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1.
Hum Immunol ; 76(4): 286-91, 2015 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-25676117

RESUMO

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(∗)23:19Q, 29:02:01. Full-length DNA sequencing of HLA-A(∗)23:19Q revealed a single polymorphism at position 619 (G>A) compared to HLA-A(∗)23:01:01. Serological typing showed only the presence of HLA-A29; HLA-A(∗)23:19Q was not detected on the cell surface. The absence of HLA-A(∗)23:19Q 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(∗)23:19Q surface expression and the presence of aberrant mRNA transcripts only, this study shows that HLA-A(∗)23:19Q is non-expressed.


Assuntos
Seleção do Doador , Antígenos HLA-A/biossíntese , Antígenos HLA-A/genética , Teste de Histocompatibilidade/métodos , Transplante de Células-Tronco , Alelos , Processamento Alternativo , Guadalupe , Humanos , Polimorfismo de Nucleotídeo Único , RNA Mensageiro/genética , Padrões de Referência , Reprodutibilidade dos Testes , Análise de Sequência de RNA
2.
Tissue Antigens ; 83(3): 147-53, 2014 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-24405442

RESUMO

Genetic polymorphism of human leukocyte antigen (HLA)-DPA1 and -DPB1 loci was studied in 154 unrelated individuals from Guadeloupe, an archipelago of five islands located in the Carribean Sea. Thirty different DPB1 and eight different DPA1 alleles were observed with a heterozygosity index of 0.87 and 0.78, respectively. This high degree of heterozygosity corresponds with those found in African populations. The DPB1* 01:01:01 allele was most frequent (0.260), followed by 02:01:02 (0.143) and 04:01:01 (0.127). The DPA1 alleles 01:03 (0.380), 02:01 (0.302), 02:02 (0.175) and 03:01 (0.123) were identified in >35 individuals each, whereas 01:04, 01:05 and 04:01 were present only once. Haplotype estimations revealed the presence of 39 different haplotypes, with DPB1*01:01:01-DPA1*02:02 and DPB1*02:01:02-DPA1*01:03 as the most frequent (0.143 and 0.140, respectively). A striking difference was observed in DPB1/DPA1 associations between DPB1*04:02 and *105:01, that have identical exon 2 sequences. DPB1*04:02 was exclusively associated with DPA1*01:03, whereas DPB1*105:01 was present with DPA1*03:01, *03:02 or *04:01. This implies that the DP molecules are actually different, and this difference is relevant to consider in studies on the function of HLA-DP molecules in transplantation. Overall, HLA-DPA1 and DPB1 allele frequencies and haplotypes of the population of Guadeloupe were most similar to African populations, with characteristic alleles and haplotypes that bespeaks the admixture with other ethnicities.


Assuntos
Alelos , Frequência do Gene/genética , Genética Populacional , Cadeias alfa de HLA-DP/genética , Cadeias beta de HLA-DP/genética , Haplótipos/genética , Adulto , Motivos de Aminoácidos , Pré-Escolar , Epitopos/química , Epitopos/imunologia , Feminino , Guadalupe , Humanos , Masculino
3.
Tissue Antigens ; 79(1): 75-6, 2012 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-21859429

RESUMO

The new HLA-B*15:220 allele shows a single-nucleotide substitution in exon 1 at position 47 (C>T) when compared to its closest allele HLA-B*15:03:01, resulting in an amino acid substitution from Ala to Val in the signal peptide at codon -9.


Assuntos
Alelos , Substituição de Aminoácidos , Éxons/genética , Antígenos HLA-B/genética , Mutação de Sentido Incorreto , Guadalupe , Humanos
4.
Tissue Antigens ; 79(1): 71-2, 2012 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-21880020

RESUMO

The new HLA-A*23:38N allele shows a single-base deletion in exon 2, resulting in a frame shift and a premature stop codon.


Assuntos
Alelos , Códon de Terminação/genética , Éxons/genética , Mutação da Fase de Leitura , Guadalupe , Antígenos HLA-A , Humanos
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