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CCR5 deficiency predisposes to fatal outcome in influenza virus infection
67
Citations
20
References
2015
Year
Inflammatory Lung DiseaseViral PathogenesisImmunologyGenetic EpidemiologyFlu VaccinationCovid-19Influenza VaccinesDisease SusceptibilityViral EvolutionPediatric EpidemiologyRespiratory InfectionPublic HealthCcr5-δ32 MutationRespiratory DiseasesVirologyEpidemiologyCcr5 GeneInfluenza EpidemicsEmerging Infectious DiseasesPathogenesisInfectious Respiratory DiseaseInfluenza VaccineInfluenza Virus InfectionMedicine
Influenza epidemics affect all age groups, although children, the elderly and those with underlying medical conditions are the most severely affected. Whereas co-morbidities are present in 50% of fatal cases, 25-50% of deaths are in apparently healthy individuals. This suggests underlying genetic determinants that govern infection severity. Although some viral factors that contribute to influenza disease are known, the role of host genetic factors remains undetermined. Data for small cohorts of influenza-infected patients are contradictory regarding the potential role of chemokine receptor 5 deficiency (CCR5-Δ32 mutation, a 32 bp deletion in the CCR5 gene) in the outcome of influenza virus infection. We tested 171 respiratory samples from influenza patients (2009 pandemic) for CCR5-Δ32 and evaluated its correlation with patient mortality. CCR5-Δ32 patients (17.4%) showed a higher mortality rate than WT individuals (4.7%; P = 0.021), which indicates that CCR5-Δ32 patients are at higher risk than the normal population of a fatal outcome in influenza infection.
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