Binding of human milk to pathogen receptor DC-SIGN varies with bile salt-stimulated lipase (BSSL) gene polymorphism

PLoS One. 2011 Feb 28;6(2):e17316. doi: 10.1371/journal.pone.0017316.

Abstract

Objective: Dendritic cells bind an array of antigens and DC-SIGN has been postulated to act as a receptor for mucosal pathogen transmission. Bile salt-stimulated lipase (BSSL) from human milk potently binds DC-SIGN and blocks DC-SIGN mediated trans-infection of CD4(+) T-lymphocytes with HIV-1. Objective was to study variation in DC-SIGN binding properties and the relation between DC-SIGN binding capacity of milk and BSSL gene polymorphisms.

Study design: ELISA and PCR were used to study DC-SIGN binding properties and BSSL exon 11 size variation for human milk derived from 269 different mothers distributed over 4 geographical regions.

Results: DC-SIGN binding properties were highly variable for milks derived from different mothers and between samplings from different geographical regions. Differences in DC-SIGN binding were correlated with a genetic polymorphism in BSSL which is related to the number of 11 amino acid repeats at the C-terminus of the protein.

Conclusion: The observed variation in DC-SIGN binding properties among milk samples may have implications for the risk of mucosal transmission of pathogens during breastfeeding.

Publication types

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

MeSH terms

  • Breast Feeding / adverse effects
  • CD4-Positive T-Lymphocytes / immunology
  • CD4-Positive T-Lymphocytes / metabolism
  • CD4-Positive T-Lymphocytes / virology
  • Cell Adhesion Molecules / metabolism*
  • DNA Repeat Expansion / genetics
  • DNA Repeat Expansion / physiology
  • Egypt
  • Female
  • Genetic Predisposition to Disease
  • Genotype
  • HIV Infections / genetics*
  • HIV Infections / immunology
  • HIV Infections / metabolism
  • HIV Infections / transmission*
  • HIV-1 / metabolism
  • HIV-1 / physiology
  • Humans
  • Infant, Newborn
  • Lectins, C-Type / metabolism*
  • Lipase / genetics*
  • Lipase / metabolism
  • Maternal Exposure / adverse effects
  • Milk, Human / metabolism*
  • Milk, Human / physiology
  • Milk, Human / virology
  • Netherlands
  • Norway
  • Polymorphism, Genetic* / physiology
  • Protein Binding / genetics
  • Receptors, Cell Surface / metabolism*
  • Sweden

Substances

  • Cell Adhesion Molecules
  • DC-specific ICAM-3 grabbing nonintegrin
  • Lectins, C-Type
  • Receptors, Cell Surface
  • CEL protein, human
  • Lipase