VEXAS综合征:一种新发现的x连锁血液病-其遗传,分子,炎症和临床景观的全面概述

IF 7.9 1区 医学 Q1 IMMUNOLOGY
Alpana Singh, Rishabh Chaudhary
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引用次数: 0

摘要

VEXAS (Vacuoles, E1 Enzyme, X-linked, Auto-inflammatory, Somatic)综合征是最近发现的一种自体炎症性疾病,主要影响50岁以上的男性。它是由于UBA1基因的体细胞突变引起的,UBA1基因是启动泛素-蛋白酶体系统所必需的x连锁基因,导致蛋白质降解失调和免疫功能障碍。临床上,VEXAS表现为多种炎症表现,包括持续发热、中性粒细胞皮肤病、耳部和鼻部软骨炎、肺部浸润、眼部炎症和静脉血栓形成,同时伴有明显的血液学异常,如巨细胞性贫血、血小板减少症、骨髓和红细胞前体空泡化和骨髓发育不良。这些系统性并发症导致高发病率和死亡率。目前,治疗策略在很大程度上仍不明确,治疗主要集中在两种主要方法上,即通过皮质类固醇、JAK抑制剂或IL-6阻断来调节炎症,以及靶向突变造血克隆或异体造血干细胞移植(AHSCT)治疗。支持性干预措施,包括红细胞和血小板输注、促红细胞生成药物、血栓预防和抗菌素预防,对于控制疾病相关并发症至关重要。本文旨在全面分析VEXAS综合征,重点介绍其遗传基础、病理生理、临床表现、诊断标准和不断发展的治疗策略。通过整合当前文献中的发现和识别正在进行的研究中的空白,本综述旨在使临床医生和研究人员对VEXAS综合征有一个全面的了解。此外,它旨在指导未来的研究,以完善诊断策略,优化治疗方法,并最终改善患者护理和临床结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

VEXAS syndrome: A newly identified X-Linked hematoinflammatory disorder – A comprehensive overview of its genetic, molecular, inflammatory, and clinical landscape

VEXAS syndrome: A newly identified X-Linked hematoinflammatory disorder – A comprehensive overview of its genetic, molecular, inflammatory, and clinical landscape
VEXAS (Vacuoles, E1 Enzyme, X-linked, Auto-inflammatory, Somatic) syndrome is a recently identified auto-inflammatory disorder predominantly affecting males over the age of 50. It arises due to somatic mutations in the UBA1 gene, an X-linked gene essential for initiating the ubiquitin-proteasome system, leading to dysregulated protein degradation and immune dysfunction. Clinically, VEXAS presents with a diverse array of inflammatory manifestations, including persistent fever, neutrophilic dermatosis, auricular and nasal chondritis, pulmonary infiltrates, ocular inflammation, and venous thrombosis, along with significant haematological abnormalities such as macrocytic anemia, thrombocytopenia, myeloid and erythroid precursor vacuolization, and bone marrow dysplasia. These systemic complications contribute to high morbidity and mortality. Currently, therapeutic strategies remain largely undefined, with treatment focusing on two primary approaches, which are modulating inflammation through corticosteroids, JAK inhibitors, or IL-6 blockade and targeting the mutant hematopoietic clone or allogeneic hematopoietic stem cell transplantation (AHSCT) therapies. Supportive interventions, including red blood cell and platelet transfusions, erythropoiesis-stimulating agents, thromboprophylaxis, and antimicrobial prophylaxis, are crucial in managing disease-associated complications. This review aims to present a comprehensive analysis of VEXAS syndrome, focusing on its genetic underpinnings, pathophysiology, clinical manifestations, diagnostic criteria, and evolving therapeutic strategies. By integrating current findings from the literature and identifying gaps in ongoing research, this review seeks to equip clinicians and researchers with a comprehensive understanding of VEXAS syndrome. Additionally, it aims to guide future investigations toward refining diagnostic strategies, optimizing therapeutic approaches, and ultimately improving patient care and clinical outcomes.
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来源期刊
Journal of autoimmunity
Journal of autoimmunity 医学-免疫学
CiteScore
27.90
自引率
1.60%
发文量
117
审稿时长
17 days
期刊介绍: The Journal of Autoimmunity serves as the primary publication for research on various facets of autoimmunity. These include topics such as the mechanism of self-recognition, regulation of autoimmune responses, experimental autoimmune diseases, diagnostic tests for autoantibodies, as well as the epidemiology, pathophysiology, and treatment of autoimmune diseases. While the journal covers a wide range of subjects, it emphasizes papers exploring the genetic, molecular biology, and cellular aspects of the field. The Journal of Translational Autoimmunity, on the other hand, is a subsidiary journal of the Journal of Autoimmunity. It focuses specifically on translating scientific discoveries in autoimmunity into clinical applications and practical solutions. By highlighting research that bridges the gap between basic science and clinical practice, the Journal of Translational Autoimmunity aims to advance the understanding and treatment of autoimmune diseases.
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