Effects of a Tolerance Induction Protocol in Renal Allograft Recipients — the Ahmedabad Experience
Article Outline
Background
The most interesting recent development in transplantation immunobiology is the clinical implementation of tolerance induction. We report our experience of megadose hematopoietic stem cell transplantation with non-myeloablative minimum conditioning in renal allograft recipients.
Methods
This was a retrospective, single-center study of 159 renal allograft biopsies from two groups of patients: one group underwent a tolerance induction protocol (TIP) before renal transplantation; the other underwent renal transplantation directly. Biopsies were classified into two subgroups to differentiate between acute and late rejection: 127 biopsies, comprising 64 from patients who underwent a TIP and 63 from controls, performed within 180 days after transplantation; and 32 biopsies, comprising 26 from patients who underwent a TIP and six from controls, performed 180 days after transplantation. All patients received cyclosporine 7 mg/kg/day, tapered to 3 mg/kg/day 3 months after transplantation, and subsequently continued at the latter dosage.
Results
There was markedly less immunologic injury (i.e. generally fewer and milder rejection episodes) evident in biopsies from patients who underwent TIP than in biopsies from controls. Cyclosporine toxicity was considerably greater in patients from the TIP versus control group (82.9% vs 40.6%).
Conclusion
TIP protects renal allografts from immunologic injury and has an unexplained cyclosporine-sparing effect.
Key words: cyclosporine nephrotoxicity , hematopoietic stem cell transplantation , immunologic injury , renal transplantation , tolerance induction protocol
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References
- High dose PBSC associated tolerance in live-related renal allograft recipients . Transplant Proc . 2000;32:2001–2002
- Megadose approach to DBMC infusion-induced allograft hyporesponsiveness in living-related renal allograft recipients . Transplant Proc . 2001;33:71–76
- High-dose peripheral blood stem cell infusion: a strategy to induce donor-specific hyporesponsiveness to allografts in pedia-tric renal transplant recipients . Pediatr Transplant . 2002;6:63–68
- Mega dose unfractionated donor bone marrow-derived cell infusion in thymus and periphery - an integrated clinical approach for tolerance in live related renal allografts . Transplant Proc . 2003;35:203–206
- The Banff 97 working classification of renal allograft pathology . Kidney Int . 1999;55:713–723
- . Cyclosporin in cadaveric renal transplantation: 5-year follow-up of a multicentre trial . Lancet . 1987;2:506–507
- . Cyclosporine-induced renal dysfunction in ex-perimental animals and humans . Kidney Int Suppl . 1995;52:S70–S74
- Morphology of cyclosporine nephrotoxicity and acute rejection in patients immunosuppressed with cyclo-sporine and prednisone . Surgery . 1983;94:225–234
- . Cyclosporine. . In: Schumacher D editors. Therapeutic Drug Monitoring. . Stanford, CT: Appleton and Lange; 1995;p. 449
PII: S1561-5413(09)60176-9
doi:10.1016/S1561-5413(09)60176-9
© 2005 The Hong Kong Society of Nephrology. Published by Elsevier Inc. All rights reserved.
