雌激素驱动免疫球蛋白G - Fc糖基化的变化。

Q2 Medicine
Kaitlyn A Lagattuta, Peter A Nigrovic
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引用次数: 5

摘要

免疫球蛋白G (IgG) Fc区的糖基化调节其参与补体和Fc受体的能力,从而提供微调效应功能的机会。调节IgG Fc聚糖的机制仍然知之甚少。月经初潮、更年期和怀孕的变化长期以来都与激素因素有关。干预研究现在证实,雌激素增强了女性和男性中IgG Fc半乳糖基化,确定了调节Fc聚糖的第一条途径,从而在性别和免疫之间建立了新的联系。这一机制可能参与胎儿-母体免疫、抗体介导的炎症以及年龄和性别特异性免疫功能的其他方面。在这里,我们回顾了从童年到老年影响IgG Fc血糖的变化,确立雌激素作用的证据,以及揭示可能为治疗干预提供信息的相关机制的研究方向。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Estrogen-Driven Changes in Immunoglobulin G Fc Glycosylation.

Glycosylation within the immunoglobulin G (IgG) Fc region modulates its ability to engage complement and Fc receptors, affording the opportunity to fine-tune effector functions. Mechanisms regulating IgG Fc glycans remain poorly understood. Changes accompanying menarche, menopause, and pregnancy have long implicated hormonal factors. Intervention studies now confirm that estrogens enhance IgG Fc galactosylation, in females and also in males, defining the first pathway modulating Fc glycans and thereby a new link between sex and immunity. This mechanism may participate in fetal-maternal immunity, antibody-mediated inflammation, and other aspects of age- and sex-specific immune function. Here we review the changes affecting the IgG Fc glycome from childhood through old age, the evidence establishing a role for estrogens, and research directions to uncover associated mechanisms that may inform therapeutic intervention.

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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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