% IMPORTANT: The following is UTF-8 encoded.  This means that in the presence
% of non-ASCII characters, it will not work with BibTeX 0.99 or older.
% Instead, you should use an up-to-date BibTeX implementation like “bibtex8” or
% “biber”.

@ARTICLE{Mnz:300306,
      author       = {C. Münz and G. R. Campbell and A. Esclatine and M. Faure
                      and P. Labonte and M. Lussignol and A. Orvedahl and N.
                      Altan-Bonnet and R. Bartenschlager$^*$ and R. Beale and M.
                      Cirone and L. Espert and J. Jung and D. Leib and F. Reggiori
                      and S. Sanyal and S. A. Spector and V. Thiel and C. Viret
                      and Y. Wei and T. Wileman and H. Wodrich},
      title        = {{A}utophagy machinery as exploited by viruses.},
      journal      = {Autophagy reports},
      volume       = {4},
      number       = {1},
      issn         = {2769-4127},
      address      = {London},
      publisher    = {Taylor $\&$ Francis Group},
      reportid     = {DKFZ-2025-00756},
      pages        = {2464986},
      year         = {2025},
      abstract     = {Viruses adapt and modulate cellular pathways to allow their
                      replication in host cells. The catabolic pathway of
                      macroautophagy, for simplicity referred to as autophagy, is
                      no exception. In this review, we discuss anti-viral
                      functions of both autophagy and select components of the
                      autophagy machinery, and how viruses have evaded them. Some
                      viruses use the membrane remodeling ability of the autophagy
                      machinery to build their replication compartments in the
                      cytosol or efficiently egress from cells in a non-lytic
                      fashion. Some of the autophagy machinery components and
                      their remodeled membranes can even be found in viral
                      particles as envelopes or single membranes around virus
                      packages that protect them during spreading and
                      transmission. Therefore, studies on autophagy regulation by
                      viral infections can reveal functions of the autophagy
                      machinery beyond lysosomal degradation of cytosolic
                      constituents. Furthermore, they can also pinpoint molecular
                      interactions with which the autophagy machinery can most
                      efficiently be manipulated, and this may be relevant to
                      develop effective disease treatments based on autophagy
                      modulation.},
      subtyp        = {Review Article},
      keywords     = {Endosomal damage (Other) / interferon (Other) / replication
                      organelle (Other) / secretory autophagy (Other) / virophagy
                      (Other)},
      cin          = {D430},
      ddc          = {610},
      cid          = {I:(DE-He78)D430-20160331},
      pnm          = {314 - Immunologie und Krebs (POF4-314)},
      pid          = {G:(DE-HGF)POF4-314},
      typ          = {PUB:(DE-HGF)16},
      pubmed       = {pmid:40201908},
      pmc          = {pmc:PMC11921968},
      doi          = {10.1080/27694127.2025.2464986},
      url          = {https://inrepo02.dkfz.de/record/300306},
}