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哮喘中靶向补体成分的价值。

The Value of Targeting Complement Components in Asthma.

机构信息

Department of Respiratory Sciences, University of Leicester, Leicester LE1 9HN, UK.

出版信息

Medicina (Kaunas). 2020 Aug 12;56(8):405. doi: 10.3390/medicina56080405.

DOI:10.3390/medicina56080405
PMID:32806638
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7466339/
Abstract

Asthma is an important respiratory illness. Though pharmacological and biological treatment is well established and is staged according to endotypes and their responses to treatment, novel avenues are being explored. Our focus is complement. In this viewpoint, we evaluate the approach to target complement in this complex hypersensitivity reaction that develops chronicity and has a personal-as well as a societal-cost.

摘要

哮喘是一种重要的呼吸道疾病。虽然药理学和生物学治疗已经得到很好的建立,并根据表型及其对治疗的反应进行分期,但新的途径正在探索中。我们关注的是补体。在这篇观点文章中,我们评估了针对这种复杂超敏反应中补体的靶标治疗方法,这种超敏反应会发展为慢性疾病,给个人和社会带来成本。

相似文献

1
The Value of Targeting Complement Components in Asthma.哮喘中靶向补体成分的价值。
Medicina (Kaunas). 2020 Aug 12;56(8):405. doi: 10.3390/medicina56080405.
2
New concepts on the therapeutic control of complement anaphylatoxin receptors.补体过敏毒素受体治疗性控制的新概念。
Mol Immunol. 2017 Sep;89:36-43. doi: 10.1016/j.molimm.2017.05.015. Epub 2017 May 30.
3
Pharmacological approach for the reduction of inflammatory and prothrombotic hyperactive state in COVID-19 positive patients by acting on complement cascade.通过作用于补体级联反应来降低 COVID-19 阳性患者的炎症和促血栓形成高反应状态的药理学方法。
Hum Immunol. 2021 Apr;82(4):264-269. doi: 10.1016/j.humimm.2021.01.007. Epub 2021 Jan 20.
4
Complement in asthma: sensitivity to activation and generation of C3a and C5a via the different complement pathways.哮喘中的补体:通过不同补体途径对C3a和C5a激活及生成的敏感性。
Transl Res. 2006 Oct;148(4):157-63. doi: 10.1016/j.trsl.2006.05.004.
5
Complement components as potential therapeutic targets for asthma treatment.补体成分作为哮喘治疗的潜在治疗靶点。
Respir Med. 2014 Apr;108(4):543-9. doi: 10.1016/j.rmed.2014.01.005. Epub 2014 Jan 15.
6
Regulation and function of anaphylatoxins and their receptors in allergic asthma.过敏毒素及其受体在过敏性哮喘中的调节作用与功能
Mol Immunol. 2017 Apr;84:51-56. doi: 10.1016/j.molimm.2016.11.013.
7
Complement factors C3a and C5a are increased in bronchoalveolar lavage fluid after segmental allergen provocation in subjects with asthma.在哮喘患者中,节段性变应原激发后,支气管肺泡灌洗液中的补体因子C3a和C5a会增加。
Am J Respir Crit Care Med. 2001 Nov 15;164(10 Pt 1):1841-3. doi: 10.1164/ajrccm.164.10.2010096.
8
The role of complement in the diagnosis and management of allergic rhinitis and allergic asthma.补体在过敏性鼻炎和过敏性哮喘的诊断和治疗中的作用。
Curr Allergy Asthma Rep. 2011 Apr;11(2):122-30. doi: 10.1007/s11882-010-0171-6.
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Eculizumab-C5 complexes express a C5a neoepitope in vivo: Consequences for interpretation of patient complement analyses.依库珠单抗 - C5复合物在体内表达C5a新表位:对患者补体分析解读的影响。
Mol Immunol. 2017 Sep;89:111-114. doi: 10.1016/j.molimm.2017.05.021. Epub 2017 Jun 10.
10
Food intake regulation by central complement system.中枢补体系统对食物摄入的调节
Adv Exp Med Biol. 2008;632:35-46.

本文引用的文献

1
Allergen-Induced C5a/C5aR1 Axis Activation in Pulmonary CD11b cDCs Promotes Pulmonary Tolerance through Downregulation of CD40.过敏原诱导的肺部 CD11b cDCs 中的 C5a/C5aR1 轴激活通过下调 CD40 促进肺部耐受。
Cells. 2020 Jan 26;9(2):300. doi: 10.3390/cells9020300.
2
Effect of C1-inhibitor in adults with mild asthma: A randomized controlled trial.C1抑制剂对轻度哮喘成人患者的影响:一项随机对照试验。
Allergy. 2020 Apr;75(4):953-955. doi: 10.1111/all.14053. Epub 2019 Oct 1.
3
Complement factor C5 inhibition reduces type 2 responses without affecting group 2 innate lymphoid cells in a house dust mite induced murine asthma model.补体因子 C5 抑制作用可减少 2 型反应,而不影响屋尘螨诱导的小鼠哮喘模型中的 2 类先天淋巴细胞。
Respir Res. 2019 Jul 24;20(1):165. doi: 10.1186/s12931-019-1136-5.
4
Epidemiology of Asthma in Children and Adults.儿童和成人哮喘的流行病学
Front Pediatr. 2019 Jun 18;7:246. doi: 10.3389/fped.2019.00246. eCollection 2019.
5
Complement-Mediated Activation of the NLRP3 Inflammasome and Its Inhibition by AAV-Mediated Delivery of CD59 in a Model of Uveitis.补体介导的 NLRP3 炎性小体激活及其在葡萄膜炎模型中通过 AAV 介导的 CD59 传递的抑制作用。
Mol Ther. 2018 Jun 6;26(6):1568-1580. doi: 10.1016/j.ymthe.2018.03.012. Epub 2018 Mar 19.
6
Role for NLRP3 Inflammasome-mediated, IL-1β-Dependent Responses in Severe, Steroid-Resistant Asthma.NLRP3 炎性小体介导体液免疫和细胞免疫应答在激素抵抗性重症哮喘中的作用。
Am J Respir Crit Care Med. 2017 Aug 1;196(3):283-297. doi: 10.1164/rccm.201609-1830OC.
7
Asthma costs and social impact.哮喘的成本与社会影响。
Asthma Res Pract. 2017 Jan 6;3:1. doi: 10.1186/s40733-016-0029-3. eCollection 2017.
8
Monoclonal antibody therapy for the treatment of asthma and chronic obstructive pulmonary disease with eosinophilic inflammation.单克隆抗体治疗哮喘和伴有嗜酸性粒细胞炎症的慢性阻塞性肺疾病。
Pharmacol Ther. 2017 Jan;169:57-77. doi: 10.1016/j.pharmthera.2016.10.016. Epub 2016 Oct 20.
9
Contribution of the anaphylatoxin receptors, C3aR and C5aR, to the pathogenesis of pulmonary fibrosis.过敏毒素受体C3aR和C5aR在肺纤维化发病机制中的作用。
FASEB J. 2016 Jun;30(6):2336-50. doi: 10.1096/fj.201500044. Epub 2016 Mar 8.
10
Complement mediators: key regulators of airway tissue remodeling in asthma.补体介质:哮喘气道组织重塑的关键调节因子。
J Transl Med. 2015 Aug 20;13:272. doi: 10.1186/s12967-015-0565-2.