Mathematical artificial intelligence design of mutation-proof COVID-19 monoclonal antibodies.

IF 0.6 Q4 COMPUTER SCIENCE, INFORMATION SYSTEMS
Jiahui Chen, Guo-Wei Wei
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Abstract

Emerging severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) variants have compromised existing vaccines and posed a grand challenge to coronavirus disease 2019 (COVID-19) prevention, control, and global economic recovery. For COVID-19 patients, one of the most effective COVID-19 medications is monoclonal antibody (mAb) therapies. The United States Food and Drug Administration (U.S. FDA) has given the emergency use authorization (EUA) to a few mAbs, including those from Regeneron, Eli Elly, etc. However, they are also undermined by SARS-CoV-2 mutations. It is imperative to develop effective mutation-proof mAbs for treating COVID-19 patients infected by all emerging variants and/or the original SARS-CoV-2. We carry out a deep mutational scanning to present the blueprint of such mAbs using algebraic topology and artificial intelligence (AI). To reduce the risk of clinical trial-related failure, we select five mAbs either with FDA EUA or in clinical trials as our starting point. We demonstrate that topological AI-designed mAbs are effective for variants of concerns and variants of interest designated by the World Health Organization (WHO), as well as the original SARS-CoV-2. Our topological AI methodologies have been validated by tens of thousands of deep mutational data and their predictions have been confirmed by results from tens of experimental laboratories and population-level statistics of genome isolates from hundreds of thousands of patients.

Abstract Image

数学人工智能设计防突变的 COVID-19 单克隆抗体。
新出现的严重急性呼吸系统综合征冠状病毒 2(SARS-CoV-2)变种破坏了现有的疫苗,并对 2019 年冠状病毒疾病(COVID-19)的预防、控制和全球经济复苏构成了巨大挑战。对于 COVID-19 患者来说,最有效的 COVID-19 药物之一是单克隆抗体(mAb)疗法。美国食品和药物管理局(U.S. FDA)已向一些 mAb 提供了紧急使用授权(EUA),其中包括 Regeneron、Eli Elly 等公司的产品。然而,它们也受到了 SARS-CoV-2 变异的影响。当务之急是开发有效的抗变异 mAbs,用于治疗感染所有新变种和/或原始 SARS-CoV-2 的 COVID-19 患者。我们利用代数拓扑学和人工智能(AI)进行了深度突变扫描,以展示此类 mAbs 的蓝图。为了降低临床试验失败的风险,我们选择了五种已获得美国食品及药物管理局(FDA)EUA 或正在进行临床试验的 mAbs 作为起点。我们证明,拓扑人工智能设计的 mAbs 对关注的变种、世界卫生组织(WHO)指定的感兴趣的变种以及原始 SARS-CoV-2 均有效。我们的拓扑人工智能方法已通过数以万计的深度变异数据进行了验证,其预测结果也得到了数十个实验实验室的结果和来自数十万患者的基因组分离物的群体级统计数据的证实。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Communications in Information and Systems
Communications in Information and Systems COMPUTER SCIENCE, INFORMATION SYSTEMS-
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