HLA-DR matched transfusions - Development of donor-specific T- and B-cell antibodies and renal allograft outcome

Citation
Mhl. Christiaans et al., HLA-DR matched transfusions - Development of donor-specific T- and B-cell antibodies and renal allograft outcome, TRANSPLANT, 67(7), 1999, pp. 1029-1035
Citations number
15
Categorie Soggetti
Medical Research Diagnosis & Treatment
Journal title
TRANSPLANTATION
ISSN journal
00411337 → ACNP
Volume
67
Issue
7
Year of publication
1999
Pages
1029 - 1035
Database
ISI
SICI code
0041-1337(19990415)67:7<1029:HMT-DO>2.0.ZU;2-T
Abstract
Background, Pretransplant blood transfusions are reported to decrease acute rejection rate and increase graft survival after renal transplantation. Th is has been attributed to matching for HLA-DR with the transfusion donor, w hich also results in a lower rate of sensitization. Methods. The development of donor-specific T- and B-cell antibodies was mea sured by National Institutes of Health and two-color fluorescence assays af ter one transfusion in 247 naive patients. Auto-cross-matches were performe d to exclude autoantibodies, Patients were grouped according to DR-matching (n=107) or nonmatching (n=140) with the transfusion donor. In 103 renal al lograft recipients, acute rejection rate and graft survival were analyzed b y Cox regression. Results. T-cell antibodies developed in 6.5% of the patients. There was no difference between the DR-matched and nonmatched group. No auto-antibodies against T-cells developed, whereas one quarter of the sera had a positive B -cell auto-cross-match. There was no difference with regard to B-cell antib odies (autoantibody-positive sera excluded) between the DR-matched (15.8%) and nonmatched (18.6%) group. Sharing of HLA A and/or B antigens did not re sult in a lower frequency of donor-directed T- or B-cell antibodies. None o f the risk factors, including DR sharing with transfusion donor, contribute d significantly towards graft survival (odds ratio for DR sharing: 1.02; 95 % confidence interval: 0.45-2.32; P=0.97), DR sharing was no risk factor to wards acute rejection either, in contrast to DR mismatch with kidney donor (odds ratio: 2.9), and use of cyclosporine versus tacrolimus (odds ratio: 4 .4). Conclusions. Development of donor-directed T-cell antibodies after one tran sfusion of leukocyte-poor blood is low and irrespective of HLA-DR match wit h transfusion donor. B-cell antibodies develop more frequently and independ ent of HLA-DR match. In 26% of the sera, B-cell auto-antibodies are detecte d. Rejection rate and graft survival are not significantly different betwee n HLA-DR-matched and nonmatched transfusions.