Lactoferrin protects neonatal rats from gut-related systemic infection

Author:

Edde Lynn12,Hipolito Ronaldo B.3,Hwang Freda F. Y.3,Headon Denis R.4,Shalwitz Robert A.5,Sherman Michael P.32

Affiliation:

1. Department of Pediatrics, University of Arizona, Tucson, Arizona 85724;

2. Department of Pediatrics, Baylor College of Medicine, Houston, Texas 77030

3. Department of Pediatrics, University of California, Davis, California 95616;

4. Agennix Incorporated, Houston, Texas 77046;

5. Ross Products Division, Abbott Laboratories, Columbus, Ohio 43215; and

Abstract

Lactoferrin is a milk protein that reportedly protects infants from gut-related, systemic infection. Proof for this concept is limited and was addressed during in vivo and in vitro studies. Neonatal rats pretreated orally with recombinant human lactoferrin (rh-LF) had less bacteremia and lower disease severity scores ( P < 0.001) after intestinal infection with Escherichia coli. Control animals had 1,000-fold more colony-forming units of E. coli per milliliter of blood than treated animals ( P < 0.001). Liver cultures from control animals had a twofold increase in bacterial counts compared with cultures from rh-LF-treated pups ( P < 0.02). Oral therapy with rh-LF + FeSO4did not alter the protective effect. In vitro studies confirmed that rh-LF interacted with the infecting bacterium and rat macrophages. An in vitro assay showed that rh-LF did not kill E. coli, but a combination of rh-LF + lysozyme was microbicidal. In vitro studies showed that rat macrophages released escalating amounts of nitric oxide and tumor necrosis factor-α when stimulated with increasing concentrations of rh-LF. The in vitro studies suggest that rh-LF may act with other “natural peptide antibiotics” or may prime macrophages to kill E. coli in vivo.

Publisher

American Physiological Society

Subject

Physiology (medical),Gastroenterology,Hepatology,Physiology

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