Transcriptional control of effector and memory CD8+ T cell differentiation

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T cell exhaustion

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Molecular Signature of CD8+ T Cell Exhaustion during Chronic Viral Infection

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Cutting Edge: Distinct Glycolytic and Lipid Oxidative Metabolic Programs Are Essential for Effector and Regulatory CD4+ T Cell Subsets

Michalek, R. D., Gerriets, V. A., Jacobs, S. R., Macintyre, A. N., MacIver, N. J., Mason, E. F., Sullivan, S. A., Nichols, A. G., & Rathmell, J. C. (2011) · The Journal of Immunology · doi:10.4049/jimmunol.1003613 · Cited by 2,091

Preferential Localization of Effector Memory Cells in Nonlymphoid Tissue

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Lineage relationship and protective immunity of memory CD8 T cell subsets

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Inflammation Directs Memory Precursor and Short-Lived Effector CD8+ T Cell Fates via the Graded Expression of T-bet Transcription Factor

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Selective expression of the interleukin 7 receptor identifies effector CD8 T cells that give rise to long-lived memory cells

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Interleukin-7 mediates the homeostasis of naïve and memory CD8 T cells in vivo

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Stem cell-like memory T cells: A perspective from the dark side

Gao, S., Liang, X., Wang, H., Bao, B., Zhang, K., Zhu, Y., & Shao, Q. (2021) · Cellular Immunology · doi:10.1016/j.cellimm.2020.104273 · Cited by 31

Kdm6b Regulates the Generation of Effector CD8+ T Cells by Inducing Chromatin Accessibility in Effector-Associated Genes

Xu, T., Schutte, A., Jimenez, L., Gonçalves, A. N. A., Keller, A., Pipkin, M. E., Nakaya, H. I., Pereira, R. M., & Martínez, G. (2021) · The Journal of Immunology · doi:10.4049/jimmunol.2001459 · Cited by 31

The transcription factor Fli1 restricts the formation of memory precursor NK cells during viral infection

Riggan, L., Ma, F., Li, J. H., Fernandez, E., Nathanson, D. A., Pellegrini, M. A., & O’Sullivan, T. E. (2022) · Nature Immunology · doi:10.1038/s41590-022-01150-0 · Cited by 37

Cancer cell membrane biomimetic mesoporous silica nanotheranostics for enhanced Ferroptosis-mediated immuogenic cell death on Gastric cancer

Guo, W., Chen, Z., Li, Z., Huang, H., Ren, Y., Li, Z., Zhao, B., Li, G., & Hu, Y. (2022) · Chemical Engineering Journal · doi:10.1016/j.cej.2022.140868 · Cited by 32

Inhibition of TGF-β1 Signaling Promotes Central Memory T Cell Differentiation

Takai, S., Schlom, J., Tucker, J., Tsang, K. Y., & Greiner, J. W. (2013) · The Journal of Immunology · doi:10.4049/jimmunol.1300472 · Cited by 36

Lack of Sprouty 1 and 2 enhances survival of effector CD8 + T cells and yields more protective memory cells

Shehata, H. M., Khan, S., Chen, E., Fields, P. E., Flavell, R. A., & Sanjabi, S. (2018) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1808320115 · Cited by 31

Cardinal features of immune memory in innate lymphocytes

Santosa, E. K., & Sun, J. C.-Y. (2023) · Nature Immunology · doi:10.1038/s41590-023-01607-w · Cited by 32

Functionalized nanowires for miRNA-mediated therapeutic programming of naïve T cells

Mon, K. J. Y., Kim, S., Dai, Z., West, J. D., Zhu, H., Jain, R., Grimson, A., Rudd, B. D., & Singh, A. K. (2024) · Nature Nanotechnology · doi:10.1038/s41565-024-01649-7 · Cited by 32

A tumor-on-a-chip for in vitro study of CAR-T cell immunotherapy in solid tumors

Liu, H., Noguera-Ortega, E., Dong, X., Lee, W. D., Chang, J., Aday, S., Li, Y., Shin, Y., Shi, X., Liousia, M., et al. (2025) · Nature Biotechnology · doi:10.1038/s41587-025-02845-z · Cited by 41

Molecular adjuvant IL-33 enhances the potency of a DNA vaccine in a lethal challenge model

Villarreal, D. O., Svoronos, N., Wise, M. C., Shedlock, D. J., Morrow, M. P., Conejo-Garcia, J. R., & Weiner, D. B. (2015) · Vaccine · doi:10.1016/j.vaccine.2015.03.086 · Cited by 31

The Characteristics of Naive-like T Cells in Tumor-infiltrating Lymphocytes From Human Lung Cancer

Sheng, S. Y., Gu, Y., Lu, C. G., Tang, Y., Zou, J. Y., Zhang, Y. Q., Wang, R. F., & Hong, H. Y. (2016) · Journal of Immunotherapy · doi:10.1097/cji.0000000000000147 · Cited by 31

CD8+ T cells lack local signals to produce IFN-γ in the skin during leishmania infection

Novais, F. O., Wong, A. C., Villareal, D. O., Beiting, D. P., & Scott, P. (2018) · Journal of Immunology · doi:10.4049/jimmunol.1701597 · Cited by 32

Heterodimeric Fc-fused IL12 shows potent antitumor activity by generating memory CD8+T cells

Jung, K., Ha, J.-H., Kim, J., Kim, J.-A., Kim, Y., Kim, Y., & Kim, Y. (2018) · OncoImmunology · doi:10.1080/2162402x.2018.1438800 · Cited by 31

Adding Indoximod to Hypofractionated Radiotherapy with Anti-PD-1 Checkpoint Blockade Enhances Early NK and CD8+ T-Cell–Dependent Tumor Activity

Watanabe, T., Gaedicke, S., Guffart, E., Firat, E., & Niedermann, G. (2019) · Clinical Cancer Research · doi:10.1158/1078-0432.ccr-19-0476 · Cited by 30

Zbtb20 Restrains CD8 T Cell Immunometabolism and Restricts Memory Differentiation and Antitumor Immunity

Sun, Y., Preiss, N. K., Valenteros, K. B., Kamal, Y., Usherwood, Y.-K., Frost, H. R., & Usherwood, E. J. (2020) · The Journal of Immunology · doi:10.4049/jimmunol.2000459 · Cited by 34

Suppressive neutrophils require PIM1 for metabolic fitness and survival during chronic viral infection

Volberding, P. J., Xin, G., Kasmani, M. Y., Khatun, A., Brown, A. K., Nguyen, C. P., Stancill, J. S., Martinez, E., Corbett, J. A., & Cui, W. (2021) · Cell Reports · doi:10.1016/j.celrep.2021.109160 · Cited by 30

Single-Cell RNA Sequencing Reveals the Immunological Profiles of Renal Allograft Rejection in Mice

Shen, Q., Wang, Y., Chen, J., Ma, L., Huang, X., Tang, S. C. W., Lan, H., Jiang, H., & Chen, J. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.693608 · Cited by 32

Regulatory roles of MicroRNA in shaping T cell function, differentiation and polarization

Naqvi, R. A., Datta, M., Khan, S. H., & Naqvi, A. R. (2021) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2021.08.003 · Cited by 32

Immunological perspectives on spatial and temporal vaccine delivery

Zhu, M. (2021) · Advanced Drug Delivery Reviews · doi:10.1016/j.addr.2021.113966 · Cited by 32

Interleukin-10 induces interferon-γ-dependent emergency myelopoiesis

Cardoso, A., Martins, A. C. M., Maceiras, A. R., Liu, W., Castro, I., Castro, A. G., Bandeira, A., Santo, J. P. D., Cumano, A., Li, Y., et al. (2021) · Cell Reports · doi:10.1016/j.celrep.2021.109887 · Cited by 36

Asymmetric cell division safeguards memory CD8 T cell development

Gräbnitz, F., Stark, D., Shlesinger, D., Petkidis, A., Borsa, M., Yermanos, A., Carr, A., Barandun, N., Wehling, A., Baláž, M., et al. (2023) · Cell Reports · doi:10.1016/j.celrep.2023.112468 · Cited by 31

Candida-Elicited Murine Th17 Cells Express High CTLA-4 Compared with Th1 Cells and Are Resistant to Costimulation Blockade

Krummey, S. M., Floyd, T. L., Liu, D., Wagener, M. E., Song, M., & Ford, M. L. (2014) · The Journal of Immunology · doi:10.4049/jimmunol.1301332 · Cited by 31

Characterization of Diabetogenic CD8+ T Cells

Garyu, J., Uduman, M., Stewart, A., Rui, J., Deng, S., Shenson, J. A., Staron, M. M., Kaech, S. M., Kleinstein, S. H., & Herold, K. C. (2016) · Journal of Biological Chemistry · doi:10.1074/jbc.m115.713362 · Cited by 32

Unexpected positive control of NFκB and miR-155 by DGKα and ζ ensures effector and memory CD8+ T cell differentiation

Yang, J., Zhang, P., Krishna, S., Wang, J., Lin, X., Huang, H., Xie, D., Gorentla, B. K., Huang, R. H., Gao, J., et al. (2016) · Oncotarget · doi:10.18632/oncotarget.8164 · Cited by 32

Local Cellular and Cytokine Cues in the Spleen Regulate In Situ T Cell Receptor Affinity, Function, and Fate of CD8 + T Cells

Seo, Y., Jothikumar, P., Suthar, M. S., Zhu, C., & Grakoui, A. (2016) · Immunity · doi:10.1016/j.immuni.2016.10.024 · Cited by 31

Formation of Tissue-Resident CD8+ T-Cell MemoryPreprint

Dijkgraaf, F. E., Kok, L., & Schumacher, T. N. (2021) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a038117 · Cited by 33

Beyond T-cell subsets: stemness and adaptation redefining immunity and immunotherapy

Zou, D., Li, X. C., & Chen, W. (2025) · Cellular and Molecular Immunology · doi:10.1038/s41423-025-01321-7 · Cited by 30

Regulation of T cell exhaustion and stemness: molecular mechanisms and implications for cancer immunotherapy

Chen, Z., Zhu, Z., Hu, T., Yao, C., & Wu, T. (2025) · Cellular and Molecular Immunology · doi:10.1038/s41423-025-01378-4 · Cited by 37

IL-2 Induction of Blimp-1 Is a Key In Vivo Signal for CD8+ Short-Lived Effector T Cell Differentiation

Boulet, S., Daudelin, J., & Labrecque, N. (2014) · The Journal of Immunology · doi:10.4049/jimmunol.1302365 · Cited by 30

Regulation of Antiviral CD8 T-Cell Responses

Kulinski, J. M., Tarakanova, V. L., & Verbsky, J. W. (2013) · Critical Reviews in Immunology · doi:10.1615/critrevimmunol.2013007909 · Cited by 29

Trans-presentation of IL-15 modulates STAT5 activation and Bcl-6 expression in TH1 cells

Cooley, I. D., Read, K. A., & Oestreich, K. J. (2015) · Scientific Reports · doi:10.1038/srep15722 · Cited by 29

Poly I:C-based rHBVvac therapeutic vaccine eliminates HBV via generation of HBV-specific CD8 + effector memory T cells

Zhao, H., Han, Q., Wang, G., Lin, A., Xu, D., Wang, Y., Zhao, L., Tian, Z., & Zhang, J. (2019) · Gut · doi:10.1136/gutjnl-2017-315588 · Cited by 32

Antigen-Induced but Not Innate Memory CD8 T Cells Express NKG2D and Are Recruited to the Lung Parenchyma upon Viral Infection

Grau, M., Valsesia, S., Mafille, J., Djebali, S., Tomkowiak, M., Mathieu, A., Laubreton, D., de Bernard, S., Jouve, P.-E., Ventre, E., et al. (2018) · The Journal of Immunology · doi:10.4049/jimmunol.1701698 · Cited by 30

Monocyte-Derived Cells in Tissue-Resident Memory T Cell Formation

Chu, K.-L., Batista, N. V., Girard, M., & Watts, T. H. (2020) · The Journal of Immunology · doi:10.4049/jimmunol.1901046 · Cited by 33

Conversations that count: Cellular interactions that drive T cell fate

Duckworth, B. C., & Groom, J. R. (2021) · Immunological Reviews · doi:10.1111/imr.12945 · Cited by 32

Chitosan Nanovaccines as Efficient Carrier Adjuvant System for IL-12 with Enhanced Protection Against HBV

Zhao, H., Wang, H., Hu, Y., Xu, D., Yin, C., Han, Q., & Zhang, J. (2021) · International Journal of Nanomedicine · doi:10.2147/ijn.s317113 · Cited by 30

Characteristics of splenic CD8+ T cell exhaustion in patients with hepatitis C

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Early Effector Cells Survive the Contraction Phase in Malaria Infection and Generate Both Central and Effector Memory T Cells

Opata, M. M., Carpio, V. H., Ibitokou, S. A., Dillon, B., Obiero, J. M., & Stephens, R. (2015) · The Journal of Immunology · doi:10.4049/jimmunol.1403216 · Cited by 30

Long-Lived Skin-Resident Memory T Cells Contribute to Concomitant Immunity in Cutaneous LeishmaniasisPreprint

Scott, P. (2020) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a038059 · Cited by 29

Functional CRISPR screens in T cells reveal new opportunities for cancer immunotherapies

Xiang, M., Li, H., Zhan, Y., Ma, D., Gao, Q., & Fang, Y. (2024) · Molecular Cancer · doi:10.1186/s12943-024-01987-z · Cited by 29

CD103–CD8+ T cells promote neurotoxic inflammation in Alzheimer’s disease via granzyme K–PAR-1 signaling

Terrabuio, E., Pietronigro, E. C., Bani, A., Bianca, V. D., Laudanna, C., Rossi, B., Finotti, G., Santos-Lima, B., Zenaro, E., Turano, E., et al. (2025) · Nature Communications · doi:10.1038/s41467-025-62405-6 · Cited by 33

Change of paradigm: CD8+ T cells as important helper for CD4+ T cells during asthma and autoimmune encephalomyelitis

Huber, M., & Lohoff, M. D. (2015) · Allergo Journal International · doi:10.1007/s40629-015-0038-4 · Cited by 29

The Second-Generation mTOR Kinase Inhibitor INK128 Exhibits Anti-inflammatory Activity in Lipopolysaccharide-Activated RAW 264.7 Cells

Pan, H., Xu, L., Ouyang, D., Wang, Y., Zha, Q.-B., Hou, X., & He, X. (2014) · Inflammation · doi:10.1007/s10753-013-9794-9 · Cited by 30

The prognostic role of circulating CD8+ T cell proliferation in patients with untreated extensive stage small cell lung cancer

An, N., Wang, H., Jia, W., Wang, J., Liu, C., Zhu, H., & Yu, J. (2019) · Journal of Translational Medicine · doi:10.1186/s12967-019-02160-7 · Cited by 29

Epigenetics of T cell fate decision

Pace, L., & Amigorena, S. (2020) · Current Opinion in Immunology · doi:10.1016/j.coi.2020.01.002 · Cited by 30

Domain binding and isotype dictate the activity of anti-human OX40 antibodies

Griffiths, J., Hussain, K., Smith, H. L., Sanders, T. J., Cox, K. L., Semmrich, M., Mårtensson, L., Kim, J., Inzhelevskaya, T., Penfold, C., et al. (2020) · Journal for ImmunoTherapy of Cancer · doi:10.1136/jitc-2020-001557 · Cited by 31

Molecular and Functional Signatures Associated with CAR T Cell Exhaustion and Impaired Clinical Response in Patients with B Cell Malignancies

Beider, K., Itzhaki, O., Schachter, J., Grushchenko-Polaq, A. H., Voevoda-Dimenshtein, V., Rosenberg, E., Ostrovsky, O., Devillers, O., Frommer, R. S., Zeltzer, L., et al. (2022) · Cells · doi:10.3390/cells11071140 · Cited by 30

Cellular Deconstruction: Finding Meaning in Individual Cell Variation

Eberwine, J. H., & Kim, J. (2015) · Trends in Cell Biology · doi:10.1016/j.tcb.2015.07.004 · Cited by 30

Integrating multiplexed imaging and multiscale modeling identifies tumor phenotype conversion as a critical component of therapeutic T cell efficacy

Hickey, J. W., Agmon, E., Horowitz, N. B., Tan, T.-K., Lamore, M., Sunwoo, J. B., Covert, M. W., & Nolan, G. P. (2024) · Cell Systems · doi:10.1016/j.cels.2024.03.004 · Cited by 32

Distinct phenotype and function of circulating Vδ1+ and Vδ2+ γδT-cells in acute and chronic hepatitis B

Chang, K., Traum, D., Park, J., Ho, S., Ojiro, K., Wong, D., Wahed, A. S., Terrault, N. A., Khalili, M., Sterling, R. K., et al. (2019) · PLoS Pathogens · doi:10.1371/journal.ppat.1007715 · Cited by 29

The elusive identity of CXCR5+ CD8 T cells in viral infection and autoimmunity: Cytotoxic, regulatory, or helper cells?

Fousteri, G., & Kuka, M. (2020) · Molecular Immunology · doi:10.1016/j.molimm.2020.01.007 · Cited by 28

Immunomodulatory Dual-Sized Microparticle System Conditions Human Antigen Presenting Cells Into a Tolerogenic Phenotype In Vitro and Inhibits Type 1 Diabetes-Specific Autoreactive T Cell Responses

Brusko, M., Stewart, J. M., Posgai, A. L., Wasserfall, C. H., Atkinson, M. A., Brusko, T. M., & Keselowsky, B. G. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.574447 · Cited by 29

Ptpn2 and KLRG1 regulate the generation and function of tissue-resident memory CD8+ T cells in skin

Hochheiser, K., Wiede, F., Wagner, T., Freestone, D., Enders, M. H., Olshansky, M., Russ, B., Nüssing, S., Bawden, E., Braun, A., et al. (2021) · The Journal of Experimental Medicine · doi:10.1084/jem.20200940 · Cited by 27

Aging‐related cell type‐specific pathophysiologic immune responses that exacerbate disease severity in aged COVID‐19 patients

Hou, Y., Zhou, Y., Gack, M. U., Luo, Y., Jehi, L., Chan, T. A.-T., Yu, H., Eng, C., Pieper, A. A., & Cheng, F. (2022) · Aging Cell · doi:10.1111/acel.13544 · Cited by 22

Patients with HIV-associated cancers have evidence of increased T cell dysfunction and exhaustion prior to cancer diagnosis

Chaudhary, O., Trotta, D., Wang, K., Wang, X., Chu, X., Bradley, C., Okulicz, J. F., Maves, R. C., Kronmann, K., Schofield, C. M., et al. (2022) · Journal for ImmunoTherapy of Cancer · doi:10.1136/jitc-2022-004564 · Cited by 29

Randomized, Double-Blind, Reference-Controlled, Phase 2a Study Evaluating the Immunogenicity and Safety of OVX836, A Nucleoprotein-Based Influenza Vaccine

Leroux‐Roels, I., Waerlop, G., Tourneur, J., Boever, F. D., Maes, C., Bruhwyler, J., Guyon-Gellin, D., Moris, P., del Campo, J. M., Willems, P., et al. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.852904 · Cited by 28

DNA architectural protein CTCF facilitates subset-specific chromatin interactions to limit the formation of memory CD8+ T cells

Quon, S., Yu, B., Russ, B. E., Tsyganov, K., Nguyen, H., Toma, C., Heeg, M., Hocker, J. D., Milner, J. J., Crotty, S., et al. (2023) · Immunity · doi:10.1016/j.immuni.2023.03.017 · Cited by 28

Exosomal noncoding RNA-mediated spatiotemporal regulation of lipid metabolism: Implications in immune evasion and chronic inflammation

Hegde, M., Kumar, A., Girisa, S., Alqahtani, M. S., Abbas, M. A. E., Goel, A., Hui, K. M., Sethi, G., & Kunnumakkara, A. B. (2023) · Cytokine & Growth Factor Reviews · doi:10.1016/j.cytogfr.2023.06.001 · Cited by 28

Exposure to lung-migrating helminth protects against murine SARS-CoV-2 infection through macrophage-dependent T cell activation

Oyesola, O. O., Hilligan, K. L., Namasivayam, S., Howard, N., Clancy, C. S., Zhao, M., Oland, S. D., Kiwanuka, K. N., Garza, N. L., Lafont, B. A. P., et al. (2023) · Science Immunology · doi:10.1126/sciimmunol.adf8161 · Cited by 33

Shortened Intervals during Heterologous Boosting Preserve Memory CD8 T Cell Function but Compromise Longevity

Thompson, E. A., Beura, L. K., Nelson, C. E., Anderson, K. G., & Vezys, V. (2016) · The Journal of Immunology · doi:10.4049/jimmunol.1501797 · Cited by 27

Long-Lived CD4+IFN-γ+ T Cells rather than Short-Lived CD4+IFN-γ+IL-10+ T Cells Initiate Rapid IL-10 Production To Suppress Anamnestic T Cell Responses during Secondary Malaria Infection

Villegas-Méndez, A., Inkson, C. A., Shaw, T. N., Strangward, P., & Couper, K. N. (2016) · The Journal of Immunology · doi:10.4049/jimmunol.1600968 · Cited by 28

Metabolic Control of Memory T-Cell Generation and StemnessPreprint

Raynor, J. L., Chapman, N. M., & Chi, H. (2021) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a037770 · Cited by 28

Tumor cell metabolic reprogramming and hypoxic immunosuppression: driving carcinogenesis to metastatic colonization

Katopodi, T., Petanidis, S., Anestakis, D., Charalampidis, C., Chatziprodromidou, I. P., Floros, G., Eskitzis, P., Zarogoulidis, P., Koulouris, C., Sevva, C. D., et al. (2024) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1325360 · Cited by 28

Combination of S1–N–Terminal and S1–C–Terminal Domain Antigens Targeting Double Receptor-Binding Domains Bolsters Protective Immunity of a Nanoparticle Vaccine against Porcine Epidemic Diarrhea Virus

Yang, D., Su, M., Guo, D., Zhao, F., Wang, M., Liu, J., Zhou, J., Sun, Y., Yang, X., Qi, S., et al. (2024) · ACS Nano · doi:10.1021/acsnano.4c00809 · Cited by 27

Inhibition of PCSK9 enhances the anti-hepatocellular carcinoma effects of TCR-T cells and anti-PD-1 immunotherapy

Xu, W., Hu, M., Lu, X., Lao, Y., Ma, N., Wang, Y., Li, J., Chen, X., Liu, S., Liu, J., et al. (2024) · International Journal of Biological Sciences · doi:10.7150/ijbs.93668 · Cited by 27

Chinese Immune Multi-Omics Atlas

Yin, J., Zheng, Y., Huang, Z., Zhou, W., Yuan, Y., Cai, P., Bai, Y., Yang, S., Gao, Y., Duan, S., et al. (2026) · Science · doi:10.1126/science.adt3130 · Cited by 36

The Transcription Factor T-Bet Is Regulated by MicroRNA-155 in Murine Anti-Viral CD8+ T Cells via SHIP-1

Hope, J. L., Stairiker, C. J., Spantidea, P. I., Gracias, D. T., Carey, A. J., Fike, A. J., van Meurs, M., Brouwers-Haspels, I., Rijsbergen, L. C., Fraietta, J. A., et al. (2017) · Frontiers in Immunology · doi:10.3389/fimmu.2017.01696 · Cited by 27

The Fate Choice Between Effector and Memory T Cell Lineages: Asymmetry, Signal Integration, and Feedback to Create Bistability

Backer, R. A., Hombrink, P., Helbig, C., & Amsen, D. (2018) · Advances in immunology · doi:10.1016/bs.ai.2017.12.003 · Cited by 27

The TNF Superfamily Molecule LIGHT Promotes the Generation of Circulating and Lung-Resident Memory CD8 T Cells following an Acute Respiratory Virus Infection

Desai, P., Tahiliani, V., Hutchinson, T. E., Dastmalchi, F., Stanfield, J., Abboud, G., Thomas, P. G., Ware, C. F., Song, J. J., Croft, M., et al. (2018) · The Journal of Immunology · doi:10.4049/jimmunol.1701499 · Cited by 27

Cheating the Hunger Games; Mechanisms Controlling Clonal Diversity of CD8 Effector and Memory Populations

Kavazović, I., Polić, B., & Wensveen, F. M. (2018) · Frontiers in Immunology · doi:10.3389/fimmu.2018.02831 · Cited by 29

Unravelling the heterogeneity and dynamic relationships of tumor-infiltrating T cells by single-cell RNA sequencing analysis

Yu, X., Zhang, L., Chaudhry, A., Rapaport, A. S., & Ouyang, W. (2020) · Journal of Leukocyte Biology · doi:10.1002/jlb.6mr0320-234r · Cited by 25

mTORC1 Signaling Controls TLR2-Mediated T-Cell Activation by Inducing TIRAP Expression

Imanishi, T., Unno, M., Kobayashi, W., Yoneda, N., Akira, S., & Saito, T. (2020) · Cell Reports · doi:10.1016/j.celrep.2020.107911 · Cited by 26

Accelerating clinical-scale production of BCMA CAR T cells with defined maturation stages

Joedicke, J. J., Großkinsky, U., Gerlach, K., Künkele, A., Höpken, U. E., & Rehm, A. (2021) · Molecular Therapy — Methods & Clinical Development · doi:10.1016/j.omtm.2021.12.005 · Cited by 27

Transcriptome Profiling of Porcine Naïve, Intermediate and Terminally Differentiated CD8+ T Cells

Lagumdzic, E., Pernold, C. P. S., Viano, M., Olgiati, S., Schmitt, M. W., Mair, K. H., & Saalmüller, A. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.849922 · Cited by 27

MicroRNA-29a attenuates CD8 T cell exhaustion and induces memory-like CD8 T cells during chronic infection

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