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Lineage relationship and protective immunity of memory CD8 T cell subsets
Abstract
Memory CD8 T cells can be divided into two subsets, central (T(CM)) and effector (T(EM)), but their lineage relationships and their ability to persist and confer protective immunity are not well understood. Our results show that T(CM) have a greater capacity than T(EM) to persist in vivo and are more efficient in mediating protective immunity because of their increased proliferative potential. We also demonstrate that, following antigen clearance, T(EM) convert to T(CM) and that the duration of this differentiation is programmed within the first week after immunization. We propose that T(CM) and T(EM) do not necessarily represent distinct subsets, but are part of a continuum in a linear naive --> effector --> T(EM) --> T(CM) differentiation pathway.
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“the central memory (CM) or effector memory (EM) differentiation states of CD4+ and CD8+ T cells have implications for durability, recirculation, tissue access, and responses upon antigen re-exposure (Kaech et al., 2002; Martin and Badovinac, 2018; Wherry 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 Wherry et al., 2003
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Cites
Dendritic cells and the control of immunity
Banchereau, J., & Steinman, R. M. (1998) · Nature · doi:10.1038/32588 · Cited by 14,496
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
Viral Immune Evasion Due to Persistence of Activated T Cells Without Effector Function
Zajac, A. J., Blattman, J. N., Murali-Krishna, K., Sourdive, D. J. D., Suresh, M., Altman, J. D., & Ahmed, R. (1998) · The Journal of Experimental Medicine · doi:10.1084/jem.188.12.2205 · Cited by 1,978
Self-citationPreferential Localization of Effector Memory Cells in Nonlymphoid Tissue
Masopust, D., Vezys, V., Marzo, A. L., & Lefrançois, L. (2001) · Science · doi:10.1126/science.1058867 · Cited by 1,952
Self-citationCounting Antigen-Specific CD8 T Cells: A Reevaluation of Bystander Activation during Viral Infection
Murali‐Krishna, K., Altman, J. D., Suresh, M., Sourdive, D. J. D., Zajac, A. J., Miller, J. D., Slansky, J. E., & Ahmed, R. (1998) · Immunity · doi:10.1016/s1074-7613(00)80470-7 · Cited by 1,918
Self-citationEffector 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
Self-citationImmunological 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-citationInterleukin-7 mediates the homeostasis of naïve and memory CD8 T cells in vivo
Schluns, K. S., Kieper, W. C., Jameson, S. C., & Lefrançois, L. (2000) · Nature Immunology · doi:10.1038/80868 · Cited by 1,619
Memory CD8+ T cells vary in differentiation phenotype in different persistent virus infections
Appay, V., Dunbar, P. R., Callan, M. F. C., Klenerman, P., Gillespie, G. M. A., Papagno, L., Ogg, G. S., King, A., Lechner, F., Spina, C. A., et al. (2002) · Nature Medicine · doi:10.1038/nm0402-379 · Cited by 1,556
Phenotypic and functional separation of memory and effector human CD8+ T cells
Hamann, D., Baars, P. A., Rep, M. H. G., Hooibrink, B., Kerkhof-Garde, S. R., Klein, M. R., & Lier, R. A. W. V. (1997) · The Journal of Experimental Medicine · doi:10.1084/jem.186.9.1407 · Cited by 1,366
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Song, K., Rabin, R. L., Hill, B. J., Rosa, S. C. D., Perfetto, S. P., Zhang, H. H., Foley, J. F., Reiner, J. S., Liu, J., Mattapallil, J. J., et al. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0409720102 · Cited by 92
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van Lint, A. L., Kleinert, L., Clarke, S. R. M., Stock, A. T., Heath, W. R., & Carbone, F. (2005) · Journal of Virology · doi:10.1128/jvi.79.23.14843-14851.2005 · Cited by 78
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Martin, D. L., & Tarleton, R. L. (2005) · The Journal of Immunology · doi:10.4049/jimmunol.174.3.1594 · Cited by 77
Iancu, E. M., Corthésy, P., Baumgaertner, P., Devêvre, E., Voelter, V., Romero, P. J., Speiser, D. E., & Rufer, N. (2009) · The Journal of Immunology · doi:10.4049/jimmunol.0803647 · Cited by 76
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Tewari, K., Nakayama, Y., & Suresh, M. (2007) · The Journal of Immunology · doi:10.4049/jimmunol.179.4.2115 · Cited by 75
Ramos, H. J., Davis, A. M., Cole, A. G., Schatzle, J. D., Forman, J., & Farrar, J. D. (2009) · Blood · doi:10.1182/blood-2008-11-188458 · Cited by 75
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Bedognetti, D., Wang, E., Sertoli, M. R., & Marincola, F. M. (2010) · Expert Review of Vaccines · doi:10.1586/erv.10.55 · Cited by 75
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del Amo, P. C., Lahoz-Beneytez, J., Boelen, L., Ahmed, R., Miners, K. L., Zhang, Y., Roger, L., Jones, R. E., Marraco, S. A. F., Speiser, D. E., et al. (2018) · PLoS Biology · doi:10.1371/journal.pbio.2005523 · Cited by 76
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Moniuszko, M., Fry, T., Tsai, W.-P., Morre, M., Assouline, B., Cortez, P., Lewis, M. G., Cairns, S., Mackall, C., & Franchini, G. (2004) · Journal of Virology · doi:10.1128/jvi.78.18.9740-9749.2004 · Cited by 74
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Redeker, A., Welten, S. P. M., & Arens, R. (2013) · European Journal of Immunology · doi:10.1002/eji.201343946 · Cited by 74
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Li, W., Jing, Z., Wang, S., Li, Q., Xing, Y., Shi, H., Li, S., & Hong, Z. (2021) · Biomaterials · doi:10.1016/j.biomaterials.2021.120726 · Cited by 74
Jia, Q., Zhou, J., Chen, G., Shi, Y., Yu, H., Guan, P. F., Lin, R., Jiang, N. J., Yu, P.-W., Li, Q.-J., et al. (2015) · OncoImmunology · doi:10.1080/2162402x.2014.1001230 · Cited by 73
Metadata
- Authors
- Wherry, E. J., Teichgräber, V., Becker, T. C., Masopust, D., Kaech, S. M., Antia, R., von Andrian, U. H., & Ahmed, R.
- Affiliations
- Emory University (US)
- Corresponding author
- Ahmed, Rafi
- Venue
- Nature Immunology
- Published
- 2003-02-03
- Volume
- 4
- Issue
- 3
- Pages
- 225-234
- ISSN
- 1529-2908 (ISSN-L)
- 1529-2916
- OpenAlex
- W2029128444
- Cited by
- 1,864
- References
- 57
- Citations by year
- 2026: 27 · 2025: 44 · 2024: 47 · 2023: 55 · 2022: 61 · 2021: 65 · 2020: 59 · 2019: 59 · 2018: 54 · 2017: 60 · 2016: 68 · 2015: 50 · 2014: 74 · 2013: 92 · 2012: 84
- FWCI
- 47.89
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- Locations
- Nature Immunology (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Institute of General Medical Sciences (T32GM008169)
- National Institute of Allergy and Infectious Diseases (AI44644, AI 30048)
- 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
- memory CD8+ T cells, central memory T cells, effector memory T cells, T cell lineage, T cell differentiation, T cell proliferation, protective immunity, antigen clearance, naive T cells, T cell persistence
- MeSH terms
- Animals, Cell Communication, Cell Division, Immunologic Memory, Listeriosis, Listeria monocytogenes, Lymphocytic Choriomeningitis, Lymphocytic choriomeningitis virus, Mice, Transgenic, CD8-Positive T-Lymphocytes, Cell Lineage, Mice
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