Rausch-Fan Xiahoui, Leutmezer Fritz, Willheim Martin, Spittler Andreas, Bohle Barbara, Ebner Christof, Jensen-Jarolim Erika, Boltz-Nitulescu George
Institute of Pathophysiology, University of Vienna, Vienna, Austria.
Int Arch Allergy Immunol. 2002 May;128(1):33-41. doi: 10.1159/000058001.
The steroid hormone 1alpha,25-dihydroxyvitamin D3 (calcitriol), in addition to its crucial role in calcium homeostasis, exerts several effects on the immune system by regulating cell proliferation, differentiation, and maturation. These effects may be exerted through the control of protooncogenes and the regulation of cytokine production.
The influence of calcitriol on cytokines secretion by human peripheral blood mononuclear cells (PBMC) isolated from healthy donors, and by allergen-specific T helper (Th) cell clones was studied. PBMC were cultured for 48 h with phorbol myristate acetate (PMA) and ionomycin in the presence or absence of calcitriol. Human Th cell clones were stimulated with either Bet v 1 allergen or anti-CD3 antibodies and PMA. Cytokines were measured in the supernatants by ELISA, and at single-cell level by FACS.
Calcitriol significantly inhibited the production of IL-2, IFN-gamma and IL-12 by PBMC, as well as the percentage of CD4+ T cells containing intracytoplasmic IL-2 and IFN-gamma. Interestingly, calcitriol-treated PBMC induced the production of IL-10 and IL-5, but not of IL-4. The effect of calcitriol was maximal at 10(-7) to 10(-9) and noneffective at 10(-11) M. Calcitriol diminished the secretion of IL-1, TNF-alpha, and MG-CSF in PBMC. Furthermore, calcitriol also decreased the secretion of IL-2 and IFN-gamma by Th1 clones, and of IL-4 by Th2 clones.
Our data strongly support the notion that calcitriol modulates the production of cytokines in a time- and concentration-dependent manner, and suggest that nonhypercalcemic derivatives of 1alpha,25-dihydroxyvitamin D(3) may be used for new immunosuppressive therapies.
类固醇激素1α,25 - 二羟基维生素D3(骨化三醇),除了在钙稳态中起关键作用外,还通过调节细胞增殖、分化和成熟对免疫系统产生多种影响。这些影响可能通过原癌基因的控制和细胞因子产生的调节来实现。
研究了骨化三醇对从健康供体分离的人外周血单个核细胞(PBMC)以及变应原特异性T辅助(Th)细胞克隆分泌细胞因子的影响。PBMC在存在或不存在骨化三醇的情况下,用佛波酯(PMA)和离子霉素培养48小时。人Th细胞克隆用Bet v 1变应原或抗CD3抗体和PMA刺激。通过ELISA在培养上清液中测量细胞因子,并通过流式细胞术在单细胞水平上测量。
骨化三醇显著抑制PBMC产生IL - 2、IFN - γ和IL - 12,以及含有胞质内IL - 2和IFN - γ的CD4 + T细胞的百分比。有趣的是,经骨化三醇处理的PBMC诱导产生IL - 10和IL - 5,但不产生IL - 4。骨化三醇的作用在10(-7)至10(-9)时最大,在10(-11)M时无作用。骨化三醇减少PBMC中IL - 1、TNF - α和MG - CSF的分泌。此外,骨化三醇还降低Th1克隆分泌IL - 2和IFN - γ,以及Th2克隆分泌IL - 4。
我们的数据有力地支持了骨化三醇以时间和浓度依赖性方式调节细胞因子产生的观点,并表明1α,25 - 二羟基维生素D(3)的非高钙血症衍生物可用于新的免疫抑制治疗。