Nimjee Shahid M, Rusconi Christopher P, Harrington Robert A, Sullenger Bruce A
University Program of Genetics, Duke University Medical Center, Durham, NC 27710, USA.
Trends Cardiovasc Med. 2005 Jan;15(1):41-5. doi: 10.1016/j.tcm.2005.01.002.
Useful additional options for anticoagulant therapy have been introduced over the last 15 years, including low-molecular-weight heparins and direct thrombin inhibitors. Despite these impressive advances, a need for safer effective anticoagulants remains. Aptamers represent a therapeutic modality that has the potential to address this unmet need. Aptamers are small nucleic acid molecules that function as direct protein inhibitors, much like monoclonal antibodies. Aptamers are delivered by parenteral administration, can be formulated to possess a very short or sustained half-life, and are purported to be nonimmunogenic. Perhaps most relevant to the development of safer anticoagulant therapies, recent studies have shown that antidotes can be rationally designed to control the pharmacologic effects of aptamers in vivo, paving the way for a new class of antidote-controlled therapeutics. This review discusses the limitations of current anticoagulant therapies, the properties of aptamers and how these properties can be exploited to address the unmet needs within this therapeutic class, and the progress to date in developing new aptamer-based anticoagulant therapies.
在过去15年里,抗凝治疗引入了一些有用的附加选项,包括低分子量肝素和直接凝血酶抑制剂。尽管取得了这些令人瞩目的进展,但对更安全有效的抗凝剂的需求仍然存在。适体代表了一种有可能满足这一未满足需求的治疗方式。适体是一种小核酸分子,其功能类似于单克隆抗体,可作为直接的蛋白质抑制剂。适体通过肠胃外给药,可被设计成具有非常短或持续的半衰期,并且据称无免疫原性。也许与更安全的抗凝治疗发展最相关的是,最近的研究表明,可以合理设计解毒剂来控制适体在体内的药理作用,为一类新型的解毒剂控制疗法铺平了道路。本综述讨论了当前抗凝治疗的局限性、适体的特性以及如何利用这些特性来满足这一治疗类别中未满足的需求,以及迄今为止开发基于适体的新型抗凝治疗的进展。