Department of Pathology, Kurume University School of Medicine, 67 Asahi-machi, Kurume, Fukuoka, 830-0011, Japan.
Department of Orthopedic Surgery, Kurume University School of Medicine, Kurume, Fukuoka, Japan.
Clin Exp Med. 2018 Nov;18(4):487-494. doi: 10.1007/s10238-018-0515-4. Epub 2018 Jun 30.
The etiology of rheumatoid arthritis (RA) is thought to involve dysfunction of the programmed cell death 1/programmed cell death ligand 1 (PD-1/PD-L1) pathway; PD-1 negatively regulates autoimmunity by interacting with its ligand, PD-L1. We therefore investigated PD-1/PD-L1 expression in synovial tissue of patients with RA. We immunohistochemically stained synovial specimens from 51 patients with RA and assessed the association between PD-1/PD-L1 expression and rheumatoid factor (RF), the total count of infiltrating T cells, C-reactive protein (CRP), and Krenn's synovitis score. PD-1 expression on infiltrating lymphocytes was detected in 34/51 RA cases (66.7%), while PD-1 expression was very mildly correlated only with the number of total infiltrating T cells (R = 0.1011, P = 0.0230). On the other hand, PD-L1 expression on synovial lining cells was observed in 37/51 RA cases (72.5%). Furthermore, a higher PD-L1 expression was significantly associated with RF positive state (P = 0.0454), and the correlations between PD-L1 expression and the number of infiltrating T cells (R = 0.5571, P < 0.0001), CRP (R = 0.4060, P < 0.0001), and Krenn's synovitis score (R = 0.7785, P < 0.0001) were confirmed. PD-1 was expressed on infiltrating lymphocytes, while PD-L1 was expressed on synovial lining cells; the expression of PD-L1 on synovial lining cells was significantly correlated with the active state of the disease. These data suggest that PD-1/PD-L1 pathway may have an important role in the pathogenesis of RA.
类风湿关节炎(RA)的病因被认为涉及程序性细胞死亡 1/程序性细胞死亡配体 1(PD-1/PD-L1)途径的功能障碍;PD-1 通过与其配体 PD-L1 相互作用来负向调节自身免疫。因此,我们研究了 RA 患者滑膜组织中的 PD-1/PD-L1 表达。我们对 51 例 RA 患者的滑膜标本进行了免疫组织化学染色,并评估了 PD-1/PD-L1 表达与类风湿因子(RF)、浸润 T 细胞总数、C 反应蛋白(CRP)和 Krenn 滑膜炎评分之间的关系。在 34/51 例 RA 病例(66.7%)中检测到浸润淋巴细胞上的 PD-1 表达,而 PD-1 表达仅与总浸润 T 细胞数量呈非常轻度相关(R=0.1011,P=0.0230)。另一方面,在 37/51 例 RA 病例中观察到滑膜衬里细胞上的 PD-L1 表达。此外,较高的 PD-L1 表达与 RF 阳性状态显著相关(P=0.0454),并且 PD-L1 表达与浸润 T 细胞数量(R=0.5571,P<0.0001)、CRP(R=0.4060,P<0.0001)和 Krenn 滑膜炎评分(R=0.7785,P<0.0001)之间存在相关性得到证实。PD-1 表达于浸润淋巴细胞,而 PD-L1 表达于滑膜衬里细胞;滑膜衬里细胞上 PD-L1 的表达与疾病的活动状态显著相关。这些数据表明,PD-1/PD-L1 途径可能在 RA 的发病机制中起重要作用。