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用肝片吸虫分泌的组织蛋白酶L蛋白酶CL1和CL2进行免疫接种,在大鼠中引发基于IgG2a抗体的优先1型反应。

Immunization with cathepsin L proteinases CL1 and CL2 secreted by Fasciola hepatica elicit a preferential type 1 response based on IgG2a antibodies in rats.

作者信息

Bentancor A, Piacenza L, Carmona C

机构信息

Unidad de Biología Parasitaria, Instituto de Higiene, Facultad de Ciencias, Av. A. Navarro 3051, CP 11600 Montevideo, Uruguay.

出版信息

J Helminthol. 2002 Sep;76(3):199-205. doi: 10.1079/JOH2002123.

Abstract

Cathepsin L proteinases (CL1 and CL2), the major components of Fasciola hepatica excretion/secretion products (E/S) are considered potential antigens of a vaccine against fascioliasis. The humoral response elicited by CL1 and CL2 in rats either immunized with the enzymes or infected with F. hepatica has been analysed, examining specific IgE and IgG subclass dynamics. The experiment was continued for 10 weeks and peripheral blood eosinophilia was also determined. Infected rats presented peaks of eosinophilia at weeks 3 and 7 post-infection, while those immunized with CL1 and CL2 were no different from controls. Total IgE in infected rats increased up to week 5, reaching 30 microg(-1) in some cases, then decreased slowly and rising again towards the end of the experiment. Determination of specific IgE, carried out in sera previously absorbed with Protein G-Sepharose, reached a peak in infected rats between weeks 2 and 5, depending on the individual. In immunized rats both total and specific IgE levels remained around the pre-immunization values. With regard to the IgG subclass responses to E/S products, in infected rats IgG1 predominated over IgG2a, and the reverse was true in rats immunized with CL1 and CL2 and tested against the respective antigens. In all cases an increase in IgG1 and IgG2a antibody titres was seen, with maximum levels being reached later (weeks 6-7) in infected rats than in immunized ones (weeks 4-5). No IgG2b or IgG2c responses were detected in any of the groups studied.

摘要

组织蛋白酶L蛋白酶(CL1和CL2)是肝片吸虫排泄/分泌产物(E/S)的主要成分,被认为是抗片形吸虫病疫苗的潜在抗原。已经分析了CL1和CL2在用这些酶免疫或感染肝片吸虫的大鼠中引发的体液反应,检测了特异性IgE和IgG亚类的动态变化。实验持续了10周,还测定了外周血嗜酸性粒细胞增多情况。感染大鼠在感染后第3周和第7周出现嗜酸性粒细胞增多高峰,而用CL1和CL2免疫的大鼠与对照组无差异。感染大鼠的总IgE在第5周前升高,某些情况下达到30μg(-1),然后缓慢下降,并在实验接近尾声时再次上升。在用蛋白G-琼脂糖预先吸附的血清中进行的特异性IgE测定显示,感染大鼠的特异性IgE在第2至5周达到峰值,具体取决于个体。在免疫大鼠中,总IgE和特异性IgE水平均维持在免疫前值左右。关于对E/S产物的IgG亚类反应,在感染大鼠中IgG1比IgG2a占优势,在用CL1和CL2免疫并针对相应抗原进行检测的大鼠中情况则相反。在所有情况下,均观察到IgG1和IgG2a抗体滴度增加,感染大鼠达到最高水平的时间(第6 - 7周)比免疫大鼠(第4 - 5周)晚。在所研究的任何组中均未检测到IgG2b或IgG2c反应。

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