Chronic Pulmonary Aspergillosis: Genomic Variant Analysis and Protein Dysfunction Susceptibility in a Brazilian Cohort
Mendes RDS, Wolff BM, Costa Siemann MR, Oliveira YG, Carvalho GFDS, Vieira LL, Moura EA, Nascimento KM, et al. (13 authors)
Genes · 2025-05
Abstract
Background/objectives Chronic pulmonary aspergillosis (CPA) is a debilitating condition often affecting immunocompetent patients with underlying structural lung diseases, particularly pulmonary tuberculosis. This study investigates single nucleotide variants (SNVs) in immunogenetic-related genes among a Brazilian cohort with CPA. Methods Twelve patients with confirmed CPA, based on ESCMID/ERS criteria, were sequenced using custom multigenic panel sequencing. Variants were annotated, classified using ACMG guidelines, and analyzed for potential impact on protein interactions and immune pathways. Results A set of SNVs in CX3CR1 , IL12B , IL4R , PTX3 , CCR5 , and IFNG genes were classified as variants of uncertain significance (VUS), but protein-protein interaction analysis suggests a potential role in immune evasion and dysfunction. Conclusions This is the first study to apply a custom multigenic panel for CPA susceptibility in a Brazilian cohort, contributing to future functional and clinical studies in fungal immunogenetics.
MeSH terms
- Humans
- Chronic Disease
- Genetic Predisposition to Disease
- Cohort Studies
- Polymorphism, Single Nucleotide
- Adult
- Aged
- Middle Aged
- Brazil
- Female
- Male
- Pulmonary Aspergillosis