Centre for Child Health Research, Telethon Institute for Child Health Research, University of Western Australia, West Perth, Australia.
Clin Exp Allergy. 2011 Jun;41(6):783-93. doi: 10.1111/j.1365-2222.2011.03762.x. Epub 2011 Apr 15.
Identified factors from milk have been shown to improve health outcomes. One specific factor, transforming growth factor-Beta (TGF)-β, has been identified previously as having the potential to impact on immunological outcomes in the newborn offspring. The primary objective of this review was to examine the published studies that have considered TGF-β in association with immunological outcomes of experimental models. We hypothesized that oral administration of TGF-β (through human milk, cow's milk, infant formula) or recombinant TGF-β delivered via gavage, may down-regulate immune activation in newborn offspring. Animal experimental studies were identified through MEDLINE, CAB Abstracts, Biological Abstracts and Scopus. Selection criteria included well-described animal populations, sample and study design, source of TGF-β, age and immunological outcomes measured and effect size. The findings were summarized temporally in tabular format, giving an overall measure of effect based on the literature available since 1994. Animal experimental studies (n=13) were included in the review to determine an association between maternal TGF-β and immunological outcomes. Overall 92% of these studies (12/13) showed a positive association with TGF-β1 or TGF-β2, demonstrating protection against immunologically related outcomes in early life in an animal model. TGF-β is important in developing and maintaining appropriate immune responses in the offspring. TGF-β delivered orally to neonatal animals provides protection against adverse immunological outcomes, corroborating and supporting findings from human studies. Animal studies provide important clues to the pathogenesis and therapeutics of immune activation and allergy in early childhood. TGF-βs are important growth factors involved in maintaining homeostasis in the intestine, regulating inflammation and allergy development and promoting oral tolerance in infants. Thus, taken as a whole, these and our other findings suggest that this cytokine in milk may influence the development of immunological outcomes in offspring.
已发现牛奶中的某些成分可改善健康状况。此前,有一种特定的成分转化生长因子-β(TGF-β)被认为有可能影响新生儿的免疫结果。本综述的主要目的是检查已考虑将 TGF-β与实验模型的免疫结果相关联的已发表研究。我们假设通过口服(母乳、牛奶、婴儿配方奶粉)或通过灌胃给予重组 TGF-β,可能会下调新生后代的免疫激活。通过 MEDLINE、CAB Abstracts、Biological Abstracts 和 Scopus 确定了动物实验研究。选择标准包括详细描述的动物种群、样本和研究设计、TGF-β 的来源、测量的年龄和免疫结果以及效应大小。将结果按时间顺序以表格形式进行总结,根据 1994 年以来的文献提供了总体效果衡量标准。本综述纳入了 13 项动物实验研究,以确定母体 TGF-β与免疫结果之间的关联。这些研究中有 92%(12/13)总体上显示出与 TGF-β1 或 TGF-β2 的正相关,表明在动物模型中对生命早期与免疫相关的结果具有保护作用。TGF-β在后代中形成和维持适当免疫反应方面很重要。口服给予新生动物 TGF-β可防止免疫不良后果,这与人类研究的发现相符,并提供了支持。动物研究为婴幼儿期免疫激活和过敏的发病机制和治疗提供了重要线索。TGF-βs 是参与维持肠道内稳态、调节炎症和过敏发展以及促进婴儿口服耐受的重要生长因子。因此,总的来说,这些研究和我们的其他发现表明,牛奶中的这种细胞因子可能会影响后代的免疫结果的发展。