Department of Biochemistry, Albert Einstein College of Medicine, Bronx, New York, United States of America.
Department of Microbiology and Immunology, Albert Einstein College of Medicine, Bronx, New York, United States of America.
PLoS Pathog. 2022 Jun 9;18(6):e1010573. doi: 10.1371/journal.ppat.1010573. eCollection 2022 Jun.
Powassan virus (POWV) is an emerging tick borne flavivirus (TBFV) that causes severe neuroinvasive disease. Currently, there are no approved treatments or vaccines to combat POWV infection. Here, we generated and characterized a nanoparticle immunogen displaying domain III (EDIII) of the POWV E glycoprotein. Immunization with POWV EDIII presented on nanoparticles resulted in significantly higher serum neutralizing titers against POWV than immunization with monomeric POWV EDIII. Furthermore, passive transfer of EDIII-reactive sera protected against POWV challenge in vivo. We isolated and characterized a panel of EDIII-specific monoclonal antibodies (mAbs) and identified several that potently inhibit POWV infection and engage distinct epitopes within the lateral ridge and C-C' loop of the EDIII. By creating a subunit-based nanoparticle immunogen with vaccine potential that elicits antibodies with protective activity against POWV infection, our findings enhance our understanding of the molecular determinants of antibody-mediated neutralization of TBFVs.
波瓦桑病毒(POWV)是一种新兴的蜱传黄病毒(TBFV),可引起严重的神经侵袭性疾病。目前,尚无针对 POWV 感染的批准治疗方法或疫苗。在这里,我们生成并表征了一种展示 POWV E 糖蛋白结构域 III(EDIII)的纳米颗粒免疫原。与单独使用 POWV EDIII 免疫相比,用纳米颗粒呈现的 POWV EDIII 进行免疫接种可显著提高针对 POWV 的血清中和滴度。此外,EDIII 反应性血清的被动转移可在体内保护免受 POWV 攻击。我们分离和表征了一组 EDIII 特异性单克隆抗体(mAb),并鉴定出几种能够有效抑制 POWV 感染并与 EDIII 侧脊和 C-C'环内的不同表位结合的 mAb。通过创建具有疫苗潜力的基于亚单位的纳米颗粒免疫原,该免疫原引发具有针对 POWV 感染的保护活性的抗体,我们的研究结果增强了我们对 TBFV 抗体介导中和的分子决定因素的理解。