MycoBiomDB – Record Details (MyCo_3484)

Biomarker Record Details

Database ID: MyCo_3484
DB IDMyCo_3484
TitleT-cell dysfunction as a potential contributing factor in post-COVID-19 mucormycosis
Year2022
PMID36305225
Fungal Diseases involvedMucormycosis
Associated Medical ConditionCOVID-19
GenusNone
SpeciesNone
OrganismNone
Ethical StatementEthical approval was taken by the Institutional Ethics Committee, King George's Medical University, Lucknow, India.
Site of InfectionNone
Opportunistic invasiveInvasive/Opportunistic
Sample typeBody fluid
Sample sourceBlood
Host GroupHuman
Host Common nameHuman
Host Scientific nameHomo sapiens
Biomarker NameCD8+ CD69+ (% CD8+)
Biomarker Full NameCD8+ CD69+ (% CD8+)
Biomarker TypeDiagnostic
BiomoleculeProtein
Geographical LocationIndia
CohortThe study included thirteen patients each of histopathologically proven post-¬ COVID mucor and non-¬ COVID mucor respectively. Fifteen age and sex matched healthy individual (HI) were also included as control. The study included histopathologically confirmed cases of mucor (13 post-¬ COVID, 13 non-¬ COVID) and 15 healthy individuals (HI).
Cohort No.26 patients and 15 control
Age GroupNone
P Valuep=.001
SensitivityNone
SpecificityNone
Positive Predictive ValueNone
MICNone
Fold ChangeNone
PathwayNone
Disease Introduction MechanismMucormycosis is an invasive fungal disease caused by inhalation of sporangiospores of order mucorales. It is distributed worldwide and associated with the increased morbidity and mortality. The exact prevalence of mucor in India is unknown but the estimated disease burden is approximately 70 times higher than the global prevalence. The most common causative agent is Rhizopus arrhizus (also known as oryzae) and less common are Lichtheimia, Apophysomyces, Rhizomucor and Cunninghamella.
TechniqueAnalytic
Analysis MethodFlow Cytometry Analysis
ELISA kitsNone
Assay DataNone
Validation Techniques usedFlow Cytometry Analysis
Up Regulation Down RegulationPositive
Sequence DataNone
External LinkNone