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细粒棘球绦虫感染小鼠抗性中间宿主模型中的免疫球蛋白谱

Immunoglobulin profiles in a murine intermediate host model of resistance for Echinococcus granulosus infection.

作者信息

Zhang Wenbao, You Hong, Li Jun, Zhang Zhuangzhi, Turson Gulinul, Aili Hasyet, Wang Jingcheng, McManus Donald P

机构信息

Molecular Parasitology Laboratory, Australian Centre for International and Tropical Health and Nutrition, The Queensland Institute of Medical Research and The University of Queensland, Brisbane, Queensland 4029, Australia.

出版信息

Parasite Immunol. 2003 Mar;25(3):161-8. doi: 10.1046/j.1365-3024.2003.00622.x.

Abstract

We have shown previously that primary infection of Chinese Kunming (CKM) mice with Echinococcus granulosus oncospheres is protective against subsequent challenge. Nine groups of mice were infected with the oncospheres of E. granulosus by different routes (intraperitoneal, subcutaneous or intravenous injection). After infection, serum was collected after different periods of time and serum antibodies were tested by ELISA against oncospheral proteins and hydatid cyst fluid antigens. The results indicated that CKM mice produced low levels of antibodies before a secondary challenge infection given 3 weeks later by a different route. Most mice did not evoke significant antibody responses against oncospheral antigens until 5 weeks after infection. The level of IgG, especially IgG1 against oncospheral antigens increased from week 4 post-infection (p.i.), to a maximum at week 9 p.i. In addition, antibodies against hydatid cyst fluid antigens increased at the same time as the recognition of oncospheral antigens. Immunoblots using hydatid cyst fluid showed that the first antigen that was recognized - an 8-kDa protein, possibly the smallest subunit of Antigen B - appeared 5-6 weeks p.i. and reactivity to this molecule was intensive at week 9 p.i. The results suggest that protection against secondary infection was not principally antibody-mediated during the initial phases of infection, when cellular immune responses may play a pivotal role in the protective mechanism.

摘要

我们之前已经表明,用细粒棘球绦虫六钩蚴对中国昆明(CKM)小鼠进行初次感染可使其免受后续攻击。将九组小鼠通过不同途径(腹腔内、皮下或静脉注射)感染细粒棘球绦虫六钩蚴。感染后,在不同时间段采集血清,并通过ELISA检测血清抗体针对六钩蚴蛋白和包虫囊肿液抗原的情况。结果表明,在3周后通过不同途径进行二次攻击感染之前,CKM小鼠产生的抗体水平较低。大多数小鼠直到感染后5周才对六钩蚴抗原引发显著的抗体反应。针对六钩蚴抗原的IgG水平,尤其是IgG1,从感染后第4周开始升高,在感染后第9周达到最高。此外,针对包虫囊肿液抗原的抗体与对六钩蚴抗原的识别同时增加。使用包虫囊肿液进行的免疫印迹显示,最早被识别的一种抗原——一种8 kDa的蛋白质,可能是抗原B的最小亚基——在感染后5 - 6周出现,并且在感染后第9周对该分子的反应性很强。结果表明,在感染的初始阶段,针对二次感染的保护作用并非主要由抗体介导,此时细胞免疫反应可能在保护机制中起关键作用。

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