Hyperimmune Bovine Colostral Anti-CS17 Antibodies Protect Against Enterotoxigenic Escherichia coli Diarrhea in a Randomized, Doubled-Blind, Placebo-Controlled Human Infection Model

Author:

Savarino Stephen J1,McKenzie Robin23,Tribble David R1,Porter Chad K1,O’Dowd Aisling1,Sincock Stephanie A1,Poole Steven T1,DeNearing Barbara2,Woods Colleen M1,Kim Hye3,Grahek Shannon L2,Brinkley Carl4,Crabb Joseph H5,Bourgeois A Louis2

Affiliation:

1. Naval Medical Research Center, Silver Spring, Maryland

2. Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland

3. Johns Hopkins School of Medicine, Baltimore, Maryland

4. Walter Reed Army Institute of Research, Silver Spring, Maryland

5. ImmuCell Corporation, Portland, Maine

Abstract

AbstractBackgroundEnterotoxigenic Escherichia coli (ETEC) commonly cause diarrhea in children living in developing countries and in travelers to those regions. ETEC are characterized by colonization factors (CFs) that mediate intestinal adherence. We assessed if bovine colostral IgG (bIgG) antibodies against a CF, CS17, or antibodies against CsbD, the minor tip subunit of CS17, would protect subjects against diarrhea following challenge with a CS17-expressing ETEC strain.MethodsAdult subjects were randomized (1:1:1) to receive oral bIgG against CS17, CsbD, or placebo. Two days prior to challenge, subjects began dosing 3 times daily with the bIgG products (or placebo). On day 3, subjects ingested 5 × 109 cfu ETEC strain LSN03-016011/A in buffer. Subjects were assessed for diarrhea for 120 hours postchallenge.ResultsA total of 36 subjects began oral prophylaxis and 35 were challenged with ETEC. While 50.0% of the placebo recipients had watery diarrhea, none of the subjects receiving anti-CS17 had diarrhea (P = .01). In contrast, diarrhea rates between placebo and anti-CsbD recipients (41.7%) were comparable (P = 1.0).ConclusionsThis is the first study to demonstrate anti-CS17 antibodies provide significant protection against ETEC expressing CS17. More research is needed to better understand why anti-CsbD was not comparably efficacious.Clinical Trials Registration. NCT00524004

Funder

US Army Medical Research and Materiel Command

Henry M. Jackson Foundation for the Advancement of Military Medicine

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Immunology and Allergy

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