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Workshop to identify critical windows of exposure for children's health: immune and respiratory systems work group summary.

机译:确定儿童健康暴露的关键窗口的研讨会:免疫和呼吸系统工作组摘要。

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摘要

Fetuses, infants, and juveniles (preadults) should not be considered simply "small adults" when it comes to toxicological risk. We present specific examples of developmental toxicants that are more toxic to children than to adults, focusing on effects on the immune and respiratory systems. We describe differences in both the pharmacokinetics of the developing immune and respiratory systems as well as changes in target organ sensitivities to toxicants. Differential windows of vulnerability during development are identified in the context of available animal models. We provide specific approaches to directly investigate differential windows of vulnerability. These approaches are based on fundamental developmental biology and the existence of discrete developmental processes within the immune and respiratory systems. The processes are likely to influence differential developmental susceptibility to toxicants, resulting in lifelong toxicological changes. We also provide a template for comparative research. Finally, we discuss the application of these data to risk assessment.
机译:当涉及毒理学风险时,不应将胎儿,婴儿和少年(脚手架)简单地视为“小成年人”。我们提供了发育毒物的具体示例,这些毒物对儿童的毒性大于对成年人的毒性,重点在于对免疫和呼吸系统的影响。我们描述了发展中的免疫系统和呼吸系统的药代动力学差异以及靶器官对毒物的敏感性变化。在可开发的动物模型的背景下,确定了发育过程中脆弱性的不同窗口。我们提供了直接调查漏洞的不同窗口的特定方法。这些方法基于基本的发育生物学以及免疫和呼吸系统内离散发育过程的存在。该过程可能会影响对毒物的不同发育敏感性,从而导致终身毒理学变化。我们还提供了比较研究的模板。最后,我们讨论了这些数据在风险评估中的应用。

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