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Image Search Results
Journal: Journal of immunology (Baltimore, Md. : 1950)
Article Title: Direct stimulation of human T cells via TLR5 and TLR7/8: flagellin and R-848 up-regulate proliferation and IFN-gamma production by memory CD4+ T cells.
doi: 10.4049/jimmunol.175.3.1551
Figure Lengend Snippet: FIGURE 5. Memory T cells are more sensitive to Pam3CSK4, flagellin, and R-848 than naive T cells. Naive (CD45RA) () and memory (CD45RO) T cells (u) were purified from CD4 T cells by FACS sorting and either unstimulated or stimulated with IL-2 (100 U/ml for cytokine production or 20 U/ml for proliferation assay) or anti-CD2 mAbs (2 g/ml) in the absence or presence of 1 g/ml Pam3CSK4, 5 g/ml flagellin, or 1 g/ml R-848. IFN- was quantified in the 48-h cell-free supernatants (A), and proliferation was determined after 72 h (B). Results are expressed as mean SD, n 3, and are representative of the data obtained with the T cells of two of six healthy donors.
Article Snippet: CD4 CD45RO T cells were separated into CCR7 and CCR7 cells by FACS sorting using FITC-labeled
Techniques: Proliferation Assay
Journal: International Journal of Molecular Sciences
Article Title: In-Depth Immune-Oncology Studies of the Tumor Microenvironment in a Humanized Melanoma Mouse Model
doi: 10.3390/ijms22031011
Figure Lengend Snippet: Immune cell subpopulations in untreated tumor-bearing animals detected by Chipcytometry (n = 3).
Article Snippet: 10 , 5 ,
Techniques:
Journal: International Journal of Molecular Sciences
Article Title: In-Depth Immune-Oncology Studies of the Tumor Microenvironment in a Humanized Melanoma Mouse Model
doi: 10.3390/ijms22031011
Figure Lengend Snippet: Multiplex staining Chipcytometry.
Article Snippet: 10 , 5 ,
Techniques: Multiplex Assay, Staining, Marker
Journal: Journal of Immunology Research
Article Title: An In Vitro Comparison of Costimulatory Domains in Chimeric Antigen Receptor T Cell for Breast Cancer Treatment
doi: 10.1155/2022/2449373
Figure Lengend Snippet: Comparison of immunophenotypes between CAR.MUC1-41BB ζ and CAR.MUC1-CD28 ζ . The phenotypic analyses of CAR T cells were performed on days 4, 11, and 14 after transduction. (a) Representative flow cytometry plot demonstrating the cell subset analyzed with fluorochrome-conjugated anti-CD3 and anti-CD56 on day 4 after T cell transduction. (b) Bar graph represents the percentage of CD3 + T cells (mean ± S.E.M from 8 donors). (c) Representative flow cytometry plot at 4 and 11 after transduction. (d) Mean percentage of CD8 + : CD4 + ratio on day 4 and day 11 after transduction is shown. Data shown are mean ± S.E.M from 6 donors. (e) Representative flow cytometry analysis of memory phenotype analyzed on days 4, 11, and 14 after transduction; CAR T cells were expanded in culture media containing IL-2 50 U/ml and stained with anti-CD45RO and anti-CD62L antibody (TEM: CD45RO + CD62L − , TCM: CD45RO + CD62L + , TN: CD45RO − CD62L + , and TE: CD45RO − CD62L − ). (f) The mean percentage of naïve (TN), central memory (TCM), effector memory (TEM), and terminal effector (TE) T cells. Data represents as mean ± S.E.M ( n = 6).
Article Snippet: For cell surface marker analysis, the following antibodies were used: CD56-PE (HCD56/Cat#130-114-551), CD4-FITC (OKT4/130-114-531), CD8-APC (SK1/130-110-679),
Techniques: Comparison, Transduction, Flow Cytometry, Staining