Application of genomics for transfusion therapy in sickle cell anemia

被引:16
作者
Chou, Stella T. [1 ]
Westhoff, Connie M. [2 ]
机构
[1] Childrens Hosp Philadelphia, Dept Pediat, Philadelphia, PA 19104 USA
[2] New York Blood Ctr, Immunohematol & Genom, New York, NY 10021 USA
基金
美国国家卫生研究院;
关键词
Red cell alloimmunization; Sickle cell anemia; Transfusion; Rh antigens; Antigen-matched; Red blood cell genotyping; RED-BLOOD-CELL; CLINICAL-SIGNIFICANCE; RH ALLELES; DISEASE; ALLOIMMUNIZATION; MANAGEMENT; CHILDREN; PHENOTYPE; STROKE; TRIAL;
D O I
10.1016/j.bcmd.2017.08.006
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The application of genomic approaches is impacting all areas of laboratory testing including transfusion medicine. Use of DNA-based test methods is particularly applicable for red cell and platelet antigen typing as the majority of genes encoding the carrier proteins and carbohydrates are now known and were cloned in the 1990's. Many of the antigenic polymorphisms are due to single nucleotide changes (SNP's) in the respective genes and DNA-arrays that target these changes have been validated by comparison with conventional serologic typing. Here we review the advances in the last decade in the application of DNA-based genotyping to transfusion therapy, specifically in sickle cell anemia (SCA), and discuss the practical integration and the value of this approach to improve outcomes and prevent complications in this patient population. The ability to test for antigens for which there are no serologic reagents is a major medical advance that promises to mitigate transfusion related morbidity and mortality due to alloimmunization.
引用
收藏
页码:148 / 154
页数:7
相关论文
共 43 条
[21]   Alloimmunization in sickle cell anemia in the era of extended red cell typing [J].
O'Suoji, Chibuzo ;
Liem, Robert I. ;
Mack, A. Kyle ;
Kingsberry, Paris ;
Ramsey, Glenn ;
Thompson, Alexis. A. .
PEDIATRIC BLOOD & CANCER, 2013, 60 (09) :1487-1491
[22]  
Osby M, 2005, ARCH PATHOL LAB MED, V129, P190
[23]   Genomic analyses of RH alleles to improve transfusion therapy in patients with sickle cell disease [J].
Reid, Marion E. ;
Hipsky, Christine Halter ;
Hue-Roye, Kim ;
Hoppe, Carolyn .
BLOOD CELLS MOLECULES AND DISEASES, 2014, 52 (04) :195-202
[24]   DNA array analysis for red blood cell antigens facilitates the transfusion support with antigen-matched blood in patients with sickle cell disease [J].
Ribeiro, K. R. ;
Guarnieri, M. H. ;
da Costa, D. C. ;
Costa, F. F. ;
Pellegrino, J., Jr. ;
Castilho, L. .
VOX SANGUINIS, 2009, 97 (02) :147-152
[25]  
ROSSE WF, 1990, BLOOD, V76, P1431
[26]   Allosensitization in patients receiving multiple blood transfusions [J].
Sakhalkar, VS ;
Roberts, K ;
Hawthorne, LM ;
McCaskill, DM ;
Veillon, DM ;
Caldito, GC ;
Cotelingam, JD .
COOLEY'S ANEMIA EIGHTH SYMPOSIUM, 2005, 1054 :495-499
[27]   A structural model for 30 rh D epitopes based on serological and DNA sequence data from partial D phenotypes [J].
Scott, ML ;
Voak, D ;
Jones, JW ;
Avent, ND ;
Liu, W ;
HughesJones, N ;
Sonneborn, H .
TRANSFUSION CLINIQUE ET BIOLOGIQUE, 1996, 3 (06) :391-396
[28]   Variant RH alleles and Rh immunisation in patients with sickle cell disease [J].
Sippert, Emilia ;
Fujita, Claudia R. ;
Machado, Debora ;
Guelsin, Glaucia ;
Gaspardi, Ane C. ;
Pellegrino, Jordao, Jr. ;
Gilli, Simone ;
Saad, Sara S. T. O. ;
Castilho, Lilian .
BLOOD TRANSFUSION, 2015, 13 (01) :72-77
[29]   International Society of Blood Transfusion Working Party on red cell immunogenetics and blood group terminology: Cancun report (2012) [J].
Storry, J. R. ;
Castilho, L. ;
Daniels, G. ;
Flegel, W. A. ;
Garratty, G. ;
de Haas, M. ;
Hyland, C. ;
Lomas-Francis, C. ;
Moulds, J. M. ;
Nogues, N. ;
Olsson, M. L. ;
Poole, J. ;
Reid, M. E. ;
Rouger, P. ;
van der Schoot, E. ;
Scott, M. ;
Tani, Y. ;
Yu, L. -C. ;
Wendel, S. ;
Westhoff, C. ;
Yahalom, V. ;
Zelinski, T. .
VOX SANGUINIS, 2014, 107 (01) :90-96
[30]   ANTIGEN-MATCHED DONOR BLOOD IN THE TRANSFUSION MANAGEMENT OF PATIENTS WITH SICKLE-CELL DISEASE [J].
TAHHAN, HR ;
HOLBROOK, CT ;
BRADDY, LR ;
BREWER, LD ;
CHRISTIE, JD .
TRANSFUSION, 1994, 34 (07) :562-569