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犬小孢子菌金属蛋白酶亚单位疫苗在豚鼠体内的免疫原性和保护效力评估。

Evaluation of immunogenicity and protective efficacy of a Microsporum canis metalloprotease subunit vaccine in guinea pigs.

作者信息

Vermout Sandy M, Brouta Frédéric D, Descamps Frédéric F, Losson Bertrand J, Mignon Bernard R

机构信息

Department of Infectious and Parasitic Diseases, Parasitology, Faculty of Veterinary Medicine, University of Liège, Liège, Belgium.

出版信息

FEMS Immunol Med Microbiol. 2004 Jan 15;40(1):75-80. doi: 10.1016/S0928-8244(03)00296-7.

Abstract

In order to identify protective immunogens against Microsporum canis infection, a purified recombinant keratinolytic metalloprotease (r-MEP3) was tested as a subunit vaccine in experimentally infected guinea pigs. Both humoral and cellular specific immune responses developing towards r-MEP3 were evaluated, by enzyme-linked immunosorbent assay and by in vitro lymphocyte transformation tests respectively. Vaccination induced a strong antibody response, and a significant but transient lymphoproliferative response against the protein. However, the protocol failed to prevent fungal invasion or development of dermatophytic lesions. These results show that under the present experimental conditions, r-MEP3 specific antibodies are not protective against a challenge exposure. They also suggest that in the same model, the induction of cell-mediated immunity towards r-MEP3 is not sufficient, indicating the need for further research in the field of specific immune mechanisms involved in M. canis dermatophytosis.

摘要

为了鉴定针对犬小孢子菌感染的保护性免疫原,一种纯化的重组角质溶解金属蛋白酶(r-MEP3)在实验感染的豚鼠中作为亚单位疫苗进行了测试。分别通过酶联免疫吸附测定和体外淋巴细胞转化试验评估了针对r-MEP3产生的体液和细胞特异性免疫反应。接种疫苗诱导了强烈的抗体反应以及针对该蛋白的显著但短暂的淋巴细胞增殖反应。然而,该方案未能预防真菌侵袭或皮肤癣菌病变的发展。这些结果表明,在目前的实验条件下,r-MEP3特异性抗体对激发暴露没有保护作用。它们还表明,在同一模型中,针对r-MEP3的细胞介导免疫诱导不足,这表明在犬小孢子菌皮肤癣菌病所涉及的特异性免疫机制领域需要进一步研究。

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