儿童不明原因急性肝炎的基因组学研究。
Genomic investigations of unexplained acute hepatitis in children.
机构信息
Infection, Immunity and Inflammation Department, Great Ormond Street Institute of Child Health, University College London, London, UK.
Section for Paediatrics, Department of Infectious Diseases, Faculty of Medicine, Imperial College London, London, UK.
出版信息
Nature. 2023 May;617(7961):564-573. doi: 10.1038/s41586-023-06003-w. Epub 2023 Mar 30.
Since its first identification in Scotland, over 1,000 cases of unexplained paediatric hepatitis in children have been reported worldwide, including 278 cases in the UK. Here we report an investigation of 38 cases, 66 age-matched immunocompetent controls and 21 immunocompromised comparator participants, using a combination of genomic, transcriptomic, proteomic and immunohistochemical methods. We detected high levels of adeno-associated virus 2 (AAV2) DNA in the liver, blood, plasma or stool from 27 of 28 cases. We found low levels of adenovirus (HAdV) and human herpesvirus 6B (HHV-6B) in 23 of 31 and 16 of 23, respectively, of the cases tested. By contrast, AAV2 was infrequently detected and at low titre in the blood or the liver from control children with HAdV, even when profoundly immunosuppressed. AAV2, HAdV and HHV-6 phylogeny excluded the emergence of novel strains in cases. Histological analyses of explanted livers showed enrichment for T cells and B lineage cells. Proteomic comparison of liver tissue from cases and healthy controls identified increased expression of HLA class 2, immunoglobulin variable regions and complement proteins. HAdV and AAV2 proteins were not detected in the livers. Instead, we identified AAV2 DNA complexes reflecting both HAdV-mediated and HHV-6B-mediated replication. We hypothesize that high levels of abnormal AAV2 replication products aided by HAdV and, in severe cases, HHV-6B may have triggered immune-mediated hepatic disease in genetically and immunologically predisposed children.
自苏格兰首次发现以来,全球已报告了超过 1000 例儿童不明原因肝炎病例,其中英国有 278 例。在这里,我们报告了对 38 例病例、66 例年龄匹配的免疫功能正常对照者和 21 例免疫功能低下的对照者的调查,使用了基因组、转录组、蛋白质组和免疫组织化学方法的组合。我们在 28 例中的 27 例中检测到高水平的腺相关病毒 2 (AAV2) DNA 在肝脏、血液、血浆或粪便中。我们发现低水平的腺病毒 (HAdV) 和人类疱疹病毒 6B (HHV-6B) 在 31 例中的 23 例和 23 例中的 16 例中分别检测到。相比之下,在 HAdV 感染的对照组儿童的血液或肝脏中,AAV2 的检测频率较低,即使免疫功能严重抑制。AAV2、HAdV 和 HHV-6 的系统发育排除了病例中新菌株的出现。对移植肝脏的组织学分析显示 T 细胞和 B 谱系细胞富集。对病例和健康对照者肝脏组织的蛋白质组比较发现 HLA 类 2、免疫球蛋白可变区和补体蛋白表达增加。在肝脏中未检测到 HAdV 和 AAV2 蛋白。相反,我们发现 AAV2 DNA 复合物反映了 HAdV 介导和 HHV-6B 介导的复制。我们假设高水平的异常 AAV2 复制产物在 HAdV 和在严重情况下 HHV-6B 的帮助下可能触发了遗传和免疫上易感儿童的免疫介导的肝疾病。