INT181526
From wiki-pain
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Sentences Mentioned In
Key: | Protein | Mutation | Event | Anatomy | Negation | Speculation | Pain term | Disease term |
-/- mice is less likely to be mediated by lack of upregulation of costimulatory molecules on APCs as we have previously reported that these mice have upregulated B7.1/2 on APCs[19]. | |||||||||||||||
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It was also shown that CpG stimulate T cells by inducing APCs to synthesize IFN-I, which then act directly on T cells via IFNAR[37]. | |||||||||||||||
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-/- mice is less likely to be mediated by lack of upregulation of costimulatory molecules on APCs as we have previously reported that these mice have upregulated B7.1/2 on APCs[19]. | |||||||||||||||
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-/- mice is less likely to be mediated by lack of upregulation of costimulatory molecules on APCs as we have previously reported that these mice have upregulated B7.1/2 on APCs[19]. | |||||||||||||||
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Second, total body irradiation as well as the absence of Tregs may result in the generalized activation of APCs [15], [16]. | |||||||||||||||
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LPS, major outer membrane constituent of Gram-negative bacteria, stimulates APCs through TLR4, induces high levels of pro-inflammatory cytokines and usually leads to a strong Th1 response (38). | |||||||||||||||
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Activation of TLRs is necessary for optimal activation of APCs to initiate and polarize adaptive immune responses against invading pathogens [56,57]. | |||||||||||||||
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The increase in VSV-specific CD8+ cells observed with VV-hTAP1,2 coinfections indicates a TAP-dependent increase in APC cross-priming and cross-presentation activity and is explained by an increase in TAP expression and peptide-transport activity in the APCs of the spleen. | |||||||||||||||
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More appropriately, the pathway is now recognized as a mechanism to activate APCs and to enhance their potential to activate T cells. | |||||||||||||||
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In contrast, CD80 and CD86 are inducible on DCs and other APCs upon stimulation. | |||||||||||||||
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To derive average connection strength per neuron (qcon), the number of excited neurons needs to be estimated, based on the excitability (SAP), neuron density (? | |||||||||||||||
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include a number of acute phase genes such as fibrinogen, serum amyloid P-component, lipocalin 2, metallothioneins, and serum amyloid A2, which were shown to be suppressed by the PPAR? | |||||||||||||||
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Many cytokines can be produced by activated APCs, and these can either be pro- or anti-inflammatory [33, 34, 69]. | |||||||||||||||
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