Craft Kelly M, Townsend Steven D
Department of Chemistry, Vanderbilt University , 7330 Stevenson Center, Nashville, Tennessee 37235, United States.
Institute of Chemical Biology, Vanderbilt University , 896 Preston Research Building, Nashville, Tennessee 37232, United States.
ACS Infect Dis. 2018 Feb 9;4(2):77-83. doi: 10.1021/acsinfecdis.7b00209. Epub 2017 Nov 15.
Each year over 3 million people die from infectious diseases with most of these deaths being poor and young children who live in low- and middle-income countries. Infectious diseases emerge for a multitude of reasons. On the social front, reasons include a breakdown of public health standards, international travel, and immigration (for financial, civil, and social reasons). At the molecular level, the modern rise of infectious diseases is tied to the juxtaposition of drug-resistant pathogens and a lack of new antimicrobials. The consequence is the possibility that humankind will return to the preantibiotic era wherein millions of people will perish from what should be trivial illnesses. Given the stakes, it is imperative that the chemistry community take leadership in delivering new antibiotic leads for clinical development. We believe this can happen through innovation in two areas. First is the development of novel chemical scaffolds to treat infections caused by multidrug-resistant pathogens. The second area, which is not exclusive to the first, is the generation of antibiotics that do not cause collateral damage to the host or the host's microbiome. Both can be enabled through advances in chemical synthesis. It is with this general philosophy in mind that we hypothesized human milk oligosaccharides (HMOs) could serve as novel chemical scaffolds for antibacterial development. We provide herein a personal account of our laboratory's progress toward the goal of using HMOs as a defense against infectious diseases.
每年有超过300万人死于传染病,其中大多数是生活在低收入和中等收入国家的贫困儿童和幼儿。传染病的出现有多种原因。在社会层面,原因包括公共卫生标准的崩溃、国际旅行和移民(出于经济、民事和社会原因)。在分子层面,传染病的现代兴起与耐药病原体的并列以及新抗菌药物的缺乏有关。其后果是人类有可能回到抗生素出现之前的时代,届时数百万人将死于本应微不足道的疾病。鉴于利害关系,化学界必须带头提供用于临床开发的新抗生素先导物。我们相信这可以通过两个领域的创新来实现。首先是开发新型化学支架,以治疗由多重耐药病原体引起的感染。第二个领域与第一个领域并非相互排斥,是开发不会对宿主或宿主微生物群造成附带损害的抗生素。这两个领域都可以通过化学合成的进展来实现。正是基于这种总体理念,我们推测人乳寡糖(HMOs)可以作为抗菌开发的新型化学支架。在此,我们介绍了我们实验室在将HMOs用作抵御传染病手段这一目标上取得的进展。