我们能通过靶向IgG糖组来抑制慢性全身炎症并延缓与年龄相关的疾病吗?

IF 4.6 2区 医学 Q1 PHARMACOLOGY & PHARMACY
Expert Opinion on Therapeutic Targets Pub Date : 2024-06-01 Epub Date: 2023-11-02 DOI:10.1080/14728222.2023.2277218
GordAn Lauc
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引用次数: 0

摘要

简介:与免疫球蛋白G相连的甘氨酸是慢性全身炎症的重要调节因子,也是衰老的关键驱动因素之一。随着年龄的增长,抑制炎症的聚糖正被促进炎症的聚糖所取代,但这种转化率是高度个体化的,并受到遗传、表观遗传和环境因素的影响。涵盖领域:这篇综述总结了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糖基化度的机制的关键研究。专家意见:IgG糖组是衰老过程的重要因素,可以通过生活方式和药物干预来调节。通过调节IgG糖组来抑制慢性全身炎症的小分子药物仍然不可用,但由于调节IgG糖基化的基因网络已经被确定,并且高通量体外筛选系统已经可用,这种高度创新的慢性全身炎症管理方法很可能很快就会开发出来。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Can we suppress chronic systemic inflammation and postpone age-related diseases by targeting the IgG glycome?

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 in vitro screening system is available, it is likely that this highly innovative approach to manage chronic systemic inflammation will be developed soon.

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来源期刊
CiteScore
8.90
自引率
1.70%
发文量
58
审稿时长
3 months
期刊介绍: The journal evaluates molecules, signalling pathways, receptors and other therapeutic targets and their potential as candidates for drug development. Articles in this journal focus on the molecular level and early preclinical studies. Articles should not include clinical information including specific drugs and clinical trials. The Editors welcome: Reviews covering novel disease targets at the molecular level and information on early preclinical studies and their implications for future drug development. Articles should not include clinical information including specific drugs and clinical trials. Original research papers reporting results of target selection and validation studies and basic mechanism of action studies for investigative and marketed drugs. The audience consists of scientists, managers and decision makers in the pharmaceutical industry, academic researchers working in the field of molecular medicine and others closely involved in R&D.
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