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恶性疟原虫环子孢子蛋白中的一种不变的“通用”T细胞表位。

An invariant, "universal" T-cell epitope in the P. falciparum circumsporozoite protein.

作者信息

Sinigaglia F, Guttinger M, Matile H, Pink J R

机构信息

Central Research Unit, F. Hoffmann-La Roche Ltd, Basle, Switzerland.

出版信息

Bull World Health Organ. 1990;68 Suppl(Suppl):94-8.

Abstract

Although there are important obstacles to malaria vaccine development, we believe they might be overcome by a strategy of searching for conserved regions of a vaccine candidate that are recognized in association with many different HLA molecules and, if necessary, deliberately modifying the conserved sequences to improve their immunogenicity for T cells. This approach is illustrated by work on the circumsporozoite (CS) protein of Plasmodium falciparum, which covers the surface of the malaria sporozoite and is the best characterized of current vaccine candidates.

摘要

尽管疟疾疫苗的研发存在重大障碍,但我们相信,通过寻找候选疫苗的保守区域(这些区域能与多种不同的HLA分子结合被识别),并在必要时有意修饰保守序列以提高其对T细胞的免疫原性的策略,这些障碍有可能被克服。恶性疟原虫环子孢子蛋白(CS蛋白)的研究就说明了这种方法,CS蛋白覆盖疟原虫子孢子表面,是目前特征最明确的候选疫苗。

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