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感染和接种疫苗的小鼠体内毛首鞭形线虫的淋巴细胞迁移抑制反应

Lymphocyte Migration Inhibition Response in Trichuris muris Infected and Vaccinated Mice.

作者信息

Gaherwal S, Prakash Mm

机构信息

Department of Biotechnology, Govt. Holkar Science College, Indore (M.P.) India.

出版信息

Iran J Parasitol. 2011 Mar;6(1):34-40.

Abstract

BACKGROUND

Immunological response of host and parasite play a key role in developing vaccination and immunization. The present study deals with the immune response and effecter mechanism, which was confirmed by migration inhibition factor (MIF).

METHODS

The present work was conducted in Parasitological Lab of Postgraduate Department of Zoology, Government Holkar Science College, Indore (M.P.) during 2006-2007. For MIF assay, lymphocytes were separated from heparinized blood of experimental and control mice. Aliquots of cell suspension were placed in four wells cut in a preparation of agarose in a Petri dish. Two wells were filled with soluble test antigen, while rest two wells were filled with medium (control wells). Petri dish was incubated overnight at 37 °C in a humidified environment at 5% CO2 in air. Cells migrated under the agarose in a circle were fixed and stained. Diameters of the migration areas were measured with ocular micrometer.

RESULTS

MIF reaction was maximum (44.2%) in the group IVEgESAg5 and minimum (10.8%) in the group IVASoAg1. The maximum MIF reaction was shown by eggs ES antigen and least by adult worm somatic antigen. The interesting observation was that migration inhibition increases as dose increased or we could say the reaction was dose dependent.

CONCLUSION

Increased value of MIF response in vaccinated mice suggested the involvement of lymphocytes in cell-mediated immunity. This study also proves that excretory-secretory (ES) antigen of eggs from Trichuris muris was more effective in imparting immunity in mice.

摘要

背景

宿主和寄生虫的免疫反应在疫苗接种和免疫过程中起着关键作用。本研究探讨了免疫反应及效应机制,这一机制通过迁移抑制因子(MIF)得以证实。

方法

本研究于2006 - 2007年在印度中央邦印多尔市政府霍尔卡科学学院动物学研究生部的寄生虫学实验室进行。对于MIF检测,从实验小鼠和对照小鼠的肝素化血液中分离淋巴细胞。将细胞悬液的等分试样置于培养皿中琼脂糖制剂上切割出的四个孔中。两个孔中加入可溶性测试抗原,其余两个孔加入培养基(对照孔)。将培养皿在37°C、5%二氧化碳的湿润空气中孵育过夜。对在琼脂糖下呈圆形迁移的细胞进行固定和染色。用目镜测微计测量迁移区域的直径。

结果

IVEgESAg5组的MIF反应最大(44.2%),IVASoAg1组最小(10.8%)。虫卵ES抗原显示出最大的MIF反应,成虫体抗原显示的反应最小。有趣的观察结果是,迁移抑制随着剂量增加而增强,或者可以说反应是剂量依赖性的。

结论

接种疫苗小鼠中MIF反应值的增加表明淋巴细胞参与了细胞介导的免疫。本研究还证明,来自鼠鞭虫虫卵的排泄 - 分泌(ES)抗原在赋予小鼠免疫力方面更有效。

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