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

S. Assawakosri, S. Kanokudom, N. Suntronwong, C. Auphimai, P. Nilyanimit, P. Vichaiwattana, T. Thongmee, T. Duangchinda, W. Chantima, P. Pakchotanon, D. Srimuan, T. Thatsanatorn, S. Klinfueng, R. Yorsaeng, N. Sudhinaraset, Nasamon Wanlapakorn, J. Mongkolsapaya, S. Honsawek, Y. Poovorawan
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引用次数: 48

Abstract

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 two-dose CoronaVac for six months were included. We studied reactogenicity and immunogenicity following a heterologous booster with the inactivated vaccine (BBIBP), the viral vector vaccine (AZD1222), and the mRNA vaccine (both BNT162B2 and mRNA-1273). We also determined immunogenicity at 3- and 6-months boosting intervals. Results. The solicited adverse events (AEs) were mild to moderate and well-tolerated. Total 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 groups. Conclusions. All four booster vaccines significantly increased binding and NAbs in individuals immunized with two doses of CoronaVac. The present evidence may benefit vaccine strategies development to thwart variants of concern, including the omicron variant. Keywords. COVID-19; Third dose; heterologous booster; omicron; mRNA-1273; BNT162b2; AZD1222; NAbs; T cells.
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在接受两剂冠状病毒疫苗接种的健康成人中,异源加强剂对组粒变异的中和活性
背景。在全球范围内实施了针对SARS-CoV-2的灭活的SARS-CoV-2疫苗(CoronaVac)。然而,已经观察到免疫力下降和突破性感染。因此,我们假设异种增强剂可能提高对δ和组粒变异的保护。方法。总共有224人完成了为期6个月的双剂量CoronaVac。我们研究了由灭活疫苗(BBIBP)、病毒载体疫苗(AZD1222)和mRNA疫苗(BNT162B2和mRNA-1273)组成的异源增强疫苗的反应原性和免疫原性。我们还在3个月和6个月的强化间隔中测定了免疫原性。结果。所征求的不良事件(ae)为轻度至中度,耐受性良好。rna -1273组RBD总免疫球蛋白(Ig)、抗RBD IgG、针对delta和omicron变体的焦点减少中和试验(FRNT50)和T细胞应答最高,其次是BNT162b2、AZD1222和BBIBP组。我们还发现,与短间隔组相比,长间隔组总Ig抗rbd更高。结论。在接种两剂冠状病毒疫苗的个体中,所有四种加强疫苗都显著增加了结合和nab。目前的证据可能有利于疫苗策略的发展,以阻止令人关注的变异,包括组粒变异。关键词。COVID-19;第三个剂量;不等的助推器;买卖;信使rna - 1273;BNT162b2;AZD1222;小伙子;T细胞。
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