Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 5 de 5
Filtrar
Más filtros











Intervalo de año de publicación
1.
Braz J Med Biol Res ; 46(2): 200-6, 2013 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-23369970

RESUMEN

Febrile neutropenia remains a frequent complication in onco-hematological patients, and changes in the circulating level of inflammatory molecules (IM) may precede the occurrence of fever. The present observational prospective study was carried out to evaluate the behavior of plasma tumor necrosis factor alpha (TNF-α), soluble TNF-α I and II receptors (sTNFRI and sTNFRII), monocyte chemoattractant protein-1 [MCP-1 or chemokine (c-c motif) ligand 2 (CCL2)], macrophage inflammatory protein-1α (MIP-1α or CCL3), eotaxin (CCL11), interleukin-8 (IL-8 or CXCL8), and interferon-inducible protein-10 (IP-10 or CXCL10) in 32 episodes of neutropenia in 26 onco-hematological patients. IM were tested on enrollment and 24-48 h before the onset of fever and within 24 h of the first occurrence of fever. Eight of 32 episodes of neutropenia did not present fever (control group) and the patients underwent IM tests on three different occasions. sTNFRI levels, measured a median of 11 h (1-15) before the onset of fever, were significantly higher in patients presenting fever during follow-up compared to controls (P = 0.02). Similar results were observed for sTNFRI and CCL2 levels (P = 0.04 for both) in non-transplanted patients. A cut-off of 1514 pg/mL for sTNFRI was able to discriminate between neutropenic patients with or without fever during follow-up, with 65% sensitivity, 87% specificity, and 93% positive predictive value. Measurement of the levels of plasma sTNFRI can be used to predict the occurrence of fever in neutropenic patients.


Asunto(s)
Citocinas/sangre , Neutropenia Febril/sangre , Neoplasias Hematológicas/sangre , Adolescente , Adulto , Anciano , Biomarcadores/sangre , Estudios de Casos y Controles , Femenino , Neoplasias Hematológicas/mortalidad , Humanos , Inflamación/sangre , Masculino , Persona de Mediana Edad , Proyectos Piloto , Valor Predictivo de las Pruebas , Estudios Prospectivos , Adulto Joven
2.
Rev. bras. pesqui. méd. biol ; Braz. j. med. biol. res;46(2): 200-206, 01/fev. 2013. tab, graf
Artículo en Inglés | LILACS | ID: lil-668769

RESUMEN

Febrile neutropenia remains a frequent complication in onco-hematological patients, and changes in the circulating level of inflammatory molecules (IM) may precede the occurrence of fever. The present observational prospective study was carried out to evaluate the behavior of plasma tumor necrosis factor alpha (TNF-α), soluble TNF-α I and II receptors (sTNFRI and sTNFRII), monocyte chemoattractant protein-1 [MCP-1 or chemokine (c-c motif) ligand 2 (CCL2)], macrophage inflammatory protein-1α (MIP-1α or CCL3), eotaxin (CCL11), interleukin-8 (IL-8 or CXCL8), and interferon-inducible protein-10 (IP-10 or CXCL10) in 32 episodes of neutropenia in 26 onco-hematological patients. IM were tested on enrollment and 24-48 h before the onset of fever and within 24 h of the first occurrence of fever. Eight of 32 episodes of neutropenia did not present fever (control group) and the patients underwent IM tests on three different occasions. sTNFRI levels, measured a median of 11 h (1-15) before the onset of fever, were significantly higher in patients presenting fever during follow-up compared to controls (P = 0.02). Similar results were observed for sTNFRI and CCL2 levels (P = 0.04 for both) in non-transplanted patients. A cut-off of 1514 pg/mL for sTNFRI was able to discriminate between neutropenic patients with or without fever during follow-up, with 65% sensitivity, 87% specificity, and 93% positive predictive value. Measurement of the levels of plasma sTNFRI can be used to predict the occurrence of fever in neutropenic patients.


Asunto(s)
Adolescente , Adulto , Anciano , Femenino , Humanos , Masculino , Persona de Mediana Edad , Adulto Joven , Citocinas/sangre , Neutropenia Febril/sangre , Neoplasias Hematológicas/sangre , Biomarcadores/sangre , Estudios de Casos y Controles , Neoplasias Hematológicas/mortalidad , Inflamación/sangre , Proyectos Piloto , Valor Predictivo de las Pruebas , Estudios Prospectivos
3.
Oral Dis ; 18(8): 816-22, 2012 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-22748084

RESUMEN

OBJECTIVE: Graft-versus-host disease is a major complication after allogenic hematopoietic stem cell transplantation. Interferon gamma is an important pro-inflammatory cytokine involved in this disease. Cytokine gene polymorphisms are associated with functional differences in cytokine expression and can alter the clinical course of graft-versus-host disease. This study aimed to investigate the association between IFN-γ levels in saliva, blood, and IFNG polymorphisms, as well as the occurrence of acute graft-versus-host disease in allogenic HSCT. SUBJECTS AND METHODS: Fifty-eight consecutive allogenic hematopoietic stem cell transplantation recipients and their donors were prospectively studied. IFN-g levels in saliva and blood were assessed by ELISA. Samples were collected weekly from 7 days before transplantation (day -7) to 100 days after allogenic HSCT (day +100) or until death. Saliva and/or blood samples were obtained from the recipients and donors to determine IFNG gene polymorphisms. RESULTS: Increased saliva and blood IFN-g levels were observed in patients that had developed aGVHD. In the saliva, the peak levels of IFN-g could be found one week before aGVHD diagnosis, while in the blood, peak levels of IFN-g could be only observed upon diagnosis. A significant association could be identified between the recipients'IFNG genotypes and the IFN-g levels in their blood, at +14 days after HSCT. No association could be observed between IFNG gene polymorphisms and the aGVHD. CONCLUSION: The present study shows that the genetic background of recipients can influence the production of IFN-g. Moreover, as IFN-g levels in the saliva and blood were found to be associated with aGVHD development, this cytokine may be a useful predictor of acute graft-versus-host disease.


Asunto(s)
Enfermedad Injerto contra Huésped/inmunología , Interferón gamma/análisis , Polimorfismo Genético/genética , Saliva/inmunología , Proteínas y Péptidos Salivales/análisis , Enfermedad Aguda , Adenina , Adolescente , Adulto , Anciano , Biomarcadores/análisis , Niño , Preescolar , Femenino , Estudios de Seguimiento , Predicción , Genotipo , Trasplante de Células Madre Hematopoyéticas/métodos , Humanos , Interferón gamma/sangre , Interferón gamma/genética , Masculino , Persona de Mediana Edad , Estudios Prospectivos , Timina , Donantes de Tejidos , Acondicionamiento Pretrasplante , Trasplante Homólogo , Resultado del Tratamiento , Adulto Joven
4.
Int J Lab Hematol ; 33(2): 117-24, 2011 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-21118380

RESUMEN

INTRODUCTION: Thrombotic complications are a main concern in patients with myeloproliferative neoplasms. Recently, a gain-of-function mutation of the gene encoding the JAK2 tyrosine kinase that results in a valine-to-phenylalanine substitution at position 617 (V617F) has been described. Since the description of the JAK2-V617F mutation and its finding in patients with splanchnic vein thrombosis without an overt myeloproliferative neoplasm, many groups have studied the prevalence of this mutation in patients with unexplained venous and arterial thrombosis. METHODS: A literature search was made using the key words thrombosis, JAK2V617F mutation, myeloproliferative neoplasms, cerebral vein thrombosis and splanchnic vein thrombosis. RESULTS: JAK2V617F is frequent in patients with splanchnic vein thrombosis, but is rare in patients with venous thrombosis at other locations or with arterial thrombosis. CONCLUSION: Routine testing for JAK2V617F is not currently recommended for patients with unexplained thromboses, except for those with splanchnic vein thrombosis. In patients with cerebral vein thrombosis, the value of testing for JAK2V617F mutation is yet to be established.


Asunto(s)
Pruebas Genéticas , Janus Quinasa 2/genética , Mutación , Trombosis/genética , Venas Cerebrales/patología , Predisposición Genética a la Enfermedad , Pruebas Genéticas/normas , Humanos , Venas Mesentéricas/patología , Trastornos Mieloproliferativos/complicaciones , Trastornos Mieloproliferativos/genética , Trombosis/etiología
5.
Oral Dis ; 16(2): 210-6, 2010 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-20374507

RESUMEN

OBJECTIVE: The purpose of this study was to investigate the use of saliva for the identification of human cytomegalovirus (HCMV) in allogeneic hematopoietic stem cell transplant patients by real time PCR compared with blood. MATERIALS AND METHODS: Saliva and blood samples were sampled weekly in 30 allogeneic hematopoietic stem cell transplant patients until 100 days after transplant. Total genomic DNA, extracted from saliva and whole-blood samples, was used for HCMV real time PCR. Nonparametric tests were performed, and P value

Asunto(s)
Citomegalovirus/aislamiento & purificación , ADN Viral/análisis , Trasplante de Células Madre Hematopoyéticas , Saliva/virología , Adolescente , Adulto , Antígenos Virales/análisis , Antígenos Virales/sangre , Antivirales/uso terapéutico , Niño , Citomegalovirus/genética , Citomegalovirus/inmunología , Infecciones por Citomegalovirus/diagnóstico , Infecciones por Citomegalovirus/tratamiento farmacológico , ADN Viral/sangre , Estudios de Factibilidad , Femenino , Estudios de Seguimiento , Ganciclovir/uso terapéutico , Humanos , Estudios Longitudinales , Masculino , Persona de Mediana Edad , Fosfoproteínas/análisis , Fosfoproteínas/sangre , Reacción en Cadena de la Polimerasa , Estudios Prospectivos , Trasplante Homólogo , Carga Viral , Proteínas de la Matriz Viral/análisis , Proteínas de la Matriz Viral/sangre , Viremia/virología , Activación Viral , Adulto Joven
SELECCIÓN DE REFERENCIAS
DETALLE DE LA BÚSQUEDA