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原发性肝癌患者红细胞免疫粘附肿瘤细胞能力与红细胞CR1基因型及活性相关性分析
引用本文:郭峰,赵书平,张乐之.原发性肝癌患者红细胞免疫粘附肿瘤细胞能力与红细胞CR1基因型及活性相关性分析[J].中华微生物学和免疫学杂志,1999,19(6).
作者姓名:郭峰  赵书平  张乐之
作者单位:第二军医大学长海医院免疫室!上海200433
摘    要:目的 研究原发性肝癌患者红细胞免疫粘附肿瘤细胞能力与红细胞CR1 基因组密度多态性及活性的相关性。方法 采用PCR 和Hind Ⅲ酶切技术测定红细胞CR1 基因组密度多态性变化,同时用ELISA 和肿瘤红细胞花环试验测定红细胞CR1 活性,并进行比较。结果 原发性肝癌患者红细胞CR1 基因型点突变比率(43-6 % ) 明显上升,与正常人(20 % ) 相比,差异有显著性( P<0-05) ;原发性肝癌患者3 种CR1 基因型的红细胞CR1 活性都明显低于正常人( P< 0-01 或 P<0-05) 。活性变化也不同。结论 原发性肝癌患者红细胞CR1 活性及免疫粘附肿瘤细胞能力下降可分为三种不同类型,即原发型、获得型和混合型。

关 键 词:肝肿瘤  红细胞  CR1基因组密度多态性  肿瘤细胞

Studies on relationships between ability of red cell adhering to tumor cells and CR1 activity and CR1 genomic density polymorphism on red cell in patients with primary hepatocarcinoma
GUO Feng,ZHAO Shuping,ZHANG Lezhi,et al..Studies on relationships between ability of red cell adhering to tumor cells and CR1 activity and CR1 genomic density polymorphism on red cell in patients with primary hepatocarcinoma[J].Chinese Journal of Microbiology and Immunology,1999,19(6).
Authors:GUO Feng  ZHAO Shuping  ZHANG Lezhi  
Institution:GUO Feng,ZHAO Shuping,ZHANG Lezhi,et al. Department of Immunology,Changhai Hospital,Shanghai 200433
Abstract:Objective To study the relationship between ability of red cell adhering to tumor cells and CR1 activity and CR1 genomic density polymorphism on red cell in patients with primary hepatocarcinoma. Methods Using PCR RFLP, ELISA and tumor erythrocyte rose test. We detected the ECR1 genomic density polymorphism and CR1 activity and ability of red cell adhering to tumor cells of 94 patients with primary hepatocarcinoma (PHC) and 80 normal individuals, respectively. Results The spot mutation rate (43.6%) of ECR1 genomic density gene in patients with PHC was higher than that (20%) in normal people ( P <0.05). Ability of three CR1 gene type erythrocytes adhering to tumor cells in patients with PHC significantly was lower than that in normal with CR1 same gene type ( P <0.01 or P <0.05). Conclusions There are three types of decrement in ability of erythrocytes adhering to tumor cells: primary type, acquired type and mixture type.
Keywords:Liver neoplasms    Erythrocytes    CR1 genomic density polymorphism    Tumor cells
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