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Sex-related differences in immune development and the expression of atopy in early childhood.

机译:儿童早期免疫发育和特应性表达的性别相关差异。

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BACKGROUND: Sex and age are known to influence the clinical expression of asthma and allergic diseases. OBJECTIVE: We sought to evaluate whether immune response profiles also vary by sex and age. METHODS: We performed a prospective birth cohort study (Childhood Origins of Asthma) designed to evaluate interactions among age, sex, immune responses, and virus infections on the development of asthma and allergic diseases. Two hundred eighty-nine subjects were enrolled at birth, and 275 maintained prospective follow-up for 3 years. Cytokine response profiles at birth, 1, and 3 years of age; rates of wheezing, atopic dermatitis, and viral illnesses; and biomarkers of atopy, including total and specific IgE levels and peripheral eosinophil counts, were evaluated. RESULTS: PHA-induced IFN-gamma responses were higher in boys at 1 year of age (median, 35 vs 19 pg/mL; P < .001) and at 3 years of age (median, 282 vs 181 pg/mL; P = .07). Among children who wheezed during the third year of life, boys had increased IFN-gamma, IL-5, and IL-13 responses at age 3 years (P < .001, P = .008, and P = .01, respectively). Boys also demonstrated increased rates of sensitization (P = .05 at year 1), total IgE levels (P = .03 at year 1 and P = .006 at year 3), and peripheral eosinophil counts (2.62 vs 1.85; P = .05 at year 3). CONCLUSION: Sex-specific differences in immune responses develop during early childhood; some of these differences developmentally proceed, whereas others occur in parallel to the clinical expression of various atopic phenotypes. CLINICAL IMPLICATIONS: The differential expression of atopic diseases between boys and girls in early childhood is accompanied by sex-specific differences in immune response profiles.
机译:背景:性别和年龄会影响哮喘和过敏性疾病的临床表达。目的:我们试图评估免疫应答谱是否也随性别和年龄而变化。方法:我们进行了一项前瞻性出生队列研究(哮喘的儿童起源),旨在评估年龄,性别,免疫反应和病毒感染之间对哮喘和过敏性疾病发展的相互作用。在出生时招募了289名受试者,并对275名受试者进行了为期3年的前瞻性随访。出生时,1、3岁时的细胞因子反应情况;喘息,特应性皮炎和病毒性疾病的发生率;评估了特应性的生物标志物,包括总的和特定的IgE水平和外周嗜酸性粒细胞计数。结果:PHA诱导的IFN-γ反应在1岁男孩(中位数,35 vs 19 pg / mL; P <.001)和3岁男孩(中位数,282 vs 181 pg / mL; P)中较高= .07)。在生命的第三年发生喘息的儿童中,男孩在3岁时的IFN-γ,IL-5和IL-13应答增加(分别为P <.001,P = .008和P = .01) 。男孩还表现出较高的致敏率(第1年P = 0.05),总IgE水平(第1年P = 0.03和第3年P = 0.006)以及外周嗜酸性粒细胞计数(2.62比1.85; P =)。第3年的05)。结论:儿童早期免疫反应存在性别特异性差异。这些差异中的一些会逐渐发展,而其他差异会与各种异位表型的临床表达同时发生。临床意义:早期儿童男孩和女孩之间特应性疾病的差异表达伴随着免疫反应谱的性别特异性差异。

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