Wellcome Trust Centre of Molecular Parasitology, Institute of Infection, Immunity and Inflammation and Glasgow Polyomics, College of Medical, Veterinary and Life Sciences, University of Glasgow, G12 8TA, UK.
Faculty of Infectious and Tropical Diseases, London School of Hygiene and Tropical Medicine, London WC1E 7HT, UK.
Parasitology. 2014 Jan;141(1):1-7. doi: 10.1017/S0031182013001224.
The need for new drugs to treat microbial infections is pressing. The great progress made in the middle part of the twentieth Century was followed by a period of relative inactivity as the medical needs relating to infectious disease in the wealthier nations receded. Growing realisation that anti-infectives are needed in many parts of the world, to treat neglected diseases as well as to combat the burgeoning risk of resistance to existing drugs, has galvanised a new wave of research into anti-microbial drugs. The transfer of knowledge from the Pharmaceutical industry relating to the importance of understanding how to target drugs successfully within the body, and improved understanding of how pathogens interact with their hosts, is driving a series of new paradigms in anti-infective drug design. Here we provide an overview of those processes as an introduction to a series of articles from experts in this area that emerged from a meeting entitled "Emerging Paradigms in Anti-Infective Drug Design" held in London on the 17th and 18th September 2012. The symposium was organised jointly by British Society for Parasitology (BSP) and the Biological & Medicinal Chemistry sector of the Royal Society of Chemistry (RSC) and held at the London School of Hygiene & Tropical Medicine. The symposium set out to cover all aspects of the identification of new therapeutic modalities for the treatment of neglected and tropical diseases. We aimed to bring together leading scientists from all the disciplines working in this field and cover the pharmacology, medicinal chemistry and drug delivery of potential new medicines. Sessions were held on: "Target diseases and targets for drugs", "Target based medicinal chemistry", "Bioavailability and chemistry", "Targeting intracellular microbes", "Alternative approaches and models", and "New anti-infectives - how do we get there?" This symposium was organised by Simon Croft (LSHTM) and Mike Barrett (University of Glasgow) for the BSP, and David Alker (David Alker Associates) and Andrew Stachulski (University of Liverpool) for the Biological & Medicinal Chemistry sector of the RSC.
治疗微生物感染的新药需求迫在眉睫。在 20 世纪中叶取得巨大进展之后,随着富裕国家与传染病相关的医疗需求减少,这方面的研究进入了相对沉寂的时期。人们越来越认识到,在世界许多地方都需要抗感染药物,不仅用于治疗被忽视的疾病,还要应对现有药物耐药性日益增加的风险,这激发了人们对抗微生物药物的新一轮研究。制药行业在了解如何成功地将药物靶向体内以及提高对病原体与宿主相互作用的理解方面的知识转移,正在推动抗感染药物设计的一系列新范例。在这里,我们概述了这些过程,作为对该领域专家从 2012 年 9 月 17 日至 18 日在伦敦举行的题为“抗感染药物设计新范例”会议上发表的一系列文章的介绍。该研讨会由英国寄生虫学会(BSP)和皇家化学学会(RSC)的生物与药物化学分会联合组织,在伦敦卫生与热带医学学院举行。研讨会涵盖了确定治疗被忽视和热带疾病的新治疗方法的各个方面。我们的目标是将该领域的所有学科的顶尖科学家聚集在一起,涵盖潜在新药的药理学、药物化学和药物输送。会议涵盖了以下内容:“目标疾病和药物靶点”、“基于靶点的药物化学”、“生物利用度和化学”、“靶向细胞内微生物”、“替代方法和模型”,以及“新的抗感染药物——我们如何实现?” 该研讨会由西蒙·克罗夫特(LSHTM)和迈克·巴雷特(格拉斯哥大学)为 BSP 组织,由大卫·阿尔克(David Alker Associates)和安德鲁·斯塔丘尔斯基(利物浦大学)为 RSC 的生物与药物化学分会组织。