| Literature DB >> 33391285 |
Anna C Fagre1, John Manhard2, Rachel Adams2, Miles Eckley1, Shijun Zhan1, Juliette Lewis1, Savannah M Rocha3, Catherine Woods2, Karina Kuo2, Wuxiang Liao2, Lin Li2, Adam Corper2, Dilip Challa2, Emily Mount2, Christine Tumanut2, Ronald B Tjalkens3, Tawfik Aboellail1, Xiaomin Fan2, Tony Schountz1.
Abstract
The emergence of COVID-19 has led to a pandemic that has caused millions of cases of disease, variable morbidity and hundreds of thousands of deaths. Currently, only remdesivir and dexamethasone have demonstrated limited efficacy, only slightly reducing disease burden, thus novel approaches for clinical management of COVID-19 are needed. We identified a panel of human monoclonal antibody clones from a yeast display library with specificity to the SARS-CoV-2 spike protein receptor binding domain that neutralized the virus in vitro. Administration of the lead antibody clone to Syrian hamsters challenged with SARS-CoV-2 significantly reduced viral load and histopathology score in the lungs. Moreover, the antibody interrupted monocyte infiltration into the lungs, which may have contributed to the reduction of disease severity by limiting immunopathological exacerbation. The use of this antibody could provide an important therapy for treatment of COVID-19 patients.Entities:
Keywords: COVID; SARS-CoV-2; coronavirus; monoclonal Ab; therapeutic antibodies
Mesh:
Substances:
Year: 2020 PMID: 33391285 PMCID: PMC7775388 DOI: 10.3389/fimmu.2020.614256
Source DB: PubMed Journal: Front Immunol ISSN: 1664-3224 Impact factor: 7.561