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黏膜相关恒定 T 细胞与巨细胞动脉炎不同疾病阶段的相关性。

Association of mucosal-associated invariant T cells with different disease phases of polymyalgia rheumatica.

机构信息

Department of Immunology, Juntendo University School of Medicine, Tokyo, Japan.

Department of Internal Medicine and Rheumatology, Juntendo University School of Medicine, Tokyo, Japan.

出版信息

Rheumatology (Oxford). 2020 Oct 1;59(10):2939-2946. doi: 10.1093/rheumatology/keaa054.

Abstract

OBJECTIVES

Although T cells are thought to be involved in the pathogenesis of PMR, whether innate-like T cells are involved in the process remains unknown.

METHODS

The serum levels of 27 cytokines/chemokines in patients with PMR were measured by a multiplex immunoassay (Bio-Plex Assay). The cytokine-producing capacity of T and innate-like T cells was assessed by intracellular cytokine staining and flow cytometry. The frequency and activated status of T and innate-like T cells were investigated by flow cytometry and their associations with clinical parameters were assessed.

RESULTS

The levels of inflammatory cytokines were associated with disease activity in PMR. The cytokine-producing capacity by CD8+ T and innate-like T cells was associated with disease activity. The frequency of HLA-DR+ CD38+ cells among CD8+ T cells was increased in patients with active disease. The frequencies of HLA-DR+ CD38+ cells among CD4+ T, mucosal-associated invariant T (MAIT) and γδ T cells were higher in patients with inactive disease. The frequency of HLA-DR+ CD38+ MAIT cells was associated with the PMR activity score and CRP levels in patients in remission.

CONCLUSION

The inflammatory cytokine-producing capacity and expression of activation markers of CD8+ T and innate-like T cells were associated with the disease activity of PMR. MAIT cell activation in patients in remission may contribute to the subclinical activity of the disease.

摘要

目的

虽然 T 细胞被认为参与了 PMR 的发病机制,但先天样 T 细胞是否参与该过程尚不清楚。

方法

采用多重免疫分析(Bio-Plex assay)检测 PMR 患者血清中 27 种细胞因子/趋化因子的水平。通过细胞内细胞因子染色和流式细胞术评估 T 细胞和先天样 T 细胞的细胞因子产生能力。通过流式细胞术研究 T 细胞和先天样 T 细胞的频率和激活状态,并评估其与临床参数的相关性。

结果

炎症细胞因子的水平与 PMR 的疾病活动度相关。CD8+T 和先天样 T 细胞的细胞因子产生能力与疾病活动度相关。在活动期患者的 CD8+T 细胞中,HLA-DR+CD38+细胞的频率增加。在非活动期患者的 CD4+T、黏膜相关不变 T(MAIT)和 γδ T 细胞中,HLA-DR+CD38+细胞的频率更高。HLA-DR+CD38+MAIT 细胞的频率与缓解期患者的 PMR 活动评分和 CRP 水平相关。

结论

CD8+T 和先天样 T 细胞的炎症细胞因子产生能力和激活标志物的表达与 PMR 的疾病活动度相关。缓解期患者 MAIT 细胞的激活可能与疾病的亚临床活动有关。

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