Molecular disease mechanisms of human antineuronal monoclonal autoantibodies

被引:13
作者
Duong, Sophie L. [1 ,2 ,3 ,4 ,5 ]
Pruess, Harald [1 ,2 ,3 ,4 ]
机构
[1] Charite Univ Med Berlin, Dept Neurol & Expt Neurol, D-10117 Berlin, Germany
[2] Free Univ Berlin, D-10117 Berlin, Germany
[3] Humboldt Univ, D-10117 Berlin, Germany
[4] German Ctr Neurodegenerat Dis DZNE Berlin, D-10117 Berlin, Germany
[5] Charite Univ Med Berlin, BIH Biomed Innovat Acad, BIH Charite Jr Clinician Scientist Program, Berlin Inst Hlth, Charitepl 1, D-10117 Berlin, Germany
关键词
NMDA RECEPTOR ENCEPHALITIS; GABA(A) RECEPTOR; B-CELLS; AUTOIMMUNE ENCEPHALITIS; SELECTIVE DEPLETION; LIMBIC ENCEPHALITIS; CASE SERIES; ANTIBODIES; ANTIGEN; PROTEIN;
D O I
10.1016/j.molmed.2022.09.011
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Autoantibodies targeting brain antigens can mediate a wide range of neurologi-cal 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) pro-vides 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 identifi-cation, atomic-level structural analyses, and the development of antibody -selective immunotherapies.
引用
收藏
页码:20 / 34
页数:15
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