• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

相似文献

1
Blockade of autoantibody-initiated tissue damage by using recombinant fab antibody fragments against pathogenic autoantigen.利用针对致病性自身抗原的重组 Fab 抗体片段阻断自身抗体引发的组织损伤。
Am J Pathol. 2010 Feb;176(2):914-25. doi: 10.2353/ajpath.2010.090744. Epub 2009 Dec 30.
2
Anti-collagen XVII single-chain Fv antibody blocks the autoimmune reaction mediated by pathogenic autoantibodies in bullous pemphigoid.抗胶原蛋白 XVII 单链 Fv 抗体可阻断大疱性类天疱疮中致病性自身抗体介导的自身免疫反应。
J Dermatol Sci. 2013 Oct;72(1):25-31. doi: 10.1016/j.jdermsci.2013.05.010. Epub 2013 Jun 13.
3
Antibodies to pathogenic epitopes on type XVII collagen cause skin fragility in a complement-dependent and -independent manner.抗 XVII 型胶原致病性表位的抗体以补体依赖和非依赖的方式导致皮肤脆弱。
J Immunol. 2012 Jun 1;188(11):5792-9. doi: 10.4049/jimmunol.1003402. Epub 2012 Apr 20.
4
Bullous pemphigoid autoantibodies directly induce blister formation without complement activation.大疱性类天疱疮自身抗体可直接诱导水疱形成,而无需补体激活。
J Immunol. 2014 Nov 1;193(9):4415-28. doi: 10.4049/jimmunol.1400095. Epub 2014 Sep 26.
5
Patients with bullous pemphigoid and linear IgA disease show a dual IgA and IgG autoimmune response to BP180.大疱性类天疱疮和线状IgA大疱性皮病患者对BP180表现出IgA和IgG双重自身免疫反应。
J Autoimmun. 2000 Nov;15(3):293-300. doi: 10.1006/jaut.2000.0437.
6
Immune Reaction to Type XVII Collagen Induces Intramolecular and Intermolecular Epitope Spreading in Experimental Bullous Pemphigoid Models.免疫反应对 XVII 型胶原诱导实验性大疱性类天疱疮模型中的分子内和分子间表位扩展。
Front Immunol. 2019 Jun 19;10:1410. doi: 10.3389/fimmu.2019.01410. eCollection 2019.
7
Human IgG1 monoclonal antibody against human collagen 17 noncollagenous 16A domain induces blisters via complement activation in experimental bullous pemphigoid model.针对人胶原蛋白 17 非胶原 16A 结构域的人 IgG1 单克隆抗体通过补体激活在实验性大疱性类天疱疮模型中诱导水疱。
J Immunol. 2010 Dec 15;185(12):7746-55. doi: 10.4049/jimmunol.1000667. Epub 2010 Nov 12.
8
Autoantibodies to bullous pemphigoid antigen 180 induce dermal-epidermal separation in cryosections of human skin.针对大疱性类天疱疮抗原180的自身抗体在人皮肤冰冻切片中诱导真皮-表皮分离。
J Invest Dermatol. 2002 Apr;118(4):664-71. doi: 10.1046/j.1523-1747.2002.01720.x.
9
Preferential Reactivity of Dipeptidyl Peptidase-IV Inhibitor-Associated Bullous Pemphigoid Autoantibodies to the Processed Extracellular Domains of BP180.二肽基肽酶-4 抑制剂相关性大疱性类天疱疮自身抗体对 BP180 细胞外结构域的优先反应性。
Front Immunol. 2019 May 29;10:1224. doi: 10.3389/fimmu.2019.01224. eCollection 2019.
10
IgG antibodies against immunodominant C-terminal epitopes of BP230 do not induce skin blistering in mice.针对BP230免疫显性C末端表位的IgG抗体不会在小鼠中诱发皮肤水疱。
Hum Immunol. 2014 Apr;75(4):354-63. doi: 10.1016/j.humimm.2014.01.005. Epub 2014 Jan 24.

引用本文的文献

1
Bullous pemphigoid.大疱性类天疱疮
Nat Rev Dis Primers. 2025 Feb 20;11(1):12. doi: 10.1038/s41572-025-00595-5.
2
Insights Into the Pathogenesis of Bullous Pemphigoid: The Role of Complement-Independent Mechanisms.大疱性类天疱疮发病机制的研究进展:补体非依赖机制的作用。
Front Immunol. 2022 Jul 7;13:912876. doi: 10.3389/fimmu.2022.912876. eCollection 2022.
3
Pemphigus and Pemphigoid: From Disease Mechanisms to Druggable Pathways.天疱疮和类天疱疮:从疾病机制到可用药的途径。
J Invest Dermatol. 2022 Mar;142(3 Pt B):907-914. doi: 10.1016/j.jid.2021.04.040. Epub 2021 Oct 29.
4
Decreased expression levels of complement regulator CD55 contribute to the development of bullous pemphigoid.补体调节蛋白CD55表达水平降低促成大疱性类天疱疮的发展。
Oncotarget. 2017 Sep 23;9(85):35517-35527. doi: 10.18632/oncotarget.21216. eCollection 2018 Oct 30.
5
BP180 Is Critical in the Autoimmunity of Bullous Pemphigoid.BP180在大疱性类天疱疮的自身免疫中起关键作用。
Front Immunol. 2017 Dec 8;8:1752. doi: 10.3389/fimmu.2017.01752. eCollection 2017.
6
Dysregulation of mCD46 and sCD46 contribute to the pathogenesis of bullous pemphigoid.mCD46 和 sCD46 的失调导致大疱性类天疱疮的发病机制。
Sci Rep. 2017 Mar 10;7(1):145. doi: 10.1038/s41598-017-00235-3.
7
Rituximab therapy in pemphigus and other autoantibody-mediated diseases.利妥昔单抗在天疱疮及其他自身抗体介导疾病中的治疗应用。
F1000Res. 2017 Jan 27;6:83. doi: 10.12688/f1000research.9476.1. eCollection 2017.
8
Kavain Inhibition of LPS-Induced TNF-α via ERK/LITAF.卡瓦因通过ERK/LITAF抑制脂多糖诱导的肿瘤坏死因子-α
Toxicol Res (Camb). 2016 Jan 1;5(1):188-196. doi: 10.1039/C5TX00164A. Epub 2015 Oct 21.
9
Mechanisms of Disease: Pemphigus and Bullous Pemphigoid.疾病机制:天疱疮和大疱性类天疱疮。
Annu Rev Pathol. 2016 May 23;11:175-97. doi: 10.1146/annurev-pathol-012615-044313. Epub 2016 Feb 22.
10
Shared VH1-46 gene usage by pemphigus vulgaris autoantibodies indicates common humoral immune responses among patients.寻常型天疱疮自身抗体对VH1-46基因的共同使用表明患者之间存在共同的体液免疫反应。
Nat Commun. 2014 Jun 19;5:4167. doi: 10.1038/ncomms5167.

本文引用的文献

1
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.
2
Systemic lupus erythematosus.系统性红斑狼疮
Lancet. 2007 Feb 17;369(9561):587-96. doi: 10.1016/S0140-6736(07)60279-7.
3
Autoantibodies in rheumatoid arthritis: a review.类风湿关节炎中的自身抗体:综述
Biomed Pharmacother. 2006 Dec;60(10):648-55. doi: 10.1016/j.biopha.2006.09.002. Epub 2006 Oct 10.
4
Role of different pathways of the complement cascade in experimental bullous pemphigoid.补体级联反应不同途径在实验性大疱性类天疱疮中的作用
J Clin Invest. 2006 Nov;116(11):2892-900. doi: 10.1172/JCI17891. Epub 2006 Oct 5.
5
Role of FcRs in animal model of autoimmune bullous pemphigoid.Fc受体在自身免疫性大疱性类天疱疮动物模型中的作用。
J Immunol. 2006 Sep 1;177(5):3398-405. doi: 10.4049/jimmunol.177.5.3398.
6
Colocalization of multiple laminin isoforms predominantly beneath hemidesmosomes in the upper lamina densa of the epidermal basement membrane.多种层粘连蛋白异构体主要共定位于表皮基底膜致密层上部半桥粒下方。
J Histochem Cytochem. 2006 Jan;54(1):109-18. doi: 10.1369/jhc.5A6701.2005. Epub 2005 Sep 20.
7
Selecting and screening recombinant antibody libraries.选择和筛选重组抗体文库。
Nat Biotechnol. 2005 Sep;23(9):1105-16. doi: 10.1038/nbt1126.
8
Mapping the binding sites of anti-BP180 immunoglobulin E autoantibodies in bullous pemphigoid.绘制大疱性类天疱疮中抗BP180免疫球蛋白E自身抗体的结合位点
J Invest Dermatol. 2005 Sep;125(3):467-72. doi: 10.1111/j.0022-202X.2005.23853.x.
9
Interventions for bullous pemphigoid.大疱性类天疱疮的干预措施。
Cochrane Database Syst Rev. 2005 Jul 20(3):CD002292. doi: 10.1002/14651858.CD002292.pub2.
10
The pathophysiology of autoimmune blistering diseases.自身免疫性水疱病的病理生理学
J Clin Invest. 2005 Apr;115(4):825-8. doi: 10.1172/JCI24855.

利用针对致病性自身抗原的重组 Fab 抗体片段阻断自身抗体引发的组织损伤。

Blockade of autoantibody-initiated tissue damage by using recombinant fab antibody fragments against pathogenic autoantigen.

机构信息

Department of Dermatology, Hokkaido University Graduate School of Medicine, N15 W7, Sapporo, 060-8638 Japan.

出版信息

Am J Pathol. 2010 Feb;176(2):914-25. doi: 10.2353/ajpath.2010.090744. Epub 2009 Dec 30.

DOI:10.2353/ajpath.2010.090744
PMID:20042683
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2808096/
Abstract

Activation of the complement cascade via the classical pathway is required for the development of tissue injury in many autoantibody-mediated diseases. It therefore makes sense to block the pathological action of autoantibodies by preventing complement activation through inhibition of autoantibody binding to the corresponding pathogenic autoantigen using targeted Fab antibody fragments. To achieve this, we use bullous pemphigoid (BP) as an example of a typical autoimmune disease. Recombinant Fabs against the non-collagenous 16th-A domain of type XVII collagen, the main pathogenic epitope for autoantibodies in BP, were generated from antibody repertoires of BP patients by phage display. Two Fabs, Fab-B4 and Fab-19, showed marked ability to inhibit the binding of BP autoantibodies and subsequent complement activation in vitro. In the in vivo experiments using type XVII collagen humanized BP model mice, these Fabs protected mice against BP autoantibody-induced blistering disease. Thus, the blocking of pathogenic epitopes using engineered Fabs appears to demonstrate efficacy and may lead to disease-specific treatments for antibody-mediated autoimmune diseases.

摘要

补体级联的经典途径激活是许多自身抗体介导的疾病中组织损伤发展所必需的。因此,通过使用针对 Fab 抗体片段靶向阻断自身抗体与相应致病自身抗原的结合来防止补体激活,从而阻断自身抗体的病理作用是有意义的。为了实现这一目标,我们以天疱疮(BP)为例,这是一种典型的自身免疫性疾病。通过噬菌体展示,从 BP 患者的抗体库中生成了针对 XVII 型胶原非胶原 16 域的重组 Fab,这是 BP 中自身抗体的主要致病表位。两种 Fab,Fab-B4 和 Fab-19,在体外显示出显著抑制 BP 自身抗体结合和随后补体激活的能力。在使用 XVII 型胶原人源化 BP 模型小鼠的体内实验中,这些 Fab 可保护小鼠免受 BP 自身抗体诱导的水疱病。因此,使用工程化 Fab 阻断致病表位似乎显示出疗效,并可能为抗体介导的自身免疫性疾病带来特异性治疗。