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抗BR3抗体:一类新型的B细胞免疫疗法,兼具细胞清除和生存阻断作用。

Anti-BR3 antibodies: a new class of B-cell immunotherapy combining cellular depletion and survival blockade.

作者信息

Lin Wei Yu, Gong Qian, Seshasayee Dhaya, Lin Zhonghua, Ou Qinglin, Ye Shiming, Suto Eric, Shu Jean, Lee Wyne Pun, Lee Ching-Wei V, Fuh Germaine, Leabman Maya, Iyer Suhasini, Howell Kathy, Gelzleichter Thomas, Beyer Joseph, Danilenko Dimitry, Yeh Sherry, DeForge Laura E, Ebens Allen, Thompson Jeffrey S, Ambrose Christine, Balazs Mercedesz, Starovasnik Melissa A, Martin Flavius

机构信息

Department of Immunology, Genentech, South San Francisco, CA 94080, USA.

出版信息

Blood. 2007 Dec 1;110(12):3959-67. doi: 10.1182/blood-2007-04-088088. Epub 2007 Aug 8.

Abstract

Removal of pathogenic B lymphocytes by depletion of monoclonal antibodies (mAbs) or deprivation of B-cell survival factors has demonstrated clinical benefit in both oncologic and immunologic diseases. Partial clinical responses and emerging data demonstrating incomplete B-cell depletion after immunotherapy fuels the need for improved therapeutic modalities. Lessons from the first generation of therapeutics directed against B-cell-specific antigens (CD20, CD22) are being applied to develop novel antibodies with additional functional attributes. We describe the generation of a novel class of B-cell-directed therapy (anti-BR3 mAbs) that combines the depleting capacity of a therapeutic mAb and blockade of B-cell-activating factor (BAFF)-BR3 B-cell survival. In mice, treatment with antagonistic anti-BR3 antibodies results in quantitatively greater reduction in some B-cell subsets and qualitatively different effects on bone marrow plasma cells compared with BR3-Fc BAFF blockade or with anti-CD20 treatment. Comparative analysis of BR3-Fc and anti-BR3 mAb reveals a lower B-cell dependence for BAFF-mediated survival in nonhuman primates than in mice. This novel class of B-cell-targeted therapies shows species characteristics in mice and primates that will guide translation to treatment of human disease.

摘要

通过单克隆抗体(mAb)清除或剥夺B细胞存活因子来去除致病性B淋巴细胞,已在肿瘤学和免疫学疾病中显示出临床益处。部分临床反应以及免疫治疗后显示B细胞清除不完全的新数据,促使人们需要改进治疗方式。第一代针对B细胞特异性抗原(CD20、CD22)的治疗方法所积累的经验,正被用于开发具有额外功能特性的新型抗体。我们描述了一类新型的B细胞导向疗法(抗BR3 mAb),它结合了治疗性mAb的清除能力和对B细胞激活因子(BAFF)-BR3 B细胞存活的阻断作用。在小鼠中,与BR3-Fc BAFF阻断或抗CD20治疗相比,用拮抗抗BR3抗体治疗会导致某些B细胞亚群在数量上有更大程度的减少,并且对骨髓浆细胞产生质的不同影响。对BR3-Fc和抗BR3 mAb的比较分析表明,与小鼠相比,非人灵长类动物中BAFF介导的存活对B细胞的依赖性更低。这类新型的B细胞靶向疗法在小鼠和灵长类动物中显示出物种特征,这将为转化为人类疾病治疗提供指导。

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