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Donor-specific transfusion: a report of the Japanese Renal Transplant Registry

T Sonoda1, M Ishibashi

  • 1Department of Urology, Osaka University Hospital, Japan.

Clinical Transplants
|January 1, 1987
PubMed

Insights

Donor-specific transfusions (DST) significantly improve renal transplant survival, especially with cyclosporine (CsA) immunosuppression. Unspecified transfusions also enhance outcomes, highlighting the benefits of blood transfusions in transplantation.

Area of Science:

  • Nephrology
  • Immunology
  • Transplantation Medicine

Background:

  • Donor-specific transfusions (DST) are a known method to improve transplant outcomes.
  • The role of DST in conjunction with different immunosuppressive regimens requires further elucidation.
  • Cyclosporine (CsA) and conventional immunosuppression represent distinct approaches to managing transplant recipients.

Purpose of the Study:

  • To investigate the impact of donor-specific transfusions (DST) on renal graft survival in HLA one haplotype-mismatched living-related transplant recipients.
  • To compare the efficacy of DST under cyclosporine (CsA) versus conventional immunosuppression.
  • To evaluate the effects of unspecified blood transfusions (UTF) in combination with DST.

Main Methods:

  • Analysis of 1,292 transplant patients from the Japanese Renal Transplant Registry.
  • Stratification of patients based on immunosuppressive therapy (CsA vs. conventional) and transfusion status (DST, DST + UTF, UTF, no transfusion).
  • Comparison of 4-year renal graft survival rates across different transfusion and immunosuppression groups.

Main Results:

  • In CsA groups, 4-year graft survival rates were: DST (93.5%), DST + UTF (91.6%), UTF (76.2%), and no transfusion (62.7%).
  • In conventional groups, 4-year graft survival rates were: DST (73.3%), DST + UTF (87.2%), UTF (73.2%), and no transfusion (69.0%).
  • The beneficial effect of DST was more pronounced with CsA than conventional immunosuppression, though DST with UTF showed a superior effect in conventional groups.

Conclusions:

  • Donor-specific transfusions (DST) significantly enhance renal graft survival, particularly when combined with cyclosporine (CsA) immunosuppression.
  • Unspecified transfusions (UTF) also contribute positively to graft survival, especially when administered alongside DST.
  • The combination of DST and CsA therapy appears to yield excellent long-term graft survival rates in HLA-mismatched living-related renal transplants.

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