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系统性硬化症患者中功能性血管紧张素转换酶 2 自身抗体的流行情况及其作用。

The prevalence and role of functional autoantibodies to angiotensin-converting-enzyme-2 in patients with systemic sclerosis.

机构信息

Department of Dermatology, School of Medicine in Katowice, Medical University of Silesia, Katowice, Poland.

Department of Internal Medicine Rheumatology and Clinical Immunology, School of Medicine in Katowice, Medical University of Silesia, Katowice, Poland.

出版信息

Autoimmunity. 2021 Jun;54(4):181-186. doi: 10.1080/08916934.2021.1916915. Epub 2021 Apr 29.

Abstract

INTRODUCTION

Systemic sclerosis (SSc) is an autoimmune disease caused by the imbalance between the activity of angiotensin II and angiotensin-(1-7). Their balance should be controlled by angiotensin-converting enzyme 2 (ACE2), which degrades angiotensin II into angiotensin-(1-7). Previously, autoantibodies to ACE2 (anti-ACE2) were identified in patients with vasculopathy due to different connective tissue diseases, including SSc, but their frequency in SSc was not further analyzed. The aim of the research was to investigate the prevalence and potential role of those anti-ACE2 antibodies in SSc patients.

MATERIALS AND METHODS

There were enrolled 27 patients with SSc and 23 healthy donors. ELISA assay determined the presence of anti-ACE2 autoantibodies in serum samples. The results were compared to plasma measurements of angiotensin-(1-7) level commercial ELISA.

RESULTS

The presence of anti-ACE2 autoantibodies was confirmed in five patients with SSc and two healthy controls. Two of those SSc subjects were anti-Scl70+, another two were double anti-Scl70+ and anti-Ro/SSA+, and anti-PM/Scl antibodies were detected in one patient. Median plasma level of Ang-(1-7) in anti-ACE2 negative patients was 47.4 pg/ml and stayed below the detection level in anti-ACE2 positive subjects. The plasma level of Ang-(1-7) was undetectable in four SSc patients, and three of them were anti-ACE2 positive.

CONCLUSIONS

Anti-ACE2 antibodies appear to be other functional autoantibodies with the potential to dysregulate the balance between Ang II and Ang-(1-7). They are non-specific for SSc and probably result from polyautoimmunity which affect some of SSc patients. Their occurrence in SSc settings may be associated with a severe depletion of plasma Ang-(1-7).

摘要

简介

系统性硬化症(SSc)是一种自身免疫性疾病,由血管紧张素 II 和血管紧张素-(1-7)的活性失衡引起。它们的平衡应该由血管紧张素转换酶 2(ACE2)控制,ACE2 将血管紧张素 II 降解为血管紧张素-(1-7)。以前,在因不同结缔组织疾病(包括 SSc)引起的血管病变患者中发现了针对 ACE2 的自身抗体(抗 ACE2),但未进一步分析它们在 SSc 中的频率。本研究旨在调查这些抗 ACE2 抗体在 SSc 患者中的患病率和潜在作用。

材料和方法

共纳入 27 例 SSc 患者和 23 例健康对照者。ELISA 法检测血清样本中抗 ACE2 自身抗体的存在。结果与商业 ELISA 检测的血浆血管紧张素-(1-7)水平进行比较。

结果

在 5 例 SSc 患者和 2 例健康对照者中证实存在抗 ACE2 自身抗体。这 5 例 SSc 患者中,有 2 例为抗 Scl70+,另外 2 例为双抗 Scl70+和抗 Ro/SSA+,1 例患者检测到抗 PM/Scl 抗体。抗 ACE2 阴性患者的平均血浆 Ang-(1-7)水平为 47.4 pg/ml,在抗 ACE2 阳性患者中仍低于检测水平。4 例 SSc 患者的血浆 Ang-(1-7)水平无法检测,其中 3 例为抗 ACE2 阳性。

结论

抗 ACE2 抗体似乎是另一种具有调节血管紧张素 II 和血管紧张素-(1-7)平衡能力的功能性自身抗体。它们对 SSc 非特异性,可能源于影响部分 SSc 患者的多器官自身免疫。它们在 SSc 环境中的出现可能与血浆 Ang-(1-7)的严重耗竭有关。

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