| Literature DB >> 27351923 |
Marlene Ballbach1, Tobias Hall, Alina Brand, Davide Neri, Anurag Singh, Iris Schaefer, Eva Herrmann, Sandra Hansmann, Rupert Handgretinger, Jasmin Kuemmerle-Deschner, Dominik Hartl, Nikolaus Rieber.
Abstract
Cryopyrin-associated periodic syndromes (CAPS) are caused by mutations in the NLRP3 gene leading to overproduction of IL-1β and other NLRP3 inflammasome products. Myeloid-derived suppressor cells (MDSCs) represent a novel innate immune cell subset capable of suppressing T-cell responses. As inflammasome products were previously found to induce MDSCs, we hypothesized that NLRP3 inflammasome-dependent factors induce the generation of MDSCs in CAPS. We studied neutrophilic MDSCs, their clinical relevance, and MDSC-inducing factors in a unique cohort of CAPS patients under anti-IL-1 therapy. Despite anti-IL-1 therapy and low clinical disease activity, CAPS patients showed significantly elevated MDSCs compared to healthy controls. MDSCs were functionally competent, as they suppressed polyclonal T-cell proliferation, as well as Th1 and Th17 responses. In addition, MDSCs decreased monocytic IL-1β secretion. Multiplex assays revealed a distinct pattern of MDSC-inducing cytokines, chemokines, and growth factors. Experimental analyses demonstrated that IL-1 cytokine family members and autoinflammation-associated alarmins differentially induced human MDSCs. Increased MDSCs might represent a novel autologous anti-inflammatory mechanism in autoinflammatory conditions and may serve as a future therapeutic target.Entities:
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Year: 2016 PMID: 27351923 PMCID: PMC6743338 DOI: 10.1159/000446615
Source DB: PubMed Journal: J Innate Immun ISSN: 1662-811X Impact factor: 7.349