Title
Detection of CMV pp65-specific CD8⁺ T cells by intracellular IFN-γ staining following peptide stimulation
Overview
This protocol describes the intracellular detection of interferon-gamma (IFN-γ) in CMV pp65-specific CD8⁺ T cells from peripheral blood mononuclear cells (PBMCs), using short-term peptide stimulation and flow cytometry. The protocol was used in the publication “Human thymopoiesis produces polyspecific CD8⁺ α/β T cells responding to multiple viral antigens” (eLife, 2017).
Materials
- PBMCs from human peripheral blood (fresh or thawed from cryopreservation)
- RPMI 1640 + 10% fetal bovine serum (FBS)
- Peptivator® CMV pp65 peptide pool (Miltenyi Biotec)
- Brefeldin A (10 μg/mL final; e.g., Sigma or BD GolgiPlug)
- Anti-IFN-γ-PE antibody (clone 4S.B3, BD Biosciences)
- Surface antibodies: CD3, CD8 (fluorochromes as desired)
- Fixation/Permeabilization Kit: BD Cytofix/Cytoperm
- Flow cytometer
Protocol
- Cell Preparation
- Resuspend PBMCs in complete RPMI medium.
- Sort the CD8⁺ memory T cell subset (e.g., CD3⁺ CD8⁺ CD45RO⁺) by flow cytometry (FACS) under sterile conditions.
- Plate 1–2×10⁶ cells per well (e.g., in 96-well round-bottom plates).
- Stimulation
- Add CMV pp65 peptide pool to a final concentration of 1 μg/mL.
- Incubate at 37 °C, 5% CO₂.
- After 2 hours, add Brefeldin A to reach 10 μg/mL final concentration.
- Continue incubation for an additional 4 hours (total 6 h).
- Surface staining
- Wash cells with PBS.
- Stain for CD3 and CD8 (and viability dye if needed) for 30 min at 4 °C.
- Fixation and Permeabilization
- Fix and permeabilize using the Cytofix/Cytoperm kit, following the manufacturer’s instructions.
- Intracellular staining
- Stain for IFN-γ (clone 4S.B3, PE-conjugated) for 30 min at 4 °C in the dark.
- Wash and resuspend in PBS + 2% FBS before acquisition.
- Flow cytometry
- Acquire on a cytometer and analyze IFN-γ⁺ CD3⁺ CD8⁺ T cells.
Controls
- Negative control: PBMCs unstimulated.
- Positive control: PBMCs unstimulated PMA/Ionomycin can be used if needed.
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