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Our Environment Shapes Us: The Importance of Environment and Sex Differences in Regulation of Autoantibody Production

机译:我们的环境塑造了我们:环境和性别差异在自身抗体生产监管中的重要性

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摘要

Consequential differences exist between the male and female immune systems’ ability to respond to pathogens, environmental insults or self-antigens, and subsequent effects on immunoregulation. In general, females when compared with their male counterparts, respond to pathogenic stimuli and vaccines more robustly, with heightened production of antibodies, pro-inflammatory cytokines, and chemokines. While the precise reasons for sex differences in immune response to different stimuli are not yet well understood, females are more resistant to infectious diseases and much more likely to develop autoimmune diseases. Intrinsic (i.e., sex hormones, sex chromosomes, etc.) and extrinsic (microbiome composition, external triggers, and immune modulators) factors appear to impact the overall outcome of immune responses between sexes. Evidence suggests that interactions between environmental contaminants [e.g., endocrine disrupting chemicals (EDCs)] and host leukocytes affect the ability of the immune system to mount a response to exogenous and endogenous insults, and/or return to normal activity following clearance of the threat. Inherently, males and females have differential immune response to external triggers. In this review, we describe how environmental chemicals, including EDCs, may have sex differential influence on the outcome of immune responses through alterations in epigenetic status (such as modulation of microRNA expression, gene methylation, or histone modification status), direct and indirect activation of the estrogen receptors to drive hormonal effects, and differential modulation of microbial sensing and composition of host microbiota. Taken together, an intriguing question develops as to how an individual’s environment directly and indirectly contributes to an altered immune response, dysregulation of autoantibody production, and influence autoimmune disease development. Few studies exist utilizing well-controlled cohorts of both sexes to explore the sex differences in response to EDC exposure and the effects on autoimmune disease development. Translational studies incorporating multiple environmental factors in animal models of autoimmune disease are necessary to determine the interrelationships that occur between potential etiopathological factors. The presence or absence of autoantibodies is not a reliable predictor of disease. Therefore, future studies should incorporate all the susceptibility/influencing factors, coupled with individual genomics, epigenomics, and proteomics, to develop a model that better predicts, diagnoses, and treats autoimmune diseases in a personalized-medicine fashion.
机译:男性和女性免疫系统对病原体,环境侵害或自身抗原的反应能力以及随后对免疫调节的影响之间存在相应的差异。通常,雌性与雄性相比,对病原性刺激和疫苗的反应更加强烈,抗体,促炎性细胞因子和趋化因子的产生增加。尽管对不同刺激的免疫反应中性别差异的确切原因尚不十分清楚,但女性对传染病的抵抗力更高,并且更有可能患上自身免疫性疾病。内在因素(即性激素,性染色体等)和外在因素(微生物组组成,外部触发因素和免疫调节剂)似乎会影响两性之间免疫反应的整体结果。有证据表明,环境污染物(例如内分泌干扰物(EDC))与宿主白细胞之间的相互作用会影响免疫系统对外源性和内源性损伤做出反应的能力,和/或在清除威胁后恢复正常活动。本质上,雄性和雌性对外部诱因具有不同的免疫反应。在这篇综述中,我们描述了环境化学物质(包括EDC)可能如何通过表观遗传状态的改变(例如微RNA表达的调节,基因甲基化或组蛋白修饰状态的改变),直接和间接激活对免疫应答的结果产生性别差异影响雌激素受体的驱动激素作用,以及微生物感测和宿主菌群组成的差异调节。综上所述,一个有趣的问题就一个人的环境如何直接或间接地导致免疫应答改变,自身抗体产生失调以及如何影响自身免疫疾病的发展而产生。很少有研究利用良好控制的男女队列来探索对EDC暴露的反应和对自身免疫性疾病发展的影响的性别差异。在自身免疫性疾病的动物模型中纳入多种环境因素的转化研究对于确定潜在的病因学因素之间的相互关系是必要的。自身抗体的存在与否不是疾病的可靠预测因子。因此,未来的研究应结合所有易感性/影响因素,并结合个体基因组学,表观基因组学和蛋白质组学,以开发出一种以个性化药物的方式更好地预测,诊断和治疗自身免疫性疾病的模型。

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