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环孢素A对大鼠同种异体移植的影响。

The effects of cyclosporin A on transplanted rat allografts.

作者信息

Strome M, Strome S, Darrell J, Wu J, Brodsky G

机构信息

Joint Center for Otolaryngology, Brigham and Women's Hospital, Boston, MA.

出版信息

Laryngoscope. 1993 Apr;103(4 Pt 1):394-8. doi: 10.1002/lary.5541030406.

Abstract

Since 1983, Cyclosporin A (CsA) has been the most successful primary drug in preventing rejection of organ transplants. This study was designed to determine the efficacy and dose response of CsA in preventing rejection of LBNF-1 rat allografts to Lewis recipients. Four groups of animals were studied. Group I served as the control, and groups II, III, and IV were given daily intramuscular doses of CsA for 1 month. The groups were given doses of 5 mg/kg, 7.5 mg/kg, and 10 mg/kg, respectively. Sixty-eight animals were transplanted to get eight viable transplanted animals at 1 month in each CsA group. Laryngeal viability was assessed with both clinical and histological parameters. Groups II, III, and IV had representative clinically viable larynges. The histology varied and had some correlation with CsA dosage. Group II evidenced changes ranging from mild to severe rejection. Group III was more homogeneous with the most severe change being characterized as mild-to-moderate rejection. Group IV was the most uniform with all representative specimens showing only limited infiltration of inflammatory cells with intact mucosa and submucosal glands (mild rejection). None of the CsA groups evidenced the squamous metaplasia characteristic of the control group. CsA can prevent rejection of laryngeal allografts from LBNF-1 donors to Lewis recipients.

摘要

自1983年以来,环孢素A(CsA)一直是预防器官移植排斥反应最成功的一线药物。本研究旨在确定CsA预防LBNF-1大鼠同种异体移植物对Lewis受体排斥反应的疗效和剂量反应。对四组动物进行了研究。第一组作为对照组,第二、三、四组每日肌肉注射CsA,持续1个月。这三组分别给予5mg/kg、7.5mg/kg和10mg/kg的剂量。移植了68只动物,以便在每个CsA组中1个月时获得8只存活的移植动物。通过临床和组织学参数评估喉的存活情况。第二、三、四组有具有代表性的临床存活喉。组织学变化多样,且与CsA剂量有一定相关性。第二组显示出从轻度到重度排斥反应的变化。第三组更为一致,最严重的变化表现为轻度至中度排斥反应。第四组最为均匀,所有代表性标本仅显示炎症细胞浸润有限,黏膜和黏膜下腺完整(轻度排斥反应)。没有一个CsA组出现对照组特有的鳞状化生。CsA可以预防LBNF-1供体的喉同种异体移植物对Lewis受体的排斥反应。

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