Saverymuttu S H, Peters A M, Lavender J P, Chadwick V S, Hodgson H J
Gut. 1985 Apr;26(4):378-83. doi: 10.1136/gut.26.4.378.
It has been suggested, on the basis of impaired granulocyte migration to skin windows, that there is a fundamental granulocyte defect in Crohn's disease. In vitro tests of granulocyte function have, however, failed to confirm this. We have studied granulocyte migration to inflamed bowel in Crohn's disease using a new approach which utilises dynamic gamma camera imaging after injection of 111In labelled autologous granulocytes. In 20 of 22 studies there was rapid migration to diseased bowel, compatible with no migration delay. Only two patients showed delays in migration of 12 and 15 minutes respectively, but neither had any clinical characteristics to distinguish them from the other 20 patients. This study shows that the majority of patients with Crohn's disease in relapse have rapid granulocyte migration to diseased bowel and provides evidence against a significant migration defect in this condition.
基于粒细胞向皮肤窗口迁移受损,有人提出克罗恩病存在根本性的粒细胞缺陷。然而,粒细胞功能的体外试验未能证实这一点。我们采用了一种新方法,在注射铟 - 111标记的自体粒细胞后利用动态γ相机成像,研究了克罗恩病患者粒细胞向发炎肠道的迁移情况。在22项研究中的20项里,粒细胞迅速迁移至患病肠道,这与无迁移延迟相符。只有两名患者的迁移分别延迟了12分钟和15分钟,但他们均无任何临床特征可将其与其他20名患者区分开来。这项研究表明,大多数处于复发期的克罗恩病患者的粒细胞能迅速迁移至患病肠道,为该病不存在显著迁移缺陷提供了证据。