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The Annals of Thoracic Surgery, Vol 44, 242-246, Copyright © 1987 by The Society of Thoracic Surgeons
WH Frist, PE Oyer, JC Baldwin, EB Stinson and NE Shumway
Although the major histocompatibility complex has been linked with the
control and expression of immune response in mammalian species, its
importance for heart transplantation has not been demonstrated. The
relationship of patient survival to human lymphocyte antigen (HLA) (A and B
loci) compatibility was studied in 164 consecutive cyclosporine- treated
patients who underwent orthotopic heart transplantation between 1980 and
1986 at Stanford University Medical Center. All patients receiving a
transplant within this time frame were included except those for whom HLA
typing was unavailable. A mismatched antigen was defined as an antigen
present in the donor but not in the recipient. The actuarial four-year
survival (Cutler-Ederer) for the 19 patients with 0 or 1 mismatch was 88
+/- 8%; for the 39 patients with 2 mismatches, 70 +/- 12%; for the 73
patients with 3 mismatches, 59 +/- 7%; and for the 33 patients with 4
mismatches, 54 +/- 14%. Both actuarial and linear rate analyses revealed no
significant correlation between HLA mismatching and rejection rate,
likelihood of death from rejection, or length of time to first episode of
rejection. Patients with 3 or 4 mismatches had significantly (p less than
0.05) more infections than those with fewer mismatches. By actuarial
analysis, a trend toward a higher number of deaths from rejection and
infection was observed in the groups with 3 and 4 mismatches, but it did
not achieve statistical significance. The data demonstrate that
well-matched HLA grafts are associated with better long-term survival and
fewer infections in cardiac transplant patients.
ARTICLES
HLA compatibility and cardiac transplant recipient survival
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