INT186804
From wiki-pain
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Sentences Mentioned In
Key: | Protein | Mutation | Event | Anatomy | Negation | Speculation | Pain term | Disease term |
TLR3 recognizes RNA and viruses, whereas TLR4 mediates the response to bacterial endotoxins and is activated due to sterile inflammation [33,34]. | |||||||||||||||
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Concerning protein localization, we found TLR3 and TLR4 proteins in glandular and epithelial cells of endometriosis patients.
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In undifferentiated G3 carcinoma, staining for TLR3 (figure 6E) and TLR4 (figure 6J) was not detectable, strengthening our findings of low TLR3 and TLR4 mRNA abundance in G3 carcinoma (figure 5B). | |||||||||||||||
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It might be that the increase in immunoreactivity for TLR2, TLR3 and TLR4 seen after allergen challenge only persists for a limited period of time. | |||||||||||||||
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Immunoreactivity for TLR3 was 1.39 ± 0.44 in controls (n = 9), 0.64 ± 0.25 in patients before allergen challenge (n = 11) and 2.22 ± 0.79 in patients after allergen challenge (n = 11). | |||||||||||||||
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TLR3, TLR8 and TLR9 are recognized by virus-derived double stranded RNA (poly-I:C), virus-derived single stranded RNA (ssRNA) and unmethylated CpG motifs, respectively. | |||||||||||||||
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Polyriboinosinic-polyribocytoidylic acid (poly I:C), a synthetic double-stranded RNA (dsRNA), is recognized by TLR3 and other intracellular receptors. | |||||||||||||||
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Moreover, TLR3 recognizes double-stranded (ds) RNA, assumed to be released by viral killing of cells. | |||||||||||||||
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The TLR3 ligation induced a MDC maturation profile with upregulation of the markers; CD40, CD83, CD86, CCR7, PDL-1, and downregulation of ICOSL, B7H3, and CCR5 (Figure 9). | |||||||||||||||
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The host innate immune Toll-like receptor 3 (TLR3) was shown previously in cells of myeloid origin to recognize the viral replicative, intermediate double-stranded RNA (dsRNA). | |||||||||||||||
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Double-stranded HCV RNA is also recognized by TLR-3, which activates IKKe/TBK-1, via TRIF (TIR-domain-containing adapter-inducing interferon-?) | |||||||||||||||
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Poly I:C12U, another analogue, is less toxic but also less stable in vivo than poly I:C, and TLR3 is essential for its recognition. | |||||||||||||||
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The host innate immune Toll-like receptor 3 (TLR3) was shown previously in cells of myeloid origin to recognize the viral replicative, intermediate double-stranded RNA (dsRNA). | |||||||||||||||
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The dsRNA binding to TLR3, mimicked in vitro by incubation with polyinosine-polycytidylic acid [Poly (I:C)], leads not only to the induction of inflammatory responses but also to the development of antigen-specific adaptive immunity [40]. | |||||||||||||||
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They can be recognized by both TLR3 [18] and the melanoma differentiation-associated gene-5 (MDA-5) [19], pattern recognition receptors that are expressed by many cell types and are involved in anti-viral immune responses [20]. | |||||||||||||||
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