Targeted suppression of human IBD-associated gut microbiota commensals by phage consortia for treatment of intestinal inflammation.
Crohn’s disease
Klebsiella pneumoniae
inflammatory bowel diseases
microbiome
microbiota
phage therapy
resistome
ulcerative colitis
Journal
Cell
ISSN: 1097-4172
Titre abrégé: Cell
Pays: United States
ID NLM: 0413066
Informations de publication
Date de publication:
04 08 2022
04 08 2022
Historique:
received:
17
03
2022
revised:
17
05
2022
accepted:
11
07
2022
entrez:
5
8
2022
pubmed:
6
8
2022
medline:
10
8
2022
Statut:
ppublish
Résumé
Human gut commensals are increasingly suggested to impact non-communicable diseases, such as inflammatory bowel diseases (IBD), yet their targeted suppression remains a daunting unmet challenge. In four geographically distinct IBD cohorts (n = 537), we identify a clade of Klebsiella pneumoniae (Kp) strains, featuring a unique antibiotics resistance and mobilome signature, to be strongly associated with disease exacerbation and severity. Transfer of clinical IBD-associated Kp strains into colitis-prone, germ-free, and colonized mice enhances intestinal inflammation. Stepwise generation of a lytic five-phage combination, targeting sensitive and resistant IBD-associated Kp clade members through distinct mechanisms, enables effective Kp suppression in colitis-prone mice, driving an attenuated inflammation and disease severity. Proof-of-concept assessment of Kp-targeting phages in an artificial human gut and in healthy volunteers demonstrates gastric acid-dependent phage resilience, safety, and viability in the lower gut. Collectively, we demonstrate the feasibility of orally administered combination phage therapy in avoiding resistance, while effectively inhibiting non-communicable disease-contributing pathobionts.
Identifiants
pubmed: 35931020
pii: S0092-8674(22)00850-9
doi: 10.1016/j.cell.2022.07.003
pii:
doi:
Types de publication
Journal Article
Research Support, N.I.H., Extramural
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
2879-2898.e24Commentaires et corrections
Type : CommentIn
Type : CommentIn
Type : CommentIn
Type : CommentIn
Informations de copyright
Copyright © 2022 Elsevier Inc. All rights reserved.
Déclaration de conflit d'intérêts
Declaration of interests H. Sokol received consultancy or lecture fees from Carenity, Abbvie, Astellas, Danone, Ferring, Mayoly Spindler, MSD, Novartis, Roche, Tillots, Enterome, Maat, BiomX, Biose, and Takeda and is a co-founder of Exeliom Bioscience. N.M. received consultancy or lecture fees from BiomX, Pfizer, Takeda, Janssen, Ferring, Nestle, and BMS and grant support from Takeda, Janssen, Abbott, Pfizer, Abbvie, Neopharm, Corundum Innovation Ltd, Mycolivia, and Nestle. S.K.-R., E.W., Y.M, Y.S., I.W., E.K., N.B.-I., D.I., H.B.-D., J.N., N.K., E.K., T.C., E.F.-G., L.Z., A.C., U.R., I.G.-S., M.G., V.L., N.Z., S.P., and M.S. are paid BiomX employees. R.S. is a scientific cofounder of Ecophage and BiomX. E.E. is a scientific cofounder of DayTwo and BiomX and an advisor to Hello Inside and Aposense. E.E. serves as a scientific advisory board member in Cell. A patent proposal has been submitted by the Weizmann Institute of Science and BiomX.