Lim Heeji, Jang Sundong, In Hyun Ju, Kim Kwangwook, Choi Eun Bee, Kim Soo Ji, Lim Hye Jung, Yim Min Su, Ouh In-Ohk, Kim Byung Chul, Do Hyeon Nam, Lee June-Woo, Kim Byoungguk, Lee Yoo-Kyoung
Division of Vaccine Development Coordination, Center for Vaccine Research National Institute of Infectious Diseases, Korea National Institute of Health, Korea Disease Control and Prevention Agency, Cheongju, Korea.
Division of Vaccine Clinical Research, Center for Vaccine Research National Institute of Infectious Diseases, Korea National Institute of Health, Korea Disease Control and Prevention Agency, Cheongju, Korea.
Infect Chemother. 2023 Mar;55(1):99-104. doi: 10.3947/ic.2022.0132.
The immunogenicity of a heterologous vaccination regimen consisting of ChAdOx1 nCoV-19 (a chimpanzee adenovirus-vectored vaccine) followed by mRNA-1273 (a lipid-nanoparticle-encapsulated mRNA-based vaccine) against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), specifically the omicron variant (B.1.1.529), is poorly studied. The aim of this study was to evaluate the neutralizing antibody activity and immunogenicity of heterologous ChAdOx1 nCoV-19 and mRNA-1273 prime-boost vaccination against wild-type (BetaCoV/Korea/KCDC03/2020), alpha, beta, gamma, delta, and omicron variants of SARS-CoV-2 in Korea. A 50% neutralizing dilution (ND50) titer was determined in serum samples using the plaque reduction neutralization test. Antibody titer decreased significantly at 3 months compared with that at 2 weeks after the 2nd dose. On comparing the ND50 titers for the above-mentioned variants of concerns, it was observed that the ND50 titer for the omicron variant was the lowest. This study provides insights into cross-vaccination effects and can be useful for further vaccination strategies in Korea.
由ChAdOx1 nCoV-19(一种黑猩猩腺病毒载体疫苗)和mRNA-1273(一种脂质纳米颗粒包裹的基于mRNA的疫苗)组成的异源疫苗接种方案针对严重急性呼吸综合征冠状病毒2(SARS-CoV-2),特别是奥密克戎变种(B.1.1.529)的免疫原性研究较少。本研究的目的是评估异源ChAdOx1 nCoV-19和mRNA-1273初免-加强接种对韩国SARS-CoV-2野生型(BetaCoV/Korea/KCDC03/2020)、阿尔法、贝塔、伽马、德尔塔和奥密克戎变种的中和抗体活性和免疫原性。使用蚀斑减少中和试验在血清样本中测定50%中和稀释度(ND50)滴度。与第二剂后2周相比,3个月时抗体滴度显著下降。在比较上述关注变种的ND50滴度时,观察到奥密克戎变种的ND50滴度最低。本研究为交叉接种效果提供了见解,对韩国进一步的疫苗接种策略可能有用。