MycoBiomDB – Record Details (MyCo_4863)

Biomarker Record Details

Database ID: MyCo_4863
DB IDMyCo_4863
TitleDivergent neuroimmune signatures in the cerebrospinal fluid predict differential gender-specific survival among patients with HIV-associated cryptococcal meningitis
Year2023
PMID38152404
Fungal Diseases involvedCryptococcal meningitis
Associated Medical ConditionHIV-AIDS
GenusCryptococcus
Speciesneoformans
OrganismCryptococcus neoformans
Ethical StatementThe studies involving humans were approved by Makerere University, School of Biomedical Sciences, College of Healt Sciences, Higher Degrees Research, and Ethics Committee. The studies were conducted in accordance with the local legislation and institutional requirements.
Site of InfectionNone
Opportunistic invasiveNone
Sample typeBody fluid
Sample sourceCerebrospinal fluid (CSF)
Host GroupHuman
Host Common nameHuman
Host Scientific nameHomo sapiens
Biomarker NameCCL11
Biomarker Full NameCCL11
Biomarker TypeDiagnostic
BiomoleculeProtein
Geographical LocationUganda
CohortWe considered baseline clinical features, CSF cryptococcal fungal burden, and CSF neuroimmune signatures with survival at 18 weeks among 419 consenting adults by“gender” (168 women and 251 men by biological sex de ned at birth).
Cohort No.419
Age GroupNone
P Valuep=0.001
SensitivityNone
SpecificityNone
Positive Predictive ValueNone
MICNone
Fold ChangeNone
PathwayNone
Disease Introduction MechanismCo-infection with the fungus Cryptococcus neoformans remains an important contributor to death among people with advanced HIV/ AIDS worldwide, despite the use of antifungal medications. Mortality with HIV-associated cryptococcal meningitis (CM) varies by location based on existing HIV prevalence. In Europe and North America, with the low prevalence of people with HIV, both the incidence and mortality rates of CM are lowest. In contrast, in low- and middle-income countries, especially in Africa, the prevalence, incidence, and mortality with both HIV and CM are high. In Uganda, Botswana, and South Africa, the 10-week mortality rates approach 50% even in closely monitored research settings, with deaths occurring within days to weeks and, sometimes, up to months after diagnosis. These observations emphasize the importance of characterizing early immune response as a possible intervention to control fungal infection in improving survival.
TechniqueImmunological assay
Analysis MethodLuminex cytokine and chemokine immunophenotyping
ELISA kitsNone
Assay DataNone
Validation Techniques usedLuminex cytokine and chemokine immunophenotyping
Up Regulation Down RegulationIncrease
Sequence DataNone
External LinkNone