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所选免疫调节剂对实验性接触反应的影响。

The effect of selected immunomodulating agents on experimental contact reactions.

作者信息

Anderson C

出版信息

Acta Derm Venereol Suppl (Stockh). 1985;116:1-48.

PMID:3901646
Abstract

A guinea pig experimental model which allows comparison of the macroscopic appearance of skin tests with the nature and degree of the dermal inflammatory cell infiltrate has been used to study the effects of cyclophosphamide, methotrexate, azathioprine and cyclosporin A on contact reactions. The immunomodulating capabilities of the agents tested are assessed by their effects on the allergic contact reaction to oxazolone, a cell-mediated delayed hypersensitivity reaction. Non-specific, anti-inflammatory actions are assessed by effects on the toxic contact reaction to croton oil. Changes are compared to findings in reference animals for each reaction. The reference materials and the uses and limitations of the experimental model are evaluated. When administered prior to sensitization, all agents enhanced the macroscopic appearance of the allergic contact reactions. Changes in the dermal cellular infiltrates were not pronounced. When administered prior to testing, cyclophosphamide, methotrexate and azathioprine caused changes compared to controls which varied in direction and degree both macroscopically and microscopically. Cyclophosphamide which was the most active agent showed non-specific, anti-inflammatory effects and caused a peripheral blood leukopenia, the level and character of which was essentially independent of the dermal cellular infiltrate of tests. Cyclosporin A demonstrated no non-specific, anti-inflammatory activity on the toxic reaction, but had by far the most pronounced immunosuppressant effect of the agents tested, with virtual quenching of both the macroscopic appearance and all aspects of the dermal cellular infiltrates of the allergic contact reaction.

摘要

一种豚鼠实验模型已被用于研究环磷酰胺、甲氨蝶呤、硫唑嘌呤和环孢素A对接触反应的影响,该模型能够将皮肤试验的宏观表现与真皮炎症细胞浸润的性质和程度进行比较。通过测试药物对恶唑酮过敏接触反应(一种细胞介导的迟发型超敏反应)的影响来评估其免疫调节能力。通过对巴豆油毒性接触反应的影响来评估非特异性抗炎作用。将每种反应的变化与参考动物的结果进行比较。对参考材料以及实验模型的用途和局限性进行了评估。在致敏前给药时,所有药物均增强了过敏接触反应的宏观表现。真皮细胞浸润的变化并不明显。在测试前给药时,与对照组相比,环磷酰胺、甲氨蝶呤和硫唑嘌呤在宏观和微观上均引起了方向和程度各异的变化。活性最强的环磷酰胺显示出非特异性抗炎作用,并导致外周血白细胞减少,其水平和特征基本上与试验的真皮细胞浸润无关。环孢素A对毒性反应未显示出非特异性抗炎活性,但在所测试的药物中具有迄今为止最显著的免疫抑制作用,几乎完全消除了过敏接触反应的宏观表现和真皮细胞浸润的各个方面。

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