Chen Zhixian, Xu Xiaojia, Song Manshu, Lin Ling
Department of Rheumatology and Immunology, The First Affiliated Hospital of Shantou University Medical College, Shantou, China.
Centre for Precision Health, Edith Cowan University, Perth, Australia.
OMICS. 2024 Dec;28(12):608-619. doi: 10.1089/omi.2024.0176. Epub 2024 Nov 25.
The crosstalk between cytokines and immunoglobulin G (IgG) -glycosylation forms a bidirectional regulatory network that significantly impacts inflammation and immune function. This review examines how various cytokines, both pro- and anti-inflammatory, modulate IgG -glycosylation, shaping antibody activity and influencing inflammatory responses. In addition, we explore how altered IgG -glycosylation patterns affect cytokine production and immune signaling, either promoting or reducing inflammation. Through a comprehensive analysis of current studies, this review underscores the dynamic relationship between cytokines and IgG -glycosylation. These insights enhance our understanding of the mechanisms underlying inflammatory diseases and contribute to improved strategies for disease prevention, diagnosis, monitoring, prognosis, and the exploration of novel treatment options. By focusing on this crosstalk, we identify new avenues for developing innovative diagnostic tools and therapies to improve patient outcomes in inflammatory diseases.
细胞因子与免疫球蛋白G(IgG)糖基化之间的相互作用形成了一个双向调节网络,该网络对炎症和免疫功能有显著影响。本综述探讨了各种促炎和抗炎细胞因子如何调节IgG糖基化,塑造抗体活性并影响炎症反应。此外,我们还探讨了改变的IgG糖基化模式如何影响细胞因子的产生和免疫信号传导,从而促进或减少炎症。通过对当前研究的全面分析,本综述强调了细胞因子与IgG糖基化之间的动态关系。这些见解加深了我们对炎症性疾病潜在机制的理解,并有助于改进疾病预防、诊断、监测、预后的策略以及探索新的治疗选择。通过关注这种相互作用,我们确定了开发创新诊断工具和疗法的新途径,以改善炎症性疾病患者的预后。