Literature DB >> 21745213

DIII Type 7 is likely the original serologically defined DIIIb.

Christine Lomas-Francis1, Christine Halter Hipsky, Randall W Velliquette, Marion E Reid.   

Abstract

BACKGROUND: Due to their homology, close proximity, and opposite orientation, RHD and RHCE can exchange nucleotides giving rise to variant alleles. Some of these variants encode the so-called partial phenotypes. The DIII partial D category has been subdivided into DIIIa, DIIIb, DIIIc, DIII Type 4, DIII Type 6, and DIII Type 7. During DNA-based screening tests, we identified a second example of DIII Type 7 in a Dce donor from South Africa. Our study describes hemagglutination tests on this sample and raises a question regarding the molecular basis of the originally defined DIIIb category. STUDY DESIGN AND METHODS: Hemagglutination and DNA testing were performed by standard techniques.
RESULTS: Red blood cells from this DIII Type 7 donor typed D+C-E-c+e+G-, DAK+ and did not react with anti-D made by people with the DIII phenotype. The allele is RHD*DIII 150C, 178C, 201A, 203A, 307C, 410T, 455C, 602G, 667G.
CONCLUSIONS: Based on the serotype and ethnicity (black African), it is likely that DIII Type 7 is the originally defined DIIIb category.
© 2011 American Association of Blood Banks.

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Year:  2011        PMID: 21745213      PMCID: PMC3193886          DOI: 10.1111/j.1537-2995.2011.03233.x

Source DB:  PubMed          Journal:  Transfusion        ISSN: 0041-1132            Impact factor:   3.157


  8 in total

1.  Weak D alleles express distinct phenotypes.

Authors:  F F Wagner; A Frohmajer; B Ladewig; N I Eicher; C B Lonicer; T H Müller; M H Siegel; W A Flegel
Journal:  Blood       Date:  2000-04-15       Impact factor: 22.113

2.  Frequency of partial D phenotypes in the south western region of France.

Authors:  F Roubinet; P A Apoil; A Blancher
Journal:  Transfus Clin Biol       Date:  1996       Impact factor: 1.406

3.  A human monoclonal anti-D antibody which detects a nonconformation-dependent epitope on the RhD protein by immunoblot.

Authors:  P A Apoil; M E Reid; G Halverson; I Mouro; Y Colin; F Roubinet; J P Cartron; A Blancher
Journal:  Br J Haematol       Date:  1997-08       Impact factor: 6.998

4.  Lack of G blood group antigen in DIIIb erythrocytes is associated with segmental DNA exchange between RH genes.

Authors:  C Rouillac; C Le Van Kim; A Blancher; F Roubinet; J P Cartron; Y Colin
Journal:  Br J Haematol       Date:  1995-02       Impact factor: 6.998

5.  RHCE*ceCF encodes partial c and partial e but not CELO, an antigen antithetical to Crawford.

Authors:  Christine Halter Hipsky; Christine Lomas-Francis; Akiko Fuchisawa; Marion E Reid; Marilyn Moulds; Joann Christensen; Pam Nickle; Sunitha Vege; Connie Westhoff
Journal:  Transfusion       Date:  2011-01       Impact factor: 3.157

6.  RHD(T201R, F223V) cluster analysis in five different ethnic groups and serologic characterization of a new Ethiopian variant DARE, the DIII type 6, and the RHD(F223V).

Authors:  Martine G H M Grootkerk-Tax; Joyce D van Wintershoven; Peter C Ligthart; Dick J van Rhenen; C Ellen van der Schoot; Petra A Maaskant-van Wijk
Journal:  Transfusion       Date:  2006-04       Impact factor: 3.157

7.  DIIIa and DIII Type 5 are encoded by the same allele and are associated with altered RHCE*ce alleles: clinical implications.

Authors:  Connie M Westhoff; Sunitha Vege; Christine Halter-Hipsky; Trina Whorley; Kim Hue-Roye; Christine Lomas-Francis; Marion E Reid
Journal:  Transfusion       Date:  2010-01-15       Impact factor: 3.157

8.  The DAU allele cluster of the RHD gene.

Authors:  Franz F Wagner; Birgit Ladewig; Katharina S Angert; Guido A Heymann; Nicole I Eicher; Willy A Flegel
Journal:  Blood       Date:  2002-07-01       Impact factor: 22.113

  8 in total

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