免疫学
人类白细胞抗原
抗原
主要组织相容性复合体
免疫性血小板减少症
血小板
免疫系统
抗原呈递
抗原处理
医学
生物
MHC I级
T细胞
作者
Yujuan Ren,Qianqian Ying,Ying Chen,Cong Liao,An‐Rong Li,Qidong Ye
摘要
<b><i>Introduction:</i></b> Major histocompatibility complex II (MHC-II)-mediated antigen presentation contributes to the pathogenesis of immune thrombocytopenia (ITP). Human leukocyte antigen (HLA)-DRB5 is an MHC-II molecule and this study aims to investigate its role and mechanisms in ITP development. <b><i>Methods:</i></b> Guinea pig anti-mouse platelet (PLT) serum-induced ITP mice received tail vein injection of HLA-DRB5 overexpressing adenoviral vector/immune receptor expressed on myeloid cells-1 (IREM-1) monoclonal antibody (mAb). PLT count changes in mice blood were assessed by a hematology analyzer. MHC-II/CD80/CD86 expression in mice blood was measured by quantitative real-time-PCR and immunofluorescence assay. CD8<sup>+</sup> T-cell proportion in mice blood was detected by flow cytometry. <b><i>Results:</i></b> HLA-DRB5 overexpression exacerbated PLT reduction since the 5th day of the establishment of ITP mice model and enhanced MHC-II/CD80/CD86 expression upregulation as well as CD8<sup>+</sup> T-cell ratio elevation in the blood of ITP mice, while its effects were reversed by IREM-1 mAb. <b><i>Conclusion:</i></b> HLA-DRB5 overexpression upregulates MHC-II-mediated antigen presentation to CD8<sup>+</sup> T cells, thus lowering PLT count in the ITP mice model.
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