, etc.) solely or predominantly expressed by or over-expressed by a tumor cell or cancer cell, such that the antigen is associated with the tumor or cancer.
• the cancer antigen can be, for example, a mutated tumor antigen or neoantigen.
• the cancer antigen can additionally be expressed by normal, non-tumor, or non-cancerous cells. However, in such cases the expression of the cancer antigen by normal, non-tumor, or non-cancerous cells is not as robust as the expression by tumor or cancer cells.
• the tumor or cancer cells can over-express the antigen or express the antigen at a significantly higher level, as compared to the expression of the antigen by normal, non-tumor or non-cancerous cells.
• the cancer antigen can additionally be expressed by cells of a different state of development or maturation.
• the cancer antigen can be additionally expressed by cells of the embryonic or fetal stage, which cells are not normally found in an adult mammal.
• the cancer antigen can be additionally expressed by stem cells or precursor cells, which cells are not normally found in an adult mammal.
• Cancer antigens are known in the art and include, for instance, the cancer antigens listed above, shared tumor antigens such as, e.g., mesothelin, CD19, CD22, CD276 (B7H3), gplOO, MART-1, Epidermal Growth Factor Receptor Variant III (EGFRVIII), TRP-1, KRAS, TRP-2, tyrosinase, NY-ESO-1 (also known as CAG-3), MAGE-1, MAGE-3, etc.
• the cancer antigen is a patient-specific neoantigen.
• a patient-specific neoantigen may arise as a consequence of a tumor- specific mutation.
• the cancer antigen can be an antigen expressed by any cell of any cancer or tumor, including the cancers and tumors described herein.
• the cancer antigen may be a cancer antigen of only one type of cancer or tumor, such that the cancer antigen is associated with or characteristic of only one type of cancer or tumor.
• the cancer antigen may be a cancer antigen (e.g., may be characteristic) of more than one type of cancer or tumor.
• the cancer antigen may be expressed by both breast and prostate cancer cells and not expressed at all by normal, non- tumor, or non-cancer cells.
• the condition which is associated with or is characterized by the antigen recognized by the TCR or CAR can be any condition.
• the condition can be a cancer or an infectious condition, e.g., a viral condition, as discussed herein.
• the cancer may be any cancer, including any of sarcoma, carcinoma, acute lymphocytic cancer, acute myeloid leukemia, alveolar rhabdomyosarcoma, bone cancer, brain cancer, breast cancer, cancer of the anus, anal canal, or anorectum, cancer of the eye, cancer of the intrahepatic bile duct, cancer of the joints, cancer of the neck, gallbladder, or pleura, head and neck cancers (e.g., cancer of the nose, nasal cavity, or middle ear, cancer of the oral cavity), cancer of the vulva, chronic lymphocytic leukemia, chronic myeloid cancer, colon cancer, esophageal cancer, cervical cancer, gastrointestinal carcinoid tumor, Hodgkin lymphoma, hypopharynx cancer, kidney cancer, larynx cancer, liver cancer, lung cancer, malignant mesothelioma, melanoma, multiple myeloma, nasopharynx cancer
• viral condition means a condition that can be transmitted from person to person or from organism to organism, and is caused by a vims.
• the viral condition is caused by a virus selected from the group consisting of herpes viruses, pox viruses, hepadnaviruses, papilloma viruses, adenoviruses, coronaviruses, orthomyxoviruses, paramyxoviruses, flaviviruses, and caliciviruses.
• the viral condition may be caused by a virus selected from the group consisting of respiratory syncytial virus (RSV), influenza vims, herpes simplex virus, Epstein-Barr vims, varicella virus, cytomegalovirus, hepatitis A vims, hepatitis B virus, hepatitis C virus, human immunodeficiency virus (HIV), human T-lymphotropic virus, calicivirus, adenovirus, and Arena virus.
• RSV respiratory syncytial virus
• influenza vims herpes simplex virus
• Epstein-Barr vims varicella virus
• cytomegalovirus cytomegalovirus
• hepatitis A vims hepatitis B virus
• hepatitis C virus hepatitis C virus
• HAV human immunodeficiency virus
• human T-lymphotropic virus calicivirus
• adenovirus adenovirus
• the viral condition may be, for example, influenza, pneumonia, herpes, hepatitis, hepatitis A, hepatitis B, hepatitis C, chronic fatigue syndrome, sudden acute respiratory syndrome (SARS), gastroenteritis, enteritis, carditis, encephalitis, bronchiolitis, respiratory papillomatosis, meningitis, HIV / AIDS, and mononucleosis.
• influenza influenza
• pneumonia herpes
• hepatitis hepatitis A
• hepatitis B hepatitis C
• chronic fatigue syndrome hepatitis
• SARS sudden acute respiratory syndrome
• gastroenteritis enteritis
• carditis carditis
• encephalitis encephalitis
• bronchiolitis respiratory papillomatosis
• meningitis HIV / AIDS
• mononucleosis mononucleosis.
• T cells for use in the partial reprogramming methods of the present disclosure can be isolated or purified from a source using any suitable technique known in the art.
• the immune cells e.g., T cells
• the immune cells may be obtained from a subject.
• Immune cells e.g., T cells
• PBMCs peripheral blood mononuclear cells
• immune cells can be obtained from a unit of blood collected from the subject using any number of techniques known to the skilled person, such as FICOLLTM separation.
• Cells may preferably be obtained from the circulating blood of an individual by apheresis.
• the apheresis product typically contains lymphocytes, including T cells, monocytes, granulocytes, B cells, other nucleated white blood cells, red blood cells, and platelets.
• the cells collected by apheresis may be washed to remove the plasma fraction, and placed in an appropriate buffer or media for subsequent processing. The cells may be washed with PBS.
• a washing step may be used, such as by using a semiautomated flowthrough centrifuge for example, the CobeTM 2991 cell processor, the Baxter Cyto-MateTM, or the like.
• the cells may be resuspended in a variety of biocompatible buffers, or other saline solution with or without buffer.
• the undesired components of the apheresis sample may be removed.
• the present disclosure relates in part to methods for partially reprogramming T cells.
• the T cells are partially reprogrammed by contacting the T cells with one or more reprogramming factors for a period of days such that one or more of the T cells form colonies attached (or partially attached) to the culture vessel surface (form T cell derived adherent cell colonies) where such adherent cells return to a functioning T cell after stimulation (reactivation) with a T cell activation agent and optionally an immunomodulatory molecule (e.g. cytokines)
• an immunomodulatory molecule e.g. cytokines
• reprogramming factors refers to any protein, polypeptide, amino acid, mRNA, DNA or small molecule capable of erasing and/or reestablishing epigenetic modifications acquired during mammalian cell development or in cell culture. Reprogramming factors can alter the differentiational state of a cell.
• Such reprogramming factors can include, but are not limited to the transcription factors, OCT4 (or OCT3/4), SOX3, KLF4 and C-MYC, discovered by Yamanaka and colleagues (see, e.g., Takahashi and Yamanaka, 2006, Cell, 136, 364-377) which are referred to herein as “OSKM” or the “Yamanaka factors.”
• Reprogramming factors refers to other factors that might alter the differentiation state of a cell, or that might enhance or alter the efficiency of cell reprogramming. Such factors are known in the art. Exemplary reprogramming factors are described in Feng et al. 2009, Cell Stem Cell Review, 4:301-313.
• the reprogramming factor is at least one of the groups consisting of KLF4, OCT3/4, SOX2, C-MYC and SV40.
• the reprogramming factor is at least one of the groups consisting of KLF4, OCT3/4, SOX2, C-MYC and SV40.
• not all of the four Yamanaka Factors are stringently necessary (see e.g., Genome Biol. 2012; 13(10):
• the isolated immune cells are contacted with OCT3/4 and SOX2.
• the isolated immune cells are contacted with OCT3/4, SOX2 and C-MYC.
• the isolated cells are contacted with OCT3/4, SOX2 and KFF4.
• the T cells are contacted with OCT3/4, SOX2 and KFF4, and either C-MYC or SV40.
• Additional reprogramming factors may be used in various embodiments to partially reprogram the isolated immune cells (e.g., T cells). Such factors include, but are not limited to, FIN28, NANOG, Esrrb, Pax5 shRNA, C/EBPa, p53 siRNA, UTF1, DNMT shRNA, Wnt3a, GEIS1, DEX4, CDH1, SV40 ET(T) and hTERT.
• reprogramming factors may upregulate or downregulate certain miRNAs involved in reprogramming.
• a reprogramming factor may upregulate or downregulate expression of one or more of the genes upstream or downstream of one or more of the Yamanaka Factors.
• the one or more reprogramming factors may include, but are not limited to, histone methyltransferase inhibitors, F-type calcium channel agonists, G9a methyltransferase inhibitors, DNA methyltransferase inhibitors, histone deacetylase inhibitors, MEK inhibitors, GSK3 inhibitors or TGF-B inhibitors. Any factor that modulates the upstream or downstream molecular pathway of the reprogramming transcription factors is contemplated for use in the partial reprogramming methods herein.
• Illustrative inhibitors include, but are not limited to BIX01294, BayK 8644, CHIR 99021, Forskolin, and RepSox.
• serine/threonine-protein kinase B-Raf (BRAF) inhibitors may be used in the reprogramming methods herein (see, e.g., US2017114323).
• BRAF serine/threonine-protein kinase B-Raf
• EGFR epidermal growth factor receptor
• VEGFR1 vascular endothelial growth factor 1
• FGFR1 fibroblast growth factor receptor 1
• the present disclosure relates to a method of producing a rejuvenated T cell, wherein the T cell is transiently contacted with at least one reprogramming factor selected from the group selected from KFF4, OCT3/4, SOX2 and C-MYC.
• the isolated immune cells e.g., T cells
• KFF4, OCT3/4, SOX2 and C-MYC and optionally SV40 are transiently contacted with KFF4, OCT3/4, SOX2 and C-MYC and optionally SV40.
• one or more reprogramming factors is transiently expressed in the isolated immune cells (e.g., T cells).
• the one or more reprogramming factors may include one or more or all of KLF4, OCT3/4, SOX2 and C-MYC; or may additionally include one or more other reprogramming factors.
• the reprogramming factors may be expressed in the isolated T cells using a gene editing technology (e.g. TALENS, CRISPR/cas) known in the art.
• the gene editing technology delivers an inducible set of reprogramming factors to be expressed in the isolated T cells.
• the nucleic acid(s) encoding the stem cell- associated gene/s is/are carried in one or more recombinant expression vectors.
• the recombinant expression vector(s) can comprise any type of nucleotides, including, but not limited to DNA and RNA, which can be single-stranded or double-stranded, synthesized or obtained in part from natural sources, and which can contain natural, non-natural or altered nucleotides.
• the recombinant expression vector(s) can comprise naturally-occurring or non- naturally-occurring internucleotide linkages, or both types of linkages.
• the vector(s) may contain regulatory nucleic acid sequences which provide for expression of the stem cell- associated genes.
• the recombinant expression vector is a viral vector.
• Suitable viral vectors include, without limitation, Sendai vims vectors, retroviral vectors, lentiviral vectors, alphaviral, vaccinia, adenoviral, adeno- associated viral, herpes viral, and fowl pox viral vectors, and preferably have a native or engineered capacity to transform immune cells (e.g., T cells).
• the viral vectors are pseudotyped with a heterologous viral envelope protein in certain embodiments, the viral vector is a lentivirus or Sendai virus vector pseudotyped with a suitable envelope, e.g., a vims envelope (see e.g., Blood Adv 2017 Oct 24;1(23):2088-2104; Mol Ther 2012 Sep;20(9):1699-712).
• the viral vector is an integration deficient lentiviral vector. Suitable viral vectors are known in the art and described, for example, in J. Biol. Chem. (2011) 286:4760-4771; Stem Cell Research & Therapy (2019) 10:185.
• the recombinant expression vector is delivered in a nanoparticle.
• the reprogramming factors are delivered using a nanoparticle.
• Such nanoparticles can be designed to deliver specific mRNA or other macromolecules to lymphocytes in a transient and dose-controlled manner. These nanoparticles can be designed to target specific cell subtypes and, upon binding to them, stimulate receptor mediated endocytosis, thereby introducing the synthetic mRNA they carry which the cells can now express. Because nuclear transport and transcription of the transgene are not required, this process is fast and efficient.
• one or more reprogramming vectors are delivered to the immune cells (e.g., T cells) in separate vectors.
• the immune cells e.g., T cells
• SOX2 are delivered in a single vector.
• the vector expressing KOS is a viral vector and is delivered at a titer of 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 15, 20, 25, or 30 MOIs (Multiplicity of Infection).
• KLF4 is delivered in a viral vector at a titer of 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 15, 20, 25, or 30 MOIs.
• cMyc is delivered in a viral vector at a titer of 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 15, 20, 25, or 30 MOIs.
• a vector expressing SV40 is further delivered to the cell and is a viral vector delivered at a titer of 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 15, 20, 25, or 30 MOIs.
• the immune cells e.g., T cells
• the T cell is contacted with a Sendai vector expressing KOS at 10 MOI, a Sendai vector expressing KLF4 at 10 MOI, a Sendai vector expressing C- MYC at 3 MOI, and a Sendai vector expressing SV40 at 5 MOI.
• the T cell is contacted with a multicistronic vector, such as a lentiviral vector, a Sendai vims vector or a non- viral vector, expressing KOSM.
• the T cells prior to being contacted with the one or more reprogramming factors the T cells are stimulated with a T cell activating agent and optionally one or more immunomodulatory molecules, for a time sufficient to stimulate and activate the T cells.
• the T cells are stimulated with tumor antigen or with autologous tumor cells or tumor cell line.
• the T cells are TILs and the TILs are stimulated with tumor target cells or tumor antigen derived therefrom, from the cancer patient, or one or more tumor- associated antigen.
• tumor-associted antigens include: AFP (alpha-fetoprotein), anb ⁇ or another integrin, BCMA, BRAF, B7-H3, B7-H6, CA9 (carbonic anhydrase 9), (carcinoembryonic antigen), Claudin 18.2, Claudin 6, c-MET, DFF3 (delta-like protein 3), DFF4, ENPP3 (ectonucleotide pyrophosphatase/phosphodiesterase family member 3),
• EpCAM EpCAM, EPG-2 (epithelial glycoprotein 2), EPG-40, ephrinB2, EPHa2 (ephrine receptor A2), ERBB dimers, estrogen receptor, ETBR (endothelin B receptor), FAP-a (fibroblast activation protein a), fetal AchR (fetal acetylcholine receptor), FBP (a folate binding protein), FCRL5, FR-a (folate receptor alpha), GCC (guanyl cyclase C), GD2, GD3, GPC2 (glypican-2), GPC3, gplOO (glycoprotein 100), GPNMB (glycoprotein NMB), GPRC5D (G Protein Coupled Receptor 5D), HER2, HER3, HER4, hepatitis B surface antigen, melanoma-associated antigen (MAGE)-Al, MAGE- A3, MAGE-A6, MART-1 (melan A), mesothelin, mucin 1 (M
• polyclonal antigen-specific (e.g., tumor-specific) T cells from cancer patients can be partially reprogrammed and rejuvenated.
• the T cells are selected, sorted, or otherwise enriched for following stimulation with an antigen, such as tumor antigen, tumor organoid, autologous tumor cells or tumor cell line.
• the T cells are enriched, selected for or sorted by selecting for cells expressing one or more cell surface markers, such as 4-1BB (CD137), PD1, LAG3, CD45, CD39, TIGIT, TIM3, CD69, 0X40, CD28, CD25, CD49d, and CTLA4.
• the T cells are enriched, selected for or sorted before activation with any of the T cell activating agents described herein.
• CD45+ T cells are selected for or enriched prior to activation with any of the activation agents described herein.
• the methods include activating the cells prior to, during and/or subsequent to the incubation of cells with the viral vector particles.
• the stimulating conditions may include incubation of cells in the presence of an agent capable of activating one or more intracellular signaling domains of one or more components of a TCR complex, such as a primary agent that specifically binds to a member of a TCR complex, e.g., CD3, and a secondary agent that specifically binds to a T cell costimulatory molecule, e.g., CD28, CD27, CD137 (4-1BB), 0X40, or ICOS, including antibodies such as those present on the surface of a solid support, such as a bead (for example, TRANSACT, Miltenyi).
• stimulating the T cells in this manner increases the efficiency of viral transduction and delivery of the reprogramming factors.
• transfection of nucleic acid is used for delivery of the reprogramming factors, prior stimulation of the T cells increases efficiency of the gene delivery.
• the T cells are preactivated, reactivated and/or expanded with one or more T cell activating and/or costimulatory and/or immunomodulatory compounds.
• the T cells are contacted with the one or more reprogramming factors for a period of about 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, or about 21 days.
• the T cells are contacted with the one or more reprogramming factors for a period of about 7 days.
• the T cells are contacted with the one or more reprogramming factors for a period of about 8 days.
• the T cells are contacted with the one or more reprogramming factors for a period of about 9 days.
• the T cells are contacted with the one or more reprogramming factors for a period of about 10 days. In certain embodiments, the T cells are contacted with the one or more reprogramming factors for a period of about 11 days. In certain embodiments, the T cells are contacted with the one or more reprogramming factors for a period of about 12 days. In certain embodiments, the T cells are contacted with the one or more reprogramming factors for a period of about 13 days. In certain embodiments, the T cells are contacted with the one or more reprogramming factors for a period of about 14 days.
• the T cells are contacted with the one or more reprogramming factors for a period of at least about 5 days and not more than about 10 days. In certain embodiments, the T cells are contacted with the one or more reprogramming factors for a period of at least about 5 days and not more than about 11 days. In certain embodiments, the T cells are contacted with the one or more reprogramming factors for a period of at least about 5 days and not more than about 12 days. In certain embodiments, the T cells are contacted with the one or more reprogramming factors for a period of at least about 5 days and not more than about 12 days.
• the T cells are contacted with the one or more reprogramming factors for a period of at least about 5 days and not more than about 13 days. [0249] In certain embodiments, the T cells are contacted with the one or more reprogramming factors for a period of at least about 6 days and not more than about 10 days. In certain embodiments, the T cells are contacted with the one or more reprogramming factors for a period of at least about 6 days and not more than about 11 days. In certain embodiments, the T cells are contacted with the one or more reprogramming factors for a period of at least about 6 days and not more than about 12 days.
• the T cells are contacted with the one or more reprogramming factors for a period of at least about 6 days and not more than about 12 days. In certain embodiments, the T cells are contacted with the one or more reprogramming factors for a period of at least about 6 days and not more than about 13 days.
• the period of time that T cells are contacted with the one or more reprogramming factors may vary depending on the amount or level of expression of the reprogramming factors. For example, in an embodiment where T cells are transduced with a viral vector expressing high levels of one or more of the reprogramming factors, a shorter time period may be required to achieve the desired partial reprogramming (formation of T cell derived adherent cells).
• T cells are transduced with a viral vector expressing low levels of one or more of the reprogramming factors and a longer time period may be required to achieve the desired partial reprogramming (formation of T cell derived adherent cells).
• an expression vector such as a viral vector, encoding the one or more reprogramming factors may comprise an inducible promoter where the expression of the partial reprogramming factors can be tuned to a desired expression level.
• the T cells are contacted with the one or more reprogramming factors for a period of about 5 - 30 days. In certain embodiments, the T cells are contacted with the one or more reprogramming factors for a period of about 5 - 25 days. In certain embodiments, the T cells are contacted with the one or more reprogramming factors for a period of about 5 - 20 days. In certain embodiments, the T cells are contacted with the one or more reprogramming factors for a period of about 5 - 15 days. In certain embodiments, the T cells are contacted with the one or more reprogramming factors for a period of about 5-13 days.
• the T cells are contacted with the one or more reprogramming factors for a period of about 5-12 days. In certain embodiments, the T cells are contacted with the one or more reprogramming factors for a period of about 6-12 days. In certain embodiments, the T cells are contacted with the one or more reprogramming factors for a period of about 6-13 days. In certain embodiments, the T cells are contacted with the one or more reprogramming factors for a period of about 7-12 days. In certain embodiments, the T cells are contacted with the one or more reprogramming factors for a period of about 7-13 days. In certain embodiments, the T cells are contacted with the one or more reprogramming factors for a period of about 7-14 days. In certain embodiments, the T cells are contacted with the one or more reprogramming factors for a period of about 6-20, 7-20, 8-20, 9-20, 10-20, 5- 18, 6-18, 7-18, 8-18, 9-18, or 10-18 days.
• somatic cells will start to dedifferentiate and lose their lineage specific epigenetic status, while they also start to acquire PSC phenotypes. These changes proceed gradually, so the longer somatic cells stay in the reprogramming process, the more PSC phenotypes they will acquire. In various embodiments of the present disclosure, the reprogramming process is stopped before the somatic cells dedifferentiate so much as to prevent them from losing their source cell functions.
• the partial reprogramming will be sufficient for the immune cell (e.g., a T cell) to form at least one cell that is attached to the culture vessel surface and to transform into an intermediate cell type referred to herein as a “T cell derived adherent cells”.
• the immune cell e.g., a T cell
• T cell derived adherent cells refers to an intermediate cell in the T cell partial reprogramming process.
• the T cell derived adherent cell attaches (at least in part) to the culture vessel surface and forms a colony during the partial reprogramming process.
• the T cell derived adherent cell is loosely attached to the culture vessel surface.
• T cell derived adherent cells differ from iPS cells (and iTSCs) in that they have not been completely reprogrammed.
• the T cell derived adherent cell colonies are loosely attached to the culture vessel surface.
• T cell derived adherent cells as described herein retain lineage stability e.g., the T cell derived adherent cells of the present disclosure retain the ability to return to the T cell lineage following culture in T cell activation/stimulation conditions (e.g., with T cell culture medium in the presence of activating and/or immunomodulating molecules, such as anti-CD3, anti-CD28, anti-CD27 antibodies and cytokines such as IL2, IL7, IL15, and the like).
• the T cell derived adherent cell is not multipotent. In certain embodiments, a T cell derived adherent cell is larger than a non-partially reprogrammed T cell or an activated T cell. In certain embodiments, T cell derived adherent cells are larger and have a more complex structure as measured by FACS analysis. In certain embodiments, the T cell derived adherent cell is SSEA4+CD3+.
• the T cell derived adherent cells express one more of the following cell surface markers as determined using flow cytometry or transcriptome analysis: CD50, CD352, CD31, Integrin b7, CD49e, CD122, CD314, HLA-DR, CD134, CD245, CD105 (Endoglin), CD366, CD39, Integrin a6b1, Integrin b5, CD71, CD164, CD10, CD63, XCR1, CD298, CD201, CD151, CD325, CD324, CD147, SSEA-3, TRA-1-81, TRA-2-54, Podoplanin, CD9, CD340, CD24, CD90, CD326, SSEA-5, SSEA4, TRA-1-60-R.
• iPS cells can be distinguished from T cell derived adherent cells by morphology. In particular, as shown in FIG. 3F, iPS cell colonies are much larger and have a more defined colony structure. iPS cells are well known in the art and are described for example in, Nishimura 2013, Cell Stem Cell 12, 114-126; Vizcardo et ak, 2013, Cell Stem Cell 12, 31-36).
• At least 10% of the T cell derived adherent cells express one or more of the following cell surface markers as determined using flow cytometry or transcriptome analysis: CD50, CD352, CD31, Integrin a6b1, Integrin b7, CD49e, CD122, CD314, HLA-DR, CD134, CD245, CD105 (Endoglin), CD366, CD39, Integrin b5, CD71,
• At least about 10% to about 80% of the T cell derived adherent cells express one or more of the following cell surface markers as determined using flow cytometry or transcriptome analysis: CD50, CD352, CD31, Integrin a6b1, Integrin b7, CD49e, CD122, CD314, HLA-DR, CD134, CD245, CD105 (Endoglin), CD366, CD39, Integrin b5, CD71, CD 164, CD10, CD63, XCR1, CD298, CD201, CD151, CD325, CD324, CD147, SSEA- 3, TRA-1-81, TRA-2-54, Podoplanin, CD9, CD340, CD24, CD90, CD326, SSEA-5, SSEA4, TRA-1-60-R.
• At least about 15% to about 80%, at least about 20% to about 75%, at least about 25% to about 75%, at least about 30% to about 50%, at least about 10%, 15%, 20%, 25%, 30%, 40%, 50%, 60%, 70%, 75%, or about 80% of the T cell derived adherent cells express one or more of the aforementioned cell surface markers as determined using assays known in the art, such as flow cytometry, gene expression or transcriptome analysis. The expression level of these markers and the % of positive cells will vary depending on the number of days of partial reprogramming.
• partial reprogramming may result in partial loss of certain markers of immune cell (e.g., a T cell) identity.
• partial reprogramming of T cells may result in a loss or reduction of expression of any one or more of CD3, CD4, CD8 (e.g., CD8aa, and/or CD8o$).
• reduction of expression may mean from about 10% to about 95% reduction in expression of the marker as measured by flow cytometry.
• the reduction in expression is a reduction in mean fluorescence intensity (MFI) of about 0.25, 0.5, 0.75, 1, 1.25, 1.5, 1.75, or 2 logs, in at least a portion of the T cell derived adherent cells.
• MFI mean fluorescence intensity
• the T cells are transiently contacted with one or more reprogramming factors for a period of time sufficient for T cell derived adherent cells to form.
• the T cells are transiently contacted with one or more reprogramming factors for a period of time sufficient for attached cell colonies to form wherein at least a portion of the attached cells express one or more of the following cell surface markers: CD50, CD352, CD31, Integrin a ⁇ b ⁇ , Integrin b7, CD49e, CD122, CD314, HLA-DR, CD134, CD245, CD 105 (Endoglin), CD366, CD39, Integrin b5, CD71, CD164, CD10, CD63, XCR1, CD298, CD201, CD151, CD325, CD324, CD147, SSEA-3, TRA-1-81, TRA-2-54, Podoplanin, CD9, CD340, CD24, CD90, CD326, SSEA-5, SSEA4, TRA-1-60-R.
• the T cells are transiently contacted with one or more reprogramming factors for a period of time sufficient for attached cell colonies to form wherein at least a portion of the attached cells express Integrin a ⁇ b ⁇ , CD9, CD90, and/or SSEA4.
• At least a portion of the T cell adherent cells express Integrin a ⁇ b ⁇ , CD9, CD90, or SSEA4, or any combination thereof. In certain embodiments, at least a portion of the T cell adherent cells expresses Integrin a ⁇ b ⁇ ; at least a portion of the T cell adherent cells expresses integrin a ⁇ b ⁇ and SSEA4, at least a portion of the T cell adherent cells express integrin a ⁇ b ⁇ , SSEA4 and CD9; or at least a portion of the T cell adherent cells express integrin a ⁇ b ⁇ , SSEA4, CD9, and CD90. In certain embodiments, at least a portion of the T cell adherent cells express SSEA4; SSEA4 and CD9; or SSEA4, CD9 and CD90.
• At least a portion of the T cell derived adherent cells express CD9 and/or CD90 which are early markers for the partial reprogramming process.
• CD9 is also known as tetraspanin-29 and has four transmembrane domains. It is involved in cell adhesion, signal transduction and cellular differentiation.
• CD90 is also known as THY-1. It is an immunoglobulin superfamily surface glycoprotein and is a marker associated with mesenchymal stem cells. It is also involved in cell adhesion and communication. While Thy-1 is expressed commonly in murine T cells, T cell Thy-1 expression in human T cell lineage is limited to specialized populations in the thymic cortex and subsets of CD4 Thl7 T cells.
• T cell derived adherent cells express CD9 and/or CD90.
• the T cell derived adherent cells express one or more of Integrin a6b1, CD164, CD9, CD63, CD90, CD71, CD326, TRA-1-81 and TRA-1-60-R, in certain embodiments as compared to stimulated and unstimulated T cells.
• the T cell derived adherent cells have decreased expression of CD352 and CD31 as compared to stimulated or unstimulated T cells.
• T cell derived adherent cells express one or more of CD164, CD9, CD63, CD90, CD71, CD326, TRA-1-81 and TRA-1-60-R.
• the disclosure provides a population of T cell derived adherent cells whose epigenetic age is at least 5% younger than the chronological age of relevant control T cells or the starting isolated T cell population.
• the present disclosure provides a population of T cell derived adherent cells whose epigenetic age is at least 5%, 6%, 7%, 8%, 9%, 10%, 15%, 20%, 25%, 30%, 35%, 40%, 45%, 50%, 55%, 60%, 65%, 70%, 75%, or at least 80% younger than the chronological age of the source isolated T cells (i.e., the isolated T cells that were contacted with the reprogramming factors).
• T cell activating agent e.g., anti-CD3, anti-CD28, one or more cytokines such as IL2, IL7,
• the cells exhibit increased expansion potential as compared to control T cells.
• the partially reprogrammed T cells expand at least 2, 3, 4, 5, 6, 7, 8, 9, 10, 11,
• the partially reprogrammed T cells expand at least about 50-2000 fold, at least about 50-1000- fold, at least 50-900-fold, at least 50-800-fold, at least 50-700-fold, at least 50-600-fold, at least 50 to 500-fold, at least 100 to 400-fold, at least 150 to 500-fold, at least 200 to 500-fold, or at least 300 to 500-fold more than control T cells that have not been partially reprogrammed.
• the partially reprogrammed T cells expand more quickly than T cells that have not been partially reprogrammed.
• the partial reprogramming methods are carried out under conditions appropriate for maintenance of the isolated T cells and/or the partially reprogrammed T cells (T cell derived adherent cells). Conditions appropriate for the maintenance and proliferation of particular cell types will be apparent to the skilled artisan. Specialized culture medium may be obtained from commercial sources, or factors necessary or desirable for enhancing the proliferation may be added to standard culture medium. Additional factors and agents may also be added to culture medium, for example, to induce expression of inducible elements in said cells or to inhibit growth of cells which are sensitive to particular agents.
• the isolated T cells are cultured in T cell culture medium (TCM) comprising commercially available media optimized for culture of T cells, such as TexMACS medium or OpTmizer Basal Medium, with the addition of one or more supplements such as OpTmizer Cell Supplement, in certain embodiments with the addition of Immune Cell Seram Replacement (e.g., a T cell serum replacement) and/or other supplements such as L- Glutamine; GlutaMAX; and/or cytokines such as IL-2, IL-7, and/or IL-15.
• TCM T cell culture medium
• the partial reprogramming phase of the methods herein are carried out using media optimized for cell reprogramming, such as but not limited to STEMFIT media (Amsbio, Abington, UK), mTESR2 (Stem Cell Technologies), and ESSENTIAL 6 or 8 (Life Technologies); STEMPRO hESC SFM (Gibco); TESR, clone-R, dMEM F12, KSR.
• media optimized for cell reprogramming such as but not limited to STEMFIT media (Amsbio, Abington, UK), mTESR2 (Stem Cell Technologies), and ESSENTIAL 6 or 8 (Life Technologies); STEMPRO hESC SFM (Gibco); TESR, clone-R, dMEM F12, KSR.
• the partial reprogramming is carried out in a media comprised of 50% T cell media and 50% stem cell media (e.g., STEMFIT or Essential 8, mTESR, TESR, clone-R, dMEM F12, KSR), optionally with the addition of one or more cytokines, such as IL2, IL7 and/or IL15.
• the partial reprogramming is carried out for a first period of time in a first media and then for a second period of time in a second media.
• the first media is 50/50 media as noted, optionally with the addition or one or more cytokines, for a period of 1, 2, 3, 4, 5, 6, days or more followed by culturing the cells in a second media which is a stem cell media (e.g., STEMFIT of Essential 8) media for 1, 2, 3, 4, 5, 6, 7, 8, 9, or more days.
• a stem cell media e.g., STEMFIT of Essential 8
• the first media is 50/50 and is used for 1, 2, or 3 days and the second media is a stem cell media (e.g., STEMFIT or Essential 8) and is used starting at day 2, 3, or 4 until formation of T cell derived adherent cells and reactivation as described further herein.
• the T cells are cultured for a first period of time in a first media and then cultured for a second period of time in a second media.
• the T cells contacted with the one or more reprogramming factors e.g., one or more of KLF4, OCT3/4, SOX2, C-MYC and SV40
• the one or more reprogramming factors are cultured in appropriate media in a culture vessel coated with recombinant human Laminin511- E8 fragment, such as iMatrix.
• the partially reprogrammed, T cell derived adherent cells are reactivated in an activation media that enables the reprogrammed immune cell (e.g., a T cell) to regain T cell identity and functionality.
• an activation media that enables the reprogrammed immune cell (e.g., a T cell) to regain T cell identity and functionality.
• the T cell derived adherent cells are reactivated immediately following partial reprogramming using one or more T cell stimulation or activation agents and/or costimulatory agents in an appropriate T cell culture media.
• the T cell derived adherent cells are reactivated immediately following partial reprogramming in a T cell culture media supplemented with one or more cytokines, such as IL2, IL7, IL15, IL21, with or without one or more T cell activating agents and/or one or more costimulatory agents.
• the T cell derived adherent cells are reactivated with one or more T cell activating and/or costimulatory and/or immunomodulatory agents as described elsewhere herein in an appropriate medium for T cell culture, such as T cell culture medium (TCM) comprising commercially available media optimized for culture of T cells, such as TexMACS medium or OpTmizer Basal Medium, with the addition of one or more supplements such as OpTmizer Cell Supplement, in certain embodiments with the addition of Immune Cell Seram Replacement (e.g., T cell serum replacement) and other supplements such as L- Glutamine; GlutaMAX; cytokines such as IL-2, IL7, and/or IL15.
• TCM T cell culture medium
• Immune Cell Seram Replacement e.g., T cell serum replacement
• other supplements such as L- Glutamine; GlutaMAX
• cytokines such as IL-2, IL7, and/or IL15.
• the stimulating or activating conditions or agents used herein may be used for preactivation, reactivation, and/or expansion phases of the methods herein.
• T cells can be activated and expanded generally using methods as described, for example, in U.S. Pats. 5,858,358; 5,883,223; 6,352,694; 6,534,055; 6,797,514; 6,867,041; 6,692,964; 6,887,466; 6,905,680; 6,905,681; 6,905,874; 7,067,318; 7,144,575; 7,172,869; 7,175,843; 7,232,566; 7,572,631; and 10,786,533.
• the T cells are contacted with a T cell activating agent, and/or a costimulatory agent, that provides a primary activation signal and an agent that provides a costimulatory signal.
• a T cell activating agent and/or a costimulatory agent, that provides a primary activation signal and an agent that provides a costimulatory signal.
• Agents that provide a primary activation signal include for example antibodies or antigen-binding fragments thereof or ligands, or target binding fragments thereof, that bind to the CD3 cell surface receptor (e.g., an anti-CD3 antibody) expressed on T cells.
• Agents that provide a costimulatory signal are known in the art and include, but are not limited to, antibodies or ligands that bind to CD28, OX-40, 4- 1BB/CD137, CD2, CD7, CD27, CD30, CD40,etc.
• the activating agents include one or more agents, e.g., ligand, which is capable of activating an intracellular signaling domain of a TCR complex.
• the agent turns on or initiates a primary TCR CD3 intracellular signaling cascade in a T cell, such as agents suitable to deliver a primary signal, e.g., to initiate activation of an IT AM-induced signal, such as those specific for a TCR component.
• the activating agent is provided in combination with or at the same time as an agent that promotes a costimulatory signal. Suitable agents that promote a costimulatory signal are known in the art and include antibodies or ligands that promote signaling of CD28, OX-40, 4-1BB/CD137, CD2, CD7, CD27, CD30, CD40, inducible
• the stimulatory and costimulatory agents for the activation steps of the methods here comprise an anti-CD3, anti-CD28, anti-41-BB, or anti-CD27 antibody for example, bound to solid support such as a bead, and/or one or more cytokines.
• the agents comprise a ligand for an activating receptor or a costimulatory receptor, e.g., a peptide/MHC complex and/or the CD27 ligand (e.g., CD70 or trimerized versions thereof), CD80, CD86 and the like.
• the stimulating and costimulatory agents are anti-CD3/anti-CD28 beads (e.g., DYNABEADS M-450 CD3/CD28 T Cell Expander, and/or ExpACT beads).
• the stimulation and/or activation may comprise adding anti-CD3 and/or anti CD28 antibody to the culture medium.
• the stimulating agents include IL-2, IL-7 and/or IL-15.
• the activating agent is a tumor antigen, in particular a tumor antigen as disclosed herein.
• the activating and/or costimulatory agents herein may be coated or adsorbed onto one or more surfaces.
• surfaces include, for example, solid surfaces, porous surfaces, semi-porous surfaces, spherical surfaces, non-spherical surfaces, rod-like surfaces, and polymeric surfaces.
• the T cells are activated (e.g., in the preactivation, reactivation or expansion phases of the methods herein) using commercially available reagents such as TRANSACT (Miltenyi Biotec).
• TRANSACT Microwave Access reagent
• the partially reprogrammed T cells are activated using TRANSACT at a ratio that allows the T cell derived adherent cells to regain its T cell identity.
• the partially reprogrammed T cells are activated with TRANSACT at 1:10, 1:50 1:100, 1:150, 1:200, 1:250, 1:300, 1:350, 1:400, 1:450, 1:500, 1:550, 1:600, 1:650, 1:700, 1:750, 1:800, 1:850, 1:900, 1:1,000, 1:2000, 1:3000, 1:4000 or 1:10,000.
• the T cell derived adherent cells are activated in an appropriate T cell activation media and cultured for sufficient time that allows the T cell derived adherent cell to regain its identity.
• the partially reprogrammed cells are activated and cultured in a T cell activation media for a period of about 1, 2, 3, 4, 5, 6, or 7 or more days. In certain embodiments, the partially reprogrammed cells are activated and cultured for about 1-20 days, for about 2-20 days, for about 3-20 days for about 4-20 days for about 5-20 days for about 6-20 days for about 7-20 days, 8-20 days, for about 9- 20 days, or for about 10-20 days.
• the partially reprogrammed cells are activated and then cultured for about 1-15 days, for about 2-15 days, for about 3-15 days, for about 4-15 days, for about 5-15 days, for about 6-15 days, for about 7-15 days, for about 8-15 days, for about 9-15 days or for about 10-15 days.
• the T cell derived adherent cells are redirected or reactivated with antigen or antigen expressing cells, such as tumor antigen expressing autologous cells or tumor antigen.
• antigen or antigen expressing cells such as tumor antigen expressing autologous cells or tumor antigen.
• the T cell derived adherent cells are reactivated with by co-culture with APC expressing tandem minigenes (i.e., tumor can be sequenced the fragments re-expressed from tandem minigenes expressed and presented by the APC). Any tumor antigens known to be associated with a cancer is contemplated for use herein.
• Non- limiting examples of antigens include: AFP (alpha-fetoprotein), anb ⁇ or another integrin, BCMA, BRAF, B7-H3, B7-H6, CA9 (carbonic anhydrase 9), (carcinoembryonic antigen), Claudin 18.2, Claudin 6, c-MET, DLL3 (delta- like protein 3), DLL4, ENPP3 (ectonucleotide pyrophosphatase/phosphodiesterase family member 3), EpCAM, EPG-2 (epithelial glycoprotein 2), EPG-40, ephrinB2, EPHa2 (ephrine receptor A2), ERBB dimers, estrogen receptor, ETBR (endothelin B receptor), FAP-a (fibroblast activation protein a), fetal AchR (fetal acetylcholine receptor), FBP (a folate binding protein), FCRL5, FR-a (folate receptor alpha), GCC (guanyl cyclase C),
• the activation media for the reactivation of the T cell derived adherent cells may further comprise an immunomodulatory molecule such as a cytokine.
• immunomodulatory molecules are lymphokines, monokines, and traditional polypeptide hormones.
• growth hormones such as human growth hormone, N-methionyl human growth hormone, and bovine growth hormone; parathyroid hormone; thyroxine; insulin; proinsulin; relaxin; prorelaxin; glycoprotein hormones such as follicle stimulating hormone (FSH), thyroid stimulating hormone (TSH), and luteinizing hormone (LH); hepatic growth factor (HGF); fibroblast growth factor (FGF); prolactin; placental lactogen; mullerian-inhibiting substance; mouse gonadotropin-associated peptide; inhibin; activin; vascular endothelial growth factor; integrin; thrombopoietin (TPO); nerve growth factors (NGFs) such as NGF-beta; platelet-growth factor; transforming growth factors (TGFs) such as TGF-alpha and TGF-beta; insulin-like growth factor-I and -II; erythropoietin (EPO); osteoin
• FSH follicle
• the partially reprogrammed and reactivated T cells herein may be further stimulated and expanded using the same methods for reactivation as described herein. Such methods for activating and expanding T cells are known in the art.
• the methods herein comprising the partial reprogramming followed by reactivation and optionally, further expansion, will be sufficient for the rejuvenated T cells to acquire any one or more of the following characteristics:
• the rejuvenated T cells have one or more sternness properties including high epigenetic plasticity.
• Other advantageous phenotypic markers that the rejuvenated cells may acquire include expression of L-selectin (CD62L), IL-7Ra, CD 132, CCR7, CD45RA, CD45RO, CD27, CD28, CD95, CXCR3, TCF7 and LFA-1.
• the rejuvenated T cells acquire T memory stem cell expression markers, e.g., are memory T cells that express CD95, CD45RA, CCR7, and CD62L and are endowed with the stem cell-like ability to self-renew and the multipotent capacity to reconstitute the entire spectrum of memory and effector T cell subsets.
• the rejuvenated T cells are "central memory T cells” or “TCM cells” which are memory T cells that express CD45RO, CCR7, and CD62L.
• rejuvenated T cells have effector memory T cell markers such as expression of CD45RO but lack of expression of CCR7 and CD62L.
• the rejuvenated T cells herein have a stem-like phenotype and have an improved capacity for proliferation.
• the rejuvenated T cells have characteristics of a naive T cell, "TN cells,” which are T cells that express CD45RA, CCR7, and CD62L, but which do not express CD95.
• TN cells are T cells that express CD45RA, CCR7, and CD62L, but which do not express CD95.
• the rejuvenated T cells may exhibit biological and phenotypic characteristics of younger T cells in terms of epigenetic signature, telomere length and functionality.
• partial reprogramming and reactivation as described herein results in T cells that are rejuvenated as can be measured by assessing the methylation status of various CpG sites in a cell’s DNA.
• Such techniques are known in the art. See, e.g., Horvath and Raj, 2018, Nature Reviews Genetics, 19:371-375.
• Various groups have established models or “epigenetic clocks” that use the methylation status of a cell to provide an estimate of that cell or tissues “biological age” using a mathematical algorithm that uses values assigned to the methylation state of a specific CpGs in the genome.
• the methylation status of various CpGs cites is used to determine whether partial reprogramming has occurred.
• the methylation status of various CpG cites is used to predict the counts of exhausted CD8 T cells. In various embodiments, the methylation status of various CpG cites is used to determine whether a population of immune cell (e.g., a T cell) is suitable for administration to a patient.
• a population of immune cell e.g., a T cell
• the “Horvath Clock” as described in Horvath and Raj is used to determine the epigenetic age of the cells described herein including the rejuvenated immune cell (e.g., a T cell).
• the Horvath Clock is used to determine whether partial reprogramming has occurred.
• the Horvath Clock is used to predict the counts of exhausted CD8 T cells.
• the Horvath clock is used to determine whether a population of imm immune cell (e.g., a T cell) is suitable for administration of patient.
• other epigenetic clocks or algorithms for example, the Hannum Clock or the Levine Clock are used. See, e.g., Hannum et ak, 2013, Mol. Cell., 49:359-369; Levine et ak, 2018, Aging, 10(4):573-591.
• rejuvenated T cells exhibit a reduced epigenetic age (eAge) as compared to control T cells (e.g., T cells that have been cultured without contact with one or more reprogramming factors).
• eAge may be determined using a known epigenetic clock determination method, such as the Horvath clock as described elsewhere herein.
• the eAge of a rejuvenated T cell as described herein is reduced by about 5%-75%, 10%-75%, 10%-50%, 15%-75%, 15%-50%, 20%-75%, or 20%-50% as compared to the eAge of an appropriate control T cell (e.g., T cell from the original donor sample prior to partial reprogramming and reactivation or chronologically age-matched T cells).
• an appropriate control T cell e.g., T cell from the original donor sample prior to partial reprogramming and reactivation or chronologically age-matched T cells.
• the eAge of a rejuvenated T cell as described herein is reduced by at least 5%, 6%, 7%, 8%, 9%, 10%, 15%, 20%, 25%, 30%, 35%, 40%, 45%, 50%, 55%, 60%, 65%, 70%, 75% or more as compared to an appropriate control T cell (e.g., T cell from the original donor sample prior to partial reprogramming or chronologically age-matched T cells).
• an appropriate control T cell e.g., T cell from the original donor sample prior to partial reprogramming or chronologically age-matched T cells.
• the present disclosure provides a population of T cells whose epigenetic age is at least 5% younger than its chronological age. In another embodiment, the present disclosure provides a population of T cells whose epigenetic age is at least 5%, 6%,
• the disclosure provides a population of T cells whose epigenetic age is at least 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, or more years younger that its chronological age.
• epigenetic age can be measured using methods known in the art, such as by measuring the Horvath epigenetic clock.
• rejuvenated T cells exhibit an epigenetic age (eAge) that is around 7-16 years of age.
• rejuvenated T cells exhibit an epigenetic age (eAge) that is reduced to around the equivalent age of puberty as compared to control T cells (e.g., T cells that have been cultured without contact to one or more reprogramming factors; e.g., compared to the chronological age of the starting cells).
• the rejuvenated T cells have increased telomere length as compared to control T cells.
• the telomere length can be measured using methods known in the art (see e.g., Rosenberg et ah, 2011, Clin Cancer Res 17, 4550- 4557) and commercially available kits (e.g., TELOTAGGG, Sigma-Aldrich).
• the telomere length is elongated by between about 0.1-3kb.
• the telomere length is elongated by about 0.1, 0.2, 0.3, 0.4, 0.5, 0.6, 0.7, 0.8, 0.9, or about 1 kb.
• the telomere is elongated by about 1.1, 1.2, 1.3, 1.4, 1.5, 1.6, 1.7, 1.8, 1.9, or 2 kb.
• the rejuvenated T cells exhibit increased expansion potential.
• the rejuvenated T cells expand 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 25, 30, 35, 40, 45, 50-fold more than control T cells that have not been partially reprogrammed or that are chronologically age-matched T cells.
• the rejuvenated T cells expand from 25-1000 fold more than chronologically age-matched control T cells or control T cells that have not been partially reprogrammed.
• the rejuvenated T cells expand from 25, 30, 40, 50, 60, 70, 80, 90, 100, 125, 150, 175, 200, 225, 250, 275, 300, 350, 400, 450, 500 fold more than chronologically age- matched control T cells or control T cells that have not been partially reprogrammed. In certain embodiments, the rejuvenated T cells expand more quickly than T cells that have not been partially reprogrammed.
• the present disclosure provides a population of T cells whose epigenetic age is at least 5% younger than its chronological age wherein the T cells do not express aberrant NK, T or B cell markers.
• the present disclosure provides a population of T cells whose epigenetic age is at least 5%, 6%, 7%, 8%, 9%, 10%, 15%, 20%, 25%, 30%, 35%, 40%, 45%, 50%, 55%, 60%, 65%, 70%, 75%, or at least 80% younger than the chronological age of the source T cells or appropriate control T cells, and wherein the T cells do not express express aberrant NK, T or B cell markers.
• the present disclosure provides a population of T cells whose epigenetic age is at least 5%, 6%, 7%, 8%, 9%, 10%, 15%, 20%, 25%, 30%, 35%, 40%, 45%, 50%, 55%, 60%, 65%, 70%, 75%, or at least 80% younger than the chronological age of the source T cells or appropriate control T cells, and wherein the T cells have a stem-like phenotype.
• the present disclosure provides a population of T cells whose epigenetic age is at least 5%, 6%, 7%, 8%, 9%, 10%, 15%, 20%, 25%, 30%, 35%, 40%, 45%, 50%, 55%, 60%, 65%, 70%, 75%, or at least 80% younger than the chronological age of the source T cells or appropriate control T cells, and wherein the T cells express CCR7, CD62L, and TCF7.
• the present disclosure provides a population of T cells whose epigenetic age is at least 5%, 6%, 7%, 8%, 9%, 10%, 15%, 20%, 25%, 30%, 35%, 40%, 45%, 50%, 55%, 60%, 65%, 70%, 75%, or at least 80% younger than the chronological age of the source T cells or appropriate control T cells, and wherein the T cells express CCR7, CD62L, and TCF7; and have an increased killing capacity as compared to appropriate control T cells. Killing capacity can be measured using assays known in the art such as those described in the Examples herein.
• the present disclosure provides a population of T cells whose epigenetic age is at least 5% younger than the chronological age of the source T cells wherein the T cells do not express NCAM1, NCR2, FCGR3A, KIR2DL4 or KIR2DS4.
• the present disclosure provides a population of T cells whose epigenetic age is at least 5%, 6%, 7%, 8%, 9%, 10%, 15%, 20%, 25%, 30%, 35%, 40%, 45%, 50%, 55%, 60%, 65%, 70%, 75%, or at least 80% younger than its chronological age and wherein the T cells do not express NCAM1, NCR2, FCGR3A, KIR2DF4, or KIR2DS4.
• the present disclosure provides a T cell whose epigenetic age is at least 5%, 6%, 7%, 8%, 9%, 10%, 15%, 20%, 25%, 30%, 35%, 40%, 45%, 50%, 55%, 60%, 65%, 70%, 75%, or at least 80% younger than its chronological age (or an appropriate control T cell) and wherein the T cell is enriched for oxidative phosphorylation, fatty acid metabolism, glycolysis and hypoxia gene sets as determined by transcriptome analysis.
• the present disclosure provides a T cell or a population of such T cells, whose epigenetic age is at least 5%, 6%, 7%, 8%, 9%, 10%, 15%, 20%, 25%, 30%, 35%, 40%, 45%, 50%, 55%, 60%, 65%, 70%, 75%, or at least 80% younger than its chronological age (or an appropriate control T cell) and wherein the T cells is enriched for both oxidative phosphorylation and glycolysis gene sets as compared to control T cells as determined by transcriptome analysis.
• the present disclosure provides T cells whose epigenetic age is at least 5%, 6%, 7%, 8%, 9%, 10%, 15%, 20%, 25%, 30%, 35%, 40%, 45%, 50%, 55%, 60%, 65%, 70%, 75%, or at least 80% younger than the chronological age of an appropriate control T cell and wherein the T cells have increased TCR repertoire diversity as compared to control T cells.
• the present disclosure provides a population of T cells whose epigenetic age is at least 5%, 6%, 7%, 8%, 9%, 10%, 15%, 20%, 25%, 30%, 35%, 40%, 45%, 50%, 55%, 60%, 65%, 70%, 75%, or at least 80% younger than its chronological age and wherein the T cells comprise an incomplete set of V, D, and J segments of T cell receptor genes.
• the present disclosure provides a population of T cells whose epigenetic age is at least 5%, 6%, 7%, 8%, 9%, 10%, 15%, 20%, 25%, 30%, 35%, 40%, 45%, 50%, 55%, 60%, 65%, 70%, 75%, or at least 80% younger than the chronological age of the source T cells; wherein the T cells do not express NCAM1, NCR2, FCGR3A, KIR2DF4, or KIR2DS4; and wherein the T cells are enriched for oxidative phosphorylation, fatty acid metabolism, glycolysis and hypoxia gene sets as determined by transcriptome analysis.
• the present disclosure provides a population of T cells whose epigenetic age is at least 5%, 6%, 7%, 8%, 9%, 10%, 15%, 20%, 25%, 30%, 35%, 40%, 45%, 50%, 55%, 60%, 65%, 70%, 75%, or at least 80% younger than the chronological age of the source T cells; wherein the T cells do not express NCAM1, NCR2, FCGR3A, KIR2DL4, or KIR2DS4; and wherein the T cells are enriched for both oxidative phosphorylation and glycolysis gene sets as compared to control T cells as determined by transcriptome analysis.
• the present disclosure provides a population of T cells whose epigenetic age is at least 5%, 6%, 7%, 8%, 9%, 10%, 15%, 20%, 25%, 30%, 35%, 40%, 45%, 50%, 55%, 60%, 65%, 70%, 75%, or at least 80% younger than the chronological age of the source T cells; wherein the T cells do not express NCAM1, NCR2, FCGR3A, KIR2DL4, or KIR2DS4; wherein the T cells are enriched for both oxidative phosphorylation and glycolysis gene sets as compared to control T cells as determined by transcriptome analysis; and wherein the T cells have increased TCR repertoire diversity as compared to control T cells.
• the present disclosure provides a population of T cells whose epigenetic age is at least 5%, 6%, 7%, 8%, 9%, 10%, 15%, 20%, 25%, 30%, 35%, 40%, 45%, 50%, 55%, 60%, 65%, 70%, 75%, or at least 80% younger than the chronological age of the source T cells; wherein the T cells do not express NCAM1, NCR2, FCGR3A, KIR2DL4, or KIR2DS4; wherein the T cells are enriched for both oxidative phosphorylation and glycolysis gene sets as compared to control T cells as determined by transcriptome analysis; wherein the T cells have increased TCR repertoire diversity as compared to control T cells; and wherein the T cells comprise an incomplete set of V, D, and J segments of T cell receptor genes.
• T cell receptor V, D, and J gene segments rearrange during T cell development to form complete variable domain exons. These gene rearrangements take place in the thymus.
• the rejuvenated T cells produced herein are produced from isolated T cells that have a rearranged TCR locus and express a TCR.
• the rejuvenated T cells produced herein are epigenetically younger than the source isolated T cells yet have a functional TCR (i.e., an incomplete set of V, D, and J segment of T cell receptor genes), which distinguishes them from the isolated T cells.
• the metabolic state of rejuvenated T cells is improved (see e.g., Cell Metabolism 14, 264-271).
• metabolic gene sets corresponding to oxidative phosphorylation, fatty acid metabolism, glycolysis and hypoxia are enriched in the rejuvenated T cells described herein as compared to appropriate controls (see e.g., Nishimura 2019 Int. J. Mol. Sci. 20:2254).
• the rejuvenated T cells described herein have upregulated glycolytic enzymes and downregulated electron transport chain subunits.
• the rejuvenated T cells herein demonstrate one or more of the following characteristics: a metabolic switch converting somatic oxidative metabolism into a glycolytic flux-dependent, mitochondria independent state; downregulated expression of age- related stress response genes in the p53 tumor suppressor pathway, including pl6INK4a, p21CIPl, Atf3, and Gadd45B; downregulation of the senescence-associated metalloprotease MMP13 and interleukin- 6; reduced senescence-associated b-galactosidase activity; reduced production of mitochondrial reactive oxygen species (ROS); restored levels of H3K9me3 and H4K20me3 (epigenetic modifications involved in the maintenance of heterochromatin) (see e.g., Ocampo, Cell.
• ROS mitochondrial reactive oxygen species
• the rejuvenated T cells herein are enriched for sternness gene signatures as compared to non-rejuvenated control T cells (see, e.g., Gattinoni et al., 2011 Nature Medicine 17(10): 1290-1297).
• the disclosure provides a method of treating a patient in need thereof with a population of rejuvenated T cells produced by the partial reprogramming and reactivation methods disclosed herein. Methods are provided for treating diseases or disorders, including cancer by administering a composition comprising the rejuvenated T cells described herein.
• the disclosure relates to a method of treating a patient in need thereof with a population of T cells produced by a method comprising (a) transiently contacting T cells with at least one reprogramming factor selected from the group consisting of KLF4, OCT3/4, SOX2 and C-MYC and optionally SV40, for a time sufficient for T cell derived adherent cell colonies form; and (c) contacting said T cell derived adherent cells with a culture medium comprising a T cell activating and/or costimulatory agent, such as anti-CD3, anti-CD28, and or one or more cytokines such as IL-2.
• the T cells are engineered to express a cell surface receptor that recognizes a specific antigenic moiety on the surface of a target cell.
• the target cell is a cancer cell.
• the disclosure relates to a method of treating a patient in need thereof with a population of rejuvenated T cells as described herein.
• the disclosure relates to a method of treating a patient in need thereof with a population of rejuvenated immune cell (e.g., a T cell) produced by the methods disclosed herein.
• a population of rejuvenated immune cell e.g., a T cell
• Methods are provided for treating diseases or disorders, including cancer, infectious disease, or autoimmune disease.
• the disclosure relates to a method of treating a patient in need thereof with a population of immune cell (e.g., a T cell) produced by a method comprising (a) isolating a plurality of immune cells (e.g., T cells) from a source; (b) transiently contacting said plurality of immune cells (e.g., T cells) with at least one reprogramming factor selected from the group consisting of KLF4, OCT3/4, SOX2 and C- MYC; and (c) contacting said immune cells (e.g., T cells) with a culture medium comprising IL-2, wherein said immune cells (e.g., T cells) are contacted with at least one reprogramming factor for a period of at least about four days.
• a population of immune cell e.g., a T cell
• the plurality of immune cells are engineered to express a cell surface receptor that recognizes a specific antigen on the surface of a target cell.
• the target cell is a cancer cell.
• the disclosure comprises a pharmaceutical composition comprising a plurality of rejuvenated T cells produced by the methods herein.
• the pharmaceutical composition comprises rejuvenated T cells produced by a method comprising (a) transiently contacting a plurality of T cells with at least one reprogramming factor selected from the group consisting of KLF4, OCT3/4, SOX2 and C- MYC; for a period time sufficient for the partially reprogrammed cells to attach to the culture vessel surface; and (b) contacting said attached reprogrammed T cells with a culture medium comprising a T cell activating agent.
• the pharmaceutical composition further comprises an additional active agent.
• the disclosure comprises a pharmaceutical composition comprising at least one rejuvenated T cell as described herein and a pharmaceutically acceptable excipient.
• the pharmaceutical composition further comprises an additional active agent.
• target doses for rejuvenated T cells can range from about 1 x 106 to about 2 x 1010 cells/kg, preferably 2x106 cells/kg. It will be appreciated that doses above and below this range may be appropriate for certain subjects, and appropriate dose levels can be determined by the healthcare provider as needed.
• the target dose is 1x105. In various embodiments the target dose is 1x106. In various embodiments the target dose is 1x107. In various embodiments the target dose is 1x108. In various embodiments the target dose is 1x109. In various embodiments the target dose is 1x1010. In various embodiments the target dose is 2x1010. Additionally, multiple doses of cells can be provided in accordance with the disclosure. In various embodiments at least 1, 2, 3, 4, 5, 6, 7, 8, 9 or 10 doses of cells are administered to the patient in need thereof.
• a method for reducing the size of a tumor in a subject comprising administering to the subject a rejuvenated T cell of the present disclosure.
• the subject has a solid tumor, or a blood malignancy such as lymphoma or leukemia.
• the rejuvenated immune cell e.g., a T cell
• the cancer is present in the bone marrow of the subject.
• the term “subject” or “patient” means an individual.
• a subject is a mammal such as a human.
• a subject can be a non-human primate.
• Non-human primates include marmosets, monkeys, chimpanzees, gorillas, orangutans, and gibbons, to name a few.
• the term “subject” also includes domesticated animals, such as cats, dogs, etc., livestock (e.g., llama, horses, cows), wild animals (e.g., deer, elk, moose, etc.,), laboratory animals (e.g., mouse, rabbit, rat, gerbil, guinea pig, etc.) and avian species (e.g., chickens, turkeys, ducks, etc.).
• livestock e.g., llama, horses, cows
• wild animals e.g., deer, elk, moose, etc.
• laboratory animals e.g., mouse, rabbit, rat, gerbil, guinea pig, etc.
• avian species e.g., chickens, turkeys, ducks, etc.
• the methods can further comprise administering one or more chemotherapeutic agents.
• the chemotherapeutic agent is a lymphodepleting (preconditioning) chemotherapeutic.
• Beneficial preconditioning treatment regimens, along with correlative beneficial biomarkers are described in U.S. Provisional Patent Applications 62/262,143 and 62/167,750. These describe, e.g., methods of conditioning a patient in need of a T cell therapy comprising administering to the patient specified beneficial doses of cyclophosphamide (between 200 mg/m2/ day and 2000 mg/m2/day) and specified doses of fludarabine (between 20 mg/m2/day and 900 mg/m2/day).
• a preferred dose regimen involves treating a patient comprising administering daily to the patient about 500 mg/m2/day of cyclophosphamide and about 60 mg/m2/day of fludarabine for three days prior to administration of a therapeutically effective amount of rejuvenated T cells to the patient.
• the rejuvenated T cells and the chemotherapeutic agent are administered each in an amount effective to treat the disease or condition in the subject.
• compositions comprising rejuvenated immune cell (e.g., T cells) disclosed herein may be administered in conjunction with any number of chemotherapeutic agents.
• chemotherapeutic agents include alkylating agents such as thiotepa and cyclophosphamide (CYTOXANTM); alkyl sulfonates such as busulfan, improsulfan and piposulfan; aziridines such as benzodopa, carboquone, meturedopa, and uredopa; ethylenimines and methylamelamines including altretamine, triethylenemelamine, trietylenephosphoramide, triethylenethiophosphaoramide and trimethylolomelamine resume; nitrogen mustards such as chlorambucil, chlornaphazine, cholophosphamide, estramustine, ifosfamide, mechlorethamine, mechlorethamine oxide hydrochloride,
• alkylating agents such as
• paclitaxel (Taxol®, Bristol-Myers Squibb) and doxetaxel (Taxotere®, Rhone- Poulenc Rorer); chlorambucil; gemcitabine; 6-thioguanine; mercaptopurine; methotrexate; platinum analogs such as cisplatin and carboplatin; vinblastine; platinum; etoposide (VP- 16); ifosfamide; mitomycin C; mitoxantrone; vincristine; vinorelbine; navelbine; novantrone; teniposide; daunomycin; aminopterin; xeloda; ibandronate; CPT-11; topoisomerase inhibitor RFS2000; difluoromethylomithine (DMFO); retinoic acid derivatives such as TargretinTM (bexarotene), PanretinTM, (alitretinoin); OntakTM (denileukin dif
• anti-hormonal agents that act to regulate or inhibit hormone action on tumors
• anti-estrogens including for example tamoxifen, raloxifene, aromatase inhibiting 4(5)-imidazoles, 4-hydroxytamoxifen, trioxifene, keoxifene, LY117018, onapristone, and toremifene (Fareston); and anti- androgens such as flutamide, nilutamide, bicalutamide, leuprolide, and goserelin; and pharmaceutically acceptable salts, acids or derivatives of any of the above.
• Combinations of chemotherapeutic agents are also administered where appropriate, including, but not limited to CHOP, i.e., Cyclophosphamide (Cytoxan®) Doxorubicin (hydroxy doxorubicin), Fludarabine, Vincristine (Oncovin®), and Prednisone.
• CHOP Cyclophosphamide
• Doxorubicin hydroxy doxorubicin
• Fludarabine Fludarabine
• Vincristine Oncovin®
• Prednisone Prednisone
• the chemotherapeutic agent is administered at the same time or within one week after the administration of the engineered cell or nucleic acid. In other embodiments, the chemotherapeutic agent is administered from 1 to 4 weeks or from 1 week to 1 month, 1 week to 2 months, 1 week to 3 months, 1 week to 6 months, 1 week to 9 months, or 1 week to 12 months after the administration of the engineered cell or nucleic acid. In other embodiments, the chemotherapeutic agent is administered at least 1 month before administering the cell or nucleic acid. In some embodiments, the methods further comprise administering two or more chemotherapeutic agents.
• additional therapeutic agents may be used in conjunction with the compositions described herein.
• additional therapeutic agents include PD-1 (or PD-L1) inhibitors such as nivolumab (Opdivo®), pembrolizumab (Keytruda®), pembrolizumab, pidilizumab, and atezolizumab (Tecentriq®).
• Additional therapeutic agents suitable for use in combination with the disclosure include, but are not limited to, ibrutinib (Imbruvica®), ofatumumab (Arzerra®), rituximah (Rituxan®), bevacizumab (Avastin®), trastuzumab (Herceptin®), trastuzumab emtansine (KADCYLA®), imatinib (Gleevec®), cetuximab (Erbitux®), panitumumab (Vectibix®), catumaxomab, ibritumomab, ofatumumab, tositumomab, brentuximab, alemtuzumab, gemtuzumab, erlotinib, gefitinib, vandetanib, afatinib, lapatinib, neratinib, axitinib, masitinib,
• the composition comprising a rejuvenated T cell can be administered with an anti-inflammatory agent.
• Anti-inflammatory agents or drugs include, but are not limited to, steroids and glucocorticoids (including betamethasone, budesonide, dexamethasone, hydrocortisone acetate, hydrocortisone, hydrocortisone, methylprednisolone, prednisolone, prednisone, triamcinolone), nonsteroidal anti-inflammatory drugs (NSAIDS) including aspirin, ibuprofen, naproxen, methotrexate, sulfasalazine, leflunomide, anti-TNF medications, cyclophosphamide and mycophenolate.
• steroids and glucocorticoids including betamethasone, budesonide, dexamethasone, hydrocortisone acetate, hydrocortisone, hydrocortisone, methylprednisolone, prednisolone, prednisone
• Exemplary NSAIDs include ibuprofen, naproxen, naproxen sodium, Cox-2 inhibitors, and sialylates.
• Exemplary analgesics include acetaminophen, oxycodone, tramadol of proporxyphene hydrochloride.
• Exemplary glucocorticoids include cortisone, dexamethasone, hydrocortisone, methylprednisolone, prednisolone, or prednisone.
• Exemplary biological response modifiers include molecules directed against cell surface markers (e.g., CD4, CD5, etc.), cytokine inhibitors, such as the TNF antagonists, (e.g., etanercept (ENBREL®), adalimumab (HUMIRA®) and infliximab (REMICADE®)), chemokine inhibitors and adhesion molecule inhibitors.
• TNF antagonists e.g., etanercept (ENBREL®), adalimumab (HUMIRA®) and infliximab (REMICADE®)
• chemokine inhibitors esion molecule inhibitors.
• adhesion molecule inhibitors include monoclonal antibodies as well as recombinant forms of molecules.
• Exemplary DMARDs include azathioprine, cyclophosphamide, cyclosporine, methotrexate, penicillamine, leflunomide, sulfasalazine, hydroxychloroquine, Gold (oral (auranofin) and intramuscular) and minocycline.
• compositions described herein are administered in conjunction with a cytokine.
• a cytokine may comprise a protein from natural sources or from recombinant cell culture, and biologically active equivalents of the native sequence cytokines.
• the isolated T cells can be genetically modified following isolation using known methods, or the T cells can be partially reprogrammed, activated and expanded in vitro prior to being genetically modified.
• the T cells are genetically modified with a recombinant TCR or CAR and then are rejuvenated using the partial reprogramming and reactivation methods described herein.
• the rejuvenated cells described herein are further activated and/or expanded in vitro.
• Methods for activating and expanding immune cells are known in the art and are described, for example, in U.S. Pat. Nos. 6,905,874; 6,867,041; 6,797,514; and WO2012/079000.
• such methods include contacting the T cells with a stimulatory (e.g., activating) agent (in certain embodiments, referred to as a T cell activating compound) (e.g., an agent that stimulates a CD3/TCR complex (for example, an anti-CD3 antibody or a CD3 agonist) and a costimulatory agent (an agent such as an antibody or ligand that stimulates CD28, ICOS, CD27, HVEM, LIGHT, CD40, 4- 1BB, 0X40, DR3, GITR, CD30, TIM1, CD2, CD226 or any combination thereof).
• a stimulatory agent e.g., activating
• a T cell activating compound e.g., an agent that stimulates a CD3/TCR complex (for example, an anti-CD3 antibody or a CD3 agonist) and a costimulatory agent (an agent such as an antibody or ligand that stimulates CD28, ICOS, CD27, HVEM, LIGHT, CD40, 4-
• the rejuvenated T cell may be activated and stimulated to proliferate with feeder cells and appropriate antibodies and cytokines using methods such as those described in U.S. Pat. Nos. 6,040,177; 5,827,642; and WO/2012129514.
• the disclosure provides a method of storing the rejuvenated T cells described herein. This involves cryopreserving the T cells such that the cells remain viable upon thawing. A fraction of the T cells can be cryopreserved by methods known in the art to provide a permanent source of such cells for the future treatment of patients afflicted with a malignancy. When needed, the cryopreserved T cells can be thawed, grown and expanded for more such cells.
• cryopreserve refers to the preservation of cells by cooling to sub-zero temperatures, such as (typically) 77 Kelvin or 196° C. (the boiling point of liquid nitrogen). Cryoprotective agents are often used at sub-zero temperatures to prevent the cells being preserved from damage due to freezing at low temperatures or warming to room temperature. Cryopreservative agents and optimal cooling rates can protect against cell injury.
• Cryoprotective agents which can be used in accordance with the disclosure include but are not limited to: dimethyl sulfoxide (DMSO) (Lovelock & Bishop, Nature, 1959, 183, 1394-1395; Ashwood-Smith, Nature, 1961, 190, 1204-1205), glycerol, polyvinylpyrrolidine (Rinfret, Ann. N.Y. Acad. Sci., 1960, 85, 576), and polyethylene glycol (Sloviter & Ravdin, Nature, 1962,
• the preferred cooling rate is l°-3° C/minute.
• the term, “substantially pure,” is used to indicate that a given component is present at a high level.
• the component is desirably the predominant component present in a composition. Preferably it is present at a level of more than 30%, of more than 50%, of more than 75%, of more than 90%, or even of more than 95%, said level being determined on a dry weight/dry weight basis with respect to the total composition under consideration. At very high levels (e.g.
• the component can be regarded as being in “pure form.”
• Biologically active substances of the present disclosure can be provided in a form that is substantially free of one or more contaminants with which the substance might otherwise be associated.
• the contaminant will be at a low level (e.g., at a level of less than 10%, less than 5%, or less than 1% on the dry weight/dry weight basis set out above).
• the cells herein are formulated by first harvesting them from their culture medium, and then washing and concentrating the cells in a medium and container system suitable for administration (a “pharmaceutically acceptable” carrier) in a treatment- effective amount.
• a medium and container system suitable for administration a “pharmaceutically acceptable” carrier
• Suitable infusion media can be any isotonic medium formulation, typically normal saline, NormosolTM R (Abbott) or Plasma-LyteTM A (Baxter), but also 5% dextrose in water or Ringer’s lactate can be utilized.
• the infusion medium can be supplemented with human serum albumin.
• Desired treatment amounts of cells in the composition is generally at least 2 cells or is more typically greater than 102 cells, and up to 106, up to and including 108 or 109 cells and can be more than 1010 cells.
• the number of cells will depend upon the desired use for which the composition is intended, and the type of cells included therein.
• the density of the desired cells is typically greater than 106 cells/ml and generally is greater than 107 cells/ml, generally 108 cells/ml or greater.
• the clinically relevant number of immune cells e.g., T cells
• T cells can be apportioned into multiple infusions that cumulatively equal or exceed 105, 106, 107, 108, 109, 1010, 1011, or 1012 cells.
• 106/kilogram 106-1011 per patient
• Rejuvenated T cell treatments may be administered multiple times at dosages within these ranges.
• the cells may be autologous, allogeneic, or heterologous to the patient undergoing therapy.
• the rejuvenated T cells of the present disclosure may be administered either alone, or as a pharmaceutical composition in combination with diluents and/or with other components such as IL-2 or other cytokines or cell populations.
• Pharmaceutical compositions of the present disclosure may comprise a rejuvenated T cell population as described herein, in combination with one or more pharmaceutically or physiologically acceptable carriers, diluents or excipients.
• compositions may comprise buffers such as neutral buffered saline, phosphate buffered saline and the like; carbohydrates such as glucose, mannose, sucrose or dextrans, mannitol; proteins; polypeptides or amino acids such as glycine; antioxidants; chelating agents such as EDTA or glutathione; adjuvants (e.g., aluminum hydroxide); and preservatives.
• buffers such as neutral buffered saline, phosphate buffered saline and the like
• carbohydrates such as glucose, mannose, sucrose or dextrans, mannitol
• proteins polypeptides or amino acids such as glycine
• antioxidants e.g., chelating agents such as EDTA or glutathione
• adjuvants e.g., aluminum hydroxide
• preservatives e.g., aluminum hydroxide
• compositions of the present application can comprise, consist essentially of, or consist of, the components disclosed.
• compositions of the disclosure may include one or more of the following: sterile diluents such as water for injection, saline solution, preferably physiological saline, Ringer’ s solution, isotonic sodium chloride, fixed oils such as synthetic mono or diglycerides which may serve as the solvent or suspending medium, polyethylene glycols, glycerin, propylene glycol or other solvents; antibacterial agents such as benzyl alcohol or methyl paraben; antioxidants such as ascorbic acid or sodium bisulfate; chelating agents such as ethylene-diaminetetraacetic acid; buffers such as acetates, citrates or phosphates and agents for the adjustment of tonicity such as sodium chloride or dextrose.
• the parenteral preparation can be enclosed in ampoules, disposable syringes or multiple dose vials made of glass or plastic.
• An injectable pharmaceutical composition is preferably sterile.
• dimerization pairs may include cyclosporine- A/cyclophilin, receptor, estrogen/estrogen receptor (optionally using tamoxifen), glucocorticoids/glucocorticoid receptor, tetracycline/tetracycline receptor, vitamin D/vitamin D receptor.
• dimerization technology can be found in e.g., WO 2014/127261, WO 2015/090229, US 2014/0286987, US 2015/0266973, US 2016/0046700, U.S. Patent No. 8,486,693, US 2014/0171649, and US 2012/0130076.
• Suitable techniques for genetic modification of the rejuvenated cells herein include use of inducible caspase-9 (U.S. Appl. Pub. No. 2011/0286980) or a thymidine kinase, before, after or at the same time, as the cells are genetically modified to express a CAR or other engineered TCR. Additional methods for introducing suicide genes and/or “on” switches include CRISPR, TALENS, MEGATALEN, zinc fingers, RNAi, siRNA, shRNA, antisense technology, and other techniques known in the art. IV. Kits
• kits e.g., pharmaceutical kits, comprising at least one reprogramming factor for contacting one or more T cells in vitro.
• Kits typically include a label indicating the intended use of the contents of the kit and instructions for use.
• label includes any writing, or recorded material supplied on or with the kit, or which otherwise accompanies the kit.
• the disclosure provides a kit for preparing one or more T cells for a T cell therapy for a subject in need thereof, the kit comprising at least one reprogramming factor selected from the group consisting of KLF4, OCT3/4, SOX2 and C-MYC, and optionally, SV40.
• the disclosure provides for a kit for preparing one or more T cells for a T cell therapy for a subject in need thereof, the kit comprising at least one expression vector capable of expression at least one reprogramming factor selected from the group consisting of KLF4, OCT3/4, SOX2 and C-MYC.
• the disclosure provides for a kit for preparing one or more T cells for a T cell therapy for a subject in need thereof, the kit comprising at least one Sendai virus vector capable of expression at least one reprogramming factor selected from the group consisting of KLF4, OCT3/4, SOX2 and C- MYC.
• the kit further comprises a Sendai virus vector capable of expressing SV40.
• the disclosure provides a kit for preparing one or more T cell vectors for a T cell therapy for a subject in need thereof, the kit comprising:
• the disclosure provides a kit for preparing one or more T cell vectors for a T cell therapy for a subject in need thereof, the kit comprising:
• a Sendai vims encoding C-MYC [0349] A Sendai vims encoding C-MYC; and [0350] A Sendai vims encoding SV40.
• the disclosure provides a kit for preparing one or more T cell vectors for a T cell therapy for a subject in need thereof, the kit comprising a multicistronic Sendai virus vector encoding KLF4, OCT3/4, SOX2, C-MYC and optionally SV40.
• the kit may further comprise a T-cell activating compound or agent.
• the T cell activating compound or agent is an anti-CD3 antibody.
• the kit comprises a costimulatory agent, such as an anti- CD28 antibody.
• the kit comprises both an anti-CD3 antibody and an anti-CD28 antibody.
• the kit may further comprise one or more appropriate culture media for culturing and/or partially reprogramming T cells.
• the kit may further comprise one or more cytokines. Such cytokines include but are not limited to IL-2, IL-7, IL-15 and IL-12.
• the present invention may be characterized by one or more of the following clauses defining various embodiments as described herein.
• the present invention relates to [1]:
• An in vitro method of producing at least one rejuvenated T cell comprises (a) contacting a population of T cells with at least one reprogramming factor selected from the group consisting of KLF4, OCT3/4, SOX2,C-MYC, and SV40, for a period of time sufficient for T cell derived adherent cells to form; wherein said T cells are not transformed into iPS or totipotent cells; and (b) contacting the T cell derived adherent cells with at least one T cell activating compound.
• the present invention relates to [2] :
• An in vitro method of producing at least one T cell comprising (a) contacting a population of T cells in a first culture medium in a culture vessel with at least one reprogramming factor selected from the group consisting of KLF4, OCT3/4, SOX2, C-MYC, and SV40, for a period of time sufficient for the T cells to form at least one colony attached to the culture vessel surface; wherein said T cells are not transformed into iPS cells or totipotent cells; and (b) contacting the at least one attached colony with at least one T cell activating compound.
• at least one reprogramming factor selected from the group consisting of KLF4, OCT3/4, SOX2, C-MYC, and SV40
• the present invention relates to [3]:
• An in vitro method of producing at least one T cell comprising (a) contacting a population of T cells in a first culture medium with at least one reprogramming factor selected from the group consisting of KLF4, OCT3/4, SOX2, C-MYC, and SV40, for a period of at least about 5 days and no more than about 10 days; wherein said T cells are not transformed into iPS cells or totipotent cells; and (b) contacting the T cells with at least one T cell activating compound.
• the present invention relates to [4] : [0361]
• An in vitro method of producing at least one T cell comprising (a) contacting a population of T cells with at least one reprogramming factor selected from the group consisting of KLF4, OCT3/4, SOX2, C-MYC, and SV40 for a period of time sufficient for the T cells to express at least one marker selected from the group consisting of integrin a ⁇ b ⁇ , SSEA4, CD9, and CD90; wherein said T cells are not transformed into iPS cells or totipotent cells; and (b) contacting the T cells with at least one T cell activating compound.
• the present invention relates to:
• [0363] The method of any one of [1] to [4] wherein the T cells are contacted with the at least one reprogramming factor for a period of time sufficient for at least a portion of the T cells to express CD3 and at least one marker selected from the group consisting of integrin a ⁇ b ⁇ , SSEA4, CD9, and CD90, preferably SSEA4 and CD3, more preferably CD3, CD9 and CD90, even more preferably CD3, SSEA4, CD9 and CD90.
• the T cell is a TCRa+TCI ⁇ + cell; a TCRg(Gamma)+TCRd(Delta) cell; a CD4+CD8o$+ double positive cell, CD4+ single positive cell (such as Thl, Th2, Thl7, Treg), a naive T cell, a central memory T cell, or effector memory T cell, or wherein the T cell expresses an activation marker after co-culture with autologous tumor cells, wherein the activation marker is 4-1BB (CD137), PD1, LAG3, CD45, CD39, TIGIT, TIM3, CD69, 0X40, CD28, CD25, CD49d, and CTLA4.
• the activation marker is 4-1BB (CD137), PD1, LAG3, CD45, CD39, TIGIT, TIM3, CD69, 0X40, CD28, CD25, CD49d, and CTLA4.
• T cells are isolated from a mammal,, preferably a human.
• the T cells are contacted with the at least one reprogramming factor, preferably KLF4, OCT3/4, SOX2 and C-MYC, for at least about 4 to 10 days, preferably for at least about 4 to 7 days, more preferably for about 5 days.
• the at least one reprogramming factor preferably KLF4, OCT3/4, SOX2 and C-MYC
• the at least one reprogramming factor is expressed in the T cell, preferably the least one reprogramming factor is expressed using a non-integrating viral vector or a nucleic acid delivered to the cell with a nanoparticle, more preferably the vector is a Sendai virus, even more preferably the at least one reprogramming factor is KLF4, OCT3/4, SOX2 and C-MYC.
• [0370] [11a] The method of any one of [1] to [11] wherein the at least one reprogramming factor is expressed in the T cell for: a) a period of time sufficient for T cell derived adherent cells to form and wherein said isolated T cells are not transformed into iPS or totipotent cells; b) about 4 days to about 10 days; c) about 4 days to about 11 days; d) about 4 days to about 12 days; e) about 4 days to about 13 days; or f) about 4 days to about 14 days.
• [0374] [15] The method of any one of [1] to [14], further comprising engineering the T cell to express a cell surface receptor, wherein said T cell is engineered prior to or after contacting said T cell with said at least one reprogramming factor, preferably said cell surface receptor is either a chimeric antigen receptor or a T cell receptor or a hybrid receptor thereof, more preferably said cell surface receptor recognizes a specific antigenic moiety on the surface of a target cell.
• resulting T cells comprise an incomplete set of V, D, and J segments of T cell receptor genes and/or further comprising measuring the epigenetic age of the resulting T cells, preferably the epigenetic age of the resulting T cells is at least 5% younger than the population of T cells prior to reprogramming.
• the resulting T cells comprise an incomplete set of V, D, and J segments of T cell receptor genes and/or further comprising measuring the epigenetic age of the resulting T cells, preferably the epigenetic age of the resulting T cells is at least 5% younger than the population of T cells prior to reprogramming and the T cells do not express NCAM1, NCR2, FCGR3A, KIR2DL4, or KIR2DS4.
• the present invention relates to [20]:
• An in vitro method of producing a T cell comprising culturing T cells in a first medium comprising IL-2 and activating said T cells with at least one antibody specific for CD3 or for CD28, or both; contacting said activated T cells with KLF4, OCT3/4, SOX2 and C- MYC, for a period of about five days to about 10 days; in a second culture medium that does not comprise IL-2, or antibody specific for CD3 or CD28; wherein said T cells are not completely reprogrammed into iPSC cells; replacing said second culture medium with a third culture medium comprising IL-2 and at least one antibody specific for CD3 and/or CD28; wherein the T cells are cultured in said third culture medium for at least about 5 days.
• the present invention relates to one or more of:
• T cell is a TCRa+TCR + cell; a TCRg(Gamma)+TCRd(Delta) cell; a CD4+CD8a + double positive cell, CD4+ single positive cell (Thl, Th2, Thl7,Treg), a naive T cell, a central memory T cell, or effector memory T cell.
• [0385] [24] The method of any one of [20] to [23], wherein the T cell expresses an activation marker after co-culture with autologous tumor cells, wherein the activation marker is 4-1BB (CD137), PD1, LAG3, CD45, CD39, TIGIT, TIM3, CD69, 0X40, CD28, CD25, CD49d, and CTLA4.
• the activation marker is 4-1BB (CD137), PD1, LAG3, CD45, CD39, TIGIT, TIM3, CD69, 0X40, CD28, CD25, CD49d, and CTLA4.
• TIL tumor infiltrating lymphocyte
• the present invention relates to [26] :
• a population of T cells whose epigenetic age is at least 5% younger than its chronological age, preferably at least 25% younger than its chronological age.
• the present invention relates to [27] :
• the present invention relates to:
• T cells are TILs, wherein at least 50% of the TILs express both CCR7 and CD62L, or wherein at least 50% of the TILs express both CCR7 and TCL7.
• [0397] [33] A population of T cells according to any one of [26] to [32] for use in therapy. [0398] [34] A population of T cells according to any one of [26] to [32], for use in a method for treating a cancer, a viral condition or an autoimmune disorder.
• the cancer is acute lymphocytic cancer, acute myeloid leukemia, alveolar rhabdomyosarcoma, bone cancer, brain cancer, breast cancer, cancer of the anus, anal canal, or anorectum, cancer of the eye, cancer of the intrahepatic bile duct, cancer of the joints, cancer of the neck, gallbladder, or pleura, head and neck cancers (e.g., cancer of the nose, nasal cavity, or middle ear, cancer of the oral cavity), cancer of the vulva, chronic lymphocytic leukemia, chronic myeloid cancer, colon cancer, esophageal cancer, cervical cancer, gastrointestinal carcinoid tumor, Hodgkin lymphoma, hypopharynx cancer, kidney cancer, larynx cancer, liver cancer, lung cancer, malignant mesothelioma, melanoma, multiple myeloma, nasopharyn
• the present invention relates to:
• a method of producing rejuvenated T cells comprising contacting a population of T cells (i) at least one reprogramming factor selected from the group consisting of KLF4, OCT3/4, SOX2 and C-MYC, and (ii) optionally SV40, for at least a period of time sufficient for at least 20% of the contacted T cells to express a ⁇ b ⁇ integrin and wherein said contacted T cells are not transformed into iPS cells; isolating said at least 20% of the contacted T cells with a binding molecule that specifically binds to a ⁇ b ⁇ integrin; contacting the isolated cells of (b) with a T cell activating and/or a T cell costimulatory agent; thereby producing rejuvenated T cells.
• the present invention relates to:
• a method of producing at least one rejuvenated T cell comprising transiently contacting the population of T cells with (i) at least one reprogramming factor selected from the group consisting of KLF4, OCT3/4, SOX2 AND C-MYC, and (ii) optionally SV40, for a period of time sufficient for T cell derived adherent cells to form; wherein said T cells are not transformed into iPS or totipotent cells; isolating a subpopulation of T cell derived adherent cells that express either a6 (CD49f) or bl (CD29) integrin or both; and contacting the isolated subpopulation with at least one T cell activating compound.
• at least one reprogramming factor selected from the group consisting of KLF4, OCT3/4, SOX2 AND C-MYC, and (ii) optionally SV40, for a period of time sufficient for T cell derived adherent cells to form; wherein said T cells are not transformed into iPS or totipotent cells; isol
• the present invention relates to:
• a population of rejuvenated T cells produced by a method comprising contacting the population of T cells with (i) at least one reprogramming factor selected from the group consisting of KLF4, OCT3/4, SOX2 AND C-MYC, and (ii) SV40, for a period of time sufficient for T cell derived adherent cells to form; wherein said T cells are not transformed into iPS or totipotent cells; isolating a subpopulation of T cell derived adherent cells that express either a6 integrin, bl integrin or both; and contacting the subpopulation of T cell derived adherent cells with at least one T cell activating compound.
• the present invention relates to:
• the present invention relates to:
• the present invention relates to:
• a T cell whose epigenetic age is at least 5%, 6%, 7%, 8%, 9%, 10%, 15%, 20%, 25%, 30%, 35%, 40%, 45%, 50%, 55%, 60%, 65%, 70%, 75%, or at least 80% younger than its chronological age (or an appropriate control T cell) and wherein the T cell is enriched for oxidative phosphorylation, fatty acid metabolism, glycolysis and hypoxia gene sets as determined by transcriptome analysis.
• a T cell whose epigenetic age is at least 5%, 6%, 7%, 8%, 9%, 10%, 15%, 20%, 25%, 30%, 35%, 40%, 45%, 50%, 55%, 60%, 65%, 70%, 75%, or at least 80% younger than its chronological age (or an appropriate control T cell) and wherein the T cell is enriched for both oxidative phosphorylation and glycolysis gene sets as compared to control T cells, as determined by transcriptome analysis.
• a T cell whose epigenetic age is at least 5%, 6%, 7%, 8%, 9%, 10%, 15%, 20%, 25%, 30%, 35%, 40%, 45%, 50%, 55%, 60%, 65%, 70%, 75%, or at least 80% younger than its chronological age (or an appropriate control T cell) and wherein the T cell does not express unconventional, NK, T or B cell markers (e.g., NCAM1, NCR2, FCGR3A, KIR2DL4, or KIR2DS4).
• unconventional, NK, T or B cell markers e.g., NCAM1, NCR2, FCGR3A, KIR2DL4, or KIR2DS4
• the present invention relates to
• a method of producing rejuvenated T cells comprising: a) contacting a population of T cells (i) at least one reprogramming factor selected from the group consisting of KLF4, OCT3/4, SOX2 and C-MYC, and (ii) optionally SV40, for at least a period of time sufficient for at least 20% of the contacted T cells to express a6b1 integrin and wherein said contacted T cells are not transformed into iPS cells; b)isolating said at least 20% of the contacted T cells with a binding molecule that specifically binds to a6b1 integrin; c) contacting the cells of (b) with a T cell activating and/or a T cell costimulatory agent; thereby producing rejuvenated T cells; [47] wherein the binding molecule that specifically binds to an a6b1 integrin is selected from Laminin-511, Laminin-511E8, an anti-CD29 antibody, and an anti-Cd49
• a method of producing a rejuvenated T cell comprising a) transiently contacting a population of T cells with (i) at least one reprogramming factor selected from the group consisting of KLF4, OCT3/4, SOX2 AND C-MYC, and (ii) optionally SV40, for a period of time sufficient for T cell derived adherent cells to form; wherein said T cells are not transformed into iPS or totipotent cells; b) isolating a subpopulation of T cell derived adherent cells that express either a6 (CD49f) or bl (CD29) integrin or both; and c) contacting the subpopulation with at least one T cell activating compound.
• a population of rejuvenated T cells produced by a method comprising: a) contacting the population of T cells with (i) at least one reprogramming factor selected from the group consisting of KLF4, OCT3/4, SOX2 AND C-MYC, and (ii) SV40, for a period of time sufficient for T cell derived adherent cells to form; wherein said T cells are not transformed into iPS or totipotent cells; b) isolating a subpopulation of T cell derived adherent cells that express either a6 integrin, bl integrin or both; and c) contacting the subpopulation of T cell derived adherent cells with at least one T cell activating compound.
• [0422] [50] A population of T cell derived adherent cells, wherein at least 70% of the cells express integrin a6 or integrin b ⁇ ; or [51] wherein at least 50% of the cells express both integrin a6 and integrin b ⁇ ; or [52] wherein at least 70% of the cells express both integrin a6 and integrin b ⁇ .
• T cells transient exposure of T cells to cell reprogramming conditions (in this case using a Sendai virus carrying four Yamanaka factors) results in partially reprogrammed T cells with reduced epigenetic age that have high proliferative capacity and retain antigen specificity.
• the treated T cells begin to de-differentiate, express markers more typically seen in stem cells (e.g., SSEA4) and attach to the culture vessel surface to form epithelial-type colonies.
• SSEA4 markers more typically seen in stem cells
• the treated cells begin to lose T cell identity (loss of CD3 and CD8 expression). Subsequent activation can guide these “T cell derived adherent cells” to recover their T cell identity and exhibit a surprisingly increased potential for expansion (250-fold in 6 days).
• Example 1 Partial Reprogramming conditions for T Cells [0425] In this experiment the reprogramming conditions for rejuvenating and improving T cell biological properties was explored.
• CD8 positive T cells isolated with MACS magnetic beads (Miltenyi Biotec) from the PBMC of a 21-year-old male (Donor 11360; cell purchased from Allcells, Alameda, CA), were stimulated with soluble CD3 (Cat. No.
• T cell culture medium with 60 II I/ml IL2
• the Sendai virus (Cytotune iPS 2.0 Sendai Reprogramming Kit, ThermoFisher) was composed of three vectors: 1) encoding KLF4-OCT3/4-SOX2 (KOS), 2) encoding KLF4; 3) encoding C- MYC. Collectively, these are known as the “Yamanaka factors” and are depicted as the “4Factors” or “4F” in the figures. Additionally, a Sendai vims vector encoding SV40 was used to increase reprogramming efficiency.
• the activated CD8 T cells were divided into four groups.
• Group #1 is a control group in which the T cells were cultured in the T cell culture medium during the entire process.
• Group #2 was not transduced with Sendai virus either and was cultured in stem cell medium (SCM) (StemFit Basic02 with bFGF, Ajinomoto) without IL2 from day 1.
• Cells for Groups #1 and #2 were seeded 50,000 cells per well of 96-well plate in triplicate.
• Group #3 was transduced with 23 multiplicity of infection (MO I) of EmGFP Sendai virus (Cytotune EmGFP Sendai Fluorescence reporter, Thermo), and 5 MOI of SV40 Sendai vims.
• Group #3 cells were plated at a density of 50,000 per well in a 24 well plate which was coated with recombinant human Laminin511-E8 fragment (iMatrix-511 , Cat. No. T304, Takara) in triplicate according to the manufacturer protocol.
• Group #4 was transduced with 10 MOI KOS Sendai vector, 10 MOI of KLF4 vector, 3 MOI of cMyc vector, and 5 MOI of SV40 vector. Cells were cultured in SCM without IL2 from day 1 and plated at a density of 80,000 cells per well in a 24-well plate coated with iMatrix-511 in quadmplicate. See FIG. 1 and Table 2 for the complete experimental design.
• the T cells in Group #4 started colony formation from day 3 or day 4. See, FIG. 2. Cells attached to the bottom of the coated plate forming colonies is not seen in normal T cell culture. The T cells in the other conditions did not show any colony formation and did not attach to the bottom of the culture plate.
• Figure 3 compares the attached cells from Group #4 (which expressed the four Yamanaka factors) with the appearance of the T cells from Group #3 (which did not express the Yamanaka factors; and instead expressed GFP). The attached cells showed colony formation and were bigger than the T cells in Group #3. This suggests that the T cell derived adherent cells were losing T cell identity.
• the T cell derived adherent cells from Group #4 are also bigger than standard activated T cells (FIG. 3D).
• FIG. 3A - 3F panels show T cells cultured under the various conditions as follows: 3A, 3C, 3E: attached colonies from Group #4; 3B: cells from Group #3; 3D: T cells cultured under standard T cell activation conditions; 3F: standard iPS cell colonies.
• the partially reprogrammed cells show a distinct morphology.
• flow cytometry analysis showed decreased CD3 marker expression in Groups #2, #3, and #4 cells all of which were in stem cell medium without IL2 from day 1. See, e.g., FIG. 4.
• CD3 is an important marker of T cell identity among lymphocytes. The reduction was conspicuous in the T cell derived adherent cells of Group #4.
• Example 2 Reactivation of Partially Reprogrammed T Cells
• the partially reprogrammed T cells were reactivated on day five using one to one- hundred diluted T cell TRANSACTTM (Miltenyi Biotec) in T cell culture medium for 2 days in a 96 well plate.
• Cells in the Group #4 condition were divided into two wells at day 5 — the floating cells were transferred to one well and the cells that were attached after being exposed to the reprogramming conditions were detached from the vessel surface, washed and transferred to another well.
• a large number of the cells from Group #3 died, likely due to the toxicity of Sendai virus. It is hypothesized that the Yamanaka factors expressed in Group #4 were able to rescue the cells from Sendai virus toxicity.
• SV40 were introduced into the T cells by Sendai virus transduction also as described above.
• the infected T cells were transferred onto iMatrix coated dishes on day 1 and were cultured in (a) T cell media + 60 II I/ml IL2 or (b) in iPS cell media 60 II I/ml IL2 for 3 days and then changed to iPS cell media without IL2 from day 4.
• the floating and attached cells were harvested for flow cytometry analysis.
• SSEA4 and CD3 expression were analyzed.
• SSEA4 is a carbohydrate epitope considered a wide-ranging stem cell marker expressed from partially reprogrammed somatic cells all the way to pluripotent stem cells.
• eAge epigenetic age
• Group #1 cells After reprogramming and subsequent T cell activation, Group #1 cells had a calculated eAge of 20.8 years, while the attached cells from Group #4 had a calculated eAge of 10.0 years old (note that cells that attach to the vessel surface during the partial reprogramming process detach from the surface upon or soon after activation. Such cells are referred to as “detached” cells to distinguish them from floating cells). This indicates that the partial reprogramming process resulted in rejuvenation of the cells from a measured eAge of 21.5 years to about 10 years. Floating cells in Group #4 had a calculated eAge of 14.5 years, and the T cells in Group #2 also had a calculated eAge of 14.6 years despite not being transduced with the four Yamanaka factors. This suggests that the stem cell culture medium itself (StemFit, Ajinomoto) contains components that provide some potential to rejuvenate cells although its contents are not publicly known. The results are summarized below in Table 3.
• Table 3 Epigenetic age of partially reprogrammed T cells Horvath Predicted counts of
• Sendai virus transductions were as follows: KOS 10MOI, KLF4 10MOI, cMyc 3MOI, SV405MOI and were carried out in TCM with 60IU/ml IL2.
• the reprogramming culture conditions were 50/50 TCM/iPS media (Stemfit) with 60IU/ml IL2 for 3 days followed by culture in Stemfit w/o IL2 until the second activation. After reprogramming for the time periods indicated, the floating cells and the attached cells were harvested. Cells were then activated with TRANSACT at 1:100 in TCM + 60 TIJ/ml IL2.
• FIG. 11 is a schematic summarizing the process for PBMC-derived CD8 T cells (see also Table 4).
• conventional cytotoxic T cells express CD8a- CD8p heterodimer.
• Non- conventional T cells for instance intraepithelial lymphocyte (IEL) and gamma deltT cells express CD8aa homodimer.
• IEL intraepithelial lymphocyte
• gamma deltT cells express CD8aa homodimer.
• FACS was used to determine whether the T cells generated using the partial rejuvenation process were able to express the canonical CD8 T cell markers. Lack of CD8 ⁇ 3 ⁇ 4P expression post-stimulation could indicate that the partially rejuvenated T cells are not conventional cytotoxic T cells.
• T cell derived adherent cell colonies reactivated with TCM from days 6-10 express CD8a and CD8p indicative of a return to a normal CD8 T cell phenotype.
• Delay of reactivation past day 10 of the current reprogramming method to return the de-differentiated T cells to the T cell phenotype resulted in an increase of CD4- CD8- population (see FIG. 12A, upper and lower panels at day 10 where the CD8a expression is shifting to the left side (lower MFI).
• CD8a negative cells are not matured T cells. After day 10, when gating on the CD8a positive population, more CD8p negative cells (CD8aa+ non-conventional T cells) were observed (see FIG. 12B day 13 FACS plots).
• Example 5 Cytokine Production Assay and Degranulation Assay of Rejuvenated NY-ESO-1 TCR Transduced T cells Demonstrate T Cell Functionality.
• CD8+ T cells genetically modified to express an NY-ESO-l-specific TCR were partially reprogrammed, stimulated with T cell activation molecules and the response to target cells pulsed with NY- ESO-1 peptide was measured.
• Peripheral blood-derived CD8+ T cells from a 42-year old male were purchased from Allcells (Alameda, CA). Cells were thawed and stimulated with TRANSACT (1/100) in TCM with IL-2 (60 IU/ml) as described in Example 4. The next day, T cells were transduced with NY-ESO-1 TCR by lentivirus vector transduction as follows:
• T cells were stimulated with a 1:100 dilution of T cell TRANSACT (Miltenyi) for 30 hours. Virus was then added to the T cells for 24 hours. Stimulation and viral infection were then terminated by addition of 7 volumes of fresh media without TRANSACT, and cells were cultured for 7 additional days in Grex-24 plates (Wilson Wolf) prior to cryopreservation in CryoStor CS10 (STEMCELL Technologies) at 3 x 107 cells/ml (see also Robbins 2008 J Immunol, 180(9) 6116-6131). Control T cells were not transduced and stimulated similarly.
• NY-ESO-1 specific T cells were thawed and stimulated with TRANSACT (1/100) in TCM with IL-2 (60 IU/ml).
• the cells were then stimulated on day 9 with TRANSACT to obtain the rejuvenated NY-ESO-1 specific T cells (second stimulation) as described above.
• the rejuvenated NY-ESO-1 -specific T cells were re-stimulated with TRANSACT again at day 16 (3rd stimulation) to expand them (see FIG. 13).
• Cytokine production and degranulation assays were carried out on day 26 as follows. Control non-transduced T cells and NY-ESO-1 specific TCR transduced T cells were thawed and stimulated with TRANSACT (1/500) in TCM with IL-2 (60 IU/ml) one week in order to expand. Non transduced T cells, NY-ESO-1 specific TCR transduced T cells and rejuvenated NY-ESO-1 specific TCR T cells were compared to effector cells. Target cells, T2 were cultured in T2 media (RPMI, 20% FCS and P/SM).
• T2 cells were pre-cultured with or without NY-ESO-1 peptide (SLLMWITQC) (lOnM) for one hour, washed and counted.
• SLLMWITQC NY-ESO-1 peptide
• One well contained 5x104 effector cells and 1x105 target cells (E:T ratio of 2:1).
• PMA/Ionomycin Cell Activation Cocktail by Biolegend
• GolgiPlug and GolgiStop were added according to manufacturer instructions.
• anti-CD107a Ab-BV421 were added in culture media (lul / well). Cells were cultured for six hours in TCM without cytokines.
• the co-cultured cells were then stained for surface antigens (PE-NY-ESO-1 tetramer, BUV395-CD8, BUV496-CD4, and BUV805-CD3). Live/dead eFluor 780 was also added to exclude dead cells. After 20 minutes cells were washed. Cells were fixed and permeabilized by BD cytofix cytoperm kit according to manufacturer instruction. The cells were then stained for intracellular cytokine expression (FITC-IFNg, APC-IL-2, and BV785-TNFa). After a 30-minute incubation, cells were washed twice and analyzed by flow cytometry using a ZE5 instrument. The FACS results were analyzed by FlowJo software.
• the frequency of IFNg +, TNFa +, IL-2 +, and CD107a + were calculated as shown in FIG. 14. The results showed that the rejuvenated NY-ESO-1+ transduced T cells retain functionality and are antigen-specific.
• cell surface proteins were profiled in activated T cells, unstimulated T cells, iPS cells and day 5 attached partially reprogrammed T cells (T cell derived adherent cells).
• the purpose of the screen was to identify markers expressed in partially reprogrammed cells that can be used to identify intermediate cells and to characterize the partial reprogramming process and cells produced using the method.
• T cell culture media was prepared as previously described.
• CD4+ and CD8+ T cells (cell ID 3046087I&K from Allcells) were thawed.
• T cells were stimulated with lOOng/ml anti-CD3 and 2ug/ml anti-CD28 (anti-human CD3 OKT3 and CD28 CD28.2 antibodies from BioLegend, San Diego, CA), plus 60IU IL-2 for three days.
• the cord blood-derived iPS cell line, NL5GFP, and tumor infiltrating lymphocyte (TIL) derived iPS cell line, hi4095 #8, were cultured in Stemfit and harvested.
• T cells and iPS cells were stained with BioLegend LEGENDScreen (BioLegend, San Diego, CA) plus anti-CD8, CD4, CD3,SSEA4, Live/Dead and expression level of 371 markers was determined using flow cytometry.
• the results of the initial screen identified 39 candidate markers as listed below, chosen based on their expression level in T cells and iPS cells. Markers were selected that showed significantly higher level in stimulated or unstimulated T cells versus iPS cells or that showed a different expression pattern between iPS cells and T-iPS cells. These markers and the ranking of their relative expression levels in stimulated or unstimulated T cells versus iPS cells are summarized in Table 5 below. The data are also shown graphically in a waterfall plot in FIG.
• FIG. 15 (stimulated T cells versus NL5iPS cells) and FIG. 16 (unstimulated T cells versus T-iPS cells).
• CD4+ and CD8+ T cells (cell ID 3046087I&K from Allcells) were thawed and stimulated with lOOng/ml anti-CD3 and 2ug/ml anti-CD28, plus 60IU IL-2. After three days, T cells were transduced with 10 MOI KOS Sendai vector, 10 MOI of KLF4 vector, 3 MOI of cMyc vector, and 5 MOI of SV40 vector as described in previous examples. After 5 days, attached cells were harvested and screened as described above for surface expression of the markers identified in the first screen. Unstimulated T cells, stimulated T cells, NL5 iPS cells and hi4095 iPS cells were used as controls.
• CD164, CD9, CD63, CD90, CD71, CD326, TRA-1-81 and TRA-1-60-R expression were found to be increased in Day 5 partially reprogrammed attached cells as compared to stimulated and unstimulated T cells, while CD352 and CD31 were downregulated.
• this second screen identified CD9 and CD90 as potential indicators of the early transition during partial reprogramming while at day 5, expression levels of known iPS cell markers SSEA3 and SSEA4 were not significantly changed.
• CD9 is also known as tetraspanin-29 and has four transmembrane domains. It is involved in cell adhesion, signal transduction and cellular differentiation.
• CD90 is also known as THY-1.
• Example 7 Stimulation signaling is critical for rejuvenated T cells to Survive and Proliferate
• T cell adherent cells were subject to TRANSACTTM (Miltenyi Biotec) activation at varying concentrations.
• T cells were partially reprogrammed using the methods described in Example 1. Briefly, CD8 positive T cells were stimulated with soluble CD3 and CD28 TRANSACTTM (Miltenyi Biotec) for 3 days in T cell culture medium with 60 IU/ml IL2. After 3 days, T cells were transduced with 10 MOI KOS Sendai vector, 10 MOI of KLF4 vector, 3 MOI of cMyc vector, and 5 MOI of SV40 vector. Cells were cultured in SCM without IL2 from day 1 and plated at a density of 80,000 cells per well in a 24- well plate coated with iMatrix-511 in quadruplicate.
• T cell derived adherent cells were detached from the vessel surface, washed and transferred to another well.
• the T cell derived adherent cells were then either reactivated with diluted T cell TRANSACTTM (Miltenyi Biotec) at a concentration of 1:500 or 1:1000, or incubated in no stimulation media at all. All cells were cultured in T cell culture medium (TCM plus IL2 at 60 IU/ml) for an additional nine days after activation. As shown in FIG. 18A, T cell derived adherent cells had largely lost expression of CD3 and CD8a.
• Example 8 Rejuvenated T Cells Show Effector Phenotype After Long Term Expansion in the Presence of IL-2
• Peripheral blood-derived CD8+ T cells from three donors (a 42-year-old male, a 37-year-old female, and a 52-year-old male) where purchased from Allcells, Alameda, CA. Cells were thawed and stimulated with TRANSACTTM (Miltenyi Biotec) at a concentration of 1:500 in TCM with IL-2 (60 IU/ml).
• TRANSACTTM Miltenyi Biotec
• Rejuvenated T cells were allowed to proliferate in vitro for 42 days. Expansion of non-rejuvenated T cells plateaued after approximately 3 weeks of expansion in vitro. See Figure 19A. Rejuvenated T cells continued to show significant expansion for up to 42 days in culture. See Figure 19B. This expansion is cytokine dependent, and rejuvenated T cells began to die within 6 days of IF-2 withdrawal. See Figure 20B and 20C.
• Cytokine production and degranulation assays were carried out on day 36 as follows. Cells were cultured in TCM without cytokines with or without PMA/Ionomycin (Cell Activation Cocktail by Biolegend). GolgiPlug and GolgiStop (BD Biosciences) was also added according to manufacturer instructions. The co-cultured cells were then stained for surface antigens (BUV395-CD8, BUV496-CD4, and BUV805-CD3). Five/dead eFluor 780 was also added to exclude dead cells. After 20 minutes cells were washed. Cells were fixed and permeabilized by BD cytofix/cytoperm kit according to manufacturer instruction.
• the cells were then stained for intracellular cytokine expression (FITC-IFNg, and APC-IF-2). After a 30-minute incubation, cells were washed twice and analyzed by flow cytometry using a ZE5 instrument. The FACS results were analyzed by FlowJo software. Single cells > Five cells > CD3+ > CD8+ CD4- cells were gated for all cells. The frequency of IFNg + and IF-2 + were calculated as shown in FIG. 21. The results showed that the rejuvenated T cells retain functionality. Usually, effector T cells express IFNg but do not express high amounts of IF2. Thus, these results suggest that the rejuvenated cells after 36 days of culture have still not reached full effector phenotype.
• Cell surface expression of CD3, CD8b, CD45RA, CCR7 and CD62F was measured by flow cytometry at day 7 and day 26. See Figure 22 and 23. Detached T cells that have undergone reprogramming demonstrate decreased CD3+CD8b+ expression, but elevated levels of CD45RA and CCR7+CD62F+ expression. By day 26, rejuvenated T cells show normal levels of CD3+CD8b+ expression, and reduced levels of CD45RA+ cells and CCR7+CD62F+ cells. See Figure 22 and 23.
• CD8+ T cells genetically modified to express an NY-ESO-1 -specific TCR were partially reprogrammed, stimulated with T cell activation molecules and the response to target cells pulsed with NY-ESO-1 peptide was measured.
• Peripheral blood-derived CD8+ T cells two different donors (#3 42-year old male and #4 37-year old female) were purchased from Allcells (Alameda, CA). 2x106 cells were thawed and stimulated with TRANS ACTTM (1:100) in TCM with IL-2 (60 IU/mL) in 1 well of a 24 well plate for each donor, as described in Example 4. The next day, T cells were transduced with NY-ESO-1 TCR by lentivirus vector transduction, as follows: First, the T cells were stimulated with a 1:100 dilution of T cell TRANSACT (Miltenyi) for 30 hours.
• Virus MOI: 5
• LentiBOOSTTM A & B Sirion Biotech
• Stimulation and viral infection were then terminated by addition of 7 mis TCM with IL-2 (60 IU/L).
• the infected T cells were washed and transferred onto iMatrix coated dishes on day 1 and the medium was changed to Stemfit w/o IL-2 (2 mL/well).
• Sample #3 density was 2.6x105 cells/well and #4 density was 1.76x105 cells/well, in triplicate.
• Stemfit was added (2 mL/well, total 4mL).
• target cells T2 and Mel624 HLA- A*02:01 positive tumor cells expressing endogenous NYESOl, were cultured in T2 media (RPMI, 20% FCS and P/SM).
• T2 cells were pre-cultured with or without NY-ESO-1 peptide (SLLMWITOC) (10 nM) for one hour, washed, and counted.
• SLLMWITOC NY-ESO-1 peptide
• PMA/Ionomycin Cell Activation Cocktail by Biolegend
• GolgiPlug and GolgiStop (BD Biosciences) were added according to manufacturer instructions.
• anti-CD107a Ab-BV421 were added in culture media (1 pL/well). Cells were cultured for six hours in TCM without cytokines. The co-cultured cells were then stained for surface antigens (PE-NY-ESO-1 tetramer, BUV395-CD8, BUV496-CD4, and BUV805- CD3). Live/dead eFluor 780 was also added to exclude dead cells. After 20 minutes, cells were washed. Cells were fixed and permeabilized by BD cytofix/cytoperm kit according to manufacturer instructions. The cells were then stained for intracellular cytokine expression (FITC-IFNg, APC-IL-2, and BV785-TNFa).
• CD8+ T cells are isolated from one or more donors genetically modified to express an NY-ESO-1 -specific TCR.
• the donor cells are thawed and stimulated with TRANSACTTM in TCM with IL-2 (60 IU/mL) in 1 well of a 24 well plate for each donor.
• T cells are transduced with a lentivirus expressing an NY-ESO-1 T cell receptor.
• the NY-ESO-1 -specific T cells are then co-cultured with T2 cells that have been pulsed with NY-ESO-1 peptide (T2+NY-ESO-1 cells).
• the cells are either enriched for NY-ESO-1 specific T cells (Group 1) or maintained as a heterogeneous mix of NY-ESO-1 -specific T cells and untransduced T cells (Group 2).
• Cells are again co-cultured with T2+NY-ESO-1 cells for the duration of reprogramming.
• Control cells are kept culturing in TCM with IL-2 (60 IU/mL) in co-culture with T2+NY-ESO-1 cells.
• NY-ESO-1 specific T cells are capable of forming T cell derived adherent cells in the presence of T2+NY-ESO-1 cells, in the absence of any further stimulation. Attached cells are harvested according to the protocol described in Example 9, and then activated again by co culture with T2+NY-ESO-1 cells.
• Example 11 Rejuvenation Enhanced T Cell Sternness Properties in Tumor Infiltrating Lymphocytes
• TILs Tumor Infiltrating Lymphocytes
• TILs were isolated from a 66-year- old donor and rejuvenated as follows. TILs were enriched by culturing tumor fragments in T cell culture media for 2 weeks. T cells were activated through overnight co-culture with autologous antigen presenting cells derived from the tumor. The T cells were then FACS sorted and CD137 (4-1BB) positive cells were isolated. One day later (Day 0), cells were either left undisturbed, or transduced with four Sendai viruses expressing KOS (KLF4, OCT3/4, SOX2), KLF4, cMyc and SV40 as previously described. Cells were then transferred to stem cell media (StemFit) and cultured for seven days.
• T cell derived adherent cells were harvested on Day 7 and reactivated with TransAct (1:500) in T cell culture media for two additional days. From Day 9, cells were cultured in normal T cell culture media. On Day 21, the rejuvenated or control cells (which had undergone the same procedure except that the cells were not transduced with the four Sendai viruses) were assessed for expression of CD62L, CCR7 and TCF7 using flow cytometry. Rejuvenated TILs exhibited enhanced proliferation (FIG. 27 A) and an enhanced expression of sternness phenotypic markers (FIG. 27B) relative to un rejuvenated controls.
• Example 12 Dynamic Analysis of Epigenetic Clock During T Cell Rejuvenation
• CD8+ T cells from a 53-year-old male, a 55-year-old male, and a 50- year-old male were stimulated with T cell TransAct®, human (Miltenyi Biotec,) at 1:500 dilution in T cell culture medium (TCM) with 60 IU/ml of IL-2 at a cell density of 1 million cells/ml in 48-well plate. All the TCM described hereinafter contains 60 IU/ml IL-2. After 26.5h activation, the cells were divided into two groups. One group underwent the rejuvenation protocol; the other group was used as control without any viral manipulation and cultured in TCM during the whole process.
• the CpG methylation status data was analyzed using the Horvath method as described in (Horvath et al., 2018, Aging 10, 1758-1775; Horvath and Raj, 2018, Nature Reviews Genetics, 19:371-375) to get skin and blood clock values.
• CD8 positive T cells from the three male donors were transduced with Yamanaka factors and SV40 according to the rejuvenation protocol depicted in FIG. 28, and compared with controls which were in non- transduced condition at each time point.
• the rejuvenated cells showed reduced CD3 and CD8b expression on day 7.
• the T cell conventional marker expression was fully recovered in the rejuvenated cells on day 13 and 18 (FIGs. 29A and 29B).
• partially reprogrammed cells reacquired expression of conventional T cell markers in only 6 days following reactivation.
• the chronological age of Donor 3 was 50 y/o.
• the eAge in the non-rejuvenated control cells varied from 46.0 to 51.4 (5.4 years variation), while the youngest age was 31.5 y/o in rejuvenated cells on day 7 which was 19.9 years younger than control eAge on day 7.
• the rejuvenated cells showed the youngest eAge on day 7, then the eAge gradually increased.
• eAge of Donor 1 rejuvenated cells reached control level on day 18, while in the case of the other two donors, rejuvenated cells continued to be younger than control.
• the partially reprogrammed T cells lose common T cell markers, (e.g., CD3 and CD8b) as measured on the detachment day (i.e., day 7).
• T cell adherent cells After re- stimulation on day 7 and culturing in T cell medium, however, the T cell adherent cells fully reacquired the T cell markers by or on day 13.
• the epigenetic clock showed the youngest epigenetic age on day 7 in the three donors tested (50, 53 and 55 years old, respectively).
• the results of this example demonstrate that, although a gradual eAge increase was observed after day 7, rejuvenated cells remain younger than control on day 13 when the rejuvenated cells showed full T cell phenotype.
• Example 13 Rejuvenation of NY-ESO-1 transduced T cells
• This example demonstrates that T cells can be genetically engineered to express a TCR specific for a desired target (e.g., NYESOl) and rejuvenated using the methods herein.
• a desired target e.g., NYESOl
• Healthy donor CD4/CD8 T cell activation On day 1, healthy human donor CD4 and CD8 T cells from two male donors (age 24 and 35) were thawed, washed once and resuspended in pre-warmed Complete TCM + IL-2 (60 IU/ml) (day-3). Cells were diluted to 2e6 cells/ml. Transact was added lOul/ml (1/100 dilution) to stimulate CD4 and CD8 T cells (see FIG. 31). On day 2, stimulated CD8+ and CD4+ T cells were counted and 7.5e+5 cells were suspended in 0.75ml of TCM + IL-2.
• Lentiviral vector encoding the NYESOl -specific TCR were made using standard protocols. NYESOl -encoding lentivirus supernatant (7.5ul, MOI; 10) and LentiBoost A&B (7.5 ul each) were added. The next day, 5.25ml of new TCM + IL-2 was added (total 6ml).
• a stock vial of T2 cells were thawed and washed once and cultured in complete RP10 medium for one week. 5e+6 cells were resuspended in complete RP10 with or without lOnM NY-ESOl peptide for 2 hours in 5% C02 incubator. After 2 hours, cells were washed and resuspended in TCM.
• control and rejuvenated NY-ESO-1 TCR Tg T cells were analyzed for their ability to kill target cells using sequential stimulation. Specifically, control and rejuvenated T cells were counted. 50,000 NY-ESO-1 tetramer+ T cells were co-cultured with 20,0000 NY- ESO-1+ HLA A02:01+ target cells (A375-Nuclight Red (NLR) or H1703-NLR) at 1:4 E:T in 24-well plates. Every 3-4 days, 25% of the culture was transferred into a new plate with fresh target cells plated at the initial seeding density. Target clearance was quantified using Incucyte.
• Rejuvenated NY-ESO-1 TCR Tg T cells required a longer time to start proliferation which could be due to recovery from the reprogramming process. However, over time they proliferated more than 100 fold more than control non-rejuvenated cells. See, e.g., FIG. 33. Epigenetic age of the control and rejuvenated NY-ESO-1 TCR Tg T cells were analyzed as depicted in FIG. 34. Compared to control T cells rejuvenated cells on day 19 showed about 8-18 years younger phenotype. More specifically, for the first donor (FIG.
• the epigenetic age of the rejuvenated CD4 T cells at day 7 (the T cell derived adherent cells) showed a 68% reduction in age as compared to the eAge of the control cells (eAge at day 19).
• the rejuvenated CD4+ T cells showed a 33% reduction in age as compared to the control cells.
• the epigenetic age of the rejuvenated CD8 T cells at day 7 showed a 70% reduction in age as compared to the control cells.
• the rejuvenated CD8 T cells showed a 45% reduction in age as compared to the control cells.
• the second donor FIG.
• the epigenetic age of the rejuvenated CD4 T cells at day 7 showed a 62% reduction in age as compared to the control cells.
• the rejuvenated CD4+ T cells showed a 27% reduction in age as compared to the control cells.
• the epigenetic age of the rejuvenated CD8 T cells at day 7 (the T cell derived adherent cells) showed a 68% reduction in age as compared to the control cells.
• the rejuvenated CD8 T cells showed a 67% reduction in age as compared to the control cells.
• FIG. 31 is a diagram of the experiment for rejuvenation of NY-ESO-1 Tg CD4 and CD8 T cells.
• CD4 or CD8 T cells were stimulated by Transact and transduced with NY-ESO-1 TCR before reprogramming.
• Cells were cultured in iPS cell culture condition from dayl to day7. On day7 cells were collected, counted, re-stimulated by Transact and kept in culture in TCM + IL-2. On day 19, control and rejuvenated cells were analyzed for cytokine production and cytotoxic activity. In a condition of sequential killing assay rejuvenated CD4 and CD8 T cells were mixed to check their synergistic effect.
• FIGS. 32A and 32B illustrate that rejuvenated NY-ESO-1 Tg CD4 (FIG. 32A) and CD8 T cells (FIG. 32B) showed a less differentiated phenotype.
• FIG. 33 illustrates that rejuvenation NY-ESO-1 Tg CD4 and CD8 T cells proliferated more than control NY-ESO-1 Tg CD4 and CD 8 T cells.
• NY-ESO-1 Tg CD4 and CD8 T cells were rejuvenated and cultured as described and cell number was counted every 3-4 days.
• Graph depicts the fold changes compared to day7 after transduction of the Reprogramming factors and their corresponding control cells over time. Representative data of four different donors.
• FIG. 34 illustrates that rejuvenated NY-ESO-1 Tg CD4 and CD8 T cells showed younger phenotype by epigenetic age analysis than control NY-ESO-1 Tg CD4 and CD8 T cells and the chronological age of the donors.
• Graphs show the mean and S.D. of the values of age analyzed from the methylation status of certain CpG sites.
• FIG. 35 illustrates that rejuvenation NY-ESO-1 Tg CD4 and CD8 T cells produced more cytokines (IFNg, IL-2 and TNFa) upon co-culture with T2 cells with NY-ESO-1 peptide.
• cytokines IFNg, IL-2 and TNFa
• FIG. 35 illustrates that rejuvenation NY-ESO-1 Tg CD4 and CD8 T cells produced more cytokines (IFNg, IL-2 and TNFa) upon co-culture with T2 cells with NY-ESO-1 peptide.
• cytokines IFNg, IL-2 and TNFa
• FIG. 36 illustrates that rejuvenated NY-ESO-1 Tg CD8 T cells persisted and retained their cytotoxic activity longer than control cells upon repeated co-culture with NY-ESO-1 expressing target cells (A375-NLR).
• Control or rejuvenated NY-ESO-1 Tg CD8 T cells were co-cultured with A375-NLR cell line. Every 3-4 days, 25% of the previous culture was transferred into a new plate with fresh targets. Growth of the target was monitored using the Incucyte ⁇ live-cell analysis system and analyzed with the Base Software Analysis Module. Graphs show the numbers of A375-NLR/image of each condition. Representative data of two different donors.
• NLR Nuclight Red
• FIG. 37 describes the enhanced cytotoxicity of rejuvenated NY-ESO-1 Tg CD8 T cells resulting from addition of rejuvenated NY-ESO-1 Tg CD4 T cells.
• exogenous IL-2 lOIU/ml
• the graphs show the numbers of A375-NLR/image of each condition. Representative data is from two different donors.
• rejuvenated NY-ESO-1 TCR Tg T cells showed a less differentiated phenotype and proliferated more than control NY-ESO-1 TCR Tg T cells. Additionally, the epigenetic age of rejuvenated NY-ESO-1 TCR Tg T cells was lower than that of the control NY-ESO-1 TCR Tg T cells. Rejuvenated NY-ESO-1 TCR Tg T cells also produced more cytokines (IL-2, IFNg and TNFa) upon coculture with target cells pulsed with the relevant NYESOl peptide.
• IL-2, IFNg and TNFa cytokines
• rejuvenated NYESOl TCR+ cells retained cytotoxic activity over a longer period of time after repeated exposure to target antigen cells than non-rejuvenated control cells. Furthermore, rejuvenated NY-ESO-1 TCR Tg CD8 T cell activity was enhanced by addition of IL-2 or Rejuvenated NY-ESO-1 TCR Tg CD4 T cells.
• This example was carried out to assess cytokine production of rejuvenated T cells .
• Rejuvenation of PBMC On Day -2, 1x106 donor cells were thawed and incubated in 1 ml, TCM + IL-2 (60 IU/ml) per well in 24-well-plate for 24 hours. The next day (i.e., Day -1) cells were counted and T cells were activated with T Cell Trans Act.Human (Miltenyi) REA 107 1:500, and subsequently incubated for 24 hours.
• Sendai vector transduction (MOI: KOS 10, KLF4 10, c-MYC 3, SV405) was performed, and a matrix-coated (iMatrix 511) plate was prepared by diluting iMatrix 511 (57.6 ul iMatrix+9ml PBS).
• 500 ul of the diluted iMatrix were added per well of a 24-well plate and kept at 37oC for >lh.
• cells were pelleted and dispensed into the iMatrix coated plate with 500 uL stem cell culture medium + bFGF per well.
• 500 ul fresh stem cell culture medium and bFGF were added to each well in 24-well plate.
• Example 15 Selective Rejuvenation of Antigen-Specific T Cells
• Step A Healthy donor CD8 T cell activation. Healthy human donor CD8 T cells were thawed, washed once and resuspended in pre-warmed Complete TCM + IL-2 (60 IU/ml). Cells were diluted to 2e6 cells/ml. Transact was added lOul/ml (1/100 dilution) to stimulate CD8 T cells.
• Step B Transduction of NY-ESO-1 TCRs.
• stimulated CD8 T cells were counted and le+6 cells were suspended in 1ml of TCM + IL-2.
• Supernatant from lentivirus vector encoding NYESOl-TCR (10 ul, MOI; 9.7) and LentiBoost A&B (12.5ul each) were added to the suspended cells.
• transduction efficiency was determined by FACS.
• 7 ml of TCM + IL-2 was added to dilute the vims.
• cells were stained using the antibody mix described in Table 6 below, and the cells were analyzed for expression of NY-ESO-1 TCRs. See FIG. 40.
• Step C Reprogramming.
• T cells with Transact activation were collected, washed with 10ml PBS, resuspended in 1ml of TCM + IL-2, and kept in culture.
• T cells co-cultured with autologous LCLs were collected and T cells were enriched by EasySepTM Human T Cell Isolation Kit, resuspended in TCM + IL-2 and kept in culture. See FIG. 41.
• Day 1 cells were collected, re-suspended in stem cell culture media and seeded in an iMatrix coated 6 well plate (2 wells per condition).
• Day 3 new stem cell culture media was added and on day 5 half of the medium was changed to new stem cell media (Fig 3A).
• Step D Detachment and re- stimulation of partially reprogrammed NY-ESO-1 TCR Tg T cells.
• Rejuvenated NY-ESO-1 Tg T Cells Proliferate. Partially reprogrammed T cells re stimulated by Transact or autologous LCLs with peptide (first stimulation by Transact) were cultured as described until day 21. The proliferation curve is shown in FIG. 45. Rejuvenated T cells re-stimulated with autologous LCL with NY-ESO-1 peptide proliferated as well as those re-stimulated with Transact.
• Example 16 Rejuvenation of CD19-CAR T Cells
• This Example CD19 CAR-T cells were produced and subjected to the partial reprogramming process and then proliferation and cytotoxicity was assessed.
• Rejuvenated CD 19 CAR T cells showed higher proliferation compared to control, as had been shown previously with NY-ESO-1 Tg CD8 T cells.
• Cytotoxicity of rejuvenated CD19 CAR T cells was tested by repeated co-culture with target cells expressing CD19 (Nalm6). After repeated co-culture, rejuvenated CAR T cells showed higher persistence and cytotoxicity.
• Step A Healthy donor CD8 T cell activation. Healthy human donor CD8 T cells were thawed, washed once and resuspended in pre-warmed Complete TCM + IL-2 (60 IU/ml) (day- 3). Cells were diluted to 2e6 cells/ml. Transact was added lOul/ml (1/100 dilution) to stimulate CD 8 T cells.
• Step B Transduction of CD19-CAR: The day after simulation with TRANSACT (day- 2), stimulated CD8 T cells were counted and 3e+5 cells were suspended in 1ml of TCM + IL- 2. Lentiviral vector encoding a CD 19 CAR and a truncated EGFR was produced using conventional methods. Virus supernatant (6ul, MOI; ) and LentiBoost A&B (lOul each) were added to the activated cells. The following day, 0.7ml of the media containing virus was removed and 1.8 mis new TCM + IL-2 was added. On day 5 after CAR transduction, cells were stained using the antibody mix in Table 7 below, and analyzed for the expression of CAR by idiotype antibody and EGFR antibody.(FIG. 46)
• Step D Re-stimulation of partially reprogrammed CD19 CAR Tg T cells.
• floating cells were collected, wells were washed with PBS, TrypLE enzyme was added, and attached cells were detached. The collected cells (floating cells + detached cells) were counted. See FIG. 47. 5e+5 cells were preserved in -80C for DNA age examination ⁇ Harvested cells (1.7e+6 and 2.3e+6 for Donors #1 and #2 respectively) were re-stimulated with Transact (1/500 dilution) in TCM + IL-2. le+6 of control cells were stimulated in the same way. On day 10, half of the medium was refreshed with new TCM + IL-2. On day 13 and after, cell counts and medium changes were performed every three or four days. Cells were cultured at the concentration of l-2e+6 cells per ml.
• Step F Assaying the ability for CAR-T cells to repeatedly clear target cells using sequential stimulation.
• Rejuvenated CD19 CAR T cells showed less differentiated phenotype. Healthy donor CD8+ T cells were activated and transduced with CD 19 CAR as described above, reprogrammed for 7 days, detached and re-stimulated by Transact. On day 13 rejuvenated CD19 CAR transduced T cells, which were distinguished by the expression of EGFRt, had a higher percentage of CCR7+ CD62L+ population and Tcfl-i- population, indicating that the rejuvenated CAR-T cells had a less differentiated more stem-like phenotype (see FIG. 47) [0522] Rejuvenated CD 19 CAR T cells proliferated more than control CD 19 CAR T cells.
• Control and rejuvenated CD 19 CAR Tg T cells were cultured in TCM + IL-2 and cell counts were monitored over time. Media was changed every 3-4 days, and the cell concentration was adjusted to stay at l-2e+6/ml. Although rejuvenated CD19 CAR Tg T cells initially showed delayed proliferation rate, day 25 marked an inflexion point, after which by day 55 rejuvenated cells exhibited over 100 fold greater expansion compared to control (see FIG. 48) [0523] Rejuvenated CD19 CAR T cells produced comparable levels of cytokines upon co culture with CD19 expressing target cells.
• cytokines IL-2, TNFa, IFNg
• control and rejuvenated CD 19 CAR T cells were analyzed by co-culturing them with target cells expressing CD19 (Nalm6) or no CD19 (Colo205) as described above.
• target cells expressing CD19 (Nalm6) or no CD19 (Colo205) Neither the control or rejuvenated CD 19 CAR Tg T cells produced cytokines upon co-culture with control Colo205 cells.
• both groups produced cytokines upon co-culture with Nalm6 at comparable levels with the exception of IFNg. (see FIG. 49).
• IFNg production was higher in rejuvenated cells as compared to control.
• a Sendai vims vector that was modified to express the four Yamanaka factors from a single multicistronic (i.e., “mSev”) vector was used for rejuvenating T cells and compared to rejuvenation with the Cytotune kit as described in previous examples.
• mSev multicistronic
• the Cytotune-iPS 2.0 Sendai reprogramming kit (i.e., “Sev”) contains 3 separate viral vectors: (KOS encoding Klf4, OCT4 and SOX2; cMyc; Klf4for reprogramming.
• an additional Sendai virus (Sev) expressing SV40 is also used to inhibit apoptosis and increase reprogramming efficiency .
• Using the cytotune kit four separate vectors have to be transduced into T cells. As discussed in further detail below, it was found that transduction with four separate viruses results in uneven co-transduction, inefficient reprogramming, and can result in significant variation in later products.
• T cells were subjected to the rejuvenation process described herein, using either (a) the multicistronic Sendai vector expressing the four Yamanaka factors (but not expressing SV40) or (b) the Cytotune Sev (+SV40).
• Step A T cell rejuvenation.
• CD8+ T cells from a 53-year-old male (Donor 1) and a 55- year-old male (Donor 2) were stimulated with T cell TransAct, human (Miltenyi Biotec, cat# 130- 111-160) at 1 :500 dilution in T cell culture medium containing 60 IU/ml of IL-2 at a cell density of 1 million cells/mL in a 48-well plate.
• T cell TransAct human (Miltenyi Biotec, cat# 130- 111-160) at 1 :500 dilution in T cell culture medium containing 60 IU/ml of IL-2 at a cell density of 1 million cells/mL in a 48-well plate.
• the inventors found that 24 hours of activation resulted in the most efficient transduction using the multicistronic Sendai virus vector (mSev). After 26 hours of stimulation with TransAct, the cells were divided into two groups (i.e., on Day 0).
• the Sev rejuvenated group was transduced with 10 MOI of Klf4-Oct3/4-Sox2, 10 MOI of Klf4, 3 MOI of cMyc (Cytotune iPS 2.0 Sendai Reprogramming Kit, Thermo) and 5 MOI of SV40, while MSev group was transduced with 5 MOI of mSev expressing all four Yamanaka factors without SV40. Cells were then cultured at 37°C.
• SCM stem cell medium
• PPROTEC cat# RL511S iMatrix- 511 coated 24-well plate at 50,000 cells/well (corresponding to day 0 counts) and cultured at 37°C (i.e., Day 1).
• 500 ul of SCM was added on days 3, 5, 7, 9. 1 ml of SCM was aspirated on day 7.
• both groups were detached on day 7, 9 and 11 using 1 ml of TrypLE Express (Thermo cat# 12604013) and incubated at 37°C for 10 min. The detached cells were harvested by pipetting.
• 1x105 cells were activated with 1:500 diluted T cell TransAct human in 200 uL of T cell culture medium at a density of 5x105 cells/ml in 96-well round bottom plate. Two days after detachment, cells were transferred to a 12-well plate and 1 ml of T cell culture medium was added to each well. Four days after detachment, cells were transferred to a 6-well plate. Thereafter, the cells were cultured with T cell culture medium with IL260 IU/ml, in a six-well plate.
• Step B Flowcytometry analysis. Cells were stained with fluorescent conjugated antibodies and viability dye (see Table 8 below). Cell phenotypes were acquired by flow cytometry in a Cytek Aurora. Table 8: Antibodies and Viability Dye for Staining
• Step C DNA extraction and epigenetic analysis
• CD8+ T cells from 2 male donors aged 53 and 55 were transduced with Sev or mSev, detached, and restimulated on day 7, 9 and 11 (see FIG. 51). After detaching and restimulating, conventional T cell markers CD3 and CD8b were fully recovered in both groups of rejuvenated cells 6 days after detachment and reactivation (see FIGs. 52A and 52B).
• the difference in cell count between the Sev and mSev groups may be caused by the lower expression levels of the reprogramming factors from the mSev vector and the absence of SV40, which increases reprogramming efficiency.
• the proliferation curves for the Sev and mSev groups are similar, indicating that the mSev reprogrammed cells acquired a similarly rejuvenated capacity for proliferation.
• mSev showed a higher TCF1+CCR7+ and higher CCR7+CD62L+ population among CD3+CD8b+ population which suggests more stem-like population in the mSev group (see FIGs. 54A and 54BA).
• Example 18 Transcriptome characterization of rejuvenated CD8+ T-cells [0542]
• high-dimensional transcriptional analysis of single cell and bulk RNAseq was used to characterize rejuvenated T cells as compared to control T cells.
• analysis of the clustered single cell RNA-seq data showed that, after seven days of reprogramming, the rejuvenated T-cells had a very different global phenotype than the control T cells.
• Most of the partially reprogrammed cells expressed the four Yamanaka factors on Day 7 but by Day 13, the expression of the transduced Yamanaka factors was at background levels.
• CD8 positive T cells from a 54-year-old male donor (Donor No. 18698) were subjected to the rejuvenation process as described below. Cells were divided into two groups, one rejuvenated as described below and the other used as control.
• CD8 positive T cells from a 53-year-old male donor, 55- year-old male donor and 50-year-old male donor were subjected to the same protocol.
• CD 8 positive T cells from each donor were stimulated with T cell TransAct, human (Miltenyi Biotec,) at 1:500 dilution in T cell culture medium containing 60 IU/ml of IL-2 at a cell density of 1 million cells/mL in a 48-well plate.
• T cell TransAct human (Miltenyi Biotec,) at 1:500 dilution in T cell culture medium containing 60 IU/ml of IL-2 at a cell density of 1 million cells/mL in a 48-well plate.
• T cell TransAct human (Miltenyi Biotec,) at 1:500 dilution in T cell culture medium containing 60 IU/ml of IL-2 at a cell density of 1 million cells/mL in a 48-well plate.
• the cells were plated on iMatrix-511 (PEPROTEC) coated 24-well plate at 50,000 cells/well (corresponding to day 0 count of 50,000) and cultured at 37°C (Day 1). On days 3 and 5, 500 ul of SCM was added to the cultures. On day 7, the T-cell derived adherent cells were incubated at 37°C for 10 minutes with 0.5 ml of TrypLE Express (Thermo) to detach the cells from the culture dish. The detached cells were then harvested by pipetting. Floating cells in the supernatant were also harvested and mixed with the detached cells. Floating cells in the first experiment were abandoned due to insufficient cell numbers.
• PEPROTEC iMatrix-511
• Dead cells were removed using EasySep Dead Cell Removal (Annexin V) kit (STEMCELL technologies) according to manufacturer’s instructions. The samples were processed twice with EasySep to increase viable cell purity.
• cDNA assessment was performed using the High sensitivity DNA kit (Agilent) on the 2100 BioAnalyzer and 150pg of full-length cDNA was used to prepare barcoded libraries for sequencing using the Nextera XT DNA Library Prep kit (Illumina) using the manufacturer’s protocol automated on the Biomek i7 workstation. Quality assessment was performed using a DNA1000 ScreenTape Assay (Agilent) with a 4200 TapeStation System. Barcoded libraries across samples were then multiplexed in an equimolar pool, purified, and sequenced using a NovaSeq 6000 system.
• Single Cell CITE-Seq data was processed using the 10X Cell Ranger software version 5.0.1 (10X Genomics) with Genome Reference Consortium Human Build 38 (GRCh38) as reference genome and default parameters.
• the reference genome was supplemented with the transduced Yamanaka factor sequences and control sequences from the Sendai vims backbone.
• the cell-gene matrix was further processed using Seurat package (see Hao et al. 2021) in R. Cell level quality control and removal of outliers were performed by visually selecting thresholds for percent mitochondria, nCount_RNA, nFeature_RNA, nCount_ADT and hashtag doublets. Cells from both rejuvenated and control samples collected from the four male donors were merged for Day 7 and Day 13 single cell transcriptome analysis.
• the filtered cell-gene matrix was globally scaled with ‘NormalizeData’ function with scale.factor parameter set to default 10000.
• ‘NormalizeData’ function with scale.factor parameter set to default 10000.
• the effects of cell cycle heterogeneity were corrected by calculating cell cycle phase scores (G2M.Score, S. Score) with ‘CellCycleScoring’ function in Seurat and then regressing out the cell cycle phase scores and percent mitochondrial reads in the function.
• Genes correlated with either of the two cell cycle phase scores (with Pearson correlation coefficient greater than 0.25) were excluded from selected features to further minimize the effects of cell cycle heterogeneity. Mitochondria, ribosome, TCR, and IG complex related genes were also excluded from the selected features.
• CD8 positive T cells from the four male donors were transduced with Yamanaka factors and SV40 (i.e., rejuvenated cells) according to the rejuvenation protocol and compared with corresponding controls which were in non-transduced condition at each time point. Cells were allowed to grow out to Days 17 and 29 in Experiments 1 and 2, respectively. As shown in FIG. 56 consistent with previous Examples, rejuvenated cells showed increased proliferation as compared to the control cells.
• RNA-seq analysis was performed on CD8+ T-cells from control and rejuvenated cells on Day 7 and Day 13 using cells from all four donors (Donor nos. 18698, 11347, 12254 and 26221). Bulk RNA-seq was performed from the same samples as used in the second experiment described above (i.e., the 53-year-old, 55-year-old, and 50-year-old males of the second experiment).
• the transduced C-MYC starts at exon 1 while endogenous cMYC is expected to start at the 5’ UTR confirming that the C-MYC seen at Day 7 is transduced while that at Day 13 is endogenous.
• Rejuvenated T cells are still expressing the four Yamanaka Factors until the day of detachment, resuspension and activation (Day 7). Exogenous expression of these factors are not detected on Day 13. Although rejuvenated T cells are still expressing C-MYC, the expression origin is endogenous.
• the rejuvenated cells were then assessed to determine whether they were metabolically different from the corresponding control T cells at both Day 7 and Day 13. Metabolic gene sets corresponding to oxidative phosphorylation, fatty acid metabolism, glycolysis and hypoxia were significantly enriched in the Day 7 and Day 13 rejuvenated cells (see FIG. 58A). Projection of these metabolic gene sets onto single-cell RNA-seq data indicated that, at Day 7, the rejuvenated cells were enriched for both glycolysis and oxidative phosphorylation. Surprisingly, while by Day 13 the rejuvenated cells shift to being either high in oxidative phosphorylation or high in glycolysis (see FIG. 58B), the cells were still significantly enriched for both these gene sets globally in comparison to control cells.
• naive gene sets (Gattinoni et al., 2011 Nature Medicine 17(10): 1290- 1297) in the rejuvenated cells and corresponding control T cells were assessed at Day 13. Gene sets corresponding to naive T cell phenotype were enriched in the Day 13 rejuvenated cells (see FIGs. 59A and 59B).
• relative T cell receptor repertoire diversity was estimated by Simpson clonality (Wong et al. J. Immunology V:197. Pp 1642-1649). T-cell repertoire diversity was estimated with Simpson Clonality metric, which ranges from 0 to 1, where 0 represents a completely uniform sample and 1 represents a monoclonal sample.
• Fower Simpson Clonality indicating increased TCR repertoire diversity, was observed in rejuvenated samples at day 7 and day 13 as compared to control T-cells. (see FIG. 75).
• the rejuvenated T cells of this Example were enriched for expression of genes associated with higher metabolic activity as compared with control cells.
• the data in this Example also suggests that rejuvenated T cells are more fit to use energy and synthesize nucleotides needed for proliferation and further explains the significantly increased proliferative capacity observed in the rejuvenated cells as compared to controls.
• the enrichment of both oxidative phosphorylation and glycolysis gene sets is associated with the metabolic shift during reprogramming of somatic cells to iPSCs (see, e.g., Nishimura 2019 Int. J. Mol. Sci.
• rejuvenated cells may have acquired some stem cell-related qualities without reprogramming to a fully pluripotent iPSC stage.
• rejuvenated T cells are enriched for gene sets corresponding to naive T cell phenotype and have increased polyclonality.
• Example 19 Rejuvenation Enhanced T Cell Sternness Properties in Tumor Infiltrating Lymphocytes
• TILs were rejuvenated from numerous different tumor types (lung adenocarcinoma, colorectal, liver, melanoma, colorectal carcinoma metastasis to the liver), using the process as described in Example 11 with differences as noted below in Table 10.
• Tumor samples were procured from the Cooperative Human Tissue Network (CHTN).
• CHTN Cooperative Human Tissue Network
• TILs were freshly isolated and either 1) enriched by magnetic bead separation for CD45+ immune cells (e.g., T cells) and used directly; 2) enriched by magnetic bead separation for CD45+ immune cells (e.g., T cells) followed by activation with TransAct (1:500) for 1 or 2 days; or 3) isolated and expanded for between 5 and 17 days in media containing 6000 II I/ml IL-2. Because the tumor samples were small, enrichment and/or expansion was needed to generate enough cells for the rejuvenation process. For the pre-activation step, TILs were activated by one of the following as outlined in Table 10 below:
• TILs were then rejuvenated as follows: TILs from the pre- activation step were transduced with 10 MOI of Klf4-Oct3/4-Sox2, 10 MOI of Klf4, 3 MOI of cMyc (Cytotune iPS 2.0 Sendai Reprogramming Kit, Thermo) and 5 MOI of SV40. Cells were then cultured at 37°C. After about 16 hours, cells were washed and suspended with stem cell medium (SCM; Stemfit Basic 02 with bFGF). The cells were plated on iMatrix-511 (PEPROTEC) coated 24- well plate at around 50,000 cells/well (corresponding to day 0 cell counts) and cultured at 37°C (Day 1).
• SCM stem cell medium
• PEPROTEC iMatrix-511
• TILs were detached on day 7 with enzyme (1 ml of TryplE Express (Thermo)) and incubated at 37°C for 10 min. The detached cells were harvested by pipetting. 1E5 cells were activated with 1:500 diluted T cell Trans Act human in 200 ul of TCM supplemented with 60 IU/mL IL2 at a density of 5x105 cells/ml in 96-well round bottom plate. Cell counts were taken at various time points as noted in the associated figures (FIGs. 60, 62, 64 and 68) out as far as day 30. Expression of surface markers associated with sternness (CD62L, CCR7, TCF7) were measured by flow cytometry at the days noted in FIGs. 61, 63 and 65. Note that at earlier time points, there were often insufficient cell numbers to assess phenotype.
• TIL can be rejuvenated using the methods herein and extend the data to several different tumor types including lung adenocarcinoma, colorectal cancer, liver cancer, melanoma, and colorectal carcinoma metastasis to the liver.
• the results show that rejuvenated TILs exhibited enhanced proliferative capacity, increased expression of phenotypic markers associated with sternness and reduced epigenetic age.
• Example 20 Rejuvenating Tumor Inflitrating Lymphocytes using mSev [0580]
• the multicistronic Sendai vector (mSev) encoding the four Yamanaka factors (without SV40) as described in Example 17 was used to rejuvenate TILs.
• TILs from 52- and 83-year-old female donors were isolated from tumor sample by mechanical dissociation on ice followed by enzymatic digestion for between about 30 to about 90 minutes and either used directly (i.e., “bulk”) or enriched by magnetic bead separation for CD45+ immune cells (e.g., T cells) followed by expansion with TransAct.
• TILs were expanded by culturing in T cell culture medium with 6000 IU/ml of IL-2 and expanded for 1 month.
• TIL were activated with T cell TransAct, human (Miltenyi Biotec) at 1:500 dilution for 1 day.
• the pre-activated TIL were then transduced with 5 MOI of mSev expressing 4 Yamanaka factors without SV40. Cells were then cultured at 37°C.
• the T cell derived adherent cells were detached using 1 mL of TryplE Express (Thermo) incubated at 37 °C for 10 min. The detached cells were then harvested by pipetting. 1x105 cells were activated with 1:500 diluted T cell TransAct human in 200 ul of T cell culture medium at a density of 5x105 cells/mL in 96-well round bottom plate. Two days after detachment, cells were transferred to a 12-well plate and 1 mL of T cell culture medium was added to each well. Four days after detachment, cells were transferred to a 6-well plate. Thereafter, the cells were cultured with T cell culture medium in a 6-well plate. On days 14 and 18, cells were stained with fluorescent conjugated antibodies and viability dye and cell phenotypes were acquired by flow cytometry in a Cytek Aurora.
• this Example indicates that the mSev vector can be used for rejuvenation of TILs.
• Example 21 Integrin «6 and Integrin b ⁇ as a marker of rejuvenated T cells
• integrin a6b1 could be a marker for T cell adherent cells which may contribute to cell adhesion and a less-differentiated phenotype(s).
• Integrins are one of the most important proteins which are involved in cell adhesion. The heterodimer transmembrane proteins bind actin cytoskeleton to extracellular matrix thereby connecting cells with the extracellular matrix. They work as not only cell adhesion molecules but also as receptors which transmit intracellular signaling that regulate cell proliferation and survival.
• T cells An important feature of the partial reprogramming of T cells described herein is cell attachment to a matrix-coated plate in the early phase, which suggests that the partially reprogrammed T cells express cell adhesion molecules, namely integrins (see, e.g., www(dot)ncbi(dot)nlm(dot)nih(dot)gov/books/NBK26867/).
• integrins see, e.g., www(dot)ncbi(dot)nlm(dot)nih(dot)gov/books/NBK26867/).
• integrins see, e.g., www(dot)ncbi(dot)nlm(dot)nih(dot)gov/books/NBK26867/.
• integrins the most dominant integrin complex is integrin a ⁇ b ⁇ (see, e.g., Ni
• Integrin a ⁇ b ⁇ is known to bind to laminin-511, which was used in the instant Example as extracellular matrix and has been used for culture of human pluripotent stem cells (see e.g., Miyazaki T. et al. Nat Commun (2012) 3, 1236).
• Step A T Cell Rejuvenation
• CD8 positive T cells from a 49-year-old female donor were stimulated with T cell TransAct, human (Miltenyi Biotec, cat# 130-111-160) for 1 day in T cell culture medium (TCM) with 60 Ill/ml of IL2 as 1 million cells/1 ml in a 48-well plate. All TCM used in this Example contained 60 IU/ml IL2. After 24h activation, transduction was carried out.
• TCM T cell culture medium
• Sendai viruses were transduced at 10 MOI of Klf4-Oct3/4-Sox2, 10 MOI of Klf4, 3 MOI of cMyc, and 5 MOI of SV40 (Cytotune iPS 2.0 Sendai Reprogramming Kit, Thermo) for 17 hours, then washed and suspended in stem cell medium (SCM) (StemFit Basic02 with bFGF, Ajinomoto) without IL2.
• SCM stem cell medium
• the cells were plated on an iMatrix-511 (PEPROTEC cat# RL511S) coated 24-well plate as 0.05 million cells/well (corresponding to day 0 count of 0.05 million).
• Step B Partially reprogrammed T cell detachment
• the partially reprogrammed T cells were separated into 3 groups. After the SCM was removed, 1 ml of TCM was added and resuspended twice by PI 000 pipet then harvested and referred to as weakly attached cells. The detached cells harvested by vigorous pipetting with 1 ml TCM were referred to as attached cells. Strongly attached cells were detached by incubating with a recombinant enzyme, TrypLE Express (Thermo cat# 12604013) for 10 minutes at 37°C. Cells were stained for viability and with fluorescent conjugated antibodies for detection of CCR7, CD3, CD45RA, CD45RO, CD8b, CD4, CD62L, CD49f, CD29, TCFl/7.
• TrypLE Express TrypLE Express
• Integrin a6 and Integrin b ⁇ was detected with CD49f antibody and CD29 antibody respectively.
• CD49f antibody and CD29 antibody were fixed and permed by Foxp3 stain buffer set (Thermo, 00-5523-00). Cell phenotypes were acquired by Cytek Aurora. Analysis and Results
• Integrin a6 and integrin b ⁇ are expressed higher in rejuvenated cells than activated T cells (i.e., control).
• activated T cells On Day 10, detached cells were compared with activated T cells which were activated on day -1 and cultured in TCM for 10 days. Integrin a6 and integrin bl expression was higher in T cell derived adherent cells than in activated T cell control (FIG. 70).
• strongly attached cells showed a higher proportion of Integrin a6 (CD49f) and Integrin b ⁇ (CD29) double positive cells than attached cells, and especially weakly attached cells, which suggested the integrin complex expression level correlates with the adhesion intensity.
• Integrin expression level decreased toward the expression level in activated control cells (FIG. 71).
• CD3 is the most common marker of T cells
• CD8 is a marker for cytotoxic T cells.
• the CD3+CD8+ population decreased in weakly attached cells, attached cells, and strongly attached cells on day 10, but this population increased by day 17 (FIG. 72).
• the day 17 result showing the reemergence of the CD3+CD8+ population confirmed that the CD3- or CD8- population (the T cell derived adherent cell population) regains T cell marker expression by T cell activation and growth in T cell culture condition. It is unclear from this experiment whether the CD3+CD8- population observed at day 10 (see FIG.
• TCF1 and CCR7 are well known markers of less differentiated T cells. Strongly attached cells showed higher expression of TCF1 and CCR7 than activated controls at both day 10 and day 17, while attached cells and weakly attached cells showed comparable expression of TCF1 and higher expression of CCR7 than activated control at both time points (FIG. 74).
• the strongly attached cells proliferated slowly directly after detachment but eventually rebounded and demonstrated robust proliferation.
• the strongly attached cells also had high TCF1 and CCR7 expression on Days 10 and 17, indicating a stem- like phenotype.
• High integrin b ⁇ expression could cause upregulation of b-catenin expression through the signaling (see, e.g., Yuzuriha et al., Stem Cell Res. 2021 May;53: 102287) which can potentially contribute less differentiated phenotype of rejuvenated T cells (see, e.g., Clin Cancer Res, 2010 Oct 1;16(19):4695-701).
• Multi-phenotype CRISPR- Cas9 Screen Identifies p38 Kinase as a Target for Adoptive Immunotherapies.
• CD8+ T cells that provide the proliferative burst after PD- 1 therapy. NATURE 537, 417-421.

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