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Image Search Results
Journal: International Journal of Nanomedicine
Article Title: Cathepsin B-Activatable Bioactive Peptide Nanocarrier for High-Efficiency Immunotherapy of Asthma
doi: 10.2147/IJN.S455633
Figure Lengend Snippet: Effect of PEG-Liker (PEG-IALLIPF), Trp, or MPP-Trp on the production of NO and Pro-inflammatory cytokines. ( A ) In Control-PBMCs, Asthma-PBMCs, Asthma-PBMCs + PEG-Liker, Asthma-PBMCs + Trp and Asthma-PBMCs + MPP-Trp group, NO production were examined by NO assay kit. Pro-inflammatory cytokines ( B ) TNF-α, ( C ) IL-1β, and ( D ) IL-6 contents in all groups were examined by ELISA assay. Data were presented as mean ± SD of three independent experiments. * P <0.05, ** P <0.01, *** P <0.001 vs Asthma-PBMCs group.
Article Snippet: The total
Techniques: Control, Enzyme-linked Immunosorbent Assay
Journal: International Journal of Nanomedicine
Article Title: Cathepsin B-Activatable Bioactive Peptide Nanocarrier for High-Efficiency Immunotherapy of Asthma
doi: 10.2147/IJN.S455633
Figure Lengend Snippet: MPP-Trp was closely correlated with the balanced Th1/Th2 level and Th1/Th2-type cytokine production. ( A ) In Control-PBMCs, Asthma-PBMCs, Asthma-PBMCs + PEG-Liker, Asthma-PBMCs + Trp and Asthma-PBMCs + MPP-Trp group, Th1 population (CD4+IFN-γ+) and Th2 population (CD4+IL-4+) were selected by flow cytometry assay. ( B ) Relative mRNA expressions of IFN-γ, IL-4, IL-13, and IL-5 in all groups were assessed by qRT-PCR. ( C ) The IFN-γ, IL-4, IL-13, and IL-5 contents in all groups were examined by ELISA assay. Data were presented as mean ± SD of three independent experiments. * P <0.05, ** P <0.01, *** P <0.001 vs Asthma-PBMCs group.
Article Snippet: The total
Techniques: Control, Flow Cytometry, Quantitative RT-PCR, Enzyme-linked Immunosorbent Assay
Journal: International Journal of Nanomedicine
Article Title: Cathepsin B-Activatable Bioactive Peptide Nanocarrier for High-Efficiency Immunotherapy of Asthma
doi: 10.2147/IJN.S455633
Figure Lengend Snippet: MPP-Trp altered cytokine gene expression and production in a concentration-dependent way. In Control-PBMCs, Asthma-PBMCs, and Asthma-PBMCs + MPP-Trp (10, 50, 100 and 200 μg/mL) group, ( A ) Th1/Th2 cytokine gene expressions (IFN-γ, IL-4, IL-13, and IL-5) were determined by RT-qPCR. ( B ) The cytokines (IFN-γ, IL-4, IL-13, and IL-5) levels in all groups were detected by ELISA. Data were presented as mean ± SD of three independent experiments. ** P <0.01, *** P <0.001 vs Control-PBMCs group; # P <0.05, ## P <0.01, ### P <0.001 vs Asthma-PBMCs group.
Article Snippet: The total
Techniques: Gene Expression, Concentration Assay, Control, Quantitative RT-PCR, Enzyme-linked Immunosorbent Assay
Journal: International Journal of Nanomedicine
Article Title: Cathepsin B-Activatable Bioactive Peptide Nanocarrier for High-Efficiency Immunotherapy of Asthma
doi: 10.2147/IJN.S455633
Figure Lengend Snippet: MPP-Trp altered cytokine gene expression and production in a time-dependent way. ( A ) In Control-PBMCs, Asthma-PBMCs, and 100 μg/mL Asthma-PBMCs + MPP-Trp (6, 12, 24, and 48 h) group, IFN-γ, IL-4, IL-13, and IL-5 mRNA levels were determined by RT-qPCR. ( B ) The Th1/Th2-type cytokines (IFN-γ, IL-4, IL-13, and IL-5) productions in all group were examined by ELISA. Data were presented as mean ± SD of three independent experiments. *** P <0.001 vs Control-PBMCs group; # P <0.05; ## P <0.01; ### P <0.001 vs Asthma-PBMCs group.
Article Snippet: The total
Techniques: Gene Expression, Control, Quantitative RT-PCR, Enzyme-linked Immunosorbent Assay
Journal: Poultry Science
Article Title: Engineered Salmonella Enteritidis vector targeting innate immune molecules provides protection against Salmonella Enteritidis and Salmonella Typhimurium
doi: 10.1016/j.psj.2025.105724
Figure Lengend Snippet: Specific cellular immune responses induced by SIRV in chickens. (A-C) Lymphocyte proliferation. PBMCs are stimulated with SE ( C50041 )-OMPs (A), SE (CVCC3949)-OMPs (B), and ST-OMPs (C), and proliferation is measured using the CCK-8 assay. (D-F) Cytokine production upon in vitro stimulation of lymphocytes. PBMCS are stimulated with SE ( C50041 )-OMPs (D), SE (CVCC3949)-OMPs (E), and ST-OMPs (F). mRNA expression levels of IFN‐γ and IL‐4 are quantified by qRT-PCR. Data are expressed as the mean ± SD of three chickens. Ns, not significant, *, P < 0.05, **, P < 0.01, ***, P < 0.001.
Article Snippet: Peripheral blood mononuclear cells (PBMCs) were isolated 1 week post-vaccination using the
Techniques: CCK-8 Assay, In Vitro, Expressing, Quantitative RT-PCR
Journal: Viruses
Article Title: The Mechanism of PEDV-Carrying CD3 + T Cells Migrate into the Intestinal Mucosa of Neonatal Piglets
doi: 10.3390/v13030469
Figure Lengend Snippet: Blood-derived CD3 + T cells could be hijacked by PEDV in vitro. Blood-derived CD3 + T cells were infected with PEDV at different times. The viral loads in blood-derived CD3 + T cells were detected by Western blotting ( a ), plaque assay ( b ), and FACS ( c ). At least three independent experiments were performed. PBMC: Peripheral blood monoculear cell; FACS: Fluorescence Activated Cell Sorte.
Article Snippet:
Techniques: Derivative Assay, In Vitro, Infection, Western Blot, Plaque Assay, Fluorescence