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大面积热烧伤后焦痂切除及同基因移植后的免疫抑制

Immunosuppression following excision of burn eschar and syngeneic grafting in major thermal trauma.

作者信息

Jacobson B K, Baker C C

出版信息

Yale J Biol Med. 1984 Sep-Oct;57(5):797-808.

Abstract

Recent reports have suggested that very early excision (less than 24 hours post-burn) and primary closure of burn wounds might circumvent the immunosuppression which follows severe thermal trauma. The total body surface are (TBSA) involved in burn injuries of human subjects at risk for significant post-burn immunosuppression is large enough to require grafting. In the present study cell-mediated immunity was measured via one-way allogeneic mixed lymphocyte reactions (MLR) in mice subjected to full-thickness scald wounds over 25-30 percent TBSA followed by escharectomy and syngeneic full-thickness skin grafting. A significant decrease in the proliferative capability of T-cells could be demonstrated on days five and seven post-treatment in unburned grafted animals (day five, 30.7 percent; day seven, 24.8 percent) over untreated normals. T-cells from animals burned but not excised also showed significant hyporesponsiveness (day five, 33.2 percent; day seven, 26.1 percent normal MLR). Animals undergoing both burning and excision showed even more profound immunosuppression (day five, 18.3 percent to 23.7 percent; day seven, 7.4 percent to 11.6 percent normal MLR). Surgical incision without excising the skin did not suppress cell-mediated immunity (day five, 90.8 percent; day seven, 90.4 percent normal MLR). When T-cells from treated animals of each group (with the exception of the incision control group) were added to normal MLR cultures, significant (greater than 50 percent) cell-mediated suppression by suppressor T-cells could be demonstrated. This study showed that the trauma of excision and grafting alone results in depression of cell-mediated immunity. These data call into question the ability of very early excision and grafting to alter the immunosuppression which follows severe thermal trauma.

摘要

最近的报告表明,极早期切除(烧伤后不到24小时)并一期闭合烧伤创面可能避免严重热损伤后的免疫抑制。有显著烧伤后免疫抑制风险的人类受试者,其烧伤累及的总体表面积(TBSA)大到足以需要植皮。在本研究中,通过单向同种异体混合淋巴细胞反应(MLR)测定细胞介导免疫,实验小鼠的TBSA有25% - 30%遭受全层烫伤,随后行焦痂切除和同基因全层皮肤移植。与未处理的正常小鼠相比,未烧伤的移植动物在治疗后第5天和第7天,T细胞增殖能力显著下降(第5天,30.7%;第7天,24.8%)。烧伤但未切除焦痂的动物的T细胞也显示出明显的低反应性(第5天,33.2%;第7天,正常MLR的26.1%)。既经历烧伤又接受切除的动物表现出更严重的免疫抑制(第5天,18.3%至23.7%;第7天,正常MLR的7.4%至11.6%)。未切除皮肤的手术切口并未抑制细胞介导免疫(第5天,90.8%;第7天,正常MLR的90.4%)。当将每组处理动物(切口对照组除外)的T细胞加入正常MLR培养物中时,可证明抑制性T细胞有显著(大于50%)的细胞介导抑制作用。本研究表明,仅切除和移植的创伤就会导致细胞介导免疫的抑制。这些数据使人质疑极早期切除和移植能否改变严重热损伤后的免疫抑制。

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本文引用的文献

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Standardized burns in mice.小鼠标准化烧伤。
Eur Surg Res. 1970;2(1):23-33. doi: 10.1159/000127494.
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Allogeneic transplantation of organ cultures without immunosuppression. An evaluation using adult mouse skin.
Transplantation. 1974 Jul;18(1):1-5. doi: 10.1097/00007890-197407000-00001.

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