Vaccine Research & Development Center, University of California Irvine, USA.
Center for Global Health, Department of Internal Medicine, University of New Mexico, USA.
Antiviral Res. 2024 May;225:105851. doi: 10.1016/j.antiviral.2024.105851. Epub 2024 Mar 7.
Currently, there are two approved vaccine regimens designed to prevent Ebola virus (EBOV) disease (EVD). Both are virus-vectored, and concerns about cold-chain storage and pre-existing immunity to the vectors warrant investigating additional vaccine strategies. Here, we have explored the utility of adjuvanted recombinant glycoproteins (GPs) from ebolaviruses Zaire (EBOV), Sudan (SUDV), and Bundibugyo (BDBV) for inducing antibody (Ab) and T cell cross-reactivity. Glycoproteins expressed in insect cells were administered to C57BL/6 mice as free protein or bound to the surface of liposomes, and formulated with toll-like receptor agonists CpG and MPLA (agonists for TLR 9 and 4, respectively), with or without the emulsions AddaVax or TiterMax. The magnitude of Ab cross-reactivity in binding and neutralization assays, and T cell cross-reactivity in antigen recall assays, correlated with phylogenetic relatedness. While most adjuvants screened induced IgG responses, a combination of CpG, MPLA and AddaVax emulsion ("IVAX-1") was the most potent and polarized in an IgG2c (Th1) direction. Breadth was also achieved by combining GPs into a trivalent (Tri-GP) cocktail with IVAX-1, which did not compromise antibody responses to individual components in binding and neutralizing assays. Th1 signature cytokines in T cell recall assays were undetectable after Tri-GP/IVAX-1 administration, despite a robust IgG2c response, although administration of Tri-GP on lipid nanoparticles in IVAX-1 elevated Th1 cytokines to detectable levels. Overall, the data indicate an adjuvanted trivalent recombinant GP approach may represent a path toward a broadly reactive, deployable vaccine against EVD.
目前,有两种经批准的疫苗方案旨在预防埃博拉病毒(EBOV)病(EVD)。这两种疫苗都是病毒载体疫苗,由于对冷链储存和对载体的预先存在的免疫的担忧,需要研究其他疫苗策略。在这里,我们探索了佐剂化重组糖蛋白(GPs)在诱导抗体(Ab)和 T 细胞交叉反应中的效用,这些糖蛋白来自扎伊尔(EBOV)、苏丹(SUDV)和邦迪布尤(BDBV)埃博拉病毒。在昆虫细胞中表达的糖蛋白作为游离蛋白或结合到脂质体表面被给予 C57BL/6 小鼠,并与 Toll 样受体激动剂 CpG 和 MPLA(分别为 TLR 9 和 4 的激动剂)联合使用,或不联合 AddaVax 或 TiterMax 乳化剂。在结合和中和测定中 Ab 交叉反应的程度,以及在抗原回忆测定中 T 细胞交叉反应的程度,与系统发生关系相关。虽然筛选出的大多数佐剂诱导 IgG 反应,但 CpG、MPLA 和 AddaVax 乳剂的组合(IVAX-1)是最有效的,在 IgG2c(Th1)方向上呈极化状态。通过将 GPs 组合成三价(Tri-GP)鸡尾酒与 IVAX-1 结合,也可以实现广度,这不会影响在结合和中和测定中对单个成分的抗体反应。尽管在 Tri-GP/IVAX-1 给药后检测到了强烈的 IgG2c 反应,但在 Tri-GP/IVAX-1 给药后,在 T 细胞回忆测定中未检测到 Th1 特征细胞因子,尽管在 IVAX-1 中的脂质纳米颗粒上给予 Tri-GP 可将 Th1 细胞因子提升到可检测水平。总体而言,数据表明,佐剂化三价重组 GP 方法可能代表了针对 EVD 的广泛反应性、可部署疫苗的一种途径。