Requiere autenticación

The Rh and RhAG blood group systems


Cite

Levine P, Burnham L, Katzin WM, Vogel P. The role of isoimmunization in the pathogenesis of erythroblastosis fetalis. Am J Obstet Gynecol 1941;42: 925–37.10.1016/S0002-9378(41)90260-0Search in Google Scholar

Freda VJ, Gorman JG, Pollack W. Rh factor: prevention of isoimmunization and clinical trial on mothers. Science 1966;151:828–30.10.1126/science.151.3712.82817746731Search in Google Scholar

Mollison PL, Hughes-Jones NC, Lindsay M, Wessely J. Suppression of primary RH immunization by passively-administered antibody. Experiments in volunteers. Vox Sang 1969;16:421–39.10.1111/j.1423-0410.1969.tb04769.xSearch in Google Scholar

Race RR, Sanger R. Blood groups in man. 6th ed. Oxford, England: Blackwell, 1975.Search in Google Scholar

Reid ME, Lomas-Francis C. The blood group antigen factsbook. 2nd ed. San Diego, CA: Academic Press, 2004.10.1016/B978-012586585-2/50007-XSearch in Google Scholar

Le van Kim C, Mouro I, Chérif-Zahar B, et al. Molecular cloning and primary structure of the human blood group RhD polypeptide. Proc Natl Acad Sci U S A 1992;89:10925–9.10.1073/pnas.89.22.10925504551438298Search in Google Scholar

Chérif-Zahar B, Bloy C, Le Van Kim C, et al. Molecular cloning and protein structure of a human blood group Rh polypeptide. Proc Natl Acad Sci U S A 1990;87:6243–7.10.1073/pnas.87.16.6243545091696722Search in Google Scholar

Arce MA, Thompson ES, Wagner S, Coyne KE, Ferdman BA, Lublin DM. Molecular cloning of RhD cDNA derived from a gene present in RhD-positive, but not RhD-negative individuals. Blood 1993;82: 651–5.10.1182/blood.V82.2.651.651Search in Google Scholar

Simsek S, de Jong CA, Cuijpers HT, et al. Sequence analysis of cDNA derived from reticulocyte mRNAs coding for Rh polypeptides and demonstration of E/e and C/c polymorphisms. Vox Sang 1994;67:203–9.10.1111/j.1423-0410.1994.tb01661.x7801613Search in Google Scholar

Blumenfeld OO, Patnaik SK. Allelic genes of blood group antigens: a source of human mutations and cSNPs documented in the Blood Group Antigen Gene Mutation Database. Hum Mutat 2004;23:8–16.10.1002/humu.1029614695527Search in Google Scholar

Landsteiner K, Wiener AS. An agglutinable factor in human blood recognized by immune sera for rhesus blood. Proc Soc Exp Biol Med 1940;43:223–4.10.3181/00379727-43-11151Search in Google Scholar

Tippett P. A speculative model for the Rh blood groups. Ann Hum Genet 1986;50:241–7.10.1111/j.1469-1809.1986.tb01045.x3128160Search in Google Scholar

Daniels G, Castilho L, Flegel WA, et al. International Society of Blood Transfusion Committee on terminology for red blood cell surface antigens: Macao report. Vox Sang 2009;96:153–6.10.1111/j.1423-0410.2008.01133.x19152607Search in Google Scholar

Scott ML, Voak D, Liu W, Jones JW, Avent ND. Epitopes on Rh proteins. Vox Sang 2000;78(Suppl 2):117–20.Search in Google Scholar

Colin Y, Chérif-Zahar B, Le Van Kim C, Raynal V, Van Huffel V, Cartron JP. Genetic basis of the RhD-positive and RhD-negative blood group polymorphism as determined by Southern analysis. Blood 1991;78: 2747–52.10.1182/blood.V78.10.2747.2747Search in Google Scholar

Singleton BK, Green CA, Avent ND, et al. The presence of an RHD pseudogene containing a 37 base pair duplication and a nonsense mutation in Africans with the Rh D-negative blood group phenotype. Blood 2000;95:12–18.10.1182/blood.V95.1.12Search in Google Scholar

Shao CP, Maas JH, Su YQ, Köhler M, Legler TJ. Molecular background of Rh D-positive, D-negative, D(el) and weak D phenotypes in Chinese. Vox Sang 2002;83:156–61.10.1046/j.1423-0410.2002.00192.x12201845Search in Google Scholar

Wagner FF, Gassner C, Müller TH, Schönitzer D, Schunter F, Flegel WA. Molecular basis of weak D phenotypes. Blood 1999;93:385–93.10.1182/blood.V93.1.385Search in Google Scholar

Sun CF, Chou CS, Lai NC, Wang WT. RHD gene polymorphisms among RhD-negative Chinese in Taiwan. Vox Sang 1998;75:52–7.10.1046/j.1423-0410.1998.7510052.xSearch in Google Scholar

Daniels G. Human blood groups. 2nd ed. Cambridge, MA: Wiley-Blackwell, 2002.10.1002/9780470987018Search in Google Scholar

Westhoff CM, Vege S, Nickle P, Hue-Roye K, Reid ME. A single nucleotide deletion in RHCE*cE responsible for the D- - haplotype in the Hispanic population. Vox Sang 2010:99 (Suppl):376.Search in Google Scholar

Beckers EA, Porcelijn L, Ligthart P, et al. The RoHar antigenic complex is associated with a limited number of D epitopes and alloanti-D production: a study of three unrelated persons and their families. Transfusion 1996;36:104–8.10.1046/j.1537-2995.1996.36296181919.x8614957Search in Google Scholar

Wallace M, Lomas-Francis C, Tippett P. The D antigen characteristic of RoHar is a partial D antigen. Vox Sang 1996;70:169–72.Search in Google Scholar

Flegel WA, Wagner FF, Chen Q, Schlanser G, Frame T, Westhoff CM, Moulds MK. The RHCE allele ceCF: the molecular basis of Crawford (RH43). Transfusion 2006:46:1334–4210.1111/j.1537-2995.2006.00901.x16934069Search in Google Scholar

Chen Q, Hustinx H, Flegel WA. The RHCE allele ceSL: the second example for D antigen expression without D-specific amino acids. Transfusion 2006;46:766–72.10.1111/j.1537-2995.2006.00795.x16686844Search in Google Scholar

Wagner FF, Ladewig B, Flegel WA.The RHCE allele ceRT: D epitope 6 expression does not require D-specific amino acids. Transfusion. 2003;43:1248–54.10.1046/j.1537-2995.2003.00495.x12919427Search in Google Scholar

Westhoff CM. Review: the Rh blood group D antigen... dominant, diverse, and difficult. Immunohematology 2005;21:155–63.10.21307/immunohematology-2019-412Search in Google Scholar

Daniels GL, Faas BH, Green CA, et al. The VS and V blood group polymorphisms in Africans: a serologic and molecular analysis. Transfusion 1998;38:951–8.10.1046/j.1537-2995.1998.381098440860.x9767746Search in Google Scholar

Brumit MC, Carnahan GE, Stubbs JR, Storry JR, Reid ME. Moderate hemolytic disease of the newborn (HDN) due to anti-Rh17 produced by a black female with an e variant phenotype. Immunohematology 2002;18:40–2.10.21307/immunohematology-2019-507Search in Google Scholar

Noizat-Pirenne F, Lee K, Pennec PY, et al. Rare RHCE phenotypes in black individuals of Afro-Caribbean origin: identification and transfusion safety. Blood 2002;100:4223–31.10.1182/blood-2002-01-022912393640Search in Google Scholar

Reid ME, Storry JR, Issitt PD, et al. Rh haplotypes that make e but not hrB usually make VS. Vox Sang 1997;72:41–4.10.1159/000461956Search in Google Scholar

Vege S, Westhoff CM. Molecular characterization of GYPB and RH in donors in the American Rare Donor Program. Immunohematology 2006;22:143–7.10.21307/immunohematology-2019-372Search in Google Scholar

Issit P, Anstee, DJ. Applied blood group serology. 4th ed. Durham, NC: Montgomery Scientific Publications, 1998.Search in Google Scholar

Afenyi-Annan A, Bandarenko N. Transfusion practices for patients with sickle cell disease at a major academic medical center. Immunohematology 2006;22:103–7.10.21307/immunohematology-2019-364Search in Google Scholar

Sesok-Pizzini DA, Friedman DF, Smith-Whitley K, Nance SJ. Transfusion support of patients with sickle cell disease at the Children’s Hospital of Philadelphia. Immunohematology 2006;22:121–5.10.21307/immunohematology-2019-368Search in Google Scholar

Petz LD. Review: evaluation of patients with immune hemolysis. Immunohematology 2004;20:167–76.10.21307/immunohematology-2019-443Search in Google Scholar

Price TH, ed. Standards for blood banks and transfusion services. 26th ed. Bethesda, MD: AABB 2009:29.Search in Google Scholar

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;45:1554–60.10.1111/j.1537-2995.2005.00586.x16181204Search in Google Scholar

Yasuda H, Ohto H, Sakuma S, Ishikawa Y. Secondary anti-D immunization by Del red blood cells. Transfusion 2005;45:1581–4.10.1111/j.1537-2995.2005.00579.x16181208Search in Google Scholar

Flegel WA, Khull SR, Wagner FF. Primary anti-D immunization by weak D type 2 RBCs. Transfusion 2000;40:428–34.10.1046/j.1537-2995.2000.40040428.x10773054Search in Google Scholar

Mota M, Fonseca NL, Rodrigues A, Kutner JM, Castilho L. Anti-D alloimmunization by weak D type 1 red blood cells with a very low antigen density. Vox Sang 2005;88:130–5.10.1111/j.1423-0410.2005.00604.x15720611Search in Google Scholar

Lacey PA, Caskey CR, Werner DJ, Moulds JJ. Fatal hemolytic disease of a newborn due to anti-D in an Rh-positive Du variant mother. Transfusion 1983;23: 91–4.10.1046/j.1537-2995.1983.23283172867.x6404025Search in Google Scholar

Vichinsky EP, Luban NL, Wright E, et al. Prospective RBC phenotype matching in a stroke-prevention trial in sickle cell anemia: a multicenter transfusion trial. Transfusion 2001;41:1086–92.10.1046/j.1537-2995.2001.41091086.x11552063Search in Google Scholar

Ambruso DR, Githens JH, Alcorn R, et al. Experience with donors matched for minor blood group antigens in patients with sickle cell anemia who are receiving chronic transfusion therapy. Transfusion 1987;27: 94–8.10.1046/j.1537-2995.1987.27187121485.x3810834Search in Google Scholar

Tahhan HR, Holbrook CT, Braddy LR, Brewer LD, Christie JD. Antigen-matched donor blood in the transfusion management of patients with sickle cell disease. Transfusion 1994;34:562–9.10.1046/j.1537-2995.1994.34794330008.x8053036Search in Google Scholar

Hashmi G, Shariff T, Zhang Y, et al. Determination of 24 minor red blood cell antigens for more than 2000 blood donors by high-throughput DNA analysis. Transfusion 2007;47:736–47.10.1111/j.1537-2995.2007.01178.x17381634Search in Google Scholar

Hopp K, Weber K, Bellissimo D, Johnson ST, Pietz B. High-throughput red blood cell antigen genotyping using a nanofluidic real-time polymerase chain reaction platform. Transfusion 2010;50:40–6.10.1111/j.1537-2995.2009.02377.x19761548Search in Google Scholar

Hillyer CD, Shaz BH, Winkler AM, Reid M. Integrating molecular technologies for red blood cell typing and compatibility testing into blood centers and transfusion services. Transfus Med Rev 2008;22: 117–32.10.1016/j.tmrv.2007.12.00218353252Search in Google Scholar

Lo YM, Hjelm NM, Fidler C, et al. Prenatal diagnosis of fetal RhD status by molecular analysis of maternal plasma. N Engl J Med 1998;339:1734–8.10.1056/NEJM1998121033924029845707Search in Google Scholar

Finning K, Martin P, Summers J, Massey E, Poole G, Daniels G. Effect of high throughput RHD typing of fetal DNA in maternal plasma on use of anti-RhD immunoglobulin in RhD negative pregnant women: prospective feasibility study. BMJ 2008;336:816–18.10.1136/bmj.39518.463206.25229233418390496Search in Google Scholar

Matassi G, Chérif-Zahar B, Raynal V, Rouger P, Cartron JP. Organization of the human RH50A gene (RHAG) and evolution of base composition of the RH gene family. Genomics 1998;47:286–93.10.1006/geno.1997.51129479501Search in Google Scholar

Tilley L, Green C, Poole J, et al. A new blood group system, RHAG: three antigens resulting from amino acid substitutions in the Rh-associated glycoprotein. Vox Sang 2010;98:151–9.10.1111/j.1423-0410.2009.01243.x19744193Search in Google Scholar

Gruswitz F, Chaudhary S, Ho JD, et al. Function of human Rh based on structure of RhCG at 2.1 A. Proc Natl Acad Sci U S A 2010;107:9638–43.10.1073/pnas.1003587107290688720457942Search in Google Scholar

International Society of Blood Transfusion (ISBT) Working Party on Red Cell Immunogenetics and Blood Group Terminology. http://ibgrl.blood.co.uk/ISBTPages/ISBTHome.htm. Accessed 1/4/2011.Search in Google Scholar

RhesusBase. http://www.uni-ulm.de/~fwagner/RH/RB/. Accessed 1/4/2011.Search in Google Scholar

NCBI Blood Group Mutation Database. http://www.ncbi. nlm.nih.gov/gv/mhc/xslcgi.cgi?cmd=bgmut/home. Accessed 1/4/2011.Search in Google Scholar

eISSN:
1930-3955
Idioma:
Inglés
Calendario de la edición:
4 veces al año
Temas de la revista:
Medicine, Clinical Medicine, Laboratory Medicine