Hartmann Anke, Quist Jennifer, Hamm Henning, Bröcker Eva-Bettina, Friedl Peter
Department of Dermatology, University of Würzburg, Würzburg, Germany.
Dermatol Surg. 2008 Jul;34(7):922-9. doi: 10.1111/j.1524-4725.2008.34178.x.
The transplantation of keratinocytes suspended in fibrin carrier represents a candidate regimen for chronic ulcer treatment in an outpatient setting. We evaluated the integration and survival of autologous individualized keratinocytes applied within fibrin matrix onto chronic venous leg ulcers in vivo. Parallel in vitro culture was used to validate keratinocyte survival and apoptosis in fibrin compared to collagen matrix carrier.
Seven patients with chronic venous leg ulcers were transplanted with autologous keratinocytes suspended in fibrin sealant after isolation and expansion from full-skin biopsy. The fibrin carrier was removed in three patients after 7 days, whereas four patients served as control with fibrin remaining. In parallel in vitro cultures, primary keratinocyte movement in fibrin as well as viability in three-dimensional (3D) fibrin versus collagen lattices was examined.
Complete ulcer healing was observed in four of seven ulcers after a mean duration of 14.5 weeks. If the fibrin layer was removed, complete wound healing occurred in three of three patients, compared to one of four in the control group. In vitro, keratinocytes formed a monolayer underneath but remained isolated and nonmobile within the fibrin matrix, suggesting reepithelialization along the lower fibrin interphase. Keratinocyte culture in 3D fibrin at clinically used concentration (90 mg/mL) caused high levels of apoptosis, similar to 3D collagen, which was prevented by diluting fibrin concentration to 3 mg/mL.
Transplantation of autologous keratinocytes suspended in fibrin is efficient in the treatment of chronic venous leg ulcers. Due to an antimigratory and survival-compromising effect, the presently used fibrin carrier should be removed after a few days of transplantation.
将角质形成细胞悬浮于纤维蛋白载体中进行移植,是门诊治疗慢性溃疡的一种可行方案。我们评估了在体内将自体个体化角质形成细胞应用于纤维蛋白基质中治疗慢性下肢静脉溃疡时的整合和存活情况。通过平行体外培养,比较纤维蛋白与胶原基质载体中角质形成细胞的存活和凋亡情况。
7例慢性下肢静脉溃疡患者,经全层皮肤活检分离并扩增后,将自体角质形成细胞悬浮于纤维蛋白封闭剂中进行移植。3例患者在7天后移除纤维蛋白载体,4例患者作为对照组,纤维蛋白保留。在平行体外培养中,检测了角质形成细胞在纤维蛋白中的迁移以及在三维(3D)纤维蛋白与胶原晶格中的活力。
7例溃疡中有4例在平均14.5周后完全愈合。如果移除纤维蛋白层,3例患者中有3例完全愈合,而对照组4例中有1例完全愈合。在体外,角质形成细胞在纤维蛋白下方形成单层,但在纤维蛋白基质中保持分离且不迁移,提示沿纤维蛋白下层界面进行再上皮化。在临床使用浓度(90mg/mL)的3D纤维蛋白中培养角质形成细胞会导致高水平凋亡,与3D胶原相似,将纤维蛋白浓度稀释至3mg/mL可防止这种情况发生。
将自体角质形成细胞悬浮于纤维蛋白中进行移植对慢性下肢静脉溃疡治疗有效。由于具有抗迁移和损害存活的作用,目前使用的纤维蛋白载体在移植几天后应予以移除。