| Literature DB >> 33374839 |
Jose Manuel Sánchez-Maldonado1,2,3, Ana Moñiz-Díez1,2,3, Rob Ter Horst4, Daniele Campa5, Antonio José Cabrera-Serrano1, Manuel Martínez-Bueno6, María Del Pilar Garrido-Collado2,3, Francisca Hernández-Mohedo2,3, Laura Fernández-Puerta2,3, Miguel Ángel López-Nevot7, Cristina Cunha8,9, Pedro Antonio González-Sierra2,3, Jan Springer10, Michaela Lackner11, Laura Alcazar-Fuoli12, Luana Fianchi13, José María Aguado14, Livio Pagano13, Elisa López-Fernández2,3, Esther Clavero2,3, Leonardo Potenza15, Mario Luppi15, Lucia Moratalla2,3, Carlos Solano16, Antonio Sampedro17, Manuel Cuenca-Estrella12, Cornelia Lass-Flörl11, Federico Canzian18, Juergen Loeffler10, Yang Li4,19, Hermann Einsele10, Mihai G Netea4,20, Lourdes Vázquez21, Agostinho Carvalho8,9, Manuel Jurado1,2,3, Juan Sainz1,2,3,22.
Abstract
Here, we assessed whether 36 single nucleotide polymorphisms (SNPs) within the TNFSF4 and MAPKAPK2 loci influence the risk of developing invasive aspergillosis (IA). We conducted a two-stage case control study including 911 high-risk patients diagnosed with hematological malignancies that were ascertained through the aspBIOmics consortium. The meta-analysis of the discovery and replication populations revealed that carriers of the TNFSF4 rs7526628T/T genotype had a significantly increased risk of developing IA (p = 0.00022). We also found that carriers of the TNFSF4 rs7526628T allele showed decreased serum levels of TNFSF14 protein (p = 0.0027), and that their macrophages had a decreased fungicidal activity (p = 0.048). In addition, we observed that each copy of the MAPKAPK2 rs12137965G allele increased the risk of IA by 60% (p = 0.0017), whereas each copy of the MAPKAPK2 rs17013271T allele was estimated to decrease the risk of developing the disease (p = 0.0029). Mechanistically, we found that carriers of the risk MAPKAPK2 rs12137965G allele showed increased numbers of CD38+IgM-IgD- plasmablasts in blood (p = 0.00086), whereas those harboring two copies of the allele had decreased serum concentrations of thymic stromal lymphopoietin (p = 0.00097). Finally, we also found that carriers of the protective MAPKAPK2 rs17013271T allele had decreased numbers of CD27-IgM-IgD- B cells (p = 0.00087) and significantly lower numbers of CD14+ and CD14+CD16- cells (p = 0.00018 and 0.00023). Altogether, these results suggest a role of the TNFSF4 and MAPKAPK2 genes in determining IA risk.Entities:
Keywords: B cells; MAPKAPK2; TNFSF14; TNFSF4; TSLP; genetic susceptibility; invasive aspergillosis; monocytes; serum biomarkers
Year: 2020 PMID: 33374839 PMCID: PMC7823601 DOI: 10.3390/jof7010004
Source DB: PubMed Journal: J Fungi (Basel) ISSN: 2309-608X