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Published in: Critical Care 1/2013

01-02-2013 | Letter

Contribution of activated platelets to plasma IL-27 levels

Authors: Hind Hamzeh-Cognasse, Pauline Damien, Kim Anh Nguyen, Fabrice Zeni, Bruno Pozzetto, Fabrice Cognasse, Olivier Garraud

Published in: Critical Care | Issue 1/2013

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Excerpt

In a recent issue of Critical Care, Wong and colleagues [1] demonstrated that the serum concentration of IL-27 in critically ill children was a predictor of infection. Our study aims at determining whether platelet activation contributes to the elevated plasma IL-27 concentration. Here we demonstrate that activation of platelets with thrombin receptor activating peptide (TRAP) significantly increased IL-27 levels in supernatants (Figure 1a). Moreover, B cells incubated in vitro with supernatants from activated platelets upregulated membrane expression of CD86, which was restored to baseline when B cells were pre-incubated with a gp130 blocking antibody (Figure 1b). Our data strongly suggest that platelet activation contributes, along with classical sources [2], to elevated plasma levels of IL-27. Recent advances place platelets as an important link between innate and adaptive immunity [3]. Indeed, platelets modulate their inflammatory response after sensing the presence of an infectious agent [4]. Therefore, platelet activation could contribute to increased plasma concentrations of IL-27 along with cytokines such as soluble CD40L [5], and thus may contribute towards immune dysregulation in patients with sepsis.
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Literature
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Metadata
Title
Contribution of activated platelets to plasma IL-27 levels
Authors
Hind Hamzeh-Cognasse
Pauline Damien
Kim Anh Nguyen
Fabrice Zeni
Bruno Pozzetto
Fabrice Cognasse
Olivier Garraud
Publication date
01-02-2013
Publisher
BioMed Central
Published in
Critical Care / Issue 1/2013
Electronic ISSN: 1364-8535
DOI
https://doi.org/10.1186/cc11925

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