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1.
Bone Marrow Transplant ; 50(10): 1321-5, 2015 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-26146809

RESUMO

Transplantation-associated thrombotic microangiopathy (TA-TMA) is a serious complication of allogeneic haematopoietic stem cell transplantation (allo-HSCT) with high mortality rate. We retrospectively studied the frequency, clinical and genetic associations and prognostic effect of TA-TMA, in a total of 425 consecutive adult patients, who underwent allo-HSCT for a malignant haematological condition between 2007 and 2013 at our single centre. TA-TMA developed in 19% of the patients. Unrelated donor type (P<0.001), acute GvHD grades II-IV (P<0.001), myeloablative conditioning regimens (P=0.003), tacrolimus-based GvHD prophylaxis (P=0.003), CMV infection (P=0.003) and carriership for HLA-DRB1*11 (P=0.034) were associated with the development of TA-TMA. Survival was adversely affected by the presence of TA-TMA (P<0.001). Among patients with TA-TMA, the outcome of HLA-DRB1*11 carriers was significantly better compared with non-carriers (P=0.003). As a new finding, our observations suggest that the presence of HLA-DRB1*11 antigen contributes to the development of TA-TMA and affects the outcome.


Assuntos
Cadeias HLA-DRB1/uso terapêutico , Transplante de Células-Tronco Hematopoéticas/efeitos adversos , Microangiopatias Trombóticas/terapia , Condicionamento Pré-Transplante/efeitos adversos , Feminino , Cadeias HLA-DRB1/imunologia , Transplante de Células-Tronco Hematopoéticas/métodos , Humanos , Masculino , Prognóstico , Estudos Retrospectivos , Análise de Sobrevida , Microangiopatias Trombóticas/etiologia , Microangiopatias Trombóticas/mortalidade , Condicionamento Pré-Transplante/métodos , Resultado do Tratamento
2.
Tissue Antigens ; 86(2): 115-21, 2015 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-26149581

RESUMO

Systematic analyses of human leukocyte antigen (HLA) profiles in different populations may increase the efficiency of bone marrow donor selection and help reconstructing human peopling history. We typed HLA-A, -B, and -DRB1 allele groups in two bone marrow donor cohorts of 2402 Hungarians and 186 Hungarian Gypsies and compared them with several Central-European, Spanish Gypsy, and Indian populations. Our results indicate that different European Gypsy populations share a common origin but diverged genetically as a consequence of founder effect and rapid genetic drift, whereas other European populations are related genetically in relation to geography. This study also suggests that while HLA-A accurately depicts the effects of genetic drift, HLA-B, and -DRB1 conserve more signatures of ancient population relationships, as a result of balancing selection.


Assuntos
Antígenos HLA-A/genética , Antígenos HLA-B/genética , Cadeias HLA-DRB1/genética , Polimorfismo Genético , Roma (Grupo Étnico) , População Branca , Adolescente , Adulto , Alelos , Transplante de Medula Óssea , Feminino , Efeito Fundador , Deriva Genética , Haplótipos , Humanos , Hungria , Masculino , Pessoa de Meia-Idade , Filogeografia , Doadores de Tecidos
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