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

Fedde Groot, Teunis B H Geijtenbeek, Rogier W Sanders, Christopher E Baldwin, Marta Sanchez-Hernandez, René Floris, Yvette van Kooyk, Esther C de Jong, Ben Berkhout

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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.

Original languageEnglish
Pages (from-to)3009-3015
Number of pages7
JournalJournal of Virology
Volume79
Issue number5
DOIs
Publication statusPublished - Mar 2005

Keywords

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

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