Vaughan Kerrie, Seymour Emily, Peters Bjoern, Sette Alessandro
Division for Vaccine Discovery, La Jolla Institute for Allergy and Immunology, 9420 Athena Circle, La Jolla, CA 92037, United States.
Division for Vaccine Discovery, La Jolla Institute for Allergy and Immunology, 9420 Athena Circle, La Jolla, CA 92037, United States.
Hum Immunol. 2014 May;75(5):440-51. doi: 10.1016/j.humimm.2014.02.013. Epub 2014 Feb 12.
The recent increase in whooping cough in vaccinated populations has been attributed to waning immunity associated with the acellular vaccine. The Immune Epitope Database (IEDB) is a repository of immune epitope data from the published literature and includes T cell and antibody epitopes for human pathogens. The IEDB conducted a review of the epitope literature, which revealed 300 Bordetella pertussis-related epitopes from 39 references. Epitope data are currently available for six virulence factors of B. pertussis: pertussis toxin, pertactin, fimbrial 2, fimbrial 3, adenylate cyclase and filamentous hemagglutinin. The majority of epitopes were defined for antibody reactivity; fewer T cell determinants were reported. Analysis of available protective correlates data revealed a number of candidate epitopes; however few are defined in humans and few have been shown to be protective. Moreover, there are a limited number of studies defining epitopes from natural infection versus whole cell or acellular/subunit vaccines. The relationship between epitope location and structural features, as well as antigenic drift (SNP analysis) was also investigated. We conclude that the cumulative data is yet insufficient to address many fundamental questions related to vaccine failure and this underscores the need for further investigation of B. pertussis immunity at the molecular level.
接种疫苗人群中百日咳近期有所增加,这归因于与无细胞疫苗相关的免疫力下降。免疫表位数据库(IEDB)是已发表文献中免疫表位数据的储存库,包括人类病原体的T细胞和抗体表位。IEDB对表位文献进行了综述,从39篇参考文献中发现了300个与百日咳博德特氏菌相关的表位。目前可获得百日咳博德特氏菌六种毒力因子的表位数据:百日咳毒素、百日咳黏附素、2型菌毛、3型菌毛、腺苷酸环化酶和丝状血凝素。大多数表位是针对抗体反应性定义的;报道的T细胞决定簇较少。对现有保护性相关数据的分析揭示了一些候选表位;然而,在人类中定义的很少,且很少被证明具有保护性。此外,从自然感染与全细胞或无细胞/亚单位疫苗中定义表位的研究数量有限。还研究了表位位置与结构特征以及抗原漂移(单核苷酸多态性分析)之间的关系。我们得出结论,累积数据仍不足以解决与疫苗失效相关的许多基本问题,这突出表明需要在分子水平上进一步研究百日咳博德特氏菌的免疫力。