The DOI matches its Crossref record; 32 of the 32 references it cites were found in a registry or an index.
Origin and differentiation of human memory CD8 T cells after vaccination
Open accessAbstract
The differentiation of human memory CD8 T cells is not well understood. Here we address this issue using the live yellow fever virus (YFV) vaccine, which induces long-term immunity in humans. We used in vivo deuterium labelling to mark CD8 T cells that proliferated in response to the virus and then assessed cellular turnover and longevity by quantifying deuterium dilution kinetics in YFV-specific CD8 T cells using mass spectrometry. This longitudinal analysis showed that the memory pool originates from CD8 T cells that divided extensively during the first two weeks after infection and is maintained by quiescent cells that divide less than once every year (doubling time of over 450 days). Although these long-lived YFV-specific memory CD8 T cells did not express effector molecules, their epigenetic landscape resembled that of effector CD8 T cells. This open chromatin profile at effector genes was maintained in memory CD8 T cells isolated even a decade after vaccination, indicating that these cells retain an epigenetic fingerprint of their effector history and remain poised to respond rapidly upon re-exposure to the pathogen.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“the generation of robust T cell responses by mRNA vaccines may have implications for long-term protective immunity, as memory CD4+ and CD8+ T cells can be exceptionally durable in other vaccine settings (Akondy et al., 2017; Hammarlund et al., 2003).”
From Rapid induction of antigen-specific CD4+ T cells is associated with coordinated humoral and cellular immunity to SARS-CoV-2 mRNA vaccination (2021) · cites this paper as Akondy et al., 2017
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Buenrostro, J. D., Giresi, P. G., Zaba, L. C., Chang, H. Y., & Greenleaf, W. J. (2013) · Nature Methods · doi:10.1038/nmeth.2688 · Cited by 6,422
Self-citationATAC-seq: a method for assaying chromatin accessibility genome-wide
Buenrostro, J. D., Wu, B., Chang, H. Y., & Greenleaf, W. J. (2015) · Current Protocols in Molecular Biology · doi:10.1002/0471142727.mb2129s109 · Cited by 3,289
Self-citationCpG islands and the regulation of transcription
Deaton, A. M., & Bird, A. (2011) · Genes & Development · doi:10.1101/gad.2037511 · Cited by 3,187
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
Self-citationA 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
Immunological memory and protective immunity: understanding their relation
Ahmed, R., & Gray, D. (1996) · Science · doi:10.1126/science.272.5258.54 · Cited by 1,775
Self-citationMolecular Signature of CD8+ T Cell Exhaustion during Chronic Viral Infection
Wherry, E. J., Ha, S., 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.2007.11.006 · Cited by 1,355
Self-citationHomeostasis of Naive and Memory T Cells
Surh, C. D., & Sprent, J. (2008) · Immunity · doi:10.1016/j.immuni.2008.11.002 · Cited by 1,193
Molecular and functional profiling of memory CD8 T cell differentiation.
Kaech, S., Hemby, S., Kersh, E., & Ahmed, R. (2002) · Cell · doi:10.1016/s0092-8674(02)01139-x · Cited by 1,081
Self-citationCytotoxic T-cell memory without antigen
Lau, L. L., Jamieson, B. D., Somasundaram, T., & Ahmed, R. (1994) · Nature · doi:10.1038/369648a0 · Cited by 657
Self-citation
Flagged first, then by citations
Cited by
Sorted by citations
Items 101–200 of 522
Ma, Y., Qiu, F., Deng, C., Li, J., Huang, Y., Wu, Z., Zhou, Y., Zhang, Y., Xiong, Y., Yao, Y., et al. (2022) · Genome Medicine · doi:10.1186/s13073-022-01021-1 · Cited by 70
Kahan, S. M., Bakshi, R. K., Ingram, J. T., Hendrickson, R. C., Lefkowitz, E. J., Crossman, D. K., Harrington, L. E., Weaver, C. T., & Zajac, A. J. (2022) · Science Immunology · doi:10.1126/sciimmunol.abl6322 · Cited by 67
Rewriting History: Epigenetic Reprogramming of CD8+ T Cell Differentiation to Enhance Immunotherapy
Zebley, C. C., Gottschalk, S. M., & Youngblood, B. (2020) · Trends in Immunology · doi:10.1016/j.it.2020.06.008 · Cited by 71
Self-citationAdenoviral-based vaccine promotes neoantigen-specific CD8 + T cell stemness and tumor rejection
D’Alise, A. M., Brasu, N., Intinis, C. D., Leoni, G., Russo, V., Langone, F., Baev, D. V., Micarelli, E., Petiti, L., Picelli, S., et al. (2022) · Science Translational Medicine · doi:10.1126/scitranslmed.abo7604 · Cited by 69
Zitti, B., Hoffer, E., Zheng, W., Pandey, R. V., Schlums, H., Casoni, G. P., Fusi, I., Nguyen, L., Kärner, J., Kokkinou, E., et al. (2023) · Immunity · doi:10.1016/j.immuni.2023.05.003 · Cited by 70
Stevenson, E. M., Ward, A. R., Truong, R., Thomas, A. S., Huang, S.-H., Dilling, T. R., Terry, S. N., Bui, J. K., Mota, T. M., Danesh, A., et al. (2021) · JCI Insight · doi:10.1172/jci.insight.142640 · Cited by 65
Distinct epigenomic landscapes underlie tissue-specific memory T cell differentiation
Buquicchio, F. A., Fonseca, R., Yan, P., Wang, F., Evrard, M., Obers, A., Gutierrez, J. C., Raposo, C. J., Belk, J. A., Dániel, B., et al. (2024) · Immunity · doi:10.1016/j.immuni.2024.06.014 · Cited by 65
Cell generation dynamics underlying naive T-cell homeostasis in adult humans
Mold, J. E., Réu, P., Olin, A., Bernard, S., Michaëlsson, J., Rane, S., Yates, A. J., Khosravi, A., Salehpour, M., Possnert, G., et al. (2019) · PLoS Biology · doi:10.1371/journal.pbio.3000383 · Cited by 70
Epigenetic Regulation of T Cell Memory: Recalling Therapeutic Implications
Tough, D. F., Rioja, I., Modis, L. K., & Prinjha, R. K. (2019) · Trends in Immunology · doi:10.1016/j.it.2019.11.008 · Cited by 67
Minervina, A. A., Pogorelyy, M. V., Komech, E. A., Карнаухов, В. К., Bächer, P., Rosati, E., Franke, A., Chudakov, D. M., Mamedov, I. Z., Lebedev, Y. B., et al. (2020) · eLife · doi:10.7554/elife.53704 · Cited by 68
Tu, W. J., McCuaig, R., Tan, A. H. Y., Hardy, K., Seddiki, N., Ali, S. S., Dahlstrom, J. E., Bean, E. G., Dunn, J., Forwood, J. K., et al. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.01228 · Cited by 67
Establishment and recall of SARS-CoV-2 spike epitope-specific CD4+ T cell memory
Wragg, K. M., Lee, W. S., Koutsakos, M., Tan, H., Amarasena, T. H., Reynaldi, A., Gare, G., Konstandopoulos, P., Field, K. R., Esterbauer, R., et al. (2022) · Nature Immunology · doi:10.1038/s41590-022-01175-5 · Cited by 68
Remembering to remember: T cell memory maintenance and plasticity
Omilusik, K. D., & Goldrath, A. W. (2019) · Current Opinion in Immunology · doi:10.1016/j.coi.2019.04.009 · Cited by 63
Costimulation through TLR2 Drives Polyfunctional CD8+ T Cell Responses
Salerno, F., Heeren, J. J. F., Guislain, A., Nicolet, B. P., & Wolkers, M. C. (2018) · The Journal of Immunology · doi:10.4049/jimmunol.1801026 · Cited by 62
Heterogeneity of human anti-viral immunity shaped by virus, tissue, age, and sex
Poon, M. M. L., Byington, E., Meng, W., Kubota, M., Matsumoto, R., Grifoni, A., Weiskopf, D., Dogra, P., Lam, N., Szabo, P. A., et al. (2021) · Cell Reports · doi:10.1016/j.celrep.2021.110071 · Cited by 62
Jaiswal, A., Verma, A., Dannenfelser, R., Melssen, M. M., Tirosh, I., Izar, B., Kim, T., Nirschl, C. J., Devi, K. S. P., Olson, W. C., et al. (2022) · Cancer Cell · doi:10.1016/j.ccell.2022.04.005 · Cited by 61
Goronzy, J. J., Hu, B., Kim, C., Jadhav, R. R., & Weyand, C. M. (2018) · Journal of Leukocyte Biology · doi:10.1002/jlb.1ri0418-160r · Cited by 60
Self-citationMapping the evolution of T cell states during response and resistance to adoptive cellular therapy
Bachireddy, P., Azizi, E., Burdziak, C., Nguyen, V. N., Ennis, C. S., Maurer, K., Park, C. Y., Choo, Z.-N., Li, S., Gohil, S. H., et al. (2021) · Cell Reports · doi:10.1016/j.celrep.2021.109992 · Cited by 55
TCR-sequencing in cancer and autoimmunity: barcodes and beyond
Pauken, K. E., Lagattuta, K. A., Lu, B. Y., Lucca, L. E., DAUD, A. I., Hafler, D. A., Kluger, H. M., Raychaudhuri, S., & Sharpe, A. H. (2022) · Trends in Immunology · doi:10.1016/j.it.2022.01.002 · Cited by 60
Transcriptome dynamics of CD4+ T cells during malaria maps gradual transit from effector to memory
Soon, M. S. F., Lee, H. J., Engel, J. A., Straube, J., Thomas, B. S., Pernold, C. P. S., Clarke, L. S., Laohamonthonkul, P., Haldar, R., Williams, C. G., et al. (2020) · Nature Immunology · doi:10.1038/s41590-020-0800-8 · Cited by 56
Borghans, J. A. M., Tesselaar, K., & de Boer, R. J. (2018) · Immunological Reviews · doi:10.1111/imr.12693 · Cited by 53
NIX-Mediated Mitophagy Promotes Effector Memory Formation in Antigen-Specific CD8+ T Cells
Gupta, S. S., Sharp, R., Hofferek, C. J., Kuai, L., Dorn, G. W., Wang, J., & Chen, M. (2019) · Cell Reports · doi:10.1016/j.celrep.2019.10.032 · Cited by 56
Self-citationTechnology meets TILs: Deciphering T cell function in the -omics era
Hudson, W. H., & Wieland, A. (2022) · Cancer Cell · doi:10.1016/j.ccell.2022.09.011 · Cited by 55
Regulation of activated T cell survival in rheumatic autoimmune diseases
Rosetti, F., Madera-Salcedo, I. K., Rodríguez‐Rodríguez, N., & Crispín, J. C. (2022) · Nature Reviews Rheumatology · doi:10.1038/s41584-021-00741-9 · Cited by 54
Li, W., & Zhang, L. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.01834 · Cited by 54
Replicative history marks transcriptional and functional disparity in the CD8+ T cell memory pool
Bresser, K., Kok, L., Swain, A. C., King, L. A., Jacobs, L., Weber, T., Perié, L., Duffy, K. R., de Boer, R. J., Scheeren, F. A., et al. (2022) · Nature Immunology · doi:10.1038/s41590-022-01171-9 · Cited by 53
Memory profiles distinguish cross-reactive and virus-specific T cell immunity to mpox
Adamo, S., Gao, Y., Sekine, T., Mily, A., Wu, J., Storgärd, E., Westergren, V., Filén, F., Treutiger, C.-J., Sandberg, J. K., et al. (2023) · Cell Host & Microbe · doi:10.1016/j.chom.2023.04.015 · Cited by 53
Reversible, tunable epigenetic silencing of TCF1 generates flexibility in the T cell memory decision
Abadie, K., Clark, E. C., Valanparambil, R. M., Ukogu, O., Yang, W., Daza, R. M., Ng, K. K. H., Fathima, J., Wang, A. L., Lee, J., et al. (2024) · Immunity · doi:10.1016/j.immuni.2023.12.006 · Cited by 53
Self-citationExpression of novel long noncoding RNAs defines virus-specific effector and memory CD8+ T cells
Hudson, W. H., Prokhnevska, N., Gensheimer, J., Akondy, R. S., McGuire, D. J., Ahmed, R., & Kissick, H. T. (2019) · Nature Communications · doi:10.1038/s41467-018-07956-7 · Cited by 52
Self-citationNel, A. E., & Miller, J. F. (2021) · ACS Nano · doi:10.1021/acsnano.1c01845 · Cited by 50
Yewdell, W. T., Smolkin, R. M., Belcheva, K. T., Mendoza, A., Michaels, A. J., Cols, M., Angeletti, D., Yewdell, J. W., & Chaudhuri, J. (2021) · Cell Reports · doi:10.1016/j.celrep.2021.109961 · Cited by 52
Campi-Azevedo, A. C., Peruhype-Magalhāes, V., Coelho-dos-Reis, J. G., Antonelli, L. R., Costa-Pereira, C., Speziali, E., Reis, L. R., Lemos, J. A., Ribeiro, J. G. L., Camacho, L. A. B., et al. (2019) · Emerging infectious diseases · doi:10.3201/eid2508.181432 · Cited by 50
Early life imprints the hierarchy of T cell clone sizes
Gaimann, M. U., Nguyen, M., Desponds, J., & Mayer, A. (2020) · eLife · doi:10.7554/elife.61639 · Cited by 50
Thom, R. E., Tipton, T. R. W., Strecker, T., Hall, Y., Boré, J. A., Maes, P., Koundouno, F. R., Fehling, S. K., Krähling, V., Steeds, K., et al. (2020) · The Lancet Infectious Diseases · doi:10.1016/s1473-3099(20)30736-2 · Cited by 50
T Cell Memory in Infection, Cancer, and Autoimmunity
Barnaba, V. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2021.811968 · Cited by 49
Comparative Immune Responses to Licensed Herpes Zoster Vaccines
Weinberg, A., Kroehl, M., Johnson, M. J., Hammes, A., Reinhold, D., Lang, N., & Levin, M. J. (2018) · The Journal of Infectious Diseases · doi:10.1093/infdis/jiy383 · Cited by 48
Defects in Antiviral T Cell Responses Inflicted by Aging-Associated miR-181a Deficiency
Kim, C., Jadhav, R. R., Gustafson, C. E., Smithey, M. J., Hirsch, A. J., Uhrlaub, J. L., Hildebrand, W. H., Nikolich‐Žugich, J., Weyand, C. M., & Goronzy, J. J. (2019) · Cell Reports · doi:10.1016/j.celrep.2019.10.044 · Cited by 47
Self-citationChng, M. H. Y., Lim, M. Q., Rouers, A., Becht, É., Lee, B. T. K., MacAry, P. A., Lye, D. C., Leo, Y., Chen, J., Fink, K., et al. (2019) · Immunity · doi:10.1016/j.immuni.2019.10.007 · Cited by 45
The ABC of Major Histocompatibility Complexes and T Cell Receptors in Health and Disease
Kedzierska, K., & Koutsakos, M. (2020) · Viral Immunology · doi:10.1089/vim.2019.0184 · Cited by 52
Influence of Age on Functional Memory T Cell Diversity
Fang, F., Cao, W., Zhu, W., Lam, N., Li, L., Gaddam, S., Wang, Y., Kim, C., Lambert, S., Zhang, H., et al. (2021) · Cell Reports · doi:10.1016/j.celrep.2021.109981 · Cited by 47
Self-citationIngels, J., Cock, L. D., Stevens, D., Mayer, R. L., Théry, F., Sanchez, G. S., Vermijlen, D., Weening, K., Smet, S. D., Lootens, N., et al. (2024) · Cell Reports Medicine · doi:10.1016/j.xcrm.2024.101516 · Cited by 49
Baliu‐Piqué, M., Verheij, M. W., Drylewicz, J., Ravesloot, L., de Boer, R. J., Koets, A. P., Tesselaar, K., & Borghans, J. A. M. (2018) · Frontiers in Immunology · doi:10.3389/fimmu.2018.02054 · Cited by 48
Functional pathways regulated by microRNA networks in CD8 T‐cell aging
Gustafson, C. E., Cavanagh, M., Jin, J., Weyand, C. M., & Goronzy, J. J. (2018) · Aging Cell · doi:10.1111/acel.12879 · Cited by 45
Self-citationT‐cell infiltration, contribution and regulation in the central nervous system post‐traumatic injury
Xu, L., Ye, X., Wang, Q., Xu, B., Zhong, J., Chen, Y., & Wang, L. (2021) · Cell Proliferation · doi:10.1111/cpr.13092 · Cited by 47
Schirrmacher, V. (2022) · Biomedicines · doi:10.3390/biomedicines10030562 · Cited by 45
Clonally heritable gene expression imparts a layer of diversity within cell types
Mold, J. E., Weissman, M. H., Ratz, M., Hagemann-Jensen, M., Hård, J., Eriksson, C., Toosi, H., Berghenstråhle, J., Ziegenhain, C., von Berlin, L., et al. (2024) · Cell Systems · doi:10.1016/j.cels.2024.01.004 · Cited by 47
The Untapped Opportunity and Challenge of Immunometabolism: A New Paradigm for Drug Discovery
Mazumdar, C., Driggers, E. M., & Turka, L. A. (2019) · Cell Metabolism · doi:10.1016/j.cmet.2019.11.014 · Cited by 47
Graham, N., Eisenhauer, P., Diehl, S. A., Pierce, K. K., Whitehead, S. S., Durbin, A. P., Kirkpatrick, B. D., Sette, A., Weiskopf, D., Boyson, J. E., et al. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.00479 · Cited by 44
Zhang, Y., Li, B., Bai, Q., Wang, P., Wei, G., Li, Z., Li, H., Qin, T., Zhou, J., Huang, Q., et al. (2021) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-021-00492-9 · Cited by 45
IL-12 Signaling Promotes TET2-Mediated DNA Demethylation During CD8 T Cell Effector Differentiation
Zebley, C. C., Abdelsamed, H. A., Ghoneim, H. E., Alli, S., Brown, C., Haydar, D., Tian, M., Harris, T. L., McGargill, M. A., Krenciute, G., et al. (2020) · Cell Reports · doi:10.1016/j.celrep.2021.109796 · Cited by 45
Self-citationDNA Methylation and Immune Memory Response
Mittelstaedt, N. N., Becker, A. L., de Freitas, D. N., Zanin, R. F., Stein, R. T., & de Souza, A. P. D. (2021) · Cells · doi:10.3390/cells10112943 · Cited by 45
Thomson, Z., He, Z., Swanson, E. G., Henderson, K., Phalen, C. G., Zaim, S. R., Pebworth, M.-P., Okada, L. Y., Heubeck, A. T., Roll, C. R., et al. (2023) · Nature Immunology · doi:10.1038/s41590-023-01641-8 · Cited by 43
Wu, D., Kolesnikov, A. V., Yin, R. M., Guest, J. D., Gowthaman, R., Shmelev, A., Serdyuk, Y. V., Dianov, D. V., Efimov, G. A., Pierce, B. G., et al. (2022) · Nature Communications · doi:10.1038/s41467-021-27669-8 · Cited by 45
Carlisle, J. W., Jansen, C. S., Cardenas, M. A., Sobierajska, E., Reyes, A. M., Greenwald, R., del Balzo, L., Prokhnevska, N., Küçük, Ö., Carthon, B. C., et al. (2022) · Journal for ImmunoTherapy of Cancer · doi:10.1136/jitc-2022-004803 · Cited by 42
Self-citationT cell exhaustion in human cancers
Kang, K., Lin, X., Chen, P., Liu, H., Liu, F., Xiong, W., Li, G., Yi, M., Li, X., Wang, H., et al. (2024) · Biochimica et Biophysica Acta (BBA) - Reviews on Cancer · doi:10.1016/j.bbcan.2024.189162 · Cited by 49
Epigenetic regulation of T cell adaptive immunity
Frias, A. B., Boi, S. K., Lan, X., & Youngblood, B. (2021) · Immunological Reviews · doi:10.1111/imr.12943 · Cited by 44
Self-citationSlamanig, S., & Nolte, M. A. (2021) · Cells · doi:10.3390/cells10061508 · Cited by 44
Numbers and odds: TCR repertoire size and its age changes impacting on T cell functions
Weng, N. (2023) · Seminars in Immunology · doi:10.1016/j.smim.2023.101810 · Cited by 47
Transient inhibition of type I interferon enhances CD8+ T cell stemness and vaccine protection
Broomfield, B. J., Tan, C. W., Qin, R. Z., Abberger, H., Duckworth, B. C., Alvarado, C., Dalit, L., Lee, C. L., Mugan, R. S., Mazrad, Z. A. I., et al. (2025) · The Journal of Experimental Medicine · doi:10.1084/jem.20241148 · Cited by 42
Good‐Jacobson, K. L. (2018) · Immunological Reviews · doi:10.1111/imr.12663 · Cited by 40
Common gamma chain cytokines and CD8 T cells in cancer
Shourian, M., Beltra, J., Bourdin, B., & Decaluwe, H. (2019) · Seminars in Immunology · doi:10.1016/j.smim.2019.101307 · Cited by 43
Current estimates of T cell kinetics in humans
Macallan, D. C., Busch, R., & Asquith, B. (2019) · Current Opinion in Systems Biology · doi:10.1016/j.coisb.2019.10.002 · Cited by 43
Epigenetics and CD8+ T cell memory*
Montacchiesi, G., & Pace, L. (2021) · Immunological Reviews · doi:10.1111/imr.13057 · Cited by 43
Chappert, P., Huetz, F., Espinasse, M., Chatonnet, F., Pannetier, L., Silva, L. D., Goetz, C., Megret, J., Sokal, A., Crickx, É., et al. (2022) · Immunity · doi:10.1016/j.immuni.2022.08.019 · Cited by 45
Quantification of T-cell dynamics during latent cytomegalovirus infection in humans
van den Berg, S. P. H., Derksen, L. Y., Drylewicz, J., Nanlohy, N. M., Beckers, L., Lanfermeijer, J., Gessel, S., Vos, M. W., Otto, S. A., de Boer, R. J., et al. (2021) · PLoS Pathogens · doi:10.1371/journal.ppat.1010152 · Cited by 40
Reva, K., Laranjinha, J. A. N., & Rocha, B. S. (2023) · Metabolites · doi:10.3390/metabo13030375 · Cited by 44
Integrating resident memory into T cell differentiation models
Rosato, P. C., Wijeyesinghe, S., Stolley, J. M., & Masopust, D. (2020) · Current Opinion in Immunology · doi:10.1016/j.coi.2020.01.001 · Cited by 40
Neoantigens in precision cancer immunotherapy: from identification to clinical applications
Zhang, Q., Jia, Q., Zhang, J., & Zhu, B. (2022) · Chinese Medical Journal · doi:10.1097/cm9.0000000000002181 · Cited by 39
Mechanisms governing bystander activation of T cells
Yosri, M., Dokhan, M., Aboagye, E., Moussawy, M. A., & Abdelsamed, H. A. (2024) · Frontiers in Immunology · doi:10.3389/fimmu.2024.1465889 · Cited by 38
Self-citationTakata, H., Kakazu, J. C., Mitchell, J. L., Kroon, E. D. M. B., Colby, D. J., Sacdalan, C., Bai, H., Ehrenberg, P. K., Geretz, A., Buranapraditkun, S., et al. (2022) · EBioMedicine · doi:10.1016/j.ebiom.2022.104253 · Cited by 43
Omilusik, K. D., & Goldrath, A. W. (2017) · Nature · doi:10.1038/d41586-017-08280-8 · Cited by 38
Paterson, S., Kar, S., Ung, S. K. A., Gardener, Z., Bergstrom, E., Ascough, S., Kalyan, M., Żyła, J., Maertzdorf, J., Mollenkopf, H., et al. (2021) · American Journal of Respiratory and Critical Care Medicine · doi:10.1164/rccm.202103-0620oc · Cited by 36
Li, S., Zhu, C., Zhou, X., Chen, L., Bo, X., Shen, Y., Guan, X., Han, X., Shan, D., Sun, L., et al. (2022) · Advanced Science · doi:10.1002/advs.202104619 · Cited by 38
Sepsis-induced changes in differentiation, maintenance, and function of memory CD8 T cell subsets
Heidarian, M., Griffith, T. S., & Badovinac, V. P. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1130009 · Cited by 41
Methods for Measuring T-Cell Memory to Vaccination: From Mouse to Man
Flaxman, A. L., & Ewer, K. (2018) · Vaccines · doi:10.3390/vaccines6030043 · Cited by 37
Valkenburg, S. A., Leung, N., Bull, M. B., Yan, L.-M., Li, A. P. Y., Poon, L. L. M., & Cowling, B. J. (2018) · Frontiers in Immunology · doi:10.3389/fimmu.2018.01479 · Cited by 36
Bannister, S., Messina, N. L., Novakovic, B., & Curtis, N. C. (2020) · Epigenetics · doi:10.1080/15592294.2020.1712814 · Cited by 35
Wimmers, F., & Pulendran, B. (2020) · Current Opinion in Immunology · doi:10.1016/j.coi.2020.05.001 · Cited by 37
Bevington, S. L., Keane, P., Soley, J. K., Tauch, S., Gajdasik, D. W., Fiancette, R., Matei‐Rascu, V., Willis, C., Withers, D. R., & Cockerill, P. N. (2020) · The EMBO Journal · doi:10.15252/embj.2020105220 · Cited by 36
T-Cell Response to Viral Hemorrhagic Fevers
Perdomo-Celis, F., Salvato, M. S., Medina-Moreno, S., & Zapata, J. C. (2019) · Vaccines · doi:10.3390/vaccines7010011 · Cited by 35
Yeo, L., Pujol‐Autonell, I., Baptista, R., Eichmann, M., Kronenberg‐Versteeg, D., Heck, S., Dolton, G. M., Sewell, A. K., Härkönen, T., Mikk, M.-L., et al. (2019) · Clinical & Experimental Immunology · doi:10.1111/cei.13391 · Cited by 36
Li, J., Li, Y., Li, W., Luo, H.-B., Xi, Y.-P., Dong, S.-H., Gao, M., Xu, P., Zhang, B.-L., Liang, Y., et al. (2019) · Genome Research · doi:10.1101/gr.240606.118 · Cited by 33
Schoonhoven, A. O.-V., de Bruijn, M. J. W., Stikker, B., Brouwer, R. W. W., Braunstahl, G., van IJcken, W. F. J., Graf, T., Huylebroeck, D., Hendriks, R. W., Stik, G., et al. (2023) · Science Immunology · doi:10.1126/sciimmunol.adg3917 · Cited by 35
Heterogeneity of memory T cells in aging
Jain, A. K., Sturmlechner, I., Weyand, C. M., & Goronzy, J. J. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1250916 · Cited by 34
Self-citationBevilacqua, A., Franco, F., Lu, Y.-T., Rahiman, N., Kao, K., Chuang, Y., Zhu, Y., Held, W., Xie, X., Gunsalus, K. C., et al. (2024) · Science Immunology · doi:10.1126/sciimmunol.adn2717 · Cited by 33
Epigenetic Maintenance of Acquired Gene Expression Programs during Memory CD8 T Cell Homeostasis
Abdelsamed, H. A., Zebley, C. C., & Youngblood, B. (2018) · Frontiers in Immunology · doi:10.3389/fimmu.2018.00006 · Cited by 33
Self-citationTissue-Resident Memory T Cells in Mice and Humans: Towards a Quantitative Ecology
Morris, S. E., Färber, D. L., & Yates, A. J. (2019) · The Journal of Immunology · doi:10.4049/jimmunol.1900767 · Cited by 33
Functional interrogation of lymphocyte subsets in alopecia areata using single-cell RNA sequencing
Lee, E. Y., Dai, Z., Jaiswal, A., Wang, E. H. C., Anandasabapathy, N., & Christiano, A. M. (2023) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2305764120 · Cited by 36
Area under Immunosurveillance: Dedicated Roles of Memory CD8 T-Cell SubsetsPreprint
Vidal, L. P., & van Gisbergen, K. P. J. M. (2020) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a037796 · Cited by 33
Behr, F. M., Beumer‐Chuwonpad, A., Kragten, N. A. M., Wesselink, T. H., Stark, R., & van Gisbergen, K. P. J. M. (2021) · European Journal of Immunology · doi:10.1002/eji.202048737 · Cited by 30
Epigenetic regulation of T cell exhaustion in cancer
Kang, T. G., Johnson, J. T., Zebley, C. C., & Youngblood, B. (2025) · Nature reviews. Cancer · doi:10.1038/s41568-025-00883-y · Cited by 36
Self-citationTissue-Specific Control of Tissue-Resident Memory T Cells
Liu, Y., Ma, C., & Zhang, N. (2018) · Critical Reviews in Immunology · doi:10.1615/critrevimmunol.2018025653 · Cited by 32
Potential functions of atypical memory B cells in Plasmodium-exposed individuals
Braddom, A. E., Batugedara, G., Bol, S. M., & Bunnik, E. M. (2020) · International Journal for Parasitology · doi:10.1016/j.ijpara.2020.08.003 · Cited by 31
Skin T cells maintain their diversity and functionality in the elderly
Koguchi‐Yoshioka, H., Hoffer, E., Cheuk, S., Matsumura, Y., Vo, S., Kjellman, P., Grema, L., Ishitsuka, Y., Nakamura, Y., Okiyama, N., et al. (2021) · Communications Biology · doi:10.1038/s42003-020-01551-7 · Cited by 31
TRIB2 safeguards naive T cell homeostasis during aging
Cao, W., Sturmlechner, I., Zhang, H., Jin, J., Hu, B., Jadhav, R. R., Fang, F., Weyand, C. M., & Goronzy, J. J. (2023) · Cell Reports · doi:10.1016/j.celrep.2023.112195 · Cited by 33
Self-citationRole of antiviral CD8+ T cell immunity to SARS-CoV-2 infection and vaccination
Karl, V., Hofmann, M., & Thimme, R. (2025) · Journal of Virology · doi:10.1128/jvi.01350-24 · Cited by 37
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
HTNV infection of CD8+ T cells is associated with disease progression in HFRS patients
Liu, R., Ma, R., Liu, Z., Hu, H., Shu, J., Hu, P., Kang, J., Zhang, Y., Han, M., Zhang, X., et al. (2021) · Communications Biology · doi:10.1038/s42003-021-02182-2 · Cited by 28
Wang, M., Zhai, R., Wang, M., Zhu, W., Zhang, J., Yu, M., Zhang, W., Ye, J., & Liu, L. (2023) · Molecular Oncology · doi:10.1002/1878-0261.13403 · Cited by 28
Simons, B. D., & Karin, O. (2024) · Immunity · doi:10.1016/j.immuni.2024.02.005 · Cited by 30
Metadata
- Authors
- Akondy, R. S., Fitch, M., Edupuganti, S., Yang, S., Kissick, H. T., Li, K. W., Youngblood, B. A., Abdelsamed, H. A., McGuire, D. J., Cohen, K. W., Alexe, G., Nagar, S., McCausland, M. M., Gupta, S., Tata, P., Haining, W. N., McElrath, M. J., Zhang, D., Hu, B., Greenleaf, W. J., Goronzy, J. J., Mulligan, M. J., Hellerstein, M., & Ahmed, R.
- Affiliations
- Emory University (US)
- University of California, Berkeley (US)
- Central South University (CN)
- KineMed (United States) (US)
- St. Jude Children's Research Hospital (US)
- Fred Hutch Cancer Center (US)
- Broad Institute (US)
- Strand Life Sciences (India) (IN)
- Stanford Medicine (US)
- Corresponding author
- Hellerstein, Marc
- Ahmed, Rafi
- ORCID
- Venue
- Nature
- Published
- 2017-12-13
- Volume
- 552
- Issue
- 7685
- Pages
- 362-367
- ISSN
- 0028-0836 (ISSN-L)
- 1476-4687
- PMC
- PMC6037316
- OpenAlex
- W2772063315
- Cited by
- 517
- References
- 32
- Citations by year
- 2026: 36 · 2025: 49 · 2024: 47 · 2023: 57 · 2022: 72 · 2021: 81 · 2020: 71 · 2019: 55 · 2018: 47 · 2017: 2
- FWCI
- 21.74
- Type
- journal article
- Language
- en
- Open access
- green
- europepmc.org
- Locations
- Nature (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- RePEc: Research Papers in Economics (submittedVersion)
- Funders
- National Institutes of Health (R01-AI43866-07)
- National Institute of Allergy and Infectious Diseases (R01AI043866, R01AI129191, UM1AI068618, UM1AI069481, U19AI057266)
- National Institute of Arthritis and Musculoskeletal and Skin Diseases (T32AR050942)
- Topics
- Life Sciences › Immunology and Microbiology › Immunology › T-cell and B-cell Immunology
- Life Sciences › Immunology and Microbiology › Immunology › Immune responses and vaccinations
- Life Sciences › Immunology and Microbiology › Immunology › Immunotherapy and Immune Responses
- Keywords
- memory CD8+ T cells, yellow fever vaccine, T cell differentiation, T cell quiescence, cell turnover, deuterium labeling, epigenetic memory, open chromatin, DNA methylation, effector T cells, naive T cells, T cell proliferation
- MeSH terms
- Animals, Cell Differentiation, Chromatin, Deuterium, Half-Life, Humans, Immunologic Memory, Radioisotope Dilution Technique, Transcription, Genetic, Yellow Fever, Yellow fever virus, CD8-Positive T-Lymphocytes, Lymphocyte Count, DNA Methylation, Gene Expression Profiling, Yellow Fever Vaccine, Epigenesis, Genetic, Cell Proliferation, Mice
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review