Genetic determinants of pediatric HIV-1 infection: vertical transmission and disease progression among children

Mol Med. 2001 Sep;7(9):583-9.

Abstract

It is very likely that perinatal human immunodeficiency virus type 1 (HIV-1) infection is influenced by a combination of virologic and host factors. A greater understanding of the role played by various risk factors for HIV-1 infection is crucial for the design of new preventive and therapeutic strategies. In recent years, a number of studies have suggested that host genetic factors are important determinants of both the susceptibility to perinatal HIV-1 infection and the subsequent pathogenesis of acquired immunodeficiency syndrome (AIDS). Control of HIV-1 infection involves the processing of specific viral peptides and their presentation to cells of the immune system by highly polymorphic human leukocyte antigen (HLA) alleles. The contribution of multiple HLA class I and II alleles in modulating pediatric HIV/AIDS outcomes has now been confirmed by several independent groups. Penetration of HIV-1 into cells is mediated by interaction between CD4 and chemokine receptors that serve as entry coreceptors. Genetic polymorphisms in chemokine ligand and chemokine receptor genes have recently been associated both with mother-to-child HIV-1 transmission and disease progression in children. These observations suggest a key role for genetic factors in pediatric HIV-1 infection. This article describes the current state of knowledge regarding host genetic influences on pediatric HIV-1 infection and discusses the role of these genes in HIV/AIDS pathogenesis.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Child
  • Disease Progression*
  • Female
  • HIV Infections / genetics*
  • HIV Infections / immunology
  • HIV Infections / transmission
  • HIV-1* / immunology
  • HIV-1* / physiology
  • HLA Antigens / genetics
  • HLA Antigens / immunology
  • Humans
  • Infant
  • Infectious Disease Transmission, Vertical*
  • Polymorphism, Genetic
  • Receptors, Chemokine / genetics
  • Receptors, Chemokine / metabolism
  • Receptors, HIV / genetics
  • Receptors, HIV / metabolism

Substances

  • HLA Antigens
  • Receptors, Chemokine
  • Receptors, HIV