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SARS-CoV-2 tetrameric RBD protein blocks viral infection and induces potent neutralizing antibody response

The pandemic of coronavirus disease 2019 (COVID-19) caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has posed serious threats to global health and economy and calls for the development of safe treatments and effective vaccines. The receptor-binding domain in the spike protein...

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Detalles Bibliográficos
Autores principales: Liu, Zheng, Yang, Chenglu, Zhang, Haokun, Cao, Guojie, Wang, Senzhen, Yin, Siwen, Wang, Yanming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9659643/
https://www.ncbi.nlm.nih.gov/pubmed/36389744
http://dx.doi.org/10.3389/fimmu.2022.960094
Descripción
Sumario:The pandemic of coronavirus disease 2019 (COVID-19) caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has posed serious threats to global health and economy and calls for the development of safe treatments and effective vaccines. The receptor-binding domain in the spike protein (S(RBD)) of SARS-CoV-2 is responsible for its binding to angiotensin-converting enzyme 2 (ACE2) receptor. It contains multiple dominant neutralizing epitopes and serves as an important antigen for the development of COVID-19 vaccines. Here, we showed that dimeric S(RBD)-Fc and tetrameric 2xS(RBD)-Fc fusion proteins bind ACE2 with different affinity and block SARS-CoV-2 pseudoviral infection. Immunization of mice with S(RBD)-Fc fusion proteins elicited high titer of RBD-specific antibodies with robust neutralizing activity against pseudoviral infections. As such, our study indicates that the polymeric S(RBD)-Fc fusion protein can serve as a treatment agent as well as a vaccine for fighting COVID-19.