Division of Nephrology- Universidade Federal São Paulo, UNIFESP, São Paulo, São Paulo, Brazil.
Division of Nephrology- Universidade Federal São Paulo, UNIFESP, São Paulo, São Paulo, Brazil.
J Ren Nutr. 2019 Sep;29(5):454-461. doi: 10.1053/j.jrn.2018.11.006. Epub 2019 Jan 25.
End-stage renal disease results in B cell lymphopenia and low levels of vitamin D. Since the link between vitamin D deficiency and B lymphocytes dysfunction are not clear in patients with end-stage renal disease, we suggest that vitamin D adequacy and factors related to the homeostasis of these cells should be investigated. B lymphocytes homeostasis is a process mainly regulated signals of grown and death as interleukin (IL)-7, B cell-activating factor (BAFF)/BAFF-receptor and CD95 expression.
As vitamin D serum levels were reduced in patients with end stage renal disease and it is associated with human B homeostasis, we evaluated the effect of cholecalciferol supplementation on dialysis.
Randomized, double blind clinical trial in dialysis patients with 25OH Vitamin D deficiency for a period of 12 weeks.
In a pilot study, we investigated the effect of cholecalciferol supplementation (100,000 UI once per week or placebo. In vitro, peripheral blood mononuclear cells isolated by Ficoll-Hypaque centrifugation from 12 healthy volunteers were incubated with healthy or uremic serum in the presence or absence of 25 (OH)DC with 5% CO.
There was an increase in the serum 25(OH)D level in the cholecalciferol group. No differences were found in BAFF and IL7 levels and CD95 and BAFF-R expression in B lymphocytes from patients on dialysis after cholecalciferol supplementation. Uremic serum induced an increase in the IL-7, BAFF, BAFF-R and CD95 expression compared with the control. However, we observed no effect of incubation of 25(OH)D3 and 1,25(OH)2D3 on the expression of IL-7, BAFF, BAFF-R and CD95 when incubated in the presence of normal or uremic serum.
Our results suggest that vitamin D is not involved in mechanisms of regulation of differentiation and survival in B lymphocytes. In conclusion, further studies are needed to explore the effects of vitamin D on B lymphocytes to better evaluate the possible impact of vitamin D on humoral response in the CKD population.
终末期肾病导致 B 细胞淋巴细胞减少和维生素 D 水平降低。由于维生素 D 缺乏与终末期肾病患者 B 淋巴细胞功能障碍之间的联系尚不清楚,我们建议应研究维生素 D 充足度以及与这些细胞内稳态相关的因素。B 细胞内稳态是一个主要由生长和死亡信号调节的过程,如白细胞介素(IL)-7、B 细胞激活因子(BAFF)/BAFF 受体和 CD95 表达。
由于终末期肾病患者的血清维生素 D 水平降低,且与人类 B 细胞内稳态相关,我们评估了补充胆钙化醇对透析的影响。
在透析患者中进行了为期 12 周的随机、双盲临床试验,25OH 维生素 D 缺乏。
在一项初步研究中,我们研究了胆钙化醇补充(100000 UI 每周一次或安慰剂)的影响。体外,通过 Ficoll-Hypaque 离心从 12 名健康志愿者的外周血单核细胞中分离出的细胞,在存在或不存在 25(OH)DC 的情况下,用健康或尿毒症血清孵育。
胆钙化醇组血清 25(OH)D 水平升高。胆钙化醇补充后,透析患者 B 淋巴细胞的 BAFF 和 IL7 水平以及 CD95 和 BAFF-R 表达无差异。与对照相比,尿毒症血清诱导 IL-7、BAFF、BAFF-R 和 CD95 的表达增加。然而,当在正常或尿毒症血清存在的情况下孵育时,我们观察到 25(OH)D3 和 1,25(OH)2D3 的孵育对 IL-7、BAFF、BAFF-R 和 CD95 的表达没有影响。
我们的结果表明,维生素 D 不参与 B 淋巴细胞分化和存活的调节机制。因此,需要进一步研究维生素 D 对 B 淋巴细胞的影响,以更好地评估维生素 D 对 CKD 人群体液反应的可能影响。