INT172078
From wiki-pain
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Sentences Mentioned In
Key: | Protein | Mutation | Event | Anatomy | Negation | Speculation | Pain term | Disease term |
Purified CD8+CD94+T cells from two groups displayed hyporesponsiveness to stimulation with anti-CD3 mAb, whereas CD8+CD94-T cells proliferated strongly (Fig. 4B). | |||||||||||||||
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In a second step, CD3 and PCNA were visualized with donkey anti-goat, conjugated to Alexa Fluor 594 (Molecular probes, Eugene, OR). | |||||||||||||||
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In order to obtain purified spleen cell populations for the real-time RT-PCR experiments, after erythrocyte lysis, the splenocytes were appropriately stained with PE anti CD11b for the mieloyd line, PE-anti-CD3 antibody for T lymphocytes and FITC anti CD19 for B lymphocytes (Miltenyi Biotec, Bologna, Italy) and the CD11b+, CD3+ CD19+ populations were purified (purity ? | |||||||||||||||
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In order to obtain purified spleen cell populations for the real-time RT-PCR experiments, after erythrocyte lysis, the splenocytes were appropriately stained with PE anti CD11b for the mieloyd line, PE-anti-CD3 antibody for T lymphocytes and FITC anti CD19 for B lymphocytes (Miltenyi Biotec, Bologna, Italy) and the CD11b+, CD3+ CD19+ populations were purified (purity ? | |||||||||||||||
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In order to obtain purified spleen cell populations for the real-time RT-PCR experiments, after erythrocyte lysis, the splenocytes were appropriately stained with PE anti CD11b for the mieloyd line, PE-anti-CD3 antibody for T lymphocytes and FITC anti CD19 for B lymphocytes (Miltenyi Biotec, Bologna, Italy) and the CD11b+, CD3+ CD19+ populations were purified (purity ? | |||||||||||||||
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Multi colored analysis with antibodies directed against CD3, NK1.1, ?? | |||||||||||||||
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Notably, multi colored analysis with antibodies directed against CD3, NK1.1, ?? | |||||||||||||||
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To calculate the percentage of CD68, IgA and CD3, one thousand lamina propria cells per biopsy were counted. | |||||||||||||||
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We evaluated Th1 cell immunity in immunized mice after vaginal challenge by quantitating the number of CD3+CD4+ cells that secrete IFN? | |||||||||||||||
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R-positive cells, most likely macrophages, often co-localised with CD3-positive T cells around vessels of the synovial tissue (data not shown). | |||||||||||||||
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The presence of CD3+ and CD45+ cells was used as an indicator of T cell infiltration and the prevalence of CD4+, CD8+, CD56+ cells as indicators of T helper, T cytotoxic and NK cells, respectively and CD1a was used as a marker for antigen presenting cells (APC). | |||||||||||||||
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CD4+CD28null T cells were identified by morphologically cell-like structures with co-localized immunostainings of CD3, CD4 and CD244, and were manually quantified in independent analyses performed by two persons. | |||||||||||||||
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secreting CD3+CD4+CD28null T cells was analysed by flow cytometry (see above).
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There was markedly increased, age-independent, proliferation of CD3? | |||||||||||||||
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It was not possible to colocalize CXCR5 and CD3 in serial sections, so a double-label immunohistochemistry technique was developed. | |||||||||||||||
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No co-localisation was observed between CCR9 and CD20 (B lymphocytes) or CD3 (T lymphocytes) respectively in either RA or non-RA synovia (data not shown). | |||||||||||||||
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Decreases of CD3 and CD4 and increases of CD8 cells occur in elderly individuals. | |||||||||||||||
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Multiparametric flow cytometry assays were performed to determine the relative importance of the subpopulations of influenza-specific CD3+CD4+ and CD3+CD8+ T cells that produce IL-2, IFN-? | |||||||||||||||
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Multiparametric flow cytometry assays were performed to determine the relative importance of the subpopulations of influenza-specific CD3+CD4+ and CD3+CD8+ T cells that produce IL-2, IFN-? | |||||||||||||||
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Phenotyping of the final products showed a patient-specific prevalence of NKT CD16+CD56+CD3+ (patient #1) or of NK CD16+CD56+CD3- (patients #2 and #3) cells. | |||||||||||||||
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