大鼠同种肝移植免疫耐受机制的研究  

Experimental study on the immunological tolerance in rat liver transplantation

在线阅读下载全文

作  者:柳东夫[1] 王兆海[2] 周光文[2] 

机构地区:[1]山东烟台毓璜顶医院器官移植中心,山东烟台264000 [2]上海第二医科大学附属瑞金医院外科,上海200025

出  处:《诊断学理论与实践》2005年第6期484-486,共3页Journal of Diagnostics Concepts & Practice

摘  要:目的:探讨与大鼠肝移植免疫耐受相关的细胞学改变。方法:分析从肝移植物分离出的移植物浸润细胞(GIC)的表现型和功能,同时比较长期生存的BN→LEW模型和急性排斥反应的DA→LEW模型。结果:通过流式细胞仪计数确定DA→LEW受体的T细胞和激活的T细胞相对比例高于BN→LEW受体;移植后第7、14和30天,GIC表现型证实所有T细胞、OX8阳性细胞(细胞毒T细胞和NK细胞)和OX39阳性细胞(IL-2受体)的相对比例在移植后第7天最高,移植后30d下降;移植后第7天急性排斥反应时GIC细胞毒T细胞活性高于长期生存者。结论:移植后第7天免疫抑制机制已存在;在长期生存的肝移植物中细胞毒T细胞的激活和浸润均受到抑制。Objective To elucidate the immunological characteristics of rat liver transplantation. Methods The graft-infiltrating cells (GIC) isolated from rat hepatic allografts were analyzed phenotypically and functionally. GIC from long-surviving recipients (Brown Norway livers into Lewis hosts) were compared with the acutely rejecting recipients (DA livers into Lewis hosts). Results The relative proportions of all the T cells and the activated T cells determined by flow cytometry were significantly higher in the acutely rejecting Lewis recipients than in the long-surviving recipients on day 7 after grafting. The phenotypic analysis of GIC on day 7, 14 and 30 after transplantation from long-surviving Lewis hosts showed that each proportion of all the T cells, the OX8-positive cells (cytotoxic T and natural killer cells) and the OX39- positive cells (IL-2 receptor) was the greatest on day 7 and decreased on day 30. The cytotoxic activity of GIC toward donor lymphocytes on day 7 was greater in the acutely rejecting than that in the long-surviving recipients. Conclusions The immunosuppressive mechanism is already present on day 7 posttransplantation, and the infiltration or activation of the cytotoxic T cells is inhibited in the long-surviving rat hepatic allografts.

关 键 词:同种异体肝移植物 浸润细胞 细胞毒T细胞 自然杀伤细胞 

分 类 号:R657.3[医药卫生—外科学]

 

参考文献:

正在载入数据...

 

二级参考文献:

正在载入数据...

 

耦合文献:

正在载入数据...

 

引证文献:

正在载入数据...

 

二级引证文献:

正在载入数据...

 

同被引文献:

正在载入数据...

 

相关期刊文献:

正在载入数据...

相关的主题
相关的作者对象
相关的机构对象