Nham Eliel, Kim Jineui, Lee Jungmin, Park Heedo, Kim Jeonghun, Lee Sohyun, Choi Jaeuk, Kim Kyung Taek, Yoon Jin Gu, Hwang Soon Young, Song Joon Young, Cheong Hee Jin, Kim Woo Joo, Park Man-Seong, Noh Ji Yun
Division of Infectious Diseases, Department of Internal Medicine, Korea University Guro Hospital, Korea University College of Medicine, Seoul 08308, Korea.
Department of Microbiology, Vaccine Innovation Center, Korea University College of Medicine, Seoul 02841, Korea.
Immune Netw. 2023 Nov 13;23(6):e43. doi: 10.4110/in.2023.23.e43. eCollection 2023 Dec.
The continuous emergence of severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) variants has provided insights for updating current coronavirus disease 2019 (COVID-19) vaccines. We examined the neutralizing activity of Abs induced by a BA.4/5-containing bivalent mRNA vaccine against Omicron subvariants BN.1 and XBB.1.5. We recruited 40 individuals who had received a monovalent COVID-19 booster dose after a primary series of COVID-19 vaccinations and will be vaccinated with a BA.4/5-containing bivalent vaccine. Sera were collected before vaccination, one month after, and three months after a bivalent booster. Neutralizing Ab (nAb) titers were measured against ancestral SARS-CoV-2 and Omicron subvariants BA.5, BN.1, and XBB.1.5. BA.4/5-containing bivalent vaccination significantly boosted nAb levels against both ancestral SARS-CoV-2 and Omicron subvariants. Participants with a history of SARS-CoV-2 infection had higher nAb titers against all examined strains than the infection-naïve group. NAb titers against BN.1 and XBB.1.5 were lower than those against the ancestral SARS-CoV-2 and BA.5 strains. These results suggest that COVID-19 vaccinations specifically targeting emerging Omicron subvariants, such as XBB.1.5, may be required to ensure better protection against SARS-CoV-2 infection, especially in high-risk groups.
严重急性呼吸综合征冠状病毒2(SARS-CoV-2)变体的不断出现为更新当前的2019冠状病毒病(COVID-19)疫苗提供了思路。我们检测了含BA.4/5的二价mRNA疫苗诱导的抗体对奥密克戎亚变体BN.1和XBB.1.5的中和活性。我们招募了40名在完成一系列COVID-19初种疫苗后接种了一剂COVID-19单价加强针且即将接种含BA.4/5的二价疫苗的个体。在接种疫苗前、接种后1个月和接种二价加强针后3个月采集血清。检测针对原始SARS-CoV-2以及奥密克戎亚变体BA.5、BN.1和XBB.1.5的中和抗体(nAb)滴度。含BA.4/5的二价疫苗接种显著提高了针对原始SARS-CoV-2和奥密克戎亚变体的nAb水平。有SARS-CoV-2感染史的参与者针对所有检测毒株的nAb滴度均高于未感染组。针对BN.1和XBB.1.5的nAb滴度低于针对原始SARS-CoV-2和BA.5毒株的滴度。这些结果表明,可能需要专门针对新兴奥密克戎亚变体(如XBB.1.5)的COVID-19疫苗接种,以确保更好地预防SARS-CoV-2感染,尤其是在高危人群中。