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Journal of fungi (Basel, Switzerland) · 2020

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.

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Sánchez-Maldonado Jose Manuel, Moñiz-Díez Ana, Ter Horst Rob, Campa Daniele, Cabrera-Serrano Antonio José, Martínez-Bueno Manuel, Garrido-Collado María Del Pilar, Hernández-Mohedo Francisca, Fernández-Puerta Laura, López-Nevot Miguel Ángel, Cunha Cristina, González-Sierra Pedro Antonio, Springer Jan, Lackner Michaela, Alcazar-Fuoli Laura, Fianchi Luana, Aguado José María, Pagano Livio, López-Fernández Elisa, Clavero Esther, Potenza Leonardo, Luppi Mario, Moratalla Lucia, Solano Carlos, Sampedro Antonio, Cuenca-Estrella Manuel, Lass-Flörl Cornelia, Pcraga Study Group, Canzian Federico, Loeffler Juergen, Li Yang, Einsele Hermann, Netea Mihai G, Vázquez Lourdes, Carvalho Agostinho, Jurado Manuel, Sainz Juan

Аннотация

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.

ИП Урсолов Владлен Сергеевич

ИНН 500118482352 · ОГРНИП 314500117700049

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