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Updated: Aug 15, 2025

Isolation, Transfection, and Culture of Primary Human Monocytes
Published on: December 16, 2019
Cardiac strain is lower among women with HIV in relation to monocyte activation
Mabel Toribio1, Magid Awadalla2, Zsofia D Drobni2
1Division of Endocrinology, Metabolism Unit, Massachusetts General Hospital and Harvard Medical School, Boston, MA, United States of America.
Insights
Women with HIV (WWH) show reduced left ventricular systolic function, indicated by lower global longitudinal strain (GLS). Inflammatory monocyte activation is linked to this dysfunction, suggesting a potential therapeutic target for heart failure prevention.
Area of Science:
- Cardiology
- Immunology
- Infectious Diseases
Background:
- Women with HIV (WWH) have an increased risk of heart failure.
- Understanding the immune and inflammatory pathways contributing to left ventricular (LV) systolic dysfunction in WWH is crucial but limited.
Purpose of the Study:
- To investigate the relationship between global longitudinal strain (GLS), a measure of LV systolic function, and monocyte activation in WWH.
- To explore potential immune pathways involved in cardiac dysfunction among WWH.
Main Methods:
- Cardiovascular magnetic resonance imaging was used to assess GLS.
- Flow cytometry was employed to measure monocyte activation.
- The study included 20 WWH and 14 women without HIV.
Main Results:
- WWH exhibited significantly lower GLS compared to women without HIV (19.4±3.0% vs. 23.1±1.9%, P<0.0001).
- HIV status independently predicted lower GLS.
- In WWH, lower GLS correlated with increased expression of HLA-DR on CD14+CD16+ monocytes and was predicted by inflammatory monocyte activation, even after adjusting for CD4+ T-cell count and viral load.
Conclusions:
- Inflammatory monocyte activation is associated with reduced LV systolic function in WWH.
- Further research is needed to confirm the role of inflammatory monocyte activation in the pathogenesis of lower GLS.
- Targeting inflammatory pathways may offer a strategy to mitigate heart failure risks in WWH.
Background:
Women with HIV (WWH) face heightened risks of heart failure; however, insights on immune/inflammatory pathways potentially contributing to left ventricular (LV) systolic dysfunction among WWH remain limited.
Setting:
Massachusetts General Hospital, Boston, Massachusetts.
Methods:
Global longitudinal strain (GLS) is a sensitive measure of LV systolic function, with lower cardiac strain predicting incident heart failure and adverse heart failure outcomes. We analyzed relationships between GLS (cardiovascular magnetic resonance imaging) and monocyte activation (flow cytometry) among 20 WWH and 14 women without HIV.
Results:
WWH had lower GLS compared to women without HIV (WWH vs. women without HIV: 19.4±3.0 vs. 23.1±1.9%, P<0.0001). Among the whole group, HIV status was an independent predictor of lower GLS. Among WWH (but not among women without HIV), lower GLS related to a higher density of expression of HLA-DR on the surface of CD14+CD16+ monocytes (ρ = -0.45, P = 0.0475). Further, among WWH, inflammatory monocyte activation predicted lower GLS, even after controlling for CD4+ T-cell count and HIV viral load.
Conclusions:
Additional studies among WWH are needed to examine the role of inflammatory monocyte activation in the pathogenesis of lower GLS and to determine whether targeting this immune pathway may mitigate risks of heart failure and/or adverse heart failure outcomes.
Trial Registration:
Clinical trials.gov registration: NCT02874703.
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