Kannarkat G T, Cook D A, Lee J-K, Chang J, Chung J, Sandy E, Paul K C, Ritz B, Bronstein J, Factor S A, Boss J M, Tansey M G
Department of Physiology, Emory University School of Medicine, Atlanta, GA.
Department of Epidemiology and Center for Occupational and Environmental Health, Fielding School of Public Health, University of California at Los Angeles, Los Angeles, CA.
NPJ Parkinsons Dis. 2015;1:15002-. doi: 10.1038/npjparkd.2015.2. Epub 2015 Apr 22.
BACKGROUND/OBJECTIVES: The common non-coding single nucleotide polymorphism (SNP) in is associated with risk for idiopathic Parkinson's disease (PD). The location of the SNP in the major histocompatibility complex class II (MHC-II) locus implicates regulation of antigen presentation as a potential mechanism by which immune responses link genetic susceptibility to environmental factors in conferring lifetime risk for PD.
For immunophenotyping, blood cells from 81 subjects were analyzed by qRT-PCR and flow cytometry. A case-control study was performed on a separate cohort of 962 subjects to determine association of pesticide exposure and the SNP with risk of PD.
Homozygosity for at this SNP was associated with heightened baseline expression and inducibility of MHC class II molecules in B cells and monocytes from peripheral blood of healthy controls and PD patients. In addition, exposure to a commonly used class of insecticide, pyrethroids, synergized with the risk conferred by this SNP (OR = 2.48, p = 0.007), thereby identifying a novel gene-environment interaction that promotes risk for PD via alterations in immune responses.
In sum, these novel findings suggest that the MHC-II locus may increase susceptibility to PD through presentation of pathogenic, immunodominant antigens and/or a shift toward a more pro-inflammatory CD4+ T cell response in response to specific environmental exposures, such as pyrethroid exposure through genetic or epigenetic mechanisms that modulate MHC-II gene expression.
背景/目的:常见的非编码单核苷酸多态性(SNP)与特发性帕金森病(PD)的风险相关。该SNP位于主要组织相容性复合体II类(MHC-II)基因座,这意味着抗原呈递的调节是一种潜在机制,通过这种机制,免疫反应将遗传易感性与环境因素联系起来,从而赋予PD终生风险。
为了进行免疫表型分析,通过qRT-PCR和流式细胞术对81名受试者的血细胞进行了分析。对另一组962名受试者进行了病例对照研究,以确定接触农药和该SNP与PD风险的关联。
该SNP的纯合性与健康对照和PD患者外周血B细胞和单核细胞中MHC II类分子的基线表达升高和诱导性增加相关。此外,接触常用的一类杀虫剂拟除虫菊酯与该SNP所带来的风险具有协同作用(OR = 2.48,p = 0.007),从而确定了一种新的基因-环境相互作用,即通过免疫反应的改变促进PD风险。
总之,这些新发现表明,MHC-II基因座可能通过呈递致病性、免疫显性抗原和/或响应特定环境暴露(如通过调节MHC-II基因表达的遗传或表观遗传机制接触拟除虫菊酯)而向更促炎的CD4+T细胞反应转变,从而增加对PD的易感性。