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TRIF signaling is essential for TLR4-driven IgE class switching

The TLR4 ligand LPS causes mouse B cells to undergo IgE and IgG1 isotype switching in the presence of IL-4. TLR4 activates two signaling pathways mediated by the adaptor molecules MyD88 and TRAM, which recruits TRIF. Following stimulation with LPS+IL-4, Tram(−/−) and Trif(−/−) B cells completely fai...

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Autores principales: Janssen, Erin, Ozcan, Esra, Liadaki, Kyriaki, Jabara, Haifa H., Manis, John, Ullas, Sumana, Akira, Shizuo, Fitzgerald, Katherine, Golenbock, Douglas, Geha, Raif S.
Formato: Artigo
Lenguaje:Inglês
Publicado: 2014
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Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC3952935/
https://ncbi.nlm.nih.gov/pubmed/24532577
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4049/jimmunol.1300909
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