Serological studies of monoclonal RH antibodies with RH1 (D), RH2 (C), RH3 (E) and RH5 (e) variant RBCs

Transfusion Clinique et Biologique

Volumn 10, Issue 5, 2003, Pages 319-323

  Noizat Pirenne, F ^a,b   Ansart Pirenne, H ^b   Menanteau C ^b   Braddock, D ^b   Rouzaud, A M ^b   Klein, M T ^b   Patereau, C ^b   Rouger, P ^b   Le Pennec, P Y ^b  

^a ETABLISSEMENT FRANÇAIS DU SANG   (France)

^b INSTITUT NATIONAL DE LA TRANSFUSION SANGUINE   (France)

Author keywords

Antibodies; Molecular biology; Monoclonal; RH system; RH variants

Indexed keywords

BLOOD GROUP E ANTIGEN; IMMUNOGLOBULIN M; MONOCLONAL ANTIBODY; RHESUS ANTIGEN; RHESUS C ANTIGEN; RHESUS D ANTIGEN; UNCLASSIFIED DRUG;

ANTIBODY SPECIFICITY; ANTIGEN EXPRESSION; ARTICLE; BLOOD GROUP RH; BLOOD GROUP RHESUS SYSTEM; ERYTHROCYTE; HUMAN; HUMAN CELL; PHENOTYPE; SEROLOGY;

EID: 0242318862     PISSN: 12467820     EISSN: None     Source Type: Journal    
DOI: 10.1016/S1246-7820(03)00106-X     Document Type: Article

References (24)

1. Wagner FW, Gassner C, Muller TH, Schonitzer D, Schunter F, Flegel WA. Molecular basis of weak D phenotypes. Blood 1999;93:385-93.
2. Muller TH, Wagner FF, Trokenbacher A, Eicher NI, Flegel WA, Schonitzer D, et al. PCR screening for common weak D types shows distributions in three Central European populations. Transfusion 2001;41:45-52.
3. Har antigenic complex is associated with a limited number of D epitopes and allo-anti-D production: a study in three unrelated individuals and their families. Transfusion 1996;36:104-8.
4. Har RH33 phenotype results from substitution of exon 5 of the RHCE gene by the corresponding exon of the RHD gene. Br J Haematol 1996;92:751-7.
5. Wagner FF, Gassner C, Eicher N, Lonicer C, Flegel WA. Characterization of D category IV type IV, DFW and DNB. Transfusion 1998;38:63S.
6. Rouillac C, Colin Y, Hughes-Jones NC, Beolet M, D'Ambrosio A-M, Cartron JP, et al. Transcript analysis of D category phenotypes predicts hybrid RhD-CE-D proteins associated with alteration of D epitopes. Blood 1995;85:2937-44.
7. Omi T, Takashi J, Tsudo N, Okuda H, Iwamoto S, Tanaka M, et al. The genomic organization of the partial D category DVa: the presence of a new partial D associated with DVa phenotype. Biochem Biophys Res Commun 1999;254:786-94.
8. Omi T, Okuda H, Iwamoto S, Kajii E, Takashi J, Tanaka M, et al. Detection of Rh23 in the partial D phenotype associated with the DVa category. Transfusion 2000;40:256-7.
9. Noizat-Pirenne F, Le Pennec PY, Mouro I, Roussel M, Boulard P, Rouger P, et al. The molecular basis of a D(C)(e) complex probably associated with the RH35 low frequency antigen. Transfusion 1999;39:103S.
10. Noizat-Pirenne F, Le Pennec PY, Mouro I, Juszczak G, Roussel M, Lauroua P, et al. Molecular background of D(C)(e) haplotypes within the Caucasian population. Transfusion 2002;42:627-33.
11. Noizat-Pirenne F, Mouro I, Le Pennec PY, Boulard P, Roussel M, et al. Evidence that serine at position 103 is not sufficient for complete C antigen expression. Transfusion 1999;39:103S.
12. Noizat-Pirenne F, Mouro I, Gane P, Okubo Y, Hori Y, Rouger P, et al. Heterogeneity of blood group RhE variants revealed by serological analysis and molecular alteration of the RHCE gene and transcript. Br J Haematol 1998;103:429-36.
13. N phenotypes. Blood 1996;87:4853-61.
14. x (Rh9) blood group specificities. Blood 1995;3:1196-201.
15. Noizat-Pirenne F, Mouro I, Le Pennec PY, Verdier M, Babinet J, Juszczak G, et al. Molecular basis of category EIV variant phenotype. Transfusion 1999;39:103S.
16. Hemker MB, Lightart PC, Berger L, Van Rhenen DJ, van der Schoot CE, Maaskant-van Wijk PA. DAR, a new RhD variant involving exons 4, 5 et 7, often in linkage with ceAR, a new Rhce variant frequently found in African Blacks. Blood 1999;94:4337-42.
17. Noizat-Pirenne F, Le Pennec PY, Mouro I, Roussel M, Vanhaeke D, Rouger P, et al. Production of anti-e like antibody in an African individual typed hrs negative and carrying altered RHce alleles. Transfusion 2000;40:9S.
18. Noizat-Pirenne F, Lee K, Le Pennec PY, Simon P, Kazup P, Bachir D, et al. Rare RHCE phenotypes in black individuals of Afro-Carribean origin: identification and transfusion safety. Blood 2002;100:4223-31.
19. Faas BHW, Beckers EAM, Wildoer Plightart PC, Overbeeke MAM, Zondervan HA, von dem Borne AEG, et al. Molecular background of VS and weak C expression in blacks. Transfusion 1997;37:38-44.
20. Daniels GL, Faas BHW, Green CA, Smart E, Maaskant-van Wijk ND, Avent ND, et al. The VS and V blood group polymorphisms in Africans: a serological and molecular analysis. Transfusion 1998;38:951-8.
21. S. J Forens Med 1960;7:96-105.
22. Noizat-Pirenne F, Mouro I, Le Pennec PY, Jusczcak G, Patereau C, Verdier M, et al. Two new alleles of the RHCE gene in Black individuals: the Rhce allele ceMO and the RhcE allele cEM1. Br J Haematol 2001;113:672-9.
23. Westhoff CM, Silberstein LE, Sipherd B, Demetry J. Altered "e" antigen expression associated with 16Cys in exon 1 of the RHce gene. Transfusion 1998;38:64s (abstract).
24. Annex 2: Rh antibodies third international workshop and symposium on monoclonal antibodies against human red blood cells and related antigens. Transfu Clin Biol 1996;6:525-33.