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与色素性视网膜炎中黄斑囊样水肿相关的眼部和全身免疫特征。

Ocular and systemic immune profiles associated with cystoid macular edema in retinitis pigmentosa.

作者信息

Tao Yan, Zhao Huanyu, Shimokawa Sakurako, Fukushima Masatoshi, Fujiwara Kohta, Hisai Takahiro, Yamamoto Kaho, Okita Ayako, Sonoda Koh-Hei, Murakami Yusuke

机构信息

Department of Ophthalmology, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.

Department of Ophthalmology, Oita University, Oita, Japan.

出版信息

Front Ophthalmol (Lausanne). 2025 Sep 5;5:1653404. doi: 10.3389/fopht.2025.1653404. eCollection 2025.

DOI:10.3389/fopht.2025.1653404
PMID:40979286
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12446031/
Abstract

PURPOSE

We aimed to investigate the local and systemic inflammatory profiles associated with cystoid macular edema (CME) in patients with retinitis pigmentosa (RP).

PATIENTS AND METHODS

Paired aqueous humor and serum samples were collected at the time of cataract surgery from 37 eyes of 37 patients with typical RP, including 29 without CME and eight with CME. The concentrations of cytokines and chemokines were determined using a multiplexed immunoassay (Q-Plex). Group comparisons were conducted to assess differences in the inflammatory molecule levels between the RP patients with and without CME. Correlations among the intraocular parameters, the systemic inflammatory molecules, and the CME status were analyzed.

RESULTS

Compared to RP patients without CME, those with CME showed significantly increased aqueous levels of interleukin 23 (IL-23) ( = 0.002), I-309 ( = 0.039), and growth-related oncogene alpha (GROα) ( = 0.042). A multiple-factor analysis further supported a potential association between CME formation and an IL-23-related inflammatory network characterized by aqueous IL-23, IL-8, GROα, eotaxin, I-309, serum IL-23, and IFN-γ.

CONCLUSION

These findings suggest that both intraocular and systemic immune activation may play a role in the development of CME in patients with RP. Specifically, IL-23-driven inflammation may be associated with macular fluid accumulation. Further longitudinal studies in larger cohorts are necessary to elucidate these relationships and explore their clinical implications.

摘要

目的

我们旨在研究视网膜色素变性(RP)患者中与黄斑囊样水肿(CME)相关的局部和全身炎症特征。

患者与方法

在白内障手术时,收集了37例典型RP患者的37只眼睛的配对房水和血清样本,其中29例无CME,8例有CME。使用多重免疫测定法(Q-Plex)测定细胞因子和趋化因子的浓度。进行组间比较以评估有和无CME的RP患者之间炎症分子水平的差异。分析了眼内参数、全身炎症分子和CME状态之间的相关性。

结果

与无CME的RP患者相比,有CME的患者房水中白细胞介素23(IL-23)(P = 0.002)、I-309(P = 0.039)和生长相关癌基因α(GROα)(P = 0.042)的水平显著升高。多因素分析进一步支持CME形成与以房水IL-23、IL-8、GROα、嗜酸性粒细胞趋化因子、I-309、血清IL-23和干扰素-γ为特征的IL-23相关炎症网络之间存在潜在关联。

结论

这些发现表明,眼内和全身免疫激活可能在RP患者CME的发生中起作用。具体而言,IL-23驱动的炎症可能与黄斑积液有关。有必要在更大的队列中进行进一步的纵向研究,以阐明这些关系并探索其临床意义。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b2ae/12446031/fa62720017dc/fopht-05-1653404-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b2ae/12446031/02ec0fa13e04/fopht-05-1653404-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b2ae/12446031/db17386ba660/fopht-05-1653404-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b2ae/12446031/a43fdaafde08/fopht-05-1653404-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b2ae/12446031/fa62720017dc/fopht-05-1653404-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b2ae/12446031/02ec0fa13e04/fopht-05-1653404-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b2ae/12446031/db17386ba660/fopht-05-1653404-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b2ae/12446031/a43fdaafde08/fopht-05-1653404-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b2ae/12446031/fa62720017dc/fopht-05-1653404-g004.jpg

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Validation of a deep learning model for the automated detection and quantification of cystoid macular oedema on optical coherence tomography in patients with retinitis pigmentosa.用于自动检测和量化色素性视网膜炎患者光学相干断层扫描中黄斑囊样水肿的深度学习模型的验证
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一项前瞻性自然史登记研究的研究方案,该研究旨在调查色素性视网膜炎中炎症标志物与疾病进展之间的关系:RP-PRIMARY研究。
Jpn J Ophthalmol. 2025 Mar 5. doi: 10.1007/s10384-025-01179-2.
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Vitreomacular traction - a review.玻璃体黄斑牵拉——综述
Eye (Lond). 2025 Mar;39(4):710-717. doi: 10.1038/s41433-024-03576-2. Epub 2025 Jan 20.
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