Treatment of oesophageal ulcerations using endoscopic transplantation of tissue-engineered autologous oral mucosal epithelial cell sheets in a canine model

被引:287
作者
Ohki, T.
Yamato, M.
Murakami, D.
Takagi, R.
Yang, J.
Namiki, H.
Okano, T.
Takasaki, K.
机构
[1] Tokyo Womens Med Univ, Inst Adv Biomed Engn & Sci, Shinjuku Ku, Tokyo 1628666, Japan
[2] Tokyo Womens Med Univ, Inst Gastroneterol, Dept Surg, Tokyo 1628666, Japan
[3] Waseda Univ, Grad Sch Sci & Engn, Tokyo, Japan
关键词
D O I
10.1136/gut.2005.088518
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background: With the recent development of endoscopic submucosal dissection (ESD), large oesophageal cancers can be removed with a single procedure, with few limits on the resectable range. However, after aggressive ESD, a major complication that arises is postoperative inflammation and stenosis that can considerably affect the patient's quality of life. Aims: To examine a novel treatment combining ESD and the endoscopic transplantation of tissue-engineered cell sheets created using autologous oral mucosal epithelial cells, in a clinically relevant large animal model. Methods: Oral mucosal epithelial cells, harvested from beagle dogs, were cultured under normal conditions at 37 degrees C, on temperature-responsive dishes. After ESD (5 cm in length, 180 degrees in range), cell sheets were harvested by a simple reduction in temperature to 20 degrees C, and transplanted by endoscopy. Results: The transplanted cell sheets were able to adhere to and survive on the underlying muscle layers in the ulcer sites, providing an intact, stratified epithelium. Four weeks after surgery, complete wound healing, with no observable stenosis, was seen in the animals receiving autologous cell sheet transplantation. By contrast, noticeable fibrin mesh and host inflammation, consistent with the intermediate stages of wound healing, were observed in the control animals that received only ESD. Conclusions: These findings in a clinically relevant canine model show the effectiveness of a novel combined endoscopic approach for the potential treatment of oesophageal cancers that can effectively enhance wound healing and possibly prevent postoperative oesophageal stenosis.
引用
收藏
页码:1704 / 1710
页数:7
相关论文
共 39 条
[1]
Host response to tissue engineered devices [J].
Babensee, JE ;
Anderson, JM ;
McIntire, LV ;
Mikos, AG .
ADVANCED DRUG DELIVERY REVIEWS, 1998, 33 (1-2) :111-139
[2]
Esophageal reconstruction with ECM and muscle tissue in a dog model [J].
Badylak, SF ;
Vorp, DA ;
Spievack, AR ;
Simmons-Byrd, A ;
Hanke, J ;
Freytes, DO ;
Thapa, A ;
Gilbert, TW ;
Nieponice, A .
JOURNAL OF SURGICAL RESEARCH, 2005, 128 (01) :87-97
[3]
MULTICENTER EXPERIENCE IN THE TREATMENT OF BURNS WITH AUTOLOGOUS AND ALLOGENIC CULTURED EPITHELIUM, FRESH OR PRESERVED IN A FROZEN STATE [J].
DELUCA, M ;
ALBANESE, E ;
BONDANZA, S ;
MEGNA, M ;
UGOZZOLI, L ;
MOLINA, F ;
CANCEDDA, R ;
SANTI, PL ;
BORMIOLI, M ;
STELLA, M ;
MAGLIACANI, G .
BURNS, 1989, 15 (05) :303-309
[4]
Devesa SS, 1998, CANCER, V83, P2049, DOI 10.1002/(SICI)1097-0142(19981115)83:10<2049::AID-CNCR1>3.3.CO
[5]
2-U
[6]
EGUCHI T, 2003, DIGEST ENDOSC, V15, P113, DOI DOI 10.1016/J.GIE.2005.08.026
[7]
Endoscopic mucosal resection of early cancer and high-grade dysplasia in Barrett's esophagus [J].
Ell, C ;
May, A ;
Gossner, L ;
Pech, O ;
Günter, E ;
Mayer, G ;
Henrich, R ;
Vieth, M ;
Müller, H ;
Seitz, G ;
Stolte, M .
GASTROENTEROLOGY, 2000, 118 (04) :670-677
[8]
Circumferential endoscopic mucosal resection in Barrett's esophagus with high-grade intraepithelial neoplasia or mucosal cancer. Preliminary results in 21 patients [J].
Giovannini, M ;
Bories, E ;
Pesenti, C ;
Moutardier, V ;
Monges, G ;
Danisi, C ;
Lelong, B ;
Delpero, JR .
ENDOSCOPY, 2004, 36 (09) :782-787
[9]
Gossner L, 2000, Gastrointest Endosc Clin N Am, V10, P461
[10]
A new endoscopic mucosal resection procedure using an insulation-tipped electrosurgical knife for rectal flat lesions: report of two cases [J].
Gotoda, T ;
Kondo, H ;
Ono, H ;
Saito, Y ;
Yamaguchi, H ;
Saito, D ;
Yokota, T .
GASTROINTESTINAL ENDOSCOPY, 1999, 50 (04) :560-563