Suppr超能文献

犬血白细胞在体外产生的组织因子活性增加与同种异体肾移植及排斥反应相关。

Increased tissue factor activity generation in vitro by canine blood leukocytes associated with allogeneic kidney transplantation and rejection.

作者信息

Rothberger H, Meredith J, Mutton T, Brown J, McGee M P

出版信息

Thromb Haemost. 1985 Feb 18;53(1):1-4.

PMID:3887634
Abstract

Using a canine model, leukocyte populations enriched for monocytes and lymphocytes were isolated from blood during three week periods after kidney allotransplantation corresponding to episodes of acute rejection. Relative to controls, these cells incubated in vitro for five hours were found to generate increased amounts of PCA (procoagulant activity) characterized as tissue factor, the extrinsic clotting pathway activator. Controls included comparable blood leukocyte populations isolated from kidney autograft recipients and healthy animals. Differences in results for these two control groups were insignificant. These contrasts observed between allografted animals and controls demonstrate that leukocyte PCA generation is stimulated by the allogeneicity of histoincompatible kidneys rather than by direct effects of organ transplantation or non-specific postoperative effects. Results of in vitro transfer experiments provide evidence that cellular stimulation or induction in vivo accounted for the PCA increases observed. Stimulation of leukocyte tissue factor generation as a consequence of allogeneic kidney transplantation may in part account for coagulopathies and fibrin deposition during kidney rejection.

摘要

利用犬类模型,在肾同种异体移植后对应急性排斥反应发作的三周内,从血液中分离出富含单核细胞和淋巴细胞的白细胞群体。与对照组相比,发现这些在体外孵育五小时的细胞产生了更多的PCA(促凝血活性),其特征为组织因子,即外源性凝血途径激活剂。对照组包括从肾自体移植受者和健康动物中分离出的可比血液白细胞群体。这两个对照组的结果差异不显著。在同种异体移植动物和对照组之间观察到的这些差异表明,白细胞PCA的产生是由组织不相容的肾脏的异基因性刺激的,而不是由器官移植的直接影响或非特异性术后影响导致的。体外转移实验的结果提供了证据,证明体内的细胞刺激或诱导是观察到的PCA增加的原因。同种异体肾移植导致的白细胞组织因子生成的刺激可能部分解释了肾排斥反应期间的凝血病和纤维蛋白沉积。

相似文献

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验