Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 4 de 4
Filtrar
Más filtros










Base de datos
Intervalo de año de publicación
2.
Clin Exp Immunol ; 173(2): 250-8, 2013 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-23607522

RESUMEN

The altered expression of micro-RNA (miRNA) has been associated with Crohn's disease (CD) and ulcerative colitis (UC). The aim of this study was to establish specific miRNA expression patterns in the serum and mucosa of inflammatory bowel disease (IBD) patients (UC and CD with colonic involvement) at different stages of the disease. Serum and biopsies from nine active CD (aCD), nine inactive CD (iCD), nine active UC (aUC) and nine inactive UC (iUC) and serum from 33 healthy subjects were collected. Up to 700 miRNAs were evaluated by the TaqMan human miRNA array. The ΔCt values were obtained using the mean expression values of all expressed miRNAs in a given sample as a normalization factor for miRNA real-time quantitative polymerase chain reaction data. The levels of serum miRNAs in CD and UC patients were different to healthy subjects. Thirteen serum miRNAs were expressed commonly in CD and UC patients. Two miRNAs were higher and four miRNAs were lower in the serum of aCD than iCD. No serum miRNA was regulated exclusively in aUC compared with iUC patients. Four miRNAs were higher and three miRNAs were lower in the mucosa of aCD than iCD. Two miRNAs were higher and three miRNAs were lower in the mucosa of aUC than iUC. No serum miRNAs coincided with tissue miRNAs in aCD and aUC patients. Our results suggest the existence of specific miRNA expression patterns associated with IBD and their different stages and support the utility of miRNA as possible biomarkers. This pilot study needs to be validated in a large prospective cohort.


Asunto(s)
Enfermedades Inflamatorias del Intestino/genética , MicroARNs/biosíntesis , Adulto , Progresión de la Enfermedad , Femenino , Marcadores Genéticos/genética , Humanos , Enfermedades Inflamatorias del Intestino/fisiopatología , Mucosa Intestinal/metabolismo , Masculino , MicroARNs/sangre , MicroARNs/genética , Análisis por Micromatrices , Persona de Mediana Edad , Transcriptoma
3.
Int J Immunopathol Pharmacol ; 21(2): 401-7, 2008.
Artículo en Inglés | MEDLINE | ID: mdl-18547485

RESUMEN

Immune reactivity towards the bacterial intestinal flora plays an important part in the pathogenesis of inflammatory bowel disease. Administration of probiotic bacteria has beneficial effects on infectious and inflammatory diseases, principally in bowel disorders. However, little is known about the administration of soluble bacterial antigens in intestinal inflammation. We investigated the therapeutic effects of colifagina in experimental colitis. To assess this effect, C57BL/6 mice with dextran sulphate sodium-induced colitis were treated with colifagina, or with a placebo, for a period of 10 days. The mice were monitored, and inflammation was assessed by disease activity index (DAI). Analysis of fecal IgA concentration and measurement of IgA and inflammatory chemokine production in organ colonic culture was performed by ELISA. Clinically and histologically, bacterial-lysate-treated mice revealed significantly fewer DAI and a reduction of colonic histological inflammation. Treatment of healthy mice with colifagina significantly increased the fecal concentration of IgA and IgA production in organ culture. Colifagina administration in DSS-treated mice significantly increased the fecal concentration of IgA and IgA production in organ culture. MIP-1, MIP-2 and RANTES concentrations in colonic organ culture were significantly lower in colifagina-treated mice than in the placebo group. The use of colifagina is effective in amelioration of murine colitis.


Asunto(s)
Colitis/tratamiento farmacológico , Probióticos/uso terapéutico , Animales , Quimiocinas/antagonistas & inhibidores , Quimiocinas/biosíntesis , Colitis/inducido químicamente , Colitis/patología , Colon/patología , Heces/microbiología , Inmunoglobulina A/inmunología , Mucosa Intestinal/patología , Masculino , Ratones , Ratones Endogámicos C57BL , Técnicas de Cultivo de Órganos
4.
Am Fam Physician ; 60(4): 1191-8, 1209-10, 1999 Sep 15.
Artículo en Inglés | MEDLINE | ID: mdl-10507748

RESUMEN

Atopic dermatitis is a common, potentially debilitating condition that can compromise quality of life. Its most frequent symptom is pruritus. Attempts to relieve the itch by scratching simply worsen the rash, creating a vicious circle. Treatment should be directed at limiting itching, repairing the skin and decreasing inflammation when necessary. Lubricants, antihistamines and topical corticosteroids are the mainstays of therapy. When required, oral corticosteroids can be used. If pruritus does not respond to treatment, other diagnoses, such as bacterial overgrowth or viral infections, should be considered. Treatment options are available for refractory atopic dermatitis, but these measures should be reserved for use in unique situations and typically require consultation with a dermatologist or an allergist.


Asunto(s)
Dermatitis Atópica/diagnóstico , Dermatitis Atópica/terapia , Corticoesteroides/uso terapéutico , Antibacterianos/uso terapéutico , Antidepresivos/uso terapéutico , Antineoplásicos/uso terapéutico , Árboles de Decisión , Dermatitis Atópica/complicaciones , Dermatitis Atópica/tratamiento farmacológico , Diagnóstico Diferencial , Antagonistas de los Receptores Histamínicos H1/uso terapéutico , Humanos , Inmunosupresores/uso terapéutico , Antagonistas de Leucotrieno/uso terapéutico , Educación del Paciente como Asunto , Fototerapia , Prurito/etiología , Breas/uso terapéutico , Materiales de Enseñanza
SELECCIÓN DE REFERENCIAS
DETALLE DE LA BÚSQUEDA
...