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2,800 results for “CD8+ T cells”
Supplemental Figures S1-S8: Direct CD137 costimulation of CD8 T cells promotes retention and innate-like function within nascent atherogenic foci
<p>Supplemental Figures and Table S1-S8 for "Direct CD137 costimulation of CD8 T cells promotes retention and innate-like function within nascent atherogenic foci" H-00088-2019, to the American Journal of Physiology-Heart and Circulatory Physiology.</p>
Activation markers plotted against nutrient sensors in CD4+ and CD8+ T-cells.
<p>Activation markers (CD69, CD25, CD71, and CD38) plotted against nutrient sensors (GLUT1, GLUT4, HK1, HK2, and CD36) in CD4+ T-cells.</p>
IL-2 inside tumor microenvironment is essential and sufficient to reinvigorate CD8+ T cells
<p>The single-cell RNA seq data of day 10 and day 20. </p>
CD4+ and CD8+ T cell responses to peptides covering SARS-CoV-2 Spike in response to mRNA vaccination in persons recovered from SARS-CoV-2 infection
<p>These files contain intracellular cytokine staining flow cytometry data for CD4+ and CD8+ T cells after exposure of serial PBMC to SARS-CoV-2 spike peptides or control antigens. PBMC are from subjects recovered from SARS-CoV-2 infection that subsequently received mRNA vaccination. The data were analyzed and exported from FlowJo version 10 as individual gated events and related Boolean subsets for four functional markers: CD40L, IFN-g, IL-2, and TNF-a. Counts and frequencies are both included.</p> <p> </p> <p><strong>Procedure for obtaining data:</strong></p> <p>Cryopreserved peripheral blood mononuclear cells (PBMC) were thawed and rested overnight. PBMC (1 x 10<sup>6</sup> per well) were stimulated with a SARS-CoV-2 spike overlapping peptide pool (JPT, 1 μg/mL each peptide; 0.4% final DMSO concentration), 0.4% DMSO as a negative control, or PHA-P (Remel; 1.6 μg/mL final concentration) as a positive control, in the presence of anti-CD28 and anti-CD49d (BD Biosciences) antibodies at 37°C for 6 hours. Brefeldin A (Sigma) was added after 2 hours. Cells were stained with Live/Dead Near IR dye (Invitrogen), treated with FACS lyse (BD Biosciences) and frozen at -80<sup>o</sup>C. For staining, the cells were thawed, washed, and permeabilized with Permeabilizing solution 2 (BD Biosciences) then stained with fluorochrome labeled monoclonal antibodies to anti-human CD3 mAb (clone UCHT) conjugated with PE-Texas Red (ECD; Beckman Coulter), anti-human CD4 mAb (clone SK3) conjugated with BV510 (Biolegend), anti-human CD8 mAb (clone SK1) conjugated with PerCP-Cy5.5 (BD Biosciences), and the activation markers anti-human CD40L mAb (clone TRAP1) conjugated with BV421 (BD Biosciences), anti-human IFNγ mAb (clone 4S.B3) conjugated with PE (BD Biosciences), anti-human IL2 mAb (clone MQ1-17H12) conjugated with APC (BD Biosciences), and anti-human TNFα mAb (clone MAb11) conjugated with FITC (BD Biosciences). Events were recorded with BD Fortessa and analyzed with FlowJo (v10 for Mac; BD). </p>
Injection of CD4 and CD8 + T Cells Anti-Cytomegalovirus (CMV) or Anti-adenovirus
ClinicalTrials.gov study NCT01325636. IPD Sharing: Not stated. Countries: 1. Publications: 1.
Is There an Association Between Innate CD8+ T Cells and the Evolution of Tyrosine Kinase Inhibitor Resistance Mutations in Phi+ Hematological Malignancies.
ClinicalTrials.gov study NCT04965649. IPD Sharing: Not stated. Countries: 1. Publications: 3.
Identification and Characterization of SARS-CoV-2 Specific CD8 T Cells in Humans
ClinicalTrials.gov study NCT04565067. IPD Sharing: UNDECIDED. Countries: 1. Publications: 1.
Clinical Safty and Efficacy Study of Infusion of iNKT Cells and CD8+T Cells in Patients With Advanced Solid Tumor
ClinicalTrials.gov study NCT03093688. IPD Sharing: NO. Countries: 1. Publications: 2.
A PET Imaging Agent to Assess the Level of Tumor Tissue-infiltrating CD8 + T Cells in Patients With Solid Tumors
ClinicalTrials.gov study NCT05126927. IPD Sharing: NO. Countries: 1. Publications: 2.
A Multi-center, Single-arm, Open, Phase I/IIa Clinical Trial to Evaluate the Efficacy and Safety of EBViNT Cell (EBV Specific Autologous CD8+ T Cell) in Patients With Treatment Failed Epstein Barr Vir
ClinicalTrials.gov study NCT03789617. IPD Sharing: NO. Countries: 1. Publications: 2.
Safety and Effectiveness of Immunotherapy With Autologous HIV-Specific CD8 Cells in HIV Infected Adults
ClinicalTrials.gov study NCT00110578. IPD Sharing: Not stated. Countries: 1. Publications: 1.
Continuous expression of TOX safeguards exhausted CD8 T cell epigenetic fate
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Data from: Bi-specific antibodies crosslink and redirect CD8+ T cells to kill cytomegalovirus-infected cells
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HIV vaccines induce CD8+ T cells with low antigen receptor sensitivity
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Immunofluorescence images: Inflammasome activation leads to cDC1-independent cross-priming of CD8 T cells by epithelial cell derived antigen
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Spatiotemporal co-dependency between macrophages and exhausted CD8 + T cells in cancer
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Raw - EBV-specific CD8 T lymphocytes and B cells during glatiramer acetate therapy in patients with MS
<p>Intracellular staining overnight</p>
Machine Learning-assisted immunophenotyping of peripheral blood identifies innate immune cells as best predictor of response to induction chemo-immunotherapy in head and neck squamous cell carcinoma – knowledge obtained from the CheckRad-CD8 trial
<p>Raw cell counts from peripheral blood immune phenotyping across individual patients.</p>
Figure 2 from: Hartati FK, Nafisah W, Sutanto A, Saati EA, Khairoh M, Sjamsiah (2024) Aqueous black rice (Oryza sativa L. indica) extract enhanced the activation of CD4+ and CD8+ T cells in mouse breast cancer model. Pharmacia 71: 1-7. https://doi.org/10.3897/pharmacia.71.e113442
Figure 2 Aqueous black rice (ABR) extract reduced the relative number of CD4+IL17+, CD4+TNFα+, and CD4+IFNγ+ cytokine production. A, C, E. were flow cytometry diagram; B, D, F. were the graph of flow cytometry results. The bar in the graph shows the calculation results as the mean ± SD of the relative number of cytokine production. *P<0.05, indicate significant different. The group in this study were normal group; Cancer, DMBA 15 mg/kg BW; Cis, DMBA 15 mg/kg BW + Cisplatin 5 mg/kg BW; ABR1, DMBA 15 mg/kg BW + aqueous black rice extract 0.2 g/kg BW; ABR2, DMBA 15 mg/kg BW + aqueous black rice extract 0.3 g/kg BW; ABR3, DMBA 15 mg/kg BW + aqueous black rice extract 0.4 g/kg BW; ABR4, DMBA 15 mg/kg BW + aqueous black rice extract 0.5 g/kg BW.
Figure 1 from: Hartati FK, Nafisah W, Sutanto A, Saati EA, Khairoh M, Sjamsiah (2024) Aqueous black rice (Oryza sativa L. indica) extract enhanced the activation of CD4+ and CD8+ T cells in mouse breast cancer model. Pharmacia 71: 1-7. https://doi.org/10.3897/pharmacia.71.e113442
Figure 1 Aqueous black rice (ABR) extract increased the relative number of CD4+CD62L- cells and CD8+CD62L- cells. A, C. Show flow cytometry diagrams, and B, D. Show graphs of the flow cytometry results. The bars in the graphs show the calculated results as the mean ± SD of the relative number of CD4+ and CD8+ cell activations. *P<0.05 indicates a significant difference. The groups in this study included the following groups: Normal; Cancer, DMBA 15 mg/kg BW; Cis, DMBA 15 mg/kg BW + Cisplatin 5 mg/kg BW; ABR1, DMBA 15 mg/kg BW + ABR extract 0.2 g/kg BW; ABR2, DMBA 15 mg/kg BW + ABR extract 0.3 g/kg BW; ABR3, DMBA 15 mg/kg BW + ABR extract 0.4 g/kg BW; and ABR4, DMBA 15 mg/kg BW + ABR extract 0.5 g/kg BW.
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International Brain Laboratory public data
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OpenNeuro
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