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1.
J Clin Virol ; 57(2): 147-51, 2013 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-23490398

RESUMEN

BACKGROUND: Information on vaccine-type HPV seroprevalence is essential for vaccine strategies; however, limited data are available on past exposure to HPV-quadrivalent vaccine types in HIV-infected woman in Brazil. OBJECTIVES: To assess the seroprevalence for HPV types 6, 11, 16 and 18 in HIV-infected and uninfected women, from Rio de Janeiro, Brazil and to investigate potential associations with age and pregnancy status. STUDY-DESIGN: 1100-sera were tested by virus-like particle (VLPs)-based ELISA for antibodies to HPV types 16, 18, 6 and 11. Statistical analysis was carried out by STATA/SE 10.1 and comparisons among HIV-infected and HIV-uninfected women were assessed by Poisson regression models with robust variance. RESULTS: HPV-6, 11, 16 and 18 seroprevalence was significantly higher among HIV-positive women (29.9%, 8.5%, 56.2% and 38.0%, respectively) compared to HIV-negative women (10.9%, 3.5%, 30.8% and 21.7%, respectively), when adjusted by age and pregnancy status. Overall, 69.4% of HIV-infected and 41.5% of HIV-uninfected women tested positive for any HPV quadrivalent vaccine type. However 4.7% and 1.1%, respectively, tested positive for all HPV vaccine type. In HIV-uninfected women who were pregnant, we found a higher HPV-11 seroprevalence (8.5% vs. 1.5%; P < 0.001) and a lower HPV 16 seroprevalence (22.6% vs. 34.2%; P = 0.010) compared to not pregnant women. HIV-uninfected women, aged 40 or more years old had a higher HPV 16 seroprevalence compared to women aged less than 40 years old. CONCLUSIONS: We did not observe a strong association between age and positive HPV antibodies nor an association between pregnancy and HPV seroprevalence. HPV seroprevalence was significantly higher among HIV-infected women compared to HIV negative women. In both populations the seroprevalence to all four HPV vaccine types was low suggesting that women may potentially benefit from the HPV vaccines.


Asunto(s)
Anticuerpos Antivirales/sangre , Infecciones por VIH/complicaciones , Papillomavirus Humano 11/inmunología , Papillomavirus Humano 16/inmunología , Papillomavirus Humano 18/inmunología , Papillomavirus Humano 6/inmunología , Infecciones por Papillomavirus/epidemiología , Complicaciones Infecciosas del Embarazo/epidemiología , Adulto , Brasil/epidemiología , Femenino , Infecciones por VIH/epidemiología , Infecciones por VIH/virología , Humanos , Infecciones por Papillomavirus/inmunología , Infecciones por Papillomavirus/virología , Vacunas contra Papillomavirus , Embarazo , Complicaciones Infecciosas del Embarazo/inmunología , Complicaciones Infecciosas del Embarazo/virología , Estudios Seroepidemiológicos
3.
Lancet ; 2(8609): 471-5, 1988 Aug 27.
Artículo en Inglés | MEDLINE | ID: mdl-2900402

RESUMEN

8 patients with bone marrow failure after a caesium-137 radiation accident were treated with recombinant human granulocyte-macrophage colony stimulating factor (rHuGM-CSF). The 7 who were evaluable had prompt increases in granulocytes and bone marrow cellularity. 2 patients died of radiation toxicity and haemorrhage and 2 of bacterial sepsis acquired before the start of rHuGM-CSF treatment. 4 patients survive, including 2 who were treated early and never became infected. This therapeutic approach to radiation-induced granulocytopenia may therefore be useful after radiation and nuclear accidents.


Asunto(s)
Accidentes , Agranulocitosis/tratamiento farmacológico , Radioisótopos de Cesio/efectos adversos , Factores Estimulantes de Colonias/uso terapéutico , Sustancias de Crecimiento/uso terapéutico , Traumatismos por Radiación/tratamiento farmacológico , Enfermedad Aguda , Adolescente , Adulto , Agranulocitosis/etiología , Agranulocitosis/mortalidad , Brasil , Niño , Factores Estimulantes de Colonias/efectos adversos , Evaluación de Medicamentos , Exposición a Riesgos Ambientales , Contaminación de Equipos , Femenino , Contaminación Radiactiva de Alimentos , Factor Estimulante de Colonias de Granulocitos y Macrófagos , Sustancias de Crecimiento/efectos adversos , Humanos , Masculino , Persona de Mediana Edad , Dosis de Radiación , Traumatismos por Radiación/etiología , Traumatismos por Radiación/mortalidad , Residuos Radiactivos/efectos adversos , Proteínas Recombinantes/efectos adversos , Proteínas Recombinantes/uso terapéutico , Factores de Tiempo
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