Disseminated intravascular coagulation in association with the delayed rejection of pig-to-baboon renal xenografts

被引:101
作者
Ierino, FL
Kozlowski, T
Siegel, JB
Shimizu, A
Colvin, RB
Banerjee, PT
Cooper, DKC
Cosimi, AB
Bach, FH
Sachs, DH
Robson, SC
机构
[1] Beth Israel Deaconess Med Ctr, Dept Surg, Ctr Immunobiol, Boston, MA 02215 USA
[2] Harvard Univ, Sch Med, Boston, MA 02215 USA
[3] Massachusetts Gen Hosp, Transplantat Biol Res Ctr, Boston, MA 02114 USA
[4] Massachusetts Gen Hosp, Dept Pathol, Boston, MA 02114 USA
[5] Massachusetts Gen Hosp, Dept Surg, Boston, MA 02114 USA
[6] BioTransplant Inc, Charlestown, MA 02129 USA
关键词
D O I
10.1097/00007890-199812150-00006
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background. Intravascular fibrin deposition and platelet sequestration occur with porcine xenograft rejection by baboons. Disseminated intravascular coagulopathy may arise either as a direct consequence of the failure to fully deplete xenoreactive natural antibodies and block complement, or because of putative cross-species molecular incompatibilities in this discordant species combination. Methods. Three baboons were conditioned with retrovirally transduced autologous bone marrow to induce tolerance to swine antigens, Xenoreactive natural antibodies and complement were depleted by plasmapheresis and the use of Gal alpha 1-3Gal column adsorptions; baboons were then splenectomized and underwent renal xenografting from inbred, miniature pigs, Soluble complement receptor type-1 with protocol immunosuppression (mycophenolate mofetil, 15-deoxyspergualin, steroids, and cyclosporine) was administered. Results. A bleeding diathesis was clinically evident from days 5 to 12 after transplantation in two baboons, Low levels of circulating C3a, C3d, and iC3b were measured despite the absence of functional circulating complement components. Profound thrombocytopenia with abnormalities in keeping with disseminated intravascular coagulopathy were observed. Prolongation of prothrombin and partial thromboplastin times was accompanied by evidence for tissue factor-mediated coagulation pathways, high levels of thrombin generation (prothrombin fragment F1+2 production and thrombin-antithrombin complex formation), fibrinogen depletion, and production of high levels of the fibrin degradation product D-dimer, Importantly, these disturbances resolved rapidly after the excision of the rejected xenografts in two surviving animals. Histopathological examination of the rejected xenografts confirmed vascular injury, fibrin deposition, platelet deposition, and localized complement activation, Conclusions. Systemic coagulation disturbances are associated with delayed xenograft rejection.
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收藏
页码:1439 / 1450
页数:12
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