Lactoferrin prevents dendritic cell-mediated human immunodeficiency virus type 1 transmission by blocking the DC-SIGN--gp120 interaction

J Virol. 2005 Mar;79(5):3009-15. doi: 10.1128/JVI.79.5.3009-3015.2005.

Abstract

One of the cell types first encountered by human immunodeficiency virus type 1 (HIV-1) following sexual transmission are dendritic cells (DC). DC capture HIV-1 through C-type lectin receptors, of which the best studied example is DC-SIGN, which mediates HIV-1 internalization. DC can keep the virus infectious for several days and are able to transmit HIV-1 to CD4(+) T cells. We tested proteins from milk and serum for their ability to block DC-mediated HIV-1 transmission, of which bovine lactoferrin (bLF) is the most potent inhibitor. bLF binds strongly to DC-SIGN, thus preventing virus capture and subsequent transmission. Interestingly, bLF is a much more efficient inhibitor of transmission than human lactoferrin. Since bLF is nontoxic and easy to purify in large quantities, it is an interesting candidate microbicide against HIV-1. Another advantage of bLF is its ability to block HIV-1 replication in T cells. DC-mediated capture of a bLF-resistant HIV-1 variant that was selected during long-term culturing in T cells could still be blocked by bLF. This underscores the usefulness of bLF as a microbicide drug to prevent HIV-1 transmission.

Publication types

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

MeSH terms

  • Animals
  • Cattle
  • Cell Adhesion Molecules / physiology*
  • Dendritic Cells / drug effects*
  • Dendritic Cells / immunology
  • Dendritic Cells / virology*
  • HIV Envelope Protein gp120 / physiology*
  • HIV Infections / immunology
  • HIV Infections / prevention & control
  • HIV Infections / transmission
  • HIV-1 / drug effects*
  • HIV-1 / pathogenicity*
  • HIV-1 / physiology
  • Humans
  • In Vitro Techniques
  • Lactoferrin / isolation & purification
  • Lactoferrin / metabolism
  • Lactoferrin / pharmacology*
  • Lectins, C-Type / physiology*
  • Protein Binding
  • Receptors, Cell Surface / physiology*
  • Species Specificity
  • Virus Replication / drug effects

Substances

  • Cell Adhesion Molecules
  • DC-specific ICAM-3 grabbing nonintegrin
  • HIV Envelope Protein gp120
  • Lectins, C-Type
  • Receptors, Cell Surface
  • Lactoferrin