| Literature DB >> 33574228 |
Ronit Rosenfeld1, Tal Noy-Porat2, Adva Mechaly2, Efi Makdasi2, Yinon Levy2, Ron Alcalay2, Reut Falach2, Moshe Aftalion2, Eyal Epstein2, David Gur2, Theodor Chitlaru2, Einat B Vitner2, Sharon Melamed2, Boaz Politi2, Ayelet Zauberman2, Shirley Lazar2, Adi Beth-Din2, Yentl Evgy2, Shmuel Yitzhaki2, Shmuel C Shapira2, Tomer Israely2, Ohad Mazor3.
Abstract
The coronavirus disease 2019 (COVID-19) pandemic, caused by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), exhibits high levels of mortality and morbidity and has dramatic consequences on human life, sociality and global economy. Neutralizing antibodies constitute a highly promising approach for treating and preventing infection by this novel pathogen. In the present study, we characterize and further evaluate the recently identified human monoclonal MD65 antibody for its ability to provide protection against a lethal SARS-CoV-2 infection of K18-hACE2 transgenic mice. Eighty percent of the untreated mice succumbed 6-9 days post-infection, while administration of the MD65 antibody as late as 3 days after exposure rescued all infected animals. In addition, the efficiency of the treatment is supported by prevention of morbidity and ablation of the load of infective virions in the lungs of treated animals. The data demonstrate the therapeutic value of human monoclonal antibodies as a life-saving treatment for severe COVID-19 infection.Entities:
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Year: 2021 PMID: 33574228 DOI: 10.1038/s41467-021-21239-8
Source DB: PubMed Journal: Nat Commun ISSN: 2041-1723 Impact factor: 14.919