Asthma, allergy and vitamin E: Current and future perspectives

被引:22
作者
Cook-Mills, Joan M. [1 ]
Averill, Samantha H.
Lajiness, Jacquelyn D.
机构
[1] Indiana Univ Sch Med, Herman B Wells Ctr Pediat Res, Dept Pediat, 1044 W Walnut St,R4-202A, Indianapolis, IN 46202 USA
基金
美国国家卫生研究院;
关键词
Allergy; Asthma; Vitamin E; alpha-Tocopherol; gamma-Tocopherol; Human; Animal models; PROTEIN-KINASE-C; DENDRITIC CELL-DIFFERENTIATION; DIETARY ANTIOXIDANT SUPPLEMENTATION; CD34(+) HEMATOPOIETIC PROGENITORS; GAMMA-TOCOPHEROL SUPPLEMENTATION; COLONY-STIMULATING FACTOR; HOUSE-DUST MITE; ALPHA-TOCOPHEROL; MATERNAL TRANSMISSION; EARLY-LIFE;
D O I
10.1016/j.freeradbiomed.2021.10.037
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Asthma and allergic disease result from interactions of environmental exposures and genetics. Vitamin E is one environmental factor that can modify development of allergy early in life and modify responses to allergen after allergen sensitization. Seemingly varied outcomes from vitamin E are consistent with the differential functions of the isoforms of vitamin E. Mechanistic studies demonstrate that the vitamin E isoforms alpha-tocopherol and gamma-tocopherol have opposite functions in regulation of allergic inflammation and development of allergic disease, with alpha-tocopherol having anti-inflammatory functions and gamma-tocopherol having pro-inflammatory functions in allergy and asthma. Moreover, global differences in prevalence of asthma by country may be a result, at least in part, of differences in consumption of these two isoforms of tocopherols. It is critical in clinical and animal studies that measurements of the isoforms of tocopherols be determined in vehicles for the treatments, and in the plasma and/or tissues before and after intervention. As allergic inflammation is modifiable by tocopheml isoforms, differential regulation by tocopherol isoforms provide a foundation for development of interventions to improve lung function in disease and raise the possibility of early life dietary interventions to limit the development of lung disease.
引用
收藏
页码:388 / 402
页数:15
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