Neutralizing Activities Against the Omicron Variant After a Heterologous Booster in Healthy Adults Receiving Two Doses of CoronaVac Vaccination

被引:46
作者
Assawakosri, Suvichada [1 ,2 ]
Kanokudom, Sitthichai [1 ,2 ]
Suntronwong, Nungruthai [1 ]
Auphimai, Chompoonut [1 ]
Nilyanimit, Pornjarim [1 ]
Vichaiwattana, Preeyaporn [1 ]
Thongmee, Thanunrat [1 ]
Duangchinda, Thaneeya [3 ]
Chantima, Warangkana [4 ,5 ]
Pakchotanon, Pattarakul [3 ]
Srimuan, Donchida [1 ]
Thatsanatorn, Thaksaporn [1 ]
Klinfueng, Sirapa [1 ]
Yorsang, Ritthideach [1 ]
Sudhinaraset, Natthinee [1 ]
Wanlapakorn, Nasamon [1 ]
Mongkolsapaya, Juthathip [6 ,7 ]
Honsawek, Sittisak [2 ]
Poovorawan, Yong [1 ,8 ]
机构
[1] Chulalongkorn Univ, Fac Med, Ctr Excellence Clin Virol, Bangkok 10330, Thailand
[2] Chulalongkorn Univ, King Chulalongkorn Mem Hosp, Fac Med, Osteoarthrit & Musculoskeleton Res Unit,Thai Red, Bangkok, Thailand
[3] Natl Sci & Technol Dev Agcy, Natl Sci & Dev Agcy, Natl Ctr Genet Engn & Biotechnol, Mol Biol Dengue & Flaviviruses Res Team, Pathum Thani, Thailand
[4] Mahidol Univ, Siriraj Hosp, Fac Med, Div Dengue Hemorrhag Fever Res, Bangkok, Thailand
[5] Mahidol Univ, Siriraj Hosp, Fac Med, Siriraj Ctr Res Excellence Dengue & Emerging Path, Bangkok, Thailand
[6] Univ Oxford, Wellcome Ctr Human Genet, Nuffield Dept Med, Oxford, England
[7] Univ Oxford, Chinese Acad Med Sci Oxford Inst, Oxford, England
[8] Royal Soc Thailand, Bangkok, Thailand
关键词
AZD1222; COVID-19; mRNA vaccine; omicron; third dose; VACCINES;
D O I
10.1093/infdis/jiac092
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background The use of an inactivated severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) vaccine (CoronaVac) against SARS-CoV-2 is implemented worldwide. However, waning immunity and breakthrough infections have been observed. Therefore, we hypothesized that the heterologous booster might improve the protection against the delta and omicron variants. Methods A total of 224 individuals who completed the 2-dose CoronaVac for 6 months were included. We studied reactogenicity and immunogenicity after a heterologous booster with the inactivated vaccine (BBIBP), the viral vector vaccine (AZD1222), and the messenger ribonucleic acid (mRNA) vaccine (both BNT162B2 and mRNA-1273). We also determined immunogenicity at 3- and 6-month boosting intervals. Results The solicited adverse events were mild to moderate and well tolerated. Total receptor binding domain (RBD) immunoglobulin (Ig), anti-RBD IgG, focus reduction neutralization test (FRNT50) against delta and omicron variants, and T-cell response were highest in the mRNA-1273 group followed by the BNT162b2, AZD1222, and BBIBP groups, respectively. We also witnessed a higher total Ig anti-RBD in the long-interval than in the short-interval group. Conclusions All 4 booster vaccines significantly increased binding and neutralizing antibodies in individuals immunized with 2 doses of CoronaVac. The present evidence may benefit vaccine strategies to thwart variants of concern, including the omicron variant. Heterologous booster vaccines significantly increased binding and neutralizing antibody in healthy adults immunized with 2 doses of CoronaVac. The present evidence may benefit vaccine strategies to combat variants of concern, including the omicron variant.
引用
收藏
页码:1372 / 1381
页数:10
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