Hemophilia and nonprogressing human immunodeficiency virus type 1 infection

Blood. 1997 Jan 1;89(1):191-200.

Abstract

Seven of 112 hemophiliacs infected with human immunodeficiency virus type-1 (HIV-1) before 1986 through contaminated plasma products are currently healthy, with CD4 T-cell counts above 500 cells/microL, and have never received antiretroviral therapy (long-term nonprogressors [LTNPs]). Seven age and sex-matched hemophiliacs infected in the same period but who have progressive HIV disease (progressors) and one additional slow-progressing individual were also studied. One hundred-fold, 20-fold, and 10-fold lower levels of full-length HIV RNA in plasma, peripheral blood mononuclear cells (PBMCs), and proviral DNA in PBMCs, respectively, were found in LTNPs compared with progressors. Plasma and cell-associated HIV RNA and proviral DNA were lower in LTNPs who tested negative for viral isolation from PBMCs or who were positive only after removal of CD8+ cells. No substantial differences were observed in the in vitro production of chemokines including RANTES, MIP-1 alpha, MIP-1 beta, MCP-1, and interleukin-8 (IL-8) in supernatants of activated PBMCs or CD8-depleted PBMCs of LTNPs, even when HIV isolation was simultaneously accomplished exclusively after removal of CD8+ cells. Low levels of HIV load and replication in peripheral blood are the strongest correlates of nonprogression in this small number of infected hemophiliacs.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • CD4 Lymphocyte Count
  • Case-Control Studies
  • Chemokines / biosynthesis
  • Cohort Studies
  • DNA, Viral / isolation & purification
  • Disease Progression
  • HIV Infections / complications*
  • HIV Infections / virology
  • HIV-1 / isolation & purification
  • HIV-1 / physiology
  • Hemophilia A / complications*
  • Humans
  • Leukocytes, Mononuclear / virology
  • Male
  • Middle Aged
  • Phenotype
  • Plasma / virology
  • Proviruses / isolation & purification
  • RNA, Viral / blood
  • Retrospective Studies
  • Survivors
  • T-Lymphocytes, Regulatory / immunology
  • Time Factors
  • Viremia / virology
  • Virus Cultivation
  • Virus Replication

Substances

  • Chemokines
  • DNA, Viral
  • RNA, Viral