首页> 外文期刊>Leprosy review >Cytokine responses to Mycobacterium leprae unique proteins differentiate between Mycobacterium leprae infected and na?ve armadillos
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Cytokine responses to Mycobacterium leprae unique proteins differentiate between Mycobacterium leprae infected and na?ve armadillos

机译:对麻风分枝杆菌独特蛋白的细胞因子应答区分麻风分枝杆菌感染和幼稚犰狳

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New diagnostic tools for early detection of leprosy are necessary to help reduce its transmission and severity. M. leprae unique proteins have been used to assess differences in human T-cell responses in leprosy patients, household contacts and endemic controls. In this study, we examined the response of M. leprae-infected armadillos to a variety of M. leprae recombinant antigen candidates currently being examined for diagnostic efficacy in humans. Among recently M. leprae infected armadillos, IFN-γ expression was enhanced after stimulation of PBMC with all M. leprae recombinant proteins except for ML2283 (mean: 2·65 Relative Quantification (RQ)). The group mean stimulation index for M. leprae proteins ML0009, ML1601, ML2478 and ML2531 averaged 35·2 RQ and was significantly higher (P<0·05) than that measured among the non-infected, na?ve group (mean 6·2 RQ). Although ML0840 tended to enhance IFN-γ levels, the mean IFN-γ transcript levels of the currently experimentally inoculated group (20·1 RQ) was not significantly different statistically (P = 0·10) from the mean of the na?ve group (7·5 RQ). Also no statistically significant differences were observed in IFN-γ transcript levels between the resistant and currently experimentally inoculated group (P>0·05) or between the resistant and the na?ve group (P>0·05) after stimulation of PBMCs with all M. leprae recombinant proteins. Only low levels of TNF-α were observed across all groups after in vitro stimulation with all the antigens examined. These data suggest that armadillos can be used effectively to help identify M. leprae specific proteins that may be applied for monitoring T-cell responses in M. leprae infected hosts as their disease progresses as well as for the early diagnosis of leprosy.
机译:必须使用新的诊断工具来及早发现麻风病,以帮助降低麻风病的传播程度和严重程度。麻风分枝杆菌独特的蛋白质已用于评估麻风病人,家庭接触者和地方性对照中人T细胞反应的差异。在这项研究中,我们检查了麻风分枝杆菌感染的犰狳对目前正在检查的人类诊断功效中对麻风分枝杆菌重组抗原候选物的反应。在最近感染麻风分枝杆菌的犰狳中,用除ML2283以外的所有麻风分枝杆菌重组蛋白刺激PBMC后,IFN-γ表达得以增强(平均:2·65相对定量(RQ))。麻风分枝杆菌蛋白ML0009,ML1601,ML2478和ML2531的组平均刺激指数平均为35·2 RQ,比未感染的纯稚组的平均刺激指数显着更高(P <0·05)(平均6· 2 RQ)。尽管ML0840倾向于增加IFN-γ的水平,但目前实验接种组(20·1 RQ)的平均IFN-γ转录水平与单纯组的平均值无统计学差异(P = 0·10)。 (7·5 RQ)。在用PBMC刺激PBMCs后,耐药菌组和目前实验组(P> 0·05)或耐药菌组与幼稚组(P> 0·05)之间的IFN-γ转录水平也没有统计学上的显着差异。所有麻风分枝杆菌重组蛋白。在用所有检查的抗原进行体外刺激后,所有组中仅观察到低水平的TNF-α。这些数据表明,犰狳可以有效地用于帮助鉴定麻风分枝杆菌特异性蛋白,这些蛋白可用于监测麻风分枝杆菌感染宿主的T细胞反应,以及其病情进展以及麻风病的早期诊断。

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