The DOI matches its Crossref record; 47 of the 47 references it cites were found in a registry or an index.
Age-associated increase in lifespan of naive CD4 T cells contributes to T-cell homeostasis but facilitates development of functional defects
Open accessAbstract
With age, T-cell generation from the thymus is much reduced, yet a substantial naïve T-cell pool is maintained even in aged animals, suggesting that naïve T cells either persist longer or turn over faster to maintain T-cell homeostasis. We found that with age, naïve CD4 T cells became progressively longer-lived. Their longer lifespan did not depend on recognition of self-peptide/class II. Newly generated naïve T cells derived from aged stem cells had a shorter lifespan, like that of young naïve T cells. Conversely, naïve CD4 T cells derived from middle-aged thymectomized mice were longer-lived in vivo, and their development of functional defects was accelerated. These observations suggest that naïve T cells develop their longer lifespan during their sojourn in the periphery. Increased longevity of naïve CD4 T cells correlated well with reduced expression of proapoptotic molecule Bim. We suggest that the intrinsic increase in longevity helps maintain naïve T-cell homeostasis but facilitates the development of functional defects in mice.
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In the citing paper
“With aging, the naïve subset shrinks along with the accumulation of highly differentiated memory cells, which often show dysregulated properties (5, 6).”
From Aging promotes reorganization of the CD4 T cell landscape toward extreme regulatory and effector phenotypes (2019) · cites this paper as [6]
In the citing paper
“Age-associated functional changes in naive murine T cells are not a consequence of replication—they at most divide once throughout life—but are a corollary of cellular longevity that even increases after thymectomy or in aged mice”
From Successful and Maladaptive T Cell Aging (2017) · cites this paper as Tsukamoto et al., 2009
Citations
Cites
Senescent cells, tumor suppression, and organismal aging: good citizens, bad neighbors
Campisi, J. (2005) · Cell · doi:10.1016/j.cell.2005.02.003 · Cited by 2,379
Changes in thymic function with age and during the treatment of HIV infection
Douek, D. C., McFarland, R. D., Keiser, P. H., Gage, E. A., Massey, J. M., Haynes, B. F., Polis, M. A., Haase, A. T., Feinberg, M. B., Sullivan#, J. L., et al. (1998) · Nature · doi:10.1038/25374 · Cited by 1,893
Bouillet, P., Metcalf, D., Huang, D. C. S., Tarlinton, D. M., Kay, T. W. H., Köntgen, F., Adams, J. M., & Strasser, A. (1999) · Science · doi:10.1126/science.286.5445.1735 · Cited by 1,504
ER Stress Triggers Apoptosis by Activating BH3-Only Protein Bim
Puthalakath, H., O’Reilly, L. A., Gunn, P., Lee, L., Kelly, P. N., Huntington, N. D., Hughes, P., Michalak, E. M., McKimm‐Breschkin, J. L., Motoyama, N., et al. (2007) · Cell · doi:10.1016/j.cell.2007.04.027 · Cited by 1,493
Green, D. R., & Evan, G. I. (2002) · Cancer Cell · doi:10.1016/s1535-6108(02)00024-7 · Cited by 1,254
Age-related changes in lymphocyte development and function
Linton, P. J., & Dorshkind, K. A. (2004) · Nature Immunology · doi:10.1038/ni1033 · Cited by 1,199
Age-Associated Characteristics of Murine Hematopoietic Stem Cells
Sudo, K., Ema, H., Morita, Y., & Nakauchi, H. (2000) · The Journal of Experimental Medicine · doi:10.1084/jem.192.9.1273 · Cited by 722
Maintaining the norm: T-cell homeostasis
Jameson, S. C. (2002) · Nature reviews. Immunology · doi:10.1038/nri853 · Cited by 597
Activated T Cell Death In Vivo Mediated by Proapoptotic Bcl-2 Family Member Bim
Hildeman, D. A., Zhu, Y., Mitchell, T. C., Bouillet, P., Strasser, A., Kappler, J. W., & Marrack, P. (2002) · Immunity · doi:10.1016/s1074-7613(02)00322-9 · Cited by 567
Cancer burden in the aged: an epidemiologic and demographic overview.
Yancik, R. (1997) · PubMed · Cited by 558
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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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Zhang, H., Okuyama, H., Jain, A. K., Jadhav, R. R., Wu, B., Sturmlechner, I., Morales, J., Ohtsuki, S., Weyand, C. M., & Goronzy, J. J. (2024) · JCI Insight · doi:10.1172/jci.insight.172848 · Cited by 8
Quantifying cellular dynamics in mice using a novel fluorescent division reporter system
Lukas, E., Hogan, T. V., Williams, C., Seddon, B. P., & Yates, A. J. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1157705 · Cited by 7
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Min, H.-J., Park, J. S., Yang, J., Yang, J., Oh, S. W., Jo, S., Cho, W.-Y., Gwon, J. G., Jung, C. W., Seol, Y., et al. (2022) · Kidney Research and Clinical Practice · doi:10.23876/j.krcp.21.097 · Cited by 7
“static proliferation of naïve T cells in thymectomized mice [19], as well as reduced T cell priming upon vaccination in ESKD patients [20], suggest that chronic inflammation is closely linked to both quantitative and qualitative defect of T cell immunity.”
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Thomas‐Vaslin, V., Six, A., Pham, H., Dansokho, C., Chaara, W., Gouritin, B., Bellier, B., & Klatzm, D. (2012) · InTech eBooks · doi:10.5772/29549 · Cited by 7
Integration of immunity with physical and cognitive function in definitions of successful aging.
Griffin, P. C., Michel, J. J., Huysman, K., Logar, A., & Vallejo, A. N. (2012) · Europe PMC (PubMed Central) · Cited by 7
Leposavić, G., Nanut, M. P., Pilipović, I., Kosec, D. J., Arsenović-Ranin, N., Stojić-Vukanić, Z., Djikić, J., & Nacka-Aleksić, M. (2013) · Immunobiology · doi:10.1016/j.imbio.2013.08.004 · Cited by 7
Rane, S., Das, R., Ranganathan, V., Prabhu, S. B., Das, A., Mattoo, H., Durdik, J. M., George, A., Rath, S., & Bal, V. (2014) · BMC Biology · doi:10.1186/s12915-014-0106-0 · Cited by 6
“As thymic output decreases with age, naïve T cells in the periphery appear to be longer-lived [16-18,31], and the average peripheral residence time of naïve T cells is greater in aged than in young individuals [32,33].”
BackgroundInfluentialShytikov, D. W. (2015) · American Journal of BioScience · doi:10.11648/j.ajbio.20150302.14 · Cited by 6
“Aged naive T-cells also have defects in their proliferation and activation [4].”
BackgroundDeng, H., Mao, G., Zhang, J., Wang, Z., & Li, D.-D. (2010) · Molecular Immunology · doi:10.1016/j.molimm.2010.07.015 · Cited by 5
Nauman, G., Danzl, N. M., Lee, J., Borsotti, C., Madley, R., Fu, J., Hölzl, M. A., Dahmani, A., Dorronsoro, A., Chavez, É., et al. (2022) · The Journal of Immunology · doi:10.4049/jimmunol.2100966 · Cited by 5
Isotopic Composition of Water as a Factor of Human Longevity
Ignatov, I., Mosin, O., & Velikov, B. (2015) · Journal of Medicine, Physiology and Biophysics · Cited by 5
Arsenović-Ranin, N., Kosec, D. J., Pilipović, I., Bufan, B., Stojić-Vukanić, Z., Radojević, K., Nacka-Aleksić, M., & Leposavić, G. (2014) · NeuroImmunoModulation · doi:10.1159/000355349 · Cited by 5
Balyan, R., Gund, R., Chawla, A. S., Khare, S., Pradhan, S. J., Rane, S., Galande, S., Durdik, J. M., George, A., Bal, V., et al. (2018) · Immunology · doi:10.1111/imm.13036 · Cited by 5
Kouamou, V., Gundidza, P., Ndhlovu, C. E., Makadzange, T., CryptoART Study Team, Chivige, E., Makaha, E., Mwarumba, T., Ross, C., Vallabhaneni, S., et al. (2023) · AIDS Research and Human Retroviruses · doi:10.1089/aid.2022.0117 · Cited by 4
Dai, Y., Lin, S., Wu, J., Yang, S., Yang, L., Wang, X., Li, J., Zhao, L., Chen, D., Zhang, B., et al. (2025) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-025-02489-0 · Cited by 3
The host immune response to Mycobacterium tuberculosis determining protection or disease progression
Saraiva, M., Branchett, W. J., Rengarajan, J., & O’Garra, A. (2026) · Nature Immunology · doi:10.1038/s41590-026-02529-z · Cited by 4
Advances in T Cell-Based Cancer Immunotherapy: From Fundamental Mechanisms to Clinical Prospects
Zhang, K., Zhang, Y., Pan, X., Wang, Y., Li, Y., Jiang, S., Zhang, Y., Chen, M., Su, W., Li, X., et al. (2025) · Molecular Pharmaceutics · doi:10.1021/acs.molpharmaceut.4c01502 · Cited by 3
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Carvalho, T. L., & Coutinho, A. (2013) · European Journal of Immunology · doi:10.1002/eji.201344029 · Cited by 3
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Hu, C., Wu, H., Zhu, Q., Cao, N., & Wang, H. (2023) · The FASEB Journal · doi:10.1096/fj.202300515r · Cited by 3
Ignatov, I., Mosin, O., & Velikov, B. (2015) · Journals & Books Hosting (International Knowledge Sharing Platform) · Cited by 3
Swain, S. L., Kugler‐Umana, O., & Tonkonogy, S. L. (2021) · Frontiers in Aging · doi:10.3389/fragi.2021.701900 · Cited by 3
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Markova, E. V., Sorokin, О. V., Гольдина, И. А., Владимирович, С. И., Knyazheva, M. A., Serenko, E. V., Bakulin, К. А., Владимирович, М. А., & Vector-BiAlgam JSC (Koltsovo settlement, N. R. (2021) · JOURNAL of SIBERIAN MEDICAL SCIENCES · doi:10.31549/2542-1174-2021-1-41-54 · Cited by 3
Rodríguez-Castañón, J. M., Mcnaughton, A., Cárdenas-Ochoa, A., Fuentes-Romero, L. L., Viveros-Rogel, M., Vergara‐Mendoza, M., Tello-Mercado, A. C., Leal-Gutiérrez, G., Romero-Carvajal, J. J., Cázares-Lara, J., et al. (2021) · AIDS Research and Human Retroviruses · doi:10.1089/aid.2020.0270 · Cited by 2
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Gao, Y., Pei, X.-Y., Jin, R., Chen, Y., Shen, H., Sun, X., Ge, Q., & Zhang, Y. (2014) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2014.10.037 · Cited by 2
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Lauer, V. (2013) · Cited by 2
Desta, A. A., Kidane, K. M., Bahta, Y. W., Ajemu, K. F., Woldegebriel, A. G., Berhe, A. A., Bezabih, N. M., Berhe, A., & Woldearegay, T. W. (2020) · BMJ Open · doi:10.1136/bmjopen-2020-038741 · Cited by 2
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Oh, S.-H., Kim, Y. W., Kim, S. H., & Chang, S.-Y. (2026) · Immune Network · doi:10.4110/in.2026.26.e15 · Cited by 2
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Ignatov, I., Mosin, O., & Velikov, B. (2015) · Journal of Health, Medicine and Nursing · Cited by 1
[A case report of rare bardet-biedl syndrome].
Cheng, S.-Q., Cao, Y.-H., Zhang, J.-S., & Qiang, H. (2013) · PubMed · Cited by 1
Ujeneza, E. L., Ndifon, W. O., Sawry, S., Fatti, G., Riou, J., Davies, M., & Nieuwoudt, M. (2021) · eLife · doi:10.7554/elife.42390 · Cited by 1
Uzenbaeva, L. B., Кижина, А. Г., Калинина, С. Н., Хижкин, Е. А., Ilyukha, V. A., Печорина, Э. Ф., & Fokina, V. O. (2021) · Advances in Gerontology · doi:10.1134/s2079057021020156 · Cited by 1
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BackgroundStojić-Vukanić, Z., Pilipović, I., Arsenović-Ranin, N., Dimitrijević, M., & Leposavić, G. (2021) · Immunology Letters · doi:10.1016/j.imlet.2021.08.003 · Cited by 1
Bolner, M. L. (2015) · Digital Commons-TMC (Texas Medical Center) · Cited by 1
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Bains, I. (2010) · UCL Discovery (University College London) · Cited by 1
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Zook, E. C. (2012) · Loyola eCommons (Loyola University of Chicago)
Hanania, N. A., & Busse, P. J. (2015) · Springer eBooks · doi:10.1007/978-3-319-23246-1_14
Heterochronic Parabiosis Studies of the Aging Immune System
Davies, J. (2016) · UA Campus Repository (The University of Arizona)
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Coder, B. (2015) · Digital Commons @ UNT Health Science Center
The Rejuvenation of the Immune System: Physiological, Cellular, and Molecular Mechanisms
Pishel, I., & Gm, B. (2016) · InTech eBooks · doi:10.5772/64046
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Raynor, J. L. (2014) · OhioLink ETD Center (Ohio Library and Information Network)
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Ecker, S., Chen, L., Pancaldi, V., Bagger, F. O., Fernández, J. M., Pau, S., Juan, D., Mann, A., Watt, S., Casale, F. P., et al. (2016)
Ismail, M. M. (2017) · American Journal of Immunology · doi:10.3844/ajisp.2017.233.252
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Seddon, B. P., Rane, S., & Yates, A. J. (2021) · Springer eBooks · doi:10.1007/978-3-030-57204-4_3
Shi, Z., Li, Y., & Jaberi‐Douraki, M. (2021) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1009413
Accumulation of Treg cells is detrimental in late-onset (aged) mouse model of multiple sclerosisPreprint
Wang, W., Thomas, R. G., Oh, J., & Su, D. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.12.16.472986
Xie, Y., Sun, J., Li, W., Jiang, H., Hu, C., Yang, J., Huang, Y., Ruan, B., & Zhu, B. (2021) · Figshare · doi:10.6084/m9.figshare.13532077
Morimoto, M., Tanaka, S., Jinguji, K., & Ikeda‐Ohtsubo, W. (2025) · Scientific Reports · doi:10.1038/s41598-025-16730-x
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McDaniel, J. M. (2012) · Digital Commons - University of South Florida (University of South Florida)
Xie, Y., Sun, J., Wei, L., Jiang, H., Hu, C., 杨介钻, Huang, Y., Ruan, B., & Zhu, B. (2021) · Figshare · doi:10.6084/m9.figshare.13532074
Xie, Y., Sun, J., Wei, L., Jiang, H., Hu, C., 杨介钻, Huang, Y., Ruan, B., & Zhu, B. (2021) · Figshare · doi:10.6084/m9.figshare.13532068
Xie, Y., Sun, J., Wei, L., Jiang, H., Hu, C., 杨介钻, Huang, Y., Ruan, B., & Zhu, B. (2021) · Figshare · doi:10.6084/m9.figshare.13532062
Xie, Y., Sun, J., Wei, L., Jiang, H., Hu, C., 杨介钻, Huang, Y., Ruan, B., & Zhu, B. (2021) · Figshare · doi:10.6084/m9.figshare.13532071
Xie, Y., Sun, J., Wei, L., Jiang, H., Hu, C., 杨介钻, Huang, Y., Ruan, B., & Zhu, B. (2021) · Figshare · doi:10.6084/m9.figshare.13532065
Chen, J., Titanji, K., Sheth, A. N., Gandhi, R. T., McMahon, D., Ofotokun, I., Weitzmann, M. N., Paris, K. D., & Dumond, J. B. (2022) · Figshare · doi:10.6084/m9.figshare.17799803
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Iwasa, Y., Hayashi, R., Hara, A., & Matsuo, K. (2026) · Bulletin of Mathematical Biology · doi:10.1007/s11538-025-01569-0
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Wang, B., Ji, L., & Bian, Q. (2026) · Science Advances · doi:10.1126/sciadv.aeg1622
Zhao, L., Zhang, X., Ren, Q., Song, X., Zhao, M., Wang, R., Du, H., Chen, Y., Xu, P., Liu, J., et al. (2026) · Advanced Science · doi:10.1002/advs.78123
Radiation and Immunity in the Context of Cytomegalovirus and Aging
Pugh, J. L. (2013) · UA Campus Repository (The University of Arizona)
Metadata
- Authors
- Tsukamoto, H., Clise-Dwyer, K., Huston, G. E., Duso, D. K., Buck, A. L., Johnson, L. L., Haynes, L., & Swain, S. L.
- Affiliations
- Trudeau Institute (US)
- Venue
- Proceedings of the National Academy of Sciences
- Publisher
- National Academy of Sciences
- Published
- 2009-10-27
- Volume
- 106
- Issue
- 43
- Pages
- 18333-18338
- ISSN
- 0027-8424 (ISSN-L)
- 1091-6490
- PMC
- PMC2759371
- OpenAlex
- W2137105060
- Cited by
- 166
- References
- 47
- Citations by year
- 2026: 7 · 2025: 7 · 2024: 4 · 2023: 7 · 2022: 9 · 2021: 21 · 2020: 8 · 2019: 2 · 2018: 7 · 2017: 14 · 2016: 9 · 2015: 15 · 2014: 16 · 2013: 12 · 2012: 11
- FWCI
- 4.03
- 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 Institutes of Health (AG021600)
- National Institute on Aging (P01AG021600, R37AG025805, AG021600, AG025805)
- Topics
- Life Sciences › Immunology and Microbiology › Immunology › T-cell and B-cell Immunology
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Aging › Genetics, Aging, and Longevity in Model Organisms
- Health Sciences › Medicine › Hematology › Hematopoietic Stem Cell Transplantation
- Keywords
- naive CD4+ T cells, T cell lifespan, aging, T cell homeostasis, thymic output, thymectomy, building information modeling, apoptosis, periphery
- MeSH terms
- Bcl-2-Like Protein 11, Aging, Animals, Cell Survival, Histocompatibility Antigens, Homeostasis, Immunity, Innate, Membrane Proteins, Proto-Oncogene Proteins, Receptors, Antigen, T-Cell, T-Lymphocytes, Thymectomy, Signal Transduction, CD4-Positive T-Lymphocytes, Apoptosis Regulatory Proteins, Mice
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