A new platelet alloantigen, Swia, located on glycoprotein Ia identified in a family with fetal and neonatal alloimmune thrombocytopenia

Transfusion

Volumn 51, Issue 8, 2011, Pages 1745-1754

  Kroll, Hartmut ^a,b,c,d   Feldmann, Korinna ^a,b,c,d   Zwingel, Claudia ^a,b,c,d   Hoch, Jochen ^a,b,c,d   Bald, Rainer ^a,b,c,d   Bein, Gregor ^a,b,c,d   Bayat, Behnaz ^a,b,c,d   Santoso, Sentot ^a,b,c,d  

^a Institute for Transfusion Medicine Dessau   (Germany)

^b JUSTUS LIEBIG UNIVERSITY   (Germany)

^c Institute of Experimental Haematology and Transfusion Medicine   (Germany)

^d Clinics for Gynaecology and Obstetrics   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

ALLOANTIGEN; ALPHA2 INTEGRIN; COMPLEMENTARY DNA; CYSTEINE; ENDONUCLEASE; FIBRINOGEN RECEPTOR; METHIONINE; SWI ALLOANTIGEN; THREONINE; UNCLASSIFIED DRUG; VERY LATE ACTIVATION ANTIGEN 2;

ALLELE; AMINO ACID SUBSTITUTION; ANALYTIC METHOD; ANIMAL CELL; ANIMAL CELL CULTURE; ANTIGEN CAPTURE ASSAY; ANTIGEN EXPRESSION; ARTICLE; BRAIN HEMORRHAGE; CONTROLLED STUDY; DISEASE SEVERITY; GENE AMPLIFICATION; GENETIC ANALYSIS; GENOTYPE; IMMUNOCHEMISTRY; MATERNAL SERUM; NEONATAL ALLOIMMUNE THROMBOCYTOPENIA; NONHUMAN; NUCLEOTIDE SEQUENCE; PHENOTYPE; POLYMERASE CHAIN REACTION; RESTRICTION FRAGMENT LENGTH POLYMORPHISM; SEQUENCE ANALYSIS; WILD TYPE;

ANIMALS; ANTIGENS, HUMAN PLATELET; CHO CELLS; CRICETINAE; CRICETULUS; FAMILY; FATAL OUTCOME; FEMALE; FETUS; HUMANS; INFANT, NEWBORN; INTEGRIN ALPHA2; MALE; PEDIGREE; PREGNANCY; THROMBOCYTOPENIA, NEONATAL ALLOIMMUNE;

EID: 80051662077     PISSN: 00411132     EISSN: 15372995     Source Type: Journal    
DOI: 10.1111/j.1537-2995.2010.03038.x     Document Type: Article

References (26)

1. Kaplan C,. Foetal and neonatal alloimmune thrombocytopenia. Orphanet J Rare Dis 2006; I: 39.
2. Mueller-Eckhardt C, Kiefel V, Grubert A, Kroll H, Weisheit M, Schmidt S, Mueller-Eckhardt G, Santoso S,. 348 cases of suspected neonatal alloimmune thrombocytopenia. Lancet 1989; I: 363-6. (Pubitemid 19103082)
3. Davoren A, Curtis BR, Aster RH, McFarland JG,. Human platelet antigen-specific alloantibodies implicated in 1162 cases of neonatal alloimmune thrombocytopenia. Transfusion 2004; 44: 1220-5. (Pubitemid 38989755)
4. Ertel K, Al-Tawil M, Santoso S, Kroll H,. Relevance of the HPA-15 (Gov) polymorphism on CD109 in alloimmune thrombocytopenic syndromes. Transfusion 2005; 45: 366-73. (Pubitemid 40389431)
5. a, a private platelet antigen on glycoprotein IIIa associated with neonatal alloimmune thrombocytopenia. Blood 1990; 76: 2296-302.
6. 1 integrin: a novel collectin/C1q receptor. Immunobiology 2007; 212: 343-53.
7. b are associated with a single amino acid polymorphism on glycoprotein Ia (integrin α2 subunit). J Clin Invest 1993; 92: 2427-32. (Pubitemid 23333551)
8. 807T gene polymorphism with myocardial infarction in younger patients. Blood 1999; 93: 2449-53. (Pubitemid 29181174)
9. a and affects collagen-induced aggregation. Blood 1999; 94: 4103-11.
10. 2 integrin. Transfusion 2009; 49: 2076-83.
11. 1 density. Blood 1998; 92: 2382-8. (Pubitemid 28452981)
12. Koh Y, Taniue A, Ishii H, Matsuyama N, Amakishi E, Hayashi T, Furata RA, Fukumori Y, Hirayama F, Yoshimura K, Nagamine T, Tamai S, Nakano S,. Neonatal alloimmune thrombocytopenia caused by an antibody specific for a newly identified allele of human platelet antigen-7. Transfusion 2010; 50: 1276-84.
13. Kuijpers RW, Simsek S, Faber NM, Goldschmeding R, van Wermerkerken RK, von dem Borne AE,. Single point mutation in human glycoprotein IIIa is associated with a new platelet-specific alloantigen (Mo) involved in neonatal alloimmune thrombocytopenia. Blood 1993; 81: 70-6. (Pubitemid 23013679)
14. 33Val mutation in β3-integrin impairs the HPA-1a epitope: the third allele of HPA-1. Transfusion 2006; 46: 790-9.
15. Peterson JA, Gitter ML, Pietz B, Bellissimo DB, Curtis BR, Aster RH,. A third allele of the HPA-5 (Br) platelet alloantigen system identified in investigating a case of neonatal thrombocytopenia. Transfusion 2010; 50: 1855-6.
16. Kiefel V,. The MAIPA assay and its applications in immunohaematology. Transfus Med 1992; 2: 181-8.
17. 3 integrin subunit. J Biol Chem 1994; 269: 8439-44.
18. Carl B, Kroll H, Bux J, Bein G, Santoso S,. B-lymphoblastoid cell lines as source of reference DNA for genotyping of human platelet and neutrophil antigens. Transfusion 2000; 40: 62-8. (Pubitemid 30053546)
19. Antonarakis SE,. Recommendations for a nomenclature system for human gene mutations. Nomenclature Working Group. Hum Mutat 1998; 11: 1-3. (Pubitemid 128679142)
20. 1. J Biol Chem 1997; 272: 28512-7.
21. 2 gene coding sequence. Blood 1997; 89: 1939-43. (Pubitemid 27132108)
22. Kroll H, Yates J, Santoso S,. Immunization against a low-frequency human platelet alloantigen in fetal alloimmune thrombocytopenia is not a single event: characterization by the combined use of reference DNA and novel allele-specific cell lines expressing recombinant antigens. Transfusion 2005; 45: 353-8. (Pubitemid 40389429)
23. a) neonatal alloimmune thrombocytopenia: clinical and immunological analysis of 39 cases. Br J Haematol 1991; 78: 425-9.
24. Ghevaert C, Rankin A, Huiskes E, Porcelijn L, Javela K, Kekomäki R, Bakchoul T, Santoso S, Nutland S, Smyth DJ, Smith GA, McBride S, Watkins NA, Ouwehand WH,. Alloantibodies against low-frequency human platelet antigens do not account for a significant proportion of cases of fetomaternal alloimmune thrombocytopenia: evidence from 1054 cases. Transfusion 2009; 49: 2084-9.
25. a) is an important cause of neonatal alloimmune thrombocytopenia. Transfusion 2005; 45: 1487-95. (Pubitemid 44194653)
26. Peterson JA, Gitter ML, Kanack A, Curtis BR, McFarland JG, Bougie D, Aster RH,. New low-frequency platelet glycoprotein polymorphisms associated with neonatal alloimmune thrombocytopenia. Transfusion 2010; 50: 324-33.