Geist C, Wöhrmann T, Schneider J, Zwingenberger K
Grunenthal GmbH, Center of Research, Aachen, Germany.
FEMS Immunol Med Microbiol. 1995 Dec;12(3-4):165-74. doi: 10.1111/j.1574-695X.1995.tb00189.x.
The Shwartzman reaction is an animal model displaying histopathological vasculitis phenomena. Extravasation and swelling due to increased vascular permeability and cellular infiltration, which are hallmarks of the Shwartzman reaction, were evaluated as leakage of i.v.-injected Evans Blue dye and by histological and immunohistological characteristics in rabbits and mice. (+/-)-Thalidomide, (-)-thalidomide, (+)-thalidomide and dexamethasone inhibited the increase of vascular permeability in the local Shwartzman reaction. Histologically, the intensity of the Shwartzman reaction was reduced. In mice thrombus formation and leukocytoclastic vasculitis was inhibited by (+/-)-thalidomide and (+)-thalidomide. ICAM-1 expression was markedly reduced after (+)-thalidomide injection. Thalidomide and dexamethasone pretreatment reduced Mac-1 expression on perivascular infiltrated granulocytes. The inhibitory effect of thalidomide on vasculitis of the Shwartzman reaction may thus be related to reduction of adhesion molecule expression.
施瓦茨曼反应是一种呈现组织病理学血管炎现象的动物模型。血管通透性增加和细胞浸润所致的血管外渗和肿胀是施瓦茨曼反应的特征,通过静脉注射伊文思蓝染料的渗漏情况以及兔和小鼠的组织学和免疫组织学特征对其进行评估。(±)-沙利度胺、(-)-沙利度胺、(+)-沙利度胺和地塞米松抑制局部施瓦茨曼反应中血管通透性的增加。组织学上,施瓦茨曼反应的强度降低。在小鼠中,(±)-沙利度胺和(+)-沙利度胺抑制血栓形成和白细胞破碎性血管炎。注射(+)-沙利度胺后,细胞间黏附分子-1(ICAM-1)表达明显降低。沙利度胺和地塞米松预处理降低了血管周围浸润粒细胞上巨噬细胞-1(Mac-1)的表达。因此,沙利度胺对施瓦茨曼反应性血管炎的抑制作用可能与黏附分子表达的降低有关。