Velez Eva M M, Maldonado Galdeano Carolina, Carmuega Esteban, Weill Ricardo, Bibas Bonet María E, Perdigón Gabriela
Centro de Referencia para Lactobacilos, CERELA-CONICET,Chacabuco 145,San Miguel de Tucumán-Tucumán,Argentina.
CESNI (Centro de Estudios Nutricionales Infantiles),Buenos Aires,Argentina.
Br J Nutr. 2015 Aug 28;114(4):566-76. doi: 10.1017/S0007114515001981. Epub 2015 Jul 16.
Orally administered probiotic micro-organisms are able to regulate the exacerbated immune response during the antigenic sensitisation process. The aim of the present study was to evaluate the potential efficacy of probiotic fermented milk (PFM) in preventing or treating allergy in an experimental model, and to investigate its underlying mechanisms. Ovoalbumin (OVA)-sensitised BALB/c mice were fed with PFM before the sensitisation procedure or fed continuously with PFM. At 7 and 15 d post-sensitisation, anti-OVA-specific IgE, IgG, IgG1 and IgG2a concentrations were measured in the serum and broncho-alveolar lavage fluid (BALF). Concentrations of interferon-γ (IFN-γ), IL-4, IL-10 and total secretory IgA (S-IgA) were measured in the supernatants of macerated lungs or in the BALF. The levels of IgA+, CD4+ and CD8+ T lymphocytes and F4/80+ cells were measured in the lungs by immunofluorescence. Inducible CD4+/CD25/Foxp3+ regulatory T (Treg) cells were evaluated in the lungs. PFM shifted the T helper (Th)2 profile response towards a Th1 response that led to the production of IgG instead of IgE, with increasing levels of IL-10 and IFN-γ that play an important role in immunomodulation exerted by PFM administration in sensitised mice. Anti-OVA-specific IgE levels were significantly decreased; however, there was no modification in the levels of anti-OVA-specific IgG and total S-IgA. PFM did not influence Treg cells in treated mice. Consumption of PFM could be a promising strategy in the amelioration of airway allergies, considering that the effect is mediated by the production of IgG through the activation of Th1 instead of the direct activation of Th2 cells to produce IgE.
口服益生菌微生物能够调节抗原致敏过程中加剧的免疫反应。本研究的目的是评估益生菌发酵乳(PFM)在实验模型中预防或治疗过敏的潜在功效,并研究其潜在机制。在致敏程序前给卵清蛋白(OVA)致敏的BALB/c小鼠喂食PFM,或持续喂食PFM。在致敏后7天和15天,测量血清和支气管肺泡灌洗液(BALF)中抗OVA特异性IgE、IgG、IgG1和IgG2a的浓度。测量研磨肺组织上清液或BALF中干扰素-γ(IFN-γ)、IL-4、IL-10和总分泌型IgA(S-IgA)的浓度。通过免疫荧光测量肺组织中IgA+、CD4+和CD8+T淋巴细胞以及F4/80+细胞的水平。评估肺组织中诱导性CD4+/CD25/Foxp3+调节性T(Treg)细胞。PFM将辅助性T(Th)2型反应转变为Th1型反应,导致产生IgG而非IgE,同时IL-10和IFN-γ水平升高,它们在PFM给药对致敏小鼠发挥的免疫调节中起重要作用。抗OVA特异性IgE水平显著降低;然而,抗OVA特异性IgG和总S-IgA水平没有变化。PFM对治疗小鼠的Treg细胞没有影响。考虑到该效应是通过激活Th1产生IgG介导的,而非直接激活Th2细胞产生IgE,食用PFM可能是改善气道过敏的一种有前景的策略。