疾病中的免疫球蛋白G糖基化。

Marija Pezer
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引用次数: 1

摘要

免疫球蛋白G (IgG)糖基化模式的改变已经在大量自身免疫和同种免疫、感染性、心脏代谢、恶性和其他疾病中被观察到。本章包含超过140项研究的更新目录,其中IgG糖基化分析在疾病环境中进行。由于已知IgG聚糖的组成可以调节其效应物的功能,因此表明患者体内IgG糖基化模式的改变可能与疾病的发生和进展有关,代表疾病病理中的易感性和/或功能性效应物。与可能与全身性炎症背景相关的大量血清IgG的糖基化模式相反,抗原特异性IgG的糖基化谱可能在几种感染性、同种异体和自身免疫性抗体依赖疾病的疾病病理中起直接作用。根据任何特定疾病的具体情况,IgG糖基化读数可能因此在未来发展成为一种有用的临床生物标志物或对当前使用的生物标志物的补充。
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Immunoglobulin G Glycosylation in Diseases.

Changes in immunoglobulin G (IgG) glycosylation pattern have been observed in a vast array of auto- and alloimmune, infectious, cardiometabolic, malignant, and other diseases. This chapter contains an updated catalog of over 140 studies within which IgG glycosylation analysis was performed in a disease setting. Since the composition of IgG glycans is known to modulate its effector functions, it is suggested that a changed IgG glycosylation pattern in patients might be involved in disease development and progression, representing a predisposition and/or a functional effector in disease pathology. In contrast to the glycopattern of bulk serum IgG, which likely relates to the systemic inflammatory background, the glycosylation profile of antigen-specific IgG probably plays a direct role in disease pathology in several infectious and allo- and autoimmune antibody-dependent diseases. Depending on the specifics of any given disease, IgG glycosylation read-out might therefore in the future be developed into a useful clinical biomarker or a supplementary to currently used biomarkers.

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来源期刊
Experientia supplementum (2012)
Experientia supplementum (2012) Medicine-Medicine (all)
CiteScore
3.30
自引率
0.00%
发文量
24
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