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成功药物研发的各个方面。

Aspects of successful drug discovery and development.

作者信息

Pauwels Rudi

机构信息

Chemin de Layaz 3, CH-1806 Saint-Légier, Switzerland.

出版信息

Antiviral Res. 2006 Sep;71(2-3):77-89. doi: 10.1016/j.antiviral.2006.05.007. Epub 2006 Jun 8.

Abstract

Despite landmark achievements (e.g. >20 new anti-HIV drugs), a number of important therapeutic challenges remain. Although an expanding array of new drug discovery technologies has become available, drug research and development (R&D) productivity in general is still low. The establishment of close functional links between specialists active in early discovery, development and the clinic can thereby contribute to overall efficiency and higher success rates of new drug candidates. One of the more qualitative discovery challenges is to improve the predictability of early stage research models in term of in vivo drug efficacy. A cell-based model using viral replication in human T cells (MT-4) is used as an example from the HIV field to highlight the role of cell-based assays as tools for new target discovery, lead finding and optimization. The development of the next generation HIV non-nucleoside reverse transcriptase inhibitors (NNRTIs) TMC125 and TMC278 and the protease inhibitor (PI) TMC114 (Prezista), further point to new fundamental strategies to combat and prevent antiviral drug resistance and to the importance of incorporating clinical and pharmaceutical aspects into lead finding and optimization, drug design and drug candidate selection. A more parallel-oriented drug discovery strategy is thus portrayed that harnesses some 'evolutionary' principles in combination with technologies that are currently rationalizing drug discovery.

摘要

尽管取得了具有里程碑意义的成就(例如20多种新型抗艾滋病毒药物),但仍存在一些重要的治疗挑战。虽然一系列不断扩展的新药发现技术已经可用,但总体而言,药物研发的效率仍然很低。在早期发现、开发和临床领域积极工作的专家之间建立紧密的功能联系,有助于提高新药候选药物的整体效率和成功率。在定性发现方面的挑战之一是提高早期研究模型在体内药物疗效方面的可预测性。以艾滋病毒领域中使用人类T细胞(MT-4)中的病毒复制的细胞模型为例,强调基于细胞的检测作为新靶点发现、先导化合物发现和优化工具的作用。下一代艾滋病毒非核苷类逆转录酶抑制剂(NNRTIs)TMC125和TMC278以及蛋白酶抑制剂(PI)TMC114(Prezista)的开发,进一步指出了对抗和预防抗病毒药物耐药性的新基本策略,以及将临床和药学方面纳入先导化合物发现和优化、药物设计和候选药物选择的重要性。因此,描绘了一种更具平行导向性的药物发现策略,该策略结合了一些“进化”原则和当前使药物发现合理化的技术。

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