The immunocompromised host: HIV infection

Proc Am Thorac Soc. 2005;2(5):423-7. doi: 10.1513/pats.200507-077JS.

Abstract

The variety of pulmonary infections encountered in HIV-infected individuals indicates that many components of the host defense network are impaired. In addition to depletion of CD4+ T cell numbers, HIV infection results in functional deficits in CD4+ T cells, CD8+ T cells, and natural killer cells. Although some components of macrophage defense are preserved, lack of activation signals from CD4+ T cells contributes to impaired defense by macrophages. There are few data examining the functional capabilities of neutrophils in the lung, but evidence from peripheral blood neutrophils indicates that defense by these cells is also impaired. An improved understanding of these events in the lung during HIV infection could lead to specific interventions aimed at restoration of deficient function.

Publication types

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

MeSH terms

  • Animals
  • Biomarkers / analysis
  • CD4-Positive T-Lymphocytes / immunology
  • CD4-Positive T-Lymphocytes / metabolism
  • CD8-Positive T-Lymphocytes / immunology
  • CD8-Positive T-Lymphocytes / metabolism
  • HIV Infections / immunology*
  • HIV Infections / physiopathology
  • Humans
  • Immunocompromised Host / immunology*
  • Killer Cells, Natural / immunology
  • Killer Cells, Natural / metabolism
  • Lung Diseases / epidemiology
  • Lung Diseases / immunology*
  • Lymphocyte Activation
  • Opportunistic Infections / immunology*
  • Opportunistic Infections / physiopathology
  • Prognosis
  • Sensitivity and Specificity
  • T-Lymphocytes, Regulatory / immunology*
  • T-Lymphocytes, Regulatory / metabolism

Substances

  • Biomarkers