Tick saliva inhibits dendritic cell migration, maturation, and function while promoting development of Th2 responses
Language English Country United States Media print
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
18424740
DOI
10.4049/jimmunol.180.9.6186
PII: 180/9/6186
Knihovny.cz E-resources
- MeSH
- CD40 Antigens immunology MeSH
- Dendritic Cells immunology MeSH
- Immune Tolerance immunology MeSH
- Ixodes immunology MeSH
- Lymph Nodes immunology MeSH
- Mice MeSH
- Cell Movement immunology MeSH
- Antigen Presentation immunology MeSH
- Saliva immunology MeSH
- Th1 Cells immunology MeSH
- Th2 Cells immunology MeSH
- Toll-Like Receptors immunology MeSH
- Animals MeSH
- Check Tag
- Mice MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- CD40 Antigens MeSH
- Toll-Like Receptors MeSH
Similarly to other blood-feeding arthropods, ticks have evolved immunosuppressive mechanisms enabling them to overcome the host immune system. Although the immunomodulatory effect of tick saliva on several cell populations of the immune system has been extensively studied, little is known about its impact on dendritic cells (DCs). We have examined the effect of Ixodes ricinus tick saliva on DC function in vitro and in vivo. Exposure of DCs to tick saliva in vitro resulted in impaired maturation, upon CD40 or TLR9, TLR3 and TLR7 ligation, as well as reduced Ag presentation capacity. Administration of tick saliva in vivo significantly inhibited maturation and early migration of DCs from inflamed skin to draining lymph nodes, and decreased the capacity of lymph node DCs to present soluble Ag to specific T cells. Moreover, saliva-exposed DCs failed to induce efficient Th1 and Th17 polarization and promoted development of Th2 responses. Our data reveal a complex inhibitory effect exerted by tick saliva on DC function. Given the role of DCs as the key instigators of adaptive immune responses, alteration of their function might represent a major mechanism of tick-mediated immune evasion.
References provided by Crossref.org
The structure and function of Iristatin, a novel immunosuppressive tick salivary cystatin
Modulation of host immunity by tick saliva
Tick sialostatins L and L2 differentially influence dendritic cell responses to Borrelia spirochetes