Publications by authors named "A N Chikaev"

The COVID-19 pandemic has uncovered the high genetic variability of the SARS-CoV-2 virus and its ability to evade the immune responses that were induced by earlier viral variants. Only a few monoclonal antibodies that have been reported to date are capable of neutralizing a broad spectrum of SARS-CoV-2 variants. Here, we report the isolation of a new broadly neutralizing human monoclonal antibody, iC1.

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The emergence of SARS-CoV-2 mutant variants has posed a significant challenge to both the prevention and treatment of COVID-19 with anti-coronaviral neutralizing antibodies. The latest viral variants demonstrate pronounced resistance to the vast majority of human monoclonal antibodies raised against the ancestral Wuhan variant. Less is known about the susceptibility of the evolved virus to camelid nanobodies developed at the start of the pandemic.

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Article Synopsis
  • SARS-CoV-2 has a high mutation rate, leading to new variants that challenge vaccine-induced immunity, particularly affecting the ability to neutralize these variants in vaccinated individuals and those who recovered from infection.
  • The study analyzed four patient groups: those vaccinated with the Gam-COVID-Vac booster, twice-infected unvaccinated individuals, breakthrough infections after vaccination, and vaccinated convalescents, focusing on their neutralizing antibody responses.
  • Results showed that individuals with hybrid immunity (from either breakthrough infections or vaccination after recovery) had significantly higher levels of virus-binding IgG and greater neutralizing activity against various SARS-CoV-2 variants compared to those with only vaccinations or infections, highlighting the protective advantage of hybrid immunity.
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The development of effective vaccines against SARS-CoV-2 remains a global health priority. Despite extensive use, the effects of Sputnik V on B cell immunity need to be explored in detail. We performed comprehensive profiling of humoral and B cell responses in a cohort of vaccinated subjects (n = 22), and demonstrate that Sputnik vaccination results in robust B cell immunity.

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The receptor-binding domain (RBD) of the protein S SARS-CoV-2 is considered to be one of the appealing targets for developing a vaccine against COVID-19. The choice of an expression system is essential when developing subunit vaccines, as it ensures the effective synthesis of the correctly folded target protein, and maintains its antigenic and immunogenic properties. Here, we describe the production of a recombinant RBD protein using prokaryotic (pRBD) and mammalian (mRBD) expression systems, and compare the immunogenicity of prokaryotic and mammalian-expressed RBD using a BALB/c mice model.

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