Monzavi-Karbassi Behjatolah, Cunto-Amesty Gina, Luo Ping, Kieber-Emmons Thomas
Dept of Pathology and Laboratory Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA.
Trends Biotechnol. 2002 May;20(5):207-14. doi: 10.1016/s0167-7799(02)01940-6.
Carbohydrate antigens are immune targets associated with a variety of pathogens and tumor cells. Unfortunately, most carbohydrates are intrinsically T cell-independent antigens, which diminishes their efficacy as immunogens. The conversion of carbohydrate epitopes to peptide mimotopes is one means to overcome the T cell-independent nature of carbohydrate antigens because peptides have an absolute requirement for T cells. Although such conversion has great potential for the development of veterinarian and human vaccines, there are issues related to the use of peptide-based immunogens as functional surrogates. Some of these issues are fundamental, pertaining to how mimicry comes about at the molecular level, and some are application oriented, directed at elucidating important immunological mechanisms. In this article the potential and caveats of this technology regarding its application in vaccine discovery are analyzed.
碳水化合物抗原是与多种病原体和肿瘤细胞相关的免疫靶点。不幸的是,大多数碳水化合物本质上是不依赖T细胞的抗原,这降低了它们作为免疫原的效力。将碳水化合物表位转化为肽模拟表位是克服碳水化合物抗原不依赖T细胞性质的一种方法,因为肽对T细胞有绝对需求。尽管这种转化在兽医和人类疫苗开发方面有很大潜力,但使用基于肽的免疫原作为功能替代物存在一些问题。其中一些问题是基础性的,涉及分子水平上模拟是如何产生的,还有一些是应用导向性的,旨在阐明重要的免疫机制。本文分析了该技术在疫苗发现应用中的潜力和注意事项。