Chimeric antigen receptor (CAR) T-cell therapies have demonstrated durable and potentially curative therapeutic efficacy against B-cell leukemia in clinical trials. A CAR strategy can target any tumor surface antigens as long as an antigen-binding receptor can be generated. New CARs that target solid tumors and have the potential to target multiple tumor types are needed. In this study, B7H6, a ligand for the NK cell activating receptor NKp30, was targeted to create a CAR that targets multiple tumor types. B7H6 is expressed on various primary human tumors, including leukemia, lymphoma and gastrointestinal stromal tumors, but it is not constitutively expressed on normal tissues. B7H6-specific CAR T cells have robust cellular cytotoxicity and interferon-γ secretion when co-cultured with B7H6+ tumor cells, and they exhibit little self-reactivity to immature dendritic cells or pro-inflammatory monocytes. In vivo, B7H6-specific CAR T cells greatly enhanced the survival of RMA/B7H6 lymphoma-bearing mice. The long-term survivor mice were protected against a B7H6-deficient tumor re-challenge. This CAR therapy also decreased tumor burden in a murine ovarian cancer model. In conclusion, B7H6-specific CARs have the potential to treat B7H6+ hematologic and solid tumors.
Chimeric antigen receptor (CAR) T-cell therapies have demonstrated durable and potentially curative therapeutic efficacy in various clinical trials.1, 2, 3, 4 CARs generally consist of a single-chain variable fragment from antibody for target recognition, fused with co-stimulation signaling domains, such as CD28 or 4-1BB, and a CD3ζ signaling domain to provide T-cell activation signals.5 This approach can target almost any tumor surface antigens as long as a specific receptor can be generated. Additionally, antigen recognition by CARs is often independent of major histocompatibility complex expression, which enables a single CAR design to be used in patients regardless of major histocompatibility complex allele expression. Although CAR strategies can target almost all types of tumors, approaches that target multiple tumor types are rare and CARs that target molecules more selectively expressed on tumors are needed.
CAR designs utilizing NK cell-activating receptors, such NKG2D and NKp30, provide a strategy that targets multiple tumor types yet maintains tumor selectivity over normal cells.6, 7, 8 Many NK cell-activating receptors recognize stress-induced ligands that are specifically expressed on tumor cells.9 For example, NKp30 recognizes B7H6, which is expressed on a diverse number of human tumor cell lines and on some primary human leukemia, lymphomas and gastrointestinal stromal tumors (GISTs).10, 11, 12 Moreover, data suggest that NK cells utilize NKp30 for tumor immune surveillance in clinical settings, such as in acute myeloid leukemia patients, a NCRdull phenotype on NK cells correlated with poor survival.13 In GIST patients, immunostimulatory forms of NKp30 correlated with a better prognosis.12 Furthermore, B7H6 mRNA is not expressed in 48 normal tissues under steady state conditions.11 This suggests that NKp30-based CARs may target multiple tumor types. However, BAG-6, another ligand for NKp30, is expressed on immature dendritic cells (iDCs) and can trigger NK cell killing of iDCs,14, 15 and NKp30-based CARs mediated self-reactivity against peripheral blood mononuclear cells (PBMCs) and iDCs.8
A potential approach to overcome the self-reactivity of NKp30-based CARs to PBMCs and iDCs is to create CARs targeting B7H6. In this study, we show that B7H6-specific CAR T cells mediate robust in vitro and in vivo activity against B7H6-expressing tumor cells with little activity against PBMCs or iDCs. Thus, a B7H6-specific CAR T-cell therapy may be beneficial for a variety of patients with hematologic or solid tumors.
Construction and expression of B7H6-specific CARs and NKp30-based CARs
To generate a CAR specific to B7H6 but not other NKp30 ligands, a single chain variable fragment from an anti-B7H6 monoclonal antibody (mAb) (47.39) was constructed by linking heavy chain variable region and light chain variable region with a (Glycine4Serine)3 linker. This anti-B7H6 single-chain variable fragment was fused with human CD28 hinge (H), transmembrane and cytoplasmic (CYP) domains, followed by a human CD3ζ CYP domain to create a B7H6-specific CAR (anti-B7H6 CAR) (Figure 1a). Wild-type (WT) NKp30 and a NKp30-based CAR (NKp30 CAR) were used for comparison with the anti-B7H6 CAR.8 T cells express WT NKp30 poorly and no specific activity is expected from this CAR, so WT NKp30 transduced T cells were used as a transduction control. The NKp30 CAR contains human CD28 transmembrane and CYP domains between the NKp30 extracellular and CD3ζ CYP domains (Figure 1a). These CARs can be expressed efficiently on the T-cell surface and confer primary and CD28 costimulatory signals through CD3ζ CYP and CD28 CYP domains upon CAR binding to its ligand.8 To assess anti-B7H6 CAR expression and to facilitate sorting of CAR+ T cells, a retroviral vector with the anti-B7H6 CAR, a furin cleavage site containing T2A sequence and a truncated human CD19 gene was also constructed (Figure 1a). Surface expression of anti-B7H6 CARs on transduced human T cells were analyzed by flow cytometry after staining T cells with soluble B7H6 or by using CD19 expression as a surrogate marker of the CAR expression (Figure 1b). Although there is potential for donor to donor variability in CAR expression, the expression of anti-B7H6 CAR on T cells from different human PBMC donors showed very similar patterns of expression (Figure 1c). NKp30 CAR and anti-B7H6 CARs can be expressed efficiently on human T cells, whereas WT NKp30 express poorly on T cells (Figure 1b), as previously shown.8
B7H6 expression on tumor cells
To identify the potential targets for anti-B7H6 CAR T-cell therapy, we screened a panel of human tumor cell lines for B7H6 expression.8 B7H6 expression was found in several hematological malignancy cell lines, including lymphoma, leukemia and multiple myeloma and in several solid tumor cell lines, including melanoma, breast cancer and pancreatic cancer cell lines. A broader survey of B7H6 expression reported that it was found on 24 out of 119 human tumor cell lines.11 As B7H6 gene is expressed in Homo sapiens and Pongo abelii but not Mus musculus, we generated B7H6-expressing murine tumors from RMA T-cell lymphoma, B16F10 melanoma and ID8 ovarian cancer cell lines, which we named as RMA/B7H6, B16F10/B7H6 and ID8/B7H6, respectively, for further in vitro and in vivo experiments (Figure 1d).
B7H6-specific CAR T cells mediate cytotoxicity against B7H6-expressing tumors
To test whether B7H6-specific CAR T cells mediate cytotoxicity, we co-cultured human anti-B7H6 CAR-T2A-tCD19 T cells with B7H6+ tumor cell lines (RMA/B7H6, K562, U937) or B7H6− tumor cell lines (RMA). We observed that human anti-B7H6 CAR T cells mediated robust cytotoxicity against B7H6+ tumors but not B7H6− tumor cells (Figure 2a). To confirm that cytotoxicity was dependent on B7H6, B7H6 was pre-blocked on K562 tumor cells with anti-B7H6 mAbs before incubating tumor cells with CAR T cells. Pre-blocking tumor cells with anti-B7H6 mAbs significantly reduced the cytotoxicity of anti-B7H6 CAR T cells to the cytotoxicity observed with Mock (untransduced) T cells (Figure 2b). We also observed that murine anti-B7H6 CAR T cells specifically killed B7H6+ but not B7H6− tumor cells when cultured with a 1:1 mixture of B7H6− and B7H6+ tumor cells (RMA and RMA/B7H6 or B16F10 and B16F10/B7H6) (Figures 2c and 2d). These data show that both human and murine anti-B7H6 CAR T cells mediate specific killing of B7H6+ tumor cells.
B7H6-specific CAR T cells produce interferon (IFN)-γ when cultured with B7H6-expressing tumors but not immature DCs or lipopolysaccharide (LPS)-, interleukin (IL)-1β- or tumor necrosis factor (TNF)-α-stimulated PBMCs
IFN-γ plays an important role in mediating adoptive T-cell therapy efficacies.16, 17, 18 To examine whether human B7H6-specific CAR T cells produce IFN-γ upon recognition of B7H6+ tumors, Mock, NKp30 CAR and anti-B7H6 CAR T cells were co-cultured with B7H6+ (RMA/B7H6, K562) or B7H6− (RMA) tumor cells. B7H6-specific CAR T cells mediated robust IFN-γ secretion (>2000 pg ml−1) when co-cultured with B7H6+ tumor cells (Figure 3a). The amount of IFN-γ secretion by anti-B7H6 CAR T cells was comparable with NKp30 CAR T cells. It is known that NK cells interact with iDCs and mediate iDC killing and IFN-γ secretion through NKp30 and BAG-6 interactions.15 As anti-B7H6 CAR does not recognize NKp30 ligands other than B7H6, anti-B7H6 CAR T cells should exhibit little reactivity to autologous PBMCs or iDCs compared with NKp30 CAR T cells. Indeed, human anti-B7H6 CAR T cells exhibit little self-reactivity to autologous PBMCs or iDCs compared with NKp30 CAR T cells (Figure 3b). By pre-blocking the ligands on iDCs with NKp30-Ig, there was a significant decrease in the IFN-γ secretion by NKp30 CAR T cells in these co-cultures, confirming the self-reactivity of NKp30 CAR T cells to iDCs is contributed by NKp30 recognition of its ligands (Figure 3c). Besides tumor cells, B7H6 has been reported to be expressed on circulating pro-inflammatory monocytes in a group of patients suffering severe sepsis or on monocytes stimulated in vitro with Toll-like receptor agonists or pro-inflammatory cytokines.19 However, we did not observe that the 47.39 mAb, which was used as the antigen-binding fragment of the B7H6-specific CAR, recognizes B7H6 expression on LPS-, IL-1β- or TNF-α-stimulated CD14+ monocytes (Figure 3d). Furthermore, co-culturing B7H6-specific CAR T cells with LPS-, IL-1β- or TNF-α-stimulated autologous PBMCs did not elicit specific IFN-γ secretion by CAR T cells. This phenomenon was consistent when CAR T cells were derived from different human donors (Figure 3e). As there is little self-reactivity against iDCs and pro-inflammatory monocytes by B7H6-specific CAR T cells, these CAR T cells should provide a broad therapeutic window.
B7H6 mRNA expression is upregulated in multiple primary human tumor types, and B7H6-specific CAR T cells react to human primary ovarian cancer
B7H6 is expressed by some subsets of hematological malignancies, such as acute nonlymphoblastic leukemia, acute lymphoblastic leukemia and lymphomas.11 To identify more primary human tumor types that potentially express B7H6, we took a data-mining approach to identify B7H6 expression in published microarray data from primary human tumor samples. By using the Oncomine database20 interface (https://www.oncomine.org) and searching with the keyword 'DKFZp686O24166', an alias of the B7H6 gene, and further filtering the results by differential analysis filter, we identified several subsets of primary tumor types expressing high amounts of B7H6 mRNA. Table 1 summarizes the tumor types (those having 15–285 different patient samples) that have more than 10% of the samples with high B7H6 mRNA expression (B7H6 mRNA amount>median gene mRNA amount in the particular microarray). Analysis showed that there was B7H6 mRNA expression in primary human lymphoma,21 ovarian cancer22 and sarcomas23 (Figures 4a–c). Her2/neu expression, a known breast cancer target, in human breast cancers is also shown24 using a similar data analysis for comparison (Figure 4d). As expected, some subsets of leukemia and lymphoma had high B7H6 mRNA expression, and this correlated with published data on B7H6 protein expression.11 Furthermore, GIST, the most common mesenchymal tumor of the gastrointestinal tract, whose clinical prognosis is correlated with immunostimulatory NKp30 isoforms, was found to have B7H6 expression.12 When B7H6-specific CAR T cells were co-cultured with primary human ovarian cancers, specific IFN-γ production was observed, and pre-incubating cancer cells with anti-B7H6 mAbs before co-culturing with CAR T cells significantly abrogated the response (Figure 4e). These findings highlighted the potential to target multiple clinically relevant tumor types with B7H6-specific CAR T-cell therapy.
Anti-B7H6 CAR T-cell therapy improved outcomes in murine lymphoma and ovarian cancer models
To study the therapeutic efficacy of anti-B7H6 CAR T cells in vivo, the B7H6-specific CAR was expressed in murine T cells. More than 99% of cells in the CAR cell preparations used for in vivo efficacy studies were CD3+ T cells (Figure 5a). This anti-B7H6 CAR can be expressed efficiently on murine T cells (Figure 5a), and these CAR T cells recognize B7H6-expressing tumors and secrete IFN-γ (Figure 5b). In a systemic T-cell lymphoma model, B6 mice injected with RMA/B7H6 tumor cells intravenously on day 0 were treated with anti-B7H6 CAR T cells intravenously on days 5, 7 and 9. Anti-B7H6 CAR T-cell therapy greatly enhanced the survival of tumor-bearing mice with 83% becoming long-term tumor-free survivors while all control mice had to be killed by day 29 (Figure 5c). Furthermore, the long-term tumor-free survivors were protected upon re-challenge with B7H6-deficient RMA tumor cells (Figure 5d). In an ovarian cancer model, ID8/B7H6 tumor cells were injected into mice intraperitoneally on day 0 and were treated with anti-B7H6 CAR T cells intraperitoneally on day 7. Tumor burden was assessed on day 42 by counting the solid tumors on the peritoneal wall and determining the number of free tumor cells in the peritoneum wash. We observed that anti-B7H6 CAR T-cell therapy greatly reduced the tumor burden of ID8/B7H6 tumor-bearing mice (Figures 5e and f).
In this study, we identified several types of primary human tumors including lymphoma, leukemia, ovarian cancer, breast cancer, renal cell carcinoma, various sarcomas and brain tumors as expressing high amount of B7H6 mRNA. The finding that B7H6 mRNA expression was upregulated in leukemia and GIST correlated well with clinical observations of NKp30-mediated immunosurveillance in these tumors.12, 13 These observations highlighted the potential broad tumor coverage of B7H6-specific CAR T-cell therapy.
Self-reactivity is a major concern for CAR T-cell therapy and can potentially cause unexpected severe adverse effects. The severity can range from manageable side effects, such as B-cell depletion caused by anti-CD19 CAR T cells1, 2, 3 to acute mortality caused by anti-ERBB2 CAR T cells.25 In this study, we created B7H6-specific CARs which maintained NKp30-based CAR tumor-targeting capacity but spared the reactivity against PBMCs and iDCs, so that these CAR T cells should be effective against tumors without recognizing normal hematopoietic cells.
B7H6 was identified as a tumor-specific ligand for NKp30.11 Quantitative reverse transcription PCR on a normal tissue array showed no detectable expression in any of the 48 normal tissues assayed.11 Recently, a study showed that B7H6 protein may be transiently induced on monocytes and neutrophils upon Toll-like receptor ligand stimulation or cytokine stimulation in vitro, and B7H6 was found on circulating pro-inflammatory monocytes in a group of patients suffering from severe sepsis conditions.19 However, we found little or no B7H6 upregulation on CD14+ monocytes upon LPS, IL-1β or TNF-α stimulation. In addition, B7H6-specific CAR T cells did not react to these activated monocytes in PBMCs. Thus, there may be other reasons for the differences of the findings in this study compared with the previous one, but it suggests that simple activation by Toll-like receptor agonists and inflammatory cytokines is not sufficient to trigger B7H6 expression on PBMCs.
The finding that B7H6 mRNA expression was upregulated in lymphoma, leukemia and GIST correlated with previous published results.11, 12 The observation that B7H6 mRNA was upregulated in some subsets of ovarian cancers also correlated with the in vitro functional data. Several subsets of tumors identified to express high amount of B7H6 mRNA have a high clinical incidence, such as diffuse large B-cell lymphoma, which is the most common form of lymphoma in adults.26 GIST is the most common form of mesenchymal tumor of the gastrointestinal tract and expresses B7H6.27 These findings highlighted the potential of targeting B7H6 for tumor immunotherapy.
Mus musculus does not express B7H6.11 Therefore, to investigate the therapeutic efficacy of B7H6-specific CAR T cells in immunocompetent mice, the human B7H6 gene was introduced into various murine tumor cell lines. Exogenously expressing B7H6 on tumor cell lines may lead to higher B7H6 expression on the cell surface than is found on primary human tumor cells. Human B7H6 may be immunogenic in mice, but we have not observed a selection for B7H6-loss variants in these models suggesting any immunogenicity is low. Although it is important to note these caveats, these B7H6 tumor models allow one to study B7H6-specific CAR T cells in animals with a competent immune system.
In conclusion, B7H6-specific CAR T cells produce cytokines and mediate cytotoxicity in the presence of B7H6+ tumor cells. B7H6-specific CAR T-cell therapy mediated robust therapeutic efficacy in murine lymphoma and ovarian cancer models. This CAR can also lead to resistance against tumor rechallenge, which may be a consequence of a broader host immune memory against other tumor antigens. Expression data indicate that subsets of lymphoma, leukemia, ovarian cancers, brain tumors, breast cancers, renal cell carcinomas and various sarcomas express B7H6. B7H6-specific CAR T-cell therapy has the potential to treat B7H6+ hematological malignancies and solid tumors.
Materials and methods
C57BL/6 (B6) mice were purchased from the National Cancer Institute (Frederick, MD, USA). Mice were 7–12 weeks old at the start of the experiments. All experiments were conducted under the approval of Dartmouth College's Institutional Animal Care and Use Committee.
Cell culture and cell lines
Bosc23, PT67, GP+E86, K562 and U937 cell lines were obtained from American Type Culture Collection (Rockville, MD, USA). An RMA subline RMA/B7H6, B16F10 subline B16F10/B7H6 and ID8 subline ID8/B7H6 were generated by transducing the parental cell lines with a dualtropic retrovirus containing the B7H6 gene (see below), followed by 1 mg ml−1 G418 (Corning, Cambridge, MA, USA) or 2 ug ml−1 Puromycin (Sigma-Aldrich, Saint Louis, MO, USA) selection for 7 days. Bosc23, PT67, GP+E86 and ID8/B7H6 cells were cultured in Dulbecco's modified Eagle's media with a high glucose concentration (4.5 g l−1), supplemented with 10% heat-inactive fetal bovine serum (Atlanta Biologicals, Lawrenceville, GA, USA), 10 mM HEPES, 0.1 mM non-essential amino acids, 1 mM sodium pyruvate, 100 U ml−1 penicillin, 100 ug ml−1 streptomycin and 50 uM 2-ME. Other cell lines were cultured in RPMI 1640 containing the same supplements as Dulbecco's modified Eagle's media. When harvesting adhesion growing cells for staining or functional assay, PBS containing 10 mM EDTA was used instead of trypsin. Trypsin treatment cleaves B7H6 from cell surface (data not shown). Human DCs were generated as described previously.8 To test PBMC activation with LPS, IL-1β or TNF-α, human blood cells from cell cones obtained from leukapheresis cell donations (Dartmouth-Hitchcock Medical Center Blood Donor Center) were cultured in 24-well plates at a cell density 3 × 106 cells per well in complete RPMI 1640 at 37 °C with 5% CO2 without or with following stimulation, LPS (1 μg ml−1; Sigma-Aldrich), IL-1β (1 ng ml−1; PeproTech, Rocky Hill, NJ, USA), TNF-α (100 ng ml−1; PeproTech) for 48 h. Cells were analyzed by flow cytometry, and CD14+ monocytes were gated for the analysis of B7H6 expression. De-identified primary ovarian cancer samples from patients were obtained at the time of primary debulking surgery performed at Dartmouth-Hitchcock Medical Center by the division of Gynecology Oncology. Informed consent was obtained prior to surgery. The patients were having primary debulking surgery with intent to remove all gross disease. Excess primary ovarian tumor tissue as well as metastatic intra-abdominal disease was separated from the resected specimens for research purposes prior to surgical pathology analysis. No tissue was removed solely for this research study. Cancer tissues were mechanically disrupted (Collagenase (catalog number: C5138; Sigma-Aldrich) treatment cleaves B7H6 from cell surface) and red blood cells in the samples were lysed with ACK lysis buffer (0.15M NH4Cl, 10 mM KHCO3, 0.1 mM EDTA, PH 7.4) before cell culture. Primary ovarian cancer cells were cultured for 2 days before using for functional assays.
Construction of B7H6-specific CAR
A B7H6-specific CAR was constructed by fusing the single change variable fragment of an anti-B7H6 hybridoma,8 clone 47.39, to the human CD28 hinge-transmembrane-cytoplasmic domains (amino acid (aa) 135–220) and a CD3ζ endodomain (aa 52–164). The construction of the anti-B7H6 single-chain variable fragment was carried out by fusing the variable region of heavy chain (VH, aa 1–134) and light chains (VL, aa 23–129) with a 15 amino acid glycine (G)-serine (S) linker (G4S)3 linker (three repeats of IndexTermGGGGS). The B7H6-specific CAR construct was then cloned into a retroviral vector pFB-neo (Stratagene, Palo Alto, CA, USA). B7H6-specific CAR-T2A-tCD19 construct was created by fusing the B7H6-specific CAR to a Furin cleavage site-SGSG-T2A sequence (IndexTermAGAGCCAAAAGGTCTGGCTCCGGTGAGGGCAGAGGAAGTCTTCTAACATGCGGTGACGTGGAGGAGAATCCCGGCCCT), followed by a truncated human CD19 (aa 1–327). All PCRs were carried out by using high-fidelity DNA polymerase Phusion (New England BioLabs, Ipswich, MA, USA).
Retrovirus production and transduction
Eighteen hours before transfection, Bosc23 or 293T cells were plated at a density of 3 × 106 cells per 10-cm plate in 10 ml complete Dulbecco's modified Eagle's media. Transfection of CAR plasmids into Bosc23 cells was performed using Lipofectamine 2000 (Life Technology, Carlsbad, CA, USA) following the manufacturer's protocols. Transfection of CAR plasmids and ψEco packaging plasmids (Gift from Patricia Ernst, Dartmouth College, Hanover, NH, USA) into 293 T cells was performed by using 20 ug of CAR vectors, plus 10 ug of ψEco packaging plasmids, with 9 ul of X-fect (Clonetech, Palo Alto, CA, USA) according to the manufacturer's protocols. Forty-eight to 72 h after transfection, ecotropic viral supernatant was harvested and filtered with 0.45 μm filter before storage at −80 °C. Virus-producing PT67 cells were generated by cross-infection with ecotropic viruses collected from the transfected Bosc23 or 293T cells, three times, followed by G418 (1 mg ml−1) selection for 7 days. Virus-producing GP+E86 cells were generated by cross-infection using dualtropic virus produced by PT67 cells, followed by G418 (1 mg ml−1) selection for 7 days. Retroviral transduction of T cells was performed as previously described.8 For experiments using B7H6-specific CAR-T2A-tCD19 T cells, T cells were activated, transduced and expanded. CD19+ cells were positively selected with anti-CD19-PE magnetic beads (STEMCELL, Vancouver, BC, Canada) and expanded for 5 days before functional assays. Greater than 99% of cells in CAR T-cell preparations derived from human PBMCs or murine splenocytes were CD3+ cells.
Production of soluble B7H6, DyLight 650- conjugated soluble B7H6 and NKp30-msIgG fusion protein.
A soluble B7H6 (extracellular domain) was prepared by cloning of the B7H6 extracellular portion (aa 25–262) into pET15b expression vector (Novagen, Madison, WI, USA). Soluble B7H6 was expressed as inclusion bodies in E.coli. Extraction of B7H6 inclusion bodies was carried out by using CelLytic B cell lysis reagent (Sigma-Aldrich). Dissolving and refolding of soluble B7H6 was carried out by using CelLytic IB inclusion body solubilization reagent (Sigma-Aldrich). Inclusion body extraction, dissolving and refolding were carried out following the manufacture's protocols. Conjugation of soluble B7H6 to DyLight 650 NHS Ester (Thermo Fisher Scientific, Waltham, MA, USA) was carried out according to the manufacturer's protocol. NKp30-msIgG fusion sequence was constructed by fusing the NKp30 extracellular portion (aa 1–135) with a murine IgG2a hinge-CH2-CH3 portion, and the construct was further cloned into a pFB-neo vector. Production of NKp30-msIgG fusion protein was performed by transiently transfecting the NKp30-msIgG plasmid into 293F cells (Life Technology) by 40 Kd PEI (Polysciences Inc, Warrington, PA, USA). Transfection was carried out by gently mixing 293F cells with DNA and PEI at a final concentration of 2 × 107 per ml cells, 12.5 ug ml−1 DNA, 25 ug ml−1 PEI and shaking it on an orbital shaker at 37 °C at 120 r.p.m. for 3 h. After 3 h, the whole mixture was diluted with Gibco FreeStyle 293 Expression Medium (Life Technology) at a 1:9 ratio to reach a final cell concentration 2 × 106 cells per ml. The culture was maintained in 37 °C shaker at 120 r.p.m. for 4 days. Cell-free culture supernatants were harvested and purified by HiTrap rProtein A HP column (GE healthcare, Waukesha, WI, USA) following the manufacturer's protocol.
Flow cytometry analysis of B7H6 expression on tumor cells were performed by staining cells with anti-B7H6 mAbs,8 followed by DyLight 649-conjugated goat anti-mouse IgG (clone: Poly4053, Biolegend, San Diego, CA, USA). For staining of mouse cells, the samples were pre-incubated with FcR block antibody (anti-mouse CD16/CD32, 2.4G2; Bio X Cell, Lebanon, NH, USA), and for staining of human cells, samples were pre-incubated with human gamma globulin (Cohn fraction, Sigma-Aldrich). Samples were analyzed by Accuri C6 cytometer (BD Biosciences, San Jose, CA, USA) and data were analyzed by Accuri or FlowJo software (TreeStar Inc, Ashland, OR, USA).
In vitro cytotoxicity assay
Lactate dehydrogenase release cytotoxicity assays were carried out with CytoTox 96 Non-Radioactive Cytotoxicity Assay Kit (Promega, Madison, WI, USA) following the manufacturer’s protocol. T cells and tumor cells were co-cultured at an Effector cell to Target cell ratio 5:1 (105:2 × 104) for 6 h in 96-well U-bottom plates in triplicates. The specific lysis was calculated by the following equation: percentage of specific lysis=((experimental release-effector spontaneous release-target spontaneous release)/target maximal release-target spontaneous release) × 100.
Flow cytotoxicity assays were carried out by labeling B7H6-negative and B7H6-positive tumor cell lines with 0.1 or 1 uM CFSE (Life Technology), respectively. B7H6-negative and B7H6-positive tumor cells were mixed at a 1:1 ratio before co-culturing with T cells at an Effector cell to Target cell ratio of 5:1 (2 × 105:4 × 104) for 8 h in triplicates. Samples were harvested and the ratio of B7H6-negative and B7H6-positive tumor cells were identified by flow cytometry. The specific lysis was calculated by the following equation: percentage of specific lysis=(1−(% of B7H6-positive tumor in B7H6-specific CAR or Mock T-cell group × % of B7H6-negative tumor in tumor only group)/( % of B7H6-negative tumor in B7H6-specific CAR or Mock T-cell group × % of B7H6-positive tumor in tumor-only group)) × 100.
Cytokine production by T cells
T cells were co-cultured with suspension tumor cells, primary ovarian cancer cells or LPS-, IL-1β-, or TNF-α-stimulated PBMCs at an Effector cell to Target cell ratio of 1:1 (105:105) in 96-well V-bottom plates or with adherent tumor cells at an Effector cell to Target cell ratio of 4:1 (105:2.5 × 104) in 96-well flat-bottom plates in triplicates. Cell-free culture medium was harvested after 24 h, the IFN-γ concentration was measured by ELISA using IFN-γ Duoset ELISA kits (R&D systems, Minneapolis, MN, USA).
Treatment of tumor-bearing mice with anti-B7H6 CAR T cells
As a systemic T-cell lymphoma model, B6 mice were injected with 1 × 105 RMA/B7H6 cells via the tail vein in 400 μl HBSS. Five, 7 and 9 days later, mice were treated with 5 × 106 Mock (untransduced) T cells or B7H6-specific CAR T cells intravenously. The health of mice were monitored, and mice were killed when moribund signs were observed. As an ovarian cancer model, B6 mice were injected with 5 × 106 ID8/B7H6 (GFP+) cells intraperitoneally in 400 μl HBSS. Seven days after tumor inoculation, mice were treated with 5 × 106 Mock T cells or B7H6-specific CAR T cells intraperitoneally. Forty-two days after initial tumor inoculation, tumor burden was measured by counting solid tumors on the peritoneal wall of each mouse (counting stopped at 100 tumors) and determining the number of suspension tumor cells (GFP+) in a peritoneal wash, as carried out previously.28
A student's t-test or analysis of variance was used to analyze differences between groups. Kaplan–Meier survival curves were used to analyze survival benefit. Statistical analysis was carried out by GraphPad Prism software (GraphPad Software, San Diego, CA, USA).
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We thank the National Cancer Institute Biological Resource Branch for providing recombinant human IL-2 and the staff of the Center for Comparative Medicine and Research in Dartmouth College for providing animal care. This work was supported by a grant from the NIH CA130911 and funds from the Center for Synthetic Immunity.
Tong Zhang and Charles Sentman are inventors on a patent application covering the B7H6 CAR described in this study. This technology has been licensed by Cardio3 Biosciences. This work is managed in compliance with the policies of Dartmouth College. Ming-Ru Wu and Leslie DeMars declare no potential conflict of interest.
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Wu, M., Zhang, T., DeMars, L. et al. B7H6-specific chimeric antigen receptors lead to tumor elimination and host antitumor immunity. Gene Ther 22, 675–684 (2015). https://doi.org/10.1038/gt.2015.29
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