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1.
Blood ; 95(6): 2084-92, 2000 Mar 15.
Artigo em Inglês | MEDLINE | ID: mdl-10706878

RESUMO

A new monoclonal antibody (MUM1p) was used to study the cell/tissue expression of human MUM1/IRF4 protein, the product of the homologous gene involved in the myeloma-associated t(6;14) (p25;q32). MUM1 was expressed in the nuclei and cytoplasm of plasma cells and a small percentage of germinal center (GC) B cells mainly located in the "light zone." Its morphologic spectrum ranged from that of centrocyte to that of a plasmablast/plasma cell, and it displayed a phenotype (MUM1(+)/Bcl-6(-)/Ki67(-)) different from that of most GC B cells (MUM1(-)/Bcl-6(+)/Ki67(+)) and mantle B cells (MUM1(-)/Bcl-6(-)/Ki67(-)). Polymerase chain reaction (PCR) analysis of single MUM1(+ )cells isolated from GCs showed that they contained rearranged Ig heavy chain genes with a varying number of V(H) somatic mutations. These findings suggest that these cells may represent surviving centrocytes and their progeny committed to exit GC and to differentiate into plasma cells. MUM1 was strongly expressed in lymphoplasmacytoid lymphoma, multiple myeloma, and approximately 75% of diffuse large B-cell lymphomas (DLCL-B). Unlike normal GC B cells, in which the expression of MUM1 and Bcl-6 were mutually exclusive, tumor cells in approximately 50% of MUM1(+) DLCL-B coexpressed MUM1 and Bcl-6, suggesting that expression of these proteins may be deregulated. In keeping with their proposed origin from GC B cells, Hodgkin and Reed-Sternberg cells of Hodgkin's disease consistently expressed MUM1. MUM1 was detected in normal and neoplastic activated T cells, and its expression usually paralleled that of CD30. These results suggest that MUM1 is involved in the late stages of B-cell differentiation and in T-cell activation and is deregulated in DLCL-B. (Blood. 2000;95:2084-2092)


Assuntos
Anticorpos Monoclonais , Linfócitos B/metabolismo , Proteínas de Ligação a DNA/metabolismo , Plasmócitos/metabolismo , Linfócitos T/metabolismo , Fatores de Transcrição/metabolismo , Linfócitos B/imunologia , Biomarcadores Tumorais/metabolismo , Western Blotting , Linhagem Celular , Homólogo 5 da Proteína Cromobox , Epitopos , Células HeLa , Humanos , Região Variável de Imunoglobulina/metabolismo , Imuno-Histoquímica , Fatores Reguladores de Interferon , Células Jurkat , Linfonodos/metabolismo , Linfoma/metabolismo , Mieloma Múltiplo/metabolismo , Plasmócitos/imunologia , Proteínas Recombinantes de Fusão/metabolismo , Linfócitos T/imunologia , Fatores de Tempo , Transfecção
2.
Minerva Ginecol ; 43(9): 419-20, 1991 Sep.
Artigo em Italiano | MEDLINE | ID: mdl-1945033

RESUMO

The paper describes the obstetric management of an unique case of twin, bicorial, biamniotic pregnancy in which the second twin born 36 days after the first. Both twins are living today.


Assuntos
Gêmeos Dizigóticos , Cesárea , Parto Obstétrico , Feminino , Humanos , Recém-Nascido , Gravidez , Resultado da Gravidez , Fatores de Tempo
3.
Minerva Ginecol ; 41(6): 299-300, 1989 Jun.
Artigo em Italiano | MEDLINE | ID: mdl-2788836

RESUMO

A 12.6% incidence of HBV markers was found among pregnant women in three Tivoli (USL RM 26) National Health Units last year (1.07% of them HBsAg): the difference between the findings of the three NH units was statistically significant.


Assuntos
Antígenos da Hepatite B/análise , Gravidez/sangue , Estudos Transversais , Feminino , Antígenos de Superfície da Hepatite B/análise , Humanos , Itália
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