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ROS Chronicles in HIV Infection: Genesis of Oxidative Stress, Associated Pathologies, and Therapeutic Strategies
R Harshithkumar1, Prachibahen Shah1, Pratiksha Jadaun1
1Division of Virology, ICMR-National Institute of Translational Virology and AIDS Research, Pune 411026, India.
Reactive oxygen species (ROS) cause oxidative stress (OS) in HIV infection, impacting viral replication and disease progression. Antioxidant therapies show promise but require further research for managing ART-related toxicities.
Area of Science:
- Biochemistry
- Immunology
- Virology
Background:
- Reactive oxygen species (ROS) are crucial signaling molecules, but excess ROS cause oxidative stress (OS).
- OS is increasingly implicated in HIV pathogenesis and associated comorbidities.
- ROS have dual roles in HIV infection, potentially triggering antiviral responses or promoting viral replication.
Purpose of the Study:
- To review mechanisms of OS generation in HIV infection.
- To explore the roles of viral proteins and antiretroviral therapy (ART) in HIV-associated OS.
- To discuss the implications of OS in HIV comorbidities and potential antioxidant interventions.
Main Methods:
- Literature review of studies on ROS, OS, and HIV.
- Analysis of viral protein contributions to ROS production.
- Examination of ART-induced OS and its pathological consequences.
Main Results:
- HIV infection, particularly through viral protein Tat and other viral proteins, significantly increases endogenous ROS production.
- ART can also contribute to OS, exacerbating pathologies in HIV-infected individuals.
- HIV patients exhibit compromised antioxidant defense systems.
Conclusions:
- OS is a key factor in HIV pathogenesis, comorbidities, and ART toxicity.
- Antioxidant therapy is a potential intervention strategy.
- Further research is needed to develop strategies mitigating ART-induced OS.
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