This program project renewal application is submitted by investigators who propose to expand and continue their studies on the unique properties of human milk. The five component subprojects and four subcontracts address the biologic consequence of specific milk components or properties through in vivo protocols conducted in animal models and humans. The subprojects generally seek to define and characterize factors in human milk that protect newborn infants from disease. Certain consequences of the luminal milk-gastrointestinal tract interaction that pertain to protection of the infant will be examined. Animals will be utilized when study of human subjects is not possible, but human infants will be studied whenever appropriate. The respective subprojects and subcontracts will consider: 1) the role of soluble milk factors in the prevention of shigellosis, 2) antibody secretion, cytotoxicity and immune regulation, 3) the relationship of the human milk phagocyte to infant health, 4) the role of the secretory immune system in rotavirus infection, 5) isolation and characterization of the protective factor(s) in human milk against heat stable enterotoxin of E. coli, and 6) the role of human milk in the prevention of campylobacter infection.

Agency
National Institute of Health (NIH)
Institute
Eunice Kennedy Shriver National Institute of Child Health & Human Development (NICHD)
Type
Research Program Projects (P01)
Project #
5P01HD013021-11
Application #
3096731
Study Section
Maternal and Child Health Research Committee (HDMC)
Project Start
1979-07-01
Project End
1992-11-30
Budget Start
1989-12-01
Budget End
1990-11-30
Support Year
11
Fiscal Year
1990
Total Cost
Indirect Cost
Name
University of Texas Health Science Center Houston
Department
Type
Schools of Medicine
DUNS #
City
Houston
State
TX
Country
United States
Zip Code
77225
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He, YingYing; Liu, ShuBai; Kling, David E et al. (2016) The human milk oligosaccharide 2'-fucosyllactose modulates CD14 expression in human enterocytes, thereby attenuating LPS-induced inflammation. Gut 65:33-46
Hao, Ning; Chen, Yutao; Xia, Ming et al. (2015) Crystal structures of GI.8 Boxer virus P dimers in complex with HBGAs, a novel evolutionary path selected by the Lewis epitope. Protein Cell 6:101-16
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