Assessment of peripheral tolerance in anti-CD4 treated C57BL/6 mouse heart transplants recipients

被引:10
作者
Han, WR [1 ]
Murray-Segal, LJ [1 ]
Mottram, PL [1 ]
机构
[1] Univ Melbourne, Dept Surg, Royal Melbourne Hosp, Melbourne, Vic 3050, Australia
基金
英国医学研究理事会;
关键词
D O I
10.1016/S0966-3274(99)80017-3
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The study was designed to compare second heart and skin grafts and in vitro assays as a means of assessing peripheral tolerance in C57BL/6 mice. Vascularized heterotopic BALB/c hearts were placed in C57BL/6 recipients treated with anti-CD4, GK1.5 (1 mg total per 20 g mouse i.p. on days 0, 1, 2, 3). Those mice in which hearts survived for >60 days were challenged with donor and third-party (CBA) skin grafts or with second heart grafts, of donor or third-party origin, attached to the carotid artery and jugular vein. In vitro alloreactivity was assessed by mixed lymphocyte reactions (MLR) and cell mediated lympholysis (CML) using recipient spleen cells. Parenchymal damage, cellular infiltration and vascular disease were assessed from the histology of long-term allografts and isografts. Allografts in untreated recipients were rapidly rejected while isografts survived > 100 days. Primary allografts in anti-CD4 treated recipients also survived > 100 days, as did donor strain secondary heart transplants given at >60 days after the first graft. Third-party hearts were rapidly rejected, as were donor and third-party skin grafts placed on recipients with long-term allografts. These recipients showed low MLR response to both donor and third-party stimulators and donor-specific suppression of CML at 60 days post graft. Long-surviving heart allografts all showed evidence of parenchymal damage and vascular intimal thickening. Thus in the BALB/c to C57BL/6 donor-recipient strain combination, hearts, but not skin grafts, could be used to demonstrate peripheral tolerance, which seemed to be both organ and major histocompatibility complex (MHC) specific. Despite long survival, BALB/c hearts all showed evidence of parenchymal damage and vascular intimal thickening, a sign of chronic rejection.
引用
收藏
页码:37 / 44
页数:8
相关论文
共 49 条
[1]   EXPERIMENTAL GRAFT ARTERIOSCLEROSIS .1. THE LEWIS-TO-F-344 ALLOGRAFT MODEL [J].
ADAMS, DH ;
TILNEY, NL ;
COLLINS, JJ ;
KARNOVSKY, MJ .
TRANSPLANTATION, 1992, 53 (05) :1115-1119
[2]  
[Anonymous], BMDP STAT SOFTWARE
[3]  
BARRETT LV, 1989, ALTERNATIVE HETEROTO
[4]  
BILLINGHAM RE, 1951, J EXP BIOL, V28, P385
[5]  
BORDER WA, 1994, NEW ENGL J MED, V331, P1286
[6]   MECHANISMS OF TRANSPLANTATION TOLERANCE [J].
CHARLTON, B ;
AUCHINCLOSS, H ;
FATHMAN, CG .
ANNUAL REVIEW OF IMMUNOLOGY, 1994, 12 :707-734
[7]   TOLERANCE IN THE MOUSE TO MAJOR HISTOCOMPATIBILITY COMPLEX-MISMATCHED HEART ALLOGRAFTS, AND TO RAT-HEART XENOGRAFTS, USING MONOCLONAL-ANTIBODIES TO CD4 AND CD8 [J].
CHEN, ZH ;
COBBOLD, S ;
METCALFE, S ;
WALDMANN, H .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1992, 22 (03) :805-810
[8]   Mechanisms of peripheral tolerance and suppression induced by monoclonal antibodies to CD4 and CD8 [J].
Cobbold, SP ;
Adams, E ;
Marshall, SE ;
Davies, JD ;
Waldmann, H .
IMMUNOLOGICAL REVIEWS, 1996, 149 :5-33
[9]  
COBBOLD SP, 1992, IMMUNOL REV, V129, P164
[10]   PRIMARILY VASCULARIZED ALLOGRAFTS OF HEARTS IN MICE - ROLE OF H-2D, H-2K, AND NON-H-2 ANTIGENS IN REJECTION [J].
CORRY, RJ ;
WINN, HJ ;
RUSSELL, PS .
TRANSPLANTATION, 1973, 16 (04) :343-350