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蛋白酪氨酸磷酸酶非受体型 22.6mRNA 在克罗恩病患者外周血单个核细胞中的表达水平的临床价值。

Clinical value of the expression levels of protein tyrosine phosphatase non-receptor type 22.6 mRNA in peripheral blood mononuclear cells in Crohn's disease.

机构信息

Department of Gastroenterology, The Central Hospital of Wuhan, Tongji Medical College, Huazhong University of Science and Technology; Key Laboratory for Molecular Diagnosis of Hubei Province, Wuhan, People's Republic of China.

出版信息

Clin Exp Immunol. 2022 Sep 29;209(3):311-315. doi: 10.1093/cei/uxac061.

DOI:10.1093/cei/uxac061
PMID:35751647
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9521657/
Abstract

OBJECTIVE

To explore the relationship between the expression levels of protein tyrosine phosphatase non-receptor type (PTPN) 22.6 mRNA in peripheral blood mononuclear cells (PBMCs) and the disease activity as well as clinical characteristics in Crohn's disease (CD) patients.

METHODS

A total of 480 subjects were enrolled. Data were collected including baseline information, expression levels of PTPN22.6 mRNA in PBMCs for all subjects, C-reactive protein (CRP) levels in serum, clinical characteristics, and disease activity for all patients. Expression levels of PTPN22.6 mRNA in PBMCs, CRP levels in serum, clinical characteristics according to Montreal Classification [8], and Crohn's disease activity index (CDAI) were the primary observation outcomes.

RESULTS

The expression levels of PTPN22.6 mRNA (P = 0.032) in PBMCs and serum CRP levels (P < 0.001) were significantly higher in active CD patients than in inactive CD patients (P = 0.032). Correlation analysis showed that there was a positive correlation between expression levels of PTPN22.6 mRNA and CDAI value (r = 0.512, P = 0.003), as well as expression levels of PTPN22.6 mRNA and CRP levels in the CD group (r = 0.456, P = 0.006). There were significantly higher expression levels of PTPN22.6 mRNA in PBMCs in patients with structuring behavior than that in patients with non-stricturing and non-penetrating (NSNP) behaviors (P = 0.018) and penetrating behaviors (P = 0.024).

CONCLUSIONS

The expression levels of PTPN22.6 mRNA can be used as an indicator to help predict CD diagnosis, disease activity, serum CRP level, and behavior type of CD disease.

摘要

目的

探讨外周血单个核细胞(PBMCs)中蛋白酪氨酸磷酸酶非受体型(PTPN)22.6 mRNA 表达水平与克罗恩病(CD)患者疾病活动度及临床特征的关系。

方法

共纳入 480 例受试者。收集所有受试者的基线信息、PBMCs 中 PTPN22.6 mRNA 表达水平、血清 C 反应蛋白(CRP)水平、临床特征和所有患者的疾病活动度等数据。PBMCs 中 PTPN22.6 mRNA 表达水平、血清 CRP 水平、根据蒙特利尔分类[8]的临床特征和克罗恩病活动指数(CDAI)为主要观察终点。

结果

活动期 CD 患者 PBMCs 中 PTPN22.6 mRNA 表达水平(P = 0.032)和血清 CRP 水平(P < 0.001)均显著高于缓解期 CD 患者。相关性分析显示,PBMCs 中 PTPN22.6 mRNA 表达水平与 CDAI 值呈正相关(r = 0.512,P = 0.003),CD 组中 PTPN22.6 mRNA 表达水平与 CRP 水平也呈正相关(r = 0.456,P = 0.006)。结构行为患者 PBMCs 中 PTPN22.6 mRNA 表达水平显著高于非狭窄非穿透(NSNP)行为和穿透行为患者(P = 0.018 和 P = 0.024)。

结论

PBMCs 中 PTPN22.6 mRNA 的表达水平可作为帮助预测 CD 诊断、疾病活动度、血清 CRP 水平和 CD 疾病行为类型的指标。

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本文引用的文献

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Characterization of T-cell Receptor Repertoire in Inflamed Tissues of Patients with Crohn's Disease Through Deep Sequencing.通过深度测序对克罗恩病患者炎症组织中T细胞受体库的特征分析
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miR-25 targets the modulator of apoptosis 1 gene in lung cancer.微小RNA-25靶向肺癌中的凋亡调节因子1基因。
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PTPN22: the archetypal non-HLA autoimmunity gene.PTPN22:典型的非 HLA 自身免疫基因。
Nat Rev Rheumatol. 2014 Oct;10(10):602-11. doi: 10.1038/nrrheum.2014.109. Epub 2014 Jul 8.
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Polymorphisms in the inflammatory pathway genes TLR2, TLR4, TLR9, LY96, NFKBIA, NFKB1, TNFA, TNFRSF1A, IL6R, IL10, IL23R, PTPN22, and PPARG are associated with susceptibility of inflammatory bowel disease in a Danish cohort.炎症通路基因TLR2、TLR4、TLR9、LY96、NFKBIA、NFKB1、TNFA、TNFRSF1A、IL6R、IL10、IL23R、PTPN22和PPARG中的多态性与丹麦队列中炎症性肠病的易感性相关。
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Imbalances of CD4(+) T-cell subgroups in Crohn's disease and their relationship with disease activity and prognosis.克罗恩病中CD4(+) T细胞亚群失衡及其与疾病活动和预后的关系。
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Autoimmunity-associated LYP-W620 does not impair thymic negative selection of autoreactive T cells.自身免疫相关的LYP-W620并不损害自身反应性T细胞的胸腺阴性选择。
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PTPN22 controls the germinal center by influencing the numbers and activity of T follicular helper cells.PTPN22 通过影响滤泡辅助性 T 细胞的数量和活性来控制生发中心。
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