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分析鸟枪弹样脉络膜视网膜炎患者外周炎症性 T 细胞亚群及其效应功能。

Analysis of peripheral inflammatory T cell subsets and their effector function in patients with Birdshot Retinochoroiditis.

机构信息

Regenerative Immunology and Aging, BIH Center for Regenerative Therapies, Charité Universitätsmedizin Berlin, Berlin, Germany.

Charité-Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin and Humboldt-Universität Zu Berlin, Augustenburger Platz 1, 13353, Berlin, Germany.

出版信息

Sci Rep. 2021 Apr 21;11(1):8604. doi: 10.1038/s41598-021-88013-0.

Abstract

Birdshot Retinochoroiditis (BSRC) is a progressive non-infectious intraocular inflammation that affects choroid and retina. Inflammatory processes have adverse effects on vision by affecting photoreceptor-bearing cells that do not regenerate. This study aimed at characterizing inflammatory CD4 and CD8 T cell subsets in the peripheral blood of active and inactive BSRCs. Furthermore, we correlated phenotypical and functional immunological analyses with clinical data. We observed a slight increase of terminally differentiated effector memory CD8 T cells expressing CD45RA (T) in blood of inactive, compared to active BSRCs. Moreover, we identified a trend for a decreased population of T2 cells and increased T1 frequencies in active BSRCs, a typical sign of ongoing autoimmune processes. Functional assays demonstrated severe and overall impairment of effector function of both, CD4 and CD8 inflammatory T cells, which might reflect T cell exhaustion. Although the eye is the main site of inflammation in BSRC, we observed altered T cell subset compositions in the peripheral blood, dependent on the disease status. Our results indicate that T cells may play a major role in BSRC pathology, although our cohort size is too limited for definitve conclusions. Future studies with larger BSRCs have to be performed.

摘要

鸟枪弹样视网膜脉络膜炎(BSRC)是一种进行性的非传染性眼内炎症,影响脉络膜和视网膜。炎症过程通过影响不具有再生能力的感光细胞对视力产生不良影响。本研究旨在描述活性和非活性 BSRC 患者外周血中的炎症性 CD4 和 CD8 T 细胞亚群。此外,我们还将表型和功能免疫学分析与临床数据相关联。与活动期 BSRC 相比,我们观察到非活动期 BSRC 患者血液中终末分化的效应记忆 CD8 T 细胞(表达 CD45RA(T))略有增加。此外,我们发现活动期 BSRC 中 T2 细胞的数量减少,T1 频率增加,这是正在进行的自身免疫过程的典型标志。功能测定表明,CD4 和 CD8 炎症性 T 细胞的效应功能严重且普遍受损,这可能反映了 T 细胞耗竭。尽管眼睛是 BSRC 炎症的主要部位,但我们观察到外周血中 T 细胞亚群组成发生改变,这取决于疾病状态。我们的研究结果表明,T 细胞可能在 BSRC 发病机制中起主要作用,尽管我们的研究样本量太小,无法得出明确的结论。未来需要对更大的 BSRC 进行研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8151/8060342/a60fc993bf46/41598_2021_88013_Fig1_HTML.jpg

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