Sparse production but preferential incorporation of recently produced naive T cells in the human peripheral pool.

N. Vrisekoop, I. den Braber, A.B. de Boer, A.F.C. Ruiter, M.T. Ackermans, S.N. van der Crabben, E.H.R. Schrijver, G.Th. Spierenburg, H.P. Sauerwein, M.D. Hazenberg, R.J. de Boer, F. Miedema, J.A.M. Borghans, K. Tesselaar

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Abstract

In mice, recent thymic emigrants (RTEs) make up a large part of the naïve T cell pool and have been suggested to be a distinct short-lived pool. In humans, however, the life span and number of RTEs are unknown. Although 2H2O labeling in young mice showed high thymic-dependent daily naïve T cell production, long term up- and down-labeling with 2H2O in human adults revealed a low daily production of naïve T cells. Using mathematical modeling, we estimated human naïve CD4 and CD8 T cell half-lives of 4.2 and 6.5 years, respectively, whereas memory CD4 and CD8 T cells had half-lives of 0.4 and 0.7 year. The estimated half-life of recently produced naïve T cells was much longer than these average half-lives. Thus, our data are incompatible with a substantial short-lived RTE population in human adults and suggest that the few naïve T cells that are newly produced are preferentially incorporated in the peripheral pool.

Original languageEnglish
Pages (from-to)6115-6120
Number of pages6
JournalProceedings of the National Academy of Sciences of the United States of America
Volume105
Issue number16
DOIs
Publication statusPublished - 2008

Keywords

  • Life sciences
  • Biomathematics and biometrics

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