As. Goldman, Modulation of the gastrointestinal tract of infants by human milk, interfaces and interactions. An evolutionary perspective, J NUTR, 130(2), 2000, pp. 426S-431S
Human milk contains agents that affect the growth, development and function
s of the epithelium, immune system or nervous system of the gastrointestina
l tract. Some human and animal studies indicate that human milk affects the
growth of intestinal villi, the development of intestinal disaccharidases,
the permeability of the gastrointestinal tract and resistance to certain i
nflammatory/immune-mediated diseases. Moreover, one cytokine in human milk,
interleukin (IL)-10, protects infant mice genetically deficient in IL-10 a
gainst an enterocolitis that resembles necrotizing enterocolitis (NEC) in h
uman premature infants, There are seven overlapping evolutionary strategies
regarding the relationships between the functions of the mammary gland and
the infant's gastrointestinal tract as follows: I) certain immunologic age
nts in human milk compensate directly for developmental delays in those sam
e agents in the recipient infant; 2) other agents in human milk do not comp
ensate directly for developmental delays in the production of those same ag
ents, but nevertheless protect the recipient; 3) agents in human milk enhan
ce functions that are poorly expressed in the recipient; 4) agents in human
milk change the physiologic state of the intestines from one adapted to in
trauterine life to one suited to extrauterine life; 5) some agents in human
milk prevent inflammation in the recipient's gastrointestinal tract; 6) su
rvival of human milk agents in the gastrointestinal tract is enhanced becau
se of delayed production of pancreatic proteases and gastric acid by newbor
n infants, antiproteases and inhibitors of gastric acid production in human
milk, inherent resistance of some human milk agents to proteolysis, and pr
otective binding of other factors in human milk; and 7) growth factors in h
uman milk aid in establishing a commensal enteric microflora.