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儿童期辅助性T细胞1和辅助性T细胞2细胞因子产生的个体发生

Ontogeny of T-helper 1 and T-helper 2 cytokine production in childhood.

作者信息

Smart J M, Kemp A S

机构信息

Department of Immunology, Royal Children's Hospital, Murdoch Children's Research Institute, Melbourne, Australia.

出版信息

Pediatr Allergy Immunol. 2001 Aug;12(4):181-7. doi: 10.1034/j.1399-3038.2001.012004181.x.

Abstract

Compared to adults, infants and young children demonstrate differences in their immune response, indicating that there is maturation or change over time and it is probable that this may be reflected in cytokine production. Cytokine responses have been demonstrated to be different in atopic and non-atopic individuals. In this study, we examined T-helper 1 (Th1) (interferon-gamma [IFN-gamma]) and T-helper 2 (Th2) (interleukin [IL]-4, IL-5, and IL-13) cytokine release from atopic and non-atopic children in response to the staphylococcal superantigen, staphylococcal enterotoxin B (SEB). In non-atopic and atopic children, IFN-gamma, IL-4, and IL-5 release was significantly related to age. Non-atopic children younger than 2 years of age were found to have significantly reduced Th2 (IL-4, IL-5, and IL-13) responses when compared with older, non-atopic children. Atopic children had a reduced IFN-gamma response when compared with non-atopics in early childhood; however, the decreased IFN-gamma response seen in early childhood did not persist after 10 years. These age-related changes in cytokine production provide further support for the concept that cytokine deviations may determine the natural history of atopic disease during early childhood. In addition, the present study indicates the necessity of age-matched controls when examining children for both Th1 (IFN-gamma) and Th2 (IL-4) cytokine release.

摘要

与成年人相比,婴幼儿的免疫反应存在差异,这表明免疫反应会随着时间推移而成熟或发生变化,并且这种变化很可能反映在细胞因子的产生上。已证实特应性个体和非特应性个体的细胞因子反应有所不同。在本研究中,我们检测了特应性和非特应性儿童在接触葡萄球菌超抗原——葡萄球菌肠毒素B(SEB)后,T辅助细胞1(Th1)(γ干扰素[IFN-γ])和T辅助细胞2(Th2)(白细胞介素[IL]-4、IL-5和IL-13)细胞因子的释放情况。在非特应性和特应性儿童中,IFN-γ、IL-4和IL-5的释放与年龄显著相关。结果发现,2岁以下的非特应性儿童与年龄较大的非特应性儿童相比,Th2(IL-4、IL-5和IL-13)反应显著降低。特应性儿童在幼儿期的IFN-γ反应比非特应性儿童低;然而,幼儿期出现的IFN-γ反应降低在10年后并未持续存在。细胞因子产生的这些与年龄相关的变化,为细胞因子偏差可能决定幼儿期特应性疾病自然病程这一概念提供了进一步支持。此外,本研究表明,在检测儿童Th1(IFN-γ)和Th2(IL-4)细胞因子释放时,需要年龄匹配的对照。

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