Healthy Volunteer Clinical Trial
Official title:
Protective Efficacy of Orally Delivered Bovine Serum Immunoglobulin (BSIgG) Specific for the Colonization Factor CS6 Following Challenge With the CS6-expressing Enterotoxigenic E. Coli (ETEC) Strain B7A
Enterotoxigenic Escherichia coli (ETEC) is a major cause of diarrhea worldwide. Vaccines and therapeutics are under development to prevent ETEC disease in children and travelers. One approach is to use passive protection (antibodies) to prevent infection. The purpose of this study are to assess the safety of serum-derived bovine immunoglobulins in healthy adult subjects when orally administered and to estimate protective efficacy of those preparations against moderate-severe diarrhea upon challenge with the ETEC strain B7A.
Enterotoxigenic Escherichia coli (ETEC) is one of the most common causes of infectious
diarrhea in children in resource limited countries, and is also a frequent cause of
traveler's diarrhea in civilian and military travelers to endemic countries. ETEC strains
express a variety of colonization factors (CF) that help them attach to the intestinal wall.
Each colonization factor has one or more surface antigens (CS). One of the major surface
antigens of ETEC is CS6 (Coli surface antigen 6).
Vaccines and treatments to prevent ETEC disease are under development. Some of these target
specific enterotoxins or colonization factors. For over 40 years, we have used ETEC human
challenge studies to understand the ETEC disease process, immune response, and more recently,
to determine whether treatments or vaccines are protective or effective in mitigating
disease. B7A is the only CS6 expressing ETEC challenge strain currently used.
A modality that has shown some success in the prevention of diarrhea is passive, oral
administration of bovine milk IgG with specific activity against viral, bacterial and
parasitic enteropathogens. Passive oral administration of Bovine Serum Immunoglobulins
(BSIgG) may protect against ETEC-mediated infectious diarrhea. The hypothesized mechanism of
protection stems from the passive administration of bovine anti-tip adhesion or fimbriae
antibodies preventing their adherence in the human small intestine (the initial step in
pathogenesis), thereby preventing downstream pathogenic processes and symptomatic illness.
This study will establish the foundation for evaluating BSIgG products against numerous ETEC
CFs.
This study will explore if anti-B7A and anti- CS6 BSIgG provides protection against oral
challenge with B7A in healthy adult volunteers. There will be two inpatient admissions of
approximately 30 subjects (up to 60 total). They will receive one of three investigational
products (IP) three times daily following meals beginning 2 days prior to challenge. Each
volunteer will be challenged with CS6 expressing ETEC B7A on Day 0. The investigational
product/placebo will be administered for a total of 7 days, or until antibiotic treatment has
been administered. The investigators hypothesize that anti-CS6 BSIgG will provide protection
against B7A mediated moderate to severe diarrhea upon challenge.
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