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APECED 与 AIRE 在自身免疫相关免疫网络难题中的位置。

APECED and the place of AIRE in the puzzle of the immune network associated with autoimmunity.

机构信息

Pediatric Allergy and Immunology, Department of Pediatrics, SBU Dr. Sami Ulus Children Hospital, Ankara, Turkey.

Division of Pediatric Immunology, Department of Pediatrics, Ihsan Dogramaci Children`s Hospital, Institute of Child Health, Hacettepe University Medical School, Ankara, Turkey.

出版信息

Scand J Immunol. 2023 Aug;98(2):e13299. doi: 10.1111/sji.13299. Epub 2023 Jun 12.

Abstract

In the last 20 years, discoveries about the autoimmune regulator (AIRE) protein and its critical role in immune tolerance have provided fundamental insights into understanding the molecular basis of autoimmunity. This review provides a comprehensive overview of the effect of AIRE on immunological tolerance and the characteristics of autoimmune diseases in Autoimmune Polyendocrinopathy-Candidiasis-Ectodermal Dystrophy (APECED), which is caused by biallelic AIRE mutations. A better understanding of the immunological mechanisms of AIRE deficiency may enlighten immune tolerance mechanisms and new diagnostic and treatment strategies for autoimmune diseases. Considering that not all clinical features of APECED are present in a given follow-up period, the diagnosis is not easy in a patient at the first visit. Longer follow-up and a multidisciplinary approach are essential for diagnosis. It is challenging to prevent endocrine and other organ damage compared with other diseases associated with multiple autoimmunities, such as FOXP3, LRBA, and CTLA4 deficiencies. Unfortunately, no curative therapy like haematopoietic stem cell transplantation or specific immunomodulation is present that is successful in the treatment.

摘要

在过去的 20 年中,对自身免疫调节因子(AIRE)蛋白及其在免疫耐受中的关键作用的发现,为理解自身免疫的分子基础提供了重要的见解。本文全面概述了 AIRE 对免疫耐受的影响以及自身免疫性多内分泌腺病-念珠菌病-外胚层发育不良(APECED)的特征,APECED 是由 AIRE 双等位基因突变引起的。更好地了解 AIRE 缺乏的免疫机制,可能会启发免疫耐受机制,并为自身免疫性疾病提供新的诊断和治疗策略。考虑到并非所有 APECED 的临床特征都在特定的随访期内出现,因此在首次就诊时,患者的诊断并不容易。更长时间的随访和多学科方法对于诊断至关重要。与其他与多种自身免疫相关的疾病(如 FOXP3、LRBA 和 CTLA4 缺乏症)相比,预防内分泌和其他器官损伤具有挑战性。不幸的是,目前尚无像造血干细胞移植或特异性免疫调节那样成功治疗的方法。

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