首页> 外文期刊>The Journal of Allergy and Clinical Immunology >Chronic caregiver stress and IgE expression, allergen-induced proliferation, and cytokine profiles in a birth cohort predisposed to atopy.
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Chronic caregiver stress and IgE expression, allergen-induced proliferation, and cytokine profiles in a birth cohort predisposed to atopy.

机译:慢性照料者的压力和IgE表达,过敏原诱导的增殖以及特应性过敏人群中的细胞因子特征。

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BACKGROUND: Psychologic stress modifies immune function and cytokine production. OBJECTIVE: We examined relationships between caregiver stress on the following markers of early childhood immune response: (1) IgE expression (n=215); (2) mitogen-induced and allergen-specific (Dermatophagoides farinae [Der f 1] and cockroach [Bla g 2]) proliferative response (n=114); and (3) subsequent cytokine expression (INF-gamma, TNF-alpha, IL-10, and IL-13) in a prospective birth cohort predisposed to atopy. METHODS: Caregiver stress was measured at 2-month intervals for the first 2 years of life and yearly thereafter by using the Perceived Stress Scale. A subsequent blood sample obtained from the children (median age, 2.1 years; range, 18-32 months) was analyzed for total serum IgE level and allergen-induced proliferation quantified as the stimulation index (SI; mean thymidine incorporation of the stimulated sample divided by that of the unstimulated sample). The relationship between stress and the proliferative response (SI >3 vs SI < or =3), and total IgE level (< or =100 IU/mL vs >100 IU/mL) was examined by using logistic regression. The relationship between cytokine levels and stress was analyzed by using linear regression. RESULTS: In adjusted analyses higher caregiver stress in the first 6 months after birth was associated with a Der f 1 SI of greater than 3 (odds ratio [OR], 1.5; 95% CI, 1.0-2.3) and nominally associated with a Bla g 2 SI of greater than 3 (OR, 1.13; 95% CI, 0.7-1.8). Higher stress between ages 6 and 18 months was associated with a high total IgE level (OR, 2.03; 95% CI, 1.1-3.6). Higher stress was significantly associated with increased production of TNF-alpha, with a suggested trend between higher stress and reduced INF-gamma production. CONCLUSION: Increased stress in early childhood was associated with an atopic immune profile in these children predisposed to atopy-asthma.
机译:背景:心理压力会改变免疫功能和细胞因子的产生。目的:我们研究了照顾者压力与儿童早期免疫反应的以下标志物之间的关系:(1)IgE表达(n = 215); (2)有丝分裂原诱导的和变应原特异的(Dermatophagoides farinae [Der f 1]和蟑螂[Bla g 2])增殖反应(n = 114); (3)在易患特应性的预期出生队列中随后的细胞因子表达(INF-γ,TNF-α,IL-10和IL-13)。方法:使用感知压力量表,以生命的头2年为间隔2个月测量照护者压力,此后每年测量一次。分析从儿童(中位年龄,2.1岁;范围,18-32个月)中获得的后续血液样本的总血清IgE水平,并将过敏原诱导的增殖量化为刺激指数(SI;受刺激样本的平均胸苷掺入量除以通过未刺激的样本)。使用logistic回归分析了压力与增殖反应(SI> 3 vs SI <或= 3)和总IgE水平(<或= 100 IU / mL vs> 100 IU / mL)之间的关系。通过线性回归分析细胞因子水平与应激之间的关系。结果:在调整后的分析中,出生后前6个月较高的照料者压力与Der f 1 SI大于3相关(奇数比[OR]为1.5; 95%CI为1.0-2.3),并且名义上与Bla相关g 2 SI大于3(OR,1.13; 95%CI,0.7-1.8)。 6至18个月大的压力与较高的总IgE水平相关(OR为2.03; 95%CI为1.1-3.6)。较高的压力与TNF-α的产量增加显着相关,这表明较高的压力与INF-γ的产量减少之间存在趋势。结论:这些早期患特应性哮喘的儿童的压力增加与特应性免疫特征有关。

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