SARS-CoV-2 Omicron variant BA. 2 neutralisation in sera of people with Comirnaty or CoronaVac vaccination, infection or breakthrough infection, Hong Kong, 2020 to 2022

被引:25
|
作者
Cheng, Samuel M. S. [1 ]
Mok, Chris Ka Pun [2 ,3 ]
Chan, Karl C. K. [1 ]
Ng, Susanna S. [4 ]
Lam, Bosco H. S. [5 ]
Luk, Leo L. H. [1 ]
Ko, Fanny W. [4 ]
Chen, Chunke [2 ,3 ]
Yiu, Karen [4 ]
Li, John K. C. [1 ]
Chan, Ken K. P. [4 ]
Tsang, Leo C. H. [1 ]
Poon, Leo L. M. [1 ,6 ]
Hui, David S. C. [4 ,7 ]
Peiris, Malik [1 ,6 ]
机构
[1] Univ Hong Kong, LKS Fac Med, Sch Publ Hlth, Hong Kong, Peoples R China
[2] Chinese Univ Hong Kong, Jockey Club Sch Publ Hlth & Primary Care, Hong Kong, Peoples R China
[3] Chinese Univ Hong Kong, Fac Med, Li Ka Shing Inst Hlth Sci, Hong Kong, Peoples R China
[4] Chinese Univ Hong Kong, Fac Med, Dept Med & Therapeut, Hong Kong, Peoples R China
[5] North Lantau Hosp, Dept Pathol, Hong Kong, Peoples R China
[6] Ctr Immunol & Infect, Shatin, Hong Kong Sci Pk, Hong Kong, Peoples R China
[7] Chinese Univ Hong Kong, Fac Med, Stanley Ho Ctr Emerging Infect Dis, Hong Kong, Peoples R China
基金
中国国家自然科学基金; 美国国家卫生研究院;
关键词
D O I
10.2807/1560-7917.ES.2022.27.18.2200178
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Background: Omicron subvariant BA.2 circulation is rapidly increasing globally. Aim: We evaluated the neutralising antibody response from vaccination or prior SARS-CoV-2 infection against symptomatic infection by BA.2 or other variants. Methods: Using 50% plaque reduction neutralisation tests (PRNT50), we assessed neutralising antibody titres to BA. 2, wild type (WT) SARS- CoV-2 and other variants in Comirnaty or CoronaVac vaccinees, with or without prior WT-SARS-CoV-2 infection. Titres were also measured for non- vaccinees convalescing from a WT-SARS- CoV-2 infection. Neutralising antibodies in BA.2 and BA.1 breakthrough infections and in BA. 2 infections affecting non- vaccinees were additionally studied. Results: In vaccinees or prior WT-SARS-CoV-2-infected people, BA.2 and BA.1 PRNT 50 titres were comparable but significantly (p < 10(-5)) lower than WT. In each group of 20 vaccinees with (i) three-doses of Comirnaty, (ii) two CoronaVac followed by one Comirnaty dose, or (iii) one dose of either vaccine after a WT-SARS-CoV-2 infection, = 19 individuals developed detectable (PRNT50 titre <= 10) antibodies to BA.2, while only 15 of 20 vaccinated with three doses of CoronaVac did. Comirnaty vaccination elicited higher titres to BA.2 than CoronaVac. In people convalescing from a WT-SARS-CoV-2 infection, a single vaccine dose induced higher BA.2 titres than three Comirnaty (p = 0.02) or CoronaVac (p = 0.00001) doses in infection-naive individuals. BA.2 infections in previously uninfected and unvaccinated individuals elicited low (PRNT50 titre <= 80) responses with little cross-neutralisation of other variants. However, vaccinees with BA.1 or BA.2 breakthrough infections had broad cross- neutralising antibodies to WT viruses, and BA.1, BA.2, Beta and Delta variants. Conclusions: Existing vaccines can be of help against the BA.2 subvariant.
引用
收藏
页码:14 / 24
页数:11
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