Positive and negative selection of T cell repertoires during differentiation in allogeneic bone marrow chimeras

Transpl Immunol. 2003 Oct-Nov;12(1):79-88. doi: 10.1016/S0966-3274(03)00012-1.

Abstract

T cells acquire immune functions during expansion and differentiation in the thymus. Mature T cells respond to peptide antigens (Ag) derived from foreign proteins when these peptide Ag are presented on the self major histocompatibility complex (MHC) molecules but not on allo-MHC. This is termed self-MHC restriction. On the other hand, T cells do not induce aggressive responses to self Ag (self-tolerance). Self-MHC restriction and self-tolerance are not genetically determined but acquired a posteriori by positive and negative selection in the thymus in harmony with the functional maturation. Allogeneic bone marrow (BM) chimera systems have been a useful strategy to elucidate mechanisms underlying positive and negative selection. In this communication, the contribution of BM chimera systems to the investigation of the world of T-ology is discussed.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Antigen-Presenting Cells / immunology
  • Antigens, Differentiation, T-Lymphocyte / analysis
  • Bone Marrow Transplantation / immunology*
  • Cell Differentiation / immunology*
  • Clonal Deletion / immunology
  • Columbidae
  • Cytochromes c / genetics
  • Cytochromes c / immunology
  • Flow Cytometry
  • Graft vs Host Reaction / immunology
  • Immune Tolerance / immunology
  • Lymphocyte Activation / immunology
  • Lymphocyte Culture Test, Mixed
  • Lymphocyte Depletion
  • Major Histocompatibility Complex / immunology
  • Mice
  • Mice, Inbred AKR
  • Mice, Inbred C57BL
  • Models, Immunological
  • Peptides / genetics
  • Peptides / immunology
  • Receptors, Antigen, T-Cell / immunology
  • T-Lymphocytes / chemistry
  • T-Lymphocytes / immunology*
  • T-Lymphocytes, Cytotoxic / immunology
  • Thymus Gland / cytology
  • Transplantation Chimera / immunology*
  • Transplantation, Homologous

Substances

  • Antigens, Differentiation, T-Lymphocyte
  • Peptides
  • Receptors, Antigen, T-Cell
  • Cytochromes c