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活动性自身免疫性视网膜病变患者对恢复蛋白的辅助性T细胞1型细胞免疫增强。

T Helper 1 Cellular Immunity Toward Recoverin Is Enhanced in Patients With Active Autoimmune Retinopathy.

作者信息

Lundy Steven K, Nikoopour Enayat, Karoukis Athanasios J, Ohara Ray, Othman Mohammad I, Tagett Rebecca, Jayasundera K Thiran, Heckenlively John R

机构信息

Department of Internal Medicine-Rheumatology, University of Michigan Medical School, Ann Arbor, MI, United States.

Graduate Training Program in Immunology, University of Michigan Medical School, Ann Arbor, MI, United States.

出版信息

Front Med (Lausanne). 2018 Sep 13;5:249. doi: 10.3389/fmed.2018.00249. eCollection 2018.

Abstract

Autoimmune retinopathy (AIR) causes rapidly progressive vision loss that is treatable but often is confused with other forms of retinal degeneration including retinitis pigmentosa (RP). Measurement of anti-retinal antibodies (ARA) by Western blot is a commonly used laboratory assay that supports the diagnosis yet does not reflect current disease activity. To search for better diagnostic indicators, this study was designed to compare immune biomarkers and responses toward the retinal protein, recoverin, between newly diagnosed AIR patients, slow progressing RP patients and healthy controls. All individuals had measurable anti-recoverin IgG and IgM antibodies by ELISA regardless of disease status or Western blot results. Many AIR patients had elevated anti-recoverin IgG1 levels and a strong cellular response toward recoverin dominated by IFNγ. RP patients and controls responded to recoverin with a lower IFNγ response that was balanced by IL-10 production. Both AIR and RP patients displayed lower levels of total peripheral blood mononuclear cells that were due to reductions of CD4 T cells. A comparison of messenger RNA (mRNA) for immune-related genes in whole blood of AIR patients versus RP patients or controls indicated lower expression of ATG5 and PTPN22 and higher expression of several genes involved in T cell signaling/transcription and adhesion. These data indicate that an immune response toward recoverin is normal in humans, but that in AIR patients the balance shifts dramatically toward higher IFNγ production and cellular activation.

摘要

自身免疫性视网膜病变(AIR)可导致迅速进展的视力丧失,这种视力丧失是可治疗的,但常常与包括色素性视网膜炎(RP)在内的其他形式的视网膜变性相混淆。通过蛋白质印迹法检测抗视网膜抗体(ARA)是一种常用的实验室检测方法,有助于诊断,但不能反映当前的疾病活动情况。为了寻找更好的诊断指标,本研究旨在比较新诊断的AIR患者、进展缓慢的RP患者和健康对照者之间的免疫生物标志物以及对视网膜蛋白恢复蛋白的反应。无论疾病状态或蛋白质印迹结果如何,所有个体通过酶联免疫吸附测定法均可检测到抗恢复蛋白IgG和IgM抗体。许多AIR患者抗恢复蛋白IgG1水平升高,并且对恢复蛋白有以干扰素γ为主导的强烈细胞反应。RP患者和对照者对恢复蛋白的反应中干扰素γ反应较低,由白细胞介素-10的产生来平衡。AIR患者和RP患者的外周血单个核细胞总数均较低,这是由于CD4 T细胞减少所致。对AIR患者与RP患者或对照者全血中免疫相关基因的信使核糖核酸(mRNA)进行比较,结果显示自噬相关蛋白5(ATG5)和蛋白酪氨酸磷酸酶非受体型22(PTPN22)的表达较低,而一些参与T细胞信号传导/转录和黏附的基因表达较高。这些数据表明,人类对恢复蛋白的免疫反应是正常的,但在AIR患者中,平衡显著向更高的干扰素γ产生和细胞活化方向转变。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/69e0/6146138/21121956aad9/fmed-05-00249-g0001.jpg

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