Carlsbad Science Foundation, Monrovia, CA, USA.
City of Hope National Medical Center, Duarte, CA, USA.
Brain Behav Immun. 2014 Jan;35:169-75. doi: 10.1016/j.bbi.2013.09.012. Epub 2013 Sep 25.
Cytokine gene variants are known to influence both infectious disease susceptibility and harm-avoidant behaviors, suggesting that these risk variants may be pleiotropically linked to instinctual disease-avoidant traits. The gamma-interferon (IFNG) +874 T>A polymorphism (rs2430561) is an ideal candidate gene variant for immune-behavioral studies. It is a functional SNP, regulating IFNG mRNA expression; it is known to modulate serotonergic activity and is therefore capable of modifying behavior; and it has previously been associated with increased susceptibility to malaria, tuberculosis, leprosy and Chagas disease. We hypothesized that the infectious disease-high-risk IFNG +874 A-allele would be associated with four personality traits previously reported as behavioral defenses against infection: Harm Avoidance (HA), Extraversion (E), Exploratory Excitability (Exp E), and Openness to Experience (O). We tested this hypothesis in a sample of 168 healthy university students from Southern California genotyped for IFNG +874 T>A and evaluated by the Temperament and Character Inventory-Revised (TCI-R) and the NEO Five-Factor Inventory (NEO-FFI). We found that the infectious disease-high-risk IFNG +874 A-allele was associated with increased HA (P=0.001) and decreased E (P=0.030) and Exp E (P=0.030). These findings suggest that the IFNG +874 A gene variant is linked both to infectious disease susceptibility and to proactive behavioral defenses that reduce infection risk in healthy subjects.
细胞因子基因变异已知会影响传染病易感性和回避行为,这表明这些风险变异可能与本能的疾病回避特征具有多效性联系。γ-干扰素(IFNG)+874 T>A 多态性(rs2430561)是免疫行为研究的理想候选基因变异。它是一种功能性 SNP,调节 IFNG mRNA 表达;已知它能调节 5-羟色胺能活性,从而能够改变行为;并且先前它与疟疾、结核病、麻风病和恰加斯病的易感性增加有关。我们假设传染病高风险 IFNG+874 A-等位基因与先前报道的四种抗感染行为防御特征有关:回避(HA)、外向性(E)、探索性兴奋(Exp E)和开放性体验(O)。我们在加利福尼亚南部的 168 名健康大学生样本中测试了这个假设,这些学生进行了 IFNG+874 T>A 基因分型,并通过气质和性格量表修订版(TCI-R)和五因素人格量表(NEO-FFI)进行了评估。我们发现,传染病高风险 IFNG+874 A-等位基因与 HA 增加(P=0.001)和 E(P=0.030)和 Exp E(P=0.030)减少有关。这些发现表明,IFNG+874 A 基因变异与传染病易感性以及降低健康受试者感染风险的主动行为防御有关。