RHD variants in Polish blood donors routinely typed as D-

Transfusion

Volumn 53, Issue 11 PART 2, 2013, Pages 2945-2953

  Orzińska, Agnieszka ^a   Guz, Katarzyna ^a   Pelc Kłopotowska, Helene ^b   Pelc Kłopotowska, Monika ^b   Bednarz, Justyna ^b   Gielezyńska, Agata ^b   Śliwa, Beata ^b   Kowalewska, Małgorzata ^b   Pawłowska, Elzbieta ^b   Włodarczyk, Bogusława ^b   Malaga, Małgorzata ^b   Zmudzin, Alicja ^b   Krzemienowska, Magdalena ^b   Srivastava, Kshitij ^b   Michalewska, Bogumiła ^b   Gabriel, Christian ^b   Flegel, Willy A ^b   Brojer, Ewa ^b  

^a INSTITUTE OF HEMATOLOGY AND TRANSFUSION MEDICINE   (Poland)

^b NATIONAL INSTITUTES OF HEALTH   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

RHO(D) ANTIGEN; BLOOD GROUP RHESUS SYSTEM;

ALLELE; ARTICLE; BLOOD DONOR; BLOOD GROUP RHESUS SYSTEM; BLOOD GROUP TYPING; BLOOD TRANSFUSION; COST BENEFIT ANALYSIS; DIAGNOSTIC TEST; ECONOMICS; GENETIC VARIABILITY; GENETICS; HUMAN; IMMUNOLOGY; MOLECULAR GENETICS; PHENOTYPE; POLAND; REPRODUCIBILITY; SEROLOGY; STATISTICS; VALIDATION STUDY; EPIDEMIOLOGY; STATISTICS AND NUMERICAL DATA;

ALLELES; BLOOD DONORS; BLOOD GROUPING AND CROSSMATCHING; BLOOD TRANSFUSION; COST-BENEFIT ANALYSIS; DIAGNOSTIC TESTS, ROUTINE; GENETIC VARIATION; HUMANS; MOLECULAR SEQUENCE DATA; PHENOTYPE; POLAND; REPRODUCIBILITY OF RESULTS; RH-HR BLOOD-GROUP SYSTEM; SEROLOGIC TESTS; VALIDATION STUDIES AS TOPIC;

EID: 84893408130     PISSN: 00411132     EISSN: 15372995     Source Type: Journal    
DOI: 10.1111/trf.12230     Document Type: Article

References (39)

1. Wagner FF, Gassner C, Muller TH, Schonitzer D, Schunter F, Flegel WA. Molecular basis of weak D phenotypes. Blood 1999;93: 385-93.
2. Wagner FF, Frohmajer A, Flegel WA. RHD positive haplotypes in D negative Europeans. BMC Genet 2001;2: 10.
3. Flegel WA. Molecular genetics and clinical applications for RH. Transfus Apher Sci 2011;44: 81-91.
4. Wagner FF. The Rhesus Base [database on the Internet] Ulm, Germany: Department of Transfusion Medicine, University Hospital, 1998. [cited 2013 Apr 24]. Available from: URL: http://www.uni-ulm.de/~fwagner/RH/RB/
5. Garratty G. Do we need to be more concerned about weak D antigens? Transfusion 2005;45: 1547-51.
6. Mota M, Fonseca N, Rodrigues A, Kutner J, Castilho L. Anti-D alloimmunization by weak D type 1 red blood cells with a very low antigen density. Transfusion 2008;88: 130-5.
7. Flegel W, Khull S, Wagner F. Primary anti-D immunization by weak D type 2 RBCs. Transfusion 2000;40: 428-34.
8. Yasuda H, Ohto H, Sakuma S, Ishikawa Y. Secondary anti-D immunization by Del red blood cells. Transfusion 2005;45: 1581-4.
9. Wagner T, Kormoczi GF, Buchta C, Vadon M, Lanzer G, Mayr WR, Legler TJ. Anti-D immunization by DEL red blood cells. Transfusion 2005;45: 520-6.
10. Kormoczi GF, Gassner C, Shao CP, Uchikawa M, Legler TJ. A comprehensive analysis of DEL types: partial DEL individuals are prone to anti-D alloimmunization. Transfusion 2005;45: 1561-67.
11. Flegel WA. Blood group genotyping in Germany. Transfusion 2007;47(Suppl 1):47S-53S.
12. Avent ND. Large-scale blood group genotyping: clinical implications. Br J Haematol 2009;144: 3-13.
13. Silvy M, Simon S, Gouvitsos J, Di Cristofaro J, Ferrera V, Chiaroni J, Bailly P. Weak D and DEL alleles detected by routine SNaPshot genotyping: identification of four novel RHD alleles. Transfusion 2011;51: 401-11.
14. Stabentheiner S, Danzer M, Niklas N, Atzmuller S, Proll J, Hackl C, Polin H, Hofer K, Gabriel C. Overcoming methodological limits of standard RHD genotyping by next-generation sequencing. Vox Sang 2011;100: 381-8.
15. Polin H, Danzer M, Hofer K, Gassner W, Gabriel C. Effective molecular RHD typing strategy for blood donations. Transfusion 2007;47: 1350-5.
16. Gassner C, Doescher A, Drnovsek TD, Rozman P, Eicher NI, Legler TJ, Lukin S, Garritsen H, Kleinrath T, Egger B, Ehling R, Kormoczi GF, Kilga-Nogler S, Schoenitzer D, Petershofen EK. Presence of RHD in serologically D-, C/E+ individuals: a European multicenter study. Transfusion 2005;45: 527-38.
17. Denomme GA, Wagner FF, Fernandes BJ, Li W, Flegel WA. Partial D, weak D types, and novel RHD alleles among 33,864 multiethnic patients: implications for anti-D alloimmunization and prevention. Transfusion 2005;45: 1554-60.
18. Polin H, Danzer M, Gaszner W, Broda DS, Louis M, Proll J, Hofer K, Gabriel C. Identification of RHD alleles with the potential of anti-D immunization among seemingly Dblood donors in Upper Austria. Transfusion 2009;49: 676-81.
19. Li Q, Hou L, Guo ZH, Ye LY, Yue DQ, Zhu ZY. Molecular basis of the RHD gene in blood donors with DEL phenotypes in Shanghai. Vox Sang 2009;97: 139-46.
20. Mota M, Dezan M, Valgueiro MC Sakashita AM, Kutner JM, Castilho L. RHD allelic identification among D- Brazilian blood donors as a routine test using pools of DNA. J Clin Lab Anal 2012;26: 104-8.
21. Fichou Y, Le Marechal C, Bryckaert L, Guerry C, Benech C, Dupont I, Jamet D, Ferec C, Chen JM. Variant screening of the RHD gene in a large cohort of subjects with D phenotype ambiguity: report of 17 novel rare alleles. Transfusion 2012;52: 759-64.
22. Christiansen M, Sorensen BS, Grunnet N. RHD positive among C/E+ and D- blood donors in Denmark. Transfusion 2010;50: 1460-4.
23. Garcia F, Rodriquez MA, Viedma M, Navarro T, Quesada S, Sierra M, Lopez M, Tejedor D, Martinez A, Barbolla L. D negative red blood cell units genotyping: variants encountered in Madrid (Spain) compared to those in Germany. Vox Sang 2010;99(Suppl 1):350.
24. Dogic V, Bingulac-Popovic J, Babic I, Hundric-Haspl Z, Jurakovic-Loncar N, Mratinovic-Mikulandra J, Vuk T, Balija M, Jukic I. Distribution of weak D types in the Croatian population. Transfus Med 2011;21: 278-9.
25. Guz K, Brojer E,Zupańska B. Implications of NA1/NA2 and SH genotyping results in the Polish population with regard to the new nomenclature of granulocyte alloantigens. Transfusion 2000;40: 490-1.
26. Brojer E, Letowska M, Gronowska A. Nucleic acid testing for virus screening in Polish blood donors. Transfus Med 2004;14: 79-80.
27. Brojer E,Zupanska B, Guz K, Orzinska A, Kalinska A. Noninvasive determination of fetal RHD status by examination of cell-free DNA in maternal plasma. Transfusion 2005;45: 1473-80.
28. Flegel WA, Zabern I, Wagner FF. Six years' experience performing RHD genotyping to confirm D- red blood cell units in Germany for preventing anti-D immunizations. Transfusion 2009;49: 465-71.
29. Chen Q, Flegel WA. Random survey for RHD alleles among D+ European persons. Transfusion 2005;45: 1183-91.
30. Lin IL, Shih MC, Hsieh MH, Liu TC, Chang SE, Lin CL. Molecular basis of weak D in Taiwanese. Ann Hematol 2003;82: 617-20.
31. Wagner FF, Frohmajer A, Ladewig B, Eicher NI, Lonicer CB, Muller TH, Siegel MH, Flegel WA. Weak D alleles express distinct phenotypes. Blood 2000;95: 2699-708.
32. Silvy M, Chapel-Fernandes S, Callebaut I, Beley S, Durousseau C, Simon S, Lauroua P, Dubosc-Marchenay N, Babault C, Mouchet C, Ferrera V, Chiaroni J, Bailly P. Characterization of novel RHD alleles: relationship between phenotype, genotype, and trimeric architecture. Transfusion 2012;52: 2020-9.
33. Huang CH, Peng J, Chen HC, Chen YX, Lin DT, Lin SW, Reid ME, Powell VI. RH locus contraction in a novel Dc-/ D - genotype resulting from separate genetic recombination events. Transfusion 2004;44: 853-59.
34. Fichou Y, Chen JM, Le Marechal C, Jamet D, Dupont I, Chuteau C, Durousseau C, Loirat M, Bailly P, Ferec C. Weak D caused by a founder deletion in the RHD gene. Transfusion 2012;52: 2348-55.
35. Avent N, Martin P, Armstrong-Fisher S, Liu W, Finning K. Evidence of genetic diversity underlying Rh D-, weak D (Du), and partial D phenotypes as determined by multiplex polymerase chain reaction analysis of the RHD gene. Blood 1997;89: 2568-77.
36. Shao C, Maas J, Su Y, Köhler M, Legler T. Molecular background of Rh D-positive, D-negative, Del and weak D phenotypes in Chinese. Vox Sang 2002;83: 156-61.
37. Kim J, Kim S, Kim C-A, Yon G, Park S. Molecular characterization of D- Korean persons: development of a diagnostic strategy. Transfusion 2005;45: 345-52.
38. Qun X, Grootkerk-Tax M, Maaskant-vanWijk P, Van Der Schoot C. Systemic analysis and zygosity determination of the RHD gene in a D-negative Chinese Han population reveals a novel D-negative RHD gene. Vox Sang 2005;88: 35-40.
39. Flegel WA, Denomme GA, Yazer MH. On the complexity of D antigen typing: a handy decision tree in the age of molecular blood group diagnostics. J Obstet Gynaecol Can 2007;29: 746-52.