Cited by 869T-cell and B-cell ImmunologyImmunotherapy and Immune ResponsesPsoriasis: Treatment and Pathogenesis

Turnover of naive- and memory-phenotype T cells.

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Tough, D F, Sprent, J·1994·The Journal of experimental medicine

Abstract

On the basis of their surface markers, T lymphocytes are divided into subsets of "naive" and "memory cells". We have defined the interrelationship and relative life spans of naive and memory T cells by examining the surface markers on murine T cells incorporating bromodeoxyuridine, a DNA precursor, given in the drinking water. Three findings are reported. First, using a new method we show that the release of newly formed naive T cells from the unmanipulated thymus is very low (confirming the findings of others with surgical approaches). Second, in thymectomized mice, T cells with a naive phenotype remain in interphase for prolonged periods; however, some of these cells divide and retain (or regain) their "naive" markers. Third, most T cells with a memory phenotype divide rapidly, but others remain in interphase for many weeks. Collectively, the data indicate that long-lived T cells have multiple phenotypes and contain a mixture of memory cells, naive (virgin) cells, and memory cells masquerading as naive cells.

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  • Naive T cells have a very long intermitotic half-life, with estimates for humans of approximately 3.5 years.

    “For example, naive T cells have a very long intermitotic half-life, with estimates for humans of approximately 3.5 years [45, 46].”

    From Clinical use of lentiviral vectors (2018) · cites this paper as [46]

    The introductory passage says that human CD45RA-high T cells can remain in interphase for years, supporting the claim of slow turnover. It does not give an intermitotic half-life or the specific estimate of approximately 3.5 years. The passage has no page label in our copy. (LLM, conf=0.86)

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References 41 · Cited by 869

Authors
Tough, D. F., & Sprent, J.
Affiliations
Scripps Research Institute (US)
Venue
The Journal of experimental medicine
Published
1994-04-01
Volume
179
Issue
4
Pages
1127-1135
ISSN
  • 0022-1007 (ISSN-L)
  • 1540-9538
OpenAlex
W2006981670
Cited by
869
References
41
Citations by year
2026: 3 · 2025: 2 · 2024: 4 · 2023: 2 · 2022: 6 · 2021: 7 · 2020: 6 · 2019: 9 · 2018: 13 · 2017: 8 · 2016: 12 · 2015: 14 · 2014: 10 · 2013: 19 · 2012: 22
FWCI
15.64
Type
journal article
Language
en
Open access
Licence
cc-by-nc-sa
Locations
  • The Journal of Experimental Medicine (publishedVersion)
  • PubMed Central (publishedVersion, cc-by-nc-sa)
  • PubMed (publishedVersion)
Funders
  • National Institutes of Health (5r01ai021487-20, 5p01ca025803-20)
  • National Cancer Institute (CA 38355, CA-25803)
  • National Institute of Allergy and Infectious Diseases (AI 21487)
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 › Psoriasis: Treatment and Pathogenesis
Keywords
naive T cells, memory T cells, T cell turnover, thymus, thymectomy, bromodeoxyuridine incorporation, T-cell markers, T cell division, T cell subsets
MeSH terms
Administration, Oral, Animals, Bromodeoxyuridine, Cell Division, Cell Line, Flow Cytometry, Immunologic Memory, Male, Mice, Inbred BALB C, Phenotype, Spleen, Thymectomy, Thymus Gland, T-Lymphocyte Subsets, Mice, SCID, Mice

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