Turnover of naive- and memory-phenotype T cells.
Open accessAbstract
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)
- ORCID
- Tough, D F
- Venue
- The Journal of experimental medicine
- Publisher
- Rockefeller University Press
- Published
- 1994-04-01
- Volume
- 179
- Issue
- 4
- Pages
- 1127-1135
- ISSN
- 0022-1007 (ISSN-L)
- 1540-9538
- PMC
- PMC2191431
- 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
- green
- www.ncbi.nlm.nih.gov
- 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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