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经辐照的子孢子疫苗可诱导细胞毒性T淋巴细胞,这些细胞毒性T淋巴细胞能够识别被感染肝细胞表面的疟疾抗原。

Irradiated sporozoite vaccine induces cytotoxic T lymphocytes that recognize malaria antigens on the surface of infected hepatocytes.

作者信息

Hoffman S L, Weiss W, Mellouk S, Sedegah M

机构信息

Infectious Diseases Department, Naval Medical Research Institute, Bethesda, MD 20814-5055.

出版信息

Immunol Lett. 1990 Aug;25(1-3):33-8. doi: 10.1016/0165-2478(90)90087-7.

Abstract

The observation that protective immunity induced by immunization with radiation attenuated Plasmodium berghei and Plasmodium yoelii sporozoites is dependent on CD8+ T lymphocytes in some strains of mice led us to speculate that immunization with sporozoites induces cytotoxic T lymphocytes (CTL) that recognize malaria antigens on the surface of malaria-infected hepatocytes. In this report we summarize a series of experiments that confirm this hypothesis. We first showed that when immune mice are challenged with live sporozoites they develop malaria-specific, CD8+ T cell-dependent infiltrates in their livers. Next we demonstrated that spleen cells from immune mice eliminate malaria infected hepatocytes from in vitro culture in an antigen specific and genetically restricted manner, indicating that these immune cells recognize malaria antigens on the surface of infected hepatocytes. Finally we defined a CTL epitope of the P. yoelii CS protein, and demonstrated that CTL against this 16-amino-acid peptide (PYCTL1) eliminate infected hepatocytes from culture in an antigenic specific, and MHC restricted manner, indicating that this 16-amino-acid peptide from the CS protein is present on the surface of the infected hepatocytes. We are currently working on constructing vaccines that induce protective CTL against PYCTL1, and identifying additional pre-erythrocytic stage targets of CTL mediated protective immunity.

摘要

用辐射减毒的伯氏疟原虫和约氏疟原虫子孢子免疫诱导的保护性免疫在某些品系小鼠中依赖于CD8 + T淋巴细胞,这一观察结果使我们推测,用子孢子免疫可诱导细胞毒性T淋巴细胞(CTL),这些CTL可识别疟原虫感染的肝细胞表面的疟疾抗原。在本报告中,我们总结了一系列证实这一假设的实验。我们首先表明,当用活子孢子攻击免疫小鼠时,它们的肝脏中会出现疟疾特异性的、依赖CD8 + T细胞的浸润。接下来我们证明,免疫小鼠的脾细胞以抗原特异性和基因限制性方式从体外培养物中清除疟原虫感染的肝细胞,这表明这些免疫细胞识别感染肝细胞表面的疟疾抗原。最后,我们确定了约氏疟原虫CS蛋白的一个CTL表位,并证明针对该16氨基酸肽(PYCTL1)的CTL以抗原特异性和MHC限制性方式从培养物中清除感染的肝细胞,这表明CS蛋白的这个16氨基酸肽存在于感染肝细胞的表面。我们目前正在致力于构建诱导针对PYCTL1的保护性CTL的疫苗,并确定CTL介导的保护性免疫的其他红细胞前期靶点。

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