The largest database of trusted experimental protocols

4 protocols using pe cy7 anti human cd8

1

Isolation of CD4+ and CD8+ T Cells

Check if the same lab product or an alternative is used in the 5 most similar protocols
For T cell isolation, blood samples were diluted with 1 volume of PBS 2% FBS, then the diluted blood was added dropwise to 1 volume of Lymphoprep (Stemcell Technologies Inc, Cat# 07811) at room temperature. Samples were centrifuged at 800g for 20 minutes at 22 °C, then the PBMCs layer was harvested, washed two times in PBS 2% FBS, and resuspended in PBS 2% FBS. CD8+ T cells were then purified by two subsequent rounds of isolation: first, T cells were enriched using the Pan T Cell Isolation kit (Miltenyi Biotec, Cat# 130-096-535); then, negative CD8 T cell isolation was performed with the CD8+ T Cell Isolation Kit, human (Miltenyi Biotec, Cat# 130-096-495) or negative CD4 T cell isolation was performed with the CD4+ T Cell Isolation Kit, human (Miltenyi Biotec, Cat# 130-096-533). Both enrichment steps were performed using an AutoMACS machine. For both mouse and human cells, CD8 T cell purity was assessed by FACS staining using mouse or human anti-CD3 and anti-CD8 antibodies at 1:100 dilution (PE/Cyanine7 anti-human CD3, BioLegend, # Cat317333; APC/Cyanine7 anti-mouse CD8a, BioLegend, Cat# 100714; FITC anti-human CD3, ThermoFisher Scientific, Cat#11-0038-42; PE/Cy7 anti-human CD8, Biolegend, Cat# 344712). Human CD4+ T cell purity was assessed using the A700 anti-human CD4 antibody, Biolegend, Cat# 317426 at 1:100 dilution.
+ Open protocol
+ Expand
2

Comprehensive T Cell Phenotyping and Functional Analysis

Check if the same lab product or an alternative is used in the 5 most similar protocols
The following cell surface fluorochrome-conjugated monoclonal antibodies were used to detect T cells phenotype: FITC anti-human CD4, PE/Cy7 anti-human CD8, PE anti-human CD3 (Biolegend, San Diego, CA, USA) and APC anti-human NKG2D (eBioscience). T cell activity was determined by staining the surface APC anti-human CD69, intracellular PE anti-human IFN-γ (BD Biosciences, San Diego, CA, USA), PE anti-human GzmB (eBioscience, San Diego, CA, USA) and PE anti-human Bcl-2 (Biolegend) antibodies. PE anti-human PD-1 and APC anti-human Tim-3 were purchased from Biolegend. FITC anti-human CD45RA, Percp-cy5.5 anti-human CCR7 and PE anti-human CD45RO were purchased from Biolegend to determine T cell subsets. APC Annexin-V and 7-Aminoactinomycin D (7-ADD) from BD Biosciences were used for apoptosis staining. APC mouse IgG1, κ isotype, PE mouse IgG1 isotype, PE/Cy7 mouse IgG2a, κ isotype, FITC mouse IgG1 isotype, PE/Cy7 mouse IgG1, κ isotype (Biolegend) were used as controls. Flow cytometry was performed on the BD LSRFortessa flow cytometer, and data were analyzed using FlowJo Version 10 software.
+ Open protocol
+ Expand
3

CD8+ T Cell Functionality Profiling

Check if the same lab product or an alternative is used in the 5 most similar protocols
Frequencies of peptide-specific CD8+ T cells were determined by tetramer staining using the PE/Cy7 anti-human CD8 mAb (#737661, Beckman Coulter, Brea, CA, USA) and 5 µg/mL of PE-labeled HLA:peptide tetramer (in-house production). Tetramers of the same HLA allotype containing irrelevant control peptides were used as negative control (Supplemental Table 2).
Functionality of peptide-specific T cells was analyzed by ICS using PE/Cy7 anti-human CD8, PacificBlue anti-human TNF (#502920), FITC anti-human CD107a (#328606, BioLegend, San Diego, CA, USA), and PE anti-human IFNγ (#506507, BD, Franklin Lakes, NJ, USA) antibodies as described previously30 (link).
Results of tetramer staining were considered positive if the frequency of peptide-specific CD8+ T cells was ≥0.1% of viable cells and at least three-fold higher than the frequency of peptide-specific cells in the negative control according to the harmonization guidelines for HLA-peptide multimer assays of the international Cancer Vaccine Consortium proficiency panel60 (link). The same evaluation criteria were applied for ICS. All samples were analyzed using a FACS-CantoTM II cytometer and FlowJo software version 10.0.7 (BD).
+ Open protocol
+ Expand
4

Isolation of CD4+ and CD8+ T Cells

Check if the same lab product or an alternative is used in the 5 most similar protocols
For T cell isolation, blood samples were diluted with 1 volume of PBS 2% FBS, then the diluted blood was added dropwise to 1 volume of Lymphoprep (Stemcell Technologies Inc, Cat# 07811) at room temperature. Samples were centrifuged at 800g for 20 minutes at 22 °C, then the PBMCs layer was harvested, washed two times in PBS 2% FBS, and resuspended in PBS 2% FBS. CD8+ T cells were then purified by two subsequent rounds of isolation: first, T cells were enriched using the Pan T Cell Isolation kit (Miltenyi Biotec, Cat# 130-096-535); then, negative CD8 T cell isolation was performed with the CD8+ T Cell Isolation Kit, human (Miltenyi Biotec, Cat# 130-096-495) or negative CD4 T cell isolation was performed with the CD4+ T Cell Isolation Kit, human (Miltenyi Biotec, Cat# 130-096-533). Both enrichment steps were performed using an AutoMACS machine. For both mouse and human cells, CD8 T cell purity was assessed by FACS staining using mouse or human anti-CD3 and anti-CD8 antibodies at 1:100 dilution (PE/Cyanine7 anti-human CD3, BioLegend, # Cat317333; APC/Cyanine7 anti-mouse CD8a, BioLegend, Cat# 100714; FITC anti-human CD3, ThermoFisher Scientific, Cat#11-0038-42; PE/Cy7 anti-human CD8, Biolegend, Cat# 344712). Human CD4+ T cell purity was assessed using the A700 anti-human CD4 antibody, Biolegend, Cat# 317426 at 1:100 dilution.
+ Open protocol
+ Expand

About PubCompare

Our mission is to provide scientists with the largest repository of trustworthy protocols and intelligent analytical tools, thereby offering them extensive information to design robust protocols aimed at minimizing the risk of failures.

We believe that the most crucial aspect is to grant scientists access to a wide range of reliable sources and new useful tools that surpass human capabilities.

However, we trust in allowing scientists to determine how to construct their own protocols based on this information, as they are the experts in their field.

Ready to get started?

Sign up for free.
Registration takes 20 seconds.
Available from any computer
No download required

Sign up now

Revolutionizing how scientists
search and build protocols!