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Mathematical artificial intelligence design of mutation-proof COVID-19 monoclonal antibodies
Author(s) -
Jiahui Chen,
Guo-Wei Wei
Publication year - 2022
Publication title -
communications in information and systems
Language(s) - English
Resource type - Journals
eISSN - 2163-4548
pISSN - 1526-7555
DOI - 10.4310/cis.2022.v22.n3.a3
Subject(s) - monoclonal antibody , covid-19 , virology , population , mutation , medicine , disease , biology , immunology , antibody , infectious disease (medical specialty) , genetics , gene , environmental health , pathology
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.

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