Background

Chimeric antigen receptor (CAR) T cells have shown remarkable efficacy in cancer immunotherapy,1 particularly to treat blood cancers. However, the therapeutic application of CAR-T cells against solid tumors is challenging.2 Compared with liquid tumors, solid tumors pose unique roadblocks to CAR-T cell treatment,2 3 including limited T-cell persistence,4 inefficient tumor infiltration,5 6 and an immunosuppressive tumor microenvironment.7 8 Even when solid tumors express targetable antigens, the antitumor efficacy of CAR-T cells would be unsatisfactory unless all the three roadblocks were overcome.

The adoptive transfer of T cells with less-differentiated phenotypes is critical for antitumor efficacy and patient outcomes, because of their increased expansion, persistence, and ability to differentiate into effector progeny.4 9 Attempts to maintain T-cell persistence and stemness have had some success, for example, the use of other homeostatic cytokines instead of interleukin (IL)-2,10 11 pharmacological inhibition of the phosphatidylinositol-4,5-bisphosphate 3-kinase(PI3K)-protein kinase B (AKT) pathway,12–14 and activation of Wnt signaling.15 In fact, AKT inhibition (AKTi) by the inhibitor AKTi-1/2 generated a significant CD62L+central memory-like CAR-T cell population.12 13 Central memory T cells (Tcms), generated by AKTi, express the lymphoid homing molecules CD62L (also known as selectin L (SELL)) and C-C motif chemokine receptor 7 (CCR7) and have enhanced replicative capacity; however, they also express few of the chemokine receptors or adhesion molecules necessary for trafficking to peripheral tissues and have limited effector function.16 Thus, a strategy to enhance Tcms’ cytotoxic potential and their ability to traffic to disease sites, which does not impair their self-renewal ability and persistence, is required.

Tissue-resident memory T cells (Trms) represent a heterogeneous T-cell population that function as both effector and memory T cells, but also express residence gene signatures, unlike effector memory T cells (Tems).17 This feature allows them to traffic to, reside in, and potentially patrol peripheral tissues.17 We wanted to equip Tcms with the properties of Trms, to enhance their cytotoxic potential and tumor infiltration. The transcription factor RUNX family transcription factor 3 (RUNX3) can program CD8+T cell residency in non-lymphoid tissues and tumors.18 Runx3-overexpression (RUNX3-OE) enhanced tumor-infiltrating lymphocyte abundance, and the expression of granzyme B and certain core tissue residency genes, while suppressing core circulating gene expression.18 Thus, Runx3-OE might equip T cells with Trm-like properties.

Herein, we combined ex vivo AKTi with Runx3-OE to generate CAR-T cells with tissue-resident and central-memory characteristics. AKTi promoted the CAR-T cell Tcm phenotype and enhanced persistence, whereas Runx3-OE promoted the CAR-T cell Trm phenotype and further enhanced persistence, effector function, and tumor residency. To the best of our knowledge, this was the first attempt to create CAR-T cells with tissue-resident and central memory characteristics, allowing them to overcome the roadblocks to treating solid tumors more comprehensively.

MethodsCell lines and mice

The KPC cell line, derived from spontaneous tumors in a KrasLSL-G12D; Trp53LSL-R172H; Pdx1-Cre mouse model, was maintained in McCoy’s 5A (Modified) Medium (Gibco) supplemented with 10% fetal bovine serum (FBS) (Cat#FBS-E500, NEWZERUM). HEK293T cells (ATCC) and Plat-E cells (Cell Biolabs) were maintained in Dulbecco’s Modified Eagle’s Medium (Gibco) supplemented with 10% FBS. Bxpc-3 cells (ATCC) were maintained in Roswell Park Memorial Institute (RPMI) 1640 medium (Gibco) supplemented with 10% FBS. KPC and Bxpc-3 cells expressing human carbonic anhydrase 9 (hCA9) was constructed by transduction with lentiviruses containing hCA9 and isolating cell clones using limiting dilution. We relied on the suppliers’ data for Mycoplasma and cell authenticity testing. All mice were purchased from the Model Animal Research Center of Nanjing University (China) and housed in the specific pathogen free facility of the First Affiliated Hospital, Zhejiang University School of Medicine, with approval from the Institutional Animal Care and Use Committee (ID 20191101).

Plasmid construction

The second-generation murine CAR (mCAR) was constructed using the murine CD8α signal peptide, anti-human-CA9 single-chain variable fragment(scFv),19 the hinge and transmembrane domains of murine CD8α, and the cytoplasmic domains of murine CD28 and CD3ζ. One copy of strep-tag II was added to the N-terminus between the signal peptide and scFv for surface detection.20 All retroviral plasmids were based on the pMSCV-IRES-GFP II (pMIGII; Cat#52107, Addgene). To achieve overexpression, genes (mCARs or others) were cloned into pMIGII through the EcoRI and BamHI sites to retain the green fluorescent protein (GFP) tag or through the EcoRI and SalI sites to replace the GFP tag. The murine Runx3 complementary DNA was linked 3’ to the mCAR sequences through a sequence encoding a P2A self-cleaving peptide to achieve co-expression. Gene fragments were generated by chemical synthesis. The final plasmids were confirmed by Sanger sequencing.

Murine primary T-cell activation and isolation

Spleen cells from 8-week-old BALB/c mice were collected and activated using anti-CD3ε and anti-CD28 antibodies for 24 hours.21 Activated T cells were enriched using Percoll gradient centrifugation.21 Residual B cells were removed using biotin anti-mouse-CD19 antibodies (BioLegend) and Streptavidin Nanobeads (BioLegend).

Retrovirus production, transduction, and T-cell expansion

The retroviral supernatant was produced in Plat-E cells,22 and concentrated by ultrafiltration using Amicon Ultra-15 (Millipore). Retrovirus transduction of T cells was performed in 6-well plates by spinning infection with polybrene.21 At 4 hours post-infection, transduced cells were resuspended and transferred to 10-cm plates for expansion in the presence of AKTi-1/2 (MedChemExpress) or vehicle (dimethyl sulfoxide). T cells were maintained in RPMI 1640 medium supplemented with 10% FBS, 100 IU/mL IL-2 (Novoprotein) and 0.05 mM 2-mercaptoethanol (Gibco).

Adoptive therapy tumor models

KPC-hCA9 cells (1×106/50 µL) were injected into the flanks of 7-week-old male nude mice. Tumor-bearing mice were randomly assigned to groups and T cells were adoptively transferred into mice via intravenous injection. Tumors were measured using electronic digital calipers and the tumor volume was calculated in cm3 (½ × length×width2). Mice were euthanized when the tumor length >1.5 cm or the tumor volume >1 cm3. No mice were excluded during the experiment. For each experiment, mice were purchased at the same time and acclimatized in the same environment for at least 1 week before the experiment.

Statistical analysis

Statistical analysis was performed using Prism software (GraphPad, V.9.0). Shapiro-Wilk test was used to confirm the normal distribution of data. Data for all experiments from at least three biological replicates were presented as means±SEM. One-way (column tables) or two-way (grouped tables) analysis of variance was used for multiple comparisons, and p values were adjusted by Tukey method. Student’s t-test was used to compare the differences between two groups. Survival curves were generated using Kaplan-Meier estimates and compared using the log-rank test. P value<0.05 was considered statistically significant.

Supplementary detailed methods and antibodies used were available (online supplemental table 1).

ResultsAKTi generated a CD62L+central memory-like CAR-T cell population with enhanced persistence but promotable cytotoxic potential

AKTi was used to preserve a CD62L+Tcm like population. We activated mouse spleen cells using anti-CD3 and CD28 antibodies for 48 hours in the presence of 0–4 µM AKTi-1/2 to determine its optimal working concentration. AKTi-1/2 at 1–2 µM significantly inhibited AKT phosphorylation, but had little effect on total AKT levels (figure 1A). Next, we performed mouse T-cell activation, purification, and retroviral transduction of the second-generation mCAR against hCA9 (online supplemental figure S1A), a protein upregulated in human pancreatic ductal adenocarcinoma (PDAC) samples.23 CAR-T cells were expanded in the presence of vehicle or 1–2 µM AKTi-1/2, which was maintained during the entire experiment (Mode1) or after retroviral transduction (Mode2) (figure 1B). AKTi-1/2 addition did not influence the retroviral transduction efficiency (online supplemental figure S1B). 1 µM AKTi-1/2 was sufficient to preserve the CD62L+Tcm like population (figure 1C,D) and inhibit AKT phosphorylation during CAR-T cell expansion (online supplemental figure S1C). The time point of AKTi-1/2 addition had little effect on the preservation of the Tcm-like population (figure 1D), because the percentage of Tcm-like cells was high and the degree of AKT phosphorylation was low in the initial stage of CAR-T cell expansion (figure 1D, online supplemental figure S1C). Interestingly, 2 µM AKTi-1/2 treatment retained more Tcm-like cells than 1 µM AKTi-1/2, but inhibited CAR-T cell expansion by approximately twofold (online supplemental figure S1D). Thus, in subsequent experiments, CAR-T cells were expanded in the presence of 1 µM AKTi-1/2 after retroviral transduction, representing the optimal concentration. Transcriptome analysis of sorted CD8+CAR T cells identified the top five most enriched genes following AKTi exposure as Sell, Ccr7, Klf2 (KLF transcription factor 2), S1pr1 (sphingosine-1-phosphate receptor 1), and Tcf7 (transcription factor 7) (figure 1E), which were all associated with T-cell lymphoid homing and persistence.24 The overexpression of Sell (encoding CD62L) was consistent with the protein expression data measured using flow cytometry. The RNA sequencing (RNA-seq) data also showed that AKTi downregulated the expression of genes and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway members associated with effector function (figure 1E, online supplemental figure S1E). The downregulation of cell cycle pathways supported the result that a high concentration of AKTi-1/2 inhibited CAR-T cell expansion (online supplemental figure S1E). We confirmed that AKTi downregulated granzyme B (GzmB) levels as well as the cytolytic ability of CD8+CAR T cells (figure 1F,G).

Figure 1

AKTi generated CD62L+central memory-like CAR-T cell population with promotable cytotoxic potential. (A) Western blotting of mouse spleen cells activated by 1 µg/mL anti-mouse CD3 and 0.5 µg/mL anti-mouse CD28 antibodies for 48 hours in the presence of 0–4 µM AKTi-1/2. AKT, Akt (pan); p-AKT, Phospho-Akt (Ser473). (B) Schema for the activation, purification, retroviral transduction (RV Td), and expansion of mouse T cells in the presence of IL-2 (100 IU/mL) and AKTi-1/2 (0–2 µM). AKTi-1/2 was maintained in the entire period (Mode1) or after retroviral transduction (Mode2). (C) Representative flow cytometry plot of CD44+CD62L+Tcm like CD8+CAR T cells. T cells were expanded in 0–2 µM AKTi-1/2 for 6 days. (D) Percentages of Tcm-like cells in CAR-T cells during the course of the culture in 0–2 µM AKTi-1/2. (E) Volcano plot of differentially expressed genes between CD8+CAR T cells expanded in 1 µM AKTi-1/2 (AKTi, Mode2) and vehicle, as quantified by messenger RNA sequencing (n=2 biological replicates each). (F) Medium fluorescence intensity of granzyme B in CD8+T cells measured by flow cytometry. (G) Target-cell lysis activity of CD8+CAR T cells following 14 hours of co-incubation with human carbonic anhydrase 9-overexpressed KPC cells (target cells). A two-way analysis of variance was used for multiple comparisons in panels D and G, and p values were adjusted by Tukey method. An unpaired two-tailed Student’s t-test was used between two groups in panel F. P value<0.05 was considered statistically significant. AKT, protein kinase B; AKTi, AKT inhibition; CAR, chimeric antigen receptor; IL, interleukin; RNA-seq, RNA sequencing; Tcm, central memory T cells.

We then adoptively transferred 5 million T cells with 50% CAR-T cells via intravenous injection into tumor-bearing nude mice (online supplemental figure S2A,B). The inguinal lymph nodes were larger in the CAR-T+AKTi group compared with those in the CAR-T group (online supplemental figure S2C). Notably, AKTi would not decrease the percentage of CD8+T cells among CD45+ immune cells or CAR-T cells among T cells (online supplemental figure S2D,E). Thus, AKTi promoted CAR-T cell expansion in lymph nodes. Furthermore, AKTi barely affected tumor infiltration: T-cell counts in tumors showed no significant change (online supplemental figure 2F,G). However, AKTi increased the CD8+CAR T count per mm3 of tumor (online supplemental figure S2H), indicating the enhanced persistence of tumor-infiltrating CAR-T cells. The tumor volume was not significantly smaller when treated using AKTi-generated CAR-T cells compared with using normal CAR-T cells (online supplemental figure S2I). AKTi-generated Tcm-like cells expressed lymphoid homing molecules CD62L and CCR7, and showed enhanced expansion but a weaker effector function; therefore, we hypothesized that equipping Tcm-like cells with Trm-like properties would improve the weakness of AKTi-generated CAR-T cells and enhance their effector function and tumor infiltration.

Runx3-OE cooperated with AKTi to generate CAR-T cells with both tissue-resident and central-memory characteristics

Transcription factor RUNX3 was reported to program T-cell Trm phenotype18; therefore we overexpressed Runx3 in the AKTi-generated CAR-T cells. To overexpress Runx3 together with CAR, the CAR and murine RUNX3 were linked by a P2A self-cleaving peptide and an N-terminal strep-tag II was added to detect surface expression (figure 2A).20 AKTi still preserved the CD62L+Tcm like population in Runx3-OE CAR-T cells (CAR-RUNX3-T) (online supplemental figure S3A), indicating that Runx3-OE did not interfere with AKTi’s effect. Then, we explored the effect of AKTi, Runx3-OE and their combination on the CAR-T cell phenotype.

Figure 2

Runx3-overexpression cooperated with AKTi to generate CAR-T cells with both tissue-resident and central memory characteristics in vitro. (A) Schematic diagram of plasmids expressing a second-generation CAR (CAR-T) against human carbonic anhydrase 9 or together with Runx3-overexpression (CAR-RUNX3-T). The CAR and murine Runx3 complementary DNA were separated by a P2A ribosomal skip sequence. The CAR-T plasmid contained a green fluorescent protein tag and the CAR-RUNX3-T plasmid contained a N-terminal Strep-tag II for detecting surface expression. (B) Heatmap of the expression of representative markers associated with Trm and Tcm phenotypes in different CD4+CAR T clusters. T cells were expanded in the presence of 100 IU/mL interleukin-2 and 1 µM AKTi-1/2 or vehicle for 6 days. The expression of markers was quantified by CyTOF and clusters were identified by PhenoGraph method. (C) t-SNE map of CD4+CAR T cells expressing different markers detected by CyTOF. Clusters with similar markers were combined. (D) t-SNE plots of representative markers detected by the CyTOF. (E) Percentages of different T-cell population in CD4+CAR T cells identified by CyTOF. CAR-T, normal CAR-T cells; CAR-RUNX3-T, Runx3-overexpressed CAR-T cells; AKTi, T cells were expended in 1 µM AKTi-1/2. A two-way analysis of variance was used for multiple comparisons in panel E, and p values were adjusted by Tukey method. P value<0.05 was considered statistically significant. AKT, protein kinase B; AKTi, AKT inhibition; CAR, chimeric antigen receptor; CyTOF, cytometry by time of flight; t-SNE, t-distributed stochastic neighbor embedding; RUNX3, RUNX family transcription factor 3; Tcm, central memory T cells; Tems, effector memory T cells; Trms, tissue-resident memory T cells.

Transcriptomic data showed that both Runx3-OE and AKTi had dynamic effects on CD4+T cells, whereas Runx3-OE had minimal effects on CD8+T cells (online supplemental figure S3B). Thus, we compared our transcriptomic data of CD4+T cells to the RNA-seq data previously published for Trms25 using clustering analysis of these core Trm markers (online supplemental figure S3C).18 Our data showed that the genes downregulated in Trms were suppressed by Runx3-OE, but upregulated by AKTi (online supplemental figure S3D), which supported Runx3-OE promotion of the Trm phenotype and AKTi promotion of the Tcm phenotype. However, the genes upregulated in Trms were intricately influenced by Runx3-OE and AKTi (online supplemental figure S3E). Perhaps the phenotype induced by Runx3-OE and AKTi was a mixture of different phenotypes.

We then measured the expression of Trm-associated markers on CD4+CAR T cells using cytometry by time of flight (CyTOF), which identified 18 clusters using the PhenoGraph method. Based on a heatmap and t-distributedstochastic neighbor embedding(t-SNE) map, clusters were divided into five groups (figure 2B–D). The Trm/effector-type (Te) group did not express Tcm marker CD62L and showed high levels of GzmB and CD69 as well as other tissue-resident markers, such as CD11a, CLA, CD49a, CD103, and CXCR6 (figure 2B–D).26 The Trm/Tcm group had high levels of both tissue-resident markers and the Tcm marker, CD62L (figure 2B–D). The Tcm groups had low levels of tissue-resident markers but high levels of CD62L. The Tcm2 group had higher levels of some tissue-resident markers (CXCR6, CLA, and CD44) than Tcm1 (figure 2B–D). AKTi significantly enriched T-cell populations with Tcm characteristics (Tcm and Trm/Tcm groups), while Runx3-OE enriched T-cell populations with Trm characteristics (Trm/Te and Trm/Tcm groups) (figure 2E). The combination of Runx3-OE and AKTi enriched a T-cell population with both Trm and Tcm characteristics (figure 2E). Thus, the CyTOF analysis proved that Runx3-OE cooperated with AKTi to generate CAR-T cells with both tissue-resident and central memory characteristics.

Runx3-OE enhanced the cytotoxic potential of CD4+CAR T cells and cooperated with AKTi to promote CAR-T cell persistence

Next, we evaluated the influence of AKTi and Runx3-OE on CAR-T cells’ cytotoxic potential. The transcriptomic data indicated that Runx3-OE upregulated gene expression associated with effector function (figure 3A, online supplemental figure S4A), including GzmB and Nkg7 (natural killer cell granule protein 7). KEGG pathway analysis showed that pathways associated with effector function were also upregulated (online supplemental figure S4B,C). AKTi inhibited the GzmB expression and the cytolytic ability of CAR-T cells (figure 3B, online supplemental figure S4D), which was consistent with our previous results (figure 1F–G), while Runx3-OE significantly enhanced the cytolytic ability of AKTi-generated CAR-T cells (figure 3B). AKTi strongly promoted the Tcm-like phenotype; therefore, we withdrew AKTi from the AKTi groups for 24 hours to recover the differentiation of CAR-T cells into other phenotypes. Although there was no significant increase in GzmB in CD8+CAR T cells after Runx3-OE, Runx3-OE did enhance the expression of GzmB in CD4+CAR T cells (figure 3C). Runx3-OE also promoted interferon (IFN)-γ and tumor necrosis factor (TNF)-α expression in CD4+CAR T cells after 6 hours of co-incubation with target cells (figure 3D, online supplemental figure S4E), which supported Runx3-OE-mediated enhancement of the effector function of CD4+CAR T cells. However, IFN-γ and TNF-α expression was downregulated slightly by Runx3-OE in CD8+CAR T cells after 6 hours of co-incubation with target cells (figure 3D, online supplemental figure S4E).

Figure 3

Runx3-overexpression enhanced the cytotoxic potential of CD4+CAR T cells and cooperated with AKTi to promote CAR-T cell persistence. (A) Volcano plot of differentially expressed genes between Runx3-overexpressed CD4+CAR T cells and normal CD4+CAR T cells, as quantified by messenger RNA sequencing (n=2 biological replicates each). (B) Target-cell lysis activity of CAR-T cells following 14 hours of co-incubation with target cells. CAR-T, normal CAR-T cells; CAR-RUNX3-T, Runx3-overexpressed CAR-T cells; AKTi, T cells were expended in 1 µM AKTi-1/2. (C) Medium fluorescence intensity of granzyme B measured by flow cytometry. Before analysis, CAR-T cells of all groups were cultured in the presence of IL-2 but no AKTi for 24 hours. (D) Percentages of IFN-γ and TNF-α expression in CAR-T cells measured by flow cytometry. CAR-T cells of all groups were co-incubated with target cells for 6 hours in the presence of IL-2. (E) Percentages of CAR-T cells in T cells during the course of the culture. (F) Growth curve of sorted CAR-T cells. CAR-T cell growth was defined as the ratio of cell count on a given day to that on day 5. (G) Representative flow cytometry histogram and (H) percentages of Ki67 expression in CAR-T cells after 7 days of expansion. A one or two-way analysis of variance was used for multiple comparisons in panels B, C, D, E, F and H, and p values were adjusted by Tukey method. P value<0.05 was considered statistically significant. AKT, protein kinase B; AKTi, AKT inhibition; CAR, chimeric antigen receptor; IFN, interferon; IL, interleukin; RUNX3, RUNX family transcription factor 3; TNF, tumor necrosis factor.

In addition, Runx3-OE enhanced the percentage of CAR-T cells among T cells and the expansion kinetics of sorted CAR-T cells in vitro, especially CD4+T cells (figure 3E–F). Runx3-OE cooperated with AKTi to preserve the Ki67-high population and inhibited the formation of a Ki67-low population on day 7, especially in CD4+T cells (figure 3G–H). These results indicated that Runx3-OE cooperated with AKTi to enhance the expansion ability of CAR-T cells.

In conclusion, Runx3-OE enhanced the cytotoxic potential of CD4+CAR T cells and cooperated with AKTi to promote CAR-T cell persistence by maintaining their proliferation.

Runx3-OE cooperated with AKTi to inhibit the terminal differentiation of CD8+ CAR T cells induced by tonic signaling

We next investigated why Runx3-OE slightly downregulated the cytolytic ability of normal CD8+CAR T cells as well as the expression of IFN-γ and TNF-α after co-incubation with target cells (figure 3B,D). The heatmap of the transcriptomic data showed high baseline levels of effector-related genes in CD8+CAR T cells (figure 4A). Meanwhile, Runx3-OE inhibited the expression of several effector-related genes, including GzmB, Prf1, and Ifng (figure 4A), which was consistent with our previous data showing the downregulated effector function mediated by Runx3-OE (figure 3B,D). We confirmed that the baseline level of IFN-γ was very high in normal CAR-T cells in vitro, but not in control T cells without retroviral transduction (figure 4B), which indicated tonic signaling of CAR-T cells. We then generated new third generation CAR-T cells based on CD28 and 4-1BB (also known as TNF receptor superfamily member 9) co-stimulation domains (online supplemental figure S5A), because 4-1BB co-stimulation could ameliorate tonic signaling-induced T-cell exhaustion.27 The third generation CAR-T cells exhibited much lower baseline levels of IFN-γ than the second generation CAR-T cells based on CD28 domains (online supplemental figure S5B), further confirming the existence of tonic signaling. Runx3-OE cooperated with AKTi to reduce the baseline expression of IFN-γ (figure 4B, online supplemental figure S5B), PD-1 (programmed cell death 1), and Tim-3 (T-cell immunoglobulin mucin 3) (figure 4C), especially in CD8+T cells. Meanwhile, Runx3-OE, but not the residual P2A peptide, contributed to the downregulation of IFN-γ (online supplemental figure S5C). Runx3-OE also slowed down the loss of CD62L on CD8+T cells during the late period of expansion (figure 4D,E). The loss of CD62L and the expression of IFN-γ, PD-1, and Tim-3 all indicated the differentiation of CAR-T cells into a terminal phenotype, which was contributed to by tonic signaling. Therefore, Runx3-OE cooperated with AKTi to inhibit CAR-T cell terminal differentiation induced by tonic signaling.

Figure 4

Runx3-overexpression cooperated with AKTi to inhibit terminal differentiation of CD8+CAR T cells induced by tonic signaling. (A) Heatmap of the expression levels of representative genes associated with effector function, as quantified by messenger RNA sequencing. CAR-T, normal CAR-T cells; RUNX3-T, Runx3-overexpressed CAR-T cells; AKTi, T cells were expended in 1 µM AKTi-1/2. (B) Representative flow cytometry histogram and percentages of IFN-γ expression in CAR-T cells. AKTi withdrawal 24 hours, CAR-T cells of all groups were cultured in the presence of interleukin-2 but no AKTi for 24 hours before analysis. Ctrl-T, T cells without retroviral transduction; CAR-RUNX3-T, Runx3-overexpressed CAR-T cells. (C) Representative flow cytometry plot and percentages of PD-1+Tim3+ cells in CAR-T cells. (D–E) Representative flow cytometry plot and percentages of CD44+CD62L+central memory T cells in CD8+CAR T cells after AKTi withdrawal. A one or two-way analysis of variance was used for multiple comparisons in panels B, C and E, and p values were adjusted by Tukey method. P value<0.05 was considered statistically significant. AKT, protein kinase B; AKTi, AKT inhibition; CAR, chimeric antigen receptor; PD-1, programmed cell death 1; RUNX3, RUNX family transcription factor 3; Tim-3, T-cell immunoglobulin mucin 3.

Runx3-OE cooperated with ex vivo AKTi to enhance both the antitumor activity of CAR-T cells and their sensitivity to PD-1 immunotherapy in vivo

Next, the antitumor efficacy of the AKTi-generated CAR-T cells with Runx3-OE was tested in vivo. We sorted GFP+ AKTi-generated CAR-T and strep-tag II+ AKTi-generated CAR-RUNX3-T cells and adoptively transferred them into tumor-bearing mice (online supplemental figure S6A). The number of CAR-T cells was increased to 5 and 10 million, respectively, to enhance the antitumor efficacy and determine the optimized CAR-T cell count for adoptive transfer. The tumor volume was smaller (online supplemental figure S6B), and overall survival (OS) was longer (online supplemental figure S6C) in the CAR-RUNX3-T groups compared with those in the CAR-T groups treated with the same number of CAR-T cells. Notably, treatment with 10 million CAR-RUNX3-T cells eliminated tumors 1 week after adoptive therapy and half of the mice still had no recurrence 90 days later (online supplemental figure S6C,D).

To further verify the contribution of Runx3-OE and AKTi to antitumor efficacy, we generated CAR-RUNX3-T and CAR-T cells in the presence of 1 µM AKTi-1/2 or vehicle. In the previous experiment, 5 million AKTi-generated CAR-RUNX3-T cells exhibited significant antitumor efficacy; therefore, we adoptively transferred 5 million CAR-T cells into tumor-bearing mice (figure 5A). Around day 18, CAR-T therapy suppressed tumor growth in all groups; however, the AKTi-generated CAR-RUNX3-T cells exhibited the best antitumor activity (figure 5B). After day 18, some tumors began to grow rapidly. We divided tumors into three groups according to their growth trend: complete response (CR, tumors disappeared without recurrence), stable disease (SD, tumors existed but grew by no more than 30% every 6 days), and progressive disease (PD, tumors grew by more than 30% every 6 days). The CAR-RUNX3-T+AKTi group showed the highest proportion of CR (5/10) and the least proportion of PD (3/10) among the four groups (figure 5C), indicating the best antitumor activity. Furthermore, AKTi-generated CAR-RUNX3-T cells responded well to PD-1 blockade while AKTi-generated CAR-T cells did not (figure 5D–F). The combination of AKTi-generated CAR-RUNX3-T cells and PD-1 blockade resulted in the smallest tumor volume and longest OS (figure 5D–F). These results confirmed the robust antitumor activity of AKTi-generated CAR-RUNX3-T cells. Thus, Runx3-OE cooperated with AKT inhibition to enhance both the antitumor activity of CAR-T cells and their sensitivity to PD-1 immunotherapy in vivo.

Figure 5

Runx3-overexpression cooperated with ex vivo AKTi to enhance both the antitumor activity of CAR-T cells and the sensitivity to PD-1 immunotherapy in vivo. (A) Schematics of experiment; 2×107 T cells with 20% CAR-T cells were adoptively transferred into tumor-bearing nude mice. (B) Tumor progression. Tumor volume was calculated in cubic centimeter (½ × length×width2). Ctrl-T, T cells without retroviral transduction; CAR-T, normal CAR-T cells; CAR-RUNX3-T, Runx3-overexpressed CAR-T cells; AKTi, T cells were expended in 1 µM AKTi-1/2. (C) Tumor progression. Tumor growth was defined as the ratio of tumor volume on a given day to that on day 0. (D) Schematics of experiment; 5×106 T cells with 50% CAR-T cells were adoptively transferred into tumor-bearing nude mice on day 0. PD-1 blockade was performed on day 3–15. (E) Tumor progression. CTRL, no adoptive therapy. (F) Survival curve. P values of survival curve in panel F were calculated by log-rank test analysis. A two-way analysis of variance was used for multiple comparisons in panels B and E, and p values were adjusted by Tukey method. P value<0.05 was considered statistically significant. AKT, protein kinase B; AKTi, AKT inhibition; CAR, chimeric antigen receptor; CR, complete response; PD, progressive disease; PD-1, programmed cell death 1; RUNX3, RUNX family transcription factor 3; SD, stable disease.

Runx3-OE cooperated with ex vivo AKTi to enrich the T-cell population with both Trm and Tcm characteristics in vivo

Next, we explored the lasting impact of Runx3-OE/AKTi-generated CAR-T cells on the in vivo phenotype. We determined the expression of Trm-associated markers on CD8+CAR T cells in lymph nodes using CyTOF, and 16 clusters were identified using PhenoGraph (figure 6A). Based on the heatmap and the t-SNE map, clusters were divided into four groups (figure 6B,C). The Trm group had high expression of CD69 as well as other tissue resident markers, such as CXCR6 and CLA (figure 6B, online supplemental figure S7A). The Trm/Tcm group had both Trm and Tcm characteristics (expression of Trm markers as well as the Tcm marker CCR7) (figure 6B, online supplemental figure S7A). The Tem groups showed low expression of both Trm marker CD69 and Tcm marker CCR7, while the Tem2 group had much lower expression of the Trm marker CXCR6 than the Tem1 group (figure 6B, online supplemental figure S7A). The combination of Runx3-OE and AKTi enriched the T-cell population with both Trm and Tcm characteristics (figure 6C). AKTi enriched T cells with Trm characteristics among Runx3-OE CAR-T cells (figure 6C), whereas Runx3-OE downregulated the Tem2 population and enriched the Tem1 population (online supplemental figure S7B). More specifically, Runx3-OE enriched clusters 2 and 3 (online supplemental figure S7C), which expressed CLA, CXCR6, and CXCR3 but did not express CD69 and CD103. Almost all the tumor-infiltrating CAR-T cells exhibited a CD69+ phenotype 30 days after adoptive therapy, whereas Runx3-OE promoted the formation of CD69+CD103+ Trm cells (figure 6D,E).

Figure 6

Runx3-overexpression cooperated with ex vivo AKTi to enrich T-cell population with both Trm and Tcm characteristics in vivo. (A) Heatmap of the expression of representative markers associated with Trm and Tcm phenotypes in different CD8+CAR T clusters. CAR-T cells were isolated from lymph nodes 14 days after CAR-T therapy. The expression of markers was quantified by CyTOF and clusters were identified by PhenoGraph method. (B) t-SNE map of CD8+CAR T cells expressing different markers detected by CyTOF. Clusters with similar markers were combined. (C) Percentages of Trm and Trm/Tcm cells in CD8+CAR T cells identified by CyTOF. CAR-T, normal CAR-T cells; CAR-RUNX3-T, Runx3-overexpressed CAR-T cells; AKTi, T cells were expended in 1 µM AKTi-1/2. (D) Representative flow cytometry plot and (G) percentages of CD69+CD103+ Trm cells in tumor-infiltrating CAR-T cells 30 days after adoptive therapy. A two-way analysis of variance was used for multiple comparisons in panels C and E, and p values were adjusted by Tukey method. P value<0.05 was considered statistically significant. AKT, protein kinase B; AKTi, AKT inhibition; CAR, ch