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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

Research output: Contribution to journal › Article › Academic › peer-review

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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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