Pore-formation by adenylate cyclase toxoid activates dendritic cells to prime CD8+ and CD4+ T cells
Jazyk angličtina Země Spojené státy americké Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
26437769
DOI
10.1038/icb.2015.87
PII: icb201587
Knihovny.cz E-zdroje
- MeSH
- adenylátcyklasový toxin genetika imunologie MeSH
- adjuvancia imunologická genetika MeSH
- aktivace lymfocytů * MeSH
- buněčná diferenciace MeSH
- CD4-pozitivní T-lymfocyty imunologie MeSH
- CD8-pozitivní T-lymfocyty imunologie MeSH
- cytokiny metabolismus MeSH
- cytotoxické proteiny tvořící póry genetika imunologie MeSH
- dendritické buňky imunologie mikrobiologie MeSH
- iontový transport MeSH
- kultivované buňky MeSH
- mitogenem aktivované proteinkinasy p38 metabolismus MeSH
- myši inbrední C57BL MeSH
- myši MeSH
- permeabilita buněčné membrány MeSH
- proteinové domény genetika imunologie MeSH
- protinádorové vakcíny imunologie MeSH
- zvířata MeSH
- Check Tag
- myši MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- adenylátcyklasový toxin MeSH
- adjuvancia imunologická MeSH
- cytokiny MeSH
- cytotoxické proteiny tvořící póry MeSH
- mitogenem aktivované proteinkinasy p38 MeSH
- protinádorové vakcíny MeSH
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 (~400 residues). In parallel, ~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. The toxoid-induced in vitro phenotypic maturation of DC involved the activity of mitogen activated protein kinases p38 and JNK and comprised increased expression of maturation markers, interleukin 6, chemokines KC and LIX and granulocyte-colony-stimulating factor secretion, prostaglandin E2 production and enhancement of chemotactic migration of DC. Moreover, i.v. injected toxoids induced maturation of splenic DC in function of their cell-permeabilizing capacity. Similarly, the capacity of DC to stimulate CD8(+) and CD4(+) T-cell responses in vitro and in vivo was dependent on the pore-forming activity of CyaA-AC(-). This reveals a novel self-adjuvanting capacity of the CyaA-AC(-) toxoid that is currently under clinical evaluation as a tool for delivery of immunotherapeutic anti-cancer CD8(+) T-cell vaccines into DC.
Department of Pneumology and BIOSS Albert Ludwig University Freiburg Germany
Faculty of Science Charles University Prague Czech Republic
Institut Pasteur Unité de Régulation Immunitaire et Vaccinologie Paris France
Institute of Microbiology of the ASCR v v i Prague; Czech Republic
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