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3.
Exp Hematol ; 36(9): 1205-15, 2008 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-18550258

RESUMO

OBJECTIVE: We aimed to create a molecular assay to monitor erythroid (red blood cell [RBC]) engraftment in any patient following allogeneic hematopoietic stem cell transplantation, independent of disease-specific mutations. MATERIALS AND METHODS: We identified 10 common single nucleotide polymorphisms (SNPs), expressed by genes encoding RBC antigens and structural proteins. These SNPs were polymerase chain reaction-amplified from total RNA extracted from peripheral blood, which contains nucleated erythroid progenitors. Mixing studies validated that each SNP can quantitatively measure donor/recipient DNA and RNA. RESULTS: We directly genotyped 23 patients who underwent hematopoietic stem cell transplantation and their human leukocyte antigen-matched donors and found a median of three informative SNPs (i.e., discordant between donor and recipient) per pair. By using the informative RBC SNPs to quantify donor-derived RBC transcripts, we compared rates of RBC engraftment in 13 patients with hemoglobinopathies vs donor mononuclear cell (white blood cell [WBC]) engraftment. Consistent with known ineffective erythropoiesis associated with hemoglobinopathies, we detected up to threefold greater RBC-specific compared to overall WBC engraftment in five of eight patients who were mixed chimeras by transplant day 30. The remaining three of eight who received ABH-incompatible grafts, demonstrated at least 0.5-fold lower RBC compared to WBC engraftment that was related to persistence of host-derived anti-isohemagglutinin antibodies. CONCLUSION: This RNA-based assay can be used to monitor RBC-specific engraftment regardless of a patient's specific hemoglobin mutation or even diagnosis. We propose that panels of expressed SNPs informative for other cell lineages can be created to comprehensively assess the impact of novel stem cell-based therapies on lineage-specific engraftment.


Assuntos
Anemia Falciforme/cirurgia , Células Eritroides/citologia , Transplante de Células-Tronco Hematopoéticas , Polimorfismo de Nucleotídeo Único , Talassemia beta/cirurgia , Adolescente , Adulto , Anemia Falciforme/sangue , Incompatibilidade de Grupos Sanguíneos , Proteínas Sanguíneas/genética , Linhagem da Célula , Criança , Pré-Escolar , Eritropoese , Feminino , Seguimentos , Frequência do Gene , Marcadores Genéticos , Genótipo , Rejeição de Enxerto/sangue , Rejeição de Enxerto/diagnóstico , Sobrevivência de Enxerto , Neoplasias Hematológicas/sangue , Neoplasias Hematológicas/cirurgia , Humanos , Masculino , Pessoa de Meia-Idade , Sensibilidade e Especificidade , Transplante Homólogo , Talassemia beta/sangue
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