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人类抗神经元单克隆自身抗体的分子疾病机制

Molecular disease mechanisms of human antineuronal monoclonal autoantibodies.

作者信息

Duong Sophie L, Prüss Harald

机构信息

Department of Neurology and Experimental Neurology, Charité - Universitätsmedizin Berlin, corporate member of Freie Universität Berlin and Humboldt-Universität zu Berlin, 10117 Berlin, Germany; German Center for Neurodegenerative Diseases (DZNE) Berlin, 10117 Berlin, Germany; Berlin Institute of Health at Charité - Universitätsmedizin Berlin, BIH Biomedical Innovation Academy, BIH Charité Junior Clinician Scientist Program, Charitéplatz 1, 10117 Berlin, Germany.

Department of Neurology and Experimental Neurology, Charité - Universitätsmedizin Berlin, corporate member of Freie Universität Berlin and Humboldt-Universität zu Berlin, 10117 Berlin, Germany; German Center for Neurodegenerative Diseases (DZNE) Berlin, 10117 Berlin, Germany.

出版信息

Trends Mol Med. 2023 Jan;29(1):20-34. doi: 10.1016/j.molmed.2022.09.011. Epub 2022 Oct 22.

Abstract

Autoantibodies targeting brain antigens can mediate a wide range of neurological symptoms ranging from epileptic seizures to psychosis to dementia. Although earlier experimental work indicated that autoantibodies can be directly pathogenic, detailed studies on disease mechanisms, biophysical autoantibody properties, and target interactions were hampered by the availability of human material and the paucity of monospecific disease-related autoantibodies. The emerging generation of patient-derived monoclonal autoantibodies (mAbs) provides a novel platform for the detailed characterization of immunobiology and autoantibody pathogenicity in vitro and in animal models. This Feature Review focuses on recent advances in mAb generation and discusses their potential as powerful scientific tools for high-resolution imaging, antigenic target identification, atomic-level structural analyses, and the development of antibody-selective immunotherapies.

摘要

靶向脑抗原的自身抗体可介导从癫痫发作到精神病再到痴呆等广泛的神经症状。尽管早期的实验工作表明自身抗体可能直接致病,但由于人类材料的可得性以及单特异性疾病相关自身抗体的匮乏,对疾病机制、生物物理自身抗体特性和靶标相互作用的详细研究受到了阻碍。新一代患者来源的单克隆自身抗体(mAb)为在体外和动物模型中详细表征免疫生物学和自身抗体致病性提供了一个新平台。本专题综述重点介绍了单克隆抗体生成方面的最新进展,并讨论了它们作为高分辨率成像、抗原靶标鉴定、原子水平结构分析以及抗体选择性免疫疗法开发等强大科学工具的潜力。

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