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新型冠状病毒感染和疫苗接种后与间质性肺病相关的抗PL-7/PL-12合成酶综合征:病例研究综述

Anti-PL-7/PL-12 antisynthetase syndrome associated with interstitial lung disease following SARS-COV-2 infection and vaccination: A case study review.

作者信息

García-Bravo Laura, Villegas Ángela, López Uceda Bárbara, Mariscal Anaís, Vadillo Cristina, Nieto Barbero M Asunción, Rodríguez-Hermosa Juan Luis, Mediero Valeros Beatriz, Plaza-Hernández José Carlos, Fernández-Arquero Miguel, Guzmán-Fulgencio María, Candelas-Rodríguez Gloria, Sánchez-Ramón Silvia, Ochoa-Grullón Juliana

机构信息

Immunology Department and IdISSC, Hospital Clínico San Carlos, 28040, Madrid, Spain.

Immunology Department, Hospital de la Santa Creu i Sant Pau, Universitat Autònoma de Barcelona, Biomedical Research Institute Sant Pau (IIB Sant Pau), 08041, Barcelona, Spain.

出版信息

Heliyon. 2024 Dec 30;11(2):e41311. doi: 10.1016/j.heliyon.2024.e41311. eCollection 2025 Jan 30.

Abstract

Cumulative evidence suggests a link between specific autoimmune diseases (AD), including idiopathic inflammatory myopathies (IIM), and SARS-CoV-2 infection or COVID-19 vaccination. Anti-synthetase syndrome (ASS), a subset of IIM, is defined by the presence of autoantibodies against aminoacyl-tRNA synthetase (anti-ARS) and is strongly associated with interstitial lung disease (ILD), a major contributor to severe complications and reduced survival. We present four clinical cases of patients who developed autoantibodies against threonyl (PL-7) and alanyl (PL-12) synthetases associated with ASS-ILD shortly after SARS-CoV-2 infection or COVID-19 vaccination. Anti-ARS autoantibodies were identified using three complementary methods: immunoblotting, western blotting (WB) and the method considered the gold standard, immunoprecipitation (IP), which ensures accurate interpretation of results. The study highlights the clinical and pathogenic overlap between ASS-ILD and SARS-CoV-2-related lung involvement.Both conditions share similar high-resolution computed tomography (HRCT) patterns, including inflammation and pulmonary fibrosis (PF), driven by IFN-γ signaling, which complicates accurate diagnosis. Our results provide novel insights into the temporal association of SARS-CoV-2 and vaccine exposure with ASS-ILD, focusing on possible molecular mimicry between viral proteins and ARS molecules as a potential mechanism. Understanding the involvement of specific anti-ARS autoantibodies (PL-7 and PL-12) and the identification of genetic predispositions (HLA-B∗08:01 and HLA-DRB1∗03:01) in these patients may be key to underpinning these autoimmune manifestations. The study underscores the importance of a multidisciplinary approach and vigilant follow-up to optimize diagnosis and management. Further research is essential to elucidate the causal relationships and molecular mechanisms behind these observations.

摘要

越来越多的证据表明,包括特发性炎性肌病(IIM)在内的特定自身免疫性疾病(AD)与严重急性呼吸综合征冠状病毒2(SARS-CoV-2)感染或2019冠状病毒病(COVID-19)疫苗接种之间存在联系。抗合成酶综合征(ASS)是IIM的一个亚型,其定义为存在针对氨酰tRNA合成酶的自身抗体(抗ARS),并且与间质性肺疾病(ILD)密切相关,ILD是严重并发症和生存率降低的主要原因。我们报告了4例患者的临床病例,这些患者在SARS-CoV-2感染或COVID-19疫苗接种后不久出现了与ASS-ILD相关的抗苏氨酰(PL-7)和丙氨酰(PL-12)合成酶自身抗体。使用三种互补方法鉴定抗ARS自身抗体:免疫印迹法、蛋白质印迹法(WB)以及被视为金标准的免疫沉淀法(IP),后者可确保对结果进行准确解读。该研究突出了ASS-ILD与SARS-CoV-2相关肺部受累之间的临床和致病重叠。这两种情况具有相似的高分辨率计算机断层扫描(HRCT)模式,包括由干扰素-γ信号传导驱动的炎症和肺纤维化(PF),这使得准确诊断变得复杂。我们的结果为SARS-CoV-2和疫苗暴露与ASS-ILD的时间关联提供了新的见解,重点关注病毒蛋白与ARS分子之间可能的分子模拟作为一种潜在机制。了解这些患者中特定抗ARS自身抗体(PL-7和PL-12)的参与情况以及遗传易感性(HLA-B∗08:01和HLA-DRB1∗03:01)的鉴定可能是支撑这些自身免疫表现的关键。该研究强调了多学科方法和密切随访对于优化诊断和管理的重要性。进一步的研究对于阐明这些观察结果背后的因果关系和分子机制至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ee88/11791273/7e85513a1a59/gr3.jpg

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