S. Assawakosri, S. Kanokudom, N. Suntronwong, Jiratchaya Puenpa, T. Duangchinda, W. Chantima, P. Pakchotanon, J. Mongkolsapaya, Nasamon Wanlapakorn, S. Honsawek, Y. Poovorawan
{"title":"Omicron BA.1, BA.2 and COVID-19 Booster Vaccination","authors":"S. Assawakosri, S. Kanokudom, N. Suntronwong, Jiratchaya Puenpa, T. Duangchinda, W. Chantima, P. Pakchotanon, J. Mongkolsapaya, Nasamon Wanlapakorn, S. Honsawek, Y. Poovorawan","doi":"10.1093/infdis/jiac158","DOIUrl":null,"url":null,"abstract":"TO THE EDITOR—In reply to the correspondence from Tjan et al [1] regarding the heterologous booster in healthy adults previously immunized with 2 doses of CoronaVac [2], the additional knowledge on immunogenicity of the booster (third dose) with BNT162b2 in BNT162b2primed individuals against the BA.2 omicron variant will help promote the vaccine uptake and coverage in themidst of a surge in BA.2 omicron worldwide. As of February 2022, the omicron variant was further classified into 4 main sublineages, BA.1, BA.1.1, BA.2, and BA.3. Moreover, an epidemiological surveillance on coronavirus disease 2019 (COVID-19) showed that BA.2 sublineages have become the dominant variant globally [3]. In Thailand, the BA.2 sublineages have been detected since the end of January 2022. The proportion of BA.2 sublineages rapidly increased and accounted for more than 90% of positive cases reported in March 2022 [Puenpa J et al. unpublished]. Potent serum neutralizing antibody (nAbs) against BA.1 was observed after the heterologous booster in individuals previously immunized with 2 doses of CoronaVac [2]. Considering the waning immunity after primary series vaccination and the high transmissibility and potential immune escape of BA.2 sublineage, we further determined the immunogenicity of the mRNA-1273 booster against BA.1 and BA.2 in AZD1222-primed individuals using the 50% focus reduction neutralization test (FRNT50) as previously described [2].","PeriodicalId":22572,"journal":{"name":"The Indonesian Journal of Infectious Diseases","volume":"15 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2022-04-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"2","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"The Indonesian Journal of Infectious Diseases","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1093/infdis/jiac158","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 2
Abstract
TO THE EDITOR—In reply to the correspondence from Tjan et al [1] regarding the heterologous booster in healthy adults previously immunized with 2 doses of CoronaVac [2], the additional knowledge on immunogenicity of the booster (third dose) with BNT162b2 in BNT162b2primed individuals against the BA.2 omicron variant will help promote the vaccine uptake and coverage in themidst of a surge in BA.2 omicron worldwide. As of February 2022, the omicron variant was further classified into 4 main sublineages, BA.1, BA.1.1, BA.2, and BA.3. Moreover, an epidemiological surveillance on coronavirus disease 2019 (COVID-19) showed that BA.2 sublineages have become the dominant variant globally [3]. In Thailand, the BA.2 sublineages have been detected since the end of January 2022. The proportion of BA.2 sublineages rapidly increased and accounted for more than 90% of positive cases reported in March 2022 [Puenpa J et al. unpublished]. Potent serum neutralizing antibody (nAbs) against BA.1 was observed after the heterologous booster in individuals previously immunized with 2 doses of CoronaVac [2]. Considering the waning immunity after primary series vaccination and the high transmissibility and potential immune escape of BA.2 sublineage, we further determined the immunogenicity of the mRNA-1273 booster against BA.1 and BA.2 in AZD1222-primed individuals using the 50% focus reduction neutralization test (FRNT50) as previously described [2].
致编辑:在Tjan等人[1]的信函中,我们回复了之前接种过2剂CoronaVac的健康成人[2]的异种增强剂,关于BNT162b2增强剂(第三剂)在BNT162b2引发的个体中对BA.2组克隆变体的免疫原性的额外知识,将有助于在全球BA.2组克隆激增期间促进疫苗的吸收和覆盖。截至2022年2月,该组粒变体进一步分为4个主要亚系,BA.1、BA.1.1、BA.2和BA.3。此外,对2019冠状病毒病(COVID-19)的流行病学监测显示,BA.2亚系已成为全球优势变异体[3]。在泰国,自2022年1月底以来一直检测到BA.2亚型。BA.2亚型的比例迅速增加,占2022年3月报告的阳性病例的90%以上[Puenpa J et al.未发表]。在先前接种过2剂CoronaVac的个体中,在异种增强剂后观察到针对BA.1的有效血清中和抗体(nab)[2]。考虑到一次系列疫苗接种后的免疫力下降,以及BA.2亚系的高传播性和潜在的免疫逃逸,我们采用先前描述的50%减焦中和试验(FRNT50)进一步确定了mRNA-1273增强剂对azd1222引物个体BA.1和BA.2的免疫原性[2]。