Verheijden Kim At, Braber Saskia, Leusink-Muis Thea, Thijssen Suzan, Boon Louis, Kraneveld Aletta D, Garssen Johan, Folkerts Gert, Willemsen Linette Em
Faculty of Science, Utrecht Institute for Pharmaceutical Sciences, Division of Pharmacology, Utrecht University, Utrecht, Netherlands.
Faculty of Veterinary Sciences, Division of Veterinary Pharmacy, Pharmacology, and Toxicology, Utrecht University, Utrecht, Netherlands.
J Nutr. 2015 Apr 1;146(4):831-837. doi: 10.3945/jn.115.224402.
In a murine model for house dust mite (HDM)-induced asthma, dietary galacto-oligosaccharides have been shown to suppress allergic symptoms. Previously, CD25+ regulatory T cells (Tregs) induced by nondigestible oligosaccharides were found to protect against allergy development.
The aim of the current study was to examine the effect of anti-CD25-induced Treg depletion in a murine HDM-induced asthma model and to study the contribution of Tregs in the protective effect of dietary intervention with galacto-oligosaccharides.
Male BALB/c mice (aged 6-8 wk) were intranasally sensitized and challenged with phosphate-buffered saline (PBS) or HDM. Two weeks before sensitization and throughout the whole experiment, mice were fed a control or 1% w/w galacto-oligosaccharide diet. Tregs were depleted by anti-mouse CD25 antibody (intraperitoneally injected). On day 14, T helper cell subtypes in lung and spleen were analyzed and cytokines were measured. Leukocyte subtypes were analyzed in the bronchoalveolar lavage fluid, and interleukin (IL)-33 and chemokines were measured in lung homogenate supernatants.
Anti-CD25 treatment depleted CD25+ Forkhead box P3+ Tregs in the lung and spleen of control and HDM-allergic mice (P < 0.0001) by >70% while increasing the percentage of activated T helper cells (P < 0.05) and type 2 T helper cells (P < 0.05). This was associated with increased IL-10, IL-4, and IL-13 concentrations in supernatants of ex vivo restimulated lung cells (P < 0.01). Bronchoalveolar lavage fluid leukocyte numbers and percentages of eosinophils and lymphocytes were greater in HDM-allergic mice compared with PBS mice (P < 0.01) but remained unaffected by the anti-CD25 treatment. Galacto-oligosaccharides decreased airway eosinophilia compared with HDM-allergic mice fed the control diet (from 47.8% ± 6.7% to 26.6% ± 8.5%, P < 0.01). This protective effect was lost in anti-CD25-treated mice (P < 0.05). In lung homogenates of HDM-allergic mice, IL-33 was increased compared with PBS mice (from 2.8 ± 0.3 to 5.4 ± 0.6 ng protein/mg, P < 0.01). Galacto-oligosaccharides abrogated the increase in IL-33 compared with HDM-allergic mice fed the control diet (3.0 ± 0.6 ng protein/mg, P < 0.05), which was abolished by the anti-CD25 treatment (P < 0.01).
Treg depletion enhances pulmonary type 2 T helper cell frequency and cytokine release in HDM-induced asthma in mice. Galacto-oligosaccharides decreased airway eosinophilia and IL-33 concentrations in the lung, which was abrogated by Treg depletion. This indicates that galacto-oligosaccharides have a beneficial effect in the prevention of HDM-induced allergic asthma by supporting pulmonary Treg function.
在屋尘螨(HDM)诱导的哮喘小鼠模型中,已证明膳食低聚半乳糖可抑制过敏症状。此前发现,不可消化的低聚糖诱导的CD25⁺调节性T细胞(Tregs)可预防过敏发展。
本研究旨在探讨在小鼠HDM诱导的哮喘模型中,抗CD25诱导的Treg耗竭的作用,并研究Tregs在低聚半乳糖膳食干预保护作用中的贡献。
雄性BALB/c小鼠(6 - 8周龄)经鼻用磷酸盐缓冲盐水(PBS)或HDM致敏并激发。在致敏前两周及整个实验过程中,给小鼠喂食对照饮食或1% w/w低聚半乳糖饮食。通过抗小鼠CD25抗体(腹腔注射)使Tregs耗竭。在第14天,分析肺和脾中的辅助性T细胞亚群并测量细胞因子。分析支气管肺泡灌洗液中的白细胞亚群,并测量肺匀浆上清液中的白细胞介素(IL)-33和趋化因子。
抗CD25治疗使对照和HDM过敏小鼠肺和脾中的CD25⁺叉头框P3⁺ Tregs减少>70%(P < 0.0001),同时增加了活化辅助性T细胞(P < 0.05)和2型辅助性T细胞(P < 0.05)的百分比。这与体外再刺激的肺细胞上清液中IL-10、IL-4和IL-13浓度增加有关(P < 0.01)。与PBS小鼠相比,HDM过敏小鼠的支气管肺泡灌洗液白细胞数量以及嗜酸性粒细胞和淋巴细胞百分比更高(P < 0.01),但抗CD25治疗对其无影响。与喂食对照饮食的HDM过敏小鼠相比,低聚半乳糖降低了气道嗜酸性粒细胞增多(从47.8% ± 6.7%降至26.6% ± 8.5%,P < 0.01)。在抗CD25治疗的小鼠中,这种保护作用消失(P < 0.05)。与PBS小鼠相比,HDM过敏小鼠肺匀浆中IL-33增加(从2.8 ± 0.3增至5.4 ± 0.6 ng蛋白/mg,P < 0.01)。与喂食对照饮食的HDM过敏小鼠相比,低聚半乳糖消除了IL-33的增加(3.0 ± 0.6 ng蛋白/mg,P < 0.05),而抗CD25治疗则消除了这种作用(P < 0.01)。
Treg耗竭增强了小鼠HDM诱导的哮喘中肺部2型辅助性T细胞频率和细胞因子释放。低聚半乳糖降低了气道嗜酸性粒细胞增多和肺中IL-33浓度,而Treg耗竭消除了这种作用。这表明低聚半乳糖通过支持肺部Treg功能,对预防HDM诱导的过敏性哮喘具有有益作用。