Antituberculosis Therapy and Gut Microbiota: Review of Potential Host Microbiota Directed-Therapies.
TB treatment
dysbiosis
gut microbiota
host directed-therapies
tuberculosis
Journal
Frontiers in cellular and infection microbiology
ISSN: 2235-2988
Titre abrégé: Front Cell Infect Microbiol
Pays: Switzerland
ID NLM: 101585359
Informations de publication
Date de publication:
2021
2021
Historique:
received:
26
02
2021
accepted:
12
11
2021
entrez:
24
12
2021
pubmed:
25
12
2021
medline:
28
1
2022
Statut:
epublish
Résumé
Tuberculosis (TB) remains a major public health concern with millions of deaths every year. The overlap with HIV infections, long treatment duration, and the emergence of drug resistance are significant obstacles to the control of the disease. Indeed, the standard first-line regimen TB treatment takes at least six months and even longer for the second-line therapy, resulting in relapses, drug resistance and re-infections. Many recent reports have also shown prolonged and significant damage of the gut microbial community (dysbiosis) from anti-TB drugs that can detrimentally persist several months after the cessation of treatment and could lead to the impairment of the immune response, and thus re-infections and drug resistance. A proposed strategy for shortening the treatment duration is thus to apply corrective measures to the dysbiosis for a faster bacterial clearance and a better treatment outcome. In this review, we will study the role of the gut microbiota in both TB infection and treatment, and its potential link with treatment duration. We will also discuss, the new concept of "Host Microbiota Directed-Therapies (HMDT)" as a potential adjunctive strategy to improve the treatment effectiveness, reduce its duration and or prevent relapses. These strategies include the use of probiotics, prebiotics, gut microbiota transfer, and other strategies. Application of this innovative solution could lead to HMDT as an adjunctive tool to shorten TB treatment, which will have enormous public health impacts for the End TB Strategy worldwide.
Identifiants
pubmed: 34950603
doi: 10.3389/fcimb.2021.673100
pmc: PMC8688706
doi:
Substances chimiques
Antitubercular Agents
0
Pharmaceutical Preparations
0
Types de publication
Journal Article
Research Support, N.I.H., Extramural
Research Support, Non-U.S. Gov't
Review
Langues
eng
Sous-ensembles de citation
IM
Pagination
673100Subventions
Organisme : FIC NIH HHS
ID : D43 TW010350
Pays : United States
Organisme : NIAID NIH HHS
ID : R21 AI148033
Pays : United States
Organisme : FIC NIH HHS
ID : D43 TW010543
Pays : United States
Informations de copyright
Copyright © 2021 Diallo, Somboro, Diabate, Baya, Kone, Sarro, Kone, Diarra, Diallo, Diakite, Doumbia, Toloba, Murphy and Maiga.
Déclaration de conflit d'intérêts
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
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