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Camelid Single-Domain Antibodies: Historical Perspective and Future Outlook

机译:骆驼单域抗体:历史观点和未来展望

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Tremendous effort has been expended over the past two and a half decades to understand many aspects of camelid heavy chain antibodies, from their biology, evolution, and immunogenetics to their potential applications in various fields of research and medicine. In this article, I present a historical perspective on the development of camelid single-domain antibodies (sdAbs or V_(H)Hs, also widely known as nanobodies) since their discovery and discuss the advantages and disadvantages of these unique molecules in various areas of research, industry, and medicine. Commercialization of camelid sdAbs exploded in 2001 with a flurry of patents issued to the Vrije Universiteit Brussel (VUB) and later taken on by the Vlaams Interuniversitair Instituut voor Biotechnologie (VIB) and, after 2002, the VIB-founded spin-off company, Ablynx. While entrepreneurial spirit has certainly catalyzed the exploration of nanobodies as marketable products, IP restrictions may be partially responsible for the relatively long time span between the discovery of these biomolecules and their entry into the pharmaceutical market. It is now anticipated that the first V_(H)H-based antibody drug, Caplacizumab, a bivalent anti-vWF antibody for treating rare blood clotting disorders, may be approved and commercialized in 2018 or shortly thereafter. This elusive first approval, along with the expiry of key patents, may substantially alter the scientific and biomedical landscape surrounding camelid sdAbs and pave the way for their emergence as mainstream biotherapeutics.
机译:在过去的两年半中,人们花费了巨大的精力来了解骆驼科重链抗体的许多方面,从其生物学,进化和免疫遗传学到它们在研究和医学各个领域的潜在应用。在本文中,自从发现骆驼单域抗体(sdAb或V_(H)Hs,也被广泛称为纳米抗体)以来,我就提出了他们的历史观点,并讨论了这些独特分子在各个领域的优缺点。研究,工业和医学。骆驼sdAb的商业化在2001年爆发,并获得了布鲁塞尔布鲁塞尔自由大学(VUB)的一系列专利,后来由弗拉姆大学国际生物技术研究所(VIB)接管,2002年之后,VIB成立的衍生公司Ablynx 。尽管企业家精神无疑促进了纳米抗体作为可销售产品的探索,但知识产权限制可能是这些生物分子的发现与进入制药市场之间相对较长时间的部分原因。现在可以预期,第一种基于V_(H)H的抗体药物Caplacizumab,一种用于治疗罕见凝血障碍的二价抗vWF抗体,将在2018年或之后不久获得批准并商业化。这种难以捉摸的首批批准以及关键专利的到期,可能会大大改变围绕骆驼科动物sdAb的科学和生物医学领域,并为它们成为主流生物治疗剂铺平道路。

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