医学
免疫学
血小板减少性紫癜
自身抗体
流式细胞术
免疫系统
CD19
CD38
血小板
抗体
B细胞
发病机制
生物
川地34
干细胞
遗传学
作者
Nagwa A. Hagag,Osama Elagamy,Mohamed El‐Shanshory,Mohamed Saad,Eslam E. Elhawary
标识
DOI:10.1080/08880018.2021.2024928
摘要
Primary immune thrombocytopenic purpura (ITP) is an autoimmune disorder with platelet destruction due to B- and T-cell dysregulation and antiplatelet autoantibodies production. Flow cytometry can be used to further characterize the B- and T-cell compartments involved in platelet destruction. This case-control study was to enumerate plasmablast cells in pediatric ITP patients and to correlate their levels with disease course. This study included 30 ITP patients and 10 controls. Identification and enumeration of Plasmablast were done by multicolor flow cytometry using specific antibody panels (CD19, CD27 & CD38) and sequential gating using FACSCanto flow cytometer and FlowJo software. We found that lymphocytes subpopulation in ITP patients and controls revealed increase in frequency of CD19 (B lymphocytes) in acute, persistent, and chronic ITP patients in comparison with controls (p < 0.001, 0.023, 0.001) respectively. Plasmablast cells could play a role in the pathogenesis of ITP and might guide therapy in ITP patients in the future.
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