The effect of spike mutations on SARS-CoV-2 neutralization.
The effect of spike mutations on SARS-CoV-2 neutralization.
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尖峰突变对SARS-CoV-2中和作用的影响
DOI:
10.1016/j.celrep.2021.108890
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发表时间:
2021-03-23
期刊:
影响因子:
8.8
通讯作者:
McCoy LE
中科院分区:
文献类型:
--
作者:
Rees-Spear C;Muir L;Griffith SA;Heaney J;Aldon Y;Snitselaar JL;Thomas P;Graham C;Seow J;Lee N;Rosa A;Roustan C;Houlihan CF;Sanders RW;Gupta RK;Cherepanov P;Stauss HJ;Nastouli E;SAFER Investigators;Doores KJ;van Gils MJ;McCoy LE
Multiple severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) vaccines show protective efficacy, which is most likely mediated by neutralizing antibodies recognizing the viral entry protein, spike. Because new SARS-CoV-2 variants are emerging rapidly, as exemplified by the B.1.1.7, B.1.351, and P.1 lineages, it is critical to understand whether antibody responses induced by infection with the original SARS-CoV-2 virus or current vaccines remain effective. In this study, we evaluate neutralization of a series of mutated spike pseudotypes based on divergence from SARS-CoV and then compare neutralization of the B.1.1.7 spike pseudotype and individual mutations. Spike-specific monoclonal antibody neutralization is reduced dramatically; in contrast, polyclonal antibodies from individuals infected in early 2020 remain active against most mutated spike pseudotypes, but potency is reduced in a minority of samples. This work highlights that changes in SARS-CoV-2 spike can alter neutralization sensitivity and underlines the need for effective real-time monitoring of emerging mutations and their effect on vaccine efficacy. SARS-CoV-2 pseudotypes produced by amino acids substitutions in SARS-CoV SARS-CoV-2 pseudotyped virus that encodes the B.1.1.7 variant spike Amino acid changes and B.1.1.7 can decrease monoclonal antibody neutralization Minimal effect on sera with only 10% losing potency against the B.1.1.7 pseudotype This study describes neutralization by antibodies and convalescent sera of SARS-CoV-2 spike mutants. Rees-Spear et al. show that SARS-CoV amino acid substitutions and the B.1.1.7 variant can block monoclonal antibody neutralization and that serum samples collected following mild illness are less resilient to spike variation than those following severe illness.
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DOI:
10.1126/science.abg3055
发表时间:
2021-04-09
期刊:
Science (New York, N.Y.)
影响因子:
--
作者:
Davies NG;Abbott S;Barnard RC;Jarvis CI;Kucharski AJ;Munday JD;Pearson CAB;Russell TW;Tully DC;Washburne AD;Wenseleers T;Gimma A;Waites W;Wong KLM;van Zandvoort K;Silverman JD;CMMID COVID-19 Working Group;COVID-19 Genomics UK (COG-UK) Consortium;Diaz-Ordaz K;Keogh R;Eggo RM;Funk S;Jit M;Atkins KE;Edmunds WJ
通讯作者:
Edmunds WJ
影响因子:
64.8
作者:
Li W;Moore MJ;Vasilieva N;Sui J;Wong SK;Berne MA;Somasundaran M;Sullivan JL;Luzuriaga K;Greenough TC;Choe H;Farzan M
通讯作者:
Farzan M
DOI:
10.1126/science.abe5901
发表时间:
2021-01-08
期刊:
Science (New York, N.Y.)
影响因子:
--
作者:
Oude Munnink BB;Sikkema RS;Nieuwenhuijse DF;Molenaar RJ;Munger E;Molenkamp R;van der Spek A;Tolsma P;Rietveld A;Brouwer M;Bouwmeester-Vincken N;Harders F;Hakze-van der Honing R;Wegdam-Blans MCA;Bouwstra RJ;GeurtsvanKessel C;van der Eijk AA;Velkers FC;Smit LAM;Stegeman A;van der Poel WHM;Koopmans MPG
通讯作者:
Koopmans MPG
影响因子:
82.9
作者:
Long, Quan-Xin;Liu, Bai-Zhong;Huang, Ai-Long
通讯作者:
Huang, Ai-Long
影响因子:
4.7
作者:
Gralinski, Lisa E.;Menachery, Vineet D.
通讯作者:
Menachery, Vineet D.