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首页> 外文期刊>Scandinavian journal of immunology. >Cytokine gene expression in healing and non-healing cases of cutaneous leishmaniasis in response to in vitro stimulation with recombinant gp63 using semi-quantitative RT-PCR.
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Cytokine gene expression in healing and non-healing cases of cutaneous leishmaniasis in response to in vitro stimulation with recombinant gp63 using semi-quantitative RT-PCR.

机译:使用半定量RT-PCR对重组gp63体外刺激产生反应的皮肤利什曼病的治愈和非治愈病例中的细胞因子基因表达。

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Objectives of this study were to test the cytokine gene expression in peripheral blood mononuclear cells (PBMCs) from cases with nonhealing and healing cutaneous leishmaniasis (CL) in response to in vitro stimulation of recombinant gp63 (rgp63) and soluble Leishmania antigen (SLA). Healing and nonhealing cases are, respectively, defined as recovered from disease and refractory to various treatments. To evaluate the type of immunological response, mRNA transcription level for interleukin (IL)-4, IL-10, IL-12 and interferon (IFN)-gamma were determined using semiquantitative reverse transcription-polymerase chain reaction (RT-PCR) technique in PBMCs of these volunteers. The results clearly demonstrated a high level of IL-4 expression in nonhealing cases of CL and a low expression level of transcripts for IFN-gamma and IL-12. In contrast, a high level of IFN-gamma and IL-12 expression and a low level of IL-4 and IL-10 expression were detected in the healing cases. These findings not only support the balance of Th1/Th2 cytokines in the inducing predominant profile in healing and nonhealing cases, but it may also show the potential of rgp63 as a proper immunogen which might induce protective responses.
机译:这项研究的目的是测试在体外刺激重组gp63(rgp63)和可溶性利什曼原虫抗原(SLA)的情况下,具有非自愈性皮肤利什曼病(CL)的患者的外周血单核细胞(PBMC)中的细胞因子基因表达。治愈和不治愈的情况分别定义为从疾病中恢复并且对各种治疗均无效。为了评估免疫应答的类型,使用半定量逆转录-聚合酶链反应(RT-PCR)技术测定了白介素(IL)-4,IL-10,IL-12和干扰素(IFN)-γ的mRNA转录水平。这些志愿者的PBMC。结果清楚地证明在CL的不愈合病例中IL-4表达水平高,而IFN-γ和IL-12的转录物表达水平低。相反,在治愈病例中检测到高水平的IFN-γ和IL-12表达以及低水平的IL-4和IL-10表达。这些发现不仅支持在治愈和不治愈的病例中,Th1 / Th2细胞因子在诱导型分布中的平衡,而且还可能表明rgp63作为适当的免疫原可能诱导保护性应答的潜力。

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