Tamminen Kirsi, Heinimäki Suvi, Gröhn Stina, Blazevic Vesna
Vaccine Development and Immunology/Vaccine Research Center, Faculty of Medicine and Health Technology, Tampere University, Arvo Ylpön katu 34, FI-33520 Tampere, Finland.
Vaccines (Basel). 2021 Jul 2;9(7):733. doi: 10.3390/vaccines9070733.
Vaccines based on mRNA and viral vectors are currently used in the frontline to combat the ongoing pandemic caused by the novel Severe Acute Respiratory Syndrome Coronavirus-2 (SARS-CoV-2). However, there is still an urgent need for alternative vaccine technologies inducing/boosting long-lasting and cross-reactive immunity in different populations. As a possible vaccine candidate, we employed the rotavirus VP6-protein platform to construct a fusion protein (FP) displaying receptor-binding domain (RBD) of SARS-CoV-2 spike protein (S) at the N-terminus of VP6. The recombinant baculovirus-insect cell produced VP6-RBD FP was proven antigenic in vitro and bound to the human angiotensin-converting enzyme 2 (hACE2) receptor. The FP was used to immunize BALB/c mice, and humoral- and T cell-mediated immune responses were investigated. SARS-CoV-2 RBD-specific T cells were induced at a high quantity; however, no RBD or S-specific antibodies were detected. The results suggest that conformational B cell epitopes might be buried inside the VP6, while RBD-specific T cell epitopes are available for T cell recognition after the processing and presentation of FP by the antigen-presenting cells. Further immunogenicity studies are needed to confirm these findings and to assess whether, under different experimental conditions, the VP6 platform may present SARS-CoV-2 antigens to B cells as well.
基于信使核糖核酸(mRNA)和病毒载体的疫苗目前被用于抗击由新型严重急性呼吸综合征冠状病毒2(SARS-CoV-2)引发的大流行的一线工作中。然而,仍然迫切需要替代疫苗技术,以在不同人群中诱导/增强持久和交叉反应性免疫。作为一种可能的候选疫苗,我们利用轮状病毒VP6蛋白平台构建了一种融合蛋白(FP),该融合蛋白在VP6的N端展示了SARS-CoV-2刺突蛋白(S)的受体结合域(RBD)。重组杆状病毒-昆虫细胞产生的VP6-RBD FP在体外被证明具有抗原性,并与人血管紧张素转换酶2(hACE2)受体结合。该融合蛋白用于免疫BALB/c小鼠,并研究了体液免疫和T细胞介导的免疫反应。大量诱导出了SARS-CoV-2 RBD特异性T细胞;然而,未检测到RBD或S特异性抗体。结果表明,构象性B细胞表位可能被掩埋在VP6内部,而RBD特异性T细胞表位在抗原呈递细胞对融合蛋白进行加工和呈递后可供T细胞识别。需要进一步的免疫原性研究来证实这些发现,并评估在不同实验条件下,VP6平台是否也能将SARS-CoV-2抗原呈递给B细胞。