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COVID-19 肺炎后继发抗信号识别颗粒抗体阳性的纤维性间质性肺病。

COVID-19 Pneumonia Followed by Anti-signal Recognition Particle Antibody-positive Fibrosing Interstitial Lung Disease.

机构信息

Department of Respiratory Medicine, Tokyo Medical and Dental University, Japan.

Department of Respiratory Physiology and Sleep Medicine, Tokyo Medical and Dental University, Japan.

出版信息

Intern Med. 2023 May 1;62(9):1323-1328. doi: 10.2169/internalmedicine.8877-21. Epub 2023 Feb 8.

DOI:10.2169/internalmedicine.8877-21
PMID:36754401
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10208788/
Abstract

Coronavirus disease 2019 (COVID-19) pneumonia is caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) and is frequently accompanied by various sequelae. Interstitial lung diseases (ILDs) are observed in COVID-19 pneumonia patients after recovery, probably due to persistent inflammation in the lungs. We herein report a case of ILD with anti-signal recognition particle antibodies following severe COVID-19 pneumonia. The patient was diagnosed with ILD three months after COVID-19 pneumonia. Although the exact mechanism is unknown, the autoantibody-induced immune response might have been the pulmonary fibrosis trigger in this patient.

摘要

新型冠状病毒病(COVID-19)肺炎由严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)引起,常伴有各种后遗症。COVID-19 肺炎患者在康复后观察到间质性肺疾病(ILD),可能是由于肺部持续炎症所致。本文报告了一例严重 COVID-19 肺炎后出现抗信号识别颗粒抗体的 ILD 病例。该患者在 COVID-19 肺炎后 3 个月被诊断为 ILD。尽管确切机制尚不清楚,但自身抗体诱导的免疫反应可能是该患者肺纤维化的触发因素。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d6d9/10208788/d907076f0b53/1349-7235-62-1323-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d6d9/10208788/7f7bf8beab57/1349-7235-62-1323-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d6d9/10208788/d907076f0b53/1349-7235-62-1323-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d6d9/10208788/7f7bf8beab57/1349-7235-62-1323-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d6d9/10208788/d907076f0b53/1349-7235-62-1323-g002.jpg

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本文引用的文献

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A Comparison of Line Blots, Enzyme-linked Immunosorbent, and RNA-immunoprecipitation Assays of Antisynthetase Antibodies in Serum Samples from 44 Patients.44 例患者血清样本中抗合成酶抗体的线印迹、酶联免疫吸附和 RNA 免疫沉淀检测比较。
Intern Med. 2022;61(3):313-322. doi: 10.2169/internalmedicine.7824-21. Epub 2022 Feb 1.
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Interstitial lung disease is not rare in immune-mediated necrotizing myopathy with anti-signal recognition particle antibodies.抗信号识别颗粒抗体相关性免疫介导坏死性肌病可并发间质性肺病。
BMC Pulm Med. 2022 Jan 10;22(1):14. doi: 10.1186/s12890-021-01802-1.
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Clinical characteristics of interstitial lung diseases positive to different anti-synthetase antibodies.
不同抗合成酶抗体阳性的间质性肺疾病的临床特征
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Onset of dermatomyositis in close association with COVID-19-a first case reported.皮肌炎与新型冠状病毒肺炎密切相关发病——首例报告病例
Rheumatology (Oxford). 2021 Oct 9;60(SI):SI96. doi: 10.1093/rheumatology/keab290.
7
Clinical features of anti-synthetase syndrome associated interstitial lung disease: a retrospective cohort in China.抗合成酶综合征相关间质性肺病的临床特征:中国的一项回顾性队列研究。
BMC Pulm Med. 2021 Feb 12;21(1):57. doi: 10.1186/s12890-021-01399-5.
8
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Lancet. 2021 Jan 16;397(10270):220-232. doi: 10.1016/S0140-6736(20)32656-8. Epub 2021 Jan 8.
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