HIV and co-infections

Immunol Rev. 2013 Jul;254(1):114-42. doi: 10.1111/imr.12063.

Abstract

Despite significant reductions in morbidity and mortality secondary to availability of effective combination anti-retroviral therapy (cART), human immunodeficiency virus (HIV) infection still accounts for 1.5 million deaths annually. The majority of deaths occur in sub-Saharan Africa where rates of opportunistic co-infections are disproportionately high. In this review, we discuss the immunopathogenesis of five common infections that cause significant morbidity in HIV-infected patients globally. These include co-infection with Mycobacterium tuberculosis, Cryptococcus neoformans, hepatitis B virus, hepatitis C virus, and Plasmodium falciparum. Specifically, we review the natural history of each co-infection in the setting of HIV, the specific immune defects induced by HIV, the effects of cART on the immune response to the co-infection, the pathogenesis of immune restoration disease (IRD) associated with each infection, and advances in the areas of prevention of each co-infection via vaccination. Finally, we discuss the opportunities and gaps in knowledge for future research.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • AIDS-Related Opportunistic Infections / immunology*
  • AIDS-Related Opportunistic Infections / prevention & control
  • Africa South of the Sahara
  • Animals
  • Cryptococcosis / immunology
  • Cryptococcosis / prevention & control
  • HIV Infections / drug therapy
  • HIV Infections / immunology*
  • Hepatitis B / immunology
  • Hepatitis B / prevention & control
  • Hepatitis C / immunology
  • Hepatitis C / prevention & control
  • Humans
  • Malaria / immunology
  • Malaria / prevention & control
  • Tuberculosis / immunology
  • Tuberculosis / prevention & control