The interaction of monocyte chemoattractant protein-1 and tumour necrosis factor-alpha in Mycobacterium tuberculosis-induced HIV-1 replication at sites of active tuberculosis

Scand J Immunol. 2009 Jun;69(6):516-20. doi: 10.1111/j.1365-3083.2009.02246.x.

Abstract

Tuberculosis (TB) is a prominent opportunistic infection in HIV-1-infected subjects and enhances HIV-1 replication. TB is associated with excess monocyte chemoattractant protein (MCP)-1 and tumour necrosis factor (TNF)-alpha activity in situ, both of which are implicated in transcriptional activation of HIV-1. The role of MCP-1 and TNF-alpha in activation of HIV-1 during TB and by Mycobacterium tuberculosis (MTB) in mononuclear cells from HIV-1/TB subjects with pleural TB was examined here. Extremely high levels of MCP-1 (as compared with TNF-alpha) protein and mRNA were found in pleural fluid and pleural fluid mononuclear cells. Levels of MCP-1 mRNA were sustained during in vitro culture of pleural fluid mononuclear cells. Neutralization of MCP-1 (but not TNF-alpha), resulted in inhibition of MTB induced HIV-1 gag/pol mRNA. Neutralization of both MCP-1 and TNF-alpha, however, abrogated the effect of anti-MCP-1 antibody on HIV-1 mRNA. LMP-420, a small molecular transcriptional inhibitor of both TNF-alpha and MCP-1 expression, did not reduce MTB-induced HIV-1 expression. These data imply that MCP-1 activity may be critical to activation of HIV-1 at sites of TB. An interplay of MCP-1 and TNF-alpha is also suggested.

Publication types

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

MeSH terms

  • AIDS-Related Opportunistic Infections / immunology
  • AIDS-Related Opportunistic Infections / metabolism*
  • Adult
  • Chemokine CCL2 / immunology
  • Chemokine CCL2 / metabolism*
  • DNA, Viral / analysis
  • HIV Infections / complications
  • HIV Infections / virology
  • HIV-1 / physiology*
  • Humans
  • Mycobacterium tuberculosis
  • RNA, Messenger / analysis
  • RNA, Viral / analysis
  • Reverse Transcriptase Polymerase Chain Reaction
  • Tuberculosis / complications
  • Tuberculosis / immunology
  • Tuberculosis / metabolism*
  • Tumor Necrosis Factor-alpha / immunology
  • Tumor Necrosis Factor-alpha / metabolism*
  • Virus Activation / physiology*
  • Virus Replication

Substances

  • CCL2 protein, human
  • Chemokine CCL2
  • DNA, Viral
  • RNA, Messenger
  • RNA, Viral
  • Tumor Necrosis Factor-alpha