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我们能否通过靶向 IgG 聚糖来抑制慢性系统性炎症并延缓与年龄相关的疾病?

Can we suppress chronic systemic inflammation and postpone age-related diseases by targeting the IgG glycome?

机构信息

University of Zagreb Faculty of Pharmacy and Biochemistry & Genos Glycoscience Research Laboratory, Zagreb, Croatia.

出版信息

Expert Opin Ther Targets. 2024 Jun;28(6):491-499. doi: 10.1080/14728222.2023.2277218. Epub 2023 Nov 2.

Abstract

INTRODUCTION

Glycans attached to immunoglobulin G are an important regulator of chronic systemic inflammation, one of the key drivers of aging. As people age, glycans that suppress inflammation are being replaced with inflammation-promoting glycans, but the rate of this conversion is highly individual and is affected by genetic, epigenetic, and environmental factors.

AREAS COVERED

This review summarizes key studies of IgG glycosylation changes in aging and disease, effects of lifestyle and pharmacological interventions, and mechanisms that regulate IgG glycosylation.

EXPERT OPINION

IgG glycome is an important contributor to the process of aging that can be modulated by both lifestyle and pharmacological interventions. Small molecule drugs that would suppress chronic systemic inflammation by modulation of the IgG glycome are still not available, but since gene network regulating IgG glycosylation has been identified and a high-throughput screening system is available, it is likely that this highly innovative approach to manage chronic systemic inflammation will be developed soon.

摘要

简介

免疫球蛋白 G 上的聚糖是慢性全身炎症的一个重要调节剂,而慢性全身炎症是衰老的关键驱动因素之一。随着人们年龄的增长,抑制炎症的聚糖被促炎聚糖所取代,但这种转换的速度具有高度个体差异,受到遗传、表观遗传和环境因素的影响。

涵盖领域

本篇综述总结了 IgG 糖基化在衰老和疾病中的变化、生活方式和药物干预的影响,以及调节 IgG 糖基化的机制等方面的关键研究。

专家意见

IgG 聚糖组是衰老过程中的一个重要贡献者,它可以通过生活方式和药物干预来调节。目前还没有能够通过调节 IgG 聚糖组来抑制慢性全身炎症的小分子药物,但由于已经确定了调节 IgG 糖基化的基因网络,并且有高通量筛选系统可用,因此很可能很快就会开发出这种管理慢性全身炎症的创新性方法。

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