{"title":"Effects of cetirizine on human eosinophil and neutrophil activation in vitro.","authors":"G M Walsh, R Moqbel, A Hartnell, A B Kay","doi":"10.1159/000235422","DOIUrl":null,"url":null,"abstract":"<p><p>The ability of cetirizine, a novel antihistamine agent, to inhibit the in vivo activation of human eosinophils, neutrophils and monocytes has been investigated using C3b- and IgG-dependent rosette formation, cytotoxicity against opsonised parasitic larvae and adherence to plasma-coated glass (PCG). The drug inhibited platelet-activating factor (PAF)-induced enhancement of eosinophil and neutrophil IgG (Fc) and complement (C3b) rosettes with an IC50 of 2 x 10(-5) M. There was also comparable inhibition of PAF-dependent enhancement of eosinophil cytotoxicity (for complement-coated schistosomula of Schistosoma mansoni). Cetirizine inhibited PAF-induced eosinophil, but not neutrophil, hyperadherence to PCG. These data support the view that cetirizine may exert some of its anti-allergic effects by inhibiting the activation of human granulocytes and that it may also selectively inhibit PAF-induced eosinophil hyperadherence.</p>","PeriodicalId":13810,"journal":{"name":"International archives of allergy and applied immunology","volume":"95 2-3","pages":"158-62"},"PeriodicalIF":0.0000,"publicationDate":"1991-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1159/000235422","citationCount":"40","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"International archives of allergy and applied immunology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1159/000235422","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 40
Abstract
The ability of cetirizine, a novel antihistamine agent, to inhibit the in vivo activation of human eosinophils, neutrophils and monocytes has been investigated using C3b- and IgG-dependent rosette formation, cytotoxicity against opsonised parasitic larvae and adherence to plasma-coated glass (PCG). The drug inhibited platelet-activating factor (PAF)-induced enhancement of eosinophil and neutrophil IgG (Fc) and complement (C3b) rosettes with an IC50 of 2 x 10(-5) M. There was also comparable inhibition of PAF-dependent enhancement of eosinophil cytotoxicity (for complement-coated schistosomula of Schistosoma mansoni). Cetirizine inhibited PAF-induced eosinophil, but not neutrophil, hyperadherence to PCG. These data support the view that cetirizine may exert some of its anti-allergic effects by inhibiting the activation of human granulocytes and that it may also selectively inhibit PAF-induced eosinophil hyperadherence.
西替利嗪(一种新型抗组胺剂)抑制人嗜酸性粒细胞、中性粒细胞和单核细胞体内活化的能力,已经通过C3b-和igg依赖的花环形成、对寄生性幼虫的细胞毒性和对血浆涂层玻璃(PCG)的粘附性进行了研究。该药物抑制血小板活化因子(PAF)诱导的嗜酸性粒细胞和中性粒细胞IgG (Fc)和补体(C3b)簇的增强,IC50为2 x 10(-5) M.此外,PAF依赖性的嗜酸性粒细胞细胞毒性增强也有类似的抑制作用(对于补体包被的曼氏血吸虫)。西替利嗪抑制paf诱导的嗜酸性粒细胞,但不抑制嗜中性粒细胞对PCG的过度粘附。这些数据支持西替利嗪可能通过抑制人粒细胞的激活来发挥其抗过敏作用的观点,并且它也可能选择性地抑制paf诱导的嗜酸性粒细胞过度粘附。