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Oral Combinational Antiretroviral Treatment in HIV-1 Infected Humanized Mice
Published on: October 6, 2022
HIV, Combination Antiretroviral Therapy, and Vascular Diseases in Men and Women
Laszlo Kovacs1, Taylor C Kress1, Eric J Belin de Chantemèle1,2
1Vascular Biology Center, Medical College of Georgia at Augusta University, Augusta, Georgia, USA.
Insights
Combination antiretroviral therapy (cART) increases life expectancy for people with HIV (PLWH) but heightens cardiovascular disease (CVD) risk. Preserving endothelial function is crucial for reducing CVD, especially in women.
Area of Science:
- Cardiovascular Science
- Infectious Disease
- Immunology
Background:
- Combination antiretroviral therapy (cART) has improved longevity for people living with HIV (PLWH).
- Cardiovascular disease (CVD) is now the leading cause of death in PLWH on cART.
- HIV-related CVD risks and manifestations differ by sex, with women facing higher risks.
Purpose of the Study:
- To investigate the etiopathology of CVD in PLWH on cART.
- To clarify the contributions of HIV infection and cART to CVD development.
- To identify key mechanisms underlying CVD risk in this population, particularly endothelial dysfunction.
Main Methods:
- Review of existing literature on HIV, cART, and CVD.
- Analysis of mechanisms contributing to endothelial dysfunction.
- Examination of sex-based differences in CVD manifestations.
Main Results:
- Both HIV infection and cART contribute to endothelial dysfunction, a precursor to atherosclerosis-associated CVD.
- Mechanisms include endothelial cell activation, inflammation, and oxidative stress, reducing nitric oxide bioavailability.
- Women with HIV exhibit distinct and potentially greater risks for CVD compared to men.
Conclusions:
- Endothelial dysfunction is a critical pathway for CVD development in PLWH on cART.
- Targeting endothelial function preservation is essential for mitigating CVD morbidity and mortality.
- Particular attention should be paid to reducing CVD risk in women living with HIV.
Abstract:
Thanks to the advent of combination antiretroviral therapy (cART), people living with human immunodeficiency virus (HIV) (PLWH) experienced a marked increase in life expectancy but are now at higher risk for cardiovascular disease (CVD), the current leading cause of death in PLWH on cART. Although HIV preponderantly affects men over women, manifestations of HIV-related CVD differ by sex with women experiencing greater risks than men. Despite extensive investigation, the etiopathology of CVD, notably the respective contribution of viral infection and cART, remain ill-defined. However, both viral infection and cART have been reported to contribute to endothelial dysfunction, the precursor and major cause of atherosclerosis-associated CVD, through mechanisms involving endothelial cell activation, inflammation, and oxidative stress, all leading to reduced nitric oxide bioavailability. Therefore, preserving endothelial function in PLWH on cART should be a main target to reduce CVD morbidity and mortality, notably in females.
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