Human memory T cells: generation, compartmentalization and homeostasis

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

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Phenotypic Analysis of Antigen-Specific T Lymphocytes

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Central Memory and Effector Memory T Cell Subsets: Function, Generation, and Maintenance

Sallusto, F., Geginat, J., & Lanzavecchia, A. (2004) · Annual Review of Immunology · doi:10.1146/annurev.immunol.22.012703.104702 · Cited by 3,067

Single-Cell Mass Cytometry of Differential Immune and Drug Responses Across a Human Hematopoietic Continuum

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

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Preferential Localization of Effector Memory Cells in Nonlymphoid Tissue

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Counting Antigen-Specific CD8 T Cells: A Reevaluation of Bystander Activation during Viral Infection

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HIV reservoir size and persistence are driven by T cell survival and homeostatic proliferation

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Reciprocal interactions of the intestinal microbiota and immune system

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T-cell quality in memory and protection: implications for vaccine design

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Jigsaw falling into place: A review and perspective of lymphoid tissue CD8+ T cells and control of HIV

Nguyen, S., Sada-Japp, A., Petrovas, C., & Betts, M. R. (2020) · Molecular Immunology · doi:10.1016/j.molimm.2020.05.016 · Cited by 12

Antiviral Innate Immune Activation in HIV-Infected Adults Negatively Affects H1/IC31-Induced Vaccine-Specific Memory CD4+T Cells

Lenz, N., Schindler, T., Kagina, B. M. N., Zhang, J. D., Lukindo, T., Mpina, M., Bang, P. F., Kromann, I., Hoff, S. T., Andersen, P. L., et al. (2015) · Clinical and Vaccine Immunology · doi:10.1128/cvi.00092-15 · Cited by 11

Multiple genetic programs contribute to CD4 T cell memory differentiation and longevity by maintaining T cell quiescence

Song, N., Sengupta, S., Khoruzhenko, S., Welsh, R. A., Kim, A., Kumar, M. R., Sønder, S. U., Sidhom, J.-W., Zhang, H., Jie, C., et al. (2020) · Cellular Immunology · doi:10.1016/j.cellimm.2020.104210 · Cited by 12

Aberrant CD8+T cells drive reproductive dysfunction in female mice with elevated IFN-γ levels

Bafor, E. E., Erwin-Cohen, R. A., Martin, T., Baker, C., Kimmel, A. E., Duverger, O., Fenimore, J. M., Ramba, M., Spindel, T., Hess, M. M., et al. (2024) · Frontiers in Immunology · doi:10.3389/fimmu.2024.1368572 · Cited by 10

Recent advances and challenges of cellular immunotherapies in lung cancer treatment

Yang, C., Liu, Y., Huang, Z., Liu, S., Zhang, X., Liu, Q., & Dai, J. (2025) · Experimental Hematology and Oncology · doi:10.1186/s40164-025-00679-8 · Cited by 13

Parenteral adenoviral boost enhances BCG induced protection, but not long term survival in a murine model of bovine TB

Kaveh, D. A., García‐Pelayo, M. C., Webb, P. R., Wooff, E. E., Bachy, V. S., & Hogarth, P. J. (2016) · Vaccine · doi:10.1016/j.vaccine.2016.06.032 · Cited by 10

Cancer immunotherapy and immunological memory

Murata, K., Tsukahara, T., & Torigoe, T. (2016) · Japanese Journal of Clinical Immunology · doi:10.2177/jsci.39.18 · 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

A transcriptome-based approach to identify functional modules within and across primary human immune cells

Mola, S., Foisy, S., Boucher, G., Major, F., Beauchamp, C., Karaky, M., Goyette, P., Lesage, S., & Rioux, J. D. (2020) · PLoS ONE · doi:10.1371/journal.pone.0233543 · Cited by 10

Altered T cell subpopulations and serum anti-TYRP2 and tyrosinase antibodies in the acute and chronic phase of alopecia areata in the C3H/HeJ mouse model

Hashimoto, K., Yamada, Y., Fujikawa, M., Sekiguchi, K., Uratsuji, H., Mori, S., Watanabe, H., & Matsumoto, T. (2021) · Journal of Dermatological Science · doi:10.1016/j.jdermsci.2021.09.001 · Cited by 10

OMIP‐021: Simultaneous quantification of human conventional and innate‐like T‐cell subsets

Gherardin, N. A., Ritchie, D. S., Godfrey, D. I., & Neeson, P. J. (2014) · Cytometry Part A · doi:10.1002/cyto.a.22475 · Cited by 10

Effect of memory CD4+ T cells’ signal transducer and activator of transcription (STATs) functional shift on cytokine-releasing properties in asthma

Chen, Z., Pan, J., Jia, Y., Li, D., Min, Z., Su, X., Yuan, H., Shen, G., Cao, S., Zhu, L., et al. (2016) · Cell Biology and Toxicology · doi:10.1007/s10565-016-9357-6 · Cited by 10

Lymphocyte subsets are influenced by positivity levels in healthy subjects before and after mild acute stress

Caprara, G. V., Nisini, R., Castellani, V., Pasquali, V., Alessandri, G., Ziparo, V., Ferlito, C., Germano, V., Diamanti, A. P., Biondo, M. I., et al. (2017) · Immunology Letters · doi:10.1016/j.imlet.2017.05.012 · Cited by 10

CCR4-targeted therapy in cutaneous T-cell lymphoma

Gniadecki, R. (2018) · The Lancet Oncology · doi:10.1016/s1470-2045(18)30449-2 · Cited by 10

Immune Responses: Primary and Secondary

Riddell, N. E. (2020) · Encyclopedia of Life Sciences · doi:10.1002/9780470015902.a0029196 · Cited by 10

Memory T Cells in Type 1 Diabetes: the Devil is in the Detail

Narsale, A. A., & Davies, J. D. (2017) · Current Diabetes Reports · doi:10.1007/s11892-017-0889-9 · Cited by 9

Altered levels of memory T cell subsets and common γc cytokines in Strongyloides stercoralis infection and partial reversal following anthelmintic treatment

Rajamanickam, A., Munisankar, S., Bhootra, Y., Dolla, C. K., Thiruvengadam, K., Nutman, T. B., & Babu, S. (2018) · PLoS neglected tropical diseases · doi:10.1371/journal.pntd.0006481 · Cited by 9

The Value of Flow Cytometry Clonality in Large Granular Lymphocyte Leukemia

Giudice, V., D’Addona, M., Montuori, N., & Selleri, C. (2021) · Cancers · doi:10.3390/cancers13184513 · Cited by 9

Peripheral differentiation patterns of human T cells

Heikkilä, N., Hetemäki, I., Sormunen, S., Isoniemi, H., Kekäläinen, E., Saramäki, J., & Arstila, T. P. (2022) · European Journal of Immunology · doi:10.1002/eji.202149465 · Cited by 10

SARS-CoV-2 mRNA vaccination–induced immunological memory in human nonlymphoid and lymphoid tissues

Proß, V., Sattler, A., Lukassen, S., Toth, L., Thole, L. M. L., Siegle, J., Stahl, C., He, A., Damm, G., Seehofer, D., et al. (2023) · Journal of Clinical Investigation · doi:10.1172/jci171797 · Cited by 11

Pregnancy dedifferentiates memory CD8+ T cells into hypofunctional cells with exhaustion-enriched programs

Pollard, J. M., Hynes, G. E., Yin, D., Mandal, M., Gounari, F., Alegre, M., & Chong, A. S. (2024) · JCI Insight · doi:10.1172/jci.insight.176381 · Cited by 9

Polyanhydride nanovaccine against H3N2 influenza A virus generates mucosal resident and systemic immunity promoting protection

Lopez, C. E., Zacharias, Z. R., Ross, K. A., Narasimhan, B., Waldschmidt, T. J., & Legge, K. L. (2024) · npj Vaccines · doi:10.1038/s41541-024-00883-3 · Cited by 9

HPV Infection–Associated Cancers: Next-Generation Technology for Diagnosis and Treatment

Trimble, C. L. (2014) · Cancer Immunology Research · doi:10.1158/2326-6066.cir-14-0152 · Cited by 9

Integrated vaccine screening system: using cellular functional capacity in vitro to assess genuine vaccine protectiveness in ruminants

Pooley, H. B., Plain, K. M., Purdie, A. C., Begg, D. J., Whittington, R. J., & de Silva, K. (2018) · Pathogens and Disease · doi:10.1093/femspd/fty029 · Cited by 9

Reduced expression of the lncRNA NRON is a potential hallmark of the CMV-amplified CD8+ T cell accumulations commonly seen in older humans

Wang, Y., Yu, X.-H., Qu, G., Qiao, F.-F., & Han, H. (2018) · Experimental Gerontology · doi:10.1016/j.exger.2018.11.004 · Cited by 9

High mRNA expression of LY6 gene family is associated with overall survival outcome in pancreatic ductal adenocarcinoma

Russ, E. U., Bhuvaneshwar, K., Wang, G., Jin, B., Gage, M. M., Madhavan, S., Gusev, Y., & Upadhyay, G. (2021) · Oncotarget · doi:10.18632/oncotarget.27880 · Cited by 9

Altered circulating CCR6+and CXCR3+ T cell subsets are associated with poor renal prognosis in MPO-ANCA-associated vasculitis

Liao, Z., Tang, J., Luo, L., Deng, S., Luo, L., Wang, F., Yuan, X., Hu, X., Feng, J., & Li, X. (2021) · Arthritis Research & Therapy · doi:10.1186/s13075-021-02576-x · Cited by 9

COVID-19 and cancer: Sailing through the tides

Mohanty, A., Agnihotri, S., Mehta, A., & Rawal, S. K. (2021) · Pathology - Research and Practice · doi:10.1016/j.prp.2021.153417 · Cited by 9

Identification of apolipoprotein B–reactive CDR3 motifs allows tracking of atherosclerosis-related memory CD4+T cells in multiple donors

Roy, P., Suthahar, S. S. A., Makings, J., & Ley, K. F. (2024) · Frontiers in Immunology · doi:10.3389/fimmu.2024.1302031 · Cited by 9

Polysaccharide-mediated combination therapy enhances anti-tumor effects by promoting the immune cycle of immunogenic cell death

Yu, X., Zhang, Q., Fan, J.-Y., Wu, T.-X., Chen, Z., Wang, H., Yu, X., Tangthianchaichana, J., Du, S., & Lu, Y. (2025) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2025.141323 · Cited by 8

Platelets as a potential new immune coordinator in T cell-mediated aplastic anemia

Tan, S., He, H., Li, Y., Shang, M., Cao, Y., Zou, D., Hu, R., Hui, W., Chang, X., Ni, J., et al. (2025) · Frontiers in Oncology · doi:10.3389/fonc.2025.1568169 · Cited by 9

Enhancing the potency of CAR-T cells against solid tumors through transcription factor engineering

Chen, R., Chen, L., Tang, Y. R., Xiaolin, S., Wang, Y., Tang, P., Shentu, X., & Sun, J. (2025) · JCI Insight · doi:10.1172/jci.insight.193048 · Cited by 9

Longitudinal Tracking of Immune Responses in COVID-19 Convalescents Reveals Absence of Neutralization Activity Against Omicron and Staggered Impairment to Other SARS-CoV-2 Variants of Concern

Odak, I., Schultze-Florey, C. R., Hammerschmidt, S. I., Ritter, C., Willenzon, S., Friedrichsen, M., Ravens, I., Sikora, R., Bayir, L. M., Jauregui, R. G., et al. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.863039 · Cited by 8

Role of germinal center and CD39highCD73+ B cells in the age-related tonsillar involution

Pastor, R., Puyssegur, J., Guardia, M., Varón, L. S., Beccaglia, G., Spada, N., de Lima, A. P., Collado, M. S., Blanco, A., Scetti, I. A., et al. (2024) · Immunity & Ageing · doi:10.1186/s12979-024-00425-4 · Cited by 8

Developmental immunology and role of host defenses in fetal and neonatal susceptibility to infection

Lewis, D. B., Weitkamp, J.-H., & Levy, O. (2024) · Elsevier eBooks · doi:10.1016/b978-0-323-79525-8.00013-5 · Cited by 7

Seasonal Influenza Vaccine Literacy and Hesitancy of Elderly Czechs: An Analysis Using the 5C Model of Psychological Antecedents

Riad, A., Truksová, V., & Koščík, M. (2024) · International Journal of Public Health · doi:10.3389/ijph.2024.1607626 · Cited by 8

Bone marrow expands the repertoire of functional T cells targeting tumor-associated antigens in patients with resectable non-small-cell lung cancer

Safi, S., Yamauchi, Y., Stamova, S., Rathinasamy, A., den Winkel, J. O., Jünger, S., Bucur, M., Umansky, L., Warth, A., Herpel, E., et al. (2019) · OncoImmunology · doi:10.1080/2162402x.2019.1671762 · Cited by 8

NKG2D Signaling Within the Pancreatic Islets Reduces NOD Diabetes and Increases Protective Central Memory CD8+ T-Cell Numbers

Admin, A., Trembath, A. P., Krausz, K. L., Sharma, N., Gerling, I., Mathews, C. E., & Markiewicz, M. A. (2020) · Diabetes · doi:10.2337/db19-0979 · Cited by 8

Programmed Death 1 Regulates Memory Phenotype CD4 T Cell Accumulation, Inhibits Expansion of the Effector Memory Phenotype Subset and Modulates Production of Effector Cytokines

Charlton, J. J., Tsoukatou, D., Mamalaki, C., & Chatzidakis, I. (2015) · PLoS ONE · doi:10.1371/journal.pone.0119200 · Cited by 8

HIV infection-induced transcriptional program in renal tubular epithelial cells activates a CXCR2-driven CD4+ T-cell chemotactic response

Chen, P., Yi, Z., Zhang, W., Klotman, M. E., & Chen, B. K. (2016) · AIDS · doi:10.1097/qad.0000000000001153 · Cited by 8

Peripheral autoreactive CD8 T‐cell frequencies are too variable to be a reliable predictor of disease progression of human type 1 diabetes

Wesley, J. D., Pfeiffer, S., Schneider, D., Friedrich, D. A., Perdue, N., Sehested‐Hansen, B., Hagopian, W., & von Herrath, M. G. (2021) · Clinical & Translational Immunology · doi:10.1002/cti2.1309 · Cited by 8

Human fetal T cells: Insights into developmental specialization and mechanisms of lineage transition

Burt, T. D., & McCune, J. M. (2023) · Immunological Reviews · doi:10.1111/imr.13195 · Cited by 8

Detection and characterization of autoreactive memory stem T-cells in children with acute immune thrombocytopenia

Zahran, A. M., El‐Badawy, O., Mahran, H. H., Gad, E. F., Saad, K., Morsy, S. G., Makboul, A., Zahran, Z. A. M., Elhoufey, A. A., Dailah, H. G., et al. (2024) · Clinical and Experimental Medicine · doi:10.1007/s10238-024-01386-0 · Cited by 7

PD-1 and ICOS are coexpressed in T follicular helper cells but define three stages of maturation of T follicular regulatory cells

Ribeiro, F., Antunes, D., Pires, A. R., Rino, J., Filipe, B., Jesus, K., Correia, R., Fonseca, V. R., Kumar, S., & Graça, L. (2025) · Science Advances · doi:10.1126/sciadv.adt8901 · Cited by 8

Epigenetic priming as a driver of memory recall and dysfunction in T cells

Metzemaekers, M., Rinzema, N. J., & Stadhouders, R. (2025) · The Journal of Experimental Medicine · doi:10.1084/jem.20241433 · Cited by 8

The Use of an Adjuvant System Improves Innate and Adaptive Immune Response When Associated with a Leishmania (Viannia) braziliensis Antigen in a Vaccine Candidate against L. (Leishmania) infantum Infection

Mathias, F. A. S., Ostolin, T. L. V. D. P., Reis, L. E. S., Cardoso, J. M. D. O., de Brito, R. C. F., Aguiar‐Soares, R. D. D. O., Roatt, B. M., Vieira, P. M. D. A., & Reis, A. B. (2023) · Vaccines · doi:10.3390/vaccines11020395 · Cited by 7

Multifaceted roles of T cells in obesity and obesity‐related complications: A narrative review

Qi, X., Li, Z., Han, J., Liu, W., Xia, P., Cai, X., Liu, X., Liu, X., Zhang, J., & Yu, P. (2023) · Obesity Reviews · doi:10.1111/obr.13621 · Cited by 13

From neglect to spotlight: the underappreciated role of B cells in cutaneous inflammatory diseases

Lee, E.-G., & Oh, J. E. (2024) · Frontiers in Immunology · doi:10.3389/fimmu.2024.1328785 · Cited by 7

Choosing T-cell sources determines CAR-T cell activity in neuroblastoma

García‐García, L., Sánchez, E. G., Ivanova, M., Pastora, K., Alcántara-Sánchez, C., García–Martínez, J., Martín-Antonio, B., Ramírez, M. R., & González‐Murillo, Á. (2024) · Frontiers in Immunology · doi:10.3389/fimmu.2024.1375833 · Cited by 7

A review of CD4+ T cell differentiation and diversity in dogs

Lang, H. P., Osum, K. C., & Friedenberg, S. G. (2024) · Veterinary Immunology and Immunopathology · doi:10.1016/j.vetimm.2024.110816 · Cited by 8

Development and validation of a mortality risk prediction model for chronic obstructive pulmonary disease: a cross-sectional study using probabilistic graphical modelling

Lovelace, T. C., Ryu, M. H., Jia, M., Castaldi, P. J., Sciurba, F. C., Hersh, C. P., & Benos, P. V. (2024) · EClinicalMedicine · doi:10.1016/j.eclinm.2024.102786 · Cited by 7

PLZF‐expressing CD4 T cells show the characteristics of terminally differentiated effector memory CD4 T cells in humans

Kim, Y., Zhu, L., Pyaram, K., Lopez, C. A., Ohye, R. G., García, J. V., Green, G. E., & Chang, C. (2018) · European Journal of Immunology · doi:10.1002/eji.201747426 · Cited by 6

CD9 expression in porcine blood CD4+ T cells delineates two subsets with phenotypic characteristics of central and effector memory cells

Álvarez, B., Revilla, C., Moreno, S., Jiménez-Marín, Á., Ramos, E. M., Martínez, P., Poderoso, T., Garrido, J. J., Ezquerra, Á., & Domı́nguez, J. (2022) · Developmental & Comparative Immunology · doi:10.1016/j.dci.2022.104431 · Cited by 7

A ubiquitous bone marrow reservoir of preexisting SARS-CoV-2-reactive memory CD4+ T lymphocytes in unexposed individuals

Li, J., Reinke, S., Yu, S., Schollmeyer, L., Liu, Y.-C., Wang, Z., Hardt, S., Hipfl, C., Hoffmann, U., Frischbutter, S., et al. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.1004656 · Cited by 7

Peptides targeting the BTLA-HVEM complex can modulate T cell immune response

Wojciechowicz, K., Kuncewicz, K., Lisowska, K. A., Wardowska, A., & Spodzieja, M. (2023) · European Journal of Pharmaceutical Sciences · doi:10.1016/j.ejps.2023.106677 · Cited by 7

Breakthrough infections by SARS-CoV-2 variants boost cross-reactive hybrid immune responses in mRNA-vaccinated Golden Syrian hamsters

Diego, J. G.-B., Singh, G., Jangra, S., Handrejk, K., Laporte, M., Chang, L. A., Zahed, S. S. E., Pache, L., Chang, M. W., Warang, P., et al. (2024) · PLoS Pathogens · doi:10.1371/journal.ppat.1011805 · Cited by 8

Selective loss of vaccine-specific memory B cells in a rhesus macaque model of chemotherapy: influence of doxorubicin on immunological memory

Ingelman-Sundberg, H. M., Saghafian‐Hedengren, S., Jahnmatz, M., Eksborg, S., Jonker, M., & Nilsson, A. (2014) · Haematologica · doi:10.3324/haematol.2014.116111 · Cited by 7

An Early Immediate Early Protein IE-1–Specific T-Cell Polyfunctionality Is Associated With a Better Control of Cytomegalovirus Reactivation in Kidney Transplantation

Dekeyser, M., Ladrière, M., Audonnet, S., Frimat, L., & Bittencourt, M. D. C. (2017) · Kidney International Reports · doi:10.1016/j.ekir.2017.02.016 · Cited by 7

Water extract of pilose antler can inhibit breast cancer progression of the mouse through modulating its immune system

Zheng, K., Fu, C., Jiang, C., Yue, X., & Ma, S. (2018) · Food and Agricultural Immunology · doi:10.1080/09540105.2018.1457012 · Cited by 7

Involvement of TNF-Producing CD8+ Effector Memory T Cells with Immunopathogenesis of Erythema Nodosum Leprosum in Leprosy Patients

Silva, P. H. L., dos Santos, L. N., Mendes, M. A., Nery, J. A. C., Sarno, E. N., & Esquenazi, D. (2019) · American Journal of Tropical Medicine and Hygiene · doi:10.4269/ajtmh.18-0517 · Cited by 7

Immunoregulatory potential of pregnancy-specific β1-glycoprotein

Timganova, V. P., Бочкова, М. С., Rayev, M. B. B., Khramtsov, P., & Анатольевна, З. С. (2021) · Medical Immunology (Russia) · doi:10.15789/1563-0625-ipo-2170 · Cited by 7

Medea: An AI agent for therapeutic reasoning across biological contextsPreprint

Sui, P., Li, M. M., Munson, B. P., Gao, S., Shen, W., Giunchiglia, V., Shen, A. N., Huang, Y., Kong, Z., Licon, K., et al. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.01.16.696667 · Cited by 13

Comprehensive profiling of the heterogeneity of molecular endotypic traits in chronic rhinosinusitis

Takahashi, H., Matsuyama, T., Kawabata‐Iwakawa, R., Kawamoto, T., & Chikamatsu, K. (2025) · Human Immunology · doi:10.1016/j.humimm.2025.111267 · Cited by 6

In utero per – and polyfluoroalkyl substances (PFAS) exposure and changes in infant T helper cell development among UPSIDE-ECHO cohort participants.

Castro-Meléndez, D., Laniewski, N. G., Jusko, T. A., Qiu, X., Lawrence, B. P., Rivera‐Núñez, Z., Brunner, J., Best, M., Macomber, A., Leger, A., et al. (2025) · Environmental Health Perspectives · doi:10.1289/ehp16726 · Cited by 7

The roles of tissue-resident memory T cells (TRMs) in diseases and vaccine development: A comprehensive review

Wei, H., Wang, Y., Jiang, S., Zhang, X., & Zhang, J. (2025) · Vaccine · doi:10.1016/j.vaccine.2025.127605 · Cited by 6

The linkage between innate and adaptive immunity: Recent advances in antigen recognition, processing, and presentation in fish

Wu, L., Ye, J., & Li, J. (2025) · Aquaculture and Fisheries · doi:10.1016/j.aaf.2025.07.002 · Cited by 6

Multiple subsets of regulatory T-cells

Kupriyanov, S., Синицкий, А. И., & Dolgushin, I. I. (2020) · Bulletin of Siberian Medicine · doi:10.20538/1682-0363-2020-3-144-155 · Cited by 6

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

Cytomegalovirus at the crossroads of immunosenescence and oncogenesis

Bouezzedine, F., Baba, R. E., Morot-Bizot, S., Diab‐Assaf, M., & Herbein, G. (2023) · Exploration of Immunology · doi:10.37349/ei.2023.00086 · Cited by 7

Vitamin D and immune system

Brown, G., Marchwicka, A., & Marcinkowska, E. (2024) · Advances in food and nutrition research · doi:10.1016/bs.afnr.2023.12.001 · Cited by 7

Intestinal tissue‐resident memory T cells maintain distinct identity from circulating memory T cells after in vitro restimulation

Beumer‐Chuwonpad, A., Behr, F. M., van Alphen, F. P. J., Kragten, N. A. M., Hoogendijk, A. J., van den Biggelaar, M., & van Gisbergen, K. P. J. M. (2024) · European Journal of Immunology · doi:10.1002/eji.202350873 · Cited by 6

The profile and prognostic significance of bone marrow T-cell differentiation subsets in adult AML at diagnosis

Sun, K., Shi, Z.-Y., Wang, Y., Xie, D., Liu, Y., Jiang, Q., Jiang, H., Huang, X., & Qin, Y. (2024) · Frontiers in Immunology · doi:10.3389/fimmu.2024.1418792 · Cited by 6

Enhancing Tumor Immunity with IL-12 and PD-1 Blockade: A Strategy for Inducing Robust Central Memory T Cell Responses in Resistant Cancer Model

Chen, F., Wu, K., Lin, S., Cui, J., Chen, X., Zeng, Z., Yuan, N., Fang, M., Liu, X., Chen, Y., et al. (2024) · Antibodies · doi:10.3390/antib13040094 · Cited by 6

A Novel Designed Anti–PD-L1/OX40 Bispecific Antibody Augments Both Peripheral and Tumor-Associated Immune Responses for Boosting Antitumor Immunity

Li, B., Gong, S., Zhang, N., Shi, B., Lv, Z., Zhang, Y., Gaowa, N., Dong, L., Wu, D., Wu, J., et al. (2024) · Molecular Cancer Therapeutics · doi:10.1158/1535-7163.mct-24-0330 · Cited by 6

Frontline workers: Mediators of mucosal immunity in community acquired pneumonia and COVID-19

Hastak, P., Andersen, C., Kelleher, A. D., & Sasson, S. C. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.983550 · Cited by 6

Donor selection for adoptive cell therapy with CD45RA− memory T cells for patients with coronavirus disease 2019, and dexamethasone and interleukin-15 effects on the phenotype, proliferation and interferon gamma release

Al‐Akioui‐Sanz, K., Pascual-Miguel, B., Díaz‐Almirón, M., Mestre‐Durán, C., Navarro‐Zapata, A., Villa, L. C., Martín-Cortázar, C., Vicario, J. L., Moreno, M. Á., Balas, A., et al. (2022) · Cytotherapy · doi:10.1016/j.jcyt.2022.12.001 · Cited by 5

Bacillus Calmette–Guérin–induced interleukin‐10 inhibits S100A8/A9 production and hinders development of T helper type 1 memory in mice

Wang, Y., Sun, Y., Zheng, Y., Yang, Y., He, L., Qu, P., Zhou, F., Xu, X., Bai, X., Chen, X., et al. (2023) · European Journal of Immunology · doi:10.1002/eji.202250204 · Cited by 6

Quantitative annotations of T-Cell repertoire specificity

Luo, J., Wang, X., Zou, Y., Chen, L., Liu, W., Zhang, W., & Li, S. C. (2023) · Briefings in Bioinformatics · doi:10.1093/bib/bbad175 · Cited by 6

A Noisy-Label-Learning Formulation for Immune Repertoire Classification and Disease-Associated Immune Receptor Sequence Identification

Chen, M., Zhao, Y., Wang, Z., He, B., & Yao, J. (2023) · International Joint Conference on Artificial Intelligence · doi:10.24963/ijcai.2023/527 · Cited by 6

Intramuscular Immunization with a Liposomal Multi-Epitope Chimeric Protein Induces Strong Cellular Immune Responses against Visceral Leishmaniasis

Agallou, M., Margaroni, M., & Karagouni, E. (2023) · Vaccines · doi:10.3390/vaccines11081384 · Cited by 6

Analyses of human immune responses to Francisella tularensis identify correlates of protection

Lindgren, H., Eneslätt, K., Golovliov, I. R., Gelhaus, H. C., & Sjöstedt, A. B. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1238391 · Cited by 6

Intranasal Immunization With Nanoparticles Containing an Orientia tsutsugamushi Protein Vaccine Candidate and a Polysorbitol Transporter Adjuvant Enhances Both Humoral and Cellular Immune Responses

Kim, C. G., Kim, W. K., Kim, N., Pyung, Y. J., Park, D., Lee, J.-C., Cho, C., Chu, H., & Yun, C. (2023) · Immune Network · doi:10.4110/in.2023.23.e47 · Cited by 6

Genome‐wide DNA methylation analysis of senescence in repetitively infected memory cytotoxic T lymphocytes

Shosaku, J. (2017) · Immunology · doi:10.1111/imm.12840 · Cited by 6

IgG Immune Complexes Inhibit Naïve T Cell Proliferation and Suppress Effector Function in Cytotoxic T Cells

Charab, W., Rosenberger, M. G., Shivram, H., Mirazee, J. M., Donkor, M. K., Shekhar, S., Gjuka, D., Khoo, K. H. L., Kim, J. E., Iyer, V. R., et al. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.713704 · Cited by 6

The novel sphingosine-1-phosphate receptors antagonist AD2900 affects lymphocyte activation and inhibits T-cell entry into the lymph nodes

Song, J., Dagan, A., Yakhtin, Z., Gátt, S., Riley, S., Rosen, H., Or, R., & Almogi‐Hazan, O. (2017) · Oncotarget · doi:10.18632/oncotarget.18626 · Cited by 6

The effect of splenectomy on the levels of PCV-13-induced memory B- and T cells

Gazi, U., Karasartova, D., Şahiner, İ. T., Güreser, A. S., Tosun, Ö., Derici, M. K., Dolapçı, M., & Özkan, A. T. (2018) · International Journal of Clinical Practice · doi:10.1111/ijcp.13077 · Cited by 6

Intranasal immunization with protective antigen of Bacillus anthracis induces a long-term immunological memory response

Woo, S., Kang, S., Park, S., Yang, J. S., Song, M., Yun, C., & Han, S. H. (2015) · Molecular Immunology · doi:10.1016/j.molimm.2015.08.002 · Cited by 6

Editorial: Bone Marrow T Cells at the Center Stage in Immunological Memory

Rosa, F. D., & Watts, T. H. (2016) · Frontiers in Immunology · doi:10.3389/fimmu.2016.00596 · Cited by 6

How a well-adapting immune system remembersPreprint

Mayer, A., Balasubramanian, V., Walczak, A. M., & Mora, T. (2018) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/347856 · Cited by 7

A Single-Cell Perspective on Memory T-Cell DifferentiationPreprint

Kretschmer, L., Busch, D. H., & Buchholz, V. R. (2021) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a038067 · Cited by 6

Human adipose tissue as a major reservoir of cytomegalovirus-reactive T cells

Redruello-Romero, A., Benitez‐Cantos, M. S., López-Pérez, D., García-Rubio, J., Tamayo, F., Pérez-Bartivas, D., Moreno-SanJuan, S., Ruiz-Palmero, I., Puentes-Pardo, J. D., Vilchez, J. R., et al. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1303724 · Cited by 5

Current regulatory requirements for assessment of immunogenicity for gene therapy medicinal products

Mann, C. J., Giblin, J., Braun, M., Schmid, F., Sørensen, M. R., Caferra, P., Hudák, A., Letoha, T., Coderch, N., Hickling, T. P., et al. (2025) · Cell Reports Medicine · doi:10.1016/j.xcrm.2025.102422 · Cited by 6

Neoadjuvante Immuntherapie bei Kopf-Hals- Plattenepithelkarzinomen

Kürten, C. H. L., & Ferris, R. L. (2024) · Laryngo-Rhino-Otologie · doi:10.1055/a-2183-5802 · Cited by 5

Heat shock protein 90 is a chaperone regulator of HIV-1 latency

Noorsaeed, S., AlBurtamani, N., Rokan, A., & Fassati, A. (2025) · PLoS Pathogens · doi:10.1371/journal.ppat.1012524 · Cited by 5

Shared acute phase traits in effector and memory human CD8 T cells

Marraco, S. A. F., Alpern, D., Lofek, S., Lourenço, J., Bovay, A., Hajjami, H. M.-E., Delorenzi, M., Deplancke, B., & Speiser, D. E. (2021) · Current Research in Immunology · doi:10.1016/j.crimmu.2021.12.002 · Cited by 4

Immunogenicity of varicella-zoster virus vaccine by different routes of administration: Comparable vaccination efficacy of one-fifth dose intradermal vaccination to conventional subcutaneous vaccination

Nakamura-Nishimura, Y., Shinkuma, S., Miyagawa, F., Haredy, A. M., Gomi, Y., Yamanishi, K., & Asada, H. (2022) · Journal of Dermatological Science · doi:10.1016/j.jdermsci.2022.04.001 · Cited by 5

Ibrutinib combined with low‐dose histone deacetylases inhibitor chidamide synergistically enhances the anti‐tumor effect in B‐cell lymphoma

Yu, H., Mi, L., Zhang, W., Ye, Y., Li, M., Hu, D., Cao, J., Wang, D., Wang, X., Ding, N., et al. (2022) · Hematological Oncology · doi:10.1002/hon.3056 · Cited by 4

Distinct CD4+ T cell signature in ANA-positive young adult patients

Zotti, F. D., Moriconi, C., Qiu, A., Miller, A., & Hudson, K. E. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.972127 · Cited by 5

Four-Parameter FluoroSpot Assay Reveals That the Varicella Zoster Virus Elicits a Robust Memory T Cell IL-10 Response throughout Childhood

Nilsson, A., Höbinger, A., Jahnmatz, P., Tiselius, E., Laestadius, Å., Melén, E., Björkander, S., & Saghafian‐Hedengren, S. (2022) · Journal of Virology · doi:10.1128/jvi.01310-22 · Cited by 5

Rapid disease progression on immune checkpoint inhibitors in young patients with stage IV melanoma

Machiraju, D., Schäfer, S., Beckhove, P., Roth, J., Schulz, C., & Hassel, J. C. (2023) · Frontiers in Medicine · doi:10.3389/fmed.2023.1117816 · Cited by 5

Spatial map of human T cell compartmentalization and maintenance over decades of life

Thome, J. J. C., Yudanin, N., Ohmura, Y., Kubota, M., Grinshpun, B., Sathaliyawala, T., Kato, T., Lerner, H., Shen, Y., & Farber, D. L. (2014) · Cell · doi:10.1016/j.cell.2014.10.026 · Cited by 587

The diverse landscape of memory T‐cell heterogeneity

Farber, D. (2023) · Immunological Reviews · doi:10.1111/imr.13229 · Cited by 1

Location, location, location: Tissue resident memory T cells in mice and humans

Szabo, P. A., Miron, M., & Farber, D. L. (2019) · Science Immunology · doi:10.1126/sciimmunol.aas9673 · Cited by 651

Central Memory and Effector Memory T Cell Subsets: Function, Generation, and Maintenance

Sallusto, F., Geginat, J., & Lanzavecchia, A. (2004) · Annual Review of Immunology · doi:10.1146/annurev.immunol.22.012703.104702 · Cited by 3,067

Distribution and compartmentalization of human circulating and tissue-resident memory T cell subsets

Sathaliyawala, T., Kubota, M., Yudanin, N., Turner, D., Camp, P., Thome, J. J. C., Bickham, K. L., Lerner, H., Goldstein, M., Sykes, M., et al. (2013) · Immunity · doi:10.1016/j.immuni.2012.09.020 · Cited by 848