MycoBiomDB – Record Details (MyCo_1839)

Biomarker Record Details

Database ID: MyCo_1839
DB IDMyCo_1839
TitleDevelopment of surrogate markers for oral immunisation against Candida albicans
Year2003
PMID12531338
Fungal Diseases involvedOral candidiasis
Associated Medical ConditionNone
GenusCandida
Speciesalbicans
OrganismCandida albicans
Ethical StatementNone
Site of InfectionMouth
Opportunistic invasiveOpportunistic
Sample typeBody fluid
Sample sourceSaliva
Host GroupAnimal
Host Common nameMice
Host Scientific nameMus musculus
Biomarker NameIL-4
Biomarker Full NameInterleukin-4
Biomarker TypeDiagnostic
BiomoleculeProtein
Geographical LocationAustralia
CohortMale BALB/c (H-2d) and DBA/2 mice (H-2d), 6–8 weeks old. Candida albicans isolate 3630 was obtained from the National Reference Laboratory, Royal North Shore Hospital, Sydney, Australia and blastospores collected from Sabouraud dextrose broth by centrifugation, washed and adjusted to 108 blastospores/ml in PBS until use.
Cohort No.None
Age GroupNone
P Valuep<0.05
SensitivityNone
SpecificityNone
Positive Predictive ValueNone
MICNone
Fold ChangeNone
PathwayNone
Disease Introduction MechanismProgress in development of mucosal vaccines has been restricted through a lack of validated surrogate markers of protection to aid in optimising formulation, dose and vaccination strategy. Mucosal candidiasis manifest as stomatitis or vaginitis, is a common and distressing problem, while more extensive upper gastrointestinal candidiasis in immune suppressed subjects predisposes to life threatening invasive disease. Cellular immunity contains mucosal disease, while antibody enhanced phagocytic mechanisms are critical to the outcome of systemic infection. Thus a vaccine to prevent or contain mucosal infection with Candida albicans would be of considerable clinical benefit.
TechniqueELISA
Analysis MethodELISA Based
ELISA kitsELISA Kit (Pharmingen, San Diego, CA)
Assay DataNone
Validation Techniques usedELISA, RT-PCR
Up Regulation Down RegulationIncrease
Sequence DataNone
External LinkNone