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Get Free AccessLoxoribine (7‐allyl‐7,8‐dihydro‐8‐oxo‐guanosine) acts as synthetic adjuvant in anti‐tumor responses. Here we first demonstrate that loxoribine activates cells of the innate immune system selectively via the Toll‐like receptor (TLR) 7/MyD88‐dependent signaling pathway. TLR7‐ and MyD88‐deficient immune cells fail to proliferate or produce cytokines in response to loxoribine, and genetic complementation of TLR7‐deficient cells with murine or human TLR7 confers responsiveness. Subsequently we show that cellular activation by loxoribine and resiquimod (R‐848), a stimulus for TLR7 and TLR8, depends on acidification and maturation of endosomes and targets MyD88 to vesicular structures with lysosomal characteristics. This mode of TLR7 and TLR8 action resembles CpG‐DNA‐driven TLR9 activation. We thus conclude that TLR7, 8 and 9 form a functional subgroup within the TLR family that recognizes pathogen‐associated molecular patterns in endosomal/lysosomal compartments.
Florian Heil, Parviz Ahmad‐Nejad, Hiroaki Hemmi, Hubertus Hochrein, Franziska Ampenberger, Tanja Gellert, Harald Dietrich, Grayson B. Lipford, Kiyoshi Takeda, Akira Shizuo, Hermann Wagner, Stefan Bauer (2003). The Toll‐like receptor 7 (TLR7)‐specific stimulus loxoribine uncovers a strong relationship within the TLR7, 8 and 9 subfamily. European Journal of Immunology, 33(11), pp. 2987-2997, DOI: 10.1002/eji.200324238.
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Type
Article
Year
2003
Authors
12
Datasets
0
Total Files
0
Language
English
Journal
European Journal of Immunology
DOI
10.1002/eji.200324238
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