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免疫球蛋白A抗体:从保护作用到有害作用

Immunoglobulin A Antibodies: From Protection to Harmful Roles.

作者信息

Gleeson Patrick J, Camara Niels O S, Launay Pierre, Lehuen Agnès, Monteiro Renato C

机构信息

Center for Research on Inflammation, Paris Cité University, Paris, France.

INSERM, Paris, France.

出版信息

Immunol Rev. 2024 Nov;328(1):171-191. doi: 10.1111/imr.13424. Epub 2024 Nov 23.

DOI:10.1111/imr.13424
PMID:39578936
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11659943/
Abstract

Immunoglobulin A (IgA) is the most abundantly produced antibody in humans. IgA is a unique class of immunoglobulin due to its multiple molecular forms, and a defining difference between the two subclasses: IgA1 has a long hinge-region that is heavily O-glycosylated, whereas the IgA2 hinge-region is shorter but resistant to bacterial proteases prevalent at mucosal sites. IgA is essential for immune homeostasis and education. Mucosal IgA plays a crucial role in maintaining the integrity of the mucosal barrier by immune exclusion of pathobionts while facilitating colonization with certain commensals; a large part of the gut microbiota is coated with IgA. In the circulation, monomeric IgA that has not been engaged by antigen plays a discrete role in dampening inflammatory responses. Protective and harmful roles of IgA have been studied over several decades, but a new understanding of the complex role of this immunoglobulin in health and disease has been provided by recent studies. Here, we discuss the physiological and pathological roles of IgA with a special focus on the gut, kidneys, and autoimmunity. We also discuss new IgA-based therapeutic approaches.

摘要

免疫球蛋白A(IgA)是人类产生量最为丰富的抗体。由于其多种分子形式,IgA是一类独特的免疫球蛋白,并且两个亚类之间存在一个决定性差异:IgA1具有一个长的铰链区,该区域高度O-糖基化,而IgA2的铰链区较短,但对粘膜部位普遍存在的细菌蛋白酶具有抗性。IgA对于免疫稳态和免疫调节至关重要。粘膜IgA通过对致病共生菌进行免疫排斥,同时促进某些共生菌的定植,在维持粘膜屏障的完整性方面发挥着关键作用;肠道微生物群的很大一部分都被IgA覆盖。在循环系统中,未与抗原结合的单体IgA在减轻炎症反应中发挥着独特作用。几十年来人们一直在研究IgA的保护作用和有害作用,但最近的研究为这种免疫球蛋白在健康和疾病中的复杂作用提供了新的认识。在此,我们将讨论IgA的生理和病理作用,特别关注肠道、肾脏和自身免疫。我们还将讨论基于IgA的新治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1d07/11659943/d826aacdc57d/IMR-328-171-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1d07/11659943/db130bb8f8a1/IMR-328-171-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1d07/11659943/c9aeff720f5f/IMR-328-171-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1d07/11659943/afdbf0fd7035/IMR-328-171-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1d07/11659943/d826aacdc57d/IMR-328-171-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1d07/11659943/db130bb8f8a1/IMR-328-171-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1d07/11659943/c9aeff720f5f/IMR-328-171-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1d07/11659943/afdbf0fd7035/IMR-328-171-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1d07/11659943/d826aacdc57d/IMR-328-171-g002.jpg

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本文引用的文献

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The function of antibodies.抗体的功能。
Immunol Rev. 2024 Nov;328(1):113-125. doi: 10.1111/imr.13387. Epub 2024 Aug 24.
2
The gut microbiota posttranslationally modifies IgA1 in autoimmune glomerulonephritis.肠道微生物群在自身免疫性肾小球肾炎中对 IgA1 进行翻译后修饰。
Sci Transl Med. 2024 Mar 27;16(740):eadl6149. doi: 10.1126/scitranslmed.adl6149.
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Immunology of Kidney Disease.肾脏疾病免疫学
Annu Rev Immunol. 2024 Jun;42(1):207-233. doi: 10.1146/annurev-immunol-090122-045843. Epub 2024 Jun 14.
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Each N-glycan on human IgA and J-chain uniquely affects oligomericity and stability.人 IgA 和 J 链上的每个 N-聚糖独特地影响寡聚体形成和稳定性。
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Divergent metabolic programmes control two populations of MAIT cells that protect the lung.不同的代谢程序控制着保护肺部的两个 MAIT 细胞群。
Nat Cell Biol. 2023 Jun;25(6):877-891. doi: 10.1038/s41556-023-01152-6. Epub 2023 May 25.
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Targeting MAIT cells as a cellular adjuvant for humoral immunity: a new player in a very old game.针对 MAIT 细胞作为体液免疫的细胞佐剂:一个非常古老游戏中的新角色。
Immunol Cell Biol. 2023 Jul;101(6):470-472. doi: 10.1111/imcb.12648. Epub 2023 May 3.
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Antagonizing FcαR1 (CD89) as treatment in IgA-mediated chronic inflammation and autoimmunity.拮抗 FcαR1(CD89)治疗 IgA 介导的慢性炎症和自身免疫。
Front Immunol. 2023 Apr 4;14:1118539. doi: 10.3389/fimmu.2023.1118539. eCollection 2023.
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MAIT cells activate dendritic cells to promote T cell differentiation and induce humoral immunity.MAIT 细胞激活树突状细胞,促进 T 细胞分化,并诱导体液免疫。
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Identification of IgA autoantibodies targeting mesangial cells redefines the pathogenesis of IgA nephropathy.针对系膜细胞的 IgA 自身抗体的鉴定重新定义了 IgA 肾病的发病机制。
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Gut-kidney axis in IgA nephropathy: Role on mesangial cell metabolism and inflammation.IgA肾病中的肠-肾轴:对系膜细胞代谢和炎症的作用
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