Transcriptional control of effector and memory CD8+ T cell differentiation

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

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T cell exhaustion

Wherry, E. J. (2011) · Nature Immunology · doi:10.1038/ni.2035 · Cited by 4,062

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

Wherry, E. J., Ha, S.-J., Kaech, S. M., Haining, W. N., Sarkar, S., Kalia, V., Subramaniam, S., Blattman, J. N., Barber, D. L., & Ahmed, R. (2007) · Immunity · doi:10.1016/j.immuni.2007.09.006 · Cited by 2,103

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

Wherry, E. J., Teichgräber, V., Becker, T. C., Masopust, D., Kaech, S. M., Antia, R., von Andrian, U. H., & Ahmed, R. (2003) · Nature Immunology · doi:10.1038/ni889 · Cited by 1,864

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

Kaech, S. M., Tan, J. T., Wherry, E. J., Konieczny, B. T., Surh, C. D., & Ahmed, R. (2003) · Nature Immunology · doi:10.1038/ni1009 · Cited by 1,830

Immunological memory and protective immunity: understanding their relation

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

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A randomized phase 2 trial of idiotype vaccination and adoptive autologous T-cell transfer in patients with multiple myeloma

Qazilbash, M. H., Saini, N. Y., Cha, S.-C., Wang, Z., Stadtmauer, E. A., Baladandayuthapani, V., Lin, H. Y., Tross, B., Honhar, M., Rao, S. S., et al. (2021) · Blood · doi:10.1182/blood.2020008493 · Cited by 25

Circulating naïve and effector memory T cells correlate with prognosis in head and neck squamous cell carcinoma

Takahashi, H., Sakakura, K., Ida, S., Kawabata‐Iwakawa, R., Matsuyama, T., Tada, H., Mito, I., & Chikamatsu, K. (2021) · Cancer Science · doi:10.1111/cas.15195 · Cited by 25

High proportion of circulating CD8 + CD28- senescent T cells is an independent predictor of distant metastasis in nasopharyngeal carcinoma after radiotherapy

Xu, X., Wei, F., Xiao, L., Wu, R., Wei, B., Huang, S., Yi, J., & Cui, W. (2023) · Journal of Translational Medicine · doi:10.1186/s12967-023-03912-2 · Cited by 27

iPSC-derived hypoimmunogenic tissue resident memory T cells mediate robust anti-tumor activity against cervical cancer

Furukawa, Y., Ishii, M., Ando, J., Ikeda, K., Igarashi, K. J., Kinoshita, S., Azusawa, Y., Toyota, T., Honda, T., Nakanishi, M., et al. (2023) · Cell Reports Medicine · doi:10.1016/j.xcrm.2023.101327 · Cited by 25

AMPK : A metabolic switch for CD 8+ T ‐cell memory

Araki, K., & Ahmed, R. (2013) · European Journal of Immunology · doi:10.1002/eji.201343483 · Cited by 25

Remembering one's ID/E-ntity: E/ID protein regulation of T cell memory

Omilusik, K. D., Shaw, L. A., & Goldrath, A. W. (2013) · Current Opinion in Immunology · doi:10.1016/j.coi.2013.09.004 · Cited by 25

Combination of TLR1/2 and TLR3 ligands enhances CD4+ T cell longevity and antibody responses by modulating type I IFN production

Lee, B. R., Jeong, S. K., Ahn, B. C., Lee, B.-J., Shin, S. J., Yum, J. S., & Ha, S. (2016) · Scientific Reports · doi:10.1038/srep32526 · Cited by 27

Programming of donor T cells using allogeneic δ-like ligand 4–positive dendritic cells to reduce GVHD in mice

Mochizuki, K., Meng, L., Mochizuki, I., Tong, Q., He, S., Liu, Y., Purushe, J., Fung, H. C. H., Zaidi, M. R., Zhang, Y., et al. (2016) · Blood · doi:10.1182/blood-2015-05-644476 · Cited by 25

Contrasting Roles of the PD-1 Signaling Pathway in Dendritic Cell-Mediated Induction and Regulation of HIV-1-Specific Effector T Cell Functions

García-Bates, T. M., Palma, M. L., Shen, C., Gambotto, A. A., Macatangay, B. J. C., Ferris, R. L., Rinaldo, C. R., & Mailliard, R. B. (2018) · Journal of Virology · doi:10.1128/jvi.02035-18 · Cited by 25

The chemokine receptor CXCR3 promotes CD8 + T cell–dependent lung pathology during influenza pathogenesis

Guo, K., Yombo, D. J. K., Wang, Z., Navaeiseddighi, Z., Xu, J., Schmit, T., Ahamad, N., Tripathi, J. K., Kumar, B. D., Mathur, R., et al. (2024) · Science Advances · doi:10.1126/sciadv.adj1120 · Cited by 25

Regulatory mechanisms that control T‐follicular helper and T‐helper 1 cell flexibility

Weinmann, A. S. (2013) · Immunology and Cell Biology · doi:10.1038/icb.2013.49 · Cited by 24

Modes of Communication between T Cells and Relevance for Immune Responses

Uhl, L. F. K., & Gérard, A. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21082674 · Cited by 24

The functions of EZH2 in immune cells: Principles for novel immunotherapies

Shao, F.-F., Chen, B.-J., & Wu, G. (2020) · Journal of Leukocyte Biology · doi:10.1002/jlb.1ru0520-311r · Cited by 23

Runx proteins and transcriptional mechanisms that govern memory CD8 T cell development

Pipkin, M. E. (2021) · Immunological Reviews · doi:10.1111/imr.12954 · Cited by 24

CD8+ T-cell immunity orchestrated by iNKT cells

Qin, Y., Bao, X., & Zheng, M. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2022.1109347 · Cited by 24

Hobit and human effector T‐cell differentiation: The beginning of a long journey

Braun, J., Frentsch, M., & Thiel, A. (2015) · European Journal of Immunology · doi:10.1002/eji.201545959 · Cited by 24

Enhancement of CD 8+ T‐cell memory by removal of a vaccinia virus nuclear factor‐κB inhibitor

Ren, H., Ferguson, B. J., de Motes, C. M., Sumner, R. P., Harman, L. E. R., & Smith, G. L. (2014) · Immunology · doi:10.1111/imm.12422 · Cited by 24

HIV Skews the Lineage-Defining Transcriptional Profile of Mycobacterium tuberculosis–Specific CD4+ T Cells

Riou, C., Strickland, N., Soares, A. P., Corleis, B., Kwon, D. S., Wherry, E. J., Wilkinson, R. J., & Burgers, W. A. (2016) · The Journal of Immunology · doi:10.4049/jimmunol.1502094 · Cited by 24

Divergent Effects of a Transient Corticosteroid Therapy on Virus-Specific Quiescent and Effector CD8+ T Cells

Kumar, D., & Sehrawat, S. (2019) · Frontiers in Immunology · doi:10.3389/fimmu.2019.01521 · Cited by 24

Dietary Regulation of Memory T Cells

Collins, N. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21124363 · Cited by 25

C-Myc regulation by costimulatory signals modulates the generation of CD8 + memory T cells during viral infection

Haque, M. M., Song, J., Fino, K. K., Wang, Y., Sandhu, P., Song, X., Norbury, C. C., Ni, B., Fang, D., Salek‐Ardakani, S., et al. (2016) · Open Biology · doi:10.1098/rsob.150208 · Cited by 24

Immunological roles for resistin and related adipokines in obesity-associated tumors

Zhang, J., Lu, E., Deng, L., Zhu, Y., Lu, X., Li, X., Li, F., Yan, Y., Han, J.-Y., Li, Y., et al. (2024) · International Immunopharmacology · doi:10.1016/j.intimp.2024.112911 · Cited by 25

T Cell Exhaustion in Cancer Immunotherapy: Heterogeneity, Mechanisms, and Therapeutic Opportunities

Yang, Y. P., Yao, X., Wang, Q., Yang, M., Li, R., Qin, J., Zhuang, J., & Sun, C. (2026) · Advanced Science · doi:10.1002/advs.202520634 · Cited by 27

Blood and beyond: Properties of circulating and tissue‐resident human virus‐specific αβ CD8+ T cells

van Aalderen, M. C., Remmerswaal, E. B. M., ten Berge, I. J. M., & van Lier, R. A. W. (2014) · European Journal of Immunology · doi:10.1002/eji.201344269 · Cited by 24

Unveiling the heterogeneity of NKT cells in the liver through single cell RNA sequencing

Shen, H., Gu, C., Tao, L., Liu, H., Guo, F., & Liu, X. (2020) · Scientific Reports · doi:10.1038/s41598-020-76659-1 · Cited by 23

Early-phenotype CAR-T cells for the treatment of pediatric cancers

Meyran, D., Terry, R. L., Zhu, J. J., Haber, M., Ziegler, D. S., Ekert, P. G., Trapani, J. A., Darcy, P. K., & Neeson, P. J. (2021) · Annals of Oncology · doi:10.1016/j.annonc.2021.07.018 · Cited by 24

Meta-Analysis of Two Human RNA-seq Datasets to Determine Periodontitis Diagnostic Biomarkers and Drug Target Candidates

Moreno, C. M., Bybee, E., Freitas, C. M. T., Pickett, B. E., & Weber, K. S. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23105580 · Cited by 21

Shaping Heterogeneity of Naive CD8+ T Cell Pools

Lee, S., Lee, G.-W., Kim, H.-O., & Cho, J.-H. (2023) · Immune Network · doi:10.4110/in.2023.23.e2 · Cited by 23

Co-infection of mice with SARS-CoV-2 and Mycobacterium tuberculosis limits early viral replication but does not affect mycobacterial loads

Baker, P. J., Amaral, E. P., Castro, E., Bohrer, A. C., Torres-Juárez, F., Jordan, C. M., Nelson, C. E., Barber, D. L., Johnson, R. F., Hilligan, K. L., et al. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1240419 · Cited by 20

Regulation of IFN‐γ production by ZFP36L2 in T cells is time‐dependent

Zandhuis, N. D., Guislain, A., Popalzij, A., Engels, S., Popović, B., Turner, M., & Wolkers, M. C. (2024) · European Journal of Immunology · doi:10.1002/eji.202451018 · Cited by 22

Memory T Cells in Transplantation

Su, C. A., & Fairchild, R. L. (2014) · Current Transplantation Reports · doi:10.1007/s40472-014-0018-5 · Cited by 24

Transcription Factor Bcl11b Controls Effector and Memory CD8 T cell Fate Decision and Function during Poxvirus Infection

Abboud, G., Stanfield, J., Tahiliani, V., Desai, P., Hutchinson, T. E., Lorentsen, K. J., Cho, J. J., Avram, D., & Salek‐Ardakani, S. (2016) · Frontiers in Immunology · doi:10.3389/fimmu.2016.00425 · Cited by 23

Existence and stability of periodic solutions of an impulsive differential equation and application to CD8 T-cell differentiation

Girel, S., & Fabien Crauste, A. (2018) · Journal of Mathematical Biology · doi:10.1007/s00285-018-1220-3 · Cited by 23

Reactive glia promote development of CD103+CD69+ CD8+ T‐cells through programmed cell death‐ligand 1 (PD‐L1)

Prasad, S., Hu, S., Sheng, W. S., Chauhan, P., & Lokensgard, J. R. (2018) · Immunity Inflammation and Disease · doi:10.1002/iid3.221 · Cited by 24

Peptide Antigen Concentration Modulates Digital NFAT1 Activation in Primary Mouse Naive CD8+ T Cells as Measured by Flow Cytometry of Isolated Cell Nuclei

Gallagher, M. P., Conley, J. M., & Berg, L. J. (2018) · ImmunoHorizons · doi:10.4049/immunohorizons.1800032 · Cited by 25

Chronic virus infection compromises memory bystander T cell function in an IL-6/STAT1-dependent manner

Barnstorf, I., Borsa, M., Baumann, N. S., Pallmer, K., Yermanos, A., Joller, N., Spörri, R., Welten, S. P. M., Kräutler, N. J., & Oxenius, A. (2019) · The Journal of Experimental Medicine · doi:10.1084/jem.20181589 · Cited by 22

Dynamic changes in immune cell profile in head and neck squamous cell carcinoma: Immunomodulatory effects of chemotherapy

Takahashi, H., Sakakura, K., Mito, I., Ida, S., & Chikamatsu, K. (2016) · Cancer Science · doi:10.1111/cas.12976 · Cited by 23

Increased PD-L1 Expression May Be Associated With the Cytokine Storm and CD8+ T-Cell Exhaustion in Severe COVID-19

Chen, J., & Vitetta, L. (2021) · The Journal of Infectious Diseases · doi:10.1093/infdis/jiab061 · Cited by 23

SIRT7 regulates T-cell antitumor immunity through modulation BCAA and fatty acid metabolism

Hu, Z., Chen, Y., Lei, J., Wang, K., Pan, Z., Zhang, L., Xu, X., Li, W., Zhang, L., Qin, X. Y., et al. (2025) · Cell Death and Differentiation · doi:10.1038/s41418-025-01490-y · Cited by 25

Deciphering the deterministic role of TCR signaling in T cell fate determination

Qin, Z., & Xu, T. (2025) · Frontiers in Immunology · doi:10.3389/fimmu.2025.1562248 · Cited by 30

Transcription factors early growth response gene (Egr) 2 and 3 control inflammatory responses of tolerant T cells

Omodho, B., Miao, T., Symonds, A. L. J., Singh, R. K., Li, S., & Wang, P. (2018) · Immunity Inflammation and Disease · doi:10.1002/iid3.210 · Cited by 22

Loss of the orphan nuclear receptor NR2F6 enhances CD8+ T-cell memory via IFN-γ

Jakic, B., Olson, W. J., Siegmund, K., Klepsch, V., Kimpel, J., Labi, V., Zehn, D., Baier, G., & Hermann‐Kleiter, N. (2021) · Cell Death and Disease · doi:10.1038/s41419-021-03470-9 · Cited by 22

Polymeric Pathogen-Like Particles-Based Combination Adjuvants Elicit Potent Mucosal T Cell Immunity to Influenza A Virus

Kingstad-Bakke, B. A., Toy, R., Lee, W., Pradhan, P., Vogel, G., Marinaik, C. B., Larsen, A., Gates, D. E., Luu, T., Pandey, B., et al. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2020.559382 · Cited by 22

Role of tissue-resident memory T cells in the pathophysiology of allergic contact dermatitis

Lefevre, M.-A., Vocanson, M., & Nosbaum, A. (2021) · Current Opinion in Allergy and Clinical Immunology · doi:10.1097/aci.0000000000000763 · Cited by 23

The role of protease-activated receptor 1 signaling in CD8 T cell effector functions

Chen, H., Smith, M., Herz, J., Li, T., Hasley, R. B., Saout, C. L., Zhu, Z., Cheng, J., Gronda, A., Martina, J. A., et al. (2021) · iScience · doi:10.1016/j.isci.2021.103387 · Cited by 22

TCR-induced FOXP3 expression by CD8+ T cells impairs their anti-tumor activity

Lozano, T., Conde, E., Martín-Otal, C., Navarro, F. C., Lasarte-Cía, A., Nasrallah, R., Alignani, D., Gorraiz, M., Sarobe, P., Romero, J. P., et al. (2021) · Cancer Letters · doi:10.1016/j.canlet.2021.12.030 · Cited by 22

Single-Cell RNA sequencing reveals immune cell dynamics and local intercellular communication in acute murine cardiac allograft rejection

Chen, Z., Xu, H., Li, Y., Zhang, X., Cui, J., Zou, Y., Yu, J., Wu, J., & Xia, J. (2022) · Theranostics · doi:10.7150/thno.75543 · Cited by 23

Tissue-resident memory T cells in the era of (Neo) adjuvant melanoma management

Plunkett, K. R., Armitage, J. D., Inderjeeth, A., McDonnell, A. M., Waithman, J. C., & Lau, P. K. H. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.1048758 · Cited by 25

Tumor Immune Microenvironment Predicts the Pathologic Response Of Neoadjuvant Chemoimmunotherapy In Locally Advanced And Oligometastatic Non–Small Cell Lung Cancer

Han, R. F., Zhang, Y., Wang, T., Xiao, H., Luo, Z., Shen, C., Li, J., Zhao, C., Li, L., Zhu, M., et al. (2022) · Cancer Science · doi:10.1111/cas.15778 · Cited by 20

Single-cell NAD(H) levels predict clonal lymphocyte expansion dynamics

Turner, L. H., Le, T. N. V., Cross, E. W., Queriault, C., Knight, M., Trihemasava, K., Davis, J. G., Schaefer, P. M., Nguyen, J., Xu, J. P., et al. (2024) · Science Immunology · doi:10.1126/sciimmunol.adj7238 · Cited by 22

αβ TCR-Mediated Recognition: Relevance to Tumor-Antigen Discovery and Cancer Immunotherapy

Reinherz, E. L. (2015) · Cancer Immunology Research · doi:10.1158/2326-6066.cir-15-0042 · Cited by 23

The Role of Oncolytic Virus Immunotherapies to Subvert Cancer Immune Evasion

Workenhe, S. T., Verschoor, M. L., & Mossman, K. L. (2015) · Future Oncology · doi:10.2217/fon.14.254 · Cited by 22

IRF4 Regulates the Ratio of T-Bet to Eomesodermin in CD8+ T Cells Responding to Persistent LCMV Infection

Nayar, R., Schutten, E., Jangalwe, S., Durost, P. A., Kenney, L. L., Conley, J. M., Daniels, K. A., Brehm, M. A., Welsh, R. M., & Berg, L. J. (2015) · PLoS ONE · doi:10.1371/journal.pone.0144826 · Cited by 22

Deep Immune Profiling of an Arginine-Enriched Nutritional Intervention in Patients Undergoing Surgery

Aghaeepour, N., Kin, C., Ganio, E. A., Jensen, K. P., Gaudilliere, D. K., Tingle, M. S., Tsai, A. S., Lancero, H. L., Choisy, B., McNeil, L. S., et al. (2017) · The Journal of Immunology · doi:10.4049/jimmunol.1700421 · Cited by 23

Cancer‐driven changes link T cell frequency to muscle strength in people with cancer: a pilot study

Narsale, A. A., Moya, R., Ma, J., Anderson, L. J., Wu, D. Y., Garcia, J. M., & Davies, J. D. (2019) · Journal of Cachexia Sarcopenia and Muscle · doi:10.1002/jcsm.12424 · Cited by 22

Dynamical system modeling to simulate donor T cell response to whole exome sequencing-derived recipient peptides: Understanding randomness in alloreactivity incidence following stem cell transplantation

Kopardé, V. N., Razzaq, B. A., Suntum, T., Sabo, R., Scalora, A. F., Serrano, M. G., Jameson‐Lee, M., Hall, C., Kobulnicky, D. J., Sheth, N. U., et al. (2017) · PLoS ONE · doi:10.1371/journal.pone.0187771 · Cited by 22

T-cell receptor signal strength and epigenetic control of Bim predict memory CD8+ T-cell fate

Li, K.-P., Ladle, B. H., Kurtuluş, S., Sholl, A., Shanmuganad, S., & Hildeman, D. A. (2019) · Cell Death and Differentiation · doi:10.1038/s41418-019-0410-x · Cited by 22

IL4I1 Accelerates the Expansion of Effector CD8+ T Cells at the Expense of Memory Precursors by Increasing the Threshold of T-Cell Activation

Puiffe, M., Dupont, A., Sako, N., Gatineau, J., Cohen, J. L., Mestivier, D., Bon, A. L., Prévost‐Blondel, A., Castellano, F., & Molinier‐Frenkel, V. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.600012 · Cited by 22

Combinatorial immunotherapy induces tumor-infiltrating CD8+ T cells with distinct functional, migratory, and stem-like properties

Budimir, N., Dolina, J. S., Wei, J., Wang, X., Chen, S.-H., Santiago, P., Tu, G., Micci, L., Al-Khami, A. A., Pfister, S. X., et al. (2021) · Journal for ImmunoTherapy of Cancer · doi:10.1136/jitc-2021-003614 · Cited by 22

Multimodal stimulation screens reveal unique and shared genes limiting T cell fitness

Lin, C., Levy, P. L., Alflen, A., Apriamashvili, G., Ligtenberg, M. A., Vredevoogd, D. W., Bleijerveld, O. B., Alkan, F., Malka, Y., Hoekman, L., et al. (2024) · Cancer Cell · doi:10.1016/j.ccell.2024.02.016 · Cited by 21

Encapsulation of an EP67-Conjugated CTL Peptide Vaccine in Nanoscale Biodegradable Particles Increases the Efficacy of Respiratory Immunization and Affects the Magnitude and Memory Subsets of Vaccine-Generated Mucosal and Systemic CD8+ T Cells in a Diameter-Dependent Manner

Karuturi, B. V. K., Tallapaka, S. B., Yeapuri, P., Curran, S. M., Sanderson, S. D., & Vetro, J. A. (2017) · Molecular Pharmaceutics · doi:10.1021/acs.molpharmaceut.6b01088 · Cited by 21

Let’S Fight Cancer: Let-7 is a Tool to Enhance Antitumor Immune Responses

Pobezinsky, L. A., & Wells, A. C. (2018) · Future Oncology · doi:10.2217/fon-2018-0037 · Cited by 21

DAPK1 (death associated protein kinase 1) mediates mTORC1 activation and antiviral activities in CD8+ T cells

Wei, Z., Li, P., He, R., Liu, H., Liu, N., Xia, Y., Bi, G., Du, Q., Xia, M., Pei, L., et al. (2019) · Cellular and Molecular Immunology · doi:10.1038/s41423-019-0293-2 · Cited by 21

Exploring and analysing single cell multi-omics data with VDJView

Samir, J., Rizzetto, S., Gupta, M., & Luciani, F. (2020) · BMC Medical Genomics · doi:10.1186/s12920-020-0696-z · Cited by 22

Running to Stand Still: Naive CD8+ T Cells Actively Maintain a Program of Quiescence

Bennett, T. J., Udupa, V., & Turner, S. T. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21249773 · Cited by 19

The Energy Sensor AMPKα1 Is Critical in Rapamycin-Inhibition of mTORC1-S6K-Induced T-cell Memory

Ara, A., Xu, A., Ahmed, K. A., Leary, S. C., Islam, M. F., Wu, Z., Chibbar, R., & Xiang, J. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms23010037 · Cited by 22

DExD/H-box helicase 9 intrinsically controls CD8 + T cell–mediated antiviral response through noncanonical mechanisms

Jiao, A., Sun, C., Wang, X., Lei, L., Liu, H., Li, W., Yang, X., Zheng, H., Ding, R., Zhu, K., et al. (2022) · Science Advances · doi:10.1126/sciadv.abk2691 · Cited by 21

DELVE: feature selection for preserving biological trajectories in single-cell data

Ranek, J. S., Stallaert, W., Milner, J. J., Redick, M. A., Wolff, S. C., Beltrán, A. S., Stanley, N., & Purvis, J. E. (2024) · Nature Communications · doi:10.1038/s41467-024-46773-z · Cited by 20

Molecular control of CD4+ T cell lineage plasticity and integrity

Ellmeier, W. (2015) · International Immunopharmacology · doi:10.1016/j.intimp.2015.03.050 · Cited by 21

Appearance of cytomegalovirus‐specific T ‐cells predicts fast resolution of viremia post hematopoietic stem cell transplantation

Pelák, O., Stuchlý, J., Król, L., Hubáček, P., Keslová, P., Sedláček, P., Formánková, R., Starý, J., Hrušák, O., & Kalina, T. (2015) · Cytometry Part B Clinical Cytometry · doi:10.1002/cyto.b.21348 · Cited by 21

Role of Memory T Cells and Perspectives for Intervention in Organ Transplantation

Lin, K., Chen, S., & Chen, G. (2015) · Frontiers in Immunology · doi:10.3389/fimmu.2015.00473 · Cited by 21

Biomaterials-Based Vaccination Strategies for the Induction of CD8+T Cell Responses

Chesson, C. B., Ekpo-Otu, S., Endsley, J. J., & Rudra, J. S. (2016) · ACS Biomaterials Science & Engineering · doi:10.1021/acsbiomaterials.6b00412 · Cited by 21

Up-regulated expression of substance P in CD8+ T cells and NK1R on monocytes of atopic dermatitis

Zhang, Z., Zheng, W., Xie, H., Chai, R., Wang, J., Zhang, H., & He, S. (2017) · Journal of Translational Medicine · doi:10.1186/s12967-017-1196-6 · Cited by 21

HVEM Imprints Memory Potential on Effector CD8 T Cells Required for Protective Mucosal Immunity

Desai, P., Abboud, G., Stanfield, J., Thomas, P. G., Song, J. J., Ware, C. F., Croft, M., & Salek‐Ardakani, S. (2017) · The Journal of Immunology · doi:10.4049/jimmunol.1700959 · Cited by 22

Long noncoding RNA Malat1 is not essential for T cell development and response to LCMV infection

Yao, Y., Guo, W., Chen, J., Guo, P., Yu, G., Liu, J., Wang, F., Liu, J., You, M., Zhao, T., et al. (2018) · RNA Biology · doi:10.1080/15476286.2018.1551705 · Cited by 18

Towards multiscale modeling of the CD8+T cell response to viral infections

Baral, S., Raja, R., Sen, P., & Dixit, N. M. (2019) · WIREs Systems Biology and Medicine · doi:10.1002/wsbm.1446 · Cited by 20

Use of a glycerin-based gel sheeting in scar management.

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The role of mitochondrial transfer in the suppression of CD8+ T cell responses by Mesenchymal stem cells

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