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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

  • Czech description

Classification

  • Type

    J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database

  • CEP classification

  • 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

  • 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