Treatment of streptozotocin-induced diabetes mellitus by transplantation of islet cells plus bone marrow cells via portal vein in rats

被引:42
作者
Ikebukuro, K
Adachi, Y
Yamada, Y
Fujimoto, S
Seino, Y
Oyaizu, H
Hioki, K
Ikehara, S
机构
[1] Kansai Med Univ, Dept Pathol 1, Osaka 5708506, Japan
[2] Kansai Med Univ, Dept Surg 2, Osaka 5708506, Japan
[3] Kansai Med Univ, Transplantat Ctr, Osaka 5708506, Japan
[4] Kansai Med Univ, Dept Internal Med 1, Osaka 5708506, Japan
[5] Kyoto Univ, Grad Sch Med, Dept Metab & Clin Nutr, Kyoto 6068507, Japan
关键词
D O I
10.1097/00007890-200202270-00004
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 [免疫学];
摘要
Background. We have established a new method for the transplantation of allogeneic pancreatic islets (PIs) using sublethal irradiation (9 Gy) plus simultaneous transplantation of PIs and bone marrow cells (BMCs) via the portal vein (PV) followed by intravenous (i.v.) injection of donor BMCs (9 Gy + PV + i.v.). Methods. Approximately 600 PIs of Brown Norway (BN: RTIA(n), RTlBn) rats were transplanted into the liver of streptozotocin-induced diabetic Fischer 344 (F344: RT1A(n), RT1B(n)) rats via the PV. BMCs (3x10(8)) of BN rats were injected via the PV or i.v. into the recipients simultaneously. In some groups, additional i.v. injections of BMCs from BN rats were given 5 days after the PI transplantation. Results. All the recipients (10 of 10) in the 9 Gy + PV + i.v. group showed normoglycemia for more than 1 year, whereas PIs were rejected within 30 days after transplantation in the group of 9 Gy + i.v. + i.v. Conclusions. These results suggest that simultaneous transplantation of PIs and BMCs via the PV is effective in inducing persistent tolerance.
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页码:512 / 518
页数:7
相关论文
共 37 条
[1]
ACTIVELY ACQUIRED TOLERANCE OF FOREIGN CELLS [J].
BILLINGHAM, RE ;
BRENT, L ;
MEDAWAR, PB .
NATURE, 1953, 172 (4379) :603-606
[2]
IMPORTANCE OF HEPATIC PORTAL CIRCULATION FOR INSULIN ACTION IN STREPTOZOTOCIN-DIABETIC RATS TRANSPLANTED WITH FETAL PANCREASES [J].
BROWN, J ;
MULLEN, Y ;
CLARK, WR ;
MOLNAR, IG ;
HEININGER, D .
JOURNAL OF CLINICAL INVESTIGATION, 1979, 64 (06) :1688-1694
[3]
CALLERY MP, 1989, TRANSPLANTATION, V47, P1092
[4]
TYPE-I DIABETES - A CHRONIC AUTOIMMUNE-DISEASE OF HUMAN, MOUSE, AND RAT [J].
CASTANO, L ;
EISENBARTH, GS .
ANNUAL REVIEW OF IMMUNOLOGY, 1990, 8 :647-679
[5]
A COMPARISON OF PORTAL VERSUS SYSTEMIC VENOUS DRAINAGE IN MURINE FETAL PANCREATIC-ISLET TRANSPLANTATION [J].
CUTHBERTSON, RA ;
MANDEL, TE .
AUSTRALIAN JOURNAL OF EXPERIMENTAL BIOLOGY AND MEDICAL SCIENCE, 1986, 64 :175-184
[6]
AUTOIMMUNE DIABETES-INDUCED BY THE BETA-CELL TOXIN STZ - IMMUNITY TO THE 6O-KDA HEAT-SHOCK PROTEIN AND TO INSULIN [J].
ELIAS, D ;
PRIGOZIN, H ;
POLAK, N ;
RAPOPORT, M ;
LOHSE, AW ;
COHEN, IR .
DIABETES, 1994, 43 (08) :992-998
[7]
Exner B G, 1997, Ann Transplant, V2, P77
[8]
CD8+TCR+ and CD8+TCR- cells in whole bone marrow facilitate the engraftment of hematopoietic stem cells across allogeneic barriers [J].
Gandy, KL ;
Domen, J ;
Aguila, H ;
Weissman, IL .
IMMUNITY, 1999, 11 (05) :579-590
[9]
Induction of donor-specific tolerance to rat nerve allografts with portal venous donor alloantigen and anti-ICAM-1/LFA-1 monoclonal antibodies [J].
Genden, EM ;
Mackinnon, SE ;
Yu, S ;
Flye, MW .
SURGERY, 1998, 124 (02) :448-456
[10]
THE EVOLUTION OF FUNCTION AND RESPONSE TO ARGININE CHALLENGE AND PREGNANCY OF PORTALLY AND SYSTEMICALLY PLACED ISLET CELL GRAFTS IN STREPTOZOTOCIN DIABETIC MICE [J].
GILLIES, MC ;
MANDEL, TE .
METABOLISM-CLINICAL AND EXPERIMENTAL, 1990, 39 (12) :1253-1258