| Literature DB >> 30275011 |
M Carmen Herrero-Sánchez1, Eduardo B Angomás2, Cristina de Ramón3, Juan J Tellería1,4, Luis A Corchete4,5,6, Sara Alonso1, M Del Carmen Ramos7, María J Peñarrubia3, Saioa Márquez8, Nieves Fernández8, Luis J García Frade2, Mariano Sánchez Crespo9.
Abstract
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 Candida albicans, 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.Entities:
Keywords: Dectin-1; PTX3; SNP; fungal infection; oncohematology
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Year: 2018 PMID: 30275011 PMCID: PMC6246897 DOI: 10.1128/IAI.00709-18
Source DB: PubMed Journal: Infect Immun ISSN: 0019-9567 Impact factor: 3.441