Suppr超能文献

可溶性重组补体受体1可抑制抗体介导的脱髓鞘实验性变应性脑脊髓炎中的炎症和脱髓鞘。

Soluble recombinant complement receptor 1 inhibits inflammation and demyelination in antibody-mediated demyelinating experimental allergic encephalomyelitis.

作者信息

Piddlesden S J, Storch M K, Hibbs M, Freeman A M, Lassmann H, Morgan B P

机构信息

Department of Medical Biochemistry, University of Wales College of Medicine, Cardiff, United Kingdom.

出版信息

J Immunol. 1994 Jun 1;152(11):5477-84.

PMID:8189065
Abstract

Activation of complement may contribute to tissue damage in many inflammatory diseases, including those that are clearly T cell driven. We have previously provided evidence that C is involved in tissue damage in multiple sclerosis and in the animal models of this disease, experimental allergic encephalomyelitis and Ab-mediated demyelinating experimental allergic encephalomyelitis, the latter being a model more closely resembling multiple sclerosis. The development of a soluble recombinant form of human complement receptor 1 (sCR1) with potent C-inhibiting activity both in vitro and in vivo provides a potential means of preventing C-mediated tissue damage in animal models and in human disease. Here, we describe the effects of this agent on clinical disease and pathology in Ab-mediated demyelinating experimental allergic encephalomyelitis in the rat. Daily i.p. injection of sCR1 (20 mg/kg) over 6 days completely suppressed serum C activity, reduced the severity of clinical disease (clinical score 1.33 vs 2.79 in untreated animals), inhibited central nervous system inflammation (inflammatory index 2.76 vs 6.55), and almost completely blocked demyelination (average 2.43% cord cross-section vs 8.81%). Deposition of C components C1, C3, and C9 was also markedly inhibited in sCR1-treated animals. This dramatic effect on a demyelinating disease, achieved using a well-tolerated biologic reagent, offers an exciting new prospect for therapy in multiple sclerosis.

摘要

补体激活可能在许多炎症性疾病中导致组织损伤,包括那些明显由T细胞驱动的疾病。我们之前已提供证据表明,补体(C)参与了多发性硬化症及其动物模型——实验性变应性脑脊髓炎和抗体介导的脱髓鞘性实验性变应性脑脊髓炎(后者是更类似于多发性硬化症的模型)中的组织损伤。一种具有强大的体外和体内补体抑制活性的可溶性重组人补体受体1(sCR1)的研制成功,为在动物模型和人类疾病中预防补体介导的组织损伤提供了一种潜在手段。在此,我们描述了该制剂对大鼠抗体介导的脱髓鞘性实验性变应性脑脊髓炎的临床疾病和病理学的影响。连续6天每天腹腔注射sCR1(20毫克/千克)可完全抑制血清补体活性,降低临床疾病的严重程度(临床评分:未治疗动物为2.79,而治疗动物为1.33),抑制中枢神经系统炎症(炎症指数:未治疗动物为6.55,而治疗动物为2.76),并几乎完全阻止脱髓鞘(脊髓横截面平均受累比例:未治疗动物为8.81%,而治疗动物为2.43%)。在接受sCR1治疗的动物中,补体成分C1、C3和C9的沉积也受到显著抑制。使用耐受性良好的生物制剂对脱髓鞘疾病产生的这种显著效果,为多发性硬化症的治疗提供了令人兴奋的新前景。

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