Centro de Investigación en Inmunología y Dermatología/Instituto Dermatológico de Jalisco "Dr. José Barba Rubio", Centro Universitario de Ciencias de la Salud, Universidad de Guadalajara, Zapopan, Mexico.
Doctorado en Ciencias Biomédicas con Orientación en Inmunología, Departamento de Fisiología, Centro Universitario de Ciencias de la Salud, Universidad de Guadalajara, Guadalajara, Mexico.
Mol Genet Genomic Med. 2020 Oct;8(10):e1416. doi: 10.1002/mgg3.1416. Epub 2020 Jul 23.
The macrophage migration inhibiting factor (MIF) is a protein that promotes the activation of immune cells and the production of other proinflammatory cytokines such as TNF-α, IL-1β, and IFN-γ, which have proposed to play an essential role in the pathogenesis of vitiligo. The study aimed to assess the association between MIF polymorphisms (-794 CATT and -173 G>C), MIF in situ expression, and MIF serum concentrations with susceptibility and disease activity in patients with non-segmental vitiligo (NSV) from western Mexico.
The study included 111 patients with NSV and 201 control subjects. Genotyping was performed by conventional PCR (-794 CATT ) and PCR-RFLP (-173 G>C) methods. MIF mRNA expression was quantified by real-time PCR and MIF serum concentrations were determined by ELISA kit. Histopathological samples were analyzed by automated immunohistochemistry.
The MIF polymorphisms were associated with NSV susceptibility. Serum concentrations of MIF were higher in patients with active NSV and correlated negatively with the years of evolution. The depigmented skin from patients with active vitiligo showed a high expression of MIF.
MIF polymorphisms increase the risk of NSV in the western Mexican population. The serum concentrations of MIF and in situ expression are associated with active NSV.
巨噬细胞移动抑制因子(MIF)是一种促进免疫细胞激活和其他促炎细胞因子如 TNF-α、IL-1β 和 IFN-γ产生的蛋白质,这些细胞因子被认为在白癜风的发病机制中发挥着重要作用。本研究旨在评估 MIF 多态性(-794 CATT 和-173 G>C)、MIF 原位表达和 MIF 血清浓度与来自墨西哥西部的非节段性白癜风(NSV)患者的易感性和疾病活动之间的关系。
本研究纳入了 111 名 NSV 患者和 201 名对照者。通过常规 PCR(-794 CATT)和 PCR-RFLP(-173 G>C)方法进行基因分型。通过实时 PCR 定量 MIF mRNA 表达,通过 ELISA 试剂盒测定 MIF 血清浓度。通过自动化免疫组织化学分析组织病理学样本。
MIF 多态性与 NSV 易感性相关。活动期 NSV 患者的 MIF 血清浓度较高,且与疾病进展时间呈负相关。活动期白癜风患者的脱色皮肤显示 MIF 高表达。
MIF 多态性增加了墨西哥西部人群患 NSV 的风险。MIF 的血清浓度和原位表达与活动期 NSV 相关。