In vivo tracking of T cells in humans unveils decade-long survival and activity of genetically modified T memory stem cells

Two subsets of memory T lymphocytes with distinct homing potentials and effector functions

Sallusto, F., Lenig, D., Förster, R., Lipp, M., & Lanzavecchia, A. (1999) · Nature · doi:10.1038/44385 · Cited by 5,846

GREAT improves functional interpretation of cis-regulatory regions

McLean, C. Y., Bristor, D., Hiller, M., Clarke, S. L., Schaar, B. T., Lowe, C. B., Wenger, A. M., & Bejerano, G. (2010) · Nature Biotechnology · doi:10.1038/nbt.1630 · Cited by 4,502

A human memory T cell subset with stem cell–like properties

Gattinoni, L., Lugli, E., Ji, Y., Pos, Z., Paulos, C. M., Quigley, M. F., Almeida, J. R., Gostick, E., Yu, Z., Carpenito, C., et al. (2011) · Nature Medicine · doi:10.1038/nm.2446 · Cited by 1,974

Transcriptional control of effector and memory CD8+ T cell differentiation

Kaech, S. M., & Cui, W. (2012) · Nature Reviews Immunology · doi:10.1038/nri3307 · Cited by 1,628

T Lymphocyte-Directed Gene Therapy for ADA − SCID: Initial Trial Results After 4 Years

Blaese, R. M., Culver, K. W., Miller, A. D., Carter, C. S., Fleisher, T. A., Clerici, M., Shearer, G. M., Chang, L., Chiang, Y. L., Tolstoshev, P., et al. (1995) · Science · doi:10.1126/science.270.5235.475 · Cited by 1,546

Insertional mutagenesis combined with acquired somatic mutations causes leukemogenesis following gene therapy of SCID-X1 patients

Howe, S. J., Mansour, M. R., Schwarzwaelder, K., Bartholomae, C., Hubank, M., Kempski, H., Brugman, M. H., Pike-Overzet, K., Chatters, S. J., de Ridder, D., et al. (2008) · Journal of Clinical Investigation · doi:10.1172/jci35798 · Cited by 1,286

Lentiviral Hematopoietic Stem Cell Gene Therapy Benefits Metachromatic Leukodystrophy

Biffi, A., Montini, E., Lorioli, L., Cesani, M., Fumagalli, F., Plati, T., Baldoli, C., Martino, S., Calabria, A., Canale, S., et al. (2013) · Science · doi:10.1126/science.1233158 · Cited by 1,180

Correction of ADA-SCID by Stem Cell Gene Therapy Combined with Nonmyeloablative Conditioning

Aiuti, A., Slavin, S., Aker, M., Ficara, F., Deola, S., Mortellaro, A., Morecki, S., Andolfi, G., Tabucchi, A., Carlucci, F., et al. (2002) · Science · doi:10.1126/science.1070104 · Cited by 1,142

Lentiviral Hematopoietic Stem Cell Gene Therapy in Patients with Wiskott-Aldrich Syndrome

Aiuti, A., Biasco, L., Scaramuzza, S., Ferrua, F., Cicalese, M. P., Baricordi, C., Dionisio, F., Calabria, A., Giannelli, S., Castiello, M. C., et al. (2013) · Science · doi:10.1126/science.1233151 · Cited by 1,025

Gene Therapy for Immunodeficiency Due to Adenosine Deaminase Deficiency

Aiuti, A., Cattaneo, F., Galimberti, S., Benninghoff, U., Cassani, B., Callegaro, L., Scaramuzza, S., Andolfi, G., Mirolo, M., Brigida, I., et al. (2009) · New England Journal of Medicine · doi:10.1056/nejmoa0805817 · Cited by 1,018

Platelets in Wiskott-Aldrich syndrome: Victims or executioners?

Sereni, L. P., Castiello, M. C., & VILLA, A. M. (2017) · Journal of Leukocyte Biology · doi:10.1189/jlb.5mr0617-257r · Cited by 16

Antigen-specific CD8+ memory stem T cells generated from human peripheral blood effectively eradicate allogeneic targets in mice

Guan, L., Li, X., Wei, J., Liang, Z., Yang, J. X., Weng, X., & Wu, X. (2018) · Stem Cell Research & Therapy · doi:10.1186/s13287-018-1080-1 · Cited by 16

c-MPL provides tumor-targeted T-cell receptor-transgenic T cells with costimulation and cytokine signals

Nishimura, C., Brenner, D. A., Mukherjee, M., Hirsch, R. A., Ott, L. C., Wu, M., Liu, H., Dakhova, O., Orange, J. S., Brenner, M. K., et al. (2017) · Blood · doi:10.1182/blood-2017-02-769463 · Cited by 15

Prevention and treatment of relapse after stem cell transplantation by cellular therapies

Falkenburg, F., Ruggiero, E., Bonini, C., Porter, D., Miller, J. C., Malard, F., Mohty, M., Kröger, N. M., & Kolb, H. J. (2018) · Bone Marrow Transplantation · doi:10.1038/s41409-018-0227-0 · Cited by 14

Cancer-reactive memory T cells from bone marrow: Spontaneous induction and therapeutic potential (Review)

Schirrmacher, V. (2015) · International Journal of Oncology · doi:10.3892/ijo.2015.3197 · Cited by 16

Precise CRISPR-Cas9 gene repair in autologous memory T cells to treat familial hemophagocytic lymphohistiocytosis

Li, X., Wirtz, T., Weber, T., Lebedin, M. Y., Lowenstein, E. D., Sommermann, T. G., Zach, A., Yasuda, T., de la Rosa, K., Chu, V. T., et al. (2024) · Science Immunology · doi:10.1126/sciimmunol.adi0042 · Cited by 14

Integration Site Analysis in Gene Therapy Patients: Expectations and Reality

Biasco, L. (2017) · Human Gene Therapy · doi:10.1089/hum.2017.183 · Cited by 14

Precision medicine in the clinical management of respiratory tract infections including multidrug-resistant tuberculosis

Rao, M., Ligeiro, D., & Maeurer, M. J. (2019) · Current Opinion in Pulmonary Medicine · doi:10.1097/mcp.0000000000000575 · Cited by 13

Bioprocess considerations for T‐cell therapy: Investigating the impact of agitation, dissolved oxygen, and pH on T‐cell expansion and differentiation

Amini, A., Wiegmann, V., Patel, H., Veraitch, F. S., & Baganz, F. (2020) · Biotechnology and Bioengineering · doi:10.1002/bit.27468 · Cited by 12

Modulation of Determinant Factors to Improve Therapeutic Combinations with Immune Checkpoint Inhibitors

Dosset, M., Joseph, E. L. M., Vargas, T. R., & Apétoh, L. (2020) · Cells · doi:10.3390/cells9071727 · Cited by 12

Stem-like T cells and niches: Implications in human health and disease

Yi, L., & Li, Y. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.907172 · Cited by 15

Harnessing Biomaterials to Amplify Immunity in Aged Mice through T Memory Stem Cells

Hasani‐Sadrabadi, M. M., Majedi, F. S., Zárubová, J., Thauland, T. J., Arumugaswami, V., Hsiai, T. K., Bouchard, L., Butte, M. J., & Li, S. (2024) · ACS Nano · doi:10.1021/acsnano.3c08559 · Cited by 11

Functional role of UNC13D in immune diseases and its therapeutic applications

Duong, V.-T., Lee, D., Kim, Y. H., & Oh, S. (2024) · Frontiers in Immunology · doi:10.3389/fimmu.2024.1460882 · Cited by 11

Secretion of 4-1BB Ligand Crosslinked to PD-1 Checkpoint Inhibitor Potentiates Chimeric Antigen Receptor T Cell Solid Tumor Efficacy

Dunn, Z. S., Qu, Y., MacMullan, M. A., Chen, X., Cinay, G. E., & Wang, P. (2023) · Human Gene Therapy · doi:10.1089/hum.2022.068 · Cited by 12

Preferential Homing of Tumor-specific and Functional CD8+ Stem Cell-like Memory T Cells to the Bone Marrow

Wu, K., Li, Y., Zhang, S., Zhou, N., Liu, B., Pan, T. S., Zhang, X., Luo, H., Huang, Z., Li, X., et al. (2019) · Journal of Immunotherapy · doi:10.1097/cji.0000000000000273 · Cited by 11

T memory stem cells after allogeneic haematopoietic cell transplantation: unique long‐term kinetics and influence of chronic graft‐versus‐host disease

Jimbo, K., Konuma, T., Watanabe, E., Kohara, C., Mizukami, M., Nagai, E., Oiwa‐Monna, M., Mizusawa, M., Isobe, M., Kato, S., et al. (2019) · British Journal of Haematology · doi:10.1111/bjh.15995 · Cited by 11

Immunophenotypic Analysis of CAR-T Cells

de Azevedo, J. T. C., Mizukami, A., Moço, P. D., & Malmegrim, K. C. R. (2019) · Methods in molecular biology · doi:10.1007/978-1-0716-0146-4_14 · Cited by 11

A novel mechanism linking memory stem cells with innate immunity in protection against HIV-1 infection

Wang, Y., Whittall, T., Neil, S. J. D., Britton, G., Mistry, M., Rerks‐Ngarm, S., Pitisuttithum, P., Kaewkungwal, J., Nitayaphan, S., Yu, X., et al. (2017) · Scientific Reports · doi:10.1038/s41598-017-01188-3 · Cited by 10

CD4 + T Memory Stem Cells Correlate with Disease Progression in Chronically HIV-1-Infected Patients

Lu, X., Song, B., Weng, W., Xia, H., Su, B., Wu, H., Zhang, T., Li, W., & Gao, Y. (2017) · Viral Immunology · doi:10.1089/vim.2017.0017 · Cited by 10

Normal Numbers of Stem Cell Memory T Cells Despite Strongly Reduced Naive T Cells Support Intact Memory T Cell Compartment in Ataxia Telangiectasia

Weitering, T. J., Melsen, J. E., Dam, M. M. V. O.-T., Weemaes, C. M. R., Schilham, M. W., & van der Burg, M. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.686333 · Cited by 10

Immunomodulatory Effects of IFNα on T and NK Cells in Chronic Myeloid Leukemia Patients in Deep Molecular Response Preparing for Treatment Discontinuation

Puzzolo, M. C., Breccia, M., Mariglia, P., Colafigli, G., Pepe, S., Scalzulli, E., Mariggiò, E., Latagliata, R., Guarini, A. R., & Foà, R. (2022) · Journal of Clinical Medicine · doi:10.3390/jcm11195594 · Cited by 9

Gene Edited T Cell Therapies for Inborn Errors of Immunity

Fox, T. A., Houghton, B. C., & Booth, C. (2022) · Frontiers in Genome Editing · doi:10.3389/fgeed.2022.899294 · Cited by 9

The dark side of T memory stem cells

Gattinoni, L. (2015) · Blood · doi:10.1182/blood-2015-04-640631 · Cited by 10

Generating stem-like memory T cells with antioxidants for adoptive cell transfer immunotherapy of cancer

Pilipow, K., Scamardella, E., & Lugli, E. (2020) · Methods in enzymology on CD-ROM/Methods in enzymology · doi:10.1016/bs.mie.2019.08.016 · Cited by 8

Allogeneic and other innovative chimeric antigen receptor platforms

Jallouk, A. P., Sengsayadeth, S. M., Savani, B. N., Dholaria, B., & Oluwole, O. O. (2024) · Clinical Hematology International · doi:10.46989/001c.121404 · Cited by 8

Long-term lymphoid progenitors independently sustain naïve T and NK cell production in humans

Izotova, N., Rivat, C., Baricordi, C., Blanco, E., Pellin, D., Watt, E., Gkazi, S. A., Adams, S. P., Gilmour, K. C., Xu‐Bayford, J., et al. (2021) · Nature Communications · doi:10.1038/s41467-021-21834-9 · Cited by 8

T cell therapies-are T memory stem cells the answer?

Flynn, J. K., & Gorry, P. R. (2015) · Europe PMC (PubMed Central) · doi:10.3978/j.issn.2305-5839.2015.08.13 · Cited by 8

Infusion of CCR5 Gene-Edited T Cells Allows Immune Reconstitution, HIV Reservoir Decay, and Long-Term Virological ControlPreprint

Zeidan, J., Sharma, A., Lee, G., Raad, A., Fromentin, R., Fourati, S., Ghneim, K., Sánchez, G. P., Benne, C., Canderan, G., et al. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.02.28.433290 · Cited by 8

First pediatric B-acute lymphoblastic leukemia patient treated with anti-CD19 chimeric antigen receptor T-cell therapy: Long-term remission or early cure?

Bouzianas, D. G., & Bouziana, S. D. (2024) · Human Vaccines & Immunotherapeutics · doi:10.1080/21645515.2024.2321678 · Cited by 8

IS-Seq: a bioinformatics pipeline for integration sites analysis with comprehensive abundance quantification methods

Yan, A., Baricordi, C., Nguyen, Q., Barbarossa, L., Loperfido, M., & Biasco, L. (2023) · BMC Bioinformatics · doi:10.1186/s12859-023-05390-1 · Cited by 7

Tracking the progeny of adoptively transferred virus-specific T cells in patients posttransplant using TCR sequencing

Huisman, W., Roex, M. C. J., Hageman, L., Koster, E. A. S., Veld, S. A. J., Hoogstraten, C., van Balen, P., van Egmond, H. M., van Bergen, C. A. M., Einsele, H., et al. (2022) · Blood Advances · doi:10.1182/bloodadvances.2022007270 · Cited by 7

Phenotypic and Immunometabolic Aspects on Stem Cell Memory and Resident Memory CD8+ T Cells

Manna, M. P. L., Azgomi, M. S., Tamburini, B., Badami, G. D., Mohammadnezhad, L., Dieli, F., & Caccamo, N. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.884148 · Cited by 6

Approaches for refining and furthering the development of CAR-based T cell therapies for solid malignancies

Hull, C., & Maher, J. F. (2021) · Expert Opinion on Drug Discovery · doi:10.1080/17460441.2021.1929920 · Cited by 6

The Vast Universe of T Cell Diversity: Subsets of Memory Cells and Their Differentiation

Jandus, C., Martínez-Usatorre, A., Viganó, S., Zhang, L., & Romero, P. J. (2016) · Methods in molecular biology · doi:10.1007/978-1-4939-6548-9_1 · Cited by 8

Activation of Cell-Intrinsic Signaling in CAR-T Cells via a Chimeric IL7R Domain

Vorri, S. C., Holl, N. J., Leeming, M. G., Apostolova, P., Marple, A., Ravich, J. W., Canbaz, A. A., Rahnama, R., Choe, J., Modi, A., et al. (2024) · Cancer Research Communications · doi:10.1158/2767-9764.crc-24-0286 · Cited by 4

Chimeric antigen receptor T cell therapy based on stem cell‐like memory T cells enhances anti‐tumour effects in multiple myeloma

Liu, Z., Xu, X., Wang, Y., Cao, P., Song, J., Ding, K., Liu, H., & Fu, R. (2025) · Clinical and Translational Medicine · doi:10.1002/ctm2.70264 · Cited by 4

Gene Therapy for Primary Immunodeficiencies

Cicalese, M. P., & Aiuti, A. (2018) · Springer eBooks · doi:10.1007/978-3-319-77674-3_21 · Cited by 4

Gene transfer and genome editing of T cells for cancer immunotherapy: from allogeneic HSCT to TCR gene editing

Bonini, C. (2025) · Hematology · doi:10.1182/hematology.2025000681 · Cited by 3

Advancing adoptive T cell therapy in ovarian cancer: barriers, innovations, and emerging platforms

Santos, G. N. D. S., DeJohn, C. R., Hess, S. M., Zsíros, E., & McGray, A. R. (2026) · Journal for ImmunoTherapy of Cancer · doi:10.1136/jitc-2025-013285 · Cited by 3

Twenty-five years of gene therapy for genetic diseases and leukemia: The road to marketing authorization of the first ex vivo gene therapies

Bordignon, C. (2017) · Journal of Autoimmunity · doi:10.1016/j.jaut.2017.07.005 · Cited by 3

Hematopoietic Stem Cell Fates and the Cellular Hierarchy of Mammalian Hematopoiesis: from Transplantation Models to New Insights from in Situ Analyses

Shaban, D., Najm, N., Droin, L., & Nijnik, A. (2024) · Stem Cell Reviews and Reports · doi:10.1007/s12015-024-10782-8 · Cited by 3

Allogeneic gene-edited HIV-specific CAR-T cells secreting PD-1 blocking scFv enhance anti-HIV activity in vitroPreprint

Pan, H., Wang, J., Liang, H., Jiang, Z., Zhao, L., Wang, Y., Yang, X., Liang, Z., Shen, X., Lin, Q., et al. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.01.14.476413 · Cited by 3

Comparative engraftment and clonality of macaque HSPCs expanded on human umbilical vein endothelial cells versus non-expanded cells

Srivastava, S. K., Truitt, L. L., Wu, C., Glaser, A., Nolan, D. J., Ginsberg, M. D., Espinoza, D. A., Koelle, S., Yabe, I. M., Yu, K., et al. (2021) · Molecular Therapy — Methods & Clinical Development · doi:10.1016/j.omtm.2021.02.009 · Cited by 2

A decade of CD4+ chimeric antigen receptor T-cell evolution in two chronic lymphocytic leukemia patients: were chronic lymphocytic leukemia cells present?

Bouzianas, D. G., & Bouziana, S. D. (2023) · Exploration of Targeted Anti-tumor Therapy · doi:10.37349/etat.2023.00186 · Cited by 2

Как методы молекулярной биологии повлияли на понимание устройства кроветворной системы

Bigildeev, A., Петинати, Н. А., & Дризе, Н. И. (2019) · Molecular Biology · doi:10.1134/s0026898419050021 · Cited by 2

TRACE-Seq Reveals Clonal Reconstitution Dynamics of Gene Targeted Human Hematopoietic Stem CellsPreprint

Sharma, R., Dever, D. P., Lee, C. M., Azizi, A., Pan, Y., Camarena, J., Köhnke, T., Bao, G., Porteus, M. H., & Majeti, R. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.05.25.115329 · Cited by 2

El control judicial de los defectos del veredicto

Torres, M. L. G. (2003) · Tribunales de justicia: Revista española de derecho procesal · Cited by 2

TGF-β: A silent player regulating CD8 T cell memory

Zambrano-Romero, J. D., Ríos-Ramírez, D. B., García-Rasilla, V. Y., Ruiz-Medina, B. E., & Licona-Limón, P. (2025) · Clinical Immunology · doi:10.1016/j.clim.2025.110612 · Cited by 1

Distribution and function of human long-lasting T cells in aging and non-small cell lung cancer

Tan, J. X., Yu, H. R., Gu, Y., & Hong, H. (2026) · Frontiers in Immunology · doi:10.3389/fimmu.2026.1788541 · Cited by 2

What do we know about the participation of hematopoietic stem cells in hematopoiesis?

Дризе, Н. И., & Петинати, Н. А. (2015) · F1000Research · doi:10.12688/f1000research.6459.1 · Cited by 1

Investigation of the mesenchymal stem cell compartment by means of a lentiviral barcode library

Bigildeev, A., Cornils, K., Aranyossy, T., Sats, N. V., Петинати, Н. А., Shipounova, I. N., Сурин, В. Л., Pshenichnikova, O. S., Riecken, K., Fehse, B., et al. (2016) · Biochemistry (Moscow) · doi:10.1134/s0006297916040076 · Cited by 1

Role of stem cell-like memory T cells in autoimmune diseases.

Liu, Z., Jiao, Q., Xie, H., & Liu, J. (2023) · PubMed Central · doi:10.11817/j.issn.1672-7347.2023.230051 · Cited by 1

InCliniGene enables high-throughput and comprehensive in vivo clonal tracking toward clinical genomics data integration

Merelli, I., Beretta, S., Cesana, D., Gennari, A., Benedicenti, F., Spinozzi, G., Cesini, D., Montini, E., D’Agostino, D., & Calabria, A. (2023) · Database · doi:10.1093/database/baad069 · Cited by 1

A strategy to reconstitute immunity without GVHD via adoptive allogeneic Tscm therapy

Guan, L., Sun, Y., Si, Y., Yan, Q., Han, Z., Liu, Y., & Han, T. (2024) · Frontiers in Immunology · doi:10.3389/fimmu.2024.1367609 · Cited by 2

How Methods of Molecular Biology Shape Our Understanding of the Hematopoietic System

Bigildeev, A., Петинати, Н. А., & Дризе, Н. И. (2019) · Molecular Biology · doi:10.1134/s0026893319050029 · Cited by 1

A CD45RO+ stem cell memory T cell population intermediate to canonical stem cell memory and central memory T cells in human cancer.Preprint

Powell, D. J., Eiva, M. A., Brown, E. C., Pandey, V., Benton, A., Thomas, S. J., Meng, W., Rosenfeld, A. M., & Prak, E. T. L. (2022) · Research Square · doi:10.21203/rs.3.rs-1296773/v1 · Cited by 1

CAR‐T cell therapy

Franklin, J., Pophali, P. A., Jackson, Z., Wald, D. N., & Avigan, D. (2024) · Wiley eBooks · doi:10.1002/9781394180486.ch25 · Cited by 1

CD8 T Lymphocytes in Antitumor Immunity

Romero, P. J. (2016) · Elsevier eBooks · doi:10.1016/b978-0-12-374279-7.17007-9

Transcriptional control of tissue-resident memory T cell generation

Cvetkovski, F. (2019) · doi:10.7916/d8-n16c-b343

Gentherapie bei angeborenen Defekten der Immunität

Ghosh, S. (2022) · Kinder- und Jugendmedizin · doi:10.1055/a-1677-7644

Faculty Opinions recommendation of Transfer of gene-corrected T cells corrects humoral and cytotoxic defects in patients with X-linked lymphoproliferative disease.

Meyts, I., & Bucciol, G. (2020) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.733133023.793572308

Latest advances in chimeric antigen receptor T-cell immunotherapy and future directions

Chen, G. (2022) · AIP conference proceedings · doi:10.1063/5.0094791

Aurora kinase inhibitors regulate T memory stem cell phenotype in T cell receptor-engineered T cells with prolonged persistencePreprint

Yi, L., Ma, Y., Liang, X., Linghu, L., & Zheng, G. (2023) · Research Square · doi:10.21203/rs.3.rs-2352106/v1

CAR T cells recognizing CD276 and Dual-CAR T cells against CD276/FGFR4 promote rhabdomyosarcoma clearance in orthotopic mouse modelsPreprint

Timpanaro, A., Piccand, C., Dzhumashev, D., Anton-Joseph, S., Robbi, A., Moser, J. J., Rössler, J. K., & Bernasconi, M. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.09.05.555125

Additional file 3 of IS-Seq: a bioinformatics pipeline for integration sites analysis with comprehensive abundance quantification methods

Yan, A., Baricordi, C., Nguyen, Q., Barbarossa, L., Loperfido, M., & Biasco, L. (2023) · Figshare · doi:10.6084/m9.figshare.23706959

Conventional T Cell Subsets and Their Roles Within the Tumor Microenvironment

Azimnasab-sorkhabi, P., Soltani-asl, M., Ansa-Addo, E. A., & Kfoury, J. R. (2024) · Interdisciplinary cancer research · doi:10.1007/16833_2024_332

Interview with Serena Scala, PhD

(2025) · Human Gene Therapy · doi:10.1177/10430342251383877

Additional file 2 of The construction of modular universal chimeric antigen receptor T (MU-CAR-T) cells by covalent linkage of allogeneic T cells and various antibody fragments

Chen, T., Deng, J., Zhang, Y., Liu, B., Liu, R., Zhu, Y., Zhou, M., Lin, Y., Xia, B., Lin, K., et al. (2024) · Figshare · doi:10.6084/m9.figshare.25389907

Additional file 1 of CD276-CAR T cells and Dual-CAR T cells targeting CD276/FGFR4 promote rhabdomyosarcoma clearance in orthotopic mouse models

Timpanaro, A., Piccand, C., Dzhumashev, D., Anton-Joseph, S., Robbi, A., Moser, J. J., Rössler, J. K., & Bernasconi, M. (2024) · Figshare · doi:10.6084/m9.figshare.26635719

Additional file 1 of The construction of modular universal chimeric antigen receptor T (MU-CAR-T) cells by covalent linkage of allogeneic T cells and various antibody fragments

Chen, T., Deng, J., Zhang, Y., Liu, B., Liu, R., Zhu, Y., Zhou, M., Lin, Y., Xia, B., Lin, K., et al. (2024) · Figshare · doi:10.6084/m9.figshare.25389511

Additional file 2 of CD276-CAR T cells and Dual-CAR T cells targeting CD276/FGFR4 promote rhabdomyosarcoma clearance in orthotopic mouse models

Timpanaro, A., Piccand, C., Dzhumashev, D., Anton-Joseph, S., Robbi, A., Moser, J. J., Rössler, J. K., & Bernasconi, M. (2024) · Figshare · doi:10.6084/m9.figshare.26635722

Additional file 2 of IS-Seq: a bioinformatics pipeline for integration sites analysis with comprehensive abundance quantification methods

Yan, A., Baricordi, C., Nguyen, Q., Barbarossa, L., Loperfido, M., & Biasco, L. (2023) · Figshare · doi:10.6084/m9.figshare.23706956

Additional file 1 of IS-Seq: a bioinformatics pipeline for integration sites analysis with comprehensive abundance quantification methods

Yan, A., Baricordi, C., Nguyen, Q., Barbarossa, L., Loperfido, M., & Biasco, L. (2023) · Figshare · doi:10.6084/m9.figshare.23706953

CD28 : nouvelles données sur un récepteur majeur de la costimulation lymphocytaire T

Morin, S. O. (2017) · theses.fr (ABES) · doi:10.70675/cb01635fz2f63z43e2zad0cz210485c4c5cf

Novel heterozygous STAT3 mutations clarify the molecular basis of the hyper IgE syndrome

Khourieh, J. (2018) · theses.fr (ABES) · doi:10.70675/94c52966z63f4z41c8za5c4z9fca65ad04d4

Développement de stratégies d'immunothérapies cellulaires basées sur l'activation de lymphocytes T CD4+ humains à l'aide de cellules présentatrices d'antigène artificielles.

Couture, A. (2018) · theses.fr (ABES) · doi:10.70675/3e0f658aza405z4fc6zbf7cz53eaebf43500

Preclinical development of a T cell based gene therapy to treat IPEX syndrom

Delville, M. (2019) · theses.fr (ABES) · doi:10.70675/a98fdc5dz0036z4620z848ez66c60ea7bd96

Nanotechnology for next-generation CAR T-Cell manufacturing

Schvartzman, M., & Ghassemi, S. (2026) · Frontiers in Immunology · doi:10.3389/fimmu.2026.1896088

Long-term tracking of transplanted T cells

Colmone, A. C. (2015) · Science · doi:10.1126/science.347.6222.623-e

T cell therapies-are T memory stem cells the answer?

Flynn, J. K., & Gorry, P. R. (2015) · Europe PMC (PubMed Central) · doi:10.3978/j.issn.2305-5839.2015.08.13 · Cited by 8

Tracking genetically engineered lymphocytes long-term reveals the dynamics of T cell immunological memory

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