Department of Pediatrics, University of Wisconsin-Madison, Madison, WI.
Institute of Molecular Virology, University of Wisconsin-Madison, Madison, WI.
Chest. 2019 May;155(5):1018-1025. doi: 10.1016/j.chest.2018.12.012. Epub 2019 Jan 17.
Human rhinoviruses (RVs) are picornaviruses that can cause a variety of upper and lower respiratory tract illnesses, including the common cold, bronchitis, pneumonia, and exacerbations of chronic respiratory diseases such as asthma. There are currently > 160 known types of RVs classified into three species (A, B, and C) that use three different cellular membrane glycoproteins expressed in the respiratory epithelium to enter the host cell. These viral receptors are intercellular adhesion molecule 1 (used by the majority of RV-A and all RV-B types), low-density lipoprotein receptor family members (used by 12 RV-A types), and cadherin-related family member 3 (CDHR3; used by RV-C). RV-A and RV-B interactions with intercellular adhesion molecule 1 and low-density lipoprotein receptor glycoproteins are well defined and their cellular functions have been described, whereas the mechanisms of the RV-C interaction with CDHR3 and its cellular functions are being studied. A single nucleotide polymorphism (rs6967330) in CDHR3 increases cell surface expression of this protein and, as a result, also promotes RV-C infections and illnesses. There are currently no approved vaccines or antiviral therapies available to treat or prevent RV infections, which is a major unmet medical need. Understanding interactions between RV and cellular receptors could lead to new insights into the pathogenesis of respiratory illnesses as well as lead to new approaches to control respiratory illnesses caused by RV infections.
人类鼻病毒(RV)是小核糖核酸病毒科,能引起多种上、下呼吸道疾病,包括普通感冒、支气管炎、肺炎以及哮喘等慢性呼吸道疾病的恶化。目前已知有超过 160 种 RV,可分为三个种(A、B 和 C),它们利用呼吸道上皮细胞中表达的三种不同的细胞膜糖蛋白进入宿主细胞。这些病毒受体包括细胞间黏附分子 1(大多数 RV-A 和所有 RV-B 型都使用)、低密度脂蛋白受体家族成员(12 种 RV-A 型使用)和钙黏蛋白相关家族成员 3(CDHR3;RV-C 使用)。RV-A 和 RV-B 与细胞间黏附分子 1 和低密度脂蛋白受体糖蛋白的相互作用已得到很好的定义,其细胞功能也已被描述,而 RV-C 与 CDHR3 的相互作用及其细胞功能的机制正在研究中。CDHR3 中的单核苷酸多态性(rs6967330)增加了该蛋白的细胞表面表达,因此也促进了 RV-C 的感染和疾病。目前尚无批准的疫苗或抗病毒疗法可用于治疗或预防 RV 感染,这是一个重大的未满足的医疗需求。了解 RV 与细胞受体的相互作用可能为呼吸道疾病的发病机制提供新的见解,并为控制由 RV 感染引起的呼吸道疾病提供新的方法。