Previous studies from our laboratory showed that pretreatment with ultraviolet-B-irradiated donor leukocytes (UV-B DL) combined with brief peritransplant cyclosporine (CyA) resulted in indefinite survival of Wistar/Furth rat cardiac allografts in Lewis recipients. This study was designed to examine
Failure to prolong pancreatic islet allograft survival in rats with donor-specific blood transfusions and immunosuppression
โ Scribed by J. Adam Vliet; Lieuwe G. Hem; M. Jane Field; David E. R. Sutherland
- Publisher
- Springer
- Year
- 1988
- Tongue
- English
- Weight
- 351 KB
- Volume
- 1
- Category
- Article
- ISSN
- 0934-0874
No coin nor oath required. For personal study only.
โฆ Synopsis
The effects on pancreatic islet allograft survival of donor-specific blood transfusions (DST) in combination with pre-and posttransplant immunosuppression were studied. A total of 12 groups of rats (n=105) with chemically induced diabetes underwent islet allotransplantation. Multiple DST or third-party blood transfusions (TPT) were given prior to transplantation. Pretransplant immunosuppression consisted of azathioprine and prednisolone, and low-dose cyclosporinA was used for posttransplant immunosuppression. TPT, as well as separate or combined pre-and posttransplant immunosuppression without blood transfusions, did not prolong islet allograft survival. DST resulted in either primary nonfunction of the islet allografts or a markedly decreased islet allograft survival. These findings contrast with the beneficial effect of DST on whole-organ allograft survival in rats previously described by others.
๐ SIMILAR VOLUMES
## Methods remains unclear. 1 Clonal deletion, 2 suppressor T cells, 3 veto Animals. Inbred male Lewis (LEW) (RT1 1 ) and ACI(RT1 a ) rats bred at the Kumamoto University Animal Research Center (Kumamoto, Japan) were used as transplant recipients and donors, respec-Abbreviations: DST, donor-specif