Scott Andrew E, Christ William J, George Alison J, Stokes Margaret G M, Lohman Gregory J S, Guo Yuhong, Jones Matthew, Titball Richard W, Atkins Timothy P, Campbell A Stewart, Prior Joann L
Defence Science and Technology Laboratory , Porton Down, Salisbury, Wiltshire SP4 0JQ, United Kingdom.
Corden Pharma International Inc. (formerly Ancora Pharmaceuticals Inc.) , Woburn, Massachusetts 01801 United States.
Bioconjug Chem. 2016 Jun 15;27(6):1435-46. doi: 10.1021/acs.bioconjchem.5b00525. Epub 2016 May 17.
Melioidosis is an emerging infectious disease caused by Burkholderia pseudomallei and is associated with high morbidity and mortality rates in endemic areas. Antibiotic treatment is protracted and not always successful; even with appropriate therapy, up to 40% of individuals presenting with melioidosis in Thailand succumb to infection. In these circumstances, an effective vaccine has the potential to have a dramatic impact on both the scale and the severity of disease. Currently, no vaccines are licensed for human use. A leading vaccine candidate is the capsular polysaccharide consisting of a homopolymer of unbranched 1→3 linked 2-O-acetyl-6-deoxy-β-d-manno-heptopyranose. Here, we present the chemical synthesis of this challenging antigen using a novel modular disaccharide assembly approach. The resulting hexasaccharide was coupled to the nontoxic Hc domain of tetanus toxin as a carrier protein to promote recruitment of T-cell help and provide a scaffold for antigen display. Mice immunized with the glycoconjugate developed IgM and IgG responses capable of recognizing native capsule, and were protected against infection with over 120 × LD50 of B. pseudomallei strain K96243. This is the first report of the chemical synthesis of an immunologically relevant and protective hexasaccharide fragment of the capsular polysaccharide of B. pseudomallei and serves as the rational starting point for the development of an effective licensed vaccine for this emerging infectious disease.
类鼻疽是由类鼻疽伯克霍尔德菌引起的一种新发传染病,在流行地区与高发病率和死亡率相关。抗生素治疗疗程长且并非总能成功;即使采用适当的治疗方法,在泰国出现类鼻疽症状的患者中仍有高达40%会死于感染。在这种情况下,一种有效的疫苗有可能对疾病的规模和严重程度产生巨大影响。目前,尚无获批用于人类的疫苗。一种主要的候选疫苗是由无分支的1→3连接的2-O-乙酰基-6-脱氧-β-D-甘露庚糖同聚物组成的荚膜多糖。在此,我们使用一种新型的模块化二糖组装方法展示了这种具有挑战性的抗原的化学合成。将所得的六糖与破伤风毒素的无毒Hc结构域偶联作为载体蛋白,以促进T细胞辅助的募集并为抗原展示提供支架。用该糖缀合物免疫的小鼠产生了能够识别天然荚膜的IgM和IgG反应,并对超过120×半数致死剂量的类鼻疽伯克霍尔德菌K96243菌株感染具有保护作用。这是关于类鼻疽伯克霍尔德菌荚膜多糖具有免疫相关性和保护性的六糖片段化学合成的首次报道,为开发针对这种新发传染病的有效获批疫苗提供了合理的起点。