Proteome-wide Epitope Prediction: Leveraging Bioinformatic Technologies in Rational Vaccine Design

Lindsay M. W. Piel, S. White
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Abstract

Vaccine development began in the 1790’s when Edward Jenner used cowpox to confer protection against the smallpox virus [1]. The field of vaccinology has greatly expanded since then, wherein vaccination has been a valuable tool in the decline of many diseases [1,2]. While Jenner’s use of cowpox shares attributes to a live-attenuated vaccine, there are alternate methods of vaccination, which include subunit, conjugate, mRNA, viral vector, and toxoid vaccines [2-4]. Development of these methods was facilitated through greater understanding of the immune response, elucidation of both host and pathogen genetic diversity, and advancement of laboratory techniques [1-3]. The most recent notable advancement in vaccine production was the development of a nucleic acid vaccine to combat the SARS-CoV-2 virus [1]. While advancement in vaccine methodology can be readily seen, many subunit-based vaccines end up generating a predominantly B-cell driven response [1,5].
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蛋白质组范围内的表位预测:利用生物信息学技术进行合理的疫苗设计
疫苗开发始于1790年代,当时爱德华·詹纳使用牛痘来提供对抗天花病毒的保护[1]。从那时起,疫苗接种学的领域大大扩展,其中疫苗接种是减少许多疾病的宝贵工具[1,2]。虽然詹纳对牛痘的使用与减毒活疫苗有共同的特点,但也有其他疫苗接种方法,包括亚单位、偶联物、信使核糖核酸、病毒载体和类毒素疫苗[2-4]。通过进一步了解免疫反应、阐明宿主和病原体的遗传多样性以及实验室技术的进步,促进了这些方法的发展[1-3]。疫苗生产的最新显著进展是开发了一种对抗严重急性呼吸系统综合征冠状病毒2型的核酸疫苗[1]。虽然疫苗方法的进步显而易见,但许多基于亚单位的疫苗最终产生了主要由B细胞驱动的反应[1,5]。
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