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Abcam
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Image Search Results
Journal: Allergy, Asthma, and Clinical Immunology : Official Journal of the Canadian Society of Allergy and Clinical Immunology
Article Title: T-cell phenotypes in chronic rhinosinusitis with nasal polyps in Japanese patients
doi: 10.1186/s13223-015-0100-2
Figure Lengend Snippet: The number of inflammatory cells, expression of cytokines and transcription factors in normalized relative quantities (NRQ), described as median (IQR) in the tissue of nasal polyps of ECRS and non-ECRS patients, and normal controls
Article Snippet: The following primary antibodies were used for identifying inflammatory cells in the specimens: anti-CD3 (rabbit monoclonal, clone SP7; Nichirei, Tokyo, Japan),
Techniques: Expressing
Journal: Allergy, Asthma, and Clinical Immunology : Official Journal of the Canadian Society of Allergy and Clinical Immunology
Article Title: T-cell phenotypes in chronic rhinosinusitis with nasal polyps in Japanese patients
doi: 10.1186/s13223-015-0100-2
Figure Lengend Snippet: Photomicrographs showing immunohistochemical staining for CD3 (T-cells; a ), FOXP3 ( b ), CD4 ( c ) and CD8 ( d ) in non-ECRS polyps. Scale bar 100 μm
Article Snippet: The following primary antibodies were used for identifying inflammatory cells in the specimens: anti-CD3 (rabbit monoclonal, clone SP7; Nichirei, Tokyo, Japan),
Techniques: Immunohistochemical staining, Staining
Journal: Allergy, Asthma, and Clinical Immunology : Official Journal of the Canadian Society of Allergy and Clinical Immunology
Article Title: T-cell phenotypes in chronic rhinosinusitis with nasal polyps in Japanese patients
doi: 10.1186/s13223-015-0100-2
Figure Lengend Snippet: The number of inflammatory cells in mucosal specimens. The number of CD3 positive cells (T cells) ( a ), CD4 positive cells ( b ) and CD8 positive cells ( c ) per field in the ECRS and non-ECRS polyps, as well as the non-CRS controls. Data in box-and-whisker plots represent the median, lower and upper quartile and the minimum to maximum value. ×, outliers ( † p < 0.005, **p < 0.01, *p < 0.05)
Article Snippet: The following primary antibodies were used for identifying inflammatory cells in the specimens: anti-CD3 (rabbit monoclonal, clone SP7; Nichirei, Tokyo, Japan),
Techniques: Whisker Assay
Journal: Journal for Immunotherapy of Cancer
Article Title: High endothelial venule is a surrogate biomarker for T-cell inflamed tumor microenvironment and prognosis in gastric cancer
doi: 10.1136/jitc-2021-003353
Figure Lengend Snippet: HEV density was a surrogate marker for T-cell inflamed TME. (A) HEV expression (detected by MECA-79 staining) in surgically resected GC tissue was categorized into low and high status based on the median value of HEV density (27.8/cm 2 ). Lymphocytes were stained with anti-CD8 and anti-CD4 antibodies for evaluating their relationship with HEV density. Scale bars: 200 µm. (B) Quantification of the MECA-79 area and the CD8 + and CD4 + areas according to the HEV-low and HEV-high groups was performed, and their significant correlations are shown. Values are presented as mean±SEM. (C) The differences in the expression of 730 immune-related genes were evaluated, and genes for immune checkpoints, TME, and chemokines varied with HEV density. (D) Volcano plot summarizing the effects of HEV density on immune-related gene expression. Red line, p<0.05. (E) GO term enrichment analysis revealed 13 statistically significant biological processes controlled by differentially expressed genes among patients with high HEV density. *P<0.05. GC, gastric cancer; GO, gene ontology; HEV, high endothelial venule; IFN, interferon; MHC, major histocompatibility complex; TME, tumor microenvironment; TNF, tumor necrosis factor.
Article Snippet: They were then incubated with anti-peripheral node addressin (PNAd) (rat, clone MECA-79; Santa Cruz), anti-CD8 (rabbit, clone SP57; Ventana),
Techniques: Marker, Expressing, Staining
Journal: Journal for Immunotherapy of Cancer
Article Title: High endothelial venule is a surrogate biomarker for T-cell inflamed tumor microenvironment and prognosis in gastric cancer
doi: 10.1136/jitc-2021-003353
Figure Lengend Snippet: Immune-related gene expression profile explained the anti-tumor immunity of HEV-high GC. (A) HEV-high GC had increased expression of immune cell subsets, including dendritic cells, cytotoxic and helper T cells, and B cells. (B) Fold changes of gene expression of immune cell subsets in HEV-high GC compared to HEV-low GC. Values are presented as mean±SEM. *P<0.05. (C) Gene expression of immune-modulating chemokines and interleukins was higher in HEV-high GC. (D) Fold changes of chemokines and interleukins in HEV-high GC compared with HEV-low GC. Values are presented as mean±SEM. *P<0.05. (E) Comparison of gene expression related to TME, type I or II interferon, Th1 and Th2 response, EC–LC interaction, and inhibitory and agonistic immune checkpoint between HEV-high and HEV-low GC. Values are presented as mean±SEM. *P<0.05. EC, endothelial cell; GC, gastric cancer; HEV, high endothelial venule; IC, immune checkpoint; IFN, interferon; LC, lymphocyte; NK, natural killer; TME, tumor microenvironment.
Article Snippet: They were then incubated with anti-peripheral node addressin (PNAd) (rat, clone MECA-79; Santa Cruz), anti-CD8 (rabbit, clone SP57; Ventana),
Techniques: Expressing