Fieguth A, Feldbrügge H, Gerich T, Kleemann W J, Tröger H D
Institute of Legal Medicine, Hannover Medical School, Carl-Neuberg-Strasse 1, 30625 Hannover, Germany.
Forensic Sci Int. 2003 Jan 28;131(2-3):156-61. doi: 10.1016/s0379-0738(02)00428-0.
Fibronectin, MRP8, MRP14 and defensin were detected immunohistochemically in 46 surgically treated, fresh (hours old) human wounds and in wounds of 13 individuals who died immediately from fatal trauma (airplane crashes or train rollovers). In immediate fatal trauma, it was not possible to detect fibronectin outside of bleeding areas nor could inflammatory cells be visualized in the interstitium using MRP8, MRP14, or defensin antibodies. Fibronectin staining could be regularly demonstrated in wounds at least 20 min-old. Granulocytic infiltrates limited to the perivasal space could be detected 20-30 min after infliction of the wound expressing MRP8, MRP14 and defensin. It was also possible to detect fibronectin networks and MRP8-, MRP14-, and defensin-positive granulocytes and macrophages in particular wounds up to 30 days-old. No differences between the expression of MRP8 and MRP14 could be demonstrated in the wounds, the majority of which were only several hours old. As wound age increased, the number of defensin-positive granulocytes detected decreased. The immunohistochemical detection of fibronectin is a useful way to demonstrate vitality in fresh wounds, beginning about 20-30 min post-trauma. However, detection of MRP8, MRP14 and defensin provides no advantage over the routine histological detection of granulocytes and macrophages in wounds under 1-2 days old.
采用免疫组织化学方法,对46例接受手术治疗的新鲜(伤后数小时)人类伤口,以及13例因致命创伤(飞机坠毁或火车侧翻)立即死亡者的伤口进行了纤连蛋白、MRP8、MRP14和防御素检测。在立即致命的创伤中,在出血区域之外无法检测到纤连蛋白,使用MRP8、MRP14或防御素抗体也无法在间质中观察到炎性细胞。至少伤后20分钟的伤口中可经常见到纤连蛋白染色。在伤口形成后20 - 30分钟,可在表达MRP8、MRP14和防御素的伤口中检测到局限于血管周围间隙的粒细胞浸润。在长达30天的特定伤口中,也有可能检测到纤连蛋白网络以及MRP8、MRP14和防御素阳性的粒细胞和巨噬细胞。在大多数仅数小时龄的伤口中,未发现MRP8和MRP14表达存在差异。随着伤口年龄增加,检测到的防御素阳性粒细胞数量减少。纤连蛋白的免疫组织化学检测是一种显示新鲜伤口活力的有用方法,始于创伤后约20 - 30分钟。然而,对于1 - 2日龄以内的伤口,检测MRP8、MRP14和防御素相比常规组织学检测粒细胞和巨噬细胞并无优势。