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Infect Immun ; 86(12)2018 12.
Artículo en Inglés | MEDLINE | ID: mdl-30275011

RESUMEN

High-risk hematological malignancies are a privileged setting for infection by opportunistic microbes, with invasive mycosis being one of the most serious complications. Recently, genetic background has emerged as an unanticipated risk factor. For this reason, polymorphisms for genes encoding archetypal receptors involved in the opsonic and nonopsonic clearance of microbes, pentraxin-3 (PTX3) and Dectin-1, respectively, were studied and correlated with the risk of infection. Fungal, bacterial, and viral infections were registered for a group of 198 patients with high-risk hematological malignancies. Polymorphisms for the pentraxin-3 gene (PTX3) showed a significant association with the risk of fungal infection by Candida spp. and, especially, by Aspergillus spp. This link remained even for patients undergoing antifungal prophylaxis, thus demonstrating the clinical relevance of PTX3 in the defense against fungi. CLEC7A polymorphisms did not show any definite correlation with the risk of invasive mycosis, nor did they influence the expression of Dectin-1 isoforms generated by alternative splicing. The PTX3 mRNA expression level was significantly lower in samples from healthy volunteers who showed these polymorphisms, although no differences were observed in the extents of induction elicited by bacterial lipopolysaccharide and heat-killed Candidaalbicans, thus suggesting that the expression of PTX3 at the start of infection may influence the clinical outcome. PTX3 mRNA expression can be a good biomarker to establish proper antifungal prophylaxis in immunodepressed patients.


Asunto(s)
Proteína C-Reactiva/genética , Neoplasias Hematológicas/complicaciones , Lectinas Tipo C/genética , Infecciones Oportunistas/inmunología , Fagocitosis , Componente Amiloide P Sérico/genética , Adolescente , Adulto , Anciano , Anciano de 80 o más Años , Antifúngicos/uso terapéutico , Aspergilosis/inmunología , Candidiasis/inmunología , Niño , Preescolar , Femenino , Neoplasias Hematológicas/inmunología , Humanos , Masculino , Persona de Mediana Edad , Infecciones Oportunistas/microbiología , Infecciones Oportunistas/virología , Polimorfismo Genético , Estudios Retrospectivos , Factores de Riesgo , Adulto Joven
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