Natural antibodies to CCR5 from breast milk block infection of macrophages and dendritic cells with primary R5-tropic HIV-1

J Immunol. 2005 Jun 1;174(11):7202-9. doi: 10.4049/jimmunol.174.11.7202.

Abstract

In the present study, we demonstrate that breast milk of 66% and 83% of HIV-seronegative and seropositive women, respectively, contains natural Abs of the secretory IgA and IgG isotypes directed against the CCR5 coreceptor for R5-tropic strains of HIV-1. Abs to CCR5 were affinity purified on a matrix to which a synthetic peptide corresponding to the second extracellular loop of CCR5 had been coupled. The purified Abs bound to the CCR5 peptide in a dose-dependent fashion and to both native CCR5 expressed by Chinese hamster ovary cells transfected with CCR5 gene, macrophages, and immature dendritic cells. Although the avidity differed, the amount of anti-CCR5 Abs did not significantly differ between breast milk of HIV-seropositive and -seronegative women. Purified anti-CCR5 Abs inhibited up to 75% infection of macrophages and dendritic cells with HIV(BaL) and HIV(JR-CSF). Our observations provide evidence for a role of natural Abs to CCR5 in breast milk in controlling transmissibility of HIV through breastfeeding.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Anti-HIV Agents / metabolism
  • Anti-HIV Agents / pharmacology
  • Antibodies, Blocking / metabolism
  • Antibodies, Blocking / physiology*
  • Antibody Affinity
  • Binding Sites, Antibody
  • CCR5 Receptor Antagonists
  • CHO Cells
  • Cells, Cultured
  • Cricetinae
  • Dendritic Cells / immunology*
  • Dendritic Cells / virology*
  • Dose-Response Relationship, Immunologic
  • Female
  • HIV Infections / immunology
  • HIV Infections / prevention & control
  • HIV-1 / immunology*
  • HIV-1 / pathogenicity
  • Humans
  • Macrophages / immunology*
  • Macrophages / virology*
  • Milk, Human / immunology*
  • Molecular Sequence Data
  • Peptide Fragments / antagonists & inhibitors
  • Peptide Fragments / immunology
  • Peptide Fragments / metabolism
  • Receptors, CCR5 / immunology*
  • Receptors, CCR5 / metabolism
  • Receptors, CCR5 / physiology

Substances

  • Anti-HIV Agents
  • Antibodies, Blocking
  • CCR5 Receptor Antagonists
  • Peptide Fragments
  • Receptors, CCR5