Breast-feeding is the predominant transmission route for HIV-1 infection in children. However, the vast majority of breast-fed infants do not become HIV- infected despite continuous exposure to the virus through their mothers' milk over many months. What protects breast-fed infants from HIV-1 infection? HIV-1 entry across the infant's mucosal barrier is partially mediated through binding of the viral envelope glycoprotein gp120 to the glycan binding domain of DC-SIGN on mucosal dendritic cells. DC-SIGN not only binds to the glycans on gp120, but has an even higher binding affinity for the Lewis antigens, which are also glycans and compete with gp120 for DC-SIGN binding. One liter of human milk contains 5-10 g unbound oligosaccharides, complex glycans, which carry Lewis blood group antigens. We hypothesize that human milk oligosaccharides (HMO) compete with HIV-1-gp120 for DC-SIGN binding, reduce HIV-1-transmission through breast milk, and protect a majority of infants from HIV-1-infection. Our Preliminary Results in two independent in vitro assays show that HMO indeed reduce gp120-binding to DC-SIGN by more than 80%. However, HMO consist of more than 150 different oligosaccharides. Which ones are most effective? AIM1 uses Frontal-Affinity-Chromatography Mass Spectrometry to identify individual HMO with high binding affinity for DC-SIGN.
AIM2 then uses the two already established in vitro assays to assess whether the identified HMO inhibit HIV-1- gp120 binding to DC-SIGN. The results will guide in vitro and in vivo studies investigating whether the identified oligosaccharides reduce HIV-1 infection. Other viruses such as Hepatitis C, Ebola or Dengue, also use DC-SIGN as their entry point. The identified milk oligosaccharides could serve as drug design temples to fight these devastating diseases. ? ?

Public Health Relevance

Although breast-feeding transmits the HIV-1 virus from mothers to their infants, breast milk contains compounds that protect a majority of infants from infection. Preliminary Results support our hypothesis that human milk oligosaccharides are part of this protective mechanism.
We aim at identifying those individual human milk oligosaccharides that are most effective in reducing HIV-1 infection. ? ? ? ?

Agency
National Institute of Health (NIH)
Institute
Eunice Kennedy Shriver National Institute of Child Health & Human Development (NICHD)
Type
Small Research Grants (R03)
Project #
1R03HD059717-01
Application #
7555022
Study Section
AIDS Discovery and Development of Therapeutics Study Section (ADDT)
Program Officer
Ryan, Kevin W
Project Start
2008-08-07
Project End
2009-06-30
Budget Start
2008-08-07
Budget End
2009-06-30
Support Year
1
Fiscal Year
2008
Total Cost
$68,877
Indirect Cost
Name
Sanford-Burnham Medical Research Institute
Department
Type
DUNS #
020520466
City
La Jolla
State
CA
Country
United States
Zip Code
92037
Bode, Lars (2015) The functional biology of human milk oligosaccharides. Early Hum Dev 91:619-22