PHENOTYPING AUTOLOGOUS RED-CELLS WITHIN 1 DAY AFTER ALLOGENEIC BLOOD-TRANSFUSION BY USING IMMUNOMAGNETIC ISOLATION OF RETICULOCYTES

Citation
A. Brun et al., PHENOTYPING AUTOLOGOUS RED-CELLS WITHIN 1 DAY AFTER ALLOGENEIC BLOOD-TRANSFUSION BY USING IMMUNOMAGNETIC ISOLATION OF RETICULOCYTES, Transfusion, 34(2), 1994, pp. 162-166
Citations number
21
Categorie Soggetti
Hematology
Journal title
ISSN journal
00411132
Volume
34
Issue
2
Year of publication
1994
Pages
162 - 166
Database
ISI
SICI code
0041-1132(1994)34:2<162:PARW1D>2.0.ZU;2-#
Abstract
Background: When a transfused patient develops multiple or weak blood group antibodies, posttransfusion phenotyping is useful in antibody id entification To perform a correct phenotyping after transfusion, isola tion of autologous red bells is necessary. However, mature autologous red cells are impossible to separate from their donor counterparts. Si nce the proportion of autologous reticulocytes compared to donor retic ulocytes increases rapidly after transfusion, selective isolation of r eticulocytes provides autologous cells for antigen typing. Study Desig n and Methods: Extensive phenotyping was performed on red cells from 1 0 surgical patients before transfusion and on red cells and reticulocy tes after the transfusion of 5 or more red cell units. Reticulocytes w ere isolated by using an antibody against the human transferrin recept or coupled to magnetic beads. Results: The data showed nearly full agr eement between pretransfusion phenotyping of red cells and posttransfu sion typing of reticulocytes. Correct phenotyping of transfused patien ts could be obtained 8 to 10 hours after transfusion using isolated re ticulocytes. Conclusion: This method is helpful in selecting compatibl e blood when patients have developed antibodies and have an urgent nee d for further transfusions.