Isogawa Masanori, Onodera Taishi, Ainai Akira, Kotaki Ryutaro, Kanno Takayuki, Saito Shinji, Tobiume Minoru, Tokunaga Kenzo, Hara Megumi, Hirota Yoshio, Suzuki Tadaki, Takahashi Yoshimasa, Tsuru Tomomi
Research Center for Vaccine Development, National Institute of Infectious Diseases, Japan Institute for Health Security, Tokyo, Japan.
Department of Virology II, National Institute of Infectious Diseases, Japan Institute for Health Security, Tokyo, Japan.
Sci Rep. 2025 May 28;15(1):18684. doi: 10.1038/s41598-025-00054-x.
mRNA and adenoviral vector vaccine platforms were used for the primary series of COVID-19 vaccines in many countries. However, the distinct immunogenic properties on these platforms remain less understood. We traced neutralizing antibodies, memory B cells, and T cells longitudinally in cohorts that received either mRNA (BNT162b2 or mRNA-1273) or adenoviral vector (ChAdOx1) vaccines with homologous or heterologous regimens (total 9 groups, n = 26-28 for each group) at 4 weeks interval. The priming and boosting effects on various immune parameters were comparably assessed between mRNA and adenoviral vector platforms. We found that initial priming by adenoviral vector vaccine elicited robust T cell responses, but B cell responses, including antibody titers, were relatively lower than those elicited by mRNA priming. The dissociation between T cell and antibody responses were exaggerated at greater extents after the homologous booster with the adenoviral vector vaccine, resulting in 5-19-fold lower antibody titers despite comparable spike-specific T cell numbers at day 28 after the boost. Robust IFN-γ and few IL-2 and IL-5 production characterized T cell functionality primed by adenoviral vector. Boosting with mRNA vaccines restored their IL-2 and IL-5 production at some extents, but the IL-5 T cell responses elicited by adenoviral vector/mRNA heterologous regimen waned faster than those by mRNA homologous regimen. Thus, our data revealed that the cytokine production of helper T cells was skewed by adenoviral vector priming, leading to the attenuated IL-2 and IL-5 responses which were prolonged even after mRNA boosting, suggesting an imprinting of T-cell functionality depending on the vaccine platform used for initial priming. These results highlight the importance of selecting vaccine platforms based on the immunogenic properties.
在许多国家,mRNA和腺病毒载体疫苗平台被用于新冠疫苗的初始系列接种。然而,这些平台上独特的免疫原性特性仍不太为人所知。我们在接受mRNA(BNT162b2或mRNA-1273)或腺病毒载体(ChAdOx1)疫苗同源或异源接种方案(共9组,每组n = 26 - 28)的队列中,每隔4周纵向追踪中和抗体、记忆B细胞和T细胞。对mRNA和腺病毒载体平台之间在各种免疫参数上的启动和加强作用进行了比较评估。我们发现,腺病毒载体疫苗的初始启动引发了强烈的T细胞反应,但包括抗体滴度在内的B细胞反应相对低于mRNA启动所引发的反应。在使用腺病毒载体疫苗进行同源加强接种后,T细胞和抗体反应之间的分离在更大程度上被放大,尽管在加强接种后第28天刺突特异性T细胞数量相当,但抗体滴度却降低了5至19倍。由腺病毒载体启动的T细胞功能以强大的IFN-γ产生以及少量的IL-2和IL-5产生为特征。用mRNA疫苗加强接种在一定程度上恢复了它们的IL-2和IL-5产生,但腺病毒载体/mRNA异源接种方案引发的IL-5 T细胞反应比mRNA同源接种方案消退得更快。因此,我们的数据表明,辅助性T细胞的细胞因子产生因腺病毒载体启动而发生偏差,导致IL-2和IL-5反应减弱,即使在mRNA加强接种后仍持续存在,这表明T细胞功能的印记取决于用于初始启动的疫苗平台。这些结果凸显了根据免疫原性特性选择疫苗平台的重要性。