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Coronaviruses

The significant immune escape of pseudotyped SARS-CoV-2 variant Omicron

, , , , , , , , , & ORCID Icon show all
Pages 1-5 | Received 07 Dec 2021, Accepted 08 Dec 2021, Published online: 21 Dec 2021
 

ABSTRACT

The emergence of Omicron/BA.1 has brought new challenges to fight against SARS-CoV-2. A large number of mutations in the Spike protein suggest that its susceptibility to immune protection elicited by the existing COVID-19 infection and vaccines may be altered. In this study, we constructed the pseudotyped SARS-CoV-2 variant Omicron. The sensitivity of 28 serum samples from COVID-19 convalescent patients infected with SARS-CoV-2 original strain was tested against pseudotyped Omicron as well as the other variants of concern (VOCs, Alpha, Beta, Gamma, Delta) and variants of interest (VOIs, Lambda, Mu). Our results indicated that the mean neutralization ED50 of these sera against Omicron decreased to 66, which is about 8.4-folds compared to the D614G reference strain (ED50 = 556), whereas the neutralization activity of other VOC and VOI pseudotyped viruses decreased only about 1.2–4.5-folds. The finding from our in vitro assay suggest that Omicron variant may lead to more significant escape from immune protection elicited by previous SARS-CoV-2 infection and perhaps even by existing COVID-19 vaccines.

This article is part of the following collections:
EMI Ten Year Celebration Collections

Acknowledgments

We thank GISAID and associated laboratories and researchers for the shared sequence information. We thank Dr. Xiaowang Qu of the University of South China for convalescent serum samples.

Authors’ contributions

Y. W. and W. H. conceived, designed and supervised the experiments; L. Z. and Y. W. wrote the manuscript; Q. L., Z. L., T. L., S. L., Q.C., and J. N. performed the neutralization experiments. X.Q. and Q.W. provided convalescent sera and patients information. All of authors approved the final manuscript.

Disclosure statement

No potential conflict of interest was reported by the author(s).

Additional information

Funding

This work was supported by the National Key Research and Development Program of China (Grant Numbers 2021YFC0863300 & 2021YFC2391700), General Program of the National Natural Science Foundation of China (Grant Numbers 82073621 & 82172244), Beijing Municipal Science and Technology Project (Grant Number Z211100002521018).