Transfusion to blood group A and O patients of group B RBCs that have been enzymatically converted to group O

被引:52
作者
Kruskall, MS
AuBuchon, JP
Anthony, KY
Herschel, L
Pickard, C
Biehl, R
Horowitz, M
Brambilla, DJ
Popovsky, MA
机构
[1] Harvard Univ, Div Lab & Transfus Med, Sch Med, Beth Israel Deaconess Med Ctr,Dept Pathol, Boston, MA 02215 USA
[2] Harvard Univ, Sch Med, Beth Israel Deaconess Med Ctr, Dept Med, Boston, MA 02215 USA
[3] Dartmouth Hitchcock Med Ctr, Dept Pathol, Lebanon, NH 03766 USA
[4] New England Res Inst, Watertown, MA 02172 USA
[5] ZymeQuest Inc, Beverly, MA USA
[6] Amer Red Cross, New England Reg, Dedham, MA USA
关键词
D O I
10.1046/j.1537-2995.2000.40111290.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND: The transfusion of ABO-incompatible RBCs is the leading cause of fatal transfusion reactions. Group O RBCs, lacking terminal immunodominant A and B sugars to which humans are immunized, are safe for transfusion to persons of any ABO blood group. With the use of a recombinant alpha -galactosidase to remove terminal galactose from group B RBCs, the safety and efficacy of enzyme-converted group-B-to-group-O (ECO) RBC components were studied in transfusion-dependent patients. STUDY DESIGN AND METHODS: Twenty-four patients (blood groups A and O) were randomly assigned to receive transfusion(s) of either ECO or control group O RBCs. If a second transfusion was given, the other blood component was administered. RESULTS: Twenty-one patients were given ECO RBCs; 18 also underwent control transfusions. One patient received only a small aliquot for RBC survival studies, instead of a full-unit transfusion, because his serum was incompatible with ECO RBCs. No adverse events occurred. Both ECO and control transfusions resulted in appropriate Hb increments and comparable Cr-51-labeled RBC survival studies. One patient developed a transient, weak-positive DAT, without hemolysis. Two weeks after transfusion, 5 of 19 evaluable ECO RBC recipients had increases in anti-B titers. CONCLUSION: ECO RBCs were comparable to group O cells for safety and efficacy in this study. The clinical significance of the increase in anti-B and of occasional serologic incompatibilities with ECO RBCs is unclear. If strategies can be developed to remove A epitopes, enzymatic conversion could be used to create a universal (group O) donor blood supply.
引用
收藏
页码:1290 / 1298
页数:9
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