Peripheral immune tolerance blocks clonal expansion but fails to prevent the differentiation of Th1 cells

J Immunol. 1998 Sep 1;161(5):2168-77.

Abstract

Clonal anergy in Ag-specific CD4+ T cells is shown in these experiments to inhibit IL-2 production and clonal expansion in vivo. We also demonstrate that the defect in IL-2 gene inducibility can be achieved in both naive and Th1-like memory T cells when repeatedly exposed to aqueous peptide Ag. Nevertheless, this induction of clonal anergy did not interfere with the capacity of naive T cells to differentiate into Th1-like effector cells, nor did it prevent such helper cells from participating in T-dependent IgG2a anti-hapten responses and delayed-type hypersensitivity reactions. Thus, clonal anergy can contribute to the development of Ag-specific immune tolerance by limiting the size of a Th cell population, but not by disrupting its effector function.

Publication types

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

MeSH terms

  • Adoptive Transfer
  • Animals
  • Antigens / administration & dosage
  • Antigens / immunology
  • Cell Differentiation / immunology
  • Cell Movement / immunology
  • Clonal Anergy / genetics
  • Clonal Anergy / immunology*
  • Hypersensitivity, Delayed / immunology
  • Immunoglobulin G / biosynthesis
  • Immunophenotyping
  • Injections, Intravenous
  • Interferon-gamma / biosynthesis
  • Interleukin-2 / biosynthesis
  • Interphase / immunology
  • Lymph Nodes / cytology
  • Lymph Nodes / immunology
  • Lymphocyte Activation
  • Lymphocyte Cooperation
  • Mice
  • Mice, Inbred BALB C
  • Mice, Nude
  • Mice, Transgenic
  • Ovalbumin / administration & dosage
  • Ovalbumin / immunology
  • Peptide Fragments / administration & dosage
  • Peptide Fragments / immunology
  • Receptors, Antigen, T-Cell / genetics
  • T-Lymphocyte Subsets / immunology
  • T-Lymphocyte Subsets / metabolism
  • T-Lymphocyte Subsets / transplantation
  • Th1 Cells / immunology*
  • Th1 Cells / metabolism

Substances

  • Antigens
  • Immunoglobulin G
  • Interleukin-2
  • OVA 323-339
  • Peptide Fragments
  • Receptors, Antigen, T-Cell
  • Interferon-gamma
  • Ovalbumin