Division of Nephrology, Department of Internal Medicine, Cardinal Tien Hospital, Yong-He Branch, Taipei 234, Taiwan.
Division of Nephrology, Department of Internal Medicine, Cardinal Tien Hospital & School of Medicine, Fu-Jen Catholic University, New Taipei City 231, Taiwan.
EPMA J. 2013 Jun 21;4(1):17. doi: 10.1186/1878-5085-4-17. eCollection 2013.
Patients on chronic hemodialysis (HD) have impaired cellular and humoral immunity. The percentage of elderly people among the total population in Taiwan is increasing dramatically, and HD is the primary alternative for renal replacement therapy when renal function declines. Activated vitamin D is widely used in HD patients with secondary hyperparathyroidism (SHPT) and is a well-known immunomodulatory agent. Personalized medicine and integrative medical approach has been a trend in current clinical practice. Can we improve their immune function using vitamin D in spite of the mineral aspect? Here, we investigated the relationship between serum 25-hydroxyvitamin D (25(OH)D) level and T cell differentiation in chronic HD patients.
Forty patients with chronic HD were enrolled. HD patients with SHPT had been treated with activated vitamin D for 3 months. Peripheral blood mononuclear cells obtained from the patients were cultured and stimulated by mitogens, and T cells were analyzed by flow cytometry. Serum 25(OH)D levels were detected by enzyme-linked immunosorbent assay.
The incidence of T cell differentiation to the T helper cell (Th)2 subtype was more prevalent in the elderly group than in the controls (p = 0.001). Th2 differentiation was also correlated with age (p = 0.004) and serum 25(OH)D levels (p < 0.05). After treated with activated vitamin D, the level of Th1 cytokines decreased while the Th2 cytokine level increased in the sera (p < 0.05). The T cell differentiation tended toward the Th2 subtype (p = 0.027) after treatment of activated vitamin D in SHPT patients.
These results demonstrated that Th2 differentiation is correlated with age and the serum 25(OH)D level of patients. Treatment with activated vitamin D influenced T cell differentiation and cytokine expression in SHPT patients. Taking vitamin D is the possible prediction and targeted treatment in the immune dysfunction in chronic HD patients.
慢性血液透析(HD)患者的细胞和体液免疫受损。在台湾,总人口中老年人的比例正在急剧增加,当肾功能下降时,HD 是肾脏替代治疗的主要选择。活性维生素 D 广泛用于伴有继发性甲状旁腺功能亢进(SHPT)的 HD 患者,是一种众所周知的免疫调节剂。个性化医学和整合医学方法是当前临床实践的趋势。我们能否在不考虑矿物质方面的情况下使用维生素 D 来改善他们的免疫功能?在这里,我们研究了慢性 HD 患者血清 25-羟维生素 D(25(OH)D)水平与 T 细胞分化之间的关系。
纳入 40 例慢性 HD 患者。SHPT 的 HD 患者已接受活性维生素 D 治疗 3 个月。从患者中获得外周血单核细胞并通过有丝分裂原培养和刺激,通过流式细胞术分析 T 细胞。通过酶联免疫吸附试验检测血清 25(OH)D 水平。
老年组 T 细胞向辅助性 T 细胞(Th)2 亚群分化的发生率高于对照组(p=0.001)。Th2 分化也与年龄(p=0.004)和血清 25(OH)D 水平相关(p<0.05)。在用活性维生素 D 治疗后,血清中 Th1 细胞因子的水平降低,而 Th2 细胞因子的水平升高(p<0.05)。在用活性维生素 D 治疗 SHPT 患者后,T 细胞分化倾向于 Th2 亚群(p=0.027)。
这些结果表明,Th2 分化与患者的年龄和血清 25(OH)D 水平相关。活性维生素 D 的治疗影响 SHPT 患者的 T 细胞分化和细胞因子表达。服用维生素 D 可能是慢性 HD 患者免疫功能障碍的预测和靶向治疗。