Cutting edge: Secondary lymphoid organs are essential for maintaining the CD4, but not CD8, naive T cell pool

J Immunol. 2001 Dec 15;167(12):6711-5. doi: 10.4049/jimmunol.167.12.6711.

Abstract

Despite declining thymic output with age, the peripheral naive T cell pool of an adult animal remains remarkably stable. Therefore, a central question in immunology is how the naive T cell pool is maintained. Here we show that the maintenance of the naive CD4, but not CD8, T cell population in the thymectomized adult mouse is dependent on the presence of secondary lymphoid tissues. This finding is explained by the inability of naive CD4 T cells to sustain normal levels of the survival molecule Bcl-2 or to undergo homeostatic proliferation in the absence of secondary lymphoid organs. Thus, naive CD4 T cells must traffic through secondary lymphoid organs to maintain a stable CD4 pool while naive CD8 T cells encounter their survival and proliferation signals outside the organized structures of secondary lymphoid tissues.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • CD4-Positive T-Lymphocytes / immunology*
  • CD8-Positive T-Lymphocytes / immunology*
  • Cells, Cultured
  • Homeostasis
  • Hyaluronan Receptors / analysis
  • Immunophenotyping
  • Lymph Nodes / immunology
  • Lymphocyte Activation
  • Lymphocyte Count
  • Lymphoid Tissue / immunology*
  • Mice
  • Mice, Inbred C57BL
  • Peyer's Patches / immunology
  • Proto-Oncogene Proteins c-bcl-2 / metabolism
  • Spleen / immunology
  • Splenectomy
  • T-Lymphocyte Subsets / classification
  • Thymectomy

Substances

  • Hyaluronan Receptors
  • Proto-Oncogene Proteins c-bcl-2