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免疫调节剂环磷酰胺、甲氨蝶呤、氢化可的松和环孢素A对肉芽肿性肠病动物模型的影响。

Effect of the immune modulating agents cyclophosphamide, methotrexate, hydrocortisone, and cyclosporin A on an animal model of granulomatous bowel disease.

作者信息

Mitchell I C, Turk J L

机构信息

Royal College of Surgeons of England, London.

出版信息

Gut. 1990 Jun;31(6):674-8. doi: 10.1136/gut.31.6.674.

Abstract

This study was undertaken to determine the effect of cyclophosphamide, methotrexate, hydrocortisone, and cyclosporin A on a model of granulomatous infiltration in the terminal ileum and draining lymph nodes of the guinea pig. Treatment groups of six animals were used and compared to untreated groups of 12. Epithelioid cell granulomas and primary macrophage granulomas were induced by the inoculation of BCG (Pasteur) and irradiated Mycobacterium leprae respectively into the terminal ileum of the guinea pig. The response to purified protein derivative of tuberculin was reduced in both groups of animals receiving any of these agents. Cyclophosphamide and methotrexate treated animals inoculated with BCG or M leprae showed a significant reduction of granulomatous infiltration at the inoculation site (p less than 0.05 and p less than 0.001 respectively). BCG inoculated animals treated with either hydrocortisone or cyclosporin A showed no reduction in granulomatous infiltration at either the inoculation site or the draining lymph nodes. By contrast M leprae inoculated animals receiving either of these agents showed a significant reduction of granulomatous infiltration at both the inoculation site (p less than 0.001) and in the primary draining lymph node (p less than 0.001). Ziehl Neelsen staining showed an increased proportion of animals with detectable acid fast bacilli (AFB) at the inoculation site in the groups receiving hydrocortisone (50%) and methotrexate (67%) compared to untreated controls (8%). No AFB were observed in any of the animals inoculated with M leprae. In conclusion, this model may be helpful in elucidating the mechanism of T lymphocyte response in Crohn's disease and the variable clinical response seen with the use of immunosuppressive agents in this condition.

摘要

本研究旨在确定环磷酰胺、甲氨蝶呤、氢化可的松和环孢素A对豚鼠回肠末端和引流淋巴结肉芽肿浸润模型的影响。使用每组6只动物的治疗组,并与每组12只未治疗的动物组进行比较。分别通过向豚鼠回肠末端接种卡介苗(巴斯德株)和经辐射的麻风分枝杆菌诱导上皮样细胞肉芽肿和原发性巨噬细胞肉芽肿。接受任何一种这些药物治疗的两组动物对结核菌素纯蛋白衍生物的反应均降低。接种卡介苗或麻风分枝杆菌的环磷酰胺和甲氨蝶呤治疗动物在接种部位的肉芽肿浸润显著减少(分别为p<0.05和p<0.001)。接种卡介苗的动物用氢化可的松或环孢素A治疗后,在接种部位或引流淋巴结的肉芽肿浸润均未减少。相比之下,接种麻风分枝杆菌的动物接受这两种药物中的任何一种后,在接种部位(p<0.001)和初级引流淋巴结(p<0.001)的肉芽肿浸润均显著减少。齐-尼氏染色显示,与未治疗的对照组(8%)相比,接受氢化可的松(50%)和甲氨蝶呤(67%)治疗的组中,接种部位可检测到抗酸杆菌(AFB)的动物比例增加。接种麻风分枝杆菌的动物中未观察到AFB。总之,该模型可能有助于阐明克罗恩病中T淋巴细胞反应的机制以及在这种情况下使用免疫抑制剂时出现的不同临床反应。

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