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通过神秘的免疫球蛋白D激活免疫反应的治疗意义

The therapeutic implications of activated immune responses via the enigmatic immunoglobulin D.

作者信息

Nguyen Tue Gia

机构信息

IgD Mab Technology (IMT) Group, Sydney, NSW, Australia.

出版信息

Int Rev Immunol. 2022;41(2):107-122. doi: 10.1080/08830185.2020.1861265. Epub 2021 Jan 7.

DOI:10.1080/08830185.2020.1861265
PMID:33410368
Abstract

Immunoglobulin D (IgD) is an enigmatic antibody and the least appreciated member of the immunoglobulin (Ig) family. Since its discovery over half a century ago, the essence of its function in the immune system has been somewhat enigmatic and less well-defined than other antibody classes. Membrane-bound IgD (mIgD) is mostly recognized as B-cell receptor (BCR) while secreted IgD (sIgD) has been recently implicated in 'arming' basophils and mast cells in mucosal innate immunity. Activations of immune responses via mIgD-BCR or sIgD by specific antigens or anti-IgD antibody thereby produce a broad and complex mix of cellular, antibody and cytokine responses from both the innate and adaptive immune systems. Such broadly activated immune responses via IgD were initially deemed to potentiate and exacerbate the onset of autoimmune and allergic conditions. Paradoxically, treatments with anti-IgD antibody suppressed and ameliorated autoimmune conditions and allergic inflammations in mouse models without compromising the host's general immune defence, demonstrating a unique and novel therapeutic application for anti-IgD antibody treatment. Herein, this review endeavored to collate and summarize the evidence of the unique characteristics and features of activated immune responses via mIgD-BCR and sIgD that revealed an unappreciated immune-regulatory function of IgD in the immune system via an amplifying loop of anti-inflammatory Th2 and tolerogenic responses, and highlighted a novel therapeutic paradigm in harnessing these immune responses to treat human autoimmune and allergic conditions.

摘要

免疫球蛋白D(IgD)是一种神秘的抗体,也是免疫球蛋白(Ig)家族中最不为人所重视的成员。自半个多世纪前被发现以来,其在免疫系统中的功能本质一直有些神秘,而且与其他抗体类别相比,其定义也不够明确。膜结合型IgD(mIgD)大多被认为是B细胞受体(BCR),而分泌型IgD(sIgD)最近被认为在黏膜固有免疫中“武装”嗜碱性粒细胞和肥大细胞。通过mIgD-BCR或sIgD被特定抗原或抗IgD抗体激活免疫反应,从而产生来自固有免疫系统和适应性免疫系统的广泛而复杂的细胞、抗体和细胞因子反应组合。这种通过IgD广泛激活的免疫反应最初被认为会增强和加剧自身免疫和过敏疾病的发作。矛盾的是,在小鼠模型中,用抗IgD抗体治疗可抑制和改善自身免疫疾病和过敏性炎症,而不会损害宿主的一般免疫防御,这表明抗IgD抗体治疗具有独特而新颖的治疗应用。在此,本综述致力于整理和总结通过mIgD-BCR和sIgD激活免疫反应的独特特征和特性的证据,这些证据揭示了IgD在免疫系统中通过抗炎性Th2和耐受性反应的放大环具有未被认识的免疫调节功能,并强调了利用这些免疫反应治疗人类自身免疫和过敏疾病的一种新的治疗模式。

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