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供体抗原和免疫抑制剂预处理对完全同种异体气管移植的影响。

The effects of pretreatment with donor antigen and immunosuppressive agents on fully allogenic tracheal graft.

作者信息

Suemitsu Ryuichi, Yoshino Ichiro, Shoji Fumihiro, Yamaguchi Masafumi, Tomita Yukihiro, Maehara Yoshihiko

机构信息

Department of Surgery and Science, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.

出版信息

J Surg Res. 2004 Nov;122(1):8-13. doi: 10.1016/j.jss.2004.04.019.

Abstract

BACKGROUND

Obliterative bronchiolitis is a major clinical problem in cases involving a transplanted lung. We examined drug-induced tolerance to a fully allogenic tracheal graft in a murine heterotopic transplantation model.

MATERIALS AND METHODS

Recipient mice (C57BL/6) were primed iv with 1 x 10(8) splenocytes of donor mice (BALB/c). Day 0 was the day of the splenocyte injection. Cyclophosphamide and Busulfan were injected intraperitoneally on day 2. On day 3, 1 x 10(7) donor bone marrow cells were intravenously injected. On day 28, a donor tracheal graft was implanted into a subcutaneous pocket. Grafts were harvested at 3-week intervals, and the degree of obstruction of the inner cavity, the condition of epithelium, and the viability of chondrocytes were examined.

RESULTS

All of the isograft controls (BALB/c) and grafts implanted in the T cell-free recipients (BALB/c-nu) showed patent, lined epithelium and viable chondrocytes. All allografts tested showed total luminal occlusion by granulative tissue and inflammatory cells, and the epithelium was totally absent. Five of 11 drug-treated grafts were completely patent, although the epithelium was almost absent and the chondrocytes were substantially destroyed. However, when the chimerism was analyzed by flow cytometry analysis of the recipient T cells, approximately 90% of the donor cells were recognized.

CONCLUSIONS

Even by this pre-treatment-induced chimerism, a transplanted allogenic trachea was not completely preserved. The present results suggest that a non-allogenic response might have contributed to the rejection.

摘要

背景

闭塞性细支气管炎是肺移植病例中的一个主要临床问题。我们在小鼠异位移植模型中研究了药物诱导的对完全同种异体气管移植物的耐受性。

材料与方法

受体小鼠(C57BL/6)经静脉注射1×10⁸供体小鼠(BALB/c)的脾细胞进行预处理。第0天为脾细胞注射日。第2天腹腔注射环磷酰胺和白消安。第3天静脉注射1×10⁷供体骨髓细胞。第28天,将供体气管移植物植入皮下囊袋。每隔3周采集移植物,检查内腔阻塞程度、上皮状况和软骨细胞活力。

结果

所有同基因对照(BALB/c)和植入无T细胞受体(BALB/c-nu)的移植物均显示管腔通畅、上皮衬里完整且软骨细胞存活。所有测试的同种异体移植物均显示管腔被肉芽组织和炎性细胞完全阻塞,且上皮完全缺失。11个药物处理的移植物中有5个完全通畅,尽管上皮几乎缺失且软骨细胞大量破坏。然而,当通过受体T细胞的流式细胞术分析嵌合现象时,约90%的供体细胞被识别。

结论

即使通过这种预处理诱导的嵌合现象,移植的同种异体气管也未得到完全保存。目前的结果表明,非同种异体反应可能促成了排斥反应。

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