Literature DB >> 18284306

A confusion in antibody identification: anti-D production after anti-hrB.

C Lomas-Francis1, R Yomtovian, C McGrath, P S Walker, M E Reid.   

Abstract

It is well known that certain combinations of alloantibodies are frequently found together. Patients with sickle cell disease (SCD) are mostly ofAfrican ancestry,and they may make anti-hrB. A transfusion of hrB- blood is often achieved by using e- (R2R2) RBCs; it is generally believed that hrB- patients readily make anti-E or a"broad-spectrum" anti-Rh34 (-HrB). We describe two multiply transfused D+ patients with SCD and a history of anti-hrB who subsequently produced anti- D. This raises the question whether anti-hrB together with anti-D is a more common antibody combination than anti-hrB with anti-E or anti-Rh34.

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Year:  2007        PMID: 18284306

Source DB:  PubMed          Journal:  Immunohematology        ISSN: 0894-203X


  2 in total

1.  Transfusion considerations concerning patients with anti-hrB and confounding co-morbid conditions: pregnancy and coagulopathy.

Authors:  Natasha M Savage; Wadicar F Nugent; Lawrence D Devoe; Roni J Bollag; Lloyd O Cook
Journal:  Blood Transfus       Date:  2010-12-27       Impact factor: 3.443

2.  Genomic analyses of RH alleles to improve transfusion therapy in patients with sickle cell disease.

Authors:  Marion E Reid; Christine Halter Hipsky; Kim Hue-Roye; Carolyn Hoppe
Journal:  Blood Cells Mol Dis       Date:  2013-12-02       Impact factor: 3.039

  2 in total

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