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Oral Combinational Antiretroviral Treatment in HIV-1 Infected Humanized Mice
Published on: October 6, 2022
The effects of untreated and treated HIV infection on bone disease
Aoife G Cotter1, Patrick W G Mallon
1aHIV Molecular Research Group, School of Medicine & Medical Science, University College Dublin bDepartment of Infectious Diseases, Mater Misericordiae University Hospital, Dublin, Ireland.
Insights
Low bone mineral density (BMD) is common in people with HIV. Earlier antiretroviral therapy (ART) initiation may help preserve BMD by mitigating immune and viral effects on bone metabolism.
Area of Science:
- Bone metabolism and HIV research
- Immunology and virology
- Antiretroviral therapy (ART) effects
Background:
- Low bone mineral density (BMD) is prevalent in individuals with HIV, linked to increased bone turnover and fracture risk.
- This review examines the mechanisms behind low BMD in HIV, considering its relationship with HIV infection, immune status, and ART.
- Understanding these factors is crucial for managing bone health in the HIV population.
Purpose of the Study:
- To review the underlying mechanisms of low bone mineral density (BMD) in HIV.
- To explore the relationship between low BMD, HIV infection, immune dysfunction, and antiretroviral therapy (ART).
- To propose strategies for mitigating BMD loss in HIV patients.
Main Methods:
- Literature review of studies on BMD in HIV patients.
- Analysis of the impact of HIV viremia and immune status on BMD.
- Examination of the role of antiretroviral therapy (ART) in bone metabolism.
Main Results:
- Significant BMD reductions observed with decreasing HIV viral load during ART initiation.
- Evidence suggests immune- or viral-mediated mechanisms contribute to low BMD pathogenesis.
- ART initiation is associated with changes in BMD, highlighting the interplay between treatment and bone health.
Conclusions:
- Bone metabolism is influenced by T cells and B cells, suggesting immune system involvement in BMD regulation.
- Earlier ART initiation at higher CD4 T-cell counts may prevent BMD loss by reducing immune and viral disturbances.
- Further research is needed to elucidate the complex interactions between HIV, the immune system, ART, and bone metabolism.
Purpose Of Review:
Low bone mineral density (BMD) is common in those with HIV, associated with higher bone turnover and a higher prevalence of fractures. This review explores low BMD in HIV, focusing on underlying mechanisms and relationships between low BMD and HIV infection, immune dysfunction, and antiretroviral therapy (ART).
Recent Findings:
Greater reductions in BMD accompanying reductions in HIV viremia at initiation of first-line or second-line ART suggest an important role for immune- or viral-mediated mechanisms in its pathogenesis.
Summary:
As bone metabolism is part-regulated by T cells and B cells, we propose that earlier initiation of ART at higher CD4 T-cell counts may attenuate BMD loss by abrogating immune- and viral-mediated disturbances in bone metabolism that accompany ART initiation. Further pathogenesis-based research is required in this field, focusing on the complex interaction between virus, immune system, ART, and bone metabolism.
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