| Literature DB >> 15972685 |
Stefan Blüml1, Stefanie Kirchberger, Valery N Bochkov, Gerhard Krönke, Karl Stuhlmeier, Otto Majdic, Gerhard J Zlabinger, Walter Knapp, Bernd R Binder, Johannes Stöckl, Norbert Leitinger.
Abstract
Maturation of dendritic cells (DCs) induced by pathogen-derived signals via TLRs is a crucial step in the initiation of an adaptive immune response and therefore has to be well controlled. In this study, we demonstrate that oxidized phospholipids (ox-PLs), which are generated during infections, apoptosis, and tissue damage, interfere with DC activation, preventing their maturation. ox-PLs blocked TLR-3- and TLR-4-mediated induction of the costimulatory molecules CD40, CD80, CD83, and CD86, the cytokines IL-12 and TNF, as well as lymphocyte stimulatory capacity. CD40 and TLR-2-mediated cytokine production was also inhibited, whereas up-regulation of costimulatory molecules via these receptors was not affected by ox-PLs. Thus, formation of ox-PLs during the course of an inflammatory response may represent a negative-feedback loop preventing excessive and sustained immune reactions through regulating DC maturation.Entities:
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Year: 2005 PMID: 15972685 DOI: 10.4049/jimmunol.175.1.501
Source DB: PubMed Journal: J Immunol ISSN: 0022-1767 Impact factor: 5.422