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Murine pattern recognition receptor dectin-1 is essential in the development of experimental autoimmune uveoretinitis

机译:鼠模式识别受体dectin-1在实验性自身免疫性葡萄膜视网膜炎的发展中至关重要

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摘要

Mycobacteria in complete Freund's adjuvant (CFA) are an essential component of immunization protocols in a number of autoimmune disease animal models including experimental autoimmune encephalomyelitis and uveoretinitis (EAE and EAU, respectively). We determined the role in EAU of two C-type lectin receptors on myeloid cells that recognize and respond to mycobacteria. Using receptor-specific antibodies and knockout mice, we demonstrated for the first time that the macrophage mannose receptor delays disease development but does not affect severity. In contrast, dectin-1 is critically involved in the development of CFA-mediated EAU. Disease severity is reduced in dectin-1 knockout mice and antibody blockade of dectin-1 during the induction, but not the effector phase, prevents EAU development. Significantly, similar blockade of dectin-1 in vivo has no effect in non-CFA-mediated, spontaneously induced or adoptive transfer models of EAU. Thus dectin-1 plays a critical role in the ability of complete Freund's adjuvant to induce EAU in mice. (C) 2015 Published by Elsevier Ltd.
机译:完全弗氏佐剂(CFA)中的分枝杆菌是许多自身免疫性疾病动物模型(包括实验性自身免疫性脑脊髓炎和葡萄膜视网膜炎(分别为EAE和EAU))中免疫方案的重要组成部分。我们确定了识别和响应分枝杆菌的髓样细胞上的两个C型凝集素受体在EAU中的作用。使用受体特异性抗体和基因敲除小鼠,我们首次证明了巨噬细胞甘露糖受体可以延缓疾病的发展,但不会影响疾病的严重性。相反,dectin-1关键参与CFA介导的EAU的发展。在dectin-1基因敲除小鼠中疾病严重程度降低,并且在诱导过程中但不是在效应子阶段阻断dectin-1抗体会阻止EAU的发展。值得注意的是,体内类似的dectin-1阻断在EAU的非CFA介导的,自发诱导的或过继的转移模型中没有作用。因此,dectin-1在完全弗氏佐剂诱导小鼠EAU的能力中起着至关重要的作用。 (C)2015由Elsevier Ltd.出版

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