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Isolation of Adipose Tissue Immune Cells
Published on: May 22, 2013
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Adipose Tissue in HIV Infection.
1Division of Infectious Diseases, Vanderbilt University School of Medicine, Nashville, Tennessee, USA.
Comprehensive Physiology
|September 16, 2017
Summary
HIV infection and antiretroviral therapy (ART) impact fat cells, altering tissue distribution and energy storage. Newer ART drugs show fewer adverse effects on adipocytes compared to older ones.
Area of Science:
- Adipose tissue biology
- Immunology
- Virology
Background:
- HIV infection and ART significantly affect adipose tissue quantity, distribution, and energy storage.
- HIV-associated lipodystrophy involves altered adipose tissue morphology and gene expression.
- HIV viral proteins and ART drugs can impair adipocyte maturation and function.
Purpose of the Study:
- To synthesize current literature on how HIV, ART, and host factors influence adipose tissue.
- To examine the effects on adipose tissue distribution, immunology, and metabolic health.
- To review impacts on adipocyte maturation, cellular regulation, and energy storage.
Main Methods:
- Literature review and synthesis.
- Analysis of gene expression and cellular morphology changes in adipocytes.
- Examination of immunological alterations in adipose tissue.
Main Results:
- HIV and ART alter adipose tissue morphology, gene expression (e.g., PPAR-γ), and cytokine signaling.
- Early ART drugs exhibited significant adipocyte toxicity; newer agents appear safer.
- HIV infection affects T cell balance and macrophage activation in adipose tissue, potentially creating a viral reservoir.
Conclusions:
- HIV and ART profoundly impact adipose tissue, influencing metabolic health and body composition.
- Understanding these interactions is crucial for managing HIV patients.
- Adipose tissue serves as a site for viral persistence and immune modulation in HIV infection.

