Safety and Efficacy of an AIEC-targeted Bacteriophage Cocktail in a Mice Colitis Model.


Journal

Journal of Crohn's & colitis
ISSN: 1876-4479
Titre abrégé: J Crohns Colitis
Pays: England
ID NLM: 101318676

Informations de publication

Date de publication:
01 Nov 2022
Historique:
pubmed: 24 8 2022
medline: 4 11 2022
entrez: 23 8 2022
Statut: ppublish

Résumé

Adherent invasive Escherichia coli [AIEC] are recovered with a high frequency from the gut mucosa of Crohn's disease patients and are believed to contribute to the dysbiosis and pathogenesis of this inflammatory bowel disease. In this context, bacteriophage therapy has been proposed for specifically targeting AIEC in the human gut with no deleterious impact on the commensal microbiota. The in vitro efficacy and specificity of a seven lytic phage cocktail [EcoActive™] was assessed against [i] 210 clinical AIEC strains, and [ii] 43 non-E. coli strains belonging to the top 12 most common bacterial genera typically associated with a healthy human microbiome. These data were supported by in vivo safety and efficacy assays conducted on healthy and AIEC-colonized mice, respectively. The EcoActive cocktail was effective in vitro against 95% of the AIEC strains and did not lyse any of the 43 non-E. coli commensal strains, in contrast to conventional antibiotics. Long-term administration of the EcoActive cocktail to healthy mice was safe and did not induce dysbiosis according to metagenomic data. Using a murine model of induced colitis of animals infected with the AIEC strain LF82, we found that a single administration of the cocktail failed to alleviate inflammatory symptoms, while mice receiving the cocktail twice a day for 15 days were protected from clinical and microscopical manifestations of inflammation. Collectively, the data support the approach of AIEC-targeted phage therapy as safe and effective treatment for reducing AIEC levels in the gut of IBD patients.

Sections du résumé

BACKGROUND AND AIMS OBJECTIVE
Adherent invasive Escherichia coli [AIEC] are recovered with a high frequency from the gut mucosa of Crohn's disease patients and are believed to contribute to the dysbiosis and pathogenesis of this inflammatory bowel disease. In this context, bacteriophage therapy has been proposed for specifically targeting AIEC in the human gut with no deleterious impact on the commensal microbiota.
METHODS METHODS
The in vitro efficacy and specificity of a seven lytic phage cocktail [EcoActive™] was assessed against [i] 210 clinical AIEC strains, and [ii] 43 non-E. coli strains belonging to the top 12 most common bacterial genera typically associated with a healthy human microbiome. These data were supported by in vivo safety and efficacy assays conducted on healthy and AIEC-colonized mice, respectively.
RESULTS RESULTS
The EcoActive cocktail was effective in vitro against 95% of the AIEC strains and did not lyse any of the 43 non-E. coli commensal strains, in contrast to conventional antibiotics. Long-term administration of the EcoActive cocktail to healthy mice was safe and did not induce dysbiosis according to metagenomic data. Using a murine model of induced colitis of animals infected with the AIEC strain LF82, we found that a single administration of the cocktail failed to alleviate inflammatory symptoms, while mice receiving the cocktail twice a day for 15 days were protected from clinical and microscopical manifestations of inflammation.
CONCLUSIONS CONCLUSIONS
Collectively, the data support the approach of AIEC-targeted phage therapy as safe and effective treatment for reducing AIEC levels in the gut of IBD patients.

Identifiants

pubmed: 35997152
pii: 6673800
doi: 10.1093/ecco-jcc/jjac064
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1617-1627

Subventions

Organisme : Ferring

Commentaires et corrections

Type : CommentIn

Informations de copyright

© The Author(s) 2022. Published by Oxford University Press on behalf of European Crohn’s and Colitis Organisation. All rights reserved. For permissions, please email: journals.permissions@oup.com.

Auteurs

Marie Titécat (M)

Univ. Lille, INSERM, CHU Lille, U1286 - Institute for Translational Research in Inflammation, Lille, France.

Christel Rousseaux (C)

Intestinal Biotech Development, 59045 Lille, France.

Caroline Dubuquoy (C)

Intestinal Biotech Development, 59045 Lille, France.

Benoît Foligné (B)

Univ. Lille, INSERM, CHU Lille, U1286 - Institute for Translational Research in Inflammation, Lille, France.

Oumaïra Rahmouni (O)

Univ. Lille, INSERM, CHU Lille, U1286 - Institute for Translational Research in Inflammation, Lille, France.

Séverine Mahieux (S)

Univ. Lille, INSERM, CHU Lille, U1286 - Institute for Translational Research in Inflammation, Lille, France.

Pierre Desreumaux (P)

Univ. Lille, INSERM, CHU Lille, U1286 - Institute for Translational Research in Inflammation, Lille, France.
Intestinal Biotech Development, 59045 Lille, France.

Joelle Woolston (J)

Intralytix, Inc., Columbia, MD 21046, USA.

Alexander Sulakvelidze (A)

Intralytix, Inc., Columbia, MD 21046, USA.

Kristin Wannerberger (K)

Ferring International Center SA, St-Prex, Switzerland.

Christel Neut (C)

Univ. Lille, INSERM, CHU Lille, U1286 - Institute for Translational Research in Inflammation, Lille, France.

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Classifications MeSH