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调节细胞存活的调控机制在患有自身免疫疾病聚集的儿童中发生改变。

Altered regulatory mechanisms governing cell survival in children affected with clustering of autoimmune disorders.

机构信息

Department of Pediatrics, Federico II University, Pansini 5, 80131, Naples, Italy.

出版信息

Ital J Pediatr. 2012 Sep 12;38:42. doi: 10.1186/1824-7288-38-42.

Abstract

Clustering of Autoimmune Diseases (CAD) is now emerging as a novel clinical entity within monogenic immune defects with a high familial occurrence. Aim of this study is to evaluate the regulatory mechanisms governing cell survival, paying a particular attention to Fas-induced apoptosis, in a cohort of 23 children affected with CAD. In 14 patients, Fas stimulation failed to induce cell apoptosis and in 1 case it was associated with Fas gene mutation. Our study highlights the importance to evaluate cell apoptosis in the group of children with CAD, which, with this regard, represents a distinct clinical entity.

摘要

自身免疫性疾病(CAD)的聚类现在作为一种新的临床实体出现在单基因免疫缺陷中,具有较高的家族发生。本研究的目的是评估控制细胞存活的调节机制,特别关注 Fas 诱导的细胞凋亡,在一组 23 名患有 CAD 的儿童中进行评估。在 14 名患者中,Fas 刺激未能诱导细胞凋亡,在 1 例中与 Fas 基因突变有关。我们的研究强调了在 CAD 患儿中评估细胞凋亡的重要性,从这方面来看,CAD 患儿代表了一种独特的临床实体。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c2a/3469397/2604280721ac/1824-7288-38-42-1.jpg

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