Center for Vaccines and Immunology, University of Georgia, Athens, GA, USA.
Department of Infectious Diseases, University of Georgia, Athens, GA, USA.
Expert Rev Vaccines. 2024 Jan-Dec;23(1):474-484. doi: 10.1080/14760584.2024.2343689. Epub 2024 Apr 23.
Anti-neuraminidase (NA) immunity correlates with the protection against influenza virus infection in both human and animal models. The aim of this review is to better understand the mechanism of anti-NA immunity, and also to evaluate the approaches on developing NA-based influenza vaccines or enhancing immune responses against NA for current influenza vaccines.
In this review, the structure of influenza neuraminidase, the contribution of anti-NA immunity to protection, as well as the efforts and challenges of targeting the immune responses to NA were discussed. We also listed some of the newly discovered anti-NA monoclonal antibodies and discussed their contribution in therapeutic as well as the antigen design of a broadly protective NA vaccine.
Targeting the immune response to both HA and NA may be critical for achieving the optimal protection since there are different mechanisms of HA and NA elicited protective immunity. Monoclonal antibodies (mAbs) that target the conserved protective lateral face or catalytic sites are effective therapeutics. The epitope discovery using monoclonal antibodies may benefit NA-based vaccine elicited broadly reactive antibody responses. Therefore, the potential for a vaccine that elicits cross-reactive antibodies against neuraminidase is a high priority for next-generation influenza vaccines.
抗神经氨酸酶(NA)免疫与人类和动物模型中对流感病毒感染的保护相关。本综述的目的是更好地了解抗 NA 免疫的机制,并评估针对当前流感疫苗开发基于 NA 的流感疫苗或增强针对 NA 的免疫反应的方法。
在本综述中,讨论了流感神经氨酸酶的结构、抗 NA 免疫对保护的贡献,以及针对 NA 的免疫反应的努力和挑战。我们还列出了一些新发现的抗 NA 单克隆抗体,并讨论了它们在治疗以及广泛保护性 NA 疫苗的抗原设计中的作用。
针对血凝素(HA)和神经氨酸酶(NA)的免疫反应可能是实现最佳保护的关键,因为 HA 和 NA 引发的保护性免疫具有不同的机制。针对保守的保护性侧表面或催化位点的单克隆抗体(mAbs)是有效的治疗方法。使用单克隆抗体进行表位发现可能有利于基于 NA 的疫苗引发广泛反应的抗体反应。因此,引发针对神经氨酸酶的交叉反应性抗体的疫苗的潜力是下一代流感疫苗的高度优先事项。