| Literature DB >> 28297677 |
Matthias I Gröschel1, Fadel Sayes2, Sung Jae Shin3, Wafa Frigui2, Alexandre Pawlik2, Mickael Orgeur2, Robin Canetti2, Nadine Honoré2, Roxane Simeone2, Tjip S van der Werf4, Wilbert Bitter5, Sang-Nae Cho3, Laleh Majlessi2, Roland Brosch6.
Abstract
Recent insights into the mechanisms by which Mycobacterium tuberculosis, the etiologic agent of human tuberculosis, is recognized by cytosolic nucleotide sensors have opened new avenues for rational vaccine design. The only licensed anti-tuberculosis vaccine, Mycobacterium bovis BCG, provides limited protection. A feature of BCG is the partial deletion of the ESX-1 type VII secretion system, which governs phagosomal rupture and cytosolic pattern recognition, key intracellular phenotypes linked to increased immune signaling. Here, by heterologously expressing the esx-1 region of Mycobacterium marinum in BCG, we engineered a low-virulence, ESX-1-proficient, recombinant BCG (BCG::ESX-1Mmar) that induces the cGas/STING/TBK1/IRF-3/type I interferon axis and enhances AIM2 and NLRP3 inflammasome activity, resulting in both higher proportions of CD8+ T cell effectors against mycobacterial antigens shared with BCG and polyfunctional CD4+ Th1 cells specific to ESX-1 antigens. Importantly, independent mouse vaccination models show that BCG::ESX-1Mmar confers superior protection relative to parental BCG against challenges with highly virulent M. tuberculosis.Entities:
Keywords: ESX/type VII secretion; Mycobacterium marinum; Mycobacterium tuberculosis; cytosolic pattern recognition; innate immune signaling; recombinant BCG; tuberculosis; vaccination
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Year: 2017 PMID: 28297677 DOI: 10.1016/j.celrep.2017.02.057
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423