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Beclin-1 Targeting for Viral Immune Escape

Journal

VIRUSES-BASEL
Volume 3, Issue 7, Pages 1166-1178

Publisher

MDPI AG
DOI: 10.3390/v3071166

Keywords

autophagy; influenza virus; HIV; HSV; KSHV; immunity; immune evasion

Categories

Funding

  1. National Cancer Institute [R01CA108609]
  2. Cancer Research Switzerland [KFS-02652-08-2010]
  3. Association for International Cancer Research [11-0516]
  4. Sassella Foundation [10/02]
  5. Vontobel Foundation
  6. Swiss National Science Foundation [310030_126995]

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Macroautophagy is a catabolic pathway in eukaryotic cells that has recently been shown to facilitate pathogen detection, pathogen restriction and pathogen-derived antigen presentation to CD4(+) T cells. Due to these protective functions during immune responses, several pathogens, including RNA and DNA viruses, have developed strategies to inhibit autophagosome generation or maturation. Interestingly, most of the respective viral proteins exert these functions via binding to Beclin-1, an essential macroautophagy protein that constitutes part of the phosphatidylinositol-3 kinase complexes that mark membranes for autophagosome generation and facilitate autophagosome fusion with lyososomes. The viruses that inhibit macroautophagy by this pathway include herpesviruses, HIV and influenza A virus. Inhibition either before or after autophagosome formation seems to benefit their viral replication by different mechanisms, which are discussed here.

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