Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 4 de 4
Filtrar
3.
J Viral Hepat ; 13(12): 821-7, 2006 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-17109681

RESUMEN

The alpha-defensin genes promoter regions contain a putative nuclear factors of activated T cells (NFAT)-binding site and it is known that hepatitis C virus (HCV) core protein activates the interleukin (IL)-2 gene transcription through the NFAT pathway. The aims of this study were to investigate if HCV affects the alpha-defensin expression in peripheral human mononuclear cells (PBMCs) and to evaluate the existence of a correlation between alpha-defensins and liver damage in patients with chronic hepatitis C. Ninety patients with chronic hepatitis C, 30 with chronic hepatitis B and 25 healthy controls were enrolled. Alpha-defensins were identified and quantified in PBMCs by mass spectrometry, enzyme-linked immunosorbent assay, antibacterial activity and mRNA levels. PBMCs from three patients and controls were stimulated with HCV core protein, hepatitis B virus core antigen and the alpha-defensin mRNAs level was quantified. We found that HCV core protein activates in vitro the alpha-defensin transcription. Alpha-defensin levels in patients with chronic hepatitis C (mean +/- SD = 1.103 +/- 0.765 ng/10(6) cells), chronic hepatitis B (0.53 +/- 0.15) and healthy controls (0.217 +/- 0.09) resulted significantly different (P < 0.001). In patients with chronic hepatitis C, the alpha-defensin levels and antibacterial activity correlate with the liver fibrosis. Our data suggest that HCV induces alpha-defensin expression. The high linear correlation of alpha-defensin levels with advancing fibrosis makes the measure of these peptides a reliable marker to evaluate fibrosis stage.


Asunto(s)
Antiinfecciosos/inmunología , Hepatitis C Crónica/inmunología , Leucocitos Mononucleares/inmunología , alfa-Defensinas/sangre , Adulto , Antiinfecciosos/metabolismo , Femenino , Expresión Génica , Hepatitis C Crónica/sangre , Hepatitis C Crónica/patología , Hepatitis C Crónica/virología , Humanos , Cirrosis Hepática/sangre , Cirrosis Hepática/inmunología , Cirrosis Hepática/virología , Masculino , Persona de Mediana Edad , Regiones Promotoras Genéticas , ARN Mensajero/biosíntesis , ARN Mensajero/genética , alfa-Defensinas/biosíntesis , alfa-Defensinas/genética , alfa-Defensinas/inmunología
4.
Parasitology ; 118 ( Pt 4): 335-8, 1999 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-10340322

RESUMEN

The C57BL6 strain of mice is highly susceptible to Plasmodium berghei sporozoite infections and consequently requires repeated immunizations with irradiated sporozoites to obtain protective immunity. After a live sporozoite challenge in the immunized hosts, hepatic-stage parasites found in the liver after 48 h are of different sizes--small schizonts corresponding to blocked forms (derived from irradiated sporozoites), and schizonts of intermediate size (derived from live sporozoites). Large schizonts corresponding to mature hepatic forms are found only in unimmunized but challenged C57BL6 mice. Using monoclonal and polyclonal antibodies directed to liver-stage parasites, different patterns of binding reactivity to the above forms are observed. More than 20% of the irradiated sporozoites transform into blocked forms after immunization and persist in the liver. Upon sporozoite challenge in such immunized animals the rate of transformation of sporozoites into hepatic parasites is less than 2%. These observations shed light on the fate of live sporozoite development in irradiated sporozoite-immunized C57BL6 mice.


Asunto(s)
Antígenos de Protozoos/inmunología , Inmunización , Hígado/parasitología , Malaria/parasitología , Plasmodium berghei/crecimiento & desarrollo , Plasmodium berghei/inmunología , Animales , Anopheles/parasitología , Anticuerpos Antiprotozoarios/inmunología , Femenino , Malaria/prevención & control , Ratones , Ratones Endogámicos C57BL , Plasmodium berghei/efectos de la radiación , Proteínas Protozoarias/inmunología
SELECCIÓN DE REFERENCIAS
DETALLE DE LA BÚSQUEDA