Decreased programmed death-1 expression on the T cells of patients with ankylosing spondylitis.

Lianlian Zhou, Yanhong Zhang, Huiying Xu, Liping Hu, Chunwu Zhang, Li Sun, Yaosheng Xie, Hong Lu, Zhuo Zhang, Wangqiang Hu, Xiangyang Lin

Journal: The American journal of the medical sciences 2015;349(6):488-92

PMID: 25881983

Abstract

BACKGROUND

Programmed death-1 (PD-1) plays a vital role in down-modulating immune responses and maintaining peripheral tolerance.

METHODS

The authors have investigated the inducible expression of PD-1 on activated T cells from patients with ankylosing spondylitis (AS). Thirty patients with AS and 31 unrelated healthy controls (HCs) were recruited in this study. The expression of PD-1 on T cells harvested from nonstimulated (t0) or stimulated cultures with phytohemagglutinin for 24 hours (t24) was determined by flow cytometry. The multiple levels of the PD-1 expression on stimulated and nonstimulated cells from each individual's sample (t24/t0) represented as the degree of the inducible effect on PD-1 expression.

RESULTS

The expression of PD-1 on nonstimulated T cells presented no significant difference between AS group and HC group (P > 0.05). After stimulation, the degree of effect on PD-1 expression of CD4+, CD4+CD25+, CD4+CD25 high, CD4+CD25 low and CD4+CD25- T cells were significantly lower in patients with AS than those in HC group (1.9 ± 0.9 versus 3.6 ± 2.3, 9.7 ± 7.4 versus 17.8 ± 12.6, 87.8 ± 48.6 versus 157.3 ± 117.0, 3.7 ± 1.4 versus 7.3 ± 2.4, 0.5 ± 0.3 versus 1.1 ± 0.6, respectively, P < 0.05). However, there was no significant difference of the effect on all lymphocytes and CD8+ T cells between patients with AS and HCs (P > 0.05).

CONCLUSIONS

The decreased inducible expression of PD-1 on active T lymphocytes, especially on CD4+CD25 high and CD4+CD25+ T cells, may be one of important factors involved in the development of AS.

Address: Department of Clinical Laboratory (LZ, HX, LH, YX, HL, ZZ, WH, XL), The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, China; Department of Clinical Laboratory (YZ), Yantai Yuhuangding Hospital, Yantai, China; and Departments of Orthpaedics Trauma (CZ) and Rheumatology (LS), The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, China.
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