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感染的肝细胞表面表达的一种疟疾热休克样决定簇是非实质肝细胞抗体依赖性细胞介导的细胞毒性机制的靶点。

A malaria heat-shock-like determinant expressed on the infected hepatocyte surface is the target of antibody-dependent cell-mediated cytotoxic mechanisms by nonparenchymal liver cells.

作者信息

Rénia L, Mattei D, Goma J, Pied S, Dubois P, Miltgen F, Nüssler A, Matile H, Menégaux F, Gentilini M

机构信息

INSERM U 313, Groupe Hospitalier Pitié-Salpêtrière, Paris, France.

出版信息

Eur J Immunol. 1990 Jul;20(7):1445-9. doi: 10.1002/eji.1830200706.

Abstract

Cultured hepatic stages of Plasmodium falciparum and P. yoelii and with a monoclonal antibody recognizing a C-terminal fragment of the P. falciparum heat-shock-like protein (Pfhsp70) revealed that synthesis of this antigen first occurs during intrahepatic development of the parasite, at the two nuclei stage. Using a variety of techniques, including scanning electron microscopy, we observed that this antigenic determinant was expressed on the infected hepatocyte membrane. Its participation in antibody-dependent cell-mediated cytotoxicity was investigated. While no effect was obtained with peripheral blood cells, we found that 25% of the schizonts were specifically lysed when using spleen cells at a killer/target ratio of 30/1. More interestingly, with nonparenchymal liver cells, up to 50% of the hepatic parasites disappeared with a killer/target ratio of 10/1.

摘要

用识别恶性疟原虫热休克样蛋白(Pfhsp70)C末端片段的单克隆抗体对恶性疟原虫和约氏疟原虫的肝期培养物进行检测,结果显示该抗原的合成首先发生在寄生虫肝内发育的双核期。通过包括扫描电子显微镜在内的多种技术,我们观察到这种抗原决定簇在受感染的肝细胞膜上表达。我们研究了其在抗体依赖性细胞介导的细胞毒性中的作用。虽然外周血细胞未产生效果,但我们发现当杀伤细胞与靶细胞比例为30/1时使用脾细胞,25%的裂殖体被特异性裂解。更有趣的是,对于非实质肝细胞,当杀伤细胞与靶细胞比例为10/1时,高达50%的肝内寄生虫消失。

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