Mycobacterium tuberculosis: immune evasion, latency and reactivation

Immunobiology. 2012 Mar;217(3):363-74. doi: 10.1016/j.imbio.2011.07.008. Epub 2011 Jul 18.

Abstract

One-third of the global human population harbours Mycobacterium tuberculosis in dormant form. This dormant or latent infection presents a major challenge for global efforts to eradicate tuberculosis, because it is a vast reservoir of potential reactivation and transmission. This article explains how the pathogen evades the host immune response to establish a latent infection, and how it emerges from a state of latency to cause reactivation disease. This review highlights the key factors responsible for immune evasion and reactivation. It concludes by identifying interesting candidates for drug or vaccine development, as well as identifying unresolved questions for the future research.

Publication types

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

MeSH terms

  • Antigen Presentation / immunology
  • CD8-Positive T-Lymphocytes / immunology
  • Complement Membrane Attack Complex / immunology
  • Granuloma / immunology
  • Granuloma / pathology
  • Humans
  • Immune Evasion*
  • Killer Cells, Natural / immunology
  • Lysosomes / metabolism
  • Mycobacterium tuberculosis / immunology*
  • Mycobacterium tuberculosis / metabolism
  • Nitric Oxide / metabolism
  • Phagosomes / metabolism
  • Reactive Nitrogen Species / metabolism
  • Tuberculosis / immunology*
  • Tuberculosis / microbiology*

Substances

  • Complement Membrane Attack Complex
  • Reactive Nitrogen Species
  • Nitric Oxide