Pore-formation by adenylate cyclase toxoid activates dendritic cells to prime CD8(+) and CD4(+) T cells
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61388971%3A_____%2F16%3A00462522" target="_blank" >RIV/61388971:_____/16:00462522 - isvavai.cz</a>
Alternative codes found
RIV/00216208:11310/16:10318652
Result on the web
<a href="http://dx.doi.org/10.1038/icb.2015.87" target="_blank" >http://dx.doi.org/10.1038/icb.2015.87</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1038/icb.2015.87" target="_blank" >10.1038/icb.2015.87</a>
Alternative languages
Result language
angličtina
Original language name
Pore-formation by adenylate cyclase toxoid activates dendritic cells to prime CD8(+) and CD4(+) T cells
Original language description
The adenylate cyclase toxin-hemolysin (CyaA) of Bordetella pertussis is a bi-functional leukotoxin. It penetrates myeloid phagocytes expressing the complement receptor 3 and delivers into their cytosol its N-terminal adenylate cyclase enzyme domain (similar to 400 residues). In parallel, similar to 1300 residue-long RTX hemolysin moiety of CyaA forms cation-selective pores and permeabilizes target cell membrane for efflux of cytosolic potassium ions. The non-enzymatic CyaA-AC(-) toxoid, has repeatedly been successfully exploited as an antigen delivery tool for stimulation of adaptive T-cell immune responses. We show that the pore-forming activity confers on the CyaA-AC(-) toxoid a capacity to trigger Toll-like receptor and inflammasome signaling-independent maturation of CD11b-expressing dendritic cells (DC). The DC maturation-inducing potency of mutant toxoid variants in vitro reflected their specifically enhanced or reduced pore-forming activity and K+ efflux.
Czech name
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Czech description
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Classification
Type
J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)
CEP classification
EE - Microbiology, virology
OECD FORD branch
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Result continuities
Project
Result was created during the realization of more than one project. More information in the Projects tab.
Continuities
I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace
Others
Publication year
2016
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
Immunology and Cell Biology
ISSN
0818-9641
e-ISSN
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Volume of the periodical
94
Issue of the periodical within the volume
4
Country of publishing house
AU - AUSTRALIA
Number of pages
12
Pages from-to
322-333
UT code for WoS article
000374348200003
EID of the result in the Scopus database
2-s2.0-84949008403