Department of Bioinformatics, Biocenter, Am Hubland, University of Würzburg, 97074 Würzburg, Germany.
Department of Pediatrics, Rheumatology and Special Immunology, University Hospital Würzburg, Pediatric Rheumatology/Special Immunology, Josef-Schneider-Str. 2, 97080 Würzburg, Germany.
Int J Mol Sci. 2021 Mar 5;22(5):2630. doi: 10.3390/ijms22052630.
We observed substantial differences in predicted Major Histocompatibility Complex II (MHCII) epitope presentation of SARS-CoV-2 proteins for different populations but only minor differences in predicted MHCI epitope presentation. A comparison of this predicted epitope MHC-coverage revealed for the early phase of infection spread (till day 15 after reaching 128 observed infection cases) highly significant negative correlations with the case fatality rate. Specifically, this was observed in different populations for MHC class II presentation of the viral spike protein (-value: 0.0733 for linear regression), the envelope protein (-value: 0.023), and the membrane protein (-value: 0.00053), indicating that the high case fatality rates of COVID-19 observed in some countries seem to be related with poor MHC class II presentation and hence weak adaptive immune response against these viral envelope proteins. Our results highlight the general importance of the SARS-CoV-2 structural proteins in immunological control in early infection spread looking at a global census in various countries and taking case fatality rate into account. Other factors such as health system and control measures become more important after the early spread. Our study should encourage further studies on MHCII alleles as potential risk factors in COVID-19 including assessment of local populations and specific allele distributions.
我们观察到不同人群中 SARS-CoV-2 蛋白的主要组织相容性复合物 II(MHCII)预测表位呈现存在显著差异,但预测的 MHCI 表位呈现差异较小。对这种预测表位 MHC 覆盖的比较表明,在感染传播的早期阶段(到达 128 例观察到的感染病例后 15 天),与病死率呈高度显著负相关。具体来说,在不同人群中,病毒刺突蛋白(-值:0.0733 用于线性回归)、包膜蛋白(-值:0.023)和膜蛋白(-值:0.00053)的 MHC II 呈现均观察到这种情况,表明在一些国家观察到的 COVID-19 高病死率似乎与 MHC II 呈现不良和因此针对这些病毒包膜蛋白的适应性免疫反应较弱有关。我们的研究结果强调了 SARS-CoV-2 结构蛋白在全球不同国家的早期感染传播中免疫控制中的普遍重要性,并考虑了病死率。其他因素,如卫生系统和控制措施,在早期传播后变得更加重要。我们的研究应鼓励进一步研究 MHCII 等位基因作为 COVID-19 的潜在危险因素,包括对当地人群和特定等位基因分布的评估。