Antibiotic-resistant Clostridioides difficile is responsible for more than 29,000 deaths in the US each year and the infection is an urgent threat (as designated by CDC) to public health. The incidence of C. difficile infection (CDI) and disease severity is increasing in recent years due to the emergence of hypervirulent and antibiotic- resistant strains. CDI is caused by the exotoxins TcdA and TcdB secreted by C. difficile in the colon of the host. Current standard treatment with antibiotics is not optimal and is accompanied by a high recurrence rate due to the disruption of host colonization resistance. Moreover, there is no approved prevention against the infection. Our goal is to develop a novel yeast-based immunoprophylactic/therapeutic against both primary and recurrent CDI. We have developed a therapeutic lead by engineering a probiotic yeast, Saccharomyces boulardii (Sb), to secrete an antitoxin ABAB (Sb-ABAB). ABAB is a fusion protein of 4 VHHs targeting 2 distinct neutralizing epitopes in TcdA and 2 in TcdB respectively. ABAB is ultrapotent in neutralizing both TcdA and TcdB and broadly active against toxins from 64 clinical isolates. Our preliminary data showed that oral Sb- ABAB protected mice from both primary and recurrent CDI. The objectives of this Fast-track SBIR are to: 1) phenotypically and genetically characterize Sb-ABAB to ensure its identity and quality; 2) determine pharmacokinetic and safety profiles of Sb-ABAB; 3) develop clinic-compatible formula of Sb-ABAB capsules; and 4) perform IND-enabling efficacy study in a piglet model of CDI. All proposed activities will be guided by an exceptional advisory/consultant team with specialized expertise in business development, biologics regulation, product development and planning, and clinical development. Upon the completion of the proposed studies, we will pursue Phase IIb for GMP manufacturing of Sb-ABAB, GLP toxicology and IND submission in the future.
Public Health Relevance Statement: Narrative Antibiotic-resistant Clostridioides difficile is responsible for more than 29,000 deaths in the US each year and the infection is an urgent threat to public health. This project is to develop novel yeast-based prevention and treatment against C. difficile infection.
Project Terms: Animals; Antibiotics; Antibiotic Agents; Antibiotic Drugs; Miscellaneous Antibiotic; Epitopes; Antigenic Determinants; Binding Determinants; antitoxin; anti-toxin; Attention; Blood Circulation; Bloodstream; Circulation; capsule; Capsules; Centers for Disease Control and Prevention (U.S.); CDC; Centers for Disease Control; Centers for Disease Control and Prevention; United States Centers for Disease Control; United States Centers for Disease Control and Prevention; Colon; Cessation of life; Death; Diarrhea; Pharmaceutical Preparations; Drugs; Medication; Pharmaceutic Preparations; drug/agent; Engineering; Excipients; Exotoxins; Freezing; Future; Genetic Identity; Biochemical Genetics; Gnotobiotic; Gnotobiotics; Goals; Human; Modern Man; Immunoglobulin A; IgA; Immunoglobulin G; 7S Gamma Globulin; IgG; Immunotherapy; Immune mediated therapy; Immunologically Directed Therapy; immune therapeutic approach; immune therapeutic interventions; immune therapeutic regimens; immune therapeutic strategy; immune therapy; immune-based therapies; immune-based treatments; immuno therapy; In Vitro; Incidence; Infection; Inflammation; Intestines; Intestinal; bowel; Lead; Pb element; heavy metal Pb; heavy metal lead; Mus; Mice; Mice Mammals; Murine; Drug Kinetics; Pharmacokinetics; Phenotype; Physiology; Powder dose form; Powders; Production; Public Health; Recurrence; Recurrent; Saccharomyces; Safety; Family suidae; Pigs; Suidae; Swine; porcine; suid; Technology; Testing; Tissues; Body Tissues; Toxicology; Toxin; Yeasts; Clostridium difficile; C diff; C difficile; C. diff; C. difficile; Clostridioides difficile; Resistance to antibiotics; Resistant to antibiotics; antibiotic drug resistance; antibiotic resistant; Antibiotic Resistance; Businesses; Chimera Protein; Fusion Protein; Chimeric Proteins; analytical method; base; Site; Clinical; Encapsulated; Phase; Biological; Ensure; Chemicals; Data Bases; data base; Databases; Development Plans; Therapeutic; Life; Oral; Clinic; Clinical Course of Disease; System; disease severity; Severity of illness; gastrointestinal; Probiotics; novel; Prevention; Regulation; Modeling; Property; response; pill; Pathogenicity Factors; Virulence Factors; Pseudomembranous Colitis; preventing; prevent; Enteric; Enteral; Dose; Data; SBIR; Small Business Innovation Research; Small Business Innovation Research Grant; Validation; developmental; Development; immunosuppressed; efficacy evaluation; intervention efficacy; therapeutic efficacy; therapeutically effective; therapy efficacy; Treatment Efficacy; reconstitute; reconstitution; standard treatment; standard care; resistance strain; resistant strain; product development; pre-clinical efficacy; preclinical efficacy; phase II study; phase 2 study; screening; Formulation; enhancer cassette; expression cassette; gene cassette; genetic cassette; integration cassette; promoter cassette; reporter cassette; resistance cassette; selectable cassette; selection cassette; stop cassette; transcription cassette; transcriptional cassette; transgene cassette; DNA cassette; microbial consortia; microbial flora; microflora; multispecies consortia; microbiota; experiment; experimental research; experimental study; efficacy study; clinical development; colonization resistance; antibiotic-associated diarrhea; host colonization; gene locus; genetic locus; genomic locus
