A kinetic study on the deletion of thymic, peripheral, and gut-associated V beta 6+ T cells in an Mls-1b BALB/c colony infected with an exogenous mouse mammary tumor virus

J Immunol. 1993 Jul 15;151(2):759-66.

Abstract

Mls-1a expression results in the deletion of T cells bearing V beta 6 chains of the TCR. However, V beta 6+ T cells are also deleted in Mls-1b BALB/c mice that have been infected with an exogenous mouse mammary tumor virus (swiss mice) via maternal milk intake, and whose open reading frame region is markedly similar to that of the provirus Mtv-7. In this report we describe the kinetics of V beta 6+ T cell deletion in the thymus, spleen, lymph nodes, and gut-associated lymphoid populations of these BALB/c mice from the early weeks of life to 6 mo of age. Deletion of V beta 6+ T cells within the CD4+ T cell population was more obvious in the thymus than in the spleen at 8 wk of age. However, the earliest incidence of deletion was observed in the gut intraepithelial lymphocyte population at 5 wk of age. Furthermore Mtv-7 (SW) transcripts were only found in the gut in the first wk of life, whereafter they could be detected in the thymus, spleen, and lymph nodes. This report suggests that after entering the intestinal tract of host mice, mouse mammary tumor virus (swiss mice) is subsequently transferred to the thymus and peripheral lymphoid organs resulting in the deletion of CD4+V beta 6+ T cells in that order.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • CD4 Antigens / analysis
  • CD4-Positive T-Lymphocytes / immunology*
  • CD8 Antigens / analysis
  • Intestines / immunology*
  • Intestines / microbiology
  • Kinetics
  • Mammary Neoplasms, Experimental / immunology*
  • Mammary Tumor Virus, Mouse* / genetics
  • Mice
  • Mice, Inbred BALB C
  • Mice, Inbred C57BL
  • Mice, Inbred DBA
  • Minor Lymphocyte Stimulatory Antigens / analysis*
  • RNA, Viral / analysis
  • Receptors, Antigen, T-Cell, alpha-beta / analysis*
  • Spleen / immunology
  • Thymus Gland / immunology
  • Thymus Gland / microbiology

Substances

  • CD4 Antigens
  • CD8 Antigens
  • Minor Lymphocyte Stimulatory Antigens
  • RNA, Viral
  • Receptors, Antigen, T-Cell, alpha-beta