Serum levels of soluble programmed death-1 (sPD-1) and soluble programmed death ligand 1(sPD-L1) in systemic lupus erythematosus: Association with activity and severity

被引:37
作者
Du, Yan [1 ]
Nie, Liuyan [1 ]
Xu, Li [1 ,2 ]
Wu, Xinyu [1 ]
Zhang, Songzhao [3 ]
Xue, Jing [1 ]
机构
[1] Zhejiang Univ, Dept Rheumatol, Sch Med, Affiliated Hosp 2, 88 Jiefang Rd, Hangzhou 310009, Peoples R China
[2] Jiaxing Univ, Affiliated Women & Children Hosp, Dept Internal Med, Jiaxing, Peoples R China
[3] Zhejiang Univ, Dept Clin Lab, Sch Med, Affiliated Hosp 2, Hangzhou, Peoples R China
基金
中国国家自然科学基金;
关键词
SLEDAI; sPD-1; sPD-L1; Systemic lupus erythematosus; T-CELL RESPONSES; DISEASE SEVERITY; PD-1; PATHWAY; PROGRESSION; EXPRESSION; SURVIVAL; PATHOGENESIS; LYMPHOMA; PREDICT; B7-H1;
D O I
10.1111/sji.12884
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The programmed cell death-1 (PD-1)/programmed cell death ligand 1 (PD-L1) pathway is an important host immunosuppression mechanism. Soluble PD-1 (sPD-1) and PD-L1 (sPD-L1) expression regulates co-inhibitory signals in autoimmune disorders. Here, we evaluated whether serum sPD-1 and sPD-L1 are involved in immune dysfunction and assessed its relationship with SLE. Blood samples were obtained from 130 patients with SLE and 44 healthy controls. Serum sPD-1 and sPD-L1 were tested by enzyme-linked immunosorbent assay (ELISA). Relevant immune parameters were analysed. Both serum sPD-1 and sPD-L1 were significantly higher in the SLE patients than in the controls. A series of severe disease clinical manifestations and laboratory features such as presence of decreased complement component 3, complement component 4 and SLEDAI >8 were associated with elevated sPD-1 and sPD-L1. Our study suggests that abnormal sPD-1 and sPD-L1 expression may be involved in the imbalance of immune regulation in SLE.
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页数:11
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