Toll-like receptors: critical proteins linking innate and acquired immunity
By Shizuo Akira, K. Takeda, T. Kaisho. Nature Immunology, 2001
5,090 citations recorded by the source corpus.
Subfields: Cancer Research, Immunology, Microbiology
View Paper: https://www.semanticscholar.org/paper/af22ab3cc99c0cc01d8b7be23f8c897465a90bb6
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In Cancer Research
In Immunology
- Shizuo Akira
- R. Medzhitov
- Taro Kawai
- O. Takeuchi
- K. Takeda
- Satoshi Uematsu
- Luke A. O'Neill
- B. Beutler
In Microbiology
Citations in the corpus
- Dendritic-cell control of pathogen-driven T-cell polarization (2003, background): “Adaptive immunity to pathogens often starts with the initiation of DC maturation after ligation of TLRs, which, therefore, are crucial proteins that link innate and adaptive immunit”
- Targeting natural killer cells and natural killer T cells in cancer (2012, background): “A recent paradigm shift in our understanding of immunity in mammals has resulted from the discovery of the recognition receptors used by the innate immune system, including the Toll-like receptors (TLRs”
- Helicobacter pylori and Gastric Cancer: Factors That Modulate Disease Risk (2010, background): “A major advance in this field has been the elucidation of the TLRs, which are activated by recognition of pathogenassociated molecular patterns (PAMPs) (6).”
- TLR signaling pathways. (2004, background): “In addition, recent accumulating evidence indicates that TLR signaling pathways consist, at least, of a MyD88-dependent pathway that is common to all TLRs, and a MyD88-independent pathway that is peculiar to the TLR3- and TLR4 signaling pathways [8].”
- TICAM-1, an adaptor molecule that participates in Toll-like receptor 3–mediated interferon-β induction (2003, background): “Ten members of the TLR family (TLR1–10) have been identified in human”
- Interaction between the gut microbiome and mucosal immune system (2017, background): “TLRs are a group of important PRRs play a vital role in the innate immune system [40].”
- NOD2 is a negative regulator of Toll-like receptor 2–mediated T helper type 1 responses (2004, background): “PGN is recognized independently of its MDP or iE-DAP components by cell surface Toll-like receptor 2 (TLR2), and cells that lack TLR2 are refractory to PGN stimulation and fail to show PGN-induced cytokine secretio”