Matz Hanover, Dooley Helen
Dept. Microbiology & Immunology, University of Maryland School of Medicine, Institute of Marine & Environmental Technology (IMET), Baltimore, MD, 21202, USA.
Dept. Microbiology & Immunology, University of Maryland School of Medicine, Institute of Marine & Environmental Technology (IMET), Baltimore, MD, 21202, USA.
Dev Comp Immunol. 2019 Jan;90:100-107. doi: 10.1016/j.dci.2018.09.007. Epub 2018 Sep 17.
Many of the most successful drugs generated in recent years are based upon monoclonal antibodies (mAbs). However, for some therapeutic and diagnostic applications mAbs are far from ideal; for example, while their relatively large size and inherent receptor binding aids their longevity in vivo it can also limit their tissue penetration. Further, their structural complexity makes them expensive to produce and prone to denaturation in non-physiological environments. Thus, researchers have been searching for alternative antigen-binding molecules that can be utilized in situations where mAbs are suboptimal tools. One potential source currently being explored are the shark-derived binding domains known as VNARs. Despite their small size VNARs can bind antigens with high specificity and high affinity. Combined with their propensity to bind epitopes that are inaccessible to conventional mAbs, and their ability to resist denaturation, VNARs are an emerging prospect for use in therapeutic, diagnostic, and biotechnological applications.
近年来研发出的许多最成功的药物都是基于单克隆抗体(mAb)。然而,对于某些治疗和诊断应用而言,单克隆抗体远非理想之选;例如,虽然它们相对较大的尺寸和固有的受体结合特性有助于其在体内的持久性,但这也会限制它们的组织穿透能力。此外,它们的结构复杂性使得生产成本高昂,并且在非生理环境中容易变性。因此,研究人员一直在寻找可在单克隆抗体并非最佳工具的情况下使用的替代抗原结合分子。目前正在探索的一个潜在来源是源自鲨鱼的称为VNARs的结合结构域。尽管VNARs尺寸小,但它们能够以高特异性和高亲和力结合抗原。再加上它们倾向于结合传统单克隆抗体无法触及的表位,以及它们抵抗变性的能力,VNARs在治疗、诊断和生物技术应用中是一个新兴的前景。