Division of Hematology, Rheumatology and Respiratory Medicine, Department of Internal Medicine, Faculty of Medicine, Kagawa University, 1750-1 Ikenobe, Miki-cho, Kita-gun, Kagawa, 761-0793, Japan.
Sci Rep. 2022 Jun 17;12(1):10175. doi: 10.1038/s41598-022-14571-6.
We investigated the effect of hydroxychloroquine (HCQ) as an add-on treatment to immunosuppressants on the expression of proinflammatory cytokines in patients with systemic lupus erythematosus. Serum levels of tumor necrosis factor (TNF)-α, interleukin (IL)-2, IL-6, IL-8, vascular endothelial growth factor (VEGF)-A, monocyte chemotactic protein-1 (MCP-1), macrophage inflammatory protein-1α (MIP-1α), and interleukin 1 receptor antagonist (IL-1ra) were measured immediately before and 3 months after treatment with oral HCQ. Among the 51 patients enrolled in the study, HCQ treatment led to significantly reduced serum levels of TNF-α, IL-6, IL-8, VEGF-A, IL-1ra, and IL-2 (p < 0.0001; p = 0.0006; p = 0.0460, p = 0.0177; p < 0.0001; p = 0.0282, respectively) and to decreased (but not significantly) levels of MIP-1α (p = 0.0746). No significant changes were observed in the serum MCP-1 levels before and after HCQ administration (p = 0.1402). Our results suggest that an add-on HCQ treatment modulates the expression of proinflammatory cytokines even in systemic lupus erythematosus patients with low disease activity.
我们研究了羟氯喹(HCQ)作为免疫抑制剂的附加治疗对系统性红斑狼疮患者促炎细胞因子表达的影响。在接受口服 HCQ 治疗前和 3 个月时,测量了血清肿瘤坏死因子(TNF)-α、白细胞介素(IL)-2、IL-6、IL-8、血管内皮生长因子(VEGF)-A、单核细胞趋化蛋白-1(MCP-1)、巨噬细胞炎性蛋白-1α(MIP-1α)和白细胞介素 1 受体拮抗剂(IL-1ra)的水平。在纳入研究的 51 例患者中,HCQ 治疗导致 TNF-α、IL-6、IL-8、VEGF-A、IL-1ra 和 IL-2 的血清水平显著降低(p<0.0001;p=0.0006;p=0.0460,p=0.0177;p<0.0001;p=0.0282,分别),MIP-1α 的水平降低(但不显著)(p=0.0746)。HCQ 给药前后血清 MCP-1 水平无明显变化(p=0.1402)。我们的结果表明,HCQ 的附加治疗甚至可以调节低疾病活动度的系统性红斑狼疮患者促炎细胞因子的表达。