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原发性和继发性微小隐孢子虫感染中细胞因子和血清免疫球蛋白谱的动态变化:Luminex® xMAP 技术的应用。

Dynamics of cytokines and immunoglobulins serum profiles in primary and secondary Cryptosporidium parvum infection: usefulness of Luminex® xMAP technology.

机构信息

Unidade de Parasitologia Médica, Grupo de Protozoários Oportunistas/VIH e Outros Protozoários, CMDT, Instituto de Higiene e Medicina Tropical, Universidade Nova de Lisboa, Lisboa 1349-008, Portugal.

出版信息

Exp Parasitol. 2013 Jan;133(1):106-13. doi: 10.1016/j.exppara.2012.11.003. Epub 2012 Nov 20.

Abstract

Infection by Cryptosporidium parvum triggers a complex array of innate and adaptive cell mediated immune response, playing an important role in controlling the infection. To date, there are no studies applying the Luminex® xMAP technology to determine profiles of cytokines and immunoglobulins in the context of an infection by C. parvum. In this study, we analyzed these immune mediators in the serum of immunocompetent mice inoculated with C. parvum oocysts, using Luminex, to understand how the immune system responds to an infection by this parasite. Animal sera were also analyzed by ELISA to determine the expressed immunoglobulin isotype profile, and compare the obtained trend with data obtained by Luminex. Specific-pathogen-free BALB/C mice were inoculated with oocysts of C. parvum at days 0 and 22. Peripheral blood was aseptically collected from sacrificed mice on several time points, and immune mediators were evaluated in serum samples. Infection was confirmed by the presence of C. parvum DNA in feces by a nested-PCR assay (60-kDa glycoprotein). Luminex results showed predominance in the secretion of IgG1 and IgG2a, confirmed by ELISA, which also showed that IgG1 is the major immunoglobulin isotype produced during the infection. The analysis of cytokines suggests a preferential Th(1) over the Th(2) response, with increased production of TNF-α, IFN-γ and GM-CSF. This work contributed to a better understanding of the immune response to the infection by C. parvum, as well as demonstrated the advantage of Luminex® xMAP technology to study immune mediators, using small sample volumes.

摘要

感染微小隐孢子虫会引发一系列复杂的先天和适应性细胞介导的免疫反应,在控制感染方面发挥着重要作用。迄今为止,尚无研究应用 Luminex® xMAP 技术来确定微小隐孢子虫感染时细胞因子和免疫球蛋白的图谱。在这项研究中,我们使用 Luminex 分析了免疫功能正常的小鼠接种微小隐孢子虫卵囊后血清中的这些免疫介质,以了解免疫系统如何对这种寄生虫的感染做出反应。还通过 ELISA 分析动物血清,以确定表达的免疫球蛋白同种型谱,并将获得的趋势与通过 Luminex 获得的数据进行比较。将无特定病原体的 BALB/C 小鼠在第 0 天和第 22 天用微小隐孢子虫卵囊接种。无菌采集牺牲小鼠的外周血,并在多个时间点采集血清样本,评估血清中的免疫介质。通过巢式 PCR 检测粪便中微小隐孢子虫 DNA(60-kDa 糖蛋白)来确认感染。Luminex 结果显示 IgG1 和 IgG2a 的分泌占优势,ELISA 结果也证实 IgG1 是感染期间产生的主要免疫球蛋白同种型。细胞因子分析表明 Th(1)反应优先于 Th(2)反应,TNF-α、IFN-γ 和 GM-CSF 的产生增加。这项工作有助于更好地了解对微小隐孢子虫感染的免疫反应,同时也展示了 Luminex® xMAP 技术在使用小样本量研究免疫介质方面的优势。

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