The Ancestral Environment Shapes Antiviral CD8+ T cell Responses across Generations

被引:14
|
作者
Post, Christina M. [1 ]
Boule, Lisbeth A. [1 ,2 ]
Burke, Catherine G. [2 ]
O'Dell, Colleen T. [1 ]
Winans, Bethany [1 ]
Lawrence, B. Paige [1 ,2 ]
机构
[1] Univ Rochester, Sch Med & Dent, Dept Environm Med, Rochester, NY 14642 USA
[2] Univ Rochester, Sch Med & Dent, Dept Microbiol & Immunol, Rochester, NY 14642 USA
基金
美国国家卫生研究院;
关键词
ARYL-HYDROCARBON RECEPTOR; EPIGENETIC TRANSGENERATIONAL INHERITANCE; DEVELOPING IMMUNE-SYSTEM; INFLUENZA-VIRUS; POLYCHLORINATED-BIPHENYLS; DEVELOPMENTAL ACTIVATION; LACTATIONAL EXPOSURE; METHYLATION STATUS; PRENATAL EXPOSURE; AH-RECEPTOR;
D O I
10.1016/j.isci.2019.09.014
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Recent studies have linked health fates of children to environmental exposures of their great grandparents. However, few studies have considered whether ancestral exposures influence immune function across generations. Here, we report transgenerational inheritance of altered T cell responses resulting from maternal (F0) exposure to the aryl hydrocarbon receptor ligand 2,3,7,8-tetrachlorodibenzo-pdioxin (TCDD). Since F0 exposure to TCDD has been linked to transgenerational transmission of reproductive problems, we asked whether maternal TCDD exposure also caused transgenerational changes in immune function. F0 exposure caused transgenerational effects on the CD8(+) T cell response to influenza virus infection in females but not in males. Outcrosses showed changes were passed through both parental lineages. These data demonstrate that F0 exposure to an aryl hydrocarbon receptor (AHR) agonist causes durable changes to immune responses that can affect subsequent generations. This has broad implications for understanding how the environment of prior generations shapes susceptibility to pathogens and antiviral immunity in later generations.
引用
收藏
页码:168 / +
页数:27
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