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Sequencing of Bacterial Microflora in Peripheral Blood: our Experience with HIV-infected Patients
Published on: June 11, 2011
Microbial translocation, immune activation, and HIV disease
Nichole R Klatt1, Nicholas T Funderburg, Jason M Brenchley
1Laboratory of Molecular Microbiology, Program in Barrier Immunity and Repair, National Institute of Allergy and Infectious Diseases (NIAID), National Institutes of Health, Bethesda, MD, USA.
Combination antiretroviral therapy (cART) improves human immunodeficiency virus (HIV) prognosis but persistent inflammation and microbial translocation contribute to increased mortality in treated individuals.
Area of Science:
- Immunology
- Virology
- Gastroenterology
Background:
- Combination antiretroviral therapy (cART) has improved human immunodeficiency virus (HIV) outcomes.
- Long-term cART treatment is associated with increased mortality in HIV-infected individuals.
- Persistent inflammation despite undetectable viremia contributes to this increased mortality.
Purpose of the Study:
- To review the mechanisms of microbial translocation in HIV infection.
- To elucidate the role of microbial translocation in immune activation and disease progression.
Main Methods:
- Literature review of studies on microbial translocation and HIV.
- Analysis of mechanisms linking gut barrier dysfunction to immune activation.
Main Results:
- Microbial translocation, the passage of microbial products from the gut, contributes to persistent immune activation.
- This immune activation is linked to increased mortality in cART-treated HIV-infected individuals.
- Chronic inflammation is a key factor in disease progression.
Conclusions:
- Microbial translocation is a significant factor in persistent immune activation and increased mortality in HIV infection.
- Targeting microbial translocation may offer new therapeutic strategies for HIV management.
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