Rajendran Madhusudan, Krammer Florian, McMahon Meagan
Department of Microbiology, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Department of Pathology, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Vaccines (Basel). 2021 Aug 2;9(8):846. doi: 10.3390/vaccines9080846.
The influenza virus neuraminidase (NA) is primarily involved in the release of progeny viruses from infected cells-a critical role for virus replication. Compared to the immuno-dominant hemagglutinin, there are fewer NA subtypes, and NA experiences a slower rate of antigenic drift and reduced immune selection pressure. Furthermore, NA inhibiting antibodies prevent viral egress, thus preventing viral spread. Anti-NA immunity can lessen disease severity, reduce viral shedding, and decrease viral lung titers in humans and various animal models. As a result, there has been a concerted effort to investigate the possibilities of incorporating immunogenic forms of NA as a vaccine antigen in future vaccine formulations. In this review, we discuss NA-based immunity and describe several human NA-specific monoclonal antibodies (mAbs) that have a broad range of protection. We also review vaccine platforms that are investigating NA antigens in pre-clinical models and their potential use for next-generation influenza virus vaccines. The evidence presented here supports the inclusion of immunogenic NA in future influenza virus vaccines.
流感病毒神经氨酸酶(NA)主要参与子代病毒从受感染细胞中的释放,这对病毒复制至关重要。与免疫显性的血凝素相比,NA亚型较少,且NA经历抗原漂移的速率较慢,免疫选择压力降低。此外,NA抑制性抗体可阻止病毒释放,从而防止病毒传播。抗NA免疫可减轻疾病严重程度、减少病毒脱落,并降低人类和各种动物模型中的病毒肺滴度。因此,人们一直在协同努力研究将免疫原性形式的NA作为未来疫苗配方中的疫苗抗原的可能性。在这篇综述中,我们讨论基于NA的免疫,并描述几种具有广泛保护作用的人源NA特异性单克隆抗体(mAb)。我们还综述了正在临床前模型中研究NA抗原的疫苗平台及其在下一代流感病毒疫苗中的潜在用途。此处提供的证据支持在未来的流感病毒疫苗中纳入免疫原性NA。