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一种对人甲状腺球蛋白而非小鼠甲状腺球蛋白诱导的自身免疫性甲状腺炎易感的新型H2A-E +转基因模型:小鼠致病表位的鉴定

A novel H2A-E+ transgenic model susceptible to human but not mouse thyroglobulin-induced autoimmune thyroiditis: identification of mouse pathogenic epitopes.

作者信息

Brown Nicholas K, McCormick Daniel J, Brusic Vladimir, David Chella S, Kong Yi-Chi M

机构信息

Department of Immunology and Microbiology, Wayne State University School of Medicine, 540 East Canfield Avenue, Detroit, MI 48201, USA.

出版信息

Cell Immunol. 2008 Jan;251(1):1-7. doi: 10.1016/j.cellimm.2008.02.002. Epub 2008 Apr 14.

Abstract

The A-E+ transgenic mouse is highly susceptible to human thyroglobulin (hTg)-induced thyroiditis, but strongly tolerant to a challenge by mouse thyroglobulin (mTg), in stark contrast to traditionally susceptible strains, wherein mTg induces stronger thyroiditis. To identify mouse thyroid epitopes recognized by destructive, hTg-primed T cells, we selected the three hTg epitopes known to be presented by H2E(b), as the basis for synthesizing potential mTg epitopes. One 15-mer peptide, mTg409, did prime T cells, elicit Ab, and induce thyroiditis. Moreover, cells primed with corresponding, pathogenic hTg410 cross-reacted with mTg409, and vice versa. mTg409 contained 4/4 anchor residues, similar to the corresponding hTg peptide. Based on this finding, a second mTg epitope, mTg179, was subsequently identified. These mTg autoepitopes, identified by using thyroiditogenic hTg epitopes, help to explain the severe thyroiditis seen in this novel A-E+ transgenic model.

摘要

A-E+转基因小鼠对人甲状腺球蛋白(hTg)诱导的甲状腺炎高度敏感,但对小鼠甲状腺球蛋白(mTg)的攻击具有很强的耐受性,这与传统的易感品系形成鲜明对比,在传统品系中mTg会诱发更强的甲状腺炎。为了鉴定被具有破坏性的、hTg致敏的T细胞识别的小鼠甲状腺表位,我们选择了已知由H2E(b)呈递的三个hTg表位,作为合成潜在mTg表位的基础。一个15聚体肽mTg409确实能致敏T细胞、引发抗体并诱发甲状腺炎。此外,用相应的致病性hTg410致敏的细胞与mTg409发生交叉反应,反之亦然。mTg409含有4/4个锚定残基,与相应的hTg肽相似。基于这一发现,随后鉴定出了第二个mTg表位mTg179。这些通过致甲状腺炎性hTg表位鉴定出的mTg自身表位,有助于解释在这种新型A-E+转基因模型中所见的严重甲状腺炎。

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Experimental autoimmune thyroiditis in the mouse.小鼠实验性自身免疫性甲状腺炎
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