Antigens for CD4 and CD8 T Cells in Tuberculosis

  1. Deborah Lewinsohn2
  1. 1La Jolla Institute for Allergy and Immunology, La Jolla, California 92037
  2. 2Oregon Health and Science University, Portland, Oregon 97239
  3. 3Portland VA Medical Center, Portland, Oregon 97239
  1. Correspondence: lewinsde{at}ohsu.edu

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.

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