免疫系统
免疫学
炎症
免疫
疾病
先天免疫系统
获得性免疫系统
生物
白细胞介素17
先天性淋巴细胞
医学
内科学
作者
Katherine Bao,R. Lee Reinhardt
出处
期刊:Cytokine
[Elsevier BV]
日期:2015-06-13
卷期号:75 (1): 25-37
被引量:275
标识
DOI:10.1016/j.cyto.2015.05.008
摘要
Allergic disease represents a significant global health burden, and disease incidence continues to rise in urban areas of the world. As such, a better understanding of the basic immune mechanisms underlying disease pathology are key to developing therapeutic interventions to both prevent disease onset as well as to ameliorate disease morbidity in those individuals already suffering from a disorder linked to type-2 inflammation. Two factors central to type-2 immunity are interleukin (IL)-4 and IL-13, which have been linked to virtually all major hallmarks associated with type-2 inflammation. Therefore, IL-4 and IL-13 and their regulatory pathways represent ideal targets to suppress disease. Despite sharing many common regulatory pathways and receptors, these cytokines perform very distinct functions during a type-2 immune response. This review summarizes the literature surrounding the function and expression of IL-4 and IL-13 in CD4+ T cells and innate immune cells. It highlights recent findings in vivo regarding the differential expression and non-canonical regulation of IL-4 and IL-13 in various immune cells, which likely play important and underappreciated roles in type-2 immunity.
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