Suppr超能文献

破解 COVID-19 之谜:针对 HLA-G 和 HLA-E 的治疗方法。

Puzzling out the COVID-19: Therapy targeting HLA-G and HLA-E.

机构信息

Laboratory Microorganismes and Active Biomolecules, Sciences Faculty of Tunis, University Tunis El Manar, Tunis, Tunisia.

出版信息

Hum Immunol. 2020 Dec;81(12):697-701. doi: 10.1016/j.humimm.2020.10.001. Epub 2020 Oct 7.

Abstract

SARS-CoV2 might conduce to rapid respiratory complications challenging healthcare systems worldwide. Immunological mechanisms associated to SARS-CoV2 infection are complex and not yet clearly elucidated. Arguments are in favour of a well host-adapted virus. Here I draw a systemic immunological representation linking actual SARS-CoV2 infection literature that hopefully might guide healthcare decisions to treat COVID-19. I suggest HLA-G and HLA-E, non classical HLA class I molecules, in the core of COVID-19 complications. These molecules are powerful in immune tolerance and might inhibit/suppress immune cells functions during SARS-CoV2 infection promoting virus subversion. Dosing soluble forms of these molecules in COVID-19 patients' plasma might help the identification of critical cases. I recommend also developing new SARS-CoV2 therapies based on the use of HLA-G and HLA-E or their specific receptors antibodies in combination with FDA approved therapeutics to combat efficiently COVID-19.

摘要

SARS-CoV2 可能导致快速的呼吸并发症,挑战全球的医疗保健系统。与 SARS-CoV2 感染相关的免疫机制复杂,尚未得到明确阐明。有观点认为该病毒与宿主高度适应。在这里,我绘制了一个系统免疫的表现形式,将实际的 SARS-CoV2 感染文献联系起来,希望能为治疗 COVID-19 的医疗保健决策提供指导。我认为 HLA-G 和 HLA-E 这两种非经典的 HLA Ⅰ类分子是 COVID-19 并发症的核心。这些分子在免疫耐受中具有强大的作用,可能在 SARS-CoV2 感染期间抑制/抑制免疫细胞的功能,从而促进病毒的颠覆。在 COVID-19 患者的血浆中添加这些分子的可溶性形式,可能有助于识别重症病例。我还建议开发基于 HLA-G 和 HLA-E 或其特异性受体抗体的 SARS-CoV2 新疗法,与 FDA 批准的治疗药物联合使用,以有效对抗 COVID-19。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1d0c/7539797/af626fd326ac/gr1_lrg.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验