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遗传性 IRAK-4 缺陷导致急性人类疱疹病毒 6 脑炎。

Inherited IRAK-4 Deficiency in Acute Human Herpesvirus-6 Encephalitis.

机构信息

Department of Molecular Biology and Genetics, Faculty of Science, İhsan Doğramacı Bilkent University, Ankara, Turkey.

Department of Pediatric Immunology, Dr. Sami Ulus Maternity and Children's Health and Diseases Training and Research Hospital, Ankara, Turkey.

出版信息

J Clin Immunol. 2023 Jan;43(1):192-205. doi: 10.1007/s10875-022-01369-4. Epub 2022 Oct 7.

DOI:10.1007/s10875-022-01369-4
PMID:36205835
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9540208/
Abstract

Human herpesvirus-6 (HHV-6) infection can rarely cause life-threatening conditions, such as encephalitis, in otherwise healthy children, with unclear pathogenesis. We studied a child who presented with acute HHV-6 encephalitis at the age of 10 months and who was homozygous for a novel missense mutation in IRAK4, encoding interleukin-1 receptor-associated kinase 4, identified by whole-exome sequencing. We tested the damaging impact of this mutation in silico by molecular dynamics simulations and in vitro by biochemical and functional experiments utilizing cell lines and patient's cells. We found that the mutation is severely hypomorphic, impairing both the expression and function of IRAK-4. Patient's leukocytes had barely detectable levels of IRAK-4 and diminished anti-viral immune responses to various stimuli inducing different Toll-like receptors and cytosolic nucleic acid sensors. Overall, these findings suggest that acute HHV-6 encephalitis can result from inborn errors of immunity to virus. This study represents the first report of isolated acute HHV-6 infection causing encephalitis in an inherited primary immunodeficiency, notably autosomal recessive (AR) partial IRAK-4 deficiency, and the first report of AR IRAK-4 deficiency presenting with a severe viral disease, notably HHV-6 encephalitis upon an acute infection, thereby expanding the clinical spectrum of IRAK-4 deficiency.

摘要

人类疱疹病毒-6 (HHV-6) 感染在其他方面健康的儿童中很少引起危及生命的情况,如脑炎,但发病机制尚不清楚。我们研究了一名 10 个月大的儿童,他因白细胞介素-1 受体相关激酶 4 (IRAK4) 发生新型错义突变而导致急性 HHV-6 脑炎,该突变是通过全外显子组测序发现的。我们通过分子动力学模拟和生化及功能实验(利用细胞系和患者细胞)在体内测试了这种突变的破坏性影响。我们发现该突变是严重的功能缺失型突变,既损害了 IRAK-4 的表达又损害了其功能。患者的白细胞 IRAK-4 水平几乎检测不到,并且对不同刺激物(诱导不同 Toll 样受体和细胞溶质核酸传感器)引起的抗病毒免疫反应减弱。总的来说,这些发现表明急性 HHV-6 脑炎可能是由针对病毒的先天性免疫缺陷引起的。本研究首次报道了孤立性急性 HHV-6 感染引起的脑炎在遗传性原发性免疫缺陷(特别是常染色体隐性 (AR) 部分 IRAK-4 缺乏症)中的发生,也是首次报道 AR IRAK-4 缺乏症以严重病毒性疾病(特别是急性感染后的 HHV-6 脑炎)为表现,从而扩展了 IRAK-4 缺乏症的临床表现谱。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bff5/9540208/a8a42eb0f80c/10875_2022_1369_Fig6_HTML.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bff5/9540208/42608c9758f6/10875_2022_1369_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bff5/9540208/2e3f4e2ee356/10875_2022_1369_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bff5/9540208/a8a42eb0f80c/10875_2022_1369_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bff5/9540208/2ef521e0f8c2/10875_2022_1369_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bff5/9540208/2901a59af483/10875_2022_1369_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bff5/9540208/df85237c8967/10875_2022_1369_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bff5/9540208/42608c9758f6/10875_2022_1369_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bff5/9540208/2e3f4e2ee356/10875_2022_1369_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bff5/9540208/a8a42eb0f80c/10875_2022_1369_Fig6_HTML.jpg

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