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Inflammasome Activation by Adenylate Cyclase Toxin Directs Th17 Responses and Protection against Bordetella pertussis
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SYSNO ASEP 0348119 Document Type J - Journal Article R&D Document Type Journal Article Subsidiary J Článek ve WOS Title Inflammasome Activation by Adenylate Cyclase Toxin Directs Th17 Responses and Protection against Bordetella pertussis Author(s) Dunne, A. (IE)
Ross, P. J. (IE)
Pospíšilová, Eva (MBU-M)
Mašín, Jiří (MBU-M) RID, ORCID
Meaney, A. (IE)
Sutton, C. E. (IE)
Iwakura, Y. (JP)
Tschopp, J. (CH)
Šebo, Peter (MBU-M) RID, ORCID
Mills, K. H. G. (IE)Source Title Journal of Immunology. - : American Association of Immunologists - ISSN 0022-1767
Roč. 187, č. 3 (2010), s. 1711-1719Number of pages 9 s. Language eng - English Country US - United States Keywords ADAPTIVE IMMUNE-RESPONSES ; IL-17-PRODUCING T-CELLS ; HOST-DEFENSE Subject RIV EC - Immunology R&D Projects GA310/08/0447 GA ČR - Czech Science Foundation (CSF) IAA500200914 GA AV ČR - Academy of Sciences of the Czech Republic (AV ČR) CEZ AV0Z50200510 - MBU-M (2005-2011) UT WOS 000280177400048 DOI 10.4049/jimmunol.1000105 Annotation In this article, we demonstrate that inflammasome-mediated IL-1b plays a critical role in promoting Ag-specific Th17 cells and in generating protective immunity against Bordetella pertussis infection. Using a murine respiratory challenge model, we demonstrated that the course of B. pertussis infection was significantly exacerbated in IL-1R type I-defective (IL-1RI2/2) mice. We found that adenylate cyclase toxin (CyaA), a key virulence factor secreted by B. pertussis, induced robust IL-1b production by dendritic cells through activation of caspase-1 and the NALP3-containing inflammasome complex. Using mutant toxins, we demonstrate that CyaA-mediated activation of caspase-1 was not dependent on adenylate cyclase enzyme activity but was dependent on the pore-forming capacity of CyaA Workplace Institute of Microbiology Contact Eliška Spurná, eliska.spurna@biomed.cas.cz, Tel.: 241 062 231 Year of Publishing 2011
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