Cell-based Flow Cytometry Assay to Measure Cytotoxic Activity

Summary

This protocol describes a sensitive, cell-based cytotoxicity assay. By enumerating the decrease in frequency of live target CD4+ T cells in the presence of an increasing number of effector CD8+ T cells, this assay allows for the direct assessment of cytolytic activity of antigen-specific CD8+ T cells.

Abstract

Cytolytic activity of CD8+ T cells is rarely evaluated. We describe here a new cell-based assay to measure the capacity of antigen-specific CD8+ T cells to kill CD4+ T cells loaded with their cognate peptide. Target CD4+ T cells are divided into two populations, labeled with two different concentrations of CFSE. One population is pulsed with the peptide of interest (CFSE-low) while the other remains un-pulsed (CFSE-high). Pulsed and un-pulsed CD4+ T cells are mixed at an equal ratio and incubated with an increasing number of purified CD8+ T cells. The specific killing of autologous target CD4+ T cells is analyzed by flow cytometry after coculture with CD8+ T cells containing the antigen-specific effector CD8+ T cells detected by peptide/MHCI tetramer staining. The specific lysis of target CD4+ T cells measured at different effector versus target ratios, allows for the calculation of lytic units, LU₃₀/10⁶ cells. This simple and straightforward assay allows for the accurate measurement of the intrinsic capacity of CD8+ T cells to kill target CD4+ T cells.

Introduction

Cytolytic activity is the major function of CD8+ T cells but is still rarely measured as assays used for this purpose are cumbersome and have been difficult to standardize. Accurate measurement of this function is of paramount importance when characterizing effector functions of CD8+ T cells, as no reliable predictors of effective cell-mediated cytotoxicity have been described yet^1,2. Here, we propose a new functional assay to measure the cytotoxic activity of antigen-specific CD8+ T cells on target CD4+ T cells. Several approaches have been developed to provide alternatives to the gold standard, chromium release assay. We present here a cell-based assay that reveals the entire process of killing as it measures the death of live target cells. This method was derived from protocols of flow cytometry-based cytotoxic assays in vivo in mice^4,5 and in vitro in humans⁶. In this protocol, the antigen-specific CD8+ T cells contained in the total CD8+ T cell population are used as effector cells and autologous CD4+ T cells are used as target cells. Effector CD8+ T cells of interest are enumerated using MHCI/peptide tetramers⁷. Death of target cells is calculated by the ratio between peptide loaded/nonloaded CD4+ T cells. We have previously shown that this method was reproducible, sensitive, specific and did not depend on the number of effector cells within the total CD8+ T cell population⁸. By enumerating both the number of effector and target cells in the coculture assay, the intrinsic capacity of CD8+ T cells to kill target cells can be calculated and expressed in lytic units⁹.

Protocol

1. Preparation of Effector CD8+ T Cells Thaw autologous cryopreserved PBMCs (2-3 vials of 50 x 106 cells) by transferring the cryovial from liquid nitrogen to a 37 °C water bath. Wash the cells by filling the tube to 50 ml with complete RPMI (4 mM L-glutamine, and 100 U/ml penicillin and streptomycin, supplemented with 10% FBS). Count PBMCs and resuspend cells at a concentration of 5 x 106/ml in complete RPMI. Add specific peptide (5 µg/ml) and IL-2 (10…

Representative Results

The schematic in Figure 1 summarizes the assay. Purified CD8+ T cells (effector cells) were resuspended in 450 µl of complete RPMI and serial dilutions were performed by adding 225 µl of CD8+ T cells to the next tube containing 225 µl of media (upper panel). Purified CD4+ T cells (target cells) were counted, split into two tubes and stained with two different concentrations of CFSE (high and low) as described in the protocol. CFSE-low CD4+ T cells were pulsed with the peptide of interest a…

Discussion

The assay described here allows for the quantification of the principal function of CD8+ T cells: the cytolytic activity. The accurate measurement of this function is of paramount importance when characterizing effector functions of CD8+ T cells, as previous studies reported discordance between this function and the cytokine secretion of antigen-specific CD8+ T cells^10,11. Due to the short coculture incubation time (6 hr) and the use of autologous target cells, there is low rate of nonspecific killing of targe…

Materials

EasySep Human CD4+ T Cell Enrichment Kit	Stem Cell	19052
EasySep Human CD8+ T Cell Enrichment Kit	Stem Cell	19053
CellTrace CFSE Cell Proliferation Kit – For Flow Cytometry	Invitrogen	C34554
Far Red LIVE/DEAD fixable dead cell	Invitrogen	L10120
Alexa Fluor 700 Mouse Anti-Human CD3	BD	557943
Brilliant Violet 650 Anti-Human CD4 Antibody	Biolegend	317435
PerCP anti-human CD8 Antibody	Biolegend	344707
RPMI 1640 Medium 1x	VWR	10-040-CV
Penicillin-Streptomycin 100x Solution	Invitrogen	15070063
Fetal Bovine Serum – Gold, Heat Inactivated	PAA	A15-252
96-well plates; Treated; U-bottom; with lid	BD Falcon	353077
25 ml sterile polystyrene, individually wrapped reservoirs	USA Scientific	2321-2230
96-well U-bottom, sterile 2 ml deep well plates	Thermo Scientific	275743
Human IL-2 (v126), research grade	Miltenyi Biotec	130-093-096
RoboSep Buffer, separation buffer	Stem cell	20104
15 ml Polypropylene Conical Tube	BD Falcon	352097
14 ml round bottom tube, polypropylene	BD Falcon	352059
The Big Easy EasySep Magnet	Stem cell	18001
PBS 1x	VWR	21-040-CV
96-well; V-bottom plate with lid	Fisher	12-565-481
Formaldehyde solution, ACS reagent, 37 wt % in H2O	Sigma-Aldrich	252549-500ML
1.5 ml screw cap microtube, conical	Sarstedt	72.692.005