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Isolation, Transfection, and Culture of Primary Human Monocytes
Published on: December 16, 2019
Higher circulating intermediate monocytes are associated with cognitive function in women with HIV
Rebecca T Veenhuis1, Dionna W Williams1,2, Erin N Shirk1
1Department of Molecular and Comparative Biology.
Insights
Higher intermediate monocyte levels in people with HIV (PWH) correlate with poorer neuropsychiatric function, suggesting a potential blood-based biomarker for cognitive decline in virally suppressed individuals.
Area of Science:
- Neuroscience
- Immunology
- Infectious Diseases
Background:
- Identifying biomarkers for neuropsychiatric dysfunction in people with HIV (PWH) is crucial.
- Monocytes are implicated in HIV-related central nervous system (CNS) dysfunction.
- Previous studies have not investigated blood monocyte subsets as predictors of neuropsychiatric function in virally suppressed PWH.
Purpose of the Study:
- To examine the association between blood monocyte subsets and neuropsychiatric function in virologically suppressed women with HIV (vsWWH).
- To determine if monocyte subsets can serve as a predictive biomarker for cognitive outcomes.
Main Methods:
- Two independent cohorts of vsWWH (n=25 and n=18) were studied.
- Whole blood samples were analyzed using flow cytometry to assess immune cell subsets.
- Neuropsychiatric assessments included a cognitive test battery and symptom questionnaires.
Main Results:
- A higher proportion of intermediate monocytes (CD14+CD16+) was associated with lower global cognitive function, executive function, and processing speed.
- This association was observed both concurrently and predictively (1 year prior) to neuropsychiatric testing.
- Higher classical monocyte proportions correlated with better cognitive performance, while no associations were found with depression or stress symptoms.
Conclusions:
- Blood intermediate monocyte percentage is a potential blood-based biomarker for cognitive dysfunction in vsWWH.
- This finding offers a novel, easily measurable indicator for monitoring neuroHIV-related cognitive changes.
- Further research can validate these monocytes subsets as predictive biomarkers in neuroHIV.
Abstract:
BACKGROUNDIdentifying a quantitative biomarker of neuropsychiatric dysfunction in people with HIV (PWH) remains a significant challenge in the neuroHIV field. The strongest evidence to date implicates the role of monocytes in central nervous system (CNS) dysfunction in HIV, yet no study has examined monocyte subsets in blood as a correlate and/or predictor of neuropsychiatric function in virally suppressed PWH.METHODSIn 2 independent cohorts of virologically suppressed women with HIV (vsWWH; n = 25 and n = 18), whole blood samples were obtained either in conjunction with neuropsychiatric assessments (neuropsychological [NP] test battery, self-report depression and stress-related symptom questionnaires) or 1 year prior to assessments. Immune cell subsets were assessed by flow cytometry.RESULTSA higher proportion of intermediate monocytes (CD14+CD16+) was associated with lower global NP function when assessing monocytes concurrently and approximately 1 year before (predictive) NP testing. The same pattern was seen for executive function (mental flexibility) and processing speed. Conversely, there were no associations with monocyte subsets and depression or stress-related symptoms. Additionally, we found that a higher proportion of classical monocytes was associated with better cognition.CONCLUSIONAlthough it is widely accepted that lentiviral infection of the CNS targets cells of monocyte-macrophage-microglial lineage and is associated with an increase in intermediate monocytes in the blood and monocyte migration into the brain, the percentage of intermediate monocytes in blood of vsWWH has not been associated with neuropsychiatric outcomes. Our findings provide evidence for a new, easily measured, blood-based cognitive biomarker in vsWWH.FUNDINGR01-MH113512, R01-MH113512-S, P30-AI094189, R01-MH112391, R01-AI127142, R00-DA044838, U01-AI35004, and P30-MH075673.
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