The effect of combination splenectomy and low-dose FK506 therapy on graft survival after liver allograft transplantation in rats

被引:8
作者
Kashu, Y [1 ]
Abe, Y [1 ]
Miyauchi, K [1 ]
Nakata, T [1 ]
Watanabe, Y [1 ]
Sato, M [1 ]
Sato, N [1 ]
Kimura, S [1 ]
机构
[1] EHIME UNIV,SCH MED,DEPT SURG 2,SHIGENOBU,EHIME 79102,JAPAN
关键词
D O I
10.1097/00007890-199605270-00019
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
The effect of splenectomy on allograft survival was investigated using orthotopic liver transplantation in a rat experimental model (ACI rat liver grafted to LEW rat). Control rats without any immunosuppressive treatment died, on average, 10.4+/-1.4 days after operation. Splenectomy alone somewhat prolonged the survival (13.4+/-2.0 days), and low-dose FK506 therapy moderately prolonged it (22.7+/-6.7 days). The graft survival period was significantly prolonged (39.7+/-6.3 days) when these two treatments were combined. The elevation of cytotoxic antiallograft antibodies was suppressed by splenectomy but not by low-dose FK506 therapy. The development of jaundice was moderately suppressed by FK506 but not by splenectomy. There was no difference between the pattern of body weight decline in either of these two groups and that in control rats. When these two treatments were combined at the same time, the elevation of cytotoxic antibodies, development of jaundice and decline of body weight were suppressed. These data indicate that B cells play an important role in the acute rejection of the rat liver allograft, at least partially via production of cytotoxic antiallograft antibody. Splenectomy or other immunosuppressive methods affecting B cells can be a supplement for immunosuppression when using reduced-dose FK506.
引用
收藏
页码:1522 / 1525
页数:4
相关论文
共 26 条
[1]
IGM AND IGG ALLOANTIBODY PRODUCTION BY SPLENOCYTES AND DEPOSITION IN RAT RENAL-ALLOGRAFTS ARE DECREASED BY DONOR-SPECIFIC BLOOD-TRANSFUSION [J].
BALDWIN, WM ;
RHOTON, K ;
SANFILIPPO, F .
TRANSPLANTATION, 1991, 51 (02) :481-485
[2]
TUMOR-NECROSIS-FACTOR-ALPHA IS AN AUTOCRINE GROWTH-FACTOR FOR NORMAL HUMAN B-CELLS [J].
BOUSSIOTIS, VA ;
NADLER, LM ;
STROMINGER, JL ;
GOLDFELD, AE .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (15) :7007-7011
[3]
CANDINAS D, 1994, TRANSPLANT P, V26, P3251
[4]
ANTI-CD2 MONOCLONAL-ANTIBODIES SYNERGIZE WITH FK506 BUT NOT WITH CYCLOSPORINE OR RAPAMYCIN TO INDUCE TOLERANCE [J].
CHAVIN, KD ;
QIN, LH ;
WOODWARD, JE ;
LIN, JX ;
BROMBERG, JS .
TRANSPLANTATION, 1994, 57 (05) :736-740
[5]
FK506 CONVERSION THERAPY IN PEDIATRIC LIVER-TRANSPLANTATION [J].
EGAWA, H ;
ESQUIVEL, CO ;
SO, SK ;
COX, K ;
CONCEPCION, W ;
LAWRENCE, L .
TRANSPLANTATION, 1994, 57 (08) :1169-1173
[6]
TRANSCRIPTION OF THE TUMOR-NECROSIS-FACTOR-ALPHA GENE IS RAPIDLY INDUCED BY ANTIIMMUNOGLOBULIN AND BLOCKED BY CYCLOSPORINE-A AND FK506 IN HUMAN B-CELLS [J].
GOLDFELD, AE ;
FLEMINGTON, EK ;
BOUSSIOTIS, VA ;
THEODOS, CM ;
TITUS, RG ;
STROMINGER, JL ;
SPECK, SH .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (24) :12198-12201
[7]
ORTHOTOPIC LIVER-TRANSPLANTATION IN THE RAT - TECHNIQUE USING CUFF FOR PORTAL-VEIN ANASTOMOSIS AND BILIARY DRAINAGE [J].
KAMADA, N ;
CALNE, RY .
TRANSPLANTATION, 1979, 28 (01) :47-50
[8]
KLINTMALM GBG, 1981, LANCET, V1, P470
[9]
LANGER A, 1993, AM J PATHOL, V143, P85
[10]
DEPLETION OF IGM XENOREACTIVE NATURAL ANTIBODIES BY INJECTION OF ANTI-MU MONOCLONAL-ANTIBODIES [J].
LATINNE, D ;
SOARES, M ;
HAVAUX, X ;
CORMONT, F ;
LESNIKOSKI, B ;
BACH, FH ;
BAZIN, H .
IMMUNOLOGICAL REVIEWS, 1994, 141 :95-125