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Cyclosporine-treated kidney transplants from living-related donors--a single center trial

K Ota1, K Takahashi, H Toma

  • 1Department of Surgery, Tokyo Women's Medical College, Japan.

Clinical Transplants
|January 1, 1988
PubMed

Insights

Cyclosporine A (CsA) improved 5-year kidney transplant survival compared to Azathioprine (AZ), but higher creatinine levels warrant further study. Donor-specific transfusion (DST) may benefit CsA-treated recipients, especially with poor tissue matching.

Area of Science:

  • Nephrology
  • Immunology
  • Transplantation

Background:

  • Cyclosporine A (CsA) is a key immunosuppressant in kidney transplantation.
  • Optimizing CsA regimens is crucial for long-term graft survival and renal function.
  • Living-related donor kidney transplantation outcomes require continuous evaluation.

Purpose of the Study:

  • To compare the efficacy of Cyclosporine A (CsA) versus Azathioprine (AZ) in living-related donor kidney transplant recipients.
  • To investigate the impact of donor-specific transfusion (DST) and crossmatch results on graft survival in CsA-treated patients.
  • To analyze rejection patterns based on antibody profiles.

Main Methods:

  • Retrospective analysis of 369 CsA-treated recipients and 160 AZ-treated controls.
  • Donor-specific transfusion (DST) performed in recipients responding to mixed lymphocyte reaction (MLR).
  • Evaluation of graft survival rates based on crossmatch status and antibody profiles.

Main Results:

  • Five-year graft survival was 78.2% with CsA versus 58.5% with AZ. CsA recipients had higher serum creatinine levels.
  • No significant difference in outcomes between DST and non-DST groups in CsA-treated recipients, suggesting DST benefit.
  • Lower graft survival in patients with transient positive crossmatch.
  • Acute rejection highest in T-cell antibody positive cases; chronic rejection highest in cold B-cell positive cases.
  • Azathioprine (AZ) combined with local graft irradiation suppressed blood group antigen antibodies.

Conclusions:

  • CsA offers superior graft survival but necessitates careful monitoring of renal function.
  • DST may be beneficial in CsA-treated recipients, particularly with suboptimal tissue matching.
  • Crossmatch status and specific antibody profiles influence rejection risk and graft outcomes.
  • Further research is needed to optimize CsA administration for long-term renal function maintenance.

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