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机构地区:[1]江西医学院上饶分院免疫学教研室,江西上饶334000
出 处:《江西医学院学报》2005年第4期16-17,22,共3页Acta Academiae Medicinae Jiangxi
摘 要:目的探讨胚胎胸腺组织移植对系统性红斑狼疮(SLE)模型鼠的治疗效果。方法将21只符合要求的BALB/c×C57BL/6F1小鼠经尾静脉注射亲代淋巴细胞混合悬液后随机分成3(A^C)组,于SLE模型建立成功后接受相应治疗方案,第25天处死模型小鼠,采用流式细胞技术检测各组小鼠外周血中CD4+/CD8+T细胞的比值;电子天平称取小鼠胸腺湿质量后计算胸腺指数;直接免疫荧光法检测肾冰冻切片免疫复合物的荧光强度;间接免疫荧光法检测血清中抗核抗体(ANA)的荧光滴度。结果①C组外周血中CD4+/CD8+T细胞的比值显著高于A组(P<0.05),但A组与B组相比,差异无显著性(P>0.05);②C组胸腺指数与B组相比,无显著性差异(P>0.05),但显著高于A组(P<0.05);③C组肾脏冰冻切片荧光强度及外周血ANA荧光滴度均低于A组和B组(P<0.05)。结论胚胎胸腺移植对SLE模型鼠有显著治疗效果,有望运用于临床SLE的治疗。Objective To evaluate the therapeutic effects of fetal thymus transplantation to the mice with systemic lupus erythematosus(SLE). Methods Twenty-one BALB/c×C57BL/6 F1 mice were divided into 3 groups after their being injected with their parental lymphocytes suspended solutions. When the models were established successfully,a therapy by adrenaline was conducted in group A: fetal thymus transplantation was in Group B;and adrenaline and fetal thymus transplantation was in Group C. At 25 days after the therapies,mice serum were detected by flow cytometry(FCM) for T cells ratio of CD4/CD8;Thymus were weighed with an elecronic equiarmhalance, then the indexes of thymus were calculated; Direct immunofluorescence technique was used to test the intensities of fluorescence of mice kidney frozen sections; The serum fluorescence titres of anti-nuclear antibodies(ANA) were tested by indirect immunofluorescence technique. Results①The T cells CD4/CD8 ratios in group C were higher than that in group A(P〈 0.05), while the ratios did not show any significant difference in group A and group B(P〉0. 05);②Thymus indexes in group C did not have any significant difference compared with that in group B(P〉0. 05) ,while the indexes in group C was higher than that in group A(P〈0. 05) ;③The fluorescence intensities of mice kidney frozen sections and ANA titres in group C were lower than those in group A and B(P〈0.05). Conclusion Fetal thymus transplantation perform significant therapeutic effects on SLE mice and it could be used in clinical treatment of SLE.
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