Stobart Christopher C, Nosek Jenna M, Moore Martin L
Department of Biological Sciences, Butler University, Indianapolis, IN, United States.
Department of Pediatrics, Emory University, Atlanta, GA, United States.
Front Microbiol. 2017 Dec 5;8:2412. doi: 10.3389/fmicb.2017.02412. eCollection 2017.
Human rhinovirus (HRV) remains a leading cause of several human diseases including the common cold. Despite considerable research over the last 60 years, development of an effective vaccine to HRV has been viewed by many as unfeasible due, in part, to the antigenic diversity of circulating HRVs in nature. Over 150 antigenically distinct types of HRV are currently known which span three species: HRV A, HRV B, and HRV C. Early attempts to develop a rhinovirus vaccine have shown that inactivated HRV is capable of serving as a strong immunogen and inducing neutralizing antibodies. Yet, limitations to virus preparation and recovery, continued identification of antigenic variants of HRV, and logistical challenges pertaining to preparing a polyvalent preparation of the magnitude required for true efficacy against circulating rhinoviruses continue to prove a daunting challenge. In this review, we describe HRV biology, antigenic diversity, and past and present advances in HRV vaccine design.
人鼻病毒(HRV)仍然是包括普通感冒在内的多种人类疾病的主要病因。尽管在过去60年里进行了大量研究,但许多人认为开发一种有效的HRV疫苗是不可行的,部分原因是自然界中传播的HRV具有抗原多样性。目前已知超过150种抗原性不同的HRV类型,它们分属于三个种:HRV A、HRV B和HRV C。早期开发鼻病毒疫苗的尝试表明,灭活的HRV能够作为一种强大的免疫原并诱导中和抗体。然而,病毒制备和回收的局限性、HRV抗原变体的持续发现,以及制备针对传播的鼻病毒真正有效的多价制剂所涉及的后勤挑战,仍然是一项艰巨的任务。在这篇综述中,我们描述了HRV的生物学特性、抗原多样性,以及HRV疫苗设计的过去和现在的进展。