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[抗体替代形式:抗体片段和新框架]

[Antibody alternative formats: antibody fragments and new frameworks].

作者信息

Kitten Olivier, Martineau Pierre

机构信息

Affilogic, Nantes, France.

IRCM, Institut de Recherche en Cancérologie de Montpellier, Inserm U1194, Université de Montpellier, Institut régional du Cancer de Montpellier, Montpellier, France.

出版信息

Med Sci (Paris). 2019 Dec;35(12):1092-1097. doi: 10.1051/medsci/2019217. Epub 2020 Jan 6.

Abstract

Antibodies are now recognized as routine molecules in many therapeutic fields, no longer restricted to oncology and inflammation. This explosion of the field leads to new needs that can be better fulfilled by molecules inspired but different from conventional antibodies. In particular, the antibody molecule has multiple functions that are not always necessary, such as its ability to recruit immune system cells, its bivalency, or its high plasma half-life. However, in most applications, its remarkable ability to recognize almost any molecular partner with high affinity and specificity must be preserved. In addition, antibodies are very large molecules, expensive to produce and having limited physicochemical properties that limit their use in aggressive media. Finally, in certain therapeutic applications, the large size of the antibody molecule may also limit its diffusion in tissues and prevent the recognition of some poorly accessible molecular structures. To address these limitations, many alternative formats to whole antibodies have been developed over the last twenty years. These new formats have found applications in many fields like biotechnology, in vitro and in vivo diagnosis, and therapy. Two large families of molecules cover this field and will be presented in this mini-review. The first family is based on antibody by reducing its size, such as classical antibody fragments (Fab, scFv) or those derived from camels or sharks (VHH, V-NAR). The second family was developed by first identifying frameworks fulfilling the desired properties, in particular the stability in extreme medium and the productivity in simple and economic systems like bacteria, then by grafting binding properties comparable to antibodies using methods based on in vitro directed molecular evolution techniques. This mini-review will focus on the most advanced molecules but the field is quickly evolving. It should be noted that many of these molecules, or even these approaches, are covered by patents and are often developed by young innovative companies, some of which have been already bought by large pharmaceutical groups.

摘要

如今,抗体在许多治疗领域已被视为常规分子,不再局限于肿瘤学和炎症领域。该领域的迅猛发展催生了新的需求,而受传统抗体启发但与之不同的分子能够更好地满足这些需求。特别是,抗体分子具有多种并非总是必需的功能,例如其招募免疫系统细胞的能力、双价性或较高的血浆半衰期。然而,在大多数应用中,必须保留其以高亲和力和特异性识别几乎任何分子伴侣的卓越能力。此外,抗体是非常大的分子,生产成本高昂,且其物理化学性质有限,这限制了它们在苛刻介质中的应用。最后,在某些治疗应用中,抗体分子的大尺寸也可能限制其在组织中的扩散,并妨碍对一些难以接近的分子结构的识别。为解决这些局限性,在过去二十年中已开发出许多替代完整抗体的形式。这些新形式已在生物技术、体外和体内诊断及治疗等许多领域得到应用。两大类分子涵盖了这一领域,将在本综述中介绍。第一类分子是通过减小抗体尺寸而衍生出来的,如经典抗体片段(Fab、scFv)或源自骆驼或鲨鱼的片段(VHH、V-NAR)。第二类分子是通过首先确定满足所需特性的框架而开发的,特别是在极端介质中的稳定性以及在细菌等简单经济系统中的生产能力,然后通过基于体外定向分子进化技术的方法嫁接与抗体相当的结合特性。本综述将聚焦于最先进的分子,但该领域发展迅速。应当指出,这些分子中的许多,甚至这些方法,都已获得专利,并且通常由年轻的创新公司开发,其中一些公司已被大型制药集团收购。

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