Cargando…

Clostridium difficile Toxoid Vaccine Candidate Confers Broad Protection against a Range of Prevalent Circulating Strains in a Nonclinical Setting

Clostridium difficile infection (CDI) is a leading cause of nosocomial and antibiotic-associated diarrhea. A vaccine, based on formalin-inactivated toxins A and B purified from anaerobic cultures of C. difficile strain VPI 10463 (toxinotype 0), has been in development for the prevention of symptomat...

Descripción completa

Detalles Bibliográficos
Autores principales: Quemeneur, Laurence, Petiot, Nadine, Arnaud-Barbe, Nadège, Hessler, Catherine, Pietrobon, Patricia J., Londoño-Hayes, Patricia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5964523/
https://www.ncbi.nlm.nih.gov/pubmed/29632249
http://dx.doi.org/10.1128/IAI.00742-17
_version_ 1783325194331357184
author Quemeneur, Laurence
Petiot, Nadine
Arnaud-Barbe, Nadège
Hessler, Catherine
Pietrobon, Patricia J.
Londoño-Hayes, Patricia
author_facet Quemeneur, Laurence
Petiot, Nadine
Arnaud-Barbe, Nadège
Hessler, Catherine
Pietrobon, Patricia J.
Londoño-Hayes, Patricia
author_sort Quemeneur, Laurence
collection PubMed
description Clostridium difficile infection (CDI) is a leading cause of nosocomial and antibiotic-associated diarrhea. A vaccine, based on formalin-inactivated toxins A and B purified from anaerobic cultures of C. difficile strain VPI 10463 (toxinotype 0), has been in development for the prevention of symptomatic CDI. We evaluated the breadth of protection conferred by this C. difficile toxoid vaccine in cross-neutralization assessments using sera from vaccinated hamsters against a collection of 165 clinical isolates. Hamster antisera raised against the C. difficile toxoid vaccine neutralized the cytotoxic activity of culture supernatants from several toxinotype 0 strains and heterologous strains from 10 different toxinotypes. Further assessments performed with purified toxins confirmed that vaccine-elicited antibodies can neutralize both A and B toxins from a variety of toxinotypes. In the hamster challenge model, the vaccine conferred significant cross-protection against disease symptoms and death caused by heterologous C. difficile strains from the most common phylogenetic clades, including the most prevalent toxinotypes.
format Online
Article
Text
id pubmed-5964523
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher American Society for Microbiology
record_format MEDLINE/PubMed
spelling pubmed-59645232018-05-30 Clostridium difficile Toxoid Vaccine Candidate Confers Broad Protection against a Range of Prevalent Circulating Strains in a Nonclinical Setting Quemeneur, Laurence Petiot, Nadine Arnaud-Barbe, Nadège Hessler, Catherine Pietrobon, Patricia J. Londoño-Hayes, Patricia Infect Immun Bacterial Infections Clostridium difficile infection (CDI) is a leading cause of nosocomial and antibiotic-associated diarrhea. A vaccine, based on formalin-inactivated toxins A and B purified from anaerobic cultures of C. difficile strain VPI 10463 (toxinotype 0), has been in development for the prevention of symptomatic CDI. We evaluated the breadth of protection conferred by this C. difficile toxoid vaccine in cross-neutralization assessments using sera from vaccinated hamsters against a collection of 165 clinical isolates. Hamster antisera raised against the C. difficile toxoid vaccine neutralized the cytotoxic activity of culture supernatants from several toxinotype 0 strains and heterologous strains from 10 different toxinotypes. Further assessments performed with purified toxins confirmed that vaccine-elicited antibodies can neutralize both A and B toxins from a variety of toxinotypes. In the hamster challenge model, the vaccine conferred significant cross-protection against disease symptoms and death caused by heterologous C. difficile strains from the most common phylogenetic clades, including the most prevalent toxinotypes. American Society for Microbiology 2018-05-22 /pmc/articles/PMC5964523/ /pubmed/29632249 http://dx.doi.org/10.1128/IAI.00742-17 Text en Copyright © 2018 Quemeneur et al. https://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Bacterial Infections
Quemeneur, Laurence
Petiot, Nadine
Arnaud-Barbe, Nadège
Hessler, Catherine
Pietrobon, Patricia J.
Londoño-Hayes, Patricia
Clostridium difficile Toxoid Vaccine Candidate Confers Broad Protection against a Range of Prevalent Circulating Strains in a Nonclinical Setting
title Clostridium difficile Toxoid Vaccine Candidate Confers Broad Protection against a Range of Prevalent Circulating Strains in a Nonclinical Setting
title_full Clostridium difficile Toxoid Vaccine Candidate Confers Broad Protection against a Range of Prevalent Circulating Strains in a Nonclinical Setting
title_fullStr Clostridium difficile Toxoid Vaccine Candidate Confers Broad Protection against a Range of Prevalent Circulating Strains in a Nonclinical Setting
title_full_unstemmed Clostridium difficile Toxoid Vaccine Candidate Confers Broad Protection against a Range of Prevalent Circulating Strains in a Nonclinical Setting
title_short Clostridium difficile Toxoid Vaccine Candidate Confers Broad Protection against a Range of Prevalent Circulating Strains in a Nonclinical Setting
title_sort clostridium difficile toxoid vaccine candidate confers broad protection against a range of prevalent circulating strains in a nonclinical setting
topic Bacterial Infections
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5964523/
https://www.ncbi.nlm.nih.gov/pubmed/29632249
http://dx.doi.org/10.1128/IAI.00742-17
work_keys_str_mv AT quemeneurlaurence clostridiumdifficiletoxoidvaccinecandidateconfersbroadprotectionagainstarangeofprevalentcirculatingstrainsinanonclinicalsetting
AT petiotnadine clostridiumdifficiletoxoidvaccinecandidateconfersbroadprotectionagainstarangeofprevalentcirculatingstrainsinanonclinicalsetting
AT arnaudbarbenadege clostridiumdifficiletoxoidvaccinecandidateconfersbroadprotectionagainstarangeofprevalentcirculatingstrainsinanonclinicalsetting
AT hesslercatherine clostridiumdifficiletoxoidvaccinecandidateconfersbroadprotectionagainstarangeofprevalentcirculatingstrainsinanonclinicalsetting
AT pietrobonpatriciaj clostridiumdifficiletoxoidvaccinecandidateconfersbroadprotectionagainstarangeofprevalentcirculatingstrainsinanonclinicalsetting
AT londonohayespatricia clostridiumdifficiletoxoidvaccinecandidateconfersbroadprotectionagainstarangeofprevalentcirculatingstrainsinanonclinicalsetting