嗜碱性粒细胞
嗜碱性粒细胞活化
类胰蛋白酶
肥大细胞
组胺
免疫学
蛋白酵素
生物标志物
生物
免疫球蛋白E
过敏
抗体
酶
生物化学
内分泌学
作者
Kenji Kabashima,Chisa Nakashima,Yumi Nonomura,Atsushi Otsuka,Chiara Cardamone,Roberta Parente,Giulia De Feo,Massimo Triggiani
摘要
Summary Mast cells and basophils play a pathogenetic role in allergic, inflammatory, and autoimmune disorders. These cells have different development, anatomical location and life span but share many similarities in mechanisms of activation and type of mediators. Mediators secreted by mast cells and basophils correlate with clinical severity in asthma, chronic urticaria, anaphylaxis, and other diseases. Therefore, effective biomarkers to measure mast cell and basophil activation in vivo could potentially have high diagnostic and prognostic values. An ideal biomarker should be specific for mast cells or basophils, easily and reproducibly detectable in blood or biological fluids and should be metabolically stable. Markers of mast cell and basophil include molecules secreted by stimulated cells and surface molecules expressed upon activation. Some markers, such as histamine and lipid mediators are common to mast cells and basophils whereas others, such as tryptase and other proteases, are relatively specific for mast cells. The best surface markers of activation expressed on mast cells and basophils are CD 63 and CD 203. While these mediators and surface molecules have been associated to a variety of diseases, none of them fulfills requirements for an optimal biomarker and search for better indicators of mast cell/basophil activation in vivo is ongoing.
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