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1.
Hum Immunol ; 77(12): 1280-1283, 2016 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-27664841

RESUMEN

Type 2 Diabetes (T2D) develops, when ß-cell insulin response fails to compensate for insulin resistance. Recent studies reported associations between the IL28B polymorphisms (rs12979860 and rs8099917) and T2D development in Hepatitis C virus (HCV) patients. To identify possible association with T2D independent from virus infection, we investigated both IL28B polymorphisms in T2D patients and healthy controls (HC). No association was found comparing the genotype and allele frequencies of both IL28B polymorphisms between T2D patients and HC. However, higher glucose levels were found in T2D patients carrying the IL28B CT/TT rs12979860 and GT/GG rs8099917 HCV risk genotypes compared to those with the protective CC and TT genotype (p=0.06 and p=0.02, respectively). Moreover, T2D patients with CT/TT rs12979860 HCV risk genotypes possessed significantly higher HbA1c levels than CC carriers (p=0.04). In conclusion, the IL28B HCV risk genotypes may influence glucose homeostasis in T2D patients without HCV.


Asunto(s)
Diabetes Mellitus Tipo 2/genética , Glucosa/metabolismo , Interleucinas/genética , Adulto , Anciano , Femenino , Frecuencia de los Genes , Estudios de Asociación Genética , Genotipo , Alemania , Humanos , Interferones , Masculino , Persona de Mediana Edad , Polimorfismo de Nucleótido Simple , Riesgo
2.
J Viral Hepat ; 20(8): 530-5, 2013 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-23808991

RESUMEN

The levels of the liver-specific microRNA-122 (miR-122) circulating extracellularly in the blood have been shown to be increased upon liver damage. However, it is unknown if the levels of serum miR-122 are altered during antiviral therapy and reflect the therapeutic success. Here, we investigated miR-122 serum levels in patients with chronic hepatitis C virus (HCV) genotype 1 infection during antiviral therapy with pegylated interferon and ribavirin. Therefore, sera from 60 patients with chronic HCV infection genotype 1 showing sustained virological response (SVR), non-response or relapse to therapy obtained at baseline, 4, 12, 24 weeks, end of treatment and follow-up were analysed retrospectively for miR-122 content by quantitative real-time reverse transcription PCR. The time courses of miR-122 were correlated with HCV RNA as well as standard liver parameters. We found that while there was no relation between serum miR-122 and HCV RNA levels at baseline, the decline in HCV RNA upon beginning of the therapy closely correlated with the reduction of serum miR-122 in the three different patient groups. Moreover, the serum miR-122 level correlated well with alanine aminotransaminase, a marker of ongoing liver damage. At follow-up serum miR-122 levels remained low in SVR, but increased to baseline levels in patients not responding or showing relapse to therapy. In contrast, the serum concentration of the ubiquitously expressed miR-16 did not change during therapy. We conclude that the serum level of miR-122 well reflects the success of interferon/ribavirin therapy in patients with chronic HCV infection.


Asunto(s)
Antivirales/uso terapéutico , Biomarcadores/sangre , Hepatitis C Crónica/tratamiento farmacológico , Hepatitis C Crónica/patología , MicroARNs/sangre , Adulto , Femenino , Estudios de Seguimiento , Humanos , Interferones/uso terapéutico , Hígado/patología , Masculino , Persona de Mediana Edad , ARN Viral/sangre , Reacción en Cadena en Tiempo Real de la Polimerasa , Ribavirina/uso terapéutico , Suero/química
3.
J Viral Hepat ; 19(11): 775-83, 2012 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-23043384

RESUMEN

The hepatitis C virus (HCV) nonstructural protein 4B (NS4B) is assumed to function as a membrane anchor and protein hub for the viral replication complex. The aim of the current work was to modulate HCV replication efficacy in the subgenomic Con1 replicon by mutations of specific sites within the aminoterminal-located basic leucine zipper (bZIP), a candidate motif for protein-protein interactions involving NS4B. Mutational sites and amino acid substitutes were determined by in-silico sequence analyses of the NS4B-bZIP motif in 357 isolates of HCV genotype 1b from the euHCVdB and LosAlamos database and consecutive analysis of conserved physico-chemical properties at bZIP specific positions. Mutants with predicted minor, medium or major reduction of replication efficacy were tested in the pFKI389neo/NS3-3'/ET plasmid replicon model. Four sites (L25, T29, V39 and W43) of crucial importance for bZIP-mediated protein interaction with predicted apolarity of respective amino acid positions were selected for mutational studies. Substitutes with physico-chemical properties matching the predicted requirements either well (T29A), moderately (L25W, V39W), or insufficiently (T29E, W43E) were associated with slightly improved, moderate and marked decreased replication efficacy, respectively. Spontaneous (T29G) and adaptive (A28G, E40G) mutations occurred in the T29E mutation isolate only and were associated with marked reduction of replication efficacy. The bZIP motif region of NS4B is crucial for RNA replication in the subgenomic Con1 replicon system. RNA replication efficacy can be modulated by site-directed mutagenesis at specific bZIP functional sites. New adaptive amino acid mutations were identified within the HCV NS4B protein.


Asunto(s)
Hepacivirus/genética , Replicón , Proteínas no Estructurales Virales/química , Proteínas no Estructurales Virales/genética , Replicación Viral/genética , Sustitución de Aminoácidos , Línea Celular , Células HEK293 , Hepacivirus/fisiología , Humanos , Leucina Zippers , Mutagénesis Sitio-Dirigida , Estructura Terciaria de Proteína , ARN Viral/genética , ARN Viral/metabolismo , Proteínas no Estructurales Virales/metabolismo
4.
Appl Opt ; 39(15): 2377-86, 2000 May 20.
Artículo en Inglés | MEDLINE | ID: mdl-18345147

RESUMEN

A newly developed UV-visible instrument for differential optical absorption spectroscopic measurements of atmospheric trace gases from balloon platforms is described. Direct solar light at daytime in the near-ultraviolet (320.6-422.6-nm) and the visible (417.6-670.7-nm) spectral ranges can be simultaneously analyzed for the atmospheric column abundances or profiles of O(3), NO(2), NO(3), BrO, OClO, O(4), H(2)O, and possibly other species (HNO(2), IO, CH(2)O). Compared with previously used balloonborne UV-visible spectrometers, the instrument has the superior properties of low mass (42 kg), low power consumption (30 W), decreased spectral drift that is caused by temperature and pressure changes, low detector dark current, and low spectrometer stray light. The three last-named characteristics are achieved by enclosure of the entire spectrometer in a pressurized and thermostated container and by inclusion of separately thermostated photodiode array detectors. The optical setup is simplified to reduce its weight. The spectral stray light is reduced by suppression of the higher-order and zero-order grating reflections by use of light traps and in the UV by addition of a dispersive prism preanalyzer. The major instrumental design characteristics and the instrumental performance as tested in the laboratory and during several stratospheric balloon flights are reported.

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