65-P: Solid phase anti-HLA antibody testing: Is a low level of antibody clinically relevant?

2007 ◽  
Vol 68 (1) ◽  
pp. S47
Author(s):  
Allen J. Norin ◽  
Ballabh Das ◽  
David Hochman ◽  
Andrew D’Onofrio ◽  
Louise Bergamini ◽  
...  
2011 ◽  
Vol 72 ◽  
pp. S47
Author(s):  
Chang Liu ◽  
Sue Pang ◽  
Donna L. Phelan ◽  
Thalachallour Mohanakumar ◽  
Gerald P. Morris

2017 ◽  
Vol 78 ◽  
pp. 228
Author(s):  
John J. Xin ◽  
Jerome G. Weidner ◽  
Rebecca L. Upchurch ◽  
Nicholas K. Brown ◽  
Susana R. Marino

2015 ◽  
Vol 32 (1) ◽  
pp. 1-8 ◽  
Author(s):  
Moshe Israeli ◽  
Marilyn S. Pollack ◽  
Carley A.E. Shaut ◽  
Anne Halpin ◽  
Nicholas R. DiPaola ◽  
...  

Author(s):  
Andrea A. Zachary ◽  
Renato M. Vega ◽  
Donna P. Lucas ◽  
Mary S. Leffell

2019 ◽  
Vol 33 (1) ◽  
pp. 18-29 ◽  
Author(s):  
Caroline Wehmeier ◽  
Gideon Hönger ◽  
Stefan Schaub

2017 ◽  
Vol 78 (7-8) ◽  
pp. 471-480 ◽  
Author(s):  
Harold C. Sullivan ◽  
Howard M. Gebel ◽  
Robert A. Bray

2016 ◽  
Vol 21 (4) ◽  
pp. 453-458 ◽  
Author(s):  
Maria P. Bettinotti ◽  
Andrea A. Zachary ◽  
Mary S. Leffell
Keyword(s):  

2019 ◽  
Vol 152 (2) ◽  
pp. 146-154 ◽  
Author(s):  
Jeremy Ryan A Peña ◽  
Robert S Makar

ABSTRACTObjectivesNo validated screening methods identify patients at risk for human leukocyte antigen (HLA) alloimmune-mediated platelet refractoriness (alloPR). We determined if bead-based HLA antibody tests could predict risk of developing HLA alloPR.MethodsHematopoietic progenitor cell transplant patients screened for HLA antibodies without prior refractoriness were identified. Phenotype bead screening results were compared between patients who later did and did not develop alloPR.ResultsSeven of 27 patients identified subsequently developed alloPR. The panel reactive antibody (PRA) and mean fluorescence intensity (MFI) of the 10 most reactive beads in the initial screen were significantly higher among patients who later developed alloPR (P < .001). Specifically, PRA of more than 30% and mean MFI of 1,500 or more in the most reactive beads identified at-risk patients. Administration of HLA-compatible platelets yielded significant posttransfusion count increments compared with routine platelets.ConclusionsHLA antibody screening by phenotype bead assay may prospectively identify at-risk patients for the development of alloPR. However, clinical trials are needed to validate these findings.


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