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寻找抗肉毒杆菌神经毒素疗法面临的挑战。

Challenges in searching for therapeutics against Botulinum Neurotoxins.

作者信息

Pirazzini Marco, Rossetto Ornella

机构信息

a Department of Biomedical Sciences , University of Padova , Padova , Italy.

出版信息

Expert Opin Drug Discov. 2017 May;12(5):497-510. doi: 10.1080/17460441.2017.1303476. Epub 2017 Mar 17.

DOI:10.1080/17460441.2017.1303476
PMID:28271909
Abstract

Botulinum neurotoxins (BoNTs) are the most potent toxins known. BoNTs are responsible for botulism, a deadly neuroparalytic syndrome caused by the inactivation of neurotransmitter release at peripheral nerve terminals. Thanks to their specificity and potency, BoNTs are both considered potential bio-weapons and therapeutics of choice for a variety of medical syndromes. Several variants of BoNTs have been identified with individual biological properties and little antigenic relation. This expands greatly the potential of BoNTs as therapeutics but poses a major safety problem, increasing the need for finding appropriate antidotes. Areas covered: The authors describe the multi-step molecular mechanism through which BoNTs enter nerve terminals and discuss the many levels at which the toxins can be inhibited. They review the outcomes of the different strategies adopted to limit neurotoxicity and counter intoxication. Potential new targets arising from the last discoveries of the mechanism of action and the approaches to promote neuromuscular junction recovery are also discussed. Expert opinion: Current drug discovery efforts have mainly focused on BoNT type A and addressed primarily light chain proteolytic activity. Development of pan-BoNT inhibitors acting independently of BoNT immunological properties and targeting a common step of the intoxication process should be encouraged.

摘要

肉毒杆菌神经毒素(BoNTs)是已知毒性最强的毒素。BoNTs可导致肉毒中毒,这是一种致命的神经麻痹综合征,由外周神经末梢神经递质释放失活引起。由于其特异性和强效性,BoNTs既被视为潜在的生物武器,也是多种医学综合征的首选治疗药物。已鉴定出几种具有个体生物学特性且抗原关系不大的BoNTs变体。这极大地扩展了BoNTs作为治疗药物的潜力,但也带来了重大安全问题,增加了寻找合适解毒剂的需求。涵盖领域:作者描述了BoNTs进入神经末梢的多步骤分子机制,并讨论了毒素可被抑制的多个层面。他们回顾了为限制神经毒性和对抗中毒所采用的不同策略的结果。还讨论了基于最新作用机制发现而产生的潜在新靶点以及促进神经肌肉接头恢复的方法。专家观点:当前的药物研发工作主要集中在A型BoNT上,主要针对轻链蛋白水解活性。应鼓励开发独立于BoNT免疫学特性并靶向中毒过程共同步骤的泛BoNT抑制剂。

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