Naïve and Memory CD4 + T Cell Survival Controlled by Clonal Abundance

Author:

Hataye Jason123,Moon James J.123,Khoruts Alexander123,Reilly Cavan123,Jenkins Marc K.123

Affiliation:

1. Department of Microbiology, Center for Immunology, University of Minnesota Medical School, Minneapolis, MN 55455, USA.

2. Department of Medicine, Center for Immunology, University of Minnesota Medical School, Minneapolis, MN 55455, USA.

3. Division of Biostatistics, University of Minnesota School of Public Health, Minneapolis, MN 55455, USA.

Abstract

Immunity to a plethora of microbes depends on a diverse repertoire of naïve lymphocytes and the production of long-lived memory cells. We present evidence here that low clonal abundance in a polyclonal repertoire favors the survival and activation of naïve CD4 + T cells as well as the survival of their memory cell progeny. The inverse relation between clonal frequency and survival suggests that intraclonal competition could help maintain an optimally diverse repertoire of T cells and an optimal environment for the generation of long-lived memory cells.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

Reference25 articles.

1. Maintaining the norm: T-cell homeostasis

2. Differential regulation of antiviral T-cell immunity results in stable CD8+ but declining CD4+ T-cell memory

3. Materials and methods are available as supporting material on Science Online.

4. Half-life and statistical data for each group in Figs. 1 and 3 are in table S1.

5. CD4+ T cell survival is not directly linked to self-MHC–induced TCR signaling

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