New approaches to making the microenvironment of the female reproductive tract hostile to HIV

Am J Reprod Immunol. 2011 Mar;65(3):334-43. doi: 10.1111/j.1600-0897.2010.00949.x. Epub 2011 Jan 12.

Abstract

The studies presented in this review explore three distinct areas with potential for inhibiting HIV infection in women. Based on emerging information from the physiology, endocrinology and immunology of the female reproductive tract (FRT), we propose unique 'works in progress' for protecting women from HIV. Various aspects of FRT immunity are suppressed by estradiol during the menstrual cycle, making women more susceptible to HIV infection. By engineering commensal Lactobacillus to secrete the anti-HIV molecule Elafin as estradiol levels increase, women could be protected from HIV infection. Selective estrogen response modifiers enhance barrier integrity and enhance secretion of protective anti-HIV molecules. Finally, understanding the interactions and regulation of FRT endogenous antimicrobials, proteases, antiproteases, etc., all of which are under hormonal control, will open new avenues to therapeutic manipulation of the FRT mucosal microenvironment. By seeking new alternatives to preventing HIV infection in women, we may finally disrupt the HIV pandemic.

Publication types

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

MeSH terms

  • Anti-HIV Agents / metabolism
  • Bacterial Physiological Phenomena
  • Elafin / genetics
  • Elafin / metabolism*
  • Estradiol / adverse effects
  • Estradiol / blood*
  • Female
  • Genitalia, Female / immunology
  • Genitalia, Female / microbiology
  • Genitalia, Female / physiology*
  • Genitalia, Female / virology*
  • HIV Infections / immunology
  • HIV Infections / metabolism
  • HIV Infections / prevention & control*
  • HIV Infections / virology
  • Humans
  • Immunity, Innate
  • Immunity, Mucosal*
  • Lactobacillus / genetics
  • Mucous Membrane / metabolism
  • Selective Estrogen Receptor Modulators / pharmacology

Substances

  • Anti-HIV Agents
  • Elafin
  • Selective Estrogen Receptor Modulators
  • Estradiol