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导致AUG大鼠发生破坏性甲状腺炎的免疫事件。

Immunological events leading to destructive thyroiditis in the AUG rat.

作者信息

Hassman R, Solic N, Jasani B, Hall R, McGregor A M

机构信息

Department of Medicine, University of Wales College of Medicine, Cardiff, UK.

出版信息

Clin Exp Immunol. 1988 Sep;73(3):410-6.

Abstract

Single or infrequent observations in patients or animals with autoimmune thyroid disease (AITD) have failed to elucidate the exact sequence of pathogenetic events leading to thyroid cell destruction. A detailed serial morphological and functional study of experimental AITD (EAITD) in the female AUG rat was therefore undertaken. Following induction of EAITD with thyroglobulin (Tg) in adjuvant antibodies to Tg were detectable one week after the initial immunization, at which stage Ia positive vascular endothelium was observed within the thyroid. This was followed by large numbers of Ia positive dendritic-like cells. With time, in almost all the animals whose titre of Tg antibody rose above a critical level, lymphocytic infiltration was observed consisting mainly of Ia positive B cell aggregates with fewer scattered T cells. This was associated with raised levels of serum TSH and concomitant focal follicular hyperplasia and necrosis. Expression of Ia was mainly restricted to the outer epithelial wall of follicular thyrocytes in direct contact with invading lymphoid cells, although occasional staining on the internal apical membrane was observed as a late event in the destructive process. The Ia expression on thyroid epithelial cells was only observed in areas of thyroid lymphoid infiltration. The immune infiltration of the thyroid in the AUG rat appears to be very similar to that observed in Hashimoto's thyroiditis, with the exception that Ia was not regularly observed on the apical surfaces of thyrocytes. Whether or not the diminished or absent epithelial Ia expression contributes to the spontaneous recovery of the disease observed in this model remains to be resolved.

摘要

对患有自身免疫性甲状腺疾病(AITD)的患者或动物进行的单次或不频繁观察,未能阐明导致甲状腺细胞破坏的发病机制事件的确切顺序。因此,对雌性AUG大鼠的实验性自身免疫性甲状腺疾病(EAITD)进行了详细的系列形态学和功能研究。在用甲状腺球蛋白(Tg)佐剂诱导EAITD后,初次免疫一周后可检测到抗Tg抗体,此时在甲状腺内观察到Ia阳性血管内皮。随后出现大量Ia阳性树突状细胞。随着时间的推移,在几乎所有Tg抗体滴度升高到临界水平以上的动物中,观察到淋巴细胞浸润,主要由Ia阳性B细胞聚集物组成,散在的T细胞较少。这与血清促甲状腺激素(TSH)水平升高以及伴随的局灶性滤泡增生和坏死有关。Ia的表达主要局限于与侵入性淋巴细胞直接接触的滤泡甲状腺细胞的外上皮壁,尽管在破坏过程后期偶尔在内顶端膜上观察到染色。甲状腺上皮细胞上的Ia表达仅在甲状腺淋巴细胞浸润区域观察到。AUG大鼠甲状腺的免疫浸润似乎与桥本甲状腺炎中观察到的非常相似,不同之处在于在甲状腺细胞顶端表面未定期观察到Ia。上皮Ia表达减少或缺失是否有助于该模型中观察到的疾病自发恢复仍有待解决。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0468/1541757/1caa06d519af/clinexpimmunol00096-0077-a.jpg

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