Myeloid-related protein (MRP)-8 from cervico-vaginal secretions activates HIV replication

AIDS. 2001 Mar 9;15(4):441-9. doi: 10.1097/00002030-200103090-00002.

Abstract

Objectives: To identify a substance found in female genital tract secretions that enhances HIV expression in infected cells.

Design: Cervico-vaginal lavages (CVL), collected in sterile normal saline, were fractionated and tested for HIV-inducing activity using HIV-infected monocytes.

Methods: To purify the component(s) of CVL that enhance HIV production, Mono-Q ion exchange chromatography followed by Superose-12 molecular sieve analysis, and SDS--PAGE were performed. The purified protein was identified by amino acid sequence analysis.

Results: SDS--PAGE of bioactive fractions showed a 14 kDa polypeptide band. Amino acid sequence analysis of selected peptides from the 14 kDa band showed 100% homology with the myeloid-related protein (MRP)-8, an inflammatory protein found in mucosal secretions. Western blot analysis revealed that bioactive CVL contained more immunoreactive MRP-8 than samples without bioactivity. The HIV-inducing activity of MRP-8 was further confirmed by showing that human recombinant MRP-8 increased HIV expression by up to 40-fold.

Conclusions: MRP-8 in cervico-vaginal secretions stimulates HIV production. Strategies aimed at blocking MRP-8 activity in the genital tract could reduce risk of sexual as well as maternal--infant transmission of HIV.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Amino Acid Sequence
  • Antigens, Differentiation / chemistry
  • Antigens, Differentiation / isolation & purification
  • Antigens, Differentiation / pharmacology*
  • Calcium-Binding Proteins / chemistry
  • Calcium-Binding Proteins / isolation & purification
  • Calcium-Binding Proteins / pharmacology*
  • Calgranulin A
  • Cell Line
  • Cervix Uteri / chemistry
  • Cervix Uteri / metabolism*
  • Female
  • HIV-1 / genetics*
  • Humans
  • Recombinant Proteins / pharmacology
  • Vagina / chemistry
  • Vagina / metabolism*
  • Virus Activation

Substances

  • Antigens, Differentiation
  • Calcium-Binding Proteins
  • Calgranulin A
  • Recombinant Proteins