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提高糖缀合物疫苗的效力:从化学缀合物到下一代构建体。

Improving efficacy of glycoconjugate vaccines: from chemical conjugates to next generation constructs.

机构信息

GSK, Siena, Italy.

GSK Vaccines Institute for Global Health S.r.l., Siena, Italy.

出版信息

Curr Opin Immunol. 2020 Aug;65:42-49. doi: 10.1016/j.coi.2020.03.015. Epub 2020 Apr 30.

DOI:10.1016/j.coi.2020.03.015
PMID:32361591
Abstract

Glycoconjugate vaccines are among the safest and most successful vaccines developed during the past 30 years. Since the first semisynthetic chemical conjugate vaccine licensed in the 1980's to protect human against Haemophilus influenzae type b infection, conjugate vaccines against Neisseria meningitidis and Streptococcus pneumoniae have been developed and registered using the same approach (i.e. bacterial growth to produce capsular polysaccharide antigen and chemical coupling to carrier protein). Other types of conjugate vaccines have been recently developed and tested in clinical trials, prepared by coupling chemically synthesized oligosaccharides to proteins, by engineering Escherichia coli to directly produce bioconjugates or by delivering the native carbohydrate antigen in engineered membrane vesicles (i.e. Generalized Modules for Membrane Antigens, GMMA). Through this review, the reader will have an insight regarding the history and the characteristics of different types of conjugate vaccines, and the attributes that might affect their immunogenicity and their potential for future applications.

摘要

糖缀合物疫苗是过去 30 年来开发的最安全、最成功的疫苗之一。自 20 世纪 80 年代首个半合成化学缀合物疫苗获得许可,用于预防人类流感嗜血杆菌 b 型感染以来,已经开发并注册了针对脑膜炎奈瑟球菌和肺炎链球菌的缀合物疫苗,采用相同的方法(即细菌生长以产生荚膜多糖抗原和化学偶联到载体蛋白)。最近已经开发并在临床试验中测试了其他类型的缀合物疫苗,这些疫苗通过将化学合成的寡糖与蛋白质偶联、通过工程大肠杆菌直接产生生物缀合物或通过在工程化膜泡中递送天然碳水化合物抗原(即广义膜抗原模块,GMMA)来制备。通过这篇综述,读者将深入了解不同类型的缀合物疫苗的历史和特点,以及可能影响其免疫原性及其未来应用潜力的属性。

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