Humoral responses to pig-to-baboon cardiac transplantation: Implications for the pathogenesis and treatment of acute vascular rejection and for accommodation

被引:74
作者
McCurry, KR
Parker, W
Cotterell, AH
Weidner, BC
Lin, SS
Daniels, LJ
Holzknecht, ZE
Byrne, GW
Diamond, LE
Logan, JS
Platt, JL
机构
[1] Duke Univ, Med Ctr, Dept Surg, Durham, NC 27710 USA
[2] Duke Univ, Med Ctr, Dept Immunol, Durham, NC 27710 USA
[3] Duke Univ, Med Ctr, Dept Pediat, Durham, NC 27710 USA
[4] Nextran, Princeton, NJ 08540 USA
关键词
D O I
10.1016/S0198-8859(97)00229-2
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Organs transplanted between phylogenetically-disparate species, such as from the pig into the primate, are subject to hyperacute and acute vascular rejection. Hyperacute rejection of a porcine organ by a primate is thought to be initiated by the binding of xenoreactive natural antibodies to Gal alpha 1-3Gal expressed on the endothelial lining of blood vessels in the xenograft. The factor(s) which initiates acute vascular rejection is uncertain; however, there is some evidence implicating xenoreactive antibodies. The nature of the humoral response which might contribute to acute vascular rejection of a porcine organ was investigated in baboons which received a porcine cardiac xenograft plus immunosuppression with methylprednisolone, azathioprine and cyclosporine. Following rejection and surgical removal of the xenografts, the serum concentration of xenoreactive antibodies increased in untreated animals but in immunosuppressed animals was similar to the concentration in preimmune serum. The antibodies in the sensitized recipients were specific for Gal alpha 1-3Gal (70-95%) and other determinants (5-30%). However, cross-blocking studies showed that, following xenotransplantation, the immunosuppressed baboons had no detectable IgM or IgG directed against "new" endothelial antigens. These results indicate that antibodies made by immunosuppressed individuals in response to xenotransplantation are much like xenoreactive natural antibodies and suggest that acute vascular rejection might in some cases be addressed by therapeutic strategies antibodies. (C) American Society for Histocompatibility and Immunogenetics, 1997, Published by Elsevier Science Inc.
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页码:91 / 105
页数:15
相关论文
共 73 条
[1]  
ABBAS AK, 1974, AM J PATHOL, V75, P271
[2]  
Alexandre G.P.J., 1989, XENOGRAFT, V25, P259
[3]   XENOGENEIC TRANSPLANTATION - A REVIEW [J].
AUCHINCLOSS, H .
TRANSPLANTATION, 1988, 46 (01) :1-20
[4]   USE OF SEQUENTIAL SKIN ALLOGRAFTS TO DEMONSTRATE SENSITIZATION INDUCED BY SHORT-TERM KIDNEY TRANSPLANTS [J].
BALLANTYNE, DL ;
NATHAN, P .
TRANSPLANTATION, 1968, 6 (03) :342-+
[5]   ACTIVATION OF INTRAGRAFT ENDOTHELIAL AND MONONUCLEAR-CELLS DURING DISCORDANT XENOGRAFT REJECTION [J].
BLAKELY, ML ;
VANDERWERF, WJ ;
BERNDT, MC ;
DALMASSO, AP ;
BACH, FH ;
HANCOCK, WW .
TRANSPLANTATION, 1994, 58 (10) :1059-1066
[6]  
BRAUER RB, 1993, J IMMUNOL, V151, P7240
[7]   Transgenic pigs expressing human CD59 and decay-accelerating factor produce an intrinsic barrier to complement-mediated damage [J].
Byrne, G ;
McCurry, KR ;
Martin, MJ ;
McClellan, SM ;
Platt, JL ;
Logan, JS .
TRANSPLANTATION, 1997, 63 (01) :149-155
[8]  
CALNE RY, 1970, TRANSPL P, V2, P550
[9]  
CHOPEK MW, 1987, TRANSPLANT P, V19, P4553
[10]  
CLARK D S, 1964, Surg Forum, V15, P144