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本文引用的文献

1
Detection of linear IgE deposits in bullous pemphigoid and mucous membrane pemphigoid: a useful clue for diagnosis.在大疱性类天疱疮和黏膜类天疱疮中检测线性 IgE 沉积:诊断的有用线索。
Br J Dermatol. 2011 Nov;165(5):1133-7. doi: 10.1111/j.1365-2133.2011.10481.x.
2
FcR-independent effects of IgE and IgG autoantibodies in bullous pemphigoid.免疫球蛋白 E 和免疫球蛋白 G 自身抗体在大疱性类天疱疮中的 FcR 非依赖性作用。
J Immunol. 2011 Jul 1;187(1):553-60. doi: 10.4049/jimmunol.1001753. Epub 2011 Jun 6.
3
A novel ELISA reveals high frequencies of BP180-specific IgE production in bullous pemphigoid.一种新型酶联免疫吸附测定法显示,大疱性类天疱疮患者中BP180特异性IgE产生的频率很高。
J Immunol Methods. 2009 Jul 31;346(1-2):18-25. doi: 10.1016/j.jim.2009.04.013. Epub 2009 May 5.
4
IgG from patients with bullous pemphigoid depletes cultured keratinocytes of the 180-kDa bullous pemphigoid antigen (type XVII collagen) and weakens cell attachment.大疱性类天疱疮患者的IgG可使培养的角质形成细胞中的180 kDa大疱性类天疱疮抗原(XVII型胶原蛋白)耗竭,并削弱细胞黏附。
J Invest Dermatol. 2009 Apr;129(4):919-26. doi: 10.1038/jid.2008.305. Epub 2009 Jan 29.
5
Pathogenicity of IgE in autoimmunity: successful treatment of bullous pemphigoid with omalizumab.IgE在自身免疫中的致病性:奥马珠单抗成功治疗大疱性类天疱疮
J Allergy Clin Immunol. 2009 Mar;123(3):704-5. doi: 10.1016/j.jaci.2008.11.035. Epub 2009 Jan 18.
6
Subepidermal blistering induced by human autoantibodies to BP180 requires innate immune players in a humanized bullous pemphigoid mouse model.在人源化大疱性类天疱疮小鼠模型中,人抗BP180自身抗体诱导的表皮下水疱形成需要天然免疫参与者。
J Autoimmun. 2008 Dec;31(4):331-8. doi: 10.1016/j.jaut.2008.08.009. Epub 2008 Oct 14.
7
A pathogenic role for IgE in autoimmunity: bullous pemphigoid IgE reproduces the early phase of lesion development in human skin grafted to nu/nu mice.IgE在自身免疫中的致病作用:大疱性类天疱疮IgE可重现移植到裸鼠的人皮肤病变发展的早期阶段。
J Invest Dermatol. 2007 Nov;127(11):2605-11. doi: 10.1038/sj.jid.5700958. Epub 2007 Jul 5.
8
Humanization of autoantigen.自身抗原人源化
Nat Med. 2007 Mar;13(3):378-83. doi: 10.1038/nm1496. Epub 2007 Feb 25.
9
IgE basement membrane zone antibodies induce eosinophil infiltration and histological blisters in engrafted human skin on SCID mice.IgE 基底膜带抗体可诱导嗜酸性粒细胞浸润,并在重症联合免疫缺陷(SCID)小鼠移植的人皮肤中形成组织学水疱。
J Invest Dermatol. 2007 May;127(5):1167-74. doi: 10.1038/sj.jid.5700681. Epub 2007 Jan 18.
10
The NC16A domain of collagen XVII plays a role in triple helix assembly and stability.胶原蛋白 XVII 的 NC16A 结构域在三螺旋组装和稳定性中发挥作用。
Biochem Biophys Res Commun. 2006 Dec 1;350(4):1032-7. doi: 10.1016/j.bbrc.2006.09.147. Epub 2006 Oct 5.

一种针对大疱性类天疱疮自身抗原BP180的IgE类单克隆抗体的功能特性

Functional characterization of an IgE-class monoclonal antibody specific for the bullous pemphigoid autoantigen, BP180.

作者信息

Messingham Kelly A N, Onoh Amber, Vanderah Elizabeth M, Giudice George J, Fairley Janet A

机构信息

Department of Dermatology, The University of Iowa, Iowa City, Iowa, USA.

出版信息

Hybridoma (Larchmt). 2012 Apr;31(2):111-7. doi: 10.1089/hyb.2011.0102.

DOI:10.1089/hyb.2011.0102
PMID:22509915
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3326270/
Abstract

BP180 (collagen XVII) is the target antigen in several autoimmune diseases including bullous pemphigoid (BP). Both IgE and IgG class autoantibodies have been shown to be pathogenic in BP; however, studies designed to elucidate the patho-mechanisms mediated specifically by the IgE-class autoantibodies are limited by the low levels (ng/mL) of IgE in human sera. In this report, we developed mouse IgE class monoclonal antibodies (MAbs) against the immunodominant NC16A domain of the human BP180 protein and characterized two of the resultant MAbs, designated 395A5 and 395D2. Epitope mapping studies revealed that both MAbs target segment 2 of NC16A, as was described for IgE and IgG class BP autoantibodies. Also similar to BP IgE, MAb 395A5 showed indirect immunofluorescence labeling of the basement membrane zone (BMZ) of human skin, stimulated histamine release from mast cells when triggered with NC16A, and induced keratinocyte production of IL-8. The 395D2 MAb was also able to trigger antigen-specific histamine release from mast cells; however, in contrast to BP IgE and 395A5, 395D2 did not label the cutaneous BMZ, nor did it induce IL-8 production in keratinocytes. In summary, these studies underscore the importance of functionally characterizing MAbs generated for use in human disease models. The 395A5 IgE class murine MAb was shown to share several key functional properties with the pathogenically active IgE produced by BP patients. We therefore expect that this MAb will prove to be a useful tool for dissecting the mechanisms used by BP180-NC16A-specific IgE antibodies in the induction of BP skin lesions.

摘要

BP180(XVII型胶原蛋白)是包括大疱性类天疱疮(BP)在内的多种自身免疫性疾病中的靶抗原。IgE和IgG类自身抗体在BP中均已被证明具有致病性;然而,旨在阐明由IgE类自身抗体特异性介导的发病机制的研究受到人血清中IgE低水平(ng/mL)的限制。在本报告中,我们开发了针对人BP180蛋白免疫显性NC16A结构域的小鼠IgE类单克隆抗体(MAb),并对其中两种命名为395A5和395D2的所得MAb进行了表征。表位作图研究表明,这两种MAb均靶向NC16A的第2段,这与IgE和IgG类BP自身抗体的情况相同。同样与BP IgE相似,MAb 395A5显示出对人皮肤基底膜带(BMZ)的间接免疫荧光标记,当用NC16A触发时可刺激肥大细胞释放组胺,并诱导角质形成细胞产生IL-8。395D2 MAb也能够触发肥大细胞释放抗原特异性组胺;然而,与BP IgE和395A5不同,395D2未标记皮肤BMZ,也未在角质形成细胞中诱导IL-8产生。总之,这些研究强调了对用于人类疾病模型的MAb进行功能表征的重要性。395A5 IgE类鼠源MAb被证明与BP患者产生的具有致病活性的IgE具有几个关键的功能特性。因此,我们预计这种MAb将被证明是剖析BP180-NC16A特异性IgE抗体在诱导BP皮肤病变中所使用机制的有用工具。