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Human monoclonal natural autoantibodies against the T-cell receptor inhibit interleukin-2 production in murine T cells

机译:抗T细胞受体的人类单克隆天然自身抗体抑制鼠T细胞中IL-2的产生

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摘要

Natural autoantibodies (NAAbs) specific for the T-cell receptor (TCR) are present in all human sera, but individuals with rheumatoid arthritis (RA) generally produce higher titres of immunoglobulin M (IgM) isotype autoantibodies (AAbs) against Vβ TCR epitopes. To investigate possible correlations between the specificity of such AAbs and their role in immunomodulation, we generated seven B-cell hetero-hybridomas, secreting monoclonal IgM NAAbs, from the synovial tissue and peripheral blood of patients with RA. Here we report three anti-TCR monoclonal autoantibodies (mAAbs) – OR2, OR5 and Syn 2H-11 – with the ability to bind subsets of murine T cells, including the ovalbumin-specific DO-11.10 clone. These antibodies did not induce apoptosis in vitro, but prevented interleukin-2 (IL-2) production by antigen-specific T cells. These findings suggest an immunomodulatory function for NAAbs to TCR V-region epitopes and serve as the foundation for testing human anti-TCR mAAbs in animal models with the eventual goal of using them as therapeutic agents in human disease.
机译:对T细胞受体(TCR)具有特异性的天然自身抗体(NAAb)存在于所有人类血清中,但类风湿关节炎(RA)的个体通常会产生更高滴度的针对VβTCR表位的免疫球蛋白M(IgM)同型自身抗体(AAb)。为了研究此类AAb的特异性与其在免疫调节中的作用之间可能的相关性,我们从RA患者的滑膜组织和外周血中产生了七个分泌单克隆IgM NAAb的B细胞异型杂交瘤。在这里,我们报告了三种抗TCR单克隆自身抗体(mAAb)– OR2,OR5和Syn 2H-11 –具有结合鼠T细胞子集的能力,包括卵白蛋白特异性DO-11.10克隆。这些抗体在体外不诱导细胞凋亡,但阻止了抗原特异性T细胞产生白介素2(IL-2)。这些发现提示NAAb对TCR V区表位具有免疫调节功能,并为在动物模型中测试人类抗TCR mAAb奠定了基础,最终目的是将其用作人类疾病的治疗剂。

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