{"title":"[治疗多发性硬化症的奥法妥木单抗--临床前和临床数据摘要]。","authors":"Juliane Klehmet, Tobias Bopp","doi":"10.1055/a-2365-0966","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong> B-cell targeted therapies are highly effective in multiple sclerosis (MS). Most of these therapies are administered intravenously at long intervals. Ofatumumab, an anti-CD20 antibody that is administered subcutaneously at low doses on a monthly basis due to its high affinity to the target structure, became available for the treatment of MS in 2021.</p><p><strong>Methods: </strong> An overview of practice-relevant immunological and clinical data on ofatumumab is provided.</p><p><strong>Results: </strong> The high affinity of ofatumumab to the target structure allows low dose and low volume administration, with the release and absorption profile after subcutaneous application allowing for high concentrations in the lymph nodes and gradual depletion of B-cells. Rapid onset of action is achieved as well as B-cell repletion within a few months in case of discontinuation of therapy. Long-term data show stable IgG levels over up to four years and high efficacy with respect to relapse rate, progression, and cognition. According to current study data, the effect compared to teriflunomide is greater the earlier therapy is initiated. Ofatumumab has a specific B-cell depletion pattern. CD20 expressing B-cell progenitor cells in the bone marrow are preserved and therefore also the inducibility and differentiation of plasma cells. The formation of a humoral immunological memory is therefore possible. Four-year study data showed no abnormalities in the rate of severe infections or malignancies.</p><p><strong>Conclusions: </strong> Ofatumumab is an innovative B-cell targeted therapy. It is highly effective with a good safety and tolerability profile, well controllable and maintains immunocompetence against pathogens.</p>","PeriodicalId":0,"journal":{"name":"","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2024-08-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"[Ofatumumab in the treatment of multiple sclerosis - A summary of preclinical and clinical data].\",\"authors\":\"Juliane Klehmet, Tobias Bopp\",\"doi\":\"10.1055/a-2365-0966\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong> B-cell targeted therapies are highly effective in multiple sclerosis (MS). Most of these therapies are administered intravenously at long intervals. Ofatumumab, an anti-CD20 antibody that is administered subcutaneously at low doses on a monthly basis due to its high affinity to the target structure, became available for the treatment of MS in 2021.</p><p><strong>Methods: </strong> An overview of practice-relevant immunological and clinical data on ofatumumab is provided.</p><p><strong>Results: </strong> The high affinity of ofatumumab to the target structure allows low dose and low volume administration, with the release and absorption profile after subcutaneous application allowing for high concentrations in the lymph nodes and gradual depletion of B-cells. Rapid onset of action is achieved as well as B-cell repletion within a few months in case of discontinuation of therapy. Long-term data show stable IgG levels over up to four years and high efficacy with respect to relapse rate, progression, and cognition. According to current study data, the effect compared to teriflunomide is greater the earlier therapy is initiated. Ofatumumab has a specific B-cell depletion pattern. CD20 expressing B-cell progenitor cells in the bone marrow are preserved and therefore also the inducibility and differentiation of plasma cells. The formation of a humoral immunological memory is therefore possible. Four-year study data showed no abnormalities in the rate of severe infections or malignancies.</p><p><strong>Conclusions: </strong> Ofatumumab is an innovative B-cell targeted therapy. It is highly effective with a good safety and tolerability profile, well controllable and maintains immunocompetence against pathogens.</p>\",\"PeriodicalId\":0,\"journal\":{\"name\":\"\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":0.0,\"publicationDate\":\"2024-08-19\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1055/a-2365-0966\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1055/a-2365-0966","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
摘要
背景:B细胞靶向疗法对多发性硬化症(MS)非常有效。这些疗法大多需要长时间静脉注射。Ofatumumab是一种抗CD20抗体,因其对靶结构的高亲和力而每月以低剂量皮下注射,于2021年开始用于治疗多发性硬化症:方法:概述了与实践相关的免疫学和临床数据:结果:ofatumumab与靶结构的高亲和力允许低剂量和小容量给药,皮下注射后的释放和吸收曲线允许淋巴结中的高浓度和B细胞的逐渐耗竭。这种疗法起效迅速,即使停止治疗,B 细胞也能在几个月内恢复。长期数据显示,IgG水平在长达四年的时间里保持稳定,在复发率、病情发展和认知能力方面具有很高的疗效。根据目前的研究数据,与特立氟胺相比,越早开始治疗疗效越好。奥法图姆单抗具有特定的 B 细胞耗竭模式。骨髓中表达 CD20 的 B 细胞祖细胞得以保留,因此浆细胞的诱导和分化也得以保留。因此有可能形成体液免疫记忆。四年的研究数据显示,严重感染或恶性肿瘤的发生率没有异常:结论:Ofatumumab是一种创新的B细胞靶向疗法。结论:奥法图姆单抗是一种创新的 B 细胞靶向疗法,它疗效显著,安全性和耐受性良好,可控性好,并能保持对病原体的免疫能力。
[Ofatumumab in the treatment of multiple sclerosis - A summary of preclinical and clinical data].
Background: B-cell targeted therapies are highly effective in multiple sclerosis (MS). Most of these therapies are administered intravenously at long intervals. Ofatumumab, an anti-CD20 antibody that is administered subcutaneously at low doses on a monthly basis due to its high affinity to the target structure, became available for the treatment of MS in 2021.
Methods: An overview of practice-relevant immunological and clinical data on ofatumumab is provided.
Results: The high affinity of ofatumumab to the target structure allows low dose and low volume administration, with the release and absorption profile after subcutaneous application allowing for high concentrations in the lymph nodes and gradual depletion of B-cells. Rapid onset of action is achieved as well as B-cell repletion within a few months in case of discontinuation of therapy. Long-term data show stable IgG levels over up to four years and high efficacy with respect to relapse rate, progression, and cognition. According to current study data, the effect compared to teriflunomide is greater the earlier therapy is initiated. Ofatumumab has a specific B-cell depletion pattern. CD20 expressing B-cell progenitor cells in the bone marrow are preserved and therefore also the inducibility and differentiation of plasma cells. The formation of a humoral immunological memory is therefore possible. Four-year study data showed no abnormalities in the rate of severe infections or malignancies.
Conclusions: Ofatumumab is an innovative B-cell targeted therapy. It is highly effective with a good safety and tolerability profile, well controllable and maintains immunocompetence against pathogens.