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Inhibitors of Viral Protein Synthesis01:30

Inhibitors of Viral Protein Synthesis

Protein synthesis is indispensable for viral replication, as viruses lack the cellular machinery required for this process and must hijack the host's translational apparatus. In response, host cells deploy a critical innate immune defense involving interferons, specialized cytokines that play a central role in inhibiting viral propagation.Upon viral detection, infected cells release interferons that bind to receptors on adjacent uninfected cells, activating the JAK-STAT signaling pathway and...

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Isolation, Transfection, and Culture of Primary Human Monocytes
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Published on: December 16, 2019

A peripheral monocyte interferon phenotype in HIV infection correlates with a decrease in magnetic resonance

Lynn Pulliam1, Hans Rempel, Bing Sun

  • 1Department of Laboratory Medicine, Veterans Affairs Medical Center, San Francisco, 94121, USA. lynn.pulliam@ucsf.edu

AIDS (London, England)
|July 14, 2011
PubMed
Summary
This summary is machine-generated.

Peripheral immune activation, driven by interferon (IFN), is linked to brain injury and cognitive issues in people with HIV. Blood markers of IFN response may help track early neural damage in HIV patients.

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Area of Science:

  • Neuroimmunology
  • Infectious Diseases
  • Neuroscience

Background:

  • Cognitive impairment affects over 35% of individuals with HIV, despite effective antiretroviral therapy (ART).
  • The relationship between peripheral immune activation and brain metabolite changes in HIV remains under investigation.

Purpose of the Study:

  • To investigate the link between peripheral immune activation and brain metabolite concentrations in HIV-infected individuals.
  • To explore the correlation between monocyte gene expression, cognitive status, and brain metabolite levels.

Main Methods:

  • Cross-sectional study of 35 HIV-positive and 8 HIV-negative adults on ART or treatment interruption.
  • Monocyte gene expression, cognitive function, and brain metabolite concentrations (N-acetylaspartate) in frontal white matter, anterior cingulate cortex, and basal ganglia were assessed using 4-Tesla proton magnetic resonance spectroscopy.
  • Correlations between metabolite concentrations, monocyte gene expression, and cognitive deficit scores were analyzed.

Main Results:

  • Monocyte gene expression revealed an interferon (IFN)-α-induced activation phenotype, with IFN genes showing the highest fold increase in HIV+ individuals.
  • Monocyte activation strongly correlated with reduced N-acetylaspartate (NAA) in the frontal white matter (FWM).
  • Plasma levels of IFN-γ inducible protein-10 (IP-10), an IFN-response gene, correlated inversely with ACC NAA, which was lower in HIV+ patients with mild cognitive impairment.

Conclusions:

  • Chronic peripheral immune activation, specifically a type 1 IFN response, is associated with neuronal injury in the FWM and ACC, contributing to cognitive dysfunction in HIV.
  • IFN-induced blood markers may serve as clinically relevant indicators for monitoring early neural damage in HIV patients.