ADENOVIRUS-TRIGGERED INNATE SIGNALLING PATHWAYS

被引:32
作者
Fejer, G. [1 ,2 ]
Freudenberg, M. [1 ]
Greber, U. F. [3 ]
Gyory, I. [1 ]
机构
[1] Max Planck Inst Immunobiol & Epigenet, Stubeweg 51, D-79108 Freiburg, Germany
[2] Peninsula Coll Med & Dent, Plymouth, Devon, England
[3] Univ Zurich, Inst Mol Life Sci, Zurich, Switzerland
来源
EUROPEAN JOURNAL OF MICROBIOLOGY AND IMMUNOLOGY | 2011年 / 1卷 / 04期
关键词
adenovirus; viral entry; endosomal escape; innate response; Toll-like receptors; type-I interferons; IL-1; IRF7;
D O I
10.1556/EuJMI.1.2011.4.3
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Adenoviruses are important infectious agents and also emerging vectors in different biomedical applications. These viruses elicit a strong innate and adaptive immune response, which influences both the course of disease and the success of the applied vectors. Several Toll-like Receptor (TLR)-dependent and -independent mechanisms contribute to these responses. Understanding of the involved viral and cellular factors is crucial for the treatment of various adenovirus diseases and the optimal design of adenovirus vector applications. Here we summarize our current understanding of the complex nature of adenovirus-induced innate immune mechanisms.
引用
收藏
页码:279 / 288
页数:10
相关论文
共 106 条
[1]   Adenovirus serotype 5 infects human dendritic cells via a coxsackievirus-adenovirus receptor-independent receptor pathway mediated by lactoferrin and DC-SIGN [J].
Adams, William C. ;
Bond, Emily ;
Havenga, Menzo J. E. ;
Holterman, Lennart ;
Goudsmit, Jaap ;
Hedestam, Gunilla B. Karlsson ;
Koup, Richard A. ;
Lore, Karin .
JOURNAL OF GENERAL VIROLOGY, 2009, 90 :1600-1610
[2]   Subversion of CtBP1-controlled macropinocytosis by human adenovirus serotype 3 [J].
Amstutz, Beat ;
Gastaldelli, Michele ;
Kalin, Stefan ;
Imelli, Nicola ;
Boucke, Karin ;
Wandeler, Eliane ;
Mercer, Jason ;
Hemmi, Silvio ;
Greber, Urs F. .
EMBO JOURNAL, 2008, 27 (07) :956-969
[3]   Adenovirus vector-induced innate inflammatory mediators, MAPK signaling, as well as adaptive immune responses are dependent upon both TLR2 and TLR9 in vivo [J].
Appledorn, Daniel M. ;
Patial, Sonika ;
McBride, Aaron ;
Godbehere, Sarah ;
Van Rooijen, Nico ;
Parameswaran, Narayanan ;
Amalfitano, Andrea .
JOURNAL OF IMMUNOLOGY, 2008, 181 (03) :2134-2144
[4]   Adenovirus type 37 uses sialic acid as a cellular receptor on Chang C cells [J].
Arnberg, N ;
Pring-Åkerblom, P ;
Wadell, G .
JOURNAL OF VIROLOGY, 2002, 76 (17) :8834-8841
[5]   Current strategies and future directions for eluding adenoviral vector immunity [J].
Bangari, Dinesh S. ;
Mittal, Suresh K. .
CURRENT GENE THERAPY, 2006, 6 (02) :215-226
[6]   Isolation of a common receptor for coxsackie B viruses and adenoviruses 2 and 5 [J].
Bergelson, JM ;
Cunningham, JA ;
Droguett, G ;
KurtJones, EA ;
Krithivas, A ;
Hong, JS ;
Horwitz, MS ;
Crowell, RL ;
Finberg, RW .
SCIENCE, 1997, 275 (5304) :1320-1323
[7]   Intracellular Toll-like Receptors [J].
Blasius, Amanda L. ;
Beutler, Bruce .
IMMUNITY, 2010, 32 (03) :305-315
[8]   Adenovirus type 7 induces interleukin-8 in a lung slice model and requires activation of Erk [J].
Booth, JL ;
Coggeshall, KM ;
Gordon, BE ;
Metcalf, JP .
JOURNAL OF VIROLOGY, 2004, 78 (08) :4156-4164
[9]   Opening of size-selective pores in endosomes during human rhinovirus serotype 2 in vivo uncoating monitored by single-organelle flow analysis [J].
Brabec, M ;
Schober, D ;
Wagner, E ;
Bayer, N ;
Murphy, RF ;
Blaas, D ;
Fuchs, R .
JOURNAL OF VIROLOGY, 2005, 79 (02) :1008-1016
[10]   Adenovirus Transport via Direct Interaction of Cytoplasmic Dynein with the Viral Capsid Hexon Subunit [J].
Bremner, K. Helen ;
Scherer, Julian ;
Yi, Julie ;
Vershinin, Michael ;
Gross, Steven P. ;
Vallee, Richard B. .
CELL HOST & MICROBE, 2009, 6 (06) :523-535