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作 者:王湘玲[1] 陈楠[1] 俞海瑾[1] 任红[1] 王伟铭[1] 倪莉燕[1]
机构地区:[1]上海交通大学附属瑞金医院肾脏科,200025
出 处:《中华风湿病学杂志》2008年第7期442-444,I0001,共4页Chinese Journal of Rheumatology
基 金:国家自然科学基金资助项目(C030204);上海市重点学科资助项目(T0201);上海市卫生局重点学科资助项目(05111001);上海高校选拔培养优秀青年教师科研专项基金资助项目(18032)
摘 要:目的探讨抗中性粒细胞胞质抗体(ANCA)对中性粒细胞表面FcγⅡ/Ⅲ(CD32/CD16)受体表达的影响及临床意义。方法提纯活动期ANCA相关性小血管炎(AASV)患者的ANCAIgG,分离健康人新鲜中性粒细胞,以ANCA刺激粒细胞1h后,流式细胞仪检测CD32/CD16的表达。流式细胞仪检测18例系统性小血管炎患者CD32/CD16的表达,以35名健康人为对照。同时对18例患者临床表现及血管炎活动情况进行评分,与CD32/CD16表达进行相关分析。结果ANCAIgG与正常人IgG相比显著上调中性粒细胞表面CD16的表达(Mnx67±23vss54±21,P〈0.01),但对CD32的表达无影响(Mnx21±8vs16±8,P〉0.05)。系统性小血管炎患者CD16表达的平均荧光强度显著高于正常人(Mnx62±12vs53±10,P〈0.01),而CD32的表达与正常人差异无统计学意义。CD16表达与伯明翰小血管炎呈显著正相关(P〈0.01)。结论ANCA相关性小血管炎患者高表达Fcγ受体,ANCA可以干预CD32/CD16受体的表达,调控Fcγ受体表达可能是系统性小血管炎的发病机制之一,监测CD16的表达水平对于判断疾病活动具参考价值。Objective The interaction between anti-neutrophil cytoplasmic antibaties (ANCA) and receptors at the Fc portion of immunoglobulins ( FcγR ) is central in the pathogenisis of primary systemic small vasculitis. The aim of this study is to investigate the role and clinical value of ANCA on the expression of neutrophils FcγⅡ/Ⅲ (CD32/CD16). Methods ANCA IgG was prepared from the sera of patients with active We-gener's granulomatosis (WG) and microscopic polyangiitis ( MPA ). Neutrophils were isolated from the blood of healthy volunteers. The expression of CD32/CD16 on neutrophils was assessed by flow cytometry after stimulated by ANCA for 1 hour. We compared the expression of CD32/CD16 between 18 primary systemic small vasculitis (PSV) patients and 35 healthy volunteers. Furthermore, the correlation was also be analyzed between the expression of CD32/CD16 and Birmingham vasculitis activity score (BVAS). Results The expression of CD16 was significantly elevated by ANCA (Mnx 67±23 vs 54±21, P〈0.01). The expression of CD16 was higher in patients than in healthy volunteers (Mnx 62±12 vs 53±10, P〈0.01), which was in correlation with BVAS (r=0.728 86, P〈0.01 ). But no such eor,'elation was found for CD32 . Conclusion ANCA may play a role in the pathogenesis of PSV by modulating the expression of the FCγR. Monitoring the expression of CD16 on neutrophils is helpful for the evaluation of PSV activity.
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