Martinez Fernando D
Arizona Respiratory Center, College of Medicine, The University of Arizona, 1501 N. Campbell Avenue, 2349, Tucson, AZ 85724-5030, USA.
Immunol Allergy Clin North Am. 2005 Nov;25(4):709-21. doi: 10.1016/j.iac.2005.09.001.
The example of complex interactions between environmental exposures and polymorphisms in the CD14 gene in predisposing for allergy-related conditions offers a good indication of the complexity of the mechanisms that determine susceptibility to these conditions. Contrary to what has been the rule for monogenic diseases, the association between genetic variations and polygenic conditions such as asthma and allergies may not always be unidirectional; that is, not always will the same alleles be associated with the conditions under study. Concepts of penetrance of genetic variations that ignore these nonlinear influences (which may affect gene-gene and gene-environment interactions) may hinder a better understanding of mechanisms of disease involved, and therefore may delay the development of preventive strategies for these common conditions. Discrepancies between well-designed genetic studies of asthma and allergies, therefore, may be suggesting something fundamental about how these diseases develop and how it will be possible to abolish them in the future.
环境暴露与CD14基因多态性之间复杂的相互作用在引发过敏相关疾病方面的例子,很好地表明了决定对这些疾病易感性的机制的复杂性。与单基因疾病的情况不同,基因变异与哮喘和过敏等多基因疾病之间的关联可能并不总是单向的;也就是说,并非总是相同的等位基因与所研究的疾病相关。忽略这些非线性影响(可能影响基因-基因和基因-环境相互作用)的基因变异外显率概念,可能会阻碍对所涉及疾病机制的更好理解,因此可能会延迟针对这些常见疾病的预防策略的开发。因此,精心设计的哮喘和过敏基因研究之间的差异,可能暗示了这些疾病如何发展以及未来如何消除它们的一些基本情况。