Evaluation of pre- and posttransplant donor-specific transfusion/cyclosporine A in non-HLA identical living donor kidney transplant recipients

被引:17
作者
Alexander, JW
Light, JA
Donaldson, LA
Delmonico, FL
Diethelm, AG
Wilkinson, A
Rosenthal, JT
Thistlethwaite, JR
Hunsicker, LG
Matas, AJ
First, MR
Reinsmoen, NL
Rose, SM
机构
[1] Univ Cincinnati, Med Ctr, Coll Med, Dept Surg, Cincinnati, OH 45267 USA
[2] Washington Hosp Ctr, Dept Transplantat, Washington, DC 20010 USA
[3] EMMES Corp, Potomac, MD 20854 USA
[4] Massachusetts Gen Hosp, Dept Surg, Boston, MA 02114 USA
[5] Univ Alabama, Sch Med, Birmingham, AL 35294 USA
[6] Univ Calif Los Angeles, Med Ctr, Dept Urol, Los Angeles, CA 90095 USA
[7] Univ Chicago, Dept Surg, Chicago, IL 60637 USA
[8] Univ Iowa, Div Nephrol, Iowa City, IA 52242 USA
[9] Univ Minnesota, Dept Surg, Minneapolis, MN 55455 USA
[10] NIAID, Genet & Transplantat Branch, Div Allergy Immunol & Transplantat, Bethesda, MD 20892 USA
关键词
D O I
10.1097/00007890-199910270-00010
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background. The beneficial effects of donor specific transfusion (DST) have become controversial in the cyclosporine era, This study was performed to evaluate the potential benefits of a new protocol for administering DSTs in the perioperative period. Methods. Non-HLA identical living donor kidney transplant recipients were randomized prospectively to control or to receive a DST 24 hr before transplant and 7-10 days posttransplant, All patients received similar immunosuppression according to protocol. Results. The protocol had 212 evaluable patients (115 transfused and 97 control). There were no differences in 1- and a-year graft and patient survival, causes of graft failure, incidence and types of infection, repeat hospitalization, or the ability to withdraw steroids. Immunological hyporesponsiveness (by mixed lymphocyte culture) occurred more frequently in transfused patients (18%) than controls (3%) (P=0.04), Blood stored for greater than or equal to 3 days was associated with fewer early rejections than blood stored less than or equal to 2 days. Overall, class II antigen mismatches were associated with more rejection episodes than class I antigen mismatches. However, transfused patients, but not control patients, with more class I antigen mismatches were more likely to have rejections. Conclusions. Administration of DSTs by the method described had no practical influence on patient or graft survival for up to 2 years. However, donor-specific hyporesponsiveness was more common in transfused patients (18 vs. 3%). Longer follow-up will be needed to determine whether DST will be associated with long-term benefit.
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收藏
页码:1117 / 1124
页数:8
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