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VIP/VPAC 轴在免疫介导的炎症性疾病中的表达:相关 miRNA 特征。

VIP/VPAC Axis Expression in Immune-Mediated Inflammatory Disorders: Associated miRNA Signatures.

机构信息

Department of Cell Biology, Facultad de Biología y Facultad de Medicina, Universidad Complutense de Madrid, 28040 Madrid, Spain.

Department of Immunology, Instituto de Investigación Princesa, Hospital Universitario de La Princesa, 28006 Madrid, Spain.

出版信息

Int J Mol Sci. 2022 Aug 2;23(15):8578. doi: 10.3390/ijms23158578.

Abstract

Few studies have considered immune-mediated inflammatory disorders (IMID) together, which is necessary to adequately understand them given they share common mechanisms. Our goal was to investigate the expression of vasoactive intestinal peptide (VIP) and its receptors VPAC1 and VPAC2 in selected IMID, analyze the effect of biological therapies on them, and identify miRNA signatures associated with their expression. Serum VIP levels and mRNA of VPAC and miRNA expression in peripheral blood mononuclear cells were analyzed from 52 patients with psoriasis, rheumatoid arthritis, Graves’ disease, or spondyloarthritis and from 38 healthy subjects. IMID patients showed higher levels of VIP and increased expression of VPAC2 compared to controls (p < 0.0001 and p < 0.0192, respectively). Receiver operating characteristic curve analysis showed that the levels of VIP or VPAC2 expression were adequate discriminators capable of identifying IMID. Treatment of IMID patients with anti-TNFα and anti-IL12/23 significantly affected serum VIP levels. We identified miRNA signatures associated with levels of serum VIP and VPAC2 expression, which correlated with IMID diagnosis of the patients. The results indicate that the expression of VIP/VPAC2 is able of identify IMIDs and open up a line of research based on the association between the VIP/VPAC axis and miRNA signatures in immune-mediated diseases.

摘要

很少有研究将免疫介导的炎症性疾病 (IMID) 一起考虑,鉴于它们具有共同的机制,有必要充分了解这些疾病。我们的目标是研究在选定的 IMID 中血管活性肠肽 (VIP) 及其受体 VPAC1 和 VPAC2 的表达,分析生物疗法对它们的影响,并确定与它们表达相关的 miRNA 特征。从 52 例银屑病、类风湿关节炎、格雷夫斯病或脊柱关节炎患者和 38 例健康对照者中分析血清 VIP 水平和外周血单个核细胞中 VPAC 的 mRNA 和 miRNA 表达。与对照组相比,IMID 患者的 VIP 水平和 VPAC2 表达增加(分别为 p < 0.0001 和 p < 0.0192)。受试者工作特征曲线分析表明,VIP 或 VPAC2 表达水平是能够识别 IMID 的有效鉴别器。用抗 TNFα 和抗 IL12/23 治疗 IMID 患者显著影响血清 VIP 水平。我们确定了与血清 VIP 和 VPAC2 表达水平相关的 miRNA 特征,这些特征与患者的 IMID 诊断相关。结果表明,VIP/VPAC2 的表达能够识别 IMIDs,并为基于 VIP/VPAC 轴与免疫介导疾病中 miRNA 特征的关联的研究开辟了一条新途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b48e/9369218/12e8bcc27a86/ijms-23-08578-g001.jpg

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