| Literature DB >> 24994465 |
Yanhui Yang1, Min Xuan2, Xian Zhang2, Donglei Zhang2, Rongfeng Fu2, Fangfang Zhou2, Li Ma2, Huiyuan Li2, Feng Xue2, Lei Zhang2, Renchi Yang3.
Abstract
IL-35 is a novel heterodimeric anti-inflammatory cytokine consisting of Epstein-Barr virus-induced gene 3 (EBI3) and the p35 subunit of IL-12. IL-35 has been shown to possess the potency of inhibiting the CD4+ effector T cells and alleviating autoimmune diseases. In the study we investigated the levels of IL-35 as well as its prospective role in immune thrombocytopenia (ITP).ELISA was adopted to measure plasma IL-35, TGF-β and IL-10 levels. The mRNA expression levels of P35 and EBI3 in peripheral blood mononuclear cells (PBMCs) were studied based on real-time quantitative PCR. The correlation between plasma cytokine levels and clinical parameters was analyzed. Significantly lower plasma IL-35 levels were found in active ITP patients compared with those in remission (p = 0.017) and the healthy controls (p < 0.001). In active ITP patients, the plasma IL-35 levels displayed a significantly positive correlation with platelet counts (r = 0.5335, p < 0.0008). Further, P35 mRNA expression levels were lower in patients with active ITP than patients in remission (p = 0.033) and normal controls (p = 0.016).Thus, for the first time, this research reported a dramatically decreased IL-35 levels in ITP patients, suggesting that IL-35 may be involved in the pathogenesis of ITP.Entities:
Keywords: ELISA; IL-35; ITP; Real-time quantitative polymerase chain reaction; p35
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Year: 2014 PMID: 24994465 DOI: 10.1016/j.humimm.2014.06.019
Source DB: PubMed Journal: Hum Immunol ISSN: 0198-8859 Impact factor: 2.850