Suppr超能文献

多发性硬化症的免疫疗法。

Immunotherapy of multiple sclerosis.

作者信息

Weiner H L, Hafler D A

机构信息

Department of Medicine, Brigham and Women's Hospital, Boston, MA 02115.

出版信息

Ann Neurol. 1988 Mar;23(3):211-22. doi: 10.1002/ana.410230302.

Abstract

Based on the assumption that multiple sclerosis is an autoimmune disease, a number of clinical trials designed to suppress the immune system or to restore immune balance in multiple sclerosis have been attempted. Depending on the disease category, the clinical goals of immunotherapy differ. Therapeutic goals include improving recovery from acute attacks, preventing or decreasing the number of relapses, and halting the disease in its progressive stage. The ultimate goal of multiple sclerosis therapy is the early treatment of patients in an attempt to halt the onset of progression. Specific strategies of immunotherapy include generation of a suppressor influence, removal of helper/inducer cells, manipulation of activated T cells, manipulation of class II major histocompatibility complex-bearing cells, alteration of lymphocyte traffic, extracorporeal removal of serum factors or cells, and manipulation of antigen-specific cells. Present treatment modalities are beginning to show some efficacy of nonspecific immunosuppression, but these treatments are limited by their toxicities. As the immunotherapy of multiple sclerosis moves to the next stage in the coming years, patients at an earlier stage of their disease will have to be treated, nontoxic forms of therapy developed, clinical trials lengthened, and a laboratory monitor of the disease developed. Given the positive effects of immunotherapy seen thus far in the disease, it is possible that appropriate immunotherapeutic intervention may provide effective treatment for the disease in the future.

摘要

基于多发性硬化症是一种自身免疫性疾病的假设,人们尝试了许多旨在抑制免疫系统或恢复多发性硬化症免疫平衡的临床试验。根据疾病类型,免疫疗法的临床目标有所不同。治疗目标包括改善急性发作后的恢复情况、预防或减少复发次数,以及在疾病进展阶段阻止病情发展。多发性硬化症治疗的最终目标是尽早治疗患者,以试图阻止病情进展的发生。免疫疗法的具体策略包括产生抑制性影响、去除辅助/诱导细胞、操控活化的T细胞、操控携带II类主要组织相容性复合体的细胞、改变淋巴细胞迁移、体外去除血清因子或细胞,以及操控抗原特异性细胞。目前的治疗方式已开始显示出一些非特异性免疫抑制的疗效,但这些治疗受到其毒性的限制。随着未来几年多发性硬化症免疫疗法进入下一阶段,疾病处于早期阶段的患者将需要接受治疗,开发无毒的治疗形式,延长临床试验时间,并建立该疾病的实验室监测方法。鉴于迄今为止在该疾病中看到的免疫疗法的积极效果,未来适当的免疫治疗干预有可能为该疾病提供有效的治疗方法。

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