自身抗体
重组DNA
医学
抗原
抗体
免疫印迹
免疫学
多发性硬化
细胞
中枢神经系统
生物
基因
生物化学
内科学
作者
Rachel Dias Molina,Lucas Piccoli Conzatti,Ana Paula Bornes da Silva,Leise Daniele Sckenal Goi,Bruna Klein da Costa,Denise Cantarelli Machado,Douglas Kazutoshi Sato
标识
DOI:10.1016/j.msard.2019.101858
摘要
Abstract
The identification of autoantibodies in central nervous system (CNS) inflammatory disorders improves diagnostic accuracy and the identification of patients with a relapsing disease. Usual methods to detect autoantibodies are usually divided into 3 categories: tissue-based assays, protein-based assays and cell-based assays (CBA). Tissue-based assays are commonly used for initial identification of autoantibodies based on staining patterns and co-localization. Once the antigen is known, autoantibodies can be detected using other antigen-specific methods based on recombinant proteins and CBA using transfected cells expressing the protein in their cell membranes. Compared to traditional methods using recombinant proteins such as ELISA and western blot, the CBA have advantage of detecting conformational sensitive antibodies using natively folded proteins in the cell membrane. This article reviews the utility of CBA into the clinical practice.
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