通过神秘免疫球蛋白D激活免疫反应的治疗意义。

IF 4.3 4区 医学 Q2 IMMUNOLOGY International Reviews of Immunology Pub Date : 2022-01-01 Epub Date: 2021-01-07 DOI:10.1080/08830185.2020.1861265
Tue Gia Nguyen
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引用次数: 2

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)家族中最不受重视的成员。自从它在半个多世纪前被发现以来,它在免疫系统中功能的本质一直有点神秘,而且比其他抗体类别更不明确。膜结合型IgD (mIgD)主要被认为是b细胞受体(BCR),而分泌型IgD (sIgD)最近被认为与粘膜先天免疫中的“武装”嗜碱性细胞和肥大细胞有关。特异性抗原或抗igd抗体通过mIgD-BCR或sIgD激活免疫反应,从而产生来自先天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。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性和过敏性疾病的发作。矛盾的是,抗igd抗体治疗抑制和改善了小鼠模型中的自身免疫性疾病和过敏性炎症,而不损害宿主的一般免疫防御,证明了抗igd抗体治疗的独特和新颖的治疗应用。在此,本综述试图整理和总结通过mIgD-BCR和sIgD激活的免疫反应的独特特征和特征的证据,揭示了IgD在免疫系统中通过抗炎Th2和耐受性反应的放大回路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性和过敏性疾病的新治疗范式。
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The therapeutic implications of activated immune responses via the enigmatic immunoglobulin D.

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.

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来源期刊
CiteScore
11.00
自引率
4.00%
发文量
24
期刊介绍: This review journal provides the most current information on basic and translational research in immunology and related fields. In addition to invited reviews, the journal accepts for publication articles and editorials on relevant topics proposed by contributors. Each issue of International Reviews of Immunology contains both solicited and unsolicited review articles, editorials, and ''In-this-Issue'' highlights. The journal also hosts reviews that position the authors'' original work relative to advances in a given field, bridging the gap between annual reviews and the original research articles. This review series is relevant to all immunologists, molecular biologists, microbiologists, translational scientists, industry researchers, and physicians who work in basic and clinical immunology, inflammatory and allergic diseases, vaccines, and additional topics relevant to medical research and drug development that connect immunology to disciplines such as oncology, cardiovascular disease, and metabolic disorders. Covered in International Reviews of Immunology: Basic and developmental immunology (innate and adaptive immunity; inflammation; and tumor and microbial immunology); Clinical research (mechanisms of disease in man pertaining to infectious diseases, autoimmunity, allergy, oncology / immunology); and Translational research (relevant to biomarkers, diagnostics, vaccines, and drug development).
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