Flower Darren R, Macdonald Isabel K, Ramakrishnan Kamna, Davies Matthew N, Doytchinova Irini A
School of Life and Health Sciences, University of Aston, Aston Triangle, Birmingham, B4 7ET, UK.
Immunome Res. 2010 Nov 3;6 Suppl 2(Suppl 2):S1. doi: 10.1186/1745-7580-6-S2-S1.
Immunoinformatics is an emergent branch of informatics science that long ago pullulated from the tree of knowledge that is bioinformatics. It is a discipline which applies informatic techniques to problems of the immune system. To a great extent, immunoinformatics is typified by epitope prediction methods. It has found disappointingly limited use in the design and discovery of new vaccines, which is an area where proper computational support is generally lacking. Most extant vaccines are not based around isolated epitopes but rather correspond to chemically-treated or attenuated whole pathogens or correspond to individual proteins extract from whole pathogens or correspond to complex carbohydrate. In this chapter we attempt to review what progress there has been in an as-yet-underexplored area of immunoinformatics: the computational discovery of whole protein antigens. The effective development of antigen prediction methods would significantly reduce the laboratory resource required to identify pathogenic proteins as candidate subunit vaccines. We begin our review by placing antigen prediction firmly into context, exploring the role of reverse vaccinology in the design and discovery of vaccines. We also highlight several competing yet ultimately complementary methodological approaches: sub-cellular location prediction, identifying antigens using sequence similarity, and the use of sophisticated statistical approaches for predicting the probability of antigen characteristics. We end by exploring how a systems immunomics approach to the prediction of immunogenicity would prove helpful in the prediction of antigens.
免疫信息学是信息科学中一个新兴的分支,它早在很久以前就从生物信息学这棵知识之树上衍生出来。它是一门将信息技术应用于免疫系统问题的学科。在很大程度上,免疫信息学以表位预测方法为代表。它在新疫苗的设计和发现方面的应用令人失望地有限,而在这个领域通常缺乏适当的计算支持。大多数现有的疫苗并非基于分离的表位,而是对应于化学处理或减毒的全病原体,或者对应于从全病原体中提取的单个蛋白质,或者对应于复杂碳水化合物。在本章中,我们试图回顾免疫信息学一个尚未充分探索的领域所取得的进展:全蛋白抗原的计算发现。抗原预测方法的有效发展将显著减少将致病蛋白鉴定为候选亚单位疫苗所需的实验室资源。我们通过将抗原预测置于恰当的背景下开始我们的综述,探讨反向疫苗学在疫苗设计和发现中的作用。我们还强调了几种相互竞争但最终互补的方法:亚细胞定位预测、利用序列相似性鉴定抗原以及使用复杂的统计方法预测抗原特征的概率。我们最后探讨系统免疫组学方法在免疫原性预测中如何有助于抗原预测。