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对并殖吸虫和片形吸虫感染大鼠体内吸虫半胱氨酸蛋白酶的抗体反应

Antibody responses to fluke cysteine proteinases in Paragonimus- and Fasciola-infected rats.

作者信息

Ikeda T

机构信息

Department of Medical Zoology, Kanazawa Medical University, Uchinada, Ishikawa, 920-02 Japan.

出版信息

J Helminthol. 1998 Sep;72(3):187-91. doi: 10.1017/s0022149x00016424.

Abstract

IgG and IgM antibody responses to fluke cysteine proteinases in Paragonimus ohirai- and Fasciola sp.-infected rats were followed by means of cystatin capture ELISA using fluke excretory-secretory products for 10 weeks after infection. The specific IgG antibodies were detectable at week 2 postinfection in all P. ohirai-infected and some Fasciola-infected rats. Levels of specific IgG antibodies increased rapidly between week 2 and 6, and slightly thereafter, in both infected groups. From week 3, specific IgG antibody levels were higher in Fasciola-infected than P. ohirai-infected rats. Sera from infected rats did not react with heterologous cysteine proteinases throughout the infection periods. In both infected groups, the kinetic patterns of specific IgM antibody responses were similar to those of specific IgG antibody responses although the ELISA levels of the IgM antibody responses were much lower. In abnormal infections with P. ohirai metacercariae x-irradiated at 2 krad, the specific IgG antibodies were detectable at week 2 postinfection with similar ELISA values to normal P. ohirai infection, but thereafter increased little. In infections with P. westermani, for which the rat is not a suitable host, even stunted worms induced a comparable specific IgG antibody response, although the response was lower than in normal infections with P. ohirai. These results indicate that cystatin capture ELISA can distinguish clearly between Paragonimus and Fasciola infections which show immunodiagnostic cross-reactivity and is useful even in the early stages of the infection and in the infection of unsuitable hosts.

摘要

利用半胱氨酸蛋白酶抑制剂捕获酶联免疫吸附测定法(ELISA),以吸虫排泄-分泌产物为抗原,对感染大平并殖吸虫和片形吸虫的大鼠体内针对吸虫半胱氨酸蛋白酶的IgG和IgM抗体反应进行了为期10周的跟踪监测。在感染后第2周,所有感染大平并殖吸虫的大鼠以及部分感染片形吸虫的大鼠体内均可检测到特异性IgG抗体。在两个感染组中,特异性IgG抗体水平在感染后第2周和第6周之间迅速升高,此后略有上升。从第3周起,感染片形吸虫的大鼠体内特异性IgG抗体水平高于感染大平并殖吸虫的大鼠。在整个感染期间,感染大鼠的血清均未与异源半胱氨酸蛋白酶发生反应。在两个感染组中,特异性IgM抗体反应的动力学模式与特异性IgG抗体反应相似,尽管IgM抗体反应的ELISA水平要低得多。在用2千拉德X射线照射的大平并殖吸虫囊蚴进行的异常感染中,感染后第2周可检测到特异性IgG抗体,其ELISA值与正常大平并殖吸虫感染相似,但此后几乎没有增加。在大鼠并非合适宿主的卫氏并殖吸虫感染中,即使是发育不良的虫体也能诱导出相当的特异性IgG抗体反应,尽管该反应低于正常大平并殖吸虫感染。这些结果表明,半胱氨酸蛋白酶抑制剂捕获ELISA能够清楚地区分显示免疫诊断交叉反应的并殖吸虫感染和片形吸虫感染,即使在感染早期以及在不合适宿主的感染中也很有用。

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