Tuberculosis vaccines update: Is an RNA-based vaccine feasible for tuberculosis?


Journal

International journal of infectious diseases : IJID : official publication of the International Society for Infectious Diseases
ISSN: 1878-3511
Titre abrégé: Int J Infect Dis
Pays: Canada
ID NLM: 9610933

Informations de publication

Date de publication:
May 2023
Historique:
received: 02 02 2023
revised: 16 03 2023
accepted: 16 03 2023
medline: 5 6 2023
pubmed: 25 3 2023
entrez: 24 3 2023
Statut: ppublish

Résumé

Despite concerted efforts, Mycobacterium tuberculosis (M.tb), the pathogen that causes tuberculosis (TB), continues to be a burden on global health, regaining its dubious distinction in 2022 as the world's biggest infectious killer with global COVID-19 deaths steadily declining. The complex nature of M.tb, coupled with different pathogenic stages, has highlighted the need for the development of novel immunization approaches to combat this ancient infectious agent. Intensive efforts over the last couple of decades have identified alternative approaches to improve upon traditional vaccines that are based on killed pathogens, live attenuated agents, or subunit recombinant antigens formulated with adjuvants. Massive funding and rapid advances in RNA-based vaccines for immunization have recently transformed the possibility of protecting global populations from viral pathogens, such as SARS-CoV-2. Similar efforts to combat bacterial pathogens such as M.tb have been significantly slower to implement. In this review, we discuss the application of a novel replicating RNA (repRNA)-based vaccine formulated and delivered in nanostructured lipids. Our preclinical data are the first to report that RNA platforms are a viable system for TB vaccines and should be pursued with high-priority M.tb antigens containing cluster of differentiation (CD4+) and CD8+ T-cell epitopes. This RNA vaccine shows promise for use against intracellular bacteria such as M.tb as demonstrated by the feasibility of construction, enhanced induction of cell-mediated and humoral immune responses, and improved bacterial burden outcomes in in vivo aerosol-challenged preclinical TB models.

Identifiants

pubmed: 36963657
pii: S1201-9712(23)00114-5
doi: 10.1016/j.ijid.2023.03.035
pmc: PMC10033141
pii:
doi:

Substances chimiques

Tuberculosis Vaccines 0
Antigens, Bacterial 0

Types de publication

Review Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

S47-S51

Subventions

Organisme : NIAID NIH HHS
ID : 75N93019C00072
Pays : United States
Organisme : NIAID NIH HHS
ID : R01 AI125160
Pays : United States
Organisme : NIAID NIH HHS
ID : R61 AI169207
Pays : United States

Informations de copyright

Copyright © 2023 The Authors. Published by Elsevier Ltd.. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of competing interest The authors declare no conflict of interest. The funders had no role in the design of the study; in the collection, analyses, or interpretation of data; in the writing of the manuscript; or in the decision to publish the results.

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Auteurs

Sasha E Larsen (SE)

Center for Global Infectious Disease Research, Seattle Children's Research Institute, Seattle, USA.

Susan L Baldwin (SL)

Center for Global Infectious Disease Research, Seattle Children's Research Institute, Seattle, USA.

Rhea N Coler (RN)

Center for Global Infectious Disease Research, Seattle Children's Research Institute, Seattle, USA; Department of Pediatrics, University of Washington School of Medicine, Seattle, USA; Department of Global Health, University of Washington, Seattle, USA. Electronic address: Rhea.Coler@seattlechildrens.org.

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