Single-cell approaches to dissect adaptive immune responses involved in autoimmunity: the case of celiac disease

被引:4
|
作者
Lindeman, Ida [1 ,2 ]
Sollid, Ludvig M. [1 ,2 ,3 ]
机构
[1] Univ Oslo, KG Jebsen Coeliac Dis Res Ctr, Oslo, Norway
[2] Oslo Univ Hosp, Dept Immunol, Oslo, Norway
[3] Univ Oslo, Inst Clin Med, Oslo, Norway
关键词
TRANSGLUTAMINASE 2-SPECIFIC AUTOANTIBODIES; IMMUNOGLOBULIN-CONTAINING CELLS; LINKED-IMMUNOSORBENT-ASSAY; T-CELLS; PLASMA-CELLS; TISSUE TRANSGLUTAMINASE; PERIPHERAL-BLOOD; INTERLEUKIN; 15; POSTTRANSLATIONAL MODIFICATION; TRANSCRIPTOMIC HETEROGENEITY;
D O I
10.1038/s41385-021-00452-0
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Single-cell analysis is a powerful technology that has found widespread use in recent years. For diseases with involvement of adaptive immunity, single-cell analysis of antigen-specific T cells and B cells is particularly informative. In autoimmune diseases, the adaptive immune system is obviously at play, yet the ability to identify the culprit T and B cells recognizing disease-relevant antigen can be difficult. Celiac disease, a widespread disorder with autoimmune components, is unique in that disease-relevant antigens for both T cells and B cells are well defined. Furthermore, the celiac disease gut lesion is readily accessible allowing for sampling of tissue-resident cells. Thus, disease-relevant T cells and B cells from the gut and blood can be studied at the level of single cells. Here we review single-cell studies providing information on such adaptive immune cells and outline some future perspectives in the area of single-cell analysis in autoimmune diseases.
引用
收藏
页码:51 / 63
页数:13
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