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Polymorphisms within the TNFSF4 and MAPKAPK2 Loci Influence the Risk of Developing Invasive Aspergillosis: A Two-Stage Case Control Study in the Context of the aspBIOmics Consortium.

Authors :
Manuel Sánchez-Maldonado, Jose
Moñiz-Díez, Ana
Horst, Rob ter
Campa, Daniele
José Cabrera-Serrano, Antonio
Martínez-Bueno, Manuel
del Pilar Garrido-Collado, María
Hernández-Mohedo, Francisca
Fernández-Puerta, Laura
Ángel López-Nevot, Miguel
Cunha, Cristina
Antonio González-Sierra, Pedro
Springer, Jan
Lackner, Michaela
Alcazar-Fuoli, Laura
Fianchi, Luana
María Aguado, José
Pagano, Livio
López-Fernández, Elisa
Clavero, Esther
Source :
Journal of Fungi; Jan2021, Vol. 7 Issue 1, p1-17, 17p
Publication Year :
2021

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<subscript>rs7526628T/T</subscript> genotype had a significantly increased risk of developing IA (p = 0.00022). We also found that carriers of the TNFSF4<subscript>rs7526628T</subscript> 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<subscript>rs12137965G</subscript> allele increased the risk of IA by 60% (p = 0.0017), whereas each copy of the MAPKAPK2<subscript>rs17013271T</subscript> allele was estimated to decrease the risk of developing the disease (p = 0.0029). Mechanistically, we found that carriers of the risk MAPKAPK2<subscript>rs12137965G</subscript> 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<subscript>rs17013271T</subscript> 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. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
2309608X
Volume :
7
Issue :
1
Database :
Complementary Index
Journal :
Journal of Fungi
Publication Type :
Academic Journal
Accession number :
149098364
Full Text :
https://doi.org/10.3390/jof7010004