Back to Search
Start Over
Modulation of dendritic cell antigen presentation by pathogens, tissue damage and secondary inflammatory signals.
- Source :
-
Current opinion in pharmacology [Curr Opin Pharmacol] 2014 Aug; Vol. 17, pp. 64-70. Date of Electronic Publication: 2014 Aug 13. - Publication Year :
- 2014
-
Abstract
- Antigen presentation by dendritic cells (DC) is regulated directly by pathogen-associated or cell death-associated cues, or indirectly by immunomodulatory molecules produced during infection or tissue damage. DC modulation by direct encounter of pathogen-associated compounds has been thoroughly studied; the effects of molecules associated with cell death are less well characterized; modulation by secondary signals remain poorly understood. In this review we describe recent studies on the role of these three categories of immunomodulatory compounds on DC. We conclude that characterization of the role of secondary immunomodulators is an area in dare need of further study. The outcomes of this endeavor will be new opportunities for the development of better vaccines and compounds applicable to the therapeutic immunomodulation of DC function.<br /> (Copyright © 2014 Elsevier Ltd. All rights reserved.)
- Subjects :
- Animals
Communicable Diseases immunology
Communicable Diseases metabolism
Dendritic Cells immunology
Drug Design
Host-Pathogen Interactions drug effects
Humans
Inflammation immunology
Inflammation metabolism
Receptors, Immunologic drug effects
Receptors, Immunologic metabolism
Anti-Inflammatory Agents therapeutic use
Antigen Presentation drug effects
Communicable Diseases drug therapy
Dendritic Cells drug effects
Immunologic Factors therapeutic use
Inflammation drug therapy
Inflammation Mediators metabolism
Signal Transduction drug effects
Subjects
Details
- Language :
- English
- ISSN :
- 1471-4973
- Volume :
- 17
- Database :
- MEDLINE
- Journal :
- Current opinion in pharmacology
- Publication Type :
- Academic Journal
- Accession number :
- 25128781
- Full Text :
- https://doi.org/10.1016/j.coph.2014.07.013