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The αIIb p.Leu841Met (Cab3(a+) ) polymorphism results in a new human platelet alloantigen involved in neonatal alloimmune thrombocytopenia.
Jallu, Vincent; Bertrand, Gerald; Bianchi, Frederic; Chenet, Christophe; Poulain, Pierre; Kaplan, Cecile.
Afiliação
  • Jallu V; Platelet Immunology Laboratory, INTS; DSIMB, INSERM, U665, France.
Transfusion ; 53(3): 554-63, 2013 Mar.
Article em En | MEDLINE | ID: mdl-22738334
BACKGROUND: Fetal-neonatal alloimmune thrombocytopenia (FNAIT) diagnosis relies on maternofetal incompatibility and alloantibody identification. Genotyping for rare platelet (PLT) polymorphisms allowed the identification of three families with suspected or confirmed maternofetal incompatibility for the αIIb-c.2614C>A mutation (Halle et al., Transfusion 2008;48:14-15). STUDY DESIGN AND METHODS: A polymerase chain reaction-sequence-specific primers amplification assay was designed to genotype the αIIb-c.2614C>A mutation. HEK293 cells expressing αIIb-Leu841 or αIIb-Met841 αIIbß3 forms were used to probe the reactivity of maternal sera from these families and to study the effects of the substitution on αIIbß3 expression and functions. RESULTS: Tested by flow cytometry (FCM), one serum sample specifically reacted with αIIb-Met841 but not with αIIb-Leu841 αIIbß3. This specificity revealed the αIIb-Leu841 polymorphism as a new alloantigen named Cab3(a+) . Cross-match testing using FCM also showed the Cab3(a+) antigen to be expressed at the PLT surface. As for anti-human PLT alloantigen (HPA)-3a (or -3b) and anti-HPA-9bw, detection of anti-Cab3(a+) alloantibodies appeared difficult and required whole PLT assays when classical monoclonal antibody-specific immobilization of PLT antigen test failed. In our FNAIT set, the immune response to Cab3(a+) maternofetal incompatibility could induce severe thrombocytopenias and life-threatening hemorrhages. The p.Leu841Met substitution has limited effects, if any, on local αIIb structure, preserving both αIIbß3 expression and functions. CONCLUSION: The Cab3(a+) polymorphism is a new rare alloantigen (allelic frequency <1%) carried by αIIb that might result in severe life-threatening thrombocytopenias. In Sub-Saharan African populations, higher Cab3(a+) gene frequencies (up to 8.2%; Halle et al., Transfusion 2008;48:14-15) and homozygous people are observed.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Antígenos de Plaquetas Humanas / Glicoproteína IIb da Membrana de Plaquetas / Trombocitopenia Neonatal Aloimune Tipo de estudo: Prognostic_studies Limite: Adult / Female / Humans / Male / Newborn / Pregnancy Idioma: En Revista: Transfusion Ano de publicação: 2013 Tipo de documento: Article País de afiliação: França País de publicação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Antígenos de Plaquetas Humanas / Glicoproteína IIb da Membrana de Plaquetas / Trombocitopenia Neonatal Aloimune Tipo de estudo: Prognostic_studies Limite: Adult / Female / Humans / Male / Newborn / Pregnancy Idioma: En Revista: Transfusion Ano de publicação: 2013 Tipo de documento: Article País de afiliação: França País de publicação: Estados Unidos