微生物组和免疫系统相互作用中的互惠性及其对疾病和健康的影响。

Enayat Nikoopour, Bhagirath Singh
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引用次数: 20

摘要

寄生在宿主体内的整个微生物正常菌群在进化过程中对其自然栖息地的适应,导致了微生物群和宿主在稳定状态下的和平共存,互惠互利。宿主和微生物群之间的这种共生关系对塑造宿主的免疫反应产生重大影响,以实现对微生物群的免疫耐受,但保留对入侵病原体的反应能力。通过操纵宿主微生物群落来扰乱这种平衡可导致免疫失调和对疾病的易感性。通过研究缺乏微生物群或改变微生物群的宿主,可以解决微生物对免疫系统影响的复杂性。相反,在缺乏免疫系统因素的情况下对微生物群的研究可以显示免疫系统如何有助于保持宿主-微生物群平衡。基因敲除模型中缺乏参与先天免疫或适应性免疫的分子会扰乱宿主和微生物群之间的平衡,进一步增加免疫失调。更好地了解微生物组与免疫系统的相互作用为鉴定生物标志物和药物靶点提供了新的机会。这将允许开发新的治疗药物来调节免疫系统,以改善健康,很少或没有毒性。宿主与微生物群相互作用的研究在设计由宿主与微生物群相互作用不平衡引起的免疫病理疾病的治疗干预措施方面具有重要意义。
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Reciprocity in microbiome and immune system interactions and its implications in disease and health.

Adaptation of the whole microbial normal flora residing in a host to its natural habitat over an evolutionary peroid has resulted in peaceful coexistence with mutual benefits for both microbiota and host in steady state. This symbiotic relationship between host and microbiota has a significant impact on shaping the immune response in the host to achieve an immune tolerance to microbiota but retaining the ability to respond to invading pathogens. Perturbation of this balance by manipulation of microbial communities in the host can lead to immune dysregulation and susceptibility to diseases. By studying the host in the absence of microbiota or with alteration of microbiota the complexity of microbial impact on the immune system can be resolved. Conversely, the study of microbiota in the absence of immune system factors can show how the immune system contributes to preservation of the host-microbiota balance. The absence of molecules involved in innate or adaptive immunity in knockout models can perturb the balance between host and microbiota further adding to more immune dysregulation. A better understanding of Microbiome-immune system interaction provides a new opportunity to identify biomarkers and drug targets. This will allow the development of new therapeutic agents for modulating the immune system to improve health with little or no toxicity. The study of interplay between host and microbiota has a promising role in the design of therapeutic interventions for immunopathological diseases arising from imbalanced host and microbiota interactions.

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