Folate Receptor-Alpha Targeted 7x19 CAR-<i>γδ</i>T Suppressed Triple-Negative Breast Cancer Xenograft Model in Mice

Ye, Xueshuai; Deng, Xinna; Wen, Junye; Li, Yang; Zhang, Mengya; Cai, Ziqi; Liu, Guan; Wang, Hezhi; Cai, Jianhui

doi:https://doi.org/10.1155/2022/2112898

Journal of Oncology

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Abstract Introduction Methods Results Discussion Conclusion Data Availability Conflicts of Interest Acknowledgments References Copyright Related Articles

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Epithelial-Mesenchymal Transition and its Impact on Tumor Metastasis

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Volume 2022 | Article ID 2112898 | https://doi.org/10.1155/2022/2112898

Folate Receptor-Alpha Targeted 7x19 CAR-γδT Suppressed Triple-Negative Breast Cancer Xenograft Model in Mice

Xueshuai Ye,^1,2Xinna Deng,²Junye Wen,²Yang Li,^1,3Mengya Zhang,³Ziqi Cai,³Guan Liu,^1,3Hezhi Wang,⁴and Jianhui Cai^1,2

Academic Editor: Qin Yuan

Received26 Nov 2021

Revised27 Dec 2021

Accepted10 Jan 2022

Published07 Mar 2022

Abstract

Background. Triple-negative breast cancer (TNBC) is the worst prognosis subtype of breast cancer due to lack of specific targets. Recent studies have shown that immunotherapy may solve that problem by targeting folate receptor-alpha (FRα). Methods. Gene modified γδ T cells were manufactured to express FRa specific chimeric antigen receptor (FRa CAR) and secrete interleukin-7 (IL-7) and chemokine C–C motif ligand 19 (CCL19). CAR-γδT cells that secrete IL-7 and CCL19 (7 × 19 CAR-γδT) were evaluated for their antitumor activity both in vitro and in vivo. Results. 7 × 19 CAR-γδT showed remarkable antitumor activity in vitro. Combined with PBMC, 7 × 19 CAR-γδT inhibited TNBC xenograft model growth superiorly compared with single-application or conventional CAR-γδT cells. Histopathological analyses showed increased DC or T cells infiltration to tumor tissues. Conclusion. Taken together, our results showed that 7 × 19 CAR-γδT have remarkable anti-TNBC tumor activity and showed a broad application prospect in the treatment of incurable TNBC patients.

1. Introduction

Triple-negative breast cancer (TNBC) is a kind of deadly disease, and there are nearly 15% of invasive breast cancer are TNBC [1]. The expression of human epidermal growth factor receptor 2 (HER2), estrogen receptor (ER), and progesterone receptor (PR) is negative in TNBC patients. Thus, endocrinotherapy and HER-2 targeted therapy were ineffective when treating TNBC, which necessitates novel treatment methods for TNBC patients. Chimeric antigen receptor (CAR) T cell had shown brilliant antitumor ability in hematologic malignancy by targeting the certain antigen such as CD19 and CD20 [2]. Second generation of CAR-T cells has an intracellular signaling domain consisting of CD3 ζ and one costimulatory molecule, such as CD28 or CD137, while the third generation CAR-T cells has nearly the same structure besides two costimulatory molecules. However, the treatment effect of second and third generation CAR-T cells is still controversial [3]. There are still many obstacles to overcome in the application of CAR-T cell therapy fighting against solid tumor. Unlike most hematologic malignancy tumor cells dispersed in the peripheral vascular or lymphatic system, solid tumor cells are the absence of ideal targets and usually grew as a lump. Aggregation and growth of tumor cells formed an immune impressive tumor microenvironment (TME), which is low oxygen, low pH, high metabolic waste, high immune-suppressive cytokines, and the upregulation of immune-checkpoint, such as PD-L1 and CTLA-4; those factor made the immune cells can hardly recognize and lyse the cancer cell [4, 5].

Besides, autologous T cells engineered to express a CAR also limit the application of CAR-T as an “off the shelf” drug to some extent. The ideal universal donor-derived T cell resources are γδT cells or HLA and MHC depleted αβ T cells. Those αβ T cells can be produced by using gene editing tools such as TALEN [6], ZFN, and CRISPR/CAS9 to disrupt the endogenous TCR and HLA class I (HLA-I) [7, 8], while the γδT cells can be safely applied in the allogeneic graft and γδT cells can secrete CXCL13 naturally, which regulated the migration of B cells [9].

CCL19 is a chemoattraction for T cells and DCs [10, 11]. DCs plays an essential role in cell immunity through antigen presentation, T cells activation, and multiple cytokine releases, which mean CCL19 may break the TME by attracted DCs infiltration. IL-7 is known to enhance the proliferation and survival of T cells [12–14]. On the one hand, IL-7 can protect the T cells form inhibitory of TME. Previous reports have suggested that IL-7 signaling can prevent or restore T-cell exhaustion by means of multiple mechanisms, including downregulating PD-1 expression and Treg cell’s function [15]. By introducing CCL19 and IL-7 into the conventional CAR structure, Koji Tamada et al. found that the 7 × 19 CAR-T can inhibit the growth of multiple types of solid tumors [16]. This research suggested that 7 × 19 CAR structure-based cell therapies may also bring hope for the TNBC treatment.

Several potential antigen targets, such as TEM8/ANTXR1 [17], NKG2D [18], MUC1 [19], and AXL, have been researched in TNBC. Folate receptor-alpha (FRα) is highly expressed in nonmucinous tumors of epithelial origin including ovarian, breast, and lung cancers and expressed at low levels on the apical surface of a subset of polarized epithelial cells, including the parotid, kidney, lung, thyroid, and breast. Specific overexpression of FRα is present in certain malignancies, including TNBC [20]. With low coordinate expression in normal tissue, FRα is an attractive target. However, the conventional second generation CAR-T targeting FRa did not inhibit tumor growth in those TNBC moderated expression model [21].

In the present study, we constructed a FRa specific mov19 scFv-based 7 × 19 CAR containing a fused CD28/CD3ζ endodomain and two 2A peptide to separate CCL19 and IL-7. Our results demonstrated that the 7 × 19 CAR-γδT cell can strongly suppress TNBC tumor in vivo through various mechanisms.

2. Methods

2.1. Cell Lines

HEK-293T cell line was purchased from American Type Culture Collection (ATCC, Manassas, VA, USA) and used for lentivirus packaging and maintained in DMEM medium supplemented with 10% FBS (Gibco, Life Technologies, Rockville, MD, USA), 100 U/mL penicillin, 100 mg/mL streptomycin sulfate (Life Technologies, Rockville, MD, USA), and 10 mmol/L HEPES. Human breast cancer line MCF-7, human TNBC cell line MDA-MB-231, MDA-MB-436, and MDA-MB-468 were used to determine the biological activity of immune cells. Human ovarian cancer cell line C30 was used as negative control. All the tumor cell lines were maintained in L15 medium supplemented with 10% FBS, 100 U/mL penicillin, and 100 mg/mL streptomycin sulfate.

2.2. CAR Construction

The 7 × 19 CAR construct was comprised of the Mov19 scFv linked to a CD8a hinge and transmembrane region, CD28 intracellular signaling motif, and CD3z signaling moiety tandems in proper order, followed by the genes encoding two 2A peptide sequence between IL-7 and CCL19 (Figure 1(a)). The conventional CAR construct containing the same elements except for the absence of IL-7 and CCL19 was generated as control (Figure 1(b)). The amino acid sequence of 7 × 19 CAR and conventional CAR was cloned in CAR trans-gene plasmids, respectively, for future use.

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Figure 1

γδ T cells were successfully separated and expanded from healthy donor PBMCs and transduced with CAR structure. (a) Schematic representation of 7 × 19 CAR and conventional CAR constructs. (b) The cells were detected by flow cytometry and representative dot plot from the same donor showing the percentage of Vγ9Vδ2 cells in PBMCs (left) and after the MACS magnetic beads sorting (right). (C) FACS analysis of sorting γδT cells transduction efficiency. The sorted γδT were stimulated with ZOL, IL-2, and IL-21 and transfected with either 7 × 19 CAR (middle) or conventional CAR (right). The untransduced γδT were treated as negative control.

2.3. Lentivirus Production

High-titer replication-defective lentiviruses were produced and concentrated according to the manufacturer’s instructions. Briefly, 293T cells were seeded in 150-cm² flask. Either 7 × 19 CAR trans-gene plasmids or conventional CAR trans-gene plasmids (15 μg) were cotransfected with 18 μg pRSV.REV, 18 μg pMDLg/p.RRE, and 7 μg pVSV-G with 174 μL lipo2000 (1 μg/μL) per flask. Supernatants were collected at 48 h after transfection and concentrated 10-fold by ultracentrifugation for 2 h at 28000 rpm with a Beckman SW32Ti rotor. Viruses were aliquoted into tubes and stored at −80°C until ready to use for titering or experiments.

2.4. Preparation of Human γδT Cells

Peripheral blood samples were obtained from healthy donors at Hebei Blood Center, Hebei, China. Informed consents were obtained from all donors in accordance with the guidelines approved by Hebei Medical University, Hebei, China. Peripheral blood mononuclear cells (PBMCs) were isolated by Ficoll-Paque density gradient centrifugation and collected from the interphase. After washing with PBS for three times, the PBMCs were cultured in RPMI-1640 complete medium supplemented with 10%FBS in adherent flask for 2–4 h. Then, the nonadherent cell was removed for sorting the positive γδT cells by using human γδT cell isolation MicroBeads Kit (Miltenyi Biotec, Germany). The sorting processes were operated according to the manufacturer’s instructions, and then, the γδT positive T cells were cultured and stimulated in RPMI-1640 complete medium supplemented with 10%FBS (R10), 300U/ml recombinant human IL-2 (R10 medium), 5 μM zoledronic acid, and 10 ng/mL IL-15 (Life Technologies, Rockville, MD, USA). αβT cell were purified from PBMCs following the same procedure by using human CD [3]+T cell isolation MicroBeads Kit, and then, the αβT cells were activated with OKT3/CD28 and cultured in R10 medium for future use.

2.5. Generation of 7 × 19 CAR-γδtγδ and CAR-γδtγδ Cells

Approximately 24 h after activation, human T cells were transduced using a spinoculation procedure. Briefly, T cells were infected with a multiplicity of infection (MOI) of 5 of the 7 × 19 CAR lentivirus vector. A mixture of cells and vectors were centrifuged at room temperature for 90 min (2500 rpm) in a table-top centrifuge (Sorvall ST 40). Then, rested T cells were used for functional analysis.

2.6. Cell Migration Assay

Chemotaxis of the B cells, αβT cells, or DCs was measured by migration through a polycarbonate filter of 5-µm pore-size in 96-well transwell chambers (Millipore, Billerica, MA, USA). The process was performed according to the manufacturer’s instruction. Briefly, 7 × 19 CAR-γδT, CAR-γδT or γδT cells were stimulated in the lower chambers, and the responder cells, including PBMCs, CFSE-labeled αβT cells, or CFSE-labeled DCs, were incubated in the upper chambers for 4 h. The cells that migrated from the upper chamber to the lower chamber were assessed and counted by flow cytometry.

2.7. Flow Cytometry Analysis

To demonstrate positive CAR expression and antigen binding capacity, T cells surface CAR expression was evaluated using recombinant FRα-Fc protein followed by PE-labeled anti-human IgG Fc gamma-specific antibody. The T cell phenotypic were measured by PE-anti-human TCRγ/δ. Expression of CCR7 in human PBMCs, αβT cells, and DC cells was detected by APC-anti-human CCR7 antibody. Human breast cancer cell line MCF-7, human TNBC tumor cell line MDA-MB-231, MDA-MB-436, MDA-MB-468, and human ovarian cancer cell line C30 cell line surface expression of FRα were measured using human PE-FRα mAb. B cell migration was identified by using the same gate as in PBMC.

All flow cytometry was conducted using a BD FACS Canto flow cytometer (BD Biosciences), and flow cytometric data were analyzed with FlowJo version 7.6.1 software.

2.8. In Vitro Stimulation of CAR-T Cells

For stimulation of FRa specific 7 × 19 CAR-T and conventional CAR-T cells, MDA-231 cells were inactivated with 50ug/ml mitomycin C for 90 min at 37 °C. Cytokine release assays were performed by coculturing 7 × 19 CAR T, conventional CAR T, or UNT cells with 1 × 10⁵ MDA-231 or C30 cells in triplicate in a 96-well flat bottom plate in a total volume of 200 μL. After 20–24 h, cocultured supernatants were collected and ELISA (Biolegend, San Diego) was performed, according to the manufacturer’s instructions, to measure the IFN-γ, IL-7, and CCL19, which were included in the culture medium. The values showed represent the mean of triplicate wells.

2.9. Cytotoxicity Assays

For cytotoxicity assay, 5 × 10 [4] MCF-7, MDA-231, or C30 cells were cultured with RPMI-1640 complete media in the presence of different effector cells ratios in 96-well Microplate. After coculturing for 12 h, tumor cell viability percentage were measured by CCK-8 kit through exhibiting the absorbance at 450 nm by a microplate reader. Cytotoxicity results were calculated using the following formula: specific lysis (%) = [1– (mixture cell experiment–medium control)/(target cell spontaneous–medium control)]×100%. All data are represented as a mean of triplicate wells.

2.10. Treatment of Breast Cancer or TNBC Xenograft Model

To evaluate the antitumor ability of 7 × 19 CAR-T in vivo, six-to-eight-week old, female nonobese diabetic/severe combined immunodeficient (NOD/SCID) mice were purchased from Charles River Laboratories (Beijing. China) and bred, treated, and maintained under specific pathogen-free (SPF) condition. Mice were inoculated subcutaneously on the right flank with either 3 × 10 [6] MDA-231 cells/0.3 ml PBS or 3 × 10 [6] MCF-7 cells/0.3 ml PBS on day 0. After tumor volume reached 150–200 mm [3], the MCF-7 cells bearing mice were randomly divided into four groups and treated with 2 × 10 [7] PBMC/0.2 ml PBS, 2 × 10 [7] γδT/0.2 ml PBS, 2 × 10 [7] CAR-γδT/0.2 ml PBS, and 2 × 10 [7] 7 × 19 CAR-γδ T/0.2 ml PBS, respectively. The MDA-231 cells bearing mice were randomly divided into six groups and treated with 2 × 10 [7] PBMC/0.2 ml PBS, 2 × 10 [7] γδT/0.2 ml PBS, 2 × 10 [7] CAR-γδT/0.2 ml PBS, 2 × 10 [7] 7 × 19 CAR-γδ-T/0.2 ml PBS, 2 × 10 [7] CAR-γδT+ 2 × 10 [7] PBMC/0.2 ml PBS, and 2 × 10 [7] 7 × 19 CAR-γδ T+ 2 × 10 [7] PBMC/0.2 ml PBS through tail vein injection, respectively. The tumor size was measured using caliper twice a week, and the tumor volumes were calculated using formula V = (length × width (2))/2. When the tumor volumes reach nearly 1500 mm³, the mice were sacrificed, and tumor samples were resected to calculate the final volume. The mice were euthanized with carbon dioxide. The euthanasia box does not contain carbon dioxide before placing the animal. After placing the animals, fill the euthanasia box with CO₂ at a rate of 10% of the replacement box volume per minute. After 10 min, the mice did not breathe, and their pupil dilated. The mice were observed for another 2 min and confirmed to be completely dead.

2.11. Histopathological and Immunofluorescence Assays

After the TNBC xenograft tumor was resected, samples were stored in paraformaldehyde fixative and then embedded in paraffin. For hematoxylin and eosin (H&E) staining, paraffin sections were first dewaxed and stained with hematoxylin. Sections were then dehydrated in an ethanol gradient and stained with eosin. In immunofluorescence (IF) analysis, anti-CD3 antibody and anti-S100 antibody were used as primary antibody and nuclei were stained with DAPI. Representative pictures from three independent experiments are shown.

2.12. Statistical Analysis

The data are reported as means and standard deviations (SDs). Statistical analysis was performed using two-way repeated-measure analysis of variance (ANOVA) for the tumor volumes. Student’s t-test was used to evaluate differences in absolute numbers of transferred T cells, cytokine secretion, and specific cytolysis. GraphPad Prism 5.0 (GraphPad Software) was used for the statistical calculations, where a value of < 0.05 was considered significant.

3. Results

3.1. Construction and Expression of Either FRα-Specific 7 × 19 CAR or Conventional CAR in γδT Cells from Peripheral Blood

The percentage of γδT in the peripheral blood varies from 3%–10% (Figure 1(b), left). Through magnetic bead negative sorting, the enriched cells were amplified by stimulation of zoledronic acid, IL-2, and IL-15, and the concentration could reach 99% (Figure1(b), right). The FRα targeting CAR-encoding lentivirus construct was generated by fusing the MOv19 scFv, CD8α hinge and transmembrane region, CD28 intracellular signaling motif, CD3ζ signaling moiety, two 2A peptide sequences to separate the conventional CAR structure, IL-7, and CCL19. Two CAR structures were named as 7 × 19 CAR or conventional CAR (Figure 1(a)). Purified γδT cells were efficiently transduced with either 7 × 19 CAR or CAR lentiviral vectors with the transduction efficiency of nearly 45% (Figure 1(c)).

3.2. CCR7 Is an Attractive Chemokine Receptor in Various Immune Cells

The chemokine CCL19 and its receptor CCR7 have a wide range of sources in the body. CCL19/CCR7 is involved in the homing of immune cells and the occurrence of inflammatory response in the body. The flow cytometry results indicated that 50% of the DC cells, the majority of PBMC, and the 100 percent of αβ T cells are CCR7 positive expression (Figure 2(a)). The bimodal distribution of αβ T indicates different fluorescence intensities, which reveals the different expression level of CCR-7 in CD4/CD8 T cells (Figure 2(a), right). The secretion of CCL19 and IL-7 was then measured using ELISA. The results show that the activated 7 × 19 CAR-γδ T can secrete CCL19 and IL-7 exclusively, while the CAR-γδ T or γδ T cannot (Figure 2(b)). Then, we performed transwell migration assays. The migration of responder T cells, DC cells, and B cells was significantly enhanced by incubation with 7 × 19 CAR-T cells compared with conventional CAR-T cells (Figures 2(c) and 2(d)).

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Figure 2

Chemotactic capacity towards γδT, CAR-γδT, and 7 × 19 CAR-γδ T cells. (a) FACS analysis of the expression of CCR7 in human dendritic cells (left), PBMCs (middle), and αβ T cells (right). (b) IL-7/CCL19 secretion of γδT, CAR-γδT, and 7 × 19 CAR-γδT were detected by ELISA, respectively ( ＜ 0.01). (c) The purified αβ T cell migrated from the upper chamber to the lower chamber and was analyzed by flow cytometry ( ＜ 0.01). (d) B cells and CFSE-labeled dendritic cells migration driven by CXCL13 and CCL19 were counted using flow cytometry. P values were calculated by Student’s two-sided t-test.

3.3. FRα Is Expressed on the Surface of TNBC Cell Lines Moderately

Using flow cytometry, surface expression of FRα protein was detected on human breast cancer cell line MCF-7, human TNBC tumor cell line MDA-MB-231, MDA-MB-436, and MDA-MB-468, and human ovarian cancer cell line C30 cell line after staining the cells with anti-FRα antibody. As shown in Figure 3. FRα is overexpressed in MCF-7 and is moderately expressed in MDA-MB-231, MDA-MB-436, and MDA-MB-468 but is negative in C30 cell line.

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Figure 3

Antitumor ability of γδT, CAR-γδT, and 7 × 19 CAR-γδ T cells both in vitro and in MCF-7 CDX model. (a) FACS analysis of the expression level of FRa in human TNBC cell line MDA-231, MDA-436, MDA-468, human breast cancer cell line MCF-7, and human ovarian cancer cell line C30. (b) FRa-specific cytotoxicity curves of γδT, CAR-γδT, and 7 × 19 CAR-γδ T cells against FRa negative expression C30 (left), FRa moderate expression MDA-MB-231 (middle), and FRa overexpression MCF-7 (right) tumor cell lines at the ratio of 1 : 1, 5 : 1, 10 : 1, respectively. (c) Histograms showed IFN-γ secretion of γδT, CAR-γδT, and 7 × 19 CAR-γδT against C30, MDA-MB-231, and MCF-7 at the ratio of 10 : 1. The IFN-γ production was detected using ELISA. (d) Tumor volume curves of FRa overexpression in MCF-7 CDX models. Quantification of tumor volumes (mm3) in the PBMC, γδT, CAR-γδT, and 7 × 19 CAR-γδ T treatment groups.

3.4. 7 × 19 CAR-γγδ T Cells Specifically Lysed FRαpos Tumor Cells In Vitro

CCK-8 assay was performed to detect the killing effects of 7 × 19 CAR-γδ T and conventional CAR-γδ T cells (effector cells). FRα^pos MCF-7 and MDA-231 cells were used as target cells, and FR^neg C30 were used as a negative control. 7 × 19 CAR-γδ T and conventional CAR-γδ T cells were cocultured with MCF-7, MDA-231, or C30 with different E : T ratios(1 : 1, 5 : 1, and 10 : 1), respectively. As shown in Figure 3(b), both of the 7 × 19 CAR-γδ T and conventional CAR-γδ T demonstrated strong cytotoxicity against FRα^pos MCF-7 and the killing efficiency was dose-dependent as the ratio of effector cells increased, but the untransduced γδ T did not show that tendency.

As a negative control, both of the 7 × 19 CAR-γδ T and conventional CAR-γδ T cells did not show obvious cytotoxicity when cocultured with FRα^neg C30 cells, and there was no statistically significant difference compared with untransduced γδ T cells. For the FRα moderate expressed MDA-231 cells, 7 × 19 CAR-γδ T and conventional CAR-γδ T can target the FRα^pos tumor cells, and the cytotoxicity was matched with the FRα expression level. Those results indicated that either 7 × 19 CAR-γδ T or conventional CAR-γδ T cells can specifically lyse tumor cells, where FRa are positively expressed.

3.5. 7 × 19 CAR-γγδ T Secrete Cytokines in Response to Tumor Stimulation

Cytokines IFN-γ in the effect cells against target cells in cocultured supernatants were detected by ELISA assay. As shown in Figure 3(c), a robust amount of IFN-γ was observed in either 7 × 19 CAR-γδT or CAR-γδT groups against MCF-7 or MDA-231. Moreover, the secretion of 7 × 19 CAR-γδT was significantly higher than that of CAR-γδT, which may be associated with the activated functions of IL-7. When 7 × 19 CAR-γδT or conventional CAR-γδT or γδT were cocultured with C30 cells, there were no significant statistical difference among these groups. Those results demonstrated that 7 × 19 CAR-γδT can activate costimulatory molecules through targeting and combining specific antigens and the cytotoxicity can be enhanced by IL-7.

3.6. 7 × 19 CAR-γδtγδ Induced Tumor Regression In Vivo

As 7 × 19 CAR-γδT and CAR-γδT can lyse FRa ^pos target cells in vitro specifically, we next evaluate its antitumor ability in vivo. In MCF-7 CDX model, the single use of 7 × 19 CAR-γδT or CAR-γδT can suppress tumor growth significantly compared with PBMC or γδT treatment groups (Figure 3(d)). Then, we applied the 7 × 19 CAR-γδT to find out its treating ability in the FRa moderate expression xenograft model. The mice were treated with certain numbers of effector cells through tail vein injection. Notably, 7 × 19 CAR-γδT + PBMC treatment group is the only effective treatment group that suppressed tumor growth prominently compared with other groups (Figure 4(b)). IF analysis indicated that 7 × 19 CAR-γδT + PBMC treatment groups induced massive T-cell infiltration in the tumor tissue, substantially higher than conventional CAR-γδT + PBMC treatment groups. Furthermore, infiltration of DCs into the tumor tissues and their colocalization with T cells were observed after treatment with 7 × 19 CAR-γδT + PBMC but not conventional CAR-γδT + PBMC cells, indicating that 7 × 19 CAR-γδT cells are capable of recruiting endogenous DCs into tumor tissues (Figures 4(d)–4(f)). The single use of the same does of CAR-γδT suppressed tumor growth for a short time after the infusion, but then, the tumor grew rapidly, which may be related to the loss of antigens, and the absence of other immune cells plays a synergy role at the tumor site. The HE analysis also displayed large areas of vacuolar necrosis of the 7 × 19 CAR-γδT + PBMC treated tumor tissues (Figures 4(c)–4(f)), while no extensive necrosis was observed in other groups.

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Figure 4

Antitumor ability of γδT, CAR-γδT, and 7 × 19 CAR-γδ T cells in FRa moderate expression MDA-MB-231 CDX model. (a) Tumor size comparison. Tumor xenografts were excised after treatment with different effector cells. One representative sample was displayed for each group. (b) Tumor volume curves of FRa overexpression MCF-7 CDX models. Quantification of tumor volumes (mm3) in the PBMC, γδT, CAR-γδT, 7 × 19 CAR-γδ T, and the combination of PBMC with either CAR-γδT or 7 × 19 CAR-γδT treatment groups. (c) H&E analysis of different treatment groups: (a–f) γδT, PBMC, CAR-γδT, 7 × 19 CAR-γδ t CAR-γδT + PBMC, 7 × 19 CAR-γδ T + PBMC treatment groups, respectively (40×). (d) Immunofluorescence (IF) analysis of T cells and DC cells infiltration into the tumor xenografts. (A–F) γδT, PBMC, CAR-γδT, 7 × 19 CAR-γδ T CAR-γδT + PBMC, and 7 × 19 CAR-γδ T + PBMC treatment groups, respectively (200×).

4. Discussion

Serval factors contribute to the unavailability of effective treatment methods for TNBC. On the one hand, due to the scarcity of ideal targets, adoptive cell therapy such as CAR-T or TCR-T cells cannot specifically recognize and bind to the tumor cells. On the other hand, the presence of tumor microenvironment (TME) in the solid tumor had also limited the cytotoxicity of immune cells.

Song et al. [21] showed the remarkable killing efficiency in gene engineered FRa antigen overexpression xenograft model, indicating that FRa is a promising target in the treatment of patients whose FRa antigen are overexpressed. In natural TNBC cell-derived xenograft (CDX) model, the second-generation CAR-T cells targeting FRa did not show that tendency. This phenomenon can be regarded as sequential antigen loss [22, 23], and it is reasonable that the FRa-CAR T can lyse the Fra-positive tumor cells specifically, but not the residual Fra-negative tumor cells, which leads to the ineffectiveness of FRa-targeting cell therapy.

γδT cells can target the tumor cells through non-MHC restricted mode naturally [24]. After the target cells were lysed, tumor antigens were took up and processed as associated peptide by γδT cells and then presented to the αβT cells [25, 26]. γδT cells can also secrete CXCL13, which regulated the migration of B cells. It may motivate the body’s innate humoral immunity to exert the antitumor response [9]. Some studies have pointed that the lifespan of γδT cells is shorter than that of αβT cells [27], which is possibly due to their inability to colonize bone marrow. This may also reduce the long-term toxicity of CAR-T to a certain extent, although it has an adverse effect on the maintenance of the body’s long-term antitumor response [28]. In addition, 7 × 19 CAR-γδT infusion can reduce the adverse effects of CAR-T-associated side effects by reducing the dose of cells in a single infusion while maintaining the long duration of the antitumor immune response by playing the role of APC and promoting the formation of memory associated phenotype antitumor T cells [29, 30].

In this study, we introduced chemokines CCL19 and IL-7 into the structure of conventional CAR, each domain was separated using 2A ligating peptides to ensure their respective functions. Either the FRa-targeting CAR-γδT or 7 × 19 CAR-γδT suppressed the FRa overexpressed MCF-7 tumor cells both in vitro and in vivo. But for the FRa moderately expressed MDA-MB-231 cells, CAR-γδT or 7 × 19 CAR-γδT can lyse the Fra-positive cells in vitro and cannot inhibit tumor growth in MDA-MB-231 CDX model when applied separately. The IHC assay found that CAR-γδT and 7 × 19CAR-γδT can hardly infiltrate to the tumor tissues. Then, we applied the combination of 7 × 19 CAR-γδT cells and PBMCs in the treatment of MDA-MB-231 CDX model. Intriguingly, after the coinfusion of 7 × 19 CAR-γδT cells and PBMCs, the tumor growth was significantly inhibited and IHC indicated that plenty of DCs and CD3 positive cells infiltrated to the tumor tissues compared with other groups.

In summary, our study presented that 7 × 19 CAR-γδT can suppress natural TNBC CDX model by lysis of the FRa positive cells and secreting CCL19 and IL-7. CCL19 can make chemotactic DC cells and αβT cells infiltrate into tumor tissue, and those αβT cells can be activated by the APC cells such as DC cells and γδT cells and played a synergistic role in fighting against the FRa-negative TNBC cells. The IL-7 enhanced the proliferation and survival ability of T cells that infiltrated into tumor tissues, which reduced the inhibitory of tumor microenvironment [30]. These results provide insights into the application of universal 7 × 19 CAR-γδT in solid tumor treatment and explored a new method to enhance the ACT antitumor ability by mobilizing the normal immune cells.

5. Conclusion

Our findings demonstrated that 7 × 19 CAR-γδT can not only lyse the target tumor cells, but also break through the TME and lyse nontarget tumor cells through motivating the body’s own immunity.

Data Availability

The analyzed datasets generated during the study are available from the corresponding author on reasonable request.

Conflicts of Interest

The authors declare that there are no conflicts of interest.

Acknowledgments

The authors thank YongqiangWu (Gene Editing Research Center, Hebei University of Science and Technology) for technical support. This work was supported by the Hebei Government Special Project of Top Talents (2014–2019) and Hebei Province Science and Technology Plan (21372406D).

References

T. G. Lyons, “Targeted therapies for triple-negative breast cancer,” Current Treatment Options in Oncology, vol. 20, no. 11, p. 82, 2019.
View at: Publisher Site | Google Scholar
J. S. Abramson, “Anti-CD19 CAR T-cell therapy for B-cell non-hodgkin lymphoma,” Transfusion Medicine Reviews, vol. 34, no. 1, pp. 29–33, 2020.
View at: Publisher Site | Google Scholar
C. Zhang, J. Liu, J. F. Zhong, and X. Zhang, “Engineering CAR-T cells,” Biomarker Research, vol. 5, no. 1, p. 22, 2017.
View at: Publisher Site | Google Scholar
J. Hamanishi, M. Mandai, N. Matsumura, K. Abiko, T. Baba, and I. Konishi, “PD-1/PD-L1 blockade in cancer treatment: perspectives and issues,” International Journal of Clinical Oncology, vol. 21, no. 3, pp. 462–473, 2016.
View at: Publisher Site | Google Scholar
B. Arneth, “Tumor microenvironment,” Medicina, vol. 56, no. 1, p. 15, 2019.
View at: Publisher Site | Google Scholar
W. Qasim, H. Zhan, S. Samarasinghe et al., “Molecular remission of infant B-ALL after infusion of universal TALEN gene-edited CAR T cells,” Science Translational Medicine, vol. 9, no. 374, Article ID eaaj2013, 2017.
View at: Publisher Site | Google Scholar
J. Zhao, Q. Lin, Y. Song, and D. Liu, “Universal CARs, universal T cells, and universal CAR T cells,” Journal of Hematology & Oncology, vol. 11, no. 1, p. 132, 2018.
View at: Publisher Site | Google Scholar
J. Eyquem, J. Mansilla-Soto, T. Giavridis et al., “Targeting a CAR to the TRAC locus with CRISPR/Cas9 enhances tumour rejection,” Nature, vol. 543, no. 7643, pp. 113–117, 2017.
View at: Publisher Site | Google Scholar
R. R. Bansal, C. R. Mackay, B. Moser, and M. Eberl, “γδIL-21 enhances the potential of human γδ T cells to provide B-cell help,” European Journal of Immunology, vol. 42, no. 1, pp. 110–119, 2012.
View at: Publisher Site | Google Scholar
R. Yoshida, “EBI1-ligand chemokine (ELC) attracts a broad spectrum of lymphocytes: activated T cells strongly up-regulate CCR7 and efficiently migrate toward ELC,” International Immunology, vol. 10, no. 7, pp. 901–910, 1998.
View at: Publisher Site | Google Scholar
S. A. Kellermann, S. Hudak, and E. R. Oldham, “The CC chemokine receptor-7 ligands 6Ckine and macrophage inflammatory protein-3 beta are potent chemoattractants for in vitro- and in vivo-derived dendritic cells,” The Journal of Immunology, vol. 162, pp. 3859–3864, 1999.
View at: Google Scholar
T. J. Fry and C. L. Mackall, “Interleukin-7: master regulator of peripheral T-cell,” 2013.
View at: Google Scholar
B. Asefa and A. R. Khaled, “homeostasis?” Trends in Immunology, vol. 22, pp. 564–571, 2001.
View at: Google Scholar
L. M. Bradley, L. Haynes, and S. L. Swain, “IL-7: maintaining T-cell memory and,” 2005.
View at: Google Scholar
M. L. Baker, W. S. Wels, and J. Koch, “Achieving homeostasis,” Trends in Immunology, vol. 26, pp. 172–176, 2005.
View at: Google Scholar
Q. Jiang, W. Q. Li, F. B. Aiello et al., “Cell biology of IL-7, a key lymphotrophin,” Cytokine & Growth Factor Reviews, vol. 16, no. 4-5, pp. 513–533, 2005.
View at: Publisher Site | Google Scholar
L. Hou, Z. Jie, Y. Liang, M. Desai, L. Soong, and J. Sun, “Type 1 interferon-induced IL-7 maintains CD8+ T-cell responses and homeostasis by suppressing PD-1 expression in viral hepatitis,” Cellular and Molecular Immunology, vol. 12, no. 2, pp. 213–222, 2015.
View at: Publisher Site | Google Scholar
K. Adachi, Y. Kano, T. Nagai, N. Okuyama, Y. Sakoda, and K. Tamada, “IL-7 and CCL19 expression in CAR-T cells improves immune cell infiltration and CAR-T cell survival in the tumor,” Nature Biotechnology, vol. 36, no. 4, pp. 346–351, 2018.
View at: Publisher Site | Google Scholar
T. T. Byrd, K. Fousek, A. Pignata et al., “TEM8/ANTXR1-Specific CAR T cells as a targeted therapy for triple-negative breast cancer,” Cancer Research, vol. 78, no. 2, pp. 489–500, 2018.
View at: Publisher Site | Google Scholar
Y. Han, W. Xie, D.-G. Song, and D. J. Powell, “Control of triple-negative breast cancer using ex vivo self-enriched, costimulated NKG2D CAR T cells,” Journal of Hematology & Oncology, vol. 11, no. 1, p. 92, 2018.
View at: Publisher Site | Google Scholar
R. Zhou, M. Yazdanifar, L. D. Roy et al., “CAR T cells targeting the tumor MUC1 glycoprotein reduce triple-negative breast cancer growth,” Frontiers in Immunology, vol. 10, p. 1149, 2019.
View at: Publisher Site | Google Scholar
W. Xia and P. S. Low, “Folate-targeted therapies for cancer,” Journal of Medicinal Chemistry, vol. 53, no. 19, pp. 6811–6824, 2010.
View at: Publisher Site | Google Scholar
D.-G. Song, Q. Ye, M. Poussin, J. A. Chacon, M. Figini, and D. J. Powell, “Effective adoptive immunotherapy of triple-negative breast cancer by folate receptor-alpha redirected CAR T cells is influenced by surface antigen expression level,” Journal of Hematology & Oncology, vol. 9, no. 1, p. 56, 2016.
View at: Publisher Site | Google Scholar
M. Hegde, M. Mukherjee, Z. Grada et al., “Tandem CAR T cells targeting HER2 and IL13Rα2 mitigate tumor antigen escape,” Journal of Clinical Investigation, vol. 126, no. 8, pp. 3036–3052, 2016.
View at: Publisher Site | Google Scholar
H. Shalabi, I. L. Kraft, H.-W. Wang et al., “Sequential loss of tumor surface antigens following chimeric antigen receptor T-cell therapies in diffuse large B-cell lymphoma,” Haematologica, vol. 103, no. 5, pp. e215–e218, 2018.
View at: Publisher Site | Google Scholar
I. Airoldi, A. Bertaina, I. Prigione et al., “γδγδ T-cell reconstitution after HLA-haploidentical hematopoietic transplantation depleted of TCR-αβ+/CD19+ lymphocytes,” Blood, vol. 125, no. 15, pp. 2349–2358, 2015.
View at: Publisher Site | Google Scholar
M. Brandes, K. Willimann, and B. Moser, “Professional antigen-presentation function by human γδ T cells,” Science, vol. 309, no. 5732, pp. 264–268, 2005.
View at: Publisher Site | Google Scholar
A. Capsomidis, G. Benthall, H. H. Van Acker et al., “Chimeric antigen receptor-engineered human gamma delta T cells: enhanced cytotoxicity with retention of cross presentation,” Molecular Therapy, vol. 26, no. 2, pp. 354–365, 2018.
View at: Publisher Site | Google Scholar
B. L. Clark and P. G. Thomas, “γδA cell for the ages: human γδ T cells across the lifespan,” International Journal of Molecular Sciences, vol. 21, no. 23, p. 8903, 2020.
View at: Publisher Site | Google Scholar
J. N. Brudno and J. N. Kochenderfer, “Recent advances in CAR T-cell toxicity: mechanisms, manifestations and management,” Blood Reviews, vol. 34, pp. 45–55, 2019.
View at: Publisher Site | Google Scholar

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Copyright © 2022 Xueshuai Ye et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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