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Autoimmunity and Inflammation in CVID: a Possible Crosstalk between Immune Activation, Gut Microbiota, and Epigenetic Modifications

机译:CVID中的自身免疫和炎症:免疫激活,肠道微生物群和表观遗传修饰之间的可能串扰

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Common variable immunodeficiency (CVID) is the most common symptomatic primary immunodeficiency among adults and is characterized by a B cell dysfunction and increased risk of respiratory tract infections with encapsulated bacteria. However, a large proportionofpatients also has inflammatory and autoimmune complications. It may seem like a paradox that immunodeficiency and inflammation/autoimmunity coexist within the same individuals. In this commentary, we propose that CVID immunopathogenesis involves an interplay of genes, environmental factors, and dysregulation of immune cells, where gut microbiota and gastrointestinal inflammation can both be important contributors or endpoints to the systemic immune activation seen in CVID, and where epigenetic mechanism may be the undiscovered link between these contributors. In our opinion, these pathways could represent novel targets for therapy in CVID directed against autoimmune and inflammatory manifestations that represent the most severe complications in these patients. Considering the heterogeneous nature of CVID, these mechanisms may not be present in all patients, and different complications may be triggered by different risk factors. CVID is really a variable disease and in the future there is clearly a need for a more personalized medicine based on both genotypic and phenotypic findings.
机译:常见的可变免疫缺陷(CVID)是成人中最常见的症状初级免疫缺陷,其特征在于B细胞功能障碍,并增加呼吸道感染的呼吸道感染具有包封的细菌。然而,大相比培养剂也具有炎症和自身免疫并发症。它看起来像一个悖论,即同一个人内免疫缺陷和炎症/自身免疫共存。在这种评论中,我们提出了CVID免疫病理学涉及基因,环境因素和免疫细胞的失调的相互作用,其中肠道微生物群和胃肠炎症都可以是CVID中所示的全身免疫激活的重要贡献者或终点,以及表观遗传机制可能是这些贡献者之间的未被发现的联系。在我们看来,这些途径可以代表针对自身免疫和炎症表现的CVID治疗的新靶点,这些毒性表现在这些患者中最严重的并发症。考虑到CVID的异质性质,所有患者中可能不存在这些机制,并且可以通过不同的危险因素引发不同的并发症。 CVID真的是一种可变疾病,在未来,显然需要基于基因型和表型发现的更个性化的药物。

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