Bispecific IgG neutralizes SARS-CoV-2 variants and prevents escape in mice
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F60162694%3A_____%2F21%3AN0000013" target="_blank" >RIV/60162694:_____/21:N0000013 - isvavai.cz</a>
Result on the web
<a href="https://www.nature.com/articles/s41586-021-03461-y" target="_blank" >https://www.nature.com/articles/s41586-021-03461-y</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1038/s41586-021-03461-y" target="_blank" >10.1038/s41586-021-03461-y</a>
Alternative languages
Result language
angličtina
Original language name
Bispecific IgG neutralizes SARS-CoV-2 variants and prevents escape in mice
Original language description
Neutralizing antibodies that target the receptor-binding domain (RBD) of the SARS-CoV-2 spike protein are among the most promising approaches against COVID-191,2. A bispecific IgG1-like molecule (CoV-X2) has been developed on the basis of C121 and C135, two antibodies derived from donors who had recovered from COVID-193. Here we show that CoV-X2 simultaneously binds two independent sites on the RBD and, unlike its parental antibodies, prevents detectable spike binding to the cellular receptor of the virus, angiotensin-converting enzyme 2 (ACE2). Furthermore, CoV-X2 neutralizes wild-type SARS-CoV-2 and its variants of concern, as well as escape mutants generated by the parental monoclonal antibodies. We also found that in a mouse model of SARS-CoV-2 infection with lung inflammation, CoV-X2 protects mice from disease and suppresses viral escape. Thus, the simultaneous targeting of non-overlapping RBD epitopes by IgG-like bispecific antibodies is feasible and effective, and combines the advantages of antibody cocktails with those of single-molecule approaches.
Czech name
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Czech description
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Classification
Type
J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database
CEP classification
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OECD FORD branch
20602 - Medical laboratory technology (including laboratory samples analysis; diagnostic technologies) (Biomaterials to be 2.9 [physical characteristics of living material as related to medical implants, devices, sensors])
Result continuities
Project
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Continuities
V - Vyzkumna aktivita podporovana z jinych verejnych zdroju
Others
Publication year
2021
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
Nature
ISSN
1476-4687
e-ISSN
0028-0836
Volume of the periodical
593
Issue of the periodical within the volume
květen 2021
Country of publishing house
GB - UNITED KINGDOM
Number of pages
23
Pages from-to
424-428
UT code for WoS article
000640199100001
EID of the result in the Scopus database
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