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接种 COVID-19 疫苗后的免疫介导性肝损伤:一项系统性综述。

Immune-mediated liver injury following COVID-19 vaccination: A systematic review.

机构信息

Department of Hepatology, Sanjay Gandhi Postgraduate Institute of Medical Sciences, Lucknow, India.

Department of Hepatology, Postgraduate Institute of Medical Education and Research, Chandigarh, India.

出版信息

Hepatol Commun. 2022 Sep;6(9):2513-2522. doi: 10.1002/hep4.1979. Epub 2022 May 4.

DOI:10.1002/hep4.1979
PMID:35507736
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9348067/
Abstract

Immune-mediated liver injury (ILI) following coronavirus disease 2019 (COVID-19) vaccination is not well-characterized. Therefore, we systematically reviewed the literature on ILI after COVID-19 vaccination. We searched PubMed, Cochrane, Ovid, Embase, and gray literature to include articles describing ILI following COVID-19 vaccination. Reports without confirmatory evidence from liver biopsy were excluded. Descriptive analysis, and study quality were reported as appropriate. Of the 1,048 articles found, 13 (good/fair quality; 23 patients) were included. Studies were primarily from Europe (n = 8), America (n = 2), Asia (n = 2), or Australia (n = 1). Patients were predominantly females (62.5%) of age 55.3 years (49.1-61.4), with an antecedent exposure to Moderna messenger RNA (mRNA)-1273 (47.8%), Pfizer-BioNTech BNT162b2 mRNA (39.2%), or ChAdOx1 nCoV-19 vaccine (13%). Pre-existing comorbidities (69.6%) were common, including liver disease in 26.1% and thyroid disorders in 13% of patients. About two-thirds of the patients were on concurrent medications (paracetamol, levothyroxine, statins, and non-steroidal anti-inflammatory drugs). Jaundice was the most common symptom (78.3%). Peak bilirubin, alanine aminotransferase, and alkaline phosphatase levels were 10.8 (6.8-14.8) mg/dl, 1,106.5 (757.0-1,702.5) U/L, and 229 (174.6-259.6) U/L, respectively. Histological findings were intense portal lymphoplasmacytic infiltrate with interface hepatitis. Steroids were used in 86.9% of patients, and complete response, recovering course, and death were reported in 56.5%, 39.1%, and 4.3% of patients, respectively. ILI following COVID-19 vaccination is rare. The diagnosis is established on temporal correlation, biochemical findings, and histopathology. Prognosis is excellent with corticosteroids. Causality establishment remains a challenge.

摘要

新型冠状病毒疾病 2019(COVID-19)疫苗接种后的免疫介导性肝损伤(ILI)尚未得到很好的描述。因此,我们系统地回顾了 COVID-19 疫苗接种后 ILI 的文献。我们搜索了 PubMed、Cochrane、Ovid、Embase 和灰色文献,以纳入描述 COVID-19 疫苗接种后 ILI 的文章。没有肝活检确认证据的报告被排除在外。适当报告了描述性分析和研究质量。在发现的 1048 篇文章中,纳入了 13 篇(质量良好/中等;23 名患者)。研究主要来自欧洲(n=8)、美洲(n=2)、亚洲(n=2)或澳大利亚(n=1)。患者主要为女性(62.5%),年龄 55.3 岁(49.1-61.4),先前接触过 Moderna 信使 RNA(mRNA)-1273(47.8%)、辉瑞-BioNTech BNT162b2 mRNA(39.2%)或 ChAdOx1 nCoV-19 疫苗(13%)。常见的合并症(69.6%)包括肝脏疾病(26.1%)和甲状腺疾病(13%)。大约三分之二的患者同时服用药物(对乙酰氨基酚、左甲状腺素、他汀类药物和非甾体抗炎药)。黄疸是最常见的症状(78.3%)。胆红素、丙氨酸氨基转移酶和碱性磷酸酶的峰值水平分别为 10.8(6.8-14.8)mg/dl、1106.5(757.0-1702.5)U/L 和 229(174.6-259.6)U/L。组织学发现为强烈的门脉淋巴浆细胞浸润伴界面肝炎。86.9%的患者使用了类固醇,56.5%、39.1%和 4.3%的患者完全缓解、恢复过程和死亡。COVID-19 疫苗接种后的 ILI 很少见。诊断是基于时间相关性、生化发现和组织病理学。使用皮质类固醇后预后良好。因果关系的建立仍然是一个挑战。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d1b4/9426384/a9d58c8d1ced/HEP4-6-2513-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d1b4/9426384/a9d58c8d1ced/HEP4-6-2513-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d1b4/9426384/a9d58c8d1ced/HEP4-6-2513-g001.jpg

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