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RNA and protein expression of HLA-A(∗)23:19Q.
Gerritsen, K E H; Voorter, C E M; Joannes, M O R F; Senden-Gijsbers, B L M G; Agis, F; Wieten, L; Tilanus, M G J.
Afiliación
  • Gerritsen KE; Department of Transplantation Immunology, Tissue Typing Laboratory, Maastricht University Medical Centre, Maastricht, The Netherlands.
  • Voorter CE; Department of Transplantation Immunology, Tissue Typing Laboratory, Maastricht University Medical Centre, Maastricht, The Netherlands.
  • Joannes MO; Laboratoire d'Hématologie-Immunologie, CHU Pointe-à-Pitre, Abymes, Guadeloupe.
  • Senden-Gijsbers BL; Department of Internal Medicine, Hematology, Maastricht University Medical Centre, Maastricht, The Netherlands.
  • Agis F; Laboratoire d'Hématologie-Immunologie, CHU Pointe-à-Pitre, Abymes, Guadeloupe.
  • Wieten L; Department of Transplantation Immunology, Tissue Typing Laboratory, Maastricht University Medical Centre, Maastricht, The Netherlands.
  • Tilanus MG; Department of Transplantation Immunology, Tissue Typing Laboratory, Maastricht University Medical Centre, Maastricht, The Netherlands. Electronic address: m.tilanus@mumc.nl.
Hum Immunol ; 76(4): 286-91, 2015 Apr.
Article en En | MEDLINE | ID: mdl-25676117
ABSTRACT
The assignment of null alleles is clinically relevant in stem cell transplantation, in particular for donor selection. It is unclear how questionable (Q) alleles, having an unknown expression profile, should be considered in matching criteria. In this study we analyzed the RNA and protein expression profile of a questionable allele encountered in a sample of the Guadeloupe population GD23Q, HLA-A(∗)2319Q, 290201. Full-length DNA sequencing of HLA-A(∗)2319Q revealed a single polymorphism at position 619 (G>A) compared to HLA-A(∗)230101. Serological typing showed only the presence of HLA-A29; HLA-A(∗)2319Q was not detected on the cell surface. The absence of HLA-A(∗)2319Q surface expression was shown by flow cytometry using a directly labeled monoclonal antibody and a panel of five indirectly labeled polyclonal antibodies all directed against HLA-A23 (HLA-A9) molecules. Allele specific amplification revealed the absence of intact full-length mRNA, but the presence of two major alternatively spliced mRNAs sequencing identified that in one variant exon 3 is missing and in the other variant introns 2 and 3 are retained. Based upon the lack of HLA-A(∗)2319Q surface expression and the presence of aberrant mRNA transcripts only, this study shows that HLA-A(∗)2319Q is non-expressed.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Prueba de Histocompatibilidad / Antígenos HLA-A / Trasplante de Células Madre / Selección de Donante Tipo de estudio: Prognostic_studies Límite: Humans País/Región como asunto: Caribe / Guadalupe Idioma: En Revista: Hum Immunol Año: 2015 Tipo del documento: Article País de afiliación: Países Bajos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Prueba de Histocompatibilidad / Antígenos HLA-A / Trasplante de Células Madre / Selección de Donante Tipo de estudio: Prognostic_studies Límite: Humans País/Región como asunto: Caribe / Guadalupe Idioma: En Revista: Hum Immunol Año: 2015 Tipo del documento: Article País de afiliación: Países Bajos