首页> 外文OA文献 >Adjuvant effect of synthetic oligodeoxyribonucleotides (CpG-ODN) from the Paracoccidioides brasiliensis gp43 gene on the Th2-Th1 immunomodulation of experimental paracoccidioidomycosis
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Adjuvant effect of synthetic oligodeoxyribonucleotides (CpG-ODN) from the Paracoccidioides brasiliensis gp43 gene on the Th2-Th1 immunomodulation of experimental paracoccidioidomycosis

机译:巴西副球菌gp43基因合成寡聚脱氧核糖核苷酸(CpG-ODN)对实验性副球孢子菌病Th2-Th1免疫调节的佐剂作用

摘要

Paracoccidioidomycosis (PCM) is caused by the dimorphic fungus Paracoccidioides brasiliensis. Immunostimulatory effects of P. brasiliensis DNA and CpG-oligodeoxyribonucleotides (CpG-ODN) have shown a Th2-Th1 immunomodulation of the isogenic murine model of susceptibility, which develops a progressive and disseminating disease. in this study, we investigated the optimum time interval and doses of CpG-ODN which are able to induce Th2-Th1 immunomodulation. the optimum concentrations for the induction of a decrease in antibody production were 0.5 and 1 mu g. Mice immunized twice with CpG-ODN and gp43 (5 and 7 days before the challenge) showed a 60% higher chance of survival compared with the control group (nonimmunized), and an increase in Th1 isotype (IgG2a) was also observed. in vitro assays of naive and preimmunized mice showed discrete cellular proliferation when stimulated by suitable concentrations of CpG-ODN. Type 1 cytokines interleukin-12 (IL-12) and interferon-gamma were increased in cell culture supernatants, but no significant difference was found in Th2 IL-4 cytokines in stimulated or nonstimulated cell cultures. Concerning the Th2-Th1 kinetics in experimental PCM models by adjuvant effect of CpG-ODN, there are still many questions to be answered and clarified. However, the gathering of data obtained in this investigation has led us to suggest that the modulation of Th2-Th1 in experimental PCM depends on time and CpG-ODN concentration.
机译:副球孢子菌病(PCM)是由巴西双歧杆菌Paracoccidioides引起的。巴西假单胞菌DNA和CpG-寡脱氧核糖核苷酸(CpG-ODN)的免疫刺激作用已显示出对易感性等基因鼠模型的Th2-Th1免疫调节,从而发展了一种进行性和传播性疾病。在这项研究中,我们研究了能够诱导Th2-Th1免疫调节的CpG-ODN的最佳时间间隔和剂量。诱导抗体产生减少的最佳浓度为0.5和1μg。与对照组(未免疫)相比,用CpG-ODN和gp43两次免疫的小鼠(攻击前5天和7天)显示出更高的存活机会,并且还观察到Th1同型(IgG2a)的增加。幼稚和预免疫小鼠的体外试验显示,当受到适当浓度的CpG-ODN刺激时,细胞会离散增殖。细胞培养上清液中1型细胞因子白细胞介素12(IL-12)和干扰素-γ升高,但是在刺激或未刺激的细胞培养物中,Th2 IL-4细胞因子均未发现明显差异。关于通过CpG-ODN的辅助作用在实验PCM模型中的Th2-Th1动力学,仍然有许多问题需要解答和澄清。然而,从这项研究中获得的数据的收集使我们提出实验性PCM中Th2-Th1的调节取决于时间和CpG-ODN浓度。

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