Antigens for CD4 and CD8 T cells in tuberculosis

Cold Spring Harb Perspect Med. 2014 May 22;4(7):a018465. doi: 10.1101/cshperspect.a018465.

Abstract

Tuberculosis (TB), caused by infection with Mycobacterium tuberculosis (MTB), represents an important cause of morbidity and mortality worldwide for which an improved vaccine and immunodiagnostics are urgently needed. CD4(+) and CD8(+) T cells play an important role in host defense to TB. Definition of the antigens recognized by these T cells is critical for improved understanding of the immunobiology of TB and for development of vaccines and diagnostics. Herein, the antigens and epitopes recognized by classically HLA class I- and II-restricted CD4(+) and CD8(+) T cells in humans infected with MTB are reviewed. Immunodominant antigens and epitopes have been defined using approaches targeting particular TB proteins or classes of proteins and by genome-wide discovery approaches. Antigens and epitopes recognized by classically restricted CD4(+) and CD8(+) T cells show extensive breadth and diversity in MTB-infected humans.

Publication types

  • Review

MeSH terms

  • Antigens, Bacterial / immunology*
  • CD4-Positive T-Lymphocytes / immunology*
  • CD4-Positive T-Lymphocytes / physiology
  • CD8-Positive T-Lymphocytes / immunology*
  • CD8-Positive T-Lymphocytes / physiology
  • Epitopes, B-Lymphocyte / immunology
  • Epitopes, T-Lymphocyte / immunology
  • Genome, Bacterial / immunology
  • HLA-D Antigens / immunology
  • Histocompatibility Antigens Class I / immunology
  • Humans
  • Immunity, Cellular / immunology
  • Mycobacterium tuberculosis / immunology
  • Tuberculosis / immunology*

Substances

  • Antigens, Bacterial
  • Epitopes, B-Lymphocyte
  • Epitopes, T-Lymphocyte
  • HLA-D Antigens
  • Histocompatibility Antigens Class I