Origin and differentiation of human memory CD8 T cells after vaccination

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

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Homeostasis of Naive and Memory T Cells

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Molecular and functional profiling of memory CD8 T cell differentiation.

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Blocking Formation of the Stable HIV Reservoir: A New Perspective for HIV-1 Cure

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Nanovaccines for Advancing Long-Lasting Immunity against Infectious Diseases

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Light‐Activated In Situ Vaccine with Enhanced Cytotoxic T Lymphocyte Infiltration and Function for Potent Cancer Immunotherapy

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Minimal immune response to booster vaccination against Yellow Fever associated with pre-existing antibodies

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Vaccination reshapes the virus-specific T cell repertoire in unexposed adults

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Divergent Clonal Differentiation Trajectories Establish CD8 + Memory T Cell Heterogeneity During Acute Viral Infections in Humans

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The generation of stem cell-like memory cells early after BNT162b2 vaccination is associated with durability of memory CD8+ T cell responses

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International expert consensus on immunotherapy for early-stage non-small cell lung cancer

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Markers of the HIV-1 reservoir

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Phenotypic and Functional Analysis of Human NK Cell Subpopulations According to the Expression of FcεRIγ and NKG2C

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The transcriptional cofactor Tle3 reciprocally controls effector and central memory CD8+ T cell fates

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Mechanical control of antigen detection and discrimination by T and B cell receptors

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Receptor signaling, transcriptional, and metabolic regulation of T cell exhaustion

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What if protective immunity is antigen—driven and not due to so‐called “memory” B and T cells?

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The role of systems biology approaches in determining molecular signatures for the development of more effective vaccines

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Phosphoinositide 3-Kinase Signaling in the Tumor Microenvironment: What Do We Need to Consider When Treating Chronic Lymphocytic Leukemia With PI3K Inhibitors?

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Identification of a human hematopoietic stem cell subset that retains memory of inflammatory stressPreprint

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Asynchronous aging and turnover of human circulating and tissue-resident memory T cells across sites

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

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Gene Regulatory Circuits in Innate and Adaptive Immune Cells

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Memories that last: Dynamics of memory T cells throughout the body

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Transcriptomic immune profiles of human flavivirus‐specific T‐cell responses

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Dietary Regulation of Memory T Cells

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Local memory CD4 T cell niches in respiratory viral infection

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Nanoparticles and trained immunity: Glimpse into the future

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KIR-HLA interactions extend human CD8+ T cell lifespan in vivo

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Immune Monitoring Reveals Fusion Peptide Priming to Imprint Cross-Clade HIV-Neutralizing Responses with a Characteristic Early B Cell Signature

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Rapid induction of antigen-specific CD4 + T cells guides coordinated humoral and cellular immune responses to SARS-CoV-2 mRNA vaccinationPreprint

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Antigen specificity shapes distinct aging trajectories of memory CD8⁺ T cells

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Memory T Cells in Flavivirus Vaccination

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Development of circulating CD4+ T‐cell memory

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Diverse CD8 T Cell Responses to Viral Infection Revealed by the Collaborative Cross

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MINCLE and TLR9 agonists synergize to induce Th1/Th17 vaccine memory and mucosal recall in mice and non-human primates

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Single cell immune profiling of dengue virus patients reveals intact immune responses to Zika virus with enrichment of innate immune signatures

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The Extracellular ATP Receptor P2RX7 Imprints a Promemory Transcriptional Signature in Effector CD8+ T Cells

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

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Phenotypes and Functions of SARS-CoV-2-Reactive T Cells

Jung, M. K., & Shin, E. (2021) · Molecules and Cells · doi:10.14348/molcells.2021.0079 · Cited by 19

Persistence of T Cell and Antibody Responses to SARS-CoV-2 Up to 9 Months after Symptom Onset

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Immune response induced by novel coronavirus infection

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The characterization of CD8 + T-cell responses in COVID-19

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YF17D‐based vaccines – standing on the shoulders of a giant

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Transcriptional programming and T cell receptor repertoires distinguish human lung and lymph node memory T cells

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Understanding T cell aging to improve anti-viral immunity

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SARS-CoV-2 inflammation durably imprints memory CD4 T cells

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A stimuli-responsive cuproptosis switch boosts persistent immunotherapy for tumor eradication

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Quantitative systems pharmacology modeling sheds light into the dose response relationship of a trispecific T cell engager in multiple myeloma

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Memory B Cells and Memory T Cells Induced by SARS-CoV-2 Booster Vaccination or Infection Show Different Dynamics and Responsiveness to the Omicron Variant

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Caveolin-mediated cytosolic delivery of spike nanoparticle enhances antitumor immunity of neoantigen vaccine for hepatocellular carcinoma

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Tet2 deletion in CD4+ T cells disrupts Th1 lineage commitment in memory cells and enhances T follicular helper cell recall responses to viral rechallenge

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Trying to See the Forest through the Trees: Deciphering the Nature of Memory Immunity to Mycobacterium tuberculosis

Orme, I. M., & Henao-Tamayo, M. I. (2018) · Frontiers in Immunology · doi:10.3389/fimmu.2018.00461 · Cited by 19

The memory of the fatty acid system

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Luteolin-mediated Kv1.3 K+ channel inhibition augments BCG vaccine efficacy against tuberculosis by promoting central memory T cell responses in mice

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Stochastic Inheritance of Division and Death Times Determines the Size and Phenotype of CD8+ T Cell Families

Pandit, A., & de Boer, R. J. (2019) · Frontiers in Immunology · doi:10.3389/fimmu.2019.00436 · Cited by 18

Eomesodermin driven IL-10 production in effector CD8+ T cells promotes a memory phenotype

Reiser, J., Sadashivaiah, K., Furusawa, A., Banerjee, A., & Singh, N. J. (2018) · Cellular Immunology · doi:10.1016/j.cellimm.2018.11.008 · Cited by 20

Yellow fever virus vaccination: an emblematic model to elucidate robust human immune responses

Bovay, A., Marraco, S. A. F., & Speiser, D. E. (2021) · Human Vaccines & Immunotherapeutics · doi:10.1080/21645515.2021.1891752 · Cited by 19

Temporal and Epigenetic Control of Plasticity and Fate Decision during CD8+T-Cell Memory DifferentiationPreprint

Pace, L. (2021) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a037754 · Cited by 19

Longitudinal Multi-omic Immune Profiling Reveals Age-Related Immune Cell Dynamics in Healthy AdultsPreprint

Gong, Q., Sharma, M., Kuan, E. L., Glass, M. C., Chander, A., Singh, M., Graybuck, L. T., Thomson, Z., LaFrance, C. M., Zaim, S. R., et al. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.09.10.612119 · Cited by 18

An in-depth understanding of the role and mechanisms of T cells in immune organ aging and age-related diseases

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Decoding T cell senescence in cancer: Is revisiting required?

Magkouta, S., Markaki, E., Evangelou, K., Petty, R., Verginis, P., & Gorgoulis, V. G. (2024) · Seminars in Cancer Biology · doi:10.1016/j.semcancer.2024.11.003 · Cited by 17

Adaptive immunomorphic hardware based on organic semiconductors and oxidized MXene heterostructures for feature information recognition

Gao, C., Yu, R., Li, E., Zhang, C., Zou, Y., Chen, H., Lin, Z., & Guo, T. (2022) · Cell Reports Physical Science · doi:10.1016/j.xcrp.2022.100930 · Cited by 17

The Naming of Memory T-Cell SubsetsPreprint

Jameson, S. C. (2020) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a037788 · Cited by 17

Autoregulated splicing of TRA2 β programs T cell fate in response to antigen-receptor stimulation

Karginov, T. A., Ménoret, A., Leclair, N. K., Harrison, A. G., Chandiran, K., Suarez-Ramirez, J. E., Yurieva, M., Karlinsey, K. S., Wang, P., O'Neill, R. J. W., et al. (2024) · Science · doi:10.1126/science.adj1979 · Cited by 19

mRNA vaccination boosts S-specific T cell memory and promotes expansion of CD45RAint TEMRA-like CD8+ T cells in COVID-19 recovered individuals

Mayer-Blackwell, K., Ryu, H., Codd, A. S., Parks, K. R., MacMillan, H. R., Cohen, K. W., Stewart, T. L., Seese, A. M., Lemos, M. P., Rosa, S. C. D., et al. (2023) · Cell Reports Medicine · doi:10.1016/j.xcrm.2023.101149 · Cited by 16

Proteostasis in T cell aging

Gressler, A. E., Leng, H., Zinecker, H., & Simon, A. K. (2023) · Seminars in Immunology · doi:10.1016/j.smim.2023.101838 · Cited by 15

Better Preventing and Mitigating the Effects of Covid-19

Maguire, G. (2020) · Future Science OA · doi:10.2144/fsoa-2020-0051 · Cited by 16

T Cell Receptor Diversity and Lineage Relationship between Virus-Specific CD8 T Cell Subsets during Chronic Lymphocytic Choriomeningitis Virus Infection

Chang, D. Y., Wieland, A., Li, Z.-R. T., Im, S. J., McGuire, D. J., Kissick, H. T., Antia, R., & Ahmed, R. (2020) · Journal of Virology · doi:10.1128/jvi.00935-20 · Cited by 17

Homeostasis and Durability of T-Cell Memory—The Resting and the Restless T-Cell Memory

Radbruch, A., McGrath, M. A., Siracusa, F., Hoffmann, U., Sercan-Alp, Ö., Hutloff, A., Tokoyoda, K., Chang, H.-D., & Dong, J. (2021) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a038083 · Cited by 16

Vaccination-induced T cell responses maintain polyclonality with high antigen receptor avidity

Kocher, K., Drost, F., Tesfaye, A. M., Moosmann, C., Schülein, C., Grotz, M., D’Ippolito, E., Graw, F., Spriewald, B. M., Busch, D. H., et al. (2025) · Science Immunology · doi:10.1126/sciimmunol.adu6730 · Cited by 14

Human CD8 T‐stem cell memory subsets phenotypic and functional characterization are defined by expression of CD122 or CXCR3

Zhao, Y., Cai, C., Samir, J., Palgen, J., Keoshkerian, E., Li, H., Bull, R. A., Luciani, F., An, H., & Lloyd, A. R. (2021) · European Journal of Immunology · doi:10.1002/eji.202049057 · Cited by 15

Epigenetic engineering for optimal chimeric antigen receptor T cell therapy

Ito, Y., & Kagoya, Y. (2022) · Cancer Science · doi:10.1111/cas.15541 · Cited by 14

Bivalent OX40 Aptamer and CpG as Dual Agonists for Cancer Immunotherapy

Jiang, T., Yang, Z., Su, Q., Fang, L., Xiang, Q., Cheng, T., Gao, Q., Mao, C., Huang, C. Z., & Zuo, H. (2025) · ACS Applied Materials & Interfaces · doi:10.1021/acsami.4c18550 · Cited by 15

HLA-B*27:05 alters immunodominance hierarchy of universal influenza-specific CD8+ T cells

Sant, S. A., Quiñones‐Parra, S. M., Koutsakos, M., Grant, E. J., Loudovaris, T., Mannering, S. I., Crowe, J., van de Sandt, C. E., Rimmelzwaan, G. F., Rossjohn, J., et al. (2020) · PLoS Pathogens · doi:10.1371/journal.ppat.1008714 · Cited by 14

New epigenetic regulators of T cell exhaustion

Kissick, H. T., & Ahmed, R. (2022) · Cancer Cell · doi:10.1016/j.ccell.2022.06.008 · Cited by 14

Impact of Diet and Nutrition on Memory T Cell Development, Maintenance and Function in the Context of Healthy Immune System

Ghosh, J., Singh, K., Choudhury, S. R., Koner, S., & Basu, N. (2022) · Acta Scientifci Nutritional Health · doi:10.31080/asnh.2022.06.1108 · Cited by 13

T cell differentiation drives the negative selection of pathogenic mitochondrial DNA variants

Franklin, I. G., Milne, P., Childs, J., Boggan, R. M., Barrow, I., Lawless, C., Gorman, G. S., Ng, Y. S., Collin, M. P., Russell, O. M., et al. (2023) · Life Science Alliance · doi:10.26508/lsa.202302271 · Cited by 14

Overexpression of early T cell differentiation-specific transcription factors transforms the terminally differentiated effector T cells into less differentiated state

Lu, H., Wang, H., Yan, L., Shao, H., Zhang, W., Shen, H., Bo, H., Tao, C., Xia, S., & Wu, F. (2020) · Cellular Immunology · doi:10.1016/j.cellimm.2020.104118 · Cited by 16

Dynamics and turnover of memory CD8 T cell responses following yellow fever vaccination

Zarnitsyna, V. I., Akondy, R. S., Ahmed, H., McGuire, D. J., Zarnitsyn, V. G., Moore, M., Johnson, P. L. F., Ahmed, R., Li, K. W., Hellerstein, M. K., et al. (2021) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1009468 · Cited by 16

DOCK2 Sets the Threshold for Entry into the Virtual Memory CD8+ T Cell Compartment by Negatively Regulating Tonic TCR Triggering

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Human haematopoietic stem cells remember inflammatory stress

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