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评估曲霉和毛霉科特异性 T 细胞和外周血单个核细胞细胞因子特征作为环境霉菌暴露的生物标志物。

Evaluation of Aspergillus and Mucorales specific T-cells and peripheral blood mononuclear cell cytokine signatures as biomarkers of environmental mold exposure.

机构信息

University Hospital of Wuerzburg, Department of Internal Medicine II, Division of Infectious Diseases, Josef-Schneider-Str. 2, 97080 Wuerzburg, Germany.

University of Wuerzburg, Biocenter, Department of Bioinformatics, Am Hubland, 97074 Wuerzburg, Germany.

出版信息

Int J Med Microbiol. 2018 Dec;308(8):1018-1026. doi: 10.1016/j.ijmm.2018.09.002. Epub 2018 Sep 3.

Abstract

Mold specific T-cells have been described as a supportive biomarker to monitor invasive mycoses and mold exposure. This study comparatively evaluated frequencies and cytokine profiles of Aspergillus fumigatus and Mucorales reactive T-cells depending on environmental mold exposure. Peripheral blood mononuclear cells (PBMCs) obtained from 35 healthy donors were stimulated with mycelial lysates of A. fumigatus and three human pathogenic Mucorales species. CD154 specific T-cells were quantified by flow cytometry. In a second cohort of 20 additional donors, flow cytometry was complemented by 13-plex cytokine assays. Mold exposure of the subjects was determined using a previously established questionnaire. Highly exposed subjects exhibited significantly greater CD154A. fumigatus and Mucorales specific naïve and memory T-helper cell frequencies. Significant correlation (r = 0.48 - 0.79) was found between A. fumigatus and Mucorales specific T-cell numbers. Logistic regression analyses revealed that combined analysis of mold specific T-cell frequencies and selected cytokine markers (A. fumigatus: IL-5 and TNF-α, R. arrhizus: IL-17A and IL-13) significantly improves classification performance, resulting in 75-90 % predictive power using 10-fold cross-validation. In conclusion, mold specific T-cell frequencies and their cytokine signatures offer promising potential in the assessment of environmental mold exposure. The cytokines identified in this pilot study should be validated in the clinical setting, e. g. in patients with hypersensitivity pneumonitis.

摘要

已经描述了针对特定 mold 的 T 细胞作为监测侵袭性真菌感染和 mold 暴露的支持性生物标志物。本研究比较评估了曲霉菌和毛霉目真菌反应性 T 细胞的频率和细胞因子谱,取决于环境 mold 暴露。从 35 名健康供体中获得外周血单核细胞(PBMC),并用烟曲霉和三种人类致病性毛霉目的菌丝体裂解物刺激。通过流式细胞术定量 CD154 特异性 T 细胞。在第二组 20 名额外供体中,流式细胞术通过 13 plex 细胞因子测定得到补充。使用先前建立的问卷确定受试者的 mold 暴露。高度暴露的受试者表现出显著更高的 CD154 烟曲霉和毛霉目特异性幼稚和记忆 T 辅助细胞频率。发现烟曲霉和毛霉目特异性 T 细胞数量之间存在显著相关性(r = 0.48 - 0.79)。逻辑回归分析表明,mold 特异性 T 细胞频率和选定细胞因子标志物(烟曲霉:IL-5 和 TNF-α,R. arrhizus:IL-17A 和 IL-13)的联合分析显著提高分类性能,使用 10 倍交叉验证的预测能力为 75-90%。总之,针对特定 mold 的 T 细胞频率及其细胞因子特征在评估环境 mold 暴露方面具有很大的潜力。本研究中确定的细胞因子应在临床环境中进行验证,例如在过敏反应性肺炎患者中。

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