Preclinical assessment of a new live ...
Type de document :
Article dans une revue scientifique: Article original
PMID :
Titre :
Preclinical assessment of a new live attenuated Mycobacterium tuberculosis Beijing-based vaccine for tuberculosis
Auteur(s) :
Levillain, Florence [Auteur]
Institut de pharmacologie et de biologie structurale [IPBS]
Kim, Hongmin [Auteur]
Yonsei University
Woong Kwon, Kee [Auteur]
Yonsei University
Clark, Simon [Auteur]
Public Health England [Salisbury] [PHE]
Cia, Felipe [Auteur]
London School of Hygiene and Tropical Medicine [LSHTM]
Malaga, Wladimir [Auteur]
Yonsei University
Lanni, Faye [Auteur]
Public Health England [Salisbury] [PHE]
Brodin, Priscille [Auteur]
Centre d’Infection et d’Immunité de Lille - INSERM U 1019 - UMR 9017 - UMR 8204 [CIIL]
Gicquel, Brigitte [Auteur]
Génétique mycobactérienne - Mycobacterial genetics
Shenzhen Univerisity [Shenzhen]
Guilhot, Christophe [Auteur]
Yonsei University
Bancroft, Gregory [Auteur]
London School of Hygiene and Tropical Medicine [LSHTM]
Williams, Ann [Auteur]
Public Health England [Salisbury] [PHE]
Jae Shin, Sung [Auteur]
Yonsei University
Poquet, Yannick [Auteur]
Institut de pharmacologie et de biologie structurale [IPBS]
Neyrolles, Olivier [Auteur correspondant]
Institut de pharmacologie et de biologie structurale [IPBS]
Institut de pharmacologie et de biologie structurale [IPBS]
Kim, Hongmin [Auteur]
Yonsei University
Woong Kwon, Kee [Auteur]
Yonsei University
Clark, Simon [Auteur]
Public Health England [Salisbury] [PHE]
Cia, Felipe [Auteur]
London School of Hygiene and Tropical Medicine [LSHTM]
Malaga, Wladimir [Auteur]
Yonsei University
Lanni, Faye [Auteur]
Public Health England [Salisbury] [PHE]
Brodin, Priscille [Auteur]
Centre d’Infection et d’Immunité de Lille - INSERM U 1019 - UMR 9017 - UMR 8204 [CIIL]
Gicquel, Brigitte [Auteur]
Génétique mycobactérienne - Mycobacterial genetics
Shenzhen Univerisity [Shenzhen]
Guilhot, Christophe [Auteur]
Yonsei University
Bancroft, Gregory [Auteur]
London School of Hygiene and Tropical Medicine [LSHTM]
Williams, Ann [Auteur]
Public Health England [Salisbury] [PHE]
Jae Shin, Sung [Auteur]
Yonsei University
Poquet, Yannick [Auteur]
Institut de pharmacologie et de biologie structurale [IPBS]
Neyrolles, Olivier [Auteur correspondant]
Institut de pharmacologie et de biologie structurale [IPBS]
Titre de la revue :
Vaccine
Pagination :
1416-1423
Éditeur :
Elsevier
Date de publication :
2020-02
ISSN :
0264-410X
Mot(s)-clé(s) en anglais :
Tuberculosis
Mycobacterium tuberculosis
BCG
Vaccine
Mycobacterium tuberculosis
BCG
Vaccine
Discipline(s) HAL :
Sciences du Vivant [q-bio]/Immunologie/Vaccinologie
Résumé en anglais : [en]
Tuberculosis still claims more lives than any other pathogen, and a vaccine better than BCG is urgently needed. One of the challenges for novel TB vaccines is to protect against all Mycobacterium tuberculosis lineages, ...
Lire la suite >Tuberculosis still claims more lives than any other pathogen, and a vaccine better than BCG is urgently needed. One of the challenges for novel TB vaccines is to protect against all Mycobacterium tuberculosis lineages, including the most virulent ones, such as the Beijing lineage. Here we developed a live attenuated M. tuberculosis mutant derived from GC1237, a Beijing strain responsible for tuberculosis outbreaks in the Canary Islands. The mutant strain is inactivated both in the Rv1503c gene, responsible for surface glycolipid synthesis, and in the two-component global regulator PhoPR. This double mutant is as safe as BCG in immunodeficient SCID mice. In immune-competent mice and guinea pigs, the mutant is as protective as BCG against M. tuberculosis strains of common lineage 4 (Euro-American). By contrast, in mice the vaccine is protective against a M. tuberculosis strain of lineage 2 (East-Asian, Beijing), while BCG is not. These results highlight differences in protection efficacy of live attenuated M. tuberculosis-derived vaccine candidates depending on their genetic background, and provide insights for the development of novel live vaccines against TB, especially in East-Asian countries where M. tuberculosis strains of the Beijing family are highly dominant.Lire moins >
Lire la suite >Tuberculosis still claims more lives than any other pathogen, and a vaccine better than BCG is urgently needed. One of the challenges for novel TB vaccines is to protect against all Mycobacterium tuberculosis lineages, including the most virulent ones, such as the Beijing lineage. Here we developed a live attenuated M. tuberculosis mutant derived from GC1237, a Beijing strain responsible for tuberculosis outbreaks in the Canary Islands. The mutant strain is inactivated both in the Rv1503c gene, responsible for surface glycolipid synthesis, and in the two-component global regulator PhoPR. This double mutant is as safe as BCG in immunodeficient SCID mice. In immune-competent mice and guinea pigs, the mutant is as protective as BCG against M. tuberculosis strains of common lineage 4 (Euro-American). By contrast, in mice the vaccine is protective against a M. tuberculosis strain of lineage 2 (East-Asian, Beijing), while BCG is not. These results highlight differences in protection efficacy of live attenuated M. tuberculosis-derived vaccine candidates depending on their genetic background, and provide insights for the development of novel live vaccines against TB, especially in East-Asian countries where M. tuberculosis strains of the Beijing family are highly dominant.Lire moins >
Langue :
Anglais
Comité de lecture :
Oui
Audience :
Internationale
Vulgarisation :
Non
Source :
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