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戈谢氏病患儿细胞毒性 T 细胞的上调。

Upregulation of Cytotoxic T-cells in pediatric patients with Gaucher disease.

机构信息

Department of Clinical Pathology, South Egypt Cancer Institute, Assiut University, Assiut, Egypt.

Department of Pediatrics, Assiut University Hospital, Assiut, Egypt.

出版信息

Sci Rep. 2022 Mar 23;12(1):4977. doi: 10.1038/s41598-022-08843-4.

Abstract

Cytotoxic (CD8) T-cells and natural killer (NK) cells have a significant immune function role. The ongoing stimulation of immunity and the excessive release of proinflammatory cytokines observed in pediatric patients with Gaucher disease (GD) can affect immune cells. Few studies have looked at the proportion of cytotoxic CD8 T-cells and their subsets in children with GD. A prospective case-control study was performed involving twenty pediatric patients with type 1 GD and twenty healthy age-matched controls. All patients received regular enzyme replacement therapy (ERT) for at least 6 months before the study. Complete blood count and flow cytometric analyses of CD8 T, Tc1, Tc2, NK, and NK T-cells were performed. GD patients showed significantly increased of CD8 T, Tc1 and significantly decreased NK cells frequencies when compared to healthy controls. However, no significant difference in Tc2 and NK T-cells was found between the studied groups. GD patients on regular ERT have increased CD8+ T-cell frequencies, predominantly Tc1, together with a reduction in NK cells than in healthy controls. These crucial immunological changes may contribute to some extent to the pathogenesis and the progression of GD.

摘要

细胞毒性 (CD8) T 细胞和自然杀伤 (NK) 细胞具有重要的免疫功能。戈谢氏病 (GD) 儿科患者持续的免疫刺激和过度释放促炎细胞因子会影响免疫细胞。很少有研究关注 GD 儿童细胞毒性 CD8 T 细胞及其亚群的比例。进行了一项前瞻性病例对照研究,涉及 20 名 1 型 GD 儿科患者和 20 名年龄匹配的健康对照者。所有患者在研究前至少接受了 6 个月的常规酶替代疗法 (ERT)。进行了 CD8 T、Tc1、Tc2、NK 和 NK T 细胞的全血细胞计数和流式细胞分析。与健康对照组相比,GD 患者的 CD8 T、Tc1 频率显著增加,NK 细胞频率显著降低。然而,两组间 Tc2 和 NK T 细胞无显著差异。接受常规 ERT 的 GD 患者的 CD8+T 细胞频率增加,主要是 Tc1,同时 NK 细胞减少,与健康对照组相比。这些关键的免疫学变化可能在一定程度上导致 GD 的发病机制和进展。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0bb3/8942997/0d8da2222bcf/41598_2022_8843_Fig1_HTML.jpg

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