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CD4 T cell memory derived from young naive cells functions well into old age, but memory generated from aged naive cells functions poorly
Open accessAbstract
Age-related declines in immune function have an impact on both primary and memory responses. In this study, we have examined the ability of naive CD4 T cells from young and aged T cell receptor transgenic mice to establish functional memory. We found that memory cells generated from young CD4 T cells responded well to antigen, even a year after generation, whereas memory cells derived from CD4 T cells from aged mice responded poorly both ex vivo and in vivo . Memory cells generated from aged naive cells proliferate less, produce reduced levels of cytokines, and exhibit reduced cognate helper function, compared with memory cells generated by using young naive cells. These results indicate that it is the age of the naive T cell when it first encounters antigen, rather than the age when it reencounters antigen, that is critical for good memory CD4 T cell function.
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“For example, previous studies performed on classical CD4 T cell subsets described reduced proliferation, lower secretion of interleukin-2 (IL-2) cytokine (7, 8), and accumulation of metabolic defects (9), along with higher production of pro-inflammatory mediators (10).”
From Aging promotes reorganization of the CD4 T cell landscape toward extreme regulatory and effector phenotypes (2019) · cites this paper as [8]
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Cites
Two subsets of memory T lymphocytes with distinct homing potentials and effector functions
Sallusto, F., Lenig, D., Förster, R., Lipp, M., & Lanzavecchia, A. (1999) · Nature · doi:10.1038/44385 · Cited by 5,846
Effector and memory T-cell differentiation: implications for vaccine development
Kaech, S. M., Wherry, E. J., & Ahmed, R. (2002) · Nature Reviews Immunology · doi:10.1038/nri778 · Cited by 1,865
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
The aging immune system: primer and prospectus
Miller, R. A. (1996) · Science · doi:10.1126/science.273.5271.70 · Cited by 1,165
Karasuyama, H., & Melchers, F. (1988) · European Journal of Immunology · doi:10.1002/eji.1830180115 · Cited by 1,090
Kaye, J. G., Hsu, M.-L., Sauron, M.-E., Jameson, S. C., Gascoigne, N. R. J., & Hedrick, S. Μ. (1989) · Nature · doi:10.1038/341746a0 · Cited by 632
Rapid Turnover of T Lymphocytes in SIV-Infected Rhesus Macaques
Mohri, H., Bonhoeffer, S., Monard, S. P., Perelson, A. S., & Ho, D. D. (1998) · Science · doi:10.1126/science.279.5354.1223 · Cited by 368
Generation and in vivo persistence of polarized Th1 and Th2 memory cells
Swain, S. L. (1994) · Immunity · doi:10.1016/1074-7613(94)90044-2 · Cited by 270
Self-citationMurasko, D. M. (2002) · Experimental Gerontology · doi:10.1016/s0531-5565(01)00210-8 · Cited by 250
Antigen-independent changes in naive CD4 T cells with aging.
Linton, P. J., Haynes, L., Klinman, N. R., & Swain, S. L. (1996) · The Journal of Experimental Medicine · doi:10.1084/jem.184.5.1891 · Cited by 248
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Research works printed but not linked: 2
- Phair, J., Kauffman, A., Bjornson, A., Adams, L. & Linnemann, C. (1978) J. Lab. Clin. Med. 92, 822-828.309499
- Miller R. A. (1999) in Fundamental Immunology ed. Paul W. E. (Lippincott-Raven Publishers Philadelphia) pp. 947-966.
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Tian, L., Choi, S.-C., Lee, H., Murakami, Y., Qi, C.-F., Sengottuvelu, M., Voss, O., Krzewski, K., & Coligan, J. E. (2016) · Cell Death and Differentiation · doi:10.1038/cdd.2015.161 · Cited by 45
Harper, E. I., Sheedy, E. F., & Stack, M. S. (2018) · Cancers · doi:10.3390/cancers10070230 · Cited by 45
Pfister, G., & Savino, W. (2008) · NeuroImmunoModulation · doi:10.1159/000156477 · Cited by 44
Ventura, M. T., Scichilone, N., Gelardi, M., Patella, V., & Ridolo, E. (2015) · Expert Review of Clinical Immunology · doi:10.1586/1744666x.2015.1081564 · Cited by 44
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Frasca, D., Diaz, A., Romero, M., & Blomberg, B. B. (2016) · Clinical & Experimental Immunology · doi:10.1111/cei.12824 · Cited by 43
Social effects on age-related and sex-specific immune cell profiles in a wild mammal
van Lieshout, S. H. J., Badás, E. P., Mason, M. W. T., Newman, C., Buesching, C. D., Macdonald, D. W., & Dugdale, H. L. (2020) · Biology Letters · doi:10.1098/rsbl.2020.0234 · Cited by 46
Alterations in dendritic cell function in aged mice: potential implications for immunotherapy design
Paula, C. B., Motta, A., Schmitz, C. R., Nunes, C. P., de Souza, A. P. D., & Bonorino, C. (2008) · Biogerontology · doi:10.1007/s10522-008-9150-x · Cited by 43
Brahmakshatriya, V., Kuang, Y., Devarajan, P., Xia, J., Zhang, W., Vong, A. M., & Swain, S. L. (2017) · The Journal of Immunology · doi:10.4049/jimmunol.1601119 · Cited by 43
Self-citationNormal Aging and Its Role in Cancer MetastasisPreprint
Fane, M. E., & Weeraratna, A. T. (2019) · Cold Spring Harbor Perspectives in Medicine · doi:10.1101/cshperspect.a037341 · Cited by 42
Vaccination of older adults: Influenza, pneumococcal disease, herpes zoster, COVID-19 and beyond
Weinberger, B. (2021) · Immunity & Ageing · doi:10.1186/s12979-021-00249-6 · Cited by 44
Effects of Aging on the Adaptive Immune Response to Respiratory Virus Infections
Fulton, R. B., & Varga, S. M. (2009) · Aging Health · doi:10.2217/ahe.09.69 · Cited by 39
Memory B cells form in aged mice despite impaired affinity maturation and germinal center kinetics
Goenka, R., Scholz, J. L., Naradikian, M. S., & Cancro, M. P. (2014) · Experimental Gerontology · doi:10.1016/j.exger.2013.12.013 · Cited by 38
Fulton, R. B., Weiss, K. A., Pewe, L. L., Harty, J. T., & Varga, S. M. (2013) · Journal of Virology · doi:10.1128/jvi.02282-12 · Cited by 38
Tarjanyi, O., Boldizsar, F., Nemeth, P., Mikecz, K., & Glant, T. T. (2009) · Immunity & Ageing · doi:10.1186/1742-4933-6-8 · Cited by 32
“In addition, diminished expression of CD40L, another costimulatory molecule, by aged T cells may not provide sufficient help to B cells [15].”
BackgroundClinical issues in renal transplantation in the elderly
Hod, T., & Goldfarb‐Rumyantzev, A. S. (2014) · Clinical Transplantation · doi:10.1111/ctr.12481 · Cited by 37
Gelfand, E. W., Joetham, A., Cui, Z.-H., Balhorn, A., Takeda, K., Taube, C., & Dakhama, A. (2004) · The Journal of Immunology · doi:10.4049/jimmunol.173.2.1298 · Cited by 36
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Goldstein, D. R. (2010) · Virulence · doi:10.4161/viru.1.4.12009 · Cited by 35
Avelino‐Silva, V. I., Ho, Y.-L., Avelino‐Silva, T. J., & dos Santos, S. D. S. (2010) · Ageing Research Reviews · doi:10.1016/j.arr.2010.10.004 · Cited by 38
Mirza, N. N., Pollock, K., Hoelzinger, D. B., Dominguez, A. L., & Lustgarten, J. (2011) · Aging Cell · doi:10.1111/j.1474-9726.2011.00730.x · Cited by 35
Denecke, C., Bedi, D. S., Ge, X., Kim, I. K.-E., Jurisch, A., Weiland, A., Habicht, A., Li, X. C., & Tullius, S. G. (2010) · PLoS ONE · doi:10.1371/journal.pone.0009232 · Cited by 34
Castro, F., Leal, B., Denny, A., Bahar, R., Lampkin, S. R., Reddick, R. L., Lu, S., & Gravekamp, C. (2009) · British Journal of Cancer · doi:10.1038/sj.bjc.6605329 · Cited by 34
Age-Related Gene Alteration in Naïve and Memory T cells Using Precise Age-Tracking Model
Yang, X., Wang, X., Lei, L., Sun, L., Jiao, A., Zhu, K. Y., Xie, T., Liu, H., Zhang, X., Su, Y., et al. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2020.624380 · Cited by 36
Age-related Deficiencies in Antigen-Specific CD4 T cell Responses: Lessons from Mouse Models.
Haynes, L., & Lefebvre, J. S. (2011) · Europe PMC (PubMed Central) · Cited by 33
Self-citationAging impairs murine B cell differentiation and function in primary and secondary lymphoid tissues.
Frasca, D., & Blomberg, B. B. (2011) · Europe PMC (PubMed Central) · Cited by 31
Age-related defects in the cytoskeleton signaling pathways of CD4 T cells
Garcia, G. G., & Miller, R. A. (2009) · Ageing Research Reviews · doi:10.1016/j.arr.2009.11.003 · Cited by 32
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Jones, S. C., Clise-Dwyer, K., Huston, G. E., Dibble, J. P., Eaton, S. M., Haynes, L., & Swain, S. L. (2008) · The Journal of Immunology · doi:10.4049/jimmunol.180.7.4465 · Cited by 30
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Torrance, B. L., & Haynes, L. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.1006710 · Cited by 28
Self-citationEffect of polysaccharides from a Korean ginseng berry on the immunosenescence of aged mice
Kim, M., Yi, Y., Kim, J., Han, S. Y., Kim, S. H., Seo, D. B., Cho, J. Y., & Shin, S. S. (2017) · Journal of Ginseng Research · doi:10.1016/j.jgr.2017.04.014 · Cited by 30
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Сергеевна, М. Ю., Tereshchenko, V., Bogdanova, D. A., & Александрович, Р. С. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms242115653 · Cited by 28
Guzzetta, G., & Kirschner, D. E. (2013) · PLoS ONE · doi:10.1371/journal.pone.0060425 · Cited by 28
Zhou, X., Hopkins, J. W., Wang, C., Brahmakshatriya, V., Swain, S. L., Kuchel, G. A., Haynes, L., & McElhaney, J. E. (2016) · Oncotarget · doi:10.18632/oncotarget.10047 · Cited by 28
Self-citationChiu, B., Stolberg, V. R., Freeman, C. M., & Chensue, S. W. (2007) · American Journal Of Pathology · doi:10.2353/ajpath.2007.061122 · Cited by 27
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Speziali, E., Santiago, A. F., Fernandes, R. M., Vaz, N. M., Menezes, J. S., & Faria, A. M. C. (2009) · Cellular Immunology · doi:10.1016/j.cellimm.2009.01.010 · Cited by 27
Akinsoji, E. O., Goldhardt, R., & Galor, A. (2018) · Drugs & Aging · doi:10.1007/s40266-018-0545-3 · Cited by 27
Leng, J., Stout-Delgado, H. W., Kavita, U., Jacobs, A., Tang, J. T., Du, W., Tussey, L., & Goldstein, D. R. (2011) · Vaccine · doi:10.1016/j.vaccine.2011.08.027 · Cited by 26
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Vesosky, B., Flaherty, D. K., Rottinghaus, E. K., Beamer, G., & Turner, J. (2006) · Experimental Gerontology · doi:10.1016/j.exger.2006.08.006 · Cited by 24
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Álvarez‐Luquín, D. D., Guevara‐Salinas, A., Arce-Sillas, A., Espinosa-Cárdenas, R., Leyva-Hernández, J., Montes-Moratilla, E. U., & Adalid-Peralta, L. V. (2021) · Journal of Translational Medicine · doi:10.1186/s12967-021-03055-2 · Cited by 18
Li, Q., Ren, W., Yuan, J., Guo, H., Shang, Y., Wang, W., Pan, J., Gao, M., & Pang, Y. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.904308 · Cited by 17
Kugler‐Umana, O., Zhang, W., Kuang, Y., Liang, J., Castonguay, C. H., Tonkonogy, S. L., Marshak‐Rothstein, A., Devarajan, P., & Swain, S. L. (2022) · Aging Cell · doi:10.1111/acel.13705 · Cited by 16
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Torrance, B. L., Cadar, A. N., Martin, D. E., Panier, H. A., Lorenzo, E. C., Bartley, J. M., Xu, M., & Haynes, L. (2023) · Frontiers in Aging · doi:10.3389/fragi.2023.1212750 · Cited by 20
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Luo, L., Lechuga‐Vieco, A. V., Sattentau, C., Borsa, M., & Simon, A. K. (2025) · EMBO Reports · doi:10.1038/s44319-025-00536-z · Cited by 14
Perkey, E., Miller, R. A., & Garcia, G. G. (2012) · The Journal of Immunology · doi:10.4049/jimmunol.1200487 · Cited by 14
Booth, J. S., Goldberg, E., Patil, S. A., Barnes, R. S., Greenwald, B. D., & Sztein, M. B. (2021) · Immunity & Ageing · doi:10.1186/s12979-021-00227-y · Cited by 14
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Taylor, J. R., Reynolds, L. M., Hou, L., Lohman, K., Cui, W., Kritchevsky, S. B., McCall, C. E., & Liu, Y. (2017) · Immunity & Ageing · doi:10.1186/s12979-017-0092-5 · Cited by 17
Klein, J., Brito, A. F., Trubin, P. A., Lu, P., Wong, P., Alpert, T., Peña-Hernández, M. A., Haynes, W. A., Kamath, K., Liu, F., et al. (2021) · The Journal of Infectious Diseases · doi:10.1093/infdis/jiab553 · Cited by 16
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Cookenham, T. S., Lanzer, K. G., Tighe, M., Ward, J. M., Reiley, W. W., & Blackman, M. A. (2021) · ImmunoHorizons · doi:10.4049/immunohorizons.2100032 · Cited by 11
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Rounis, K., Makrakis, D., Gioulbasanis, I., Ekman, S., Petris, L. D., Mavroudis, D., & Agelaki, S. (2022) · Life · doi:10.3390/life12060880 · Cited by 11
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Hakim, F. T., & Gress, R. E. (2005) · Expert Review of Clinical Immunology · doi:10.1586/1744666x.1.3.443 · Cited by 11
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Buckley, D. J., Sharma, S., Joseph, B., Fayyaz, A. H., Canizales, A., Terrebonne, K. J., & Trott, D. W. (2023) · GeroScience · doi:10.1007/s11357-023-00853-y · Cited by 9
Litjens, N. H. R., van der List, A. C. J., Klepper, M., Reijerkerk, D., Prevoo, F., & Betjes, M. G. H. (2024) · Frontiers in Immunology · doi:10.3389/fimmu.2024.1406716 · Cited by 9
Jaishwal, P., Jha, K., & Singh, S. P. (2024) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2024.134012 · Cited by 10
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Kugler‐Umana, O., Devarajan, P., & Swain, S. L. (2020) · Critical Reviews in Immunology · doi:10.1615/critrevimmunol.2020034934 · Cited by 10
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Haussig, J. M., burgold, J., Hafalla, J. C. R., Matuschewski, K., & Kooij, T. W. A. (2014) · Parasite Immunology · doi:10.1111/pim.12104 · Cited by 7
Broadway, R., Patel, N. M., Hillier, L. E., El-briri, A., Korneva, Y. S., Zinovkin, D. A., & Pranjol, M. Z. I. (2021) · Life · doi:10.3390/life11080788 · Cited by 5
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Kim, K.-H. (2009) · Journal of Ginseng Research · doi:10.5142/jgr.2009.33.3.177 · Cited by 6
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Miroshnichenko, M. I., Kolpakov, F., & Akberdin, I. R. (2025) · Viruses · doi:10.3390/v17050589 · Cited by 7
Ho, V., Low, H. B., Cui, J., Juequn, Z., Shunmuganathan, B. D. O., Gupta, R., Tan, N. Y. J., Qian, X., Purushotorman, K., SCOPE Cohort Study Group, et al. (2024) · Aging Cell · doi:10.1111/acel.14099 · Cited by 4
Multiple characteristic alterations and available therapeutic strategies of cellular senescence
Zhao, Y., Li, H., Guo, Q., & Hui, H. (2023) · Journal of Zhejiang University SCIENCE B · doi:10.1631/jzus.b2200178 · Cited by 5
Pflumm, D., Seidel, A., Klein, F. A. C., Groß, R. M., Krutzke, L., Kochanek, S., Kroschel, J., Münch, J., Stifter, K., & Schirmbeck, R. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1231274 · Cited by 5
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Metadata
- Authors
- Haynes, L., Eaton, S. M., Burns, E. M., Randall, T. D., & Swain, S. L.
- Affiliations
- Trudeau Institute (US)
- Venue
- Proceedings of the National Academy of Sciences
- Publisher
- National Academy of Sciences
- Published
- 2003-12
- Volume
- 100
- Issue
- 25
- Pages
- 15053-15058
- ISSN
- 0027-8424 (ISSN-L)
- 1091-6490
- PMC
- PMC299903
- OpenAlex
- W2091101346
- Cited by
- 270
- References
- 33
- Citations by year
- 2026: 7 · 2025: 6 · 2024: 5 · 2023: 10 · 2022: 9 · 2021: 27 · 2020: 11 · 2019: 14 · 2018: 12 · 2017: 14 · 2016: 10 · 2015: 7 · 2014: 9 · 2013: 22 · 2012: 9
- FWCI
- 2.80
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Proceedings of the National Academy of Sciences (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Institute on Aging (P01AG021600, P01AG001743, R01AG021054, AG21054, AG-01743)
- Topics
- Life Sciences › Immunology and Microbiology › Immunology › T-cell and B-cell Immunology
- Life Sciences › Immunology and Microbiology › Immunology › Immunotherapy and Immune Responses
- Life Sciences › Immunology and Microbiology › Immunology › Immune responses and vaccinations
- Keywords
- CD4+ T cell memory, naive T cells, immunosenescence, aging, T cell receptor transgenic mice, cytokine production, T cell proliferation, helper functions
- MeSH terms
- Aging, Animals, Cell Line, Cell Separation, Flow Cytometry, Immunologic Memory, Interferon-gamma, Interleukin-2, Lymphocytes, Mice, Transgenic, Microscopy, Fluorescence, Phenotype, CD4-Positive T-Lymphocytes, Interleukin-4, Interleukin-5, Cytokines, Cell Culture Techniques, Mice
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