TY - JOUR
T1 - Prophylactic Efficacy of Hyperimmune Bovine Colostral Antiadhesin Antibodies Against Enterotoxigenic Escherichia coli Diarrhea
T2 - A Randomized, Double-Blind, Placebo-Controlled, Phase 1 Trial
AU - Savarino, Stephen J.
AU - McKenzie, Robin
AU - Tribble, David R.
AU - Porter, Chad K.
AU - O'Dowd, Aisling
AU - Cantrell, Joyce A.
AU - Sincock, Stephanie A.
AU - Poole, Steven T.
AU - Denearing, Barbara
AU - Woods, Colleen M.
AU - Kim, Hye
AU - Grahek, Shannon L.
AU - Brinkley, Carl
AU - Crabb, Joseph H.
AU - Bourgeois, A. Louis
N1 - Publisher Copyright:
© The Author 2017. Published by Oxford University Press for the Infectious Diseases Society of America. All rights reserved.
PY - 2017/7/1
Y1 - 2017/7/1
N2 - Background. Tip-localized adhesive proteins of bacterial fimbriae from diverse pathogens confer protection in animal models, but efficacy in humans has not been reported. Enterotoxigenic Escherichia coli (ETEC) commonly elaborate colonization factors comprising a minor tip adhesin and major stalk-forming subunit. We assessed the efficacy of antiadhesin bovine colostral IgG (bIgG) antibodies against ETEC challenge in volunteers. Methods. Adults were randomly assigned (1:1:1) to take oral hyperimmune bIgG raised against CFA/I minor pilin subunit (CfaE) tip adhesin or colonization factor I (CFA/I) fimbraie (positive control) or placebo. Two days before challenge, volunteers began a thrice-daily, 7-day course of investigational product administered in sodium bicarbonate 15 minutes after each meal. On day 3, subjects drank 1 × 10 9 colony-forming units of colonization factor I (CFA/I)-ETEC strain H10407 with buffer. The primary efficacy endpoint was diarrhea within 120 hours of challenge. Results. After enrollment and randomization, 31 volunteers received product, underwent ETEC challenge, and were included in the per protocol efficacy analysis. Nine of 11 placebos developed diarrhea, 7 experiencing moderate to severe disease. Protective efficacy of 63% (P =.03) and 88% (P =.002) was observed in the antiadhesin bIgG and positive control groups, respectively. Conclusions. Oral administration of anti-CFA/I minor pilin subunit (CfaE) antibodies conferred significant protection against ETEC, providing the first clinical evidence that fimbrial tip adhesins function as protective antigens.
AB - Background. Tip-localized adhesive proteins of bacterial fimbriae from diverse pathogens confer protection in animal models, but efficacy in humans has not been reported. Enterotoxigenic Escherichia coli (ETEC) commonly elaborate colonization factors comprising a minor tip adhesin and major stalk-forming subunit. We assessed the efficacy of antiadhesin bovine colostral IgG (bIgG) antibodies against ETEC challenge in volunteers. Methods. Adults were randomly assigned (1:1:1) to take oral hyperimmune bIgG raised against CFA/I minor pilin subunit (CfaE) tip adhesin or colonization factor I (CFA/I) fimbraie (positive control) or placebo. Two days before challenge, volunteers began a thrice-daily, 7-day course of investigational product administered in sodium bicarbonate 15 minutes after each meal. On day 3, subjects drank 1 × 10 9 colony-forming units of colonization factor I (CFA/I)-ETEC strain H10407 with buffer. The primary efficacy endpoint was diarrhea within 120 hours of challenge. Results. After enrollment and randomization, 31 volunteers received product, underwent ETEC challenge, and were included in the per protocol efficacy analysis. Nine of 11 placebos developed diarrhea, 7 experiencing moderate to severe disease. Protective efficacy of 63% (P =.03) and 88% (P =.002) was observed in the antiadhesin bIgG and positive control groups, respectively. Conclusions. Oral administration of anti-CFA/I minor pilin subunit (CfaE) antibodies conferred significant protection against ETEC, providing the first clinical evidence that fimbrial tip adhesins function as protective antigens.
KW - adhesins
KW - bovine antibodies
KW - enteroxigenic Escherichia coli infections
KW - humans
KW - passive protection.
UR - http://www.scopus.com/inward/record.url?scp=85024484949&partnerID=8YFLogxK
U2 - 10.1093/infdis/jix144
DO - 10.1093/infdis/jix144
M3 - Article
C2 - 28541500
AN - SCOPUS:85024484949
SN - 0022-1899
VL - 216
SP - 7
EP - 13
JO - Journal of Infectious Diseases
JF - Journal of Infectious Diseases
IS - 1
ER -