The adenylate cyclase toxin from Bordetella pertussis--a novel promising vehicle for antigen delivery to dendritic cells
Language English Country Germany Media print
Document type Journal Article, Research Support, Non-U.S. Gov't, Review
PubMed
15149033
DOI
10.1078/1438-4221-00291
PII: S1438-4221(04)70196-4
Knihovny.cz E-resources
- MeSH
- Adenylate Cyclase Toxin immunology MeSH
- Antigens, Bacterial immunology MeSH
- Bordetella pertussis enzymology immunology MeSH
- CD4-Positive T-Lymphocytes immunology MeSH
- CD8-Positive T-Lymphocytes MeSH
- Dendritic Cells immunology MeSH
- Epitopes, T-Lymphocyte immunology MeSH
- Bordetella Infections immunology prevention & control MeSH
- Humans MeSH
- Histocompatibility Antigens Class I immunology MeSH
- Histocompatibility Antigens Class II immunology MeSH
- Antigen Presentation immunology MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Review MeSH
- Names of Substances
- Adenylate Cyclase Toxin MeSH
- Antigens, Bacterial MeSH
- Epitopes, T-Lymphocyte MeSH
- Histocompatibility Antigens Class I MeSH
- Histocompatibility Antigens Class II MeSH
Bordetella pertussis secretes an adenylate cyclase toxin (CyaA or ACT) that targets primarily cells expressing the alphaMbeta2 integrin (CD11b/CD18) receptor. This toxin can deliver its N-terminal catalytic AC domain (400 amino acid residues) into the cytosol directly across the cytoplasmic membrane. Various heterologous CD8+, as well as CD4+ T-cell epitopes have been engineered into genetically detoxified CyaA and the resulting toxoids were successfully used as vectors for delivery of inserted epitopes into antigen-presenting cells. Upon processing and presentation, these recombinant CyaAs trigger specific MHC class I and/or class II-restricted T-cell responses both in vitro and in vivo.
References provided by Crossref.org
Pore-formation by adenylate cyclase toxoid activates dendritic cells to prime CD8+ and CD4+ T cells