Engineering lymphocyte subsets: tools, trials and tribulations
暂无分享,去创建一个
[1] T. Eberlein,et al. Induction of Antigen-Specific CTL by Recombinant HIV Trans-Activating Fusion Protein-Pulsed Human Monocyte-Derived Dendritic Cells 1 , 2003, The Journal of Immunology.
[2] F. Bushman. Retroviral integration and human gene therapy. , 2007, The Journal of clinical investigation.
[3] T. Friedmann. A brief history of gene therapy , 1992, Nature Genetics.
[4] James L Riley,et al. Human T regulatory cell therapy: take a billion or so and call me in the morning. , 2009, Immunity.
[5] C. Macken,et al. A phase II randomized study of HIV-specific T-cell gene therapy in subjects with undetectable plasma viremia on combination antiretroviral therapy. , 2002, Molecular therapy : the journal of the American Society of Gene Therapy.
[6] S. Dzekunov,et al. A non-viral gene delivery system designed for clinical use. , 2003, Cytotherapy.
[7] K. Cornetta,et al. Cytokine-independent growth and clonal expansion of a primary human CD8+ T-cell clone following retroviral transduction with the IL-15 gene. , 2007, Blood.
[8] M. Kalos,et al. Transfer of Specificity for Human Immunodeficiency Virus Type 1 into Primary Human T Lymphocytes by Introduction of T-Cell Receptor Genes , 2000, Journal of Virology.
[9] B. Fehse,et al. Mutagenesis and oncogenesis by chromosomal insertion of gene transfer vectors. , 2006, Human gene therapy.
[10] I. Pastan,et al. Control of large, established tumor xenografts with genetically retargeted human T cells containing CD28 and CD137 domains , 2009, Proceedings of the National Academy of Sciences.
[11] T. Schumacher,et al. Functional Human Antigen-Specific T Cells Produced In Vitro Using Retroviral T Cell Receptor Transfer into Hematopoietic Progenitors1 , 2007, The Journal of Immunology.
[12] J. Melenhorst,et al. An APC for every occasion: induction and expansion of human Ag-specific CD4 and CD8 T cells using cellular and non-cellular APC. , 2004, Cytotherapy.
[13] O. Singer,et al. Use of Amplicon-6 Vectors Derived from Human Herpesvirus 6 for Efficient Expression of Membrane-Associated and -Secreted Proteins in T Cells , 2004, Journal of Virology.
[14] W. Smiddy. Economic implications of current age-related macular degeneration treatments. , 2009, Ophthalmology.
[15] Hans-Peter Kiem,et al. Foamy virus vector integration sites in normal human cells , 2006, Proceedings of the National Academy of Sciences of the United States of America.
[16] Jessica E. Bolden,et al. Anticancer activities of histone deacetylase inhibitors , 2006, Nature Reviews Drug Discovery.
[17] Dana Carroll,et al. Gene targeting using zinc finger nucleases , 2005, Nature Biotechnology.
[18] Hao Liu,et al. Virus-specific T cells engineered to coexpress tumor-specific receptors: persistence and antitumor activity in individuals with neuroblastoma , 2008, Nature Medicine.
[19] S. Rosenberg,et al. Cancer Regression in Patients After Transfer of Genetically Engineered Lymphocytes , 2006, Science.
[20] Mike Gough,et al. Adoptive transfer of effector CD8+ T cells derived from central memory cells establishes persistent T cell memory in primates. , 2008, The Journal of clinical investigation.
[21] M. Tykocinski,et al. New designs for cancer vaccine and artificial veto cells , 2003, Immunologic research.
[22] Mark Isalan,et al. Zinc-finger protein-targeted gene regulation: Genomewide single-gene specificity , 2003, Proceedings of the National Academy of Sciences of the United States of America.
[23] A. Bothwell,et al. Transduction of the cytoplasmic domain of CTLA-4 inhibits TcR-specific activation signals and prevents collagen-induced arthritis , 2008, Proceedings of the National Academy of Sciences.
[24] M. Merkenschlager,et al. RNAi and chromatin in T cell development and function. , 2008, Current opinion in immunology.
[25] Cameron S. Osborne,et al. LMO2-Associated Clonal T Cell Proliferation in Two Patients after Gene Therapy for SCID-X1 , 2003, Science.
[26] M. Zöller,et al. Characterization of Tumor Reactivity of Human Vγ9Vδ2 γδ T Cells In Vitro and in SCID Mice In Vivo1 , 2004, The Journal of Immunology.
[27] P. Muranski,et al. Adoptive immunotherapy of cancer using CD4(+) T cells. , 2009, Current opinion in immunology.
[28] Jiang Zhu,et al. Host-reactive CD8+ memory stem cells in graft-versus-host disease , 2005, Nature Medicine.
[29] M. Raffeld,et al. Helper virus induced T cell lymphoma in nonhuman primates after retroviral mediated gene transfer , 1992, The Journal of experimental medicine.
[30] J. Zúñiga-Pflücker,et al. In vitro generation of T lymphocytes from embryonic stem cell-derived prehematopoietic progenitors. , 2003, Blood.
[31] A. Klug,et al. Targeted gene knockout in mammalian cells by using engineered zinc-finger nucleases , 2008, Proceedings of the National Academy of Sciences.
[32] D. Trono,et al. Self-Inactivating Lentivirus Vector for Safe and Efficient In Vivo Gene Delivery , 1998, Journal of Virology.
[33] E. Elinav,et al. Amelioration of colitis by genetically engineered murine regulatory T cells redirected by antigen-specific chimeric receptor. , 2009, Gastroenterology.
[34] C. June,et al. Adoptive T cell therapy for cancer in the clinic. , 2007, The Journal of clinical investigation.
[35] A. Mackensen,et al. Ex vivo induction and expansion of antigen-specific cytotoxic T cells by HLA-Ig–coated artificial antigen-presenting cells , 2003, Nature Medicine.
[36] S. Rosenberg,et al. Gene therapy with human and mouse T-cell receptors mediates cancer regression and targets normal tissues expressing cognate antigen. , 2009, Blood.
[37] F. Gage,et al. In Vivo Gene Delivery and Stable Transduction of Nondividing Cells by a Lentiviral Vector , 1996, Science.
[38] S. Schwarze,et al. In vivo protein transduction: delivery of a biologically active protein into the mouse. , 1999, Science.
[39] H. Einsele,et al. Tumor Regression in Cancer Patients by Very Low Doses of a T Cell–Engaging Antibody , 2008, Science.
[40] C. Rooney,et al. Gene-engineered varicella-zoster virus reactive CD4+ cytotoxic T cells exert tumor-specific effector function. , 2007, Cancer research.
[41] M. Kay,et al. In vivo gene therapy of hemophilia B: sustained partial correction in factor IX-deficient dogs. , 1993, Science.
[42] M. Hansmann,et al. Resistance of mature T cells to oncogene transformation. , 2008, Blood.
[43] David G. Melvin,et al. Chromosomal transposition of PiggyBac in mouse embryonic stem cells , 2008, Proceedings of the National Academy of Sciences.
[44] G. Stamatoyannopoulos,et al. A capsid-modified adenovirus vector devoid of all viral genes: assessment of transduction and toxicity in human hematopoietic cells. , 2001, Molecular therapy : the journal of the American Society of Gene Therapy.
[45] C. Lohse,et al. Questionable Relevance of γδ T Lymphocytes in Renal Cell Carcinoma1 , 2008, The Journal of Immunology.
[46] Yoshimasa Tanaka,et al. Safety profile and anti-tumor effects of adoptive immunotherapy using gamma-delta T cells against advanced renal cell carcinoma: a pilot study , 2007, Cancer Immunology, Immunotherapy.
[47] Jeffrey C. Miller,et al. Highly efficient endogenous human gene correction using designed zinc-finger nucleases , 2005, Nature.
[48] Miller Ad,et al. Improved Retroviral Vectors for Gene Transfer and Expression , 1989 .
[49] O. Singer,et al. Tamplicon-7, a Novel T-Lymphotropic Vector Derived from Human Herpesvirus 7 , 1999, Journal of Virology.
[50] S. Riddell,et al. The use of anti-CD3 and anti-CD28 monoclonal antibodies to clone and expand human antigen-specific T cells. , 1990, Journal of immunological methods.
[51] K. Keyvanfar,et al. Robust Expansion of Viral Antigen-specific CD4+ and CD8+ T Cells for Adoptive T Cell Therapy Using Gene-modified Activated T Cells as Antigen Presenting Cells , 2006, Journal of immunotherapy.
[52] M. Tykocinski,et al. Hierarchical Costimulator Thresholds for Distinct Immune Responses: Application of a Novel Two-Step Fc Fusion Protein Transfer Method1 , 2000, The Journal of Immunology.
[53] Y. Okamoto,et al. Combination therapy of in vitro‐expanded natural killer T cells and α‐galactosylceramide‐pulsed antigen‐presenting cells in patients with recurrent head and neck carcinoma , 2009, Cancer science.
[54] Christof von Kalle,et al. The genotoxic potential of retroviral vectors is strongly modulated by vector design and integration site selection in a mouse model of HSC gene therapy. , 2009, The Journal of clinical investigation.
[55] E. Shpall,et al. System Sleeping Beauty the Redirecting Specificity of T-cell Populations for Cd19 Using Cited Articles Citing Articles E-mail Alerts Redirecting Specificity of T-cell Populations for Cd19 Using the Sleeping Beauty System , 2022 .
[56] R. Lopez. Human γδ-T cells in adoptive immunotherapy of malignant and infectious diseases , 2002 .
[57] M. Bonneville,et al. Self/non‐self discrimination by human γδ T cells: simple solutions for a complex issue? , 2007 .
[58] Jinjuan Wang,et al. Adoptive immunotherapy for indolent non-Hodgkin lymphoma and mantle cell lymphoma using genetically modified autologous CD20-specific T cells. , 2008, Blood.
[59] S. Sleijfer,et al. Treatment of metastatic renal cell carcinoma with autologous T-lymphocytes genetically retargeted against carbonic anhydrase IX: first clinical experience. , 2006, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[60] A. Ganser,et al. Infusion of suicide-gene-engineered donor lymphocytes after family haploidentical haemopoietic stem-cell transplantation for leukaemia (the TK007 trial): a non-randomised phase I-II study. , 2009, The Lancet. Oncology.
[61] Mitchell Kronenberg,et al. Toward an understanding of NKT cell biology: progress and paradoxes. , 2005, Annual review of immunology.
[62] M. Slovak,et al. Adoptive transfer of chimeric antigen receptor re-directed cytolytic T lymphocyte clones in patients with neuroblastoma. , 2007, Molecular therapy : the journal of the American Society of Gene Therapy.
[63] C. Dunbar,et al. Persistence and expression of the adenosine deaminase gene for 12 years and immune reaction to gene transfer components: long-term results of the first clinical gene therapy trial. , 2003, Blood.
[64] J. Blattman,et al. Adoptive immunotherapy: engineering T cell responses as biologic weapons for tumor mass destruction. , 2003, Cancer cell.
[65] E. Pamer,et al. Adoptive transfer of T-cell precursors enhances T-cell reconstitution after allogeneic hematopoietic stem cell transplantation , 2006, Nature Medicine.
[66] M. Sadelain,et al. Harnessing endogenous miR-181a to segregate transgenic antigen receptor expression in developing versus post-thymic T cells in murine hematopoietic chimeras. , 2008, The Journal of clinical investigation.
[67] K. Nakagawa,et al. Zoledronate facilitates large-scale ex vivo expansion of functional gammadelta T cells from cancer patients for use in adoptive immunotherapy. , 2008, Cytotherapy.
[68] Peter A. Jones,et al. Cellular differentiation, cytidine analogs and DNA methylation , 1980, Cell.
[69] Daniel G. Miller,et al. Unique integration profiles in a canine model of long-term repopulating cells transduced with gammaretrovirus, lentivirus, or foamy virus. , 2007, Human gene therapy.
[70] M. Rots,et al. A mosaic adenovirus possessing serotype Ad5 and serotype Ad3 knobs exhibits expanded tropism. , 2003, Virology.
[71] R. Hagedoorn,et al. αβ T-Cell Receptor Engineered γδ T Cells Mediate Effective Antileukemic Reactivity , 2006 .
[72] M. Heřmánková,et al. A conditionally replicating HIV-1 vector interferes with wild-type HIV-1 replication and spread. , 1996, Proceedings of the National Academy of Sciences of the United States of America.
[73] Y. Furukawa,et al. Transcriptional modulation using HDACi depsipeptide promotes immune cell-mediated tumor destruction of murine B16 melanoma. , 2008, The Journal of investigative dermatology.
[74] S. Rosenberg,et al. High-efficiency transfection of primary human and mouse T lymphocytes using RNA electroporation. , 2006, Molecular therapy : the journal of the American Society of Gene Therapy.
[75] K. Irvine,et al. De novo induction of a cancer/testis antigen by 5-aza-2'-deoxycytidine augments adoptive immunotherapy in a murine tumor model. , 2006, Cancer research.
[76] D. Baltimore,et al. Long-term in vivo provision of antigen-specific T cell immunity by programming hematopoietic stem cells. , 2005, Proceedings of the National Academy of Sciences of the United States of America.
[77] F. Guidi,et al. Adoptive immunotherapy by avidin-driven cytotoxic T lymphocyte-tumor bridging. , 2000, Cancer research.
[78] L. Booij,et al. First clinical experiences with ORG NC 45. , 1980, British journal of anaesthesia.
[79] M. Todaro,et al. Efficient Killing of Human Colon Cancer Stem Cells by γδ T Lymphocytes1 , 2009, The Journal of Immunology.
[80] S. Ekker,et al. Messenger RNA as a source of transposase for sleeping beauty transposon-mediated correction of hereditary tyrosinemia type I. , 2007, Molecular therapy : the journal of the American Society of Gene Therapy.
[81] A. Eguchi,et al. Efficient siRNA Delivery into Primary Cells by Peptide Transduction-dsRNA Binding Domain (PTD-DRBD) Fusion Protein , 2009, Nature Biotechnology.
[82] W. Janzen,et al. The use of diversity profiling to characterize chemical modulators of the histone deacetylases. , 2008, Life sciences.
[83] A. Lawson,et al. Activation of Resting Human Primary T Cells with Chimeric Receptors: Costimulation from CD28, Inducible Costimulator, CD134, and CD137 in Series with Signals from the TCRζ Chain , 2004, The Journal of Immunology.
[84] M. Connors,et al. Effects of CD28 costimulation on long-term proliferation of CD4+ T cells in the absence of exogenous feeder cells. , 1997, Journal of immunology.
[85] M. Bonneville,et al. IL-21-Mediated Potentiation of Antitumor Cytolytic and Proinflammatory Responses of Human Vγ9Vδ2 T Cells for Adoptive Immunotherapy1 , 2009, The Journal of Immunology.
[86] D. Trono,et al. A Third-Generation Lentivirus Vector with a Conditional Packaging System , 1998, Journal of Virology.
[87] T. Watts,et al. IL-15-Dependent Induction of 4-1BB Promotes Antigen-Independent CD8 Memory T Cell Survival1 , 2006, The Journal of Immunology.
[88] S. Rosenberg,et al. Telomere Length of Transferred Lymphocytes Correlates with In Vivo Persistence and Tumor Regression in Melanoma Patients Receiving Cell Transfer Therapy1 , 2005, The Journal of Immunology.
[89] Y. Hildebrandt,et al. Gene transfer into human T lymphocytes and natural killer cells by Ad5/F35 chimeric adenoviral vectors. , 2004, Experimental hematology.
[90] P. Rogers,et al. Expansion of human Vα24+ NKT cells by repeated stimulation with KRN7000 , 2004 .
[91] J. Orange,et al. Establishment of HIV-1 resistance in CD4+ T cells by genome editing using zinc-finger nucleases , 2008, Nature Biotechnology.
[92] M. Chamberlain. Bevacizumab plus irinotecan in recurrent glioblastoma. , 2008, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[93] A. Ulph,et al. An economic evaluation of national parks , 1981 .
[94] A. Rethwilm. Foamy virus vectors: an awaited alternative to gammaretro- and lentiviral vectors. , 2007, Current gene therapy.
[95] J. Sampson,et al. Selective modification of antigen-specific T cells by RNA electroporation. , 2008, Human gene therapy.
[96] David Allman,et al. Ex vivo expansion of polyclonal and antigen-specific cytotoxic T lymphocytes by artificial APCs expressing ligands for the T-cell receptor, CD28 and 4-1BB , 2002, Nature Biotechnology.
[97] T. Geiger,et al. Immunotherapy of autoimmune encephalomyelitis with redirected CD4+CD25+ T lymphocytes. , 2005, Blood.
[98] Z. Ballas. The use of 5-azacytidine to establish constitutive interleukin 2-producing clones of the EL4 thymoma. , 1984, Journal of immunology.
[99] E. Olson,et al. Deacetylase inhibition promotes the generation and function of regulatory T cells , 2007, Nature Medicine.
[100] H. Weiner,et al. What does the future hold for cell-based tolerogenic therapy? , 2007, Nature Reviews Immunology.
[101] Michel Sadelain,et al. Human T-lymphocyte cytotoxicity and proliferation directed by a single chimeric TCRζ /CD28 receptor , 2002, Nature Biotechnology.
[102] Mark M. Davis,et al. miR-181a Is an Intrinsic Modulator of T Cell Sensitivity and Selection , 2007, Cell.
[103] M. Tan,et al. Rapid Immune Recovery and Graft-versus-Host Disease–like Engraftment Syndrome following Adoptive Transfer of Costimulated Autologous T Cells , 2009, Clinical Cancer Research.
[104] G. Freeman,et al. High efficiency gene transfer into murine T cell clones using a retroviral vector. , 1986, Journal of immunology.
[105] W. Paul,et al. Spontaneous and Homeostatic Proliferation of CD4 T Cells Are Regulated by Different Mechanisms , 2005, The Journal of Immunology.
[106] M. Roederer,et al. T-cell quality in memory and protection: implications for vaccine design , 2008, Nature Reviews Immunology.
[107] P. Brauchli,et al. Bevacizumab in combination with paclitaxel for HER-2 negative metastatic breast cancer: an economic evaluation. , 2009, European journal of cancer.
[108] John J Rossi,et al. Genetic therapies against HIV , 2007, Nature Biotechnology.
[109] H. Heslop,et al. Adoptive T cell therapy of cancer. , 2010, Current opinion in immunology.
[110] Frederic D Bushman,et al. Analysis of lentiviral vector integration in HIV+ study subjects receiving autologous infusions of gene modified CD4+ T cells. , 2009, Molecular therapy : the journal of the American Society of Gene Therapy.
[111] U. Bunz. How Are Alkynes Scrambled? , 2005, Science.
[112] F. Bushman,et al. Insertional oncogenesis in 4 patients after retrovirus-mediated gene therapy of SCID-X1. , 2008, The Journal of clinical investigation.
[113] W. Heneine,et al. Frequent Simian Foamy Virus Infection in Persons Occupationally Exposed to Nonhuman Primates , 2004, Journal of Virology.
[114] S. Balk,et al. Selective activation, expansion, and monitoring of human iNKT cells with a monoclonal antibody specific for the TCR α‐chain CDR3 loop , 2008, European journal of immunology.
[115] J. Tolar,et al. Stable gene transfer and expression in human primary T cells by the Sleeping Beauty transposon system. , 2005, Blood.
[116] G. Bubley,et al. Loss of IFN-γ Production by Invariant NK T Cells in Advanced Cancer1 , 2001, The Journal of Immunology.
[117] M. Ferrarini,et al. Human gammadelta T cells: a nonredundant system in the immune-surveillance against cancer. , 2002, Trends in immunology.
[118] Malcolm K. Brenner,et al. Long–term restoration of immunity against Epstein–Barr virus infection by adoptive transfer of gene–modified virus–specific T lymphocytes , 1996, Nature Medicine.
[119] S. Sleijfer,et al. Gene-modified T cells for adoptive immunotherapy of renal cell cancer maintain transgene-specific immune functions in vivo , 2007, Cancer Immunology, Immunotherapy.
[120] K. Kretschmer,et al. DNA methylation controls Foxp3 gene expression , 2008, European journal of immunology.
[121] D. Baltimore,et al. Targeting lentiviral vectors to specific cell types in vivo. , 2006, Proceedings of the National Academy of Sciences of the United States of America.
[122] T. Schumacher,et al. T-cell-receptor gene therapy , 2002, Nature Reviews Immunology.
[123] Clelia Di Serio,et al. Hematopoietic stem cell gene transfer in a tumor-prone mouse model uncovers low genotoxicity of lentiviral vector integration , 2006, Nature Biotechnology.
[124] Y. Okamoto,et al. A Phase I Study of In vitro Expanded Natural Killer T Cells in Patients with Advanced and Recurrent Non–Small Cell Lung Cancer , 2006, Clinical Cancer Research.
[125] James M. Allen,et al. Successful treatment of canine leukocyte adhesion deficiency by foamy virus vectors , 2008, Nature Medicine.
[126] R. Vile,et al. Virus smuggling, tax evasion and tumor assassination , 2006, Nature Medicine.
[127] C. Bordignon,et al. Suicide gene therapy of graft-versus-host disease induced by central memory human T lymphocytes. , 2005, Blood.
[128] L. Fugger,et al. Redirecting Therapeutic T Cells against Myelin-Specific T Lymphocytes Using a Humanized Myelin Basic Protein-HLA-DR2-ζ Chimeric Receptor1 , 2008, The Journal of Immunology.
[129] M. Rimbert,et al. Phase-I study of Innacell γδ™, an autologous cell-therapy product highly enriched in γ9δ2 T lymphocytes, in combination with IL-2, in patients with metastatic renal cell carcinoma , 2008, Cancer Immunology, Immunotherapy.
[130] Mary K. Lewinski,et al. Genome-Wide Analysis of Chromosomal Features Repressing Human Immunodeficiency Virus Transcription , 2005, Journal of Virology.
[131] Antonio Lanzavecchia,et al. Understanding the generation and function of memory T cell subsets. , 2005, Current opinion in immunology.
[132] Yi Li,et al. Directed evolution of human T-cell receptors with picomolar affinities by phage display , 2005, Nature Biotechnology.
[133] P. Muranski,et al. Tumor-specific Th17-polarized cells eradicate large established melanoma. , 2008, Blood.
[134] C. Baird,et al. The pilot study. , 2000, Orthopedic nursing.
[135] Chien-Fu Hung,et al. Expression of IL‐15RA or an IL‐15/IL‐15RA fusion on CD8+ T cells modifies adoptively transferred T‐cell function in cis , 2009, European journal of immunology.
[136] Christopher B Wilson,et al. Epigenetic control of T-helper-cell differentiation , 2009, Nature Reviews Immunology.
[137] A. Clarke,et al. Creating the Costliest Orphan: The Orphan Drug Act in the Development of Ceredase™ , 1992, International Journal of Technology Assessment in Health Care.
[138] M. Capecchi,et al. Altering the genome by homologous recombination. , 1989, Science.
[139] H. Jürgens,et al. Human γδ T cells as mediators of chimaeric‐receptor redirected anti‐tumour immunity , 2004 .
[140] A. Lukas,et al. Mouse Mammary Tumor Virus Integration Site Selection in Human and Mouse Genomes , 2007, Journal of Virology.
[141] S. Yoon,et al. Adoptive immunotherapy using human peripheral blood lymphocytes transferred with RNA encoding Her-2/neu-specific chimeric immune receptor in ovarian cancer xenograft model , 2009, Cancer Gene Therapy.
[142] I. Chen,et al. Lentiviral Vectors--the Promise of Gene Therapy Within Reach? , 1999, Science.
[143] John R. Mascola,et al. Gene transfer in humans using a conditionally replicating lentiviral vector , 2006, Proceedings of the National Academy of Sciences.
[144] M. Sadelain,et al. The genetic engineering of hematopoietic stem cells: the rise of lentiviral vectors, the conundrum of the ltr, and the promise of lineage-restricted vectors. , 2007, Molecular therapy : the journal of the American Society of Gene Therapy.
[145] A. Miller,et al. Improved retroviral vectors for gene transfer and expression. , 1989, BioTechniques.
[146] M. Rollence,et al. Selective targeting of human cells by a chimeric adenovirus vector containing a modified fiber protein , 1997, Journal of virology.
[147] R. Storb,et al. Antileukemic effect of graft-versus-host disease in human recipients of allogeneic-marrow grafts. , 1979, The New England journal of medicine.
[148] R. Phillips,et al. Control of HIV-1 immune escape by CD8 T cells expressing enhanced T-cell receptor , 2008, Nature Medicine.
[149] G. Zhu,et al. CD137 stimulation delivers an antigen-independent growth signal for T lymphocytes with memory phenotype. , 2007, Blood.
[150] J. Ellis. Silencing and variegation of gammaretrovirus and lentivirus vectors. , 2005, Human gene therapy.
[151] C. June,et al. Extensive Replicative Capacity of Human Central Memory T Cells1 , 2004, The Journal of Immunology.
[152] D. Russell,et al. Foamy virus vectors , 1996, Journal of virology.
[153] B. Moser,et al. Professional Antigen-Presentation Function by Human γδ T Cells , 2005, Science.
[154] Kenneth M. Murphy,et al. Decision making in the immune system: The lineage decisions of helper T cells , 2002, Nature Reviews Immunology.
[155] Eun-Sung Kim,et al. Intranasal delivery of the cytoplasmic domain of CTLA-4 using a novel protein transduction domain prevents allergic inflammation , 2006, Nature Medicine.
[156] K. Cornetta,et al. Gene transfer into humans--immunotherapy of patients with advanced melanoma, using tumor-infiltrating lymphocytes modified by retroviral gene transduction. , 1990, The New England journal of medicine.
[157] Michel Sadelain,et al. The promise and potential pitfalls of chimeric antigen receptors. , 2009, Current Opinion in Immunology.
[158] Y. Mori. Recent topics related to human herpesvirus 6 cell tropism , 2009, Cellular microbiology.
[159] Z. Eshhar,et al. Expression of immunoglobulin-T-cell receptor chimeric molecules as functional receptors with antibody-type specificity. , 1989, Proceedings of the National Academy of Sciences of the United States of America.
[160] C. Rooney,et al. Human cytotoxic T lymphocytes with reduced sensitivity to Fas-induced apoptosis. , 2005, Blood.
[161] Donna Niedzwiecki,et al. Telomerase mRNA-Transfected Dendritic Cells Stimulate Antigen-Specific CD8+ and CD4+ T Cell Responses in Patients with Metastatic Prostate Cancer 1 , 2005, The Journal of Immunology.
[162] D. Largaespada,et al. Mammalian mutagenesis using a highly mobile somatic Sleeping Beauty transposon system , 2005, Nature.
[163] Robin Holliday,et al. DNA Modification Mechanisms and Gene Activity during Development , 1996 .
[164] C. June,et al. 4-1BB Is Superior to CD28 Costimulation for Generating CD8+ Cytotoxic Lymphocytes for Adoptive Immunotherapy1 , 2007, The Journal of Immunology.
[165] S. Goff,et al. Host restriction factors blocking retroviral replication. , 2008, Annual review of genetics.