人IL-35抑制IL-12的生物活性及其与IL-12Rβ2的相互作用。

Najmus S Mahfooz, Marlena R Merling, Tiffany A Claeys, Jack W Dowling, Adriana Forero, Richard T Robinson
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摘要

IL-35是一种免疫抑制性细胞因子,在癌症、自身免疫和传染病中发挥作用。在IL-35生物学的传统模型中,这种细胞因子的p35和Ebi3结构域分别与调节性T细胞和调节性B细胞的细胞表面的IL-12Rβ2和gp130相互作用,触发它们对Th细胞活性的抑制。在这里,我们使用人IL-12生物活性报告细胞系、蛋白质结合测定和原代人Th细胞来证明IL-35抑制Th细胞活性的额外机制,其中IL-35直接抑制IL-12与其表面受体IL-12Rβ2的结合和下游IL-12依赖性活性。IL-12与表面受体IL-12Rβ1的结合不受IL-35的影响。这些数据表明,除了通过调节性T细胞和调节性B细胞发挥作用外,人IL-35还可以直接抑制IL-12的生物活性及其与IL-12Rβ2的相互作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Human IL-35 Inhibits the Bioactivity of IL-12 and Its Interaction with IL-12Rβ2.

IL-35 is an immunosuppressive cytokine with roles in cancer, autoimmunity, and infectious disease. In the conventional model of IL-35 biology, the p35 and Ebi3 domains of this cytokine interact with IL-12Rβ2 and gp130, respectively, on the cell surface of regulatory T and regulatory B cells, triggering their suppression of Th cell activity. Here we use a human IL-12 bioactivity reporter cell line, protein binding assays, and primary human Th cells to demonstrate an additional mechanism by which IL-35 suppresses Th cell activity, wherein IL-35 directly inhibits the association of IL-12 with its surface receptor IL-12Rβ2 and downstream IL-12-dependent activities. IL-12 binding to the surface receptor IL-12Rβ1 was unaffected by IL-35. These data demonstrate that in addition to acting via regulatory T and regulatory B cells, human IL-35 can also directly suppress IL-12 bioactivity and its interaction with IL-12Rβ2.

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