HHV-8 reduces dendritic cell migration through down-regulation of cell-surface CCR6 and CCR7 and cytoskeleton

Mara Cirone1, Valeria Conte, Antonella Farina

  • 1Istituto Pasteur-Fondazione Cenci Bolognetti, Department of Experimental Medicine, La Sapienza University, Viale Regina Elena 324, 00161 Rome, Italy. Mara.cirone@uniroma1.it

Virology Journal
|May 16, 2012
PubMed
Abstract

Insights

Human Herpesvirus 8 (HHV-8) inhibits dendritic cell (DC) migration by altering chemokine receptor expression and inducing cytoskeleton changes. This viral interference with DC movement impairs immune responses against infection.

Area of Science:

  • Immunology
  • Virology
  • Cell Biology

Background:

  • Efficient immune responses require dendritic cells (DCs) to migrate to inflammation sites and lymphoid organs, guided by chemokine gradients.
  • Pathogens can evade immune detection by manipulating DC chemokine receptor expression and migration patterns.

Purpose of the Study:

  • To investigate the effect of Human Herpesvirus 8 (HHV-8) on the migratory behavior of immature and mature dendritic cells (DCs).
  • To elucidate the mechanisms by which HHV-8 influences DC migration and immune function.

Main Methods:

  • Analysis of chemokine receptor expression on DCs infected with HHV-8.
  • Assessment of chemokine-induced migration in infected and uninfected DCs.
  • Evaluation of HHV-8's impact on basal DC motility and cytoskeleton.

Main Results:

  • HHV-8 significantly inhibits the migratory behavior of both immature and mature DCs.
  • The virus alters DC chemokine receptor expression, affecting chemokine-induced migration.
  • HHV-8 induces cytoskeleton modifications, interfering with the basal motility of DCs.

Conclusions:

  • HHV-8 subverts dendritic cell migration capacity, representing a novel immune evasion strategy.
  • This disruption of DC migration by HHV-8 contributes to impaired immune functions during viral infection.