THE MECHANISM OF DISCORDANT XENOGRAFT REJECTION
- 1 December 1988
- journal article
- research article
- Published by Wolters Kluwer Health in Transplantation
- Vol. 46 (6) , 825-829
- https://doi.org/10.1097/00007890-198812000-00007
Abstract
The mechanism of discordant xenograft rejection using the guinea pig-to-rat heart graft model was studied. In this model, we found that (A) Rejection occurred rapidly, in 17.5 .+-. 8.3 min (mean .+-. SD) (n=8). (B) The graft survived longer when the recipient rat was pretreated with cobra venom facter (CVF). (C) Complement hemolytic titers in serum showed significant reduction of C3 in rejection without consumption of C4 and C2, suggesting complement activation through the alternative pathway. (D) No natural antibodies were detected in this combination. Complement-dependent cytotoxicity (CDC) titer, and hemagglutination (HA) titer were lower than .times. 1. (E) Histological examination of the rejected heart xenograft revealed a large area of myocytolysis without interstitial cellular infiltration. (F) In vitro experiments showed that rat complement attacked guinea pig erythrocytes (Egp) via the alternative pathway. These findings indicate that rejection in this discordant xenograft model of guinea pig-to-rat was caused by primary activation of complement via the alternative pathway.This publication has 4 references indexed in Scilit:
- Nucleated cell killing by complement: effects of C5b-9 channel size and extracellular Ca2+ on the lytic process.The Journal of Immunology, 1987
- Purification and characterization of a membrane protein (gp45-70) that is a cofactor for cleavage of C3b and C4b.The Journal of Experimental Medicine, 1986
- Prevention of complement activation on the homologous cell membrane of nucleated cells as well as erythrocytesEuropean Journal of Immunology, 1983
- Chromatographic Separation of the First Component of Complement and Its Assay on a Molecular BasisThe Journal of Immunology, 1963