国际眼科纵览 ›› 2026, Vol. 50 ›› Issue (1): 15-21.doi: 10.3760/cma.i.cn115500-20251009-26103

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IgG N-糖基化的结构与效应功能及其在眼病中的研究进展

廖海兵 张铭志   

  1. 汕头大学·香港中文大学联合汕头国际眼科中心,广东汕头 515041
  • 收稿日期:2025-10-09 出版日期:2026-02-22 发布日期:2026-02-22
  • 通讯作者: 张铭志,Email:zmz@jsiec.org
  • 基金资助:
    广东省普通高校重点科研平台和项目(2022LSYS006、2023KCXTD013)

Structural characteristics, effector functions, and research advances of IgG N-glycosylation in ocular diseases

Liao Haibing, Zhang Mingzhi   

  1. Joint Shantou International Eye Center of Shantou University and The Chinese University of Hongkong, Shantou Guangdong 515041, China
  • Received:2025-10-09 Online:2026-02-22 Published:2026-02-22
  • Contact: Zhang Mingzhi,Email: zmz@jsiec.org
  • Supported by:
    Key Reasearch Platforms and Project of Guangdong Provincial Universites(2022LSYS00, 2023KCXTD013)

摘要: 免疫球蛋白G(immunoglobulin G,IgG)的N-糖基化是一种关键的翻译后修饰,其结构多样性显著影响IgG的效应功能。IgG N-糖基化的合成涉及内质网和高尔基体中多种酶的协同作用。随着糖组学分析技术的进步,IgG N-糖基化在眼部疾病中的研究也备受关注。在糖尿病视网膜病变中,IgG半乳糖基化、岩藻糖基化和唾液酸化水平下降,可能通过增强补体激活与炎性反应,造成微血管损伤和神经视网膜病变;在年龄相关性黄斑变性中,疾病进展伴随糖基化模式的动态演变,早阶段可见免疫调节性改变,晚期则呈现显著促炎特征;在视神经脊髓炎谱系疾病中,急性期患者IgG半乳糖基化水平降低与疾病严重程度相关,此外,IgG Fc区及Fab区特定糖型的改变,可有效鉴别视神经脊髓炎谱系疾病与多发性硬化。IgG N-糖基化不仅为理解眼病免疫炎症机制提供了新视角,也展现出作为疾病诊断、分期及鉴别诊断生物标志物的潜力。

关键词: IgG, N-糖基化, 眼部疾病, 生物标志物

Abstract: Immunoglobulin G (IgG) N-glycosylation is a critical post-translational modification whose structural diversity significantly influences the effector functions of IgG. The biosynthesis of IgG N-glycosylation involves the coordinated action of multiple enzymes in the endoplasmic reticulum and Golgi apparatus. With advances in glycomics analysis techniques, research on IgG N-glycosylation in ocular diseases has attracted considerable attention. In diabetic retinopathy, decreased levels of IgGgalactosylation, fucosylation, and sialylation may contribute to microvascular damage and neuroretinopathy by enhancing complement activation and inflammatory responses. In age-related macular degeneration, disease progression is accompanied by dynamic changes in glycosylation patterns, with immunomodulatory alterations observed in early stages and pronounced pro-inflammatory features in advanced disease. In neuromyelitisoptica spectrum disorders, reduced IgGgalactosylation is associated with disease severity during acute phases, and specific glycoform alterations in the Fc and Fab regions of IgG can effectively differentiate neuromyelitisoptica spectrum disorders from multiple sclerosis. IgG N-glycosylation not only provides a new perspective for understanding the immune-inflammatory mechanisms underlying ocular diseases but also demonstrates potential as a biomarker for disease diagnosis, staging, and differential diagnosis.

Key words: IgG, N-glycosylation, Eye diseases, Biomarker