Association of drug abuse with inhibition of HIV-1 immune responses: studies with long-term of HIV-1 non-progressors

J Neuroimmunol. 2004 Feb;147(1-2):21-5. doi: 10.1016/j.jneuroim.2003.10.038.

Abstract

Recreational drug use has been proposed to affect the course of human immunodeficiency virus (HIV) infections. To investigate the effects of substance abuse on HIV infections, we compared virus-specific cytotoxic T lymphocyte (CTL) responses and the expression of IL-16, TGF-beta1, and CXCR4 in three different cohorts of HIV-infected patients: (1) long-term nonprogressors (LT-NPs) of HIV infection who do not use recreational drugs; (2) nondrugs using normal progressors (NPs), and (3) drugs using NPs. Our results show that LT-NPs manifest increased CTL activity and IL-16 expression and decreased expression of TGF-beta1 and CXCR4 compared to NPs, regardless of recreational drug usage. Furthermore, drugs using NPs showed significantly lower levels of CTL and IL-16 expression and increased TGF-beta1 and CXCR4 expression compared to nondrugs using NPs. Our results suggest that recreational drug use may reduce CTL and IL-16 expression and increase the expression of TGF-beta1 and CXCR4, all of which may facilitate progression of HIV infections.

Publication types

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

MeSH terms

  • Blotting, Northern
  • HIV Infections / complications*
  • HIV Infections / immunology*
  • HIV Long-Term Survivors*
  • HIV-1 / immunology*
  • Humans
  • Interleukin-16 / genetics
  • Interleukin-16 / immunology
  • Longitudinal Studies
  • RNA, Messenger / biosynthesis
  • Receptors, CXCR4 / genetics
  • Receptors, CXCR4 / immunology
  • Reverse Transcriptase Polymerase Chain Reaction / methods
  • Substance-Related Disorders / complications*
  • Substance-Related Disorders / immunology
  • Substance-Related Disorders / virology
  • T-Lymphocytes, Cytotoxic / immunology
  • Transforming Growth Factor beta / genetics
  • Transforming Growth Factor beta / immunology
  • Viral Load

Substances

  • Interleukin-16
  • RNA, Messenger
  • Receptors, CXCR4
  • Transforming Growth Factor beta