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Review

Engineering Next-Generation CAR-T Cells for Better Toxicity Management

by
Alain E. Andrea
1,
Andrada Chiron
2,3,
Stéphanie Bessoles
2 and
Salima Hacein-Bey-Abina
2,3,*
1
Laboratoire de Biochimie et Thérapies Moléculaires, Faculté de Pharmacie, Université Saint Joseph de Beyrouth, Beirut 1100, Lebanon
2
Université de Paris, CNRS, INSERM, UTCBS, Unité des Technologies Chimiques et Biologiques pour la Santé, F-75006 Paris, France
3
Clinical Immunology Laboratory, Groupe Hospitalier Universitaire Paris-Sud, Hôpital Kremlin-Bicêtre, Assistance Publique-Hôpitaux de Paris, 94275 Le-Kremlin-Bicêtre, France
*
Author to whom correspondence should be addressed.
Int. J. Mol. Sci. 2020, 21(22), 8620; https://doi.org/10.3390/ijms21228620
Submission received: 12 October 2020 / Revised: 9 November 2020 / Accepted: 13 November 2020 / Published: 16 November 2020
(This article belongs to the Special Issue Immunotherapy for Cancer)
Browse Figures
Versions Notes

Abstract

:
Immunoadoptive therapy with genetically modified T lymphocytes expressing chimeric antigen receptors (CARs) has revolutionized the treatment of patients with hematologic cancers. Although clinical outcomes in B-cell malignancies are impressive, researchers are seeking to enhance the activity, persistence, and also safety of CAR-T cell therapy—notably with a view to mitigating potentially serious or even life-threatening adverse events like on-target/off-tumor toxicity and (in particular) cytokine release syndrome. A variety of safety strategies have been developed by replacing or adding various components (such as OFF- and ON-switch CARs) or by combining multi-antigen-targeting OR-, AND- and NOT-gate CAR-T cells. This research has laid the foundations for a whole new generation of therapeutic CAR-T cells. Here, we review the most promising CAR-T cell safety strategies and the corresponding preclinical and clinical studies.

1. Introduction

For many decades, cancer therapy has relied primarily on surgery, chemotherapy, radiotherapy, and bone marrow transplantation (BMT). Recently, advances in immune response stimulation have yielded lasting remissions and have established immunotherapy as the fifth pillar of cancer therapy. In 1891, William Coley was the first physician to attempt to exploit the immune system for cancer treatment [1]. In the 1950s, the success of BMT laid the foundations for the development of adoptive cell therapy, with the infusion of cells into patients with hematological cancers proving that T cells have the power to kill cancer cells. Another key milestone was the discovery of monoclonal antibodies (mAbs) in 1975 by Georges Köhler and Cesar Milstein (the winners of the Nobel Prize in Medicine in 1984) [2]. These mAbs served as research tools before being used therapeutically. The emergence of mAbs as anti-cancer drugs was facilitated by the ability to mass-produce them in the laboratory, which led to the approval of rituximab for lymphoma treatment in 1997 [3]. In 1993, Zelig Eshhar and colleagues designed the first chimeric antigen receptor (CAR). This chimera contained the T-cell receptor (TCR)’s constant domains and the antibody’s variable domain, thus combining the latter’s high specificity and affinity with the T lymphocytes’ functional capacities (i.e., homing, tissue penetration, and cytotoxicity). The novelty of this new receptor relied on the ability to direct the specificity of genetically modified T cells towards a chosen tumor antigen in an MHC-independent context [4].
Just like immune checkpoint inhibitors [5], CAR-T cell immunotherapy is the culmination of more than 60 years of in-depth research on the immune system, genetic engineering, antibody therapy, and on the oncogenic mechanisms in hematological cancers. The development of CARs resulted from extensive research by several researchers, including not only Steven Rosenberg, Carl June, and Michel Sadelain but also Bryan Irvin and Arthur Weiss, who demonstrated that TCR-independent activation of T cells was possible. In order to study the role of the CD3 ζ chain in TCR-mediated signal transduction, these researchers constructed a chimeric protein linking CD8’s extramembrane domain and transmembrane domain (TM) to the cytoplasmic domain of the ζ chain. They noted that when expressed on a T-cell, the CD8/ζ pair is able to transduce signals (following the interaction of a ligand with the CD8 extracellular domain (ECD)) in the same way as the physiological TCR/CD3 pair [6,7] (Figure 1).
Furthermore, various studies determined the role of individual immunoreceptor tyrosine-based activation motifs (ITAMs) in the modulation of TCR/CD3 complex signaling. Experiments with T cells indicated that the cytoplasmic domains of the CD3ε and CD3ζ subunits were independently capable of providing activation signals similar to those of the intact TCR [6,8,9]. Hence, Eshhar et al. came up with the idea of reinforcing the CD8/ζ receptor’s activity by replacing the CD8 ECD with the variable fragments of a single-chain antibody (scFv) directed against a specific antigen (Figure 1). This allowed CAR-T cells to acquire a third important property: a broad target range. In contrast to the TCR, antibodies are capable of recognizing carbohydrate and lipid antigens as well as peptide antigens [10]. Moreover, the fact that antibodies (unlike the TCR) are able to bind to tumor antigens without MHC-restricted presentation allows CAR-T cells to attack tumor cells that may have down- regulated their MHC expression as an immune escape mechanism [11,12,13]. Following the advent of first-generation CARs, second- and third-generation CARs with greater stimulatory activity were created by engineering the intracellular co-stimulatory domains [14].
The generation of specific CARs (whether patient-derived (autologous) or donor-derived (allogenic)) starts with T cell collection by leukapheresis and is followed by ex vivo re-engineering and expansion of the T cells (so they express specific CARs), and then reinfusion into the patient. Upon recognition of the targeted tumor antigen, the CAR-T cells proliferate and specifically kill the cancer cells [15]. Advances in CAR-T cell therapy offer new options for treating refractory malignancies, and clinical trials in indications of various hematologic or solid cancers are ongoing. The clinical success of CD19-targeted CAR-T cell therapy in B-cell acute lymphoblastic leukemia (B-ALL) and the promising data in B-cell non-Hodgkin’s lymphoma (B-NHL) and chronic lymphocytic leukemia (CLL) are driving extensive research in this new field. These spectacular advances have led to marketing authorizations for Yescarta™ (axicabtagene ciloleucel, from Kite Pharma/Gilead) and Kymriah™ (tisagenlecleucel, from Novartis). These two biologics (both of which target CD19) were approved for the treatment of certain hematological cancers by the United States Food and Drug Administration (FDA) in 2017 and by the European Medicines Agency in 2018.
However, the effectiveness of CAR-T cell adoptive transfer is diminished by “on-target/off-tumor” effects and the appearance of adverse reactions. Indeed, potentially fatal cytokine release syndrome (CRS) occurs in up to 80% of patients treated with anti-CD19 CAR-T cells. CRS can lead to widespread organ toxicities, including cardiovascular disorders (sinus tachycardia hypotension, decreased left ventricular ejection fraction, QT prolongation, and arrhythmia), renal disorders (kidney failure, tumor lysis syndrome, elevated serum creatinine, and electrolyte disturbances such as hyponatremia, hypokalemia and hypophosphatemia), hepatic and gastrointestinal disorders (elevated serum transaminases and bilirubin, nausea, vomiting, and diarrhea), immune disorders (with an elevated risk of bacterial, viral and fungal infections), hematologic disorders (grade 3–4 anemia, leukopenia, thrombocytopenia, neutropenia, and lymphopenia, disseminated intravascular coagulation, prolongation of partial thromboplastin time or prothrombin time, and decreased fibrinogen), respiratory disorders (pulmonary edema, hypoxia, dyspnea, and pneumonitis), musculoskeletal disorders (elevated creatine kinase), and neurologic disorders (global encephalopathy, aphasia, tremor, ataxia, hemiparesis, and cranial nerve palsies). Neurological adverse events can occur either during CRS or after its resolution [16]. Therefore, the need to minimize undesirable immune responses is critical, and recent efforts to improve CAR-T cell therapy have focused on both effectiveness and safety [17]. Abbreviations used are summarized in Table 1.

2. From Conventional CAR-T Cells to Next-Generation CAR-T Cells

The CAR construct is based on genetic engineering of the coding DNA sequence, where each set of genes codes for one of the receptor’s five components: the variable fragments of a specific mAb directed against the target antigen (scFv), the hinge region, the TM domain, and the signaling domain (composed of the co-stimulatory CM domain and the CD3ζ domain) (Figure 2).
The receptor’s intracellular domain is the functional domain that enables signal transduction and T cell activation. All clinically tested CARs contain one or two co-stimulation domains (CD28 [18], 4-1BB (CD137) [19,20], OX40 [19], DAP10 [18] and/or CD27 [21]) in addition to the CD3ζ chain. However, other domains have been preclinically tested and have given rise to fourth-generation CAR-T cells (Figure 3) [22]. Given the great heterogeneity of cancer cells in solid tumors, considerable efforts are currently being made to diversify the antitumor response by playing on the recruitment of other immune cells.
The stimulation of a powerful immune response capable of eradicating both hematological cancers and solid tumors with minimal side effects is still a major challenge. There are two major criteria for target specificity: safety, and the persistence of adoptively transferred CAR-T cells. Ideally, CAR-T cells should target only tumor cells and thus spare healthy cells and tissues [23]. Selecting a valid target antigen for CAR-T cells is not easy. Firstly, the ideal target molecule must be a surface tumor antigen that is stably expressed on almost all tumor cells. Furthermore, this molecule should be expressed weakly on healthy tissues, in order to avoid “off-target” side effects associated with the destruction of healthy cells. Expression of the target antigen on vital organs (such as the brain and heart) or hematopoietic stem cells (the “on-target/off-tumor” effect) is redhibitory. For a particular cancer, truly tumor-specific antigens expressed by a large proportion of patients are rare. In contrast to tumor-specific antigens resulting from a gene mutation and expressed exclusively on tumor cells, TAAs are over-expressed on tumor cells but can also be found at low levels on normal cells [24]. A significant example of toxicity associated with the non-exclusive expression of a TAA on tumor cells is illustrated by the case of a patient with metastatic colorectal cancer who received an infusion of autologous CAR-T cells directed against the human epidermal growth factor receptor-2 (HER2)/neu (ErbB2) and who experienced acute respiratory distress and then fatal pulmonary edema [25]. This pulmonary toxicity was likely to be due to the expression of ErbB2 on pulmonary epithelial cells [25]. Thus, a candidate target antigen for CAR-T cells must fulfill stringent criteria: (i) specificity, (ii) the ability to trigger a response that is sufficiently powerful and long-lasting to destroy the target, and (iii) escape from tumor inhibitors, and (iv) limited toxicity. Based on these four criteria, researchers engineering next-generation CAR-T cells have focused on modifying the CAR and other cellular variables.

2.1. CAR-T Cells with an OFF-Switch

Several existing or emerging methods for limiting the toxicity of CAR-T cells have been suggested. These include the incorporation of an “OFF-switch” (such as suicide and elimination genes) or a small-molecule-assisted shutoff (SMASh) CAR into genetically modified T cells. Given the expression of one of these genes by CAR-T cells, an external molecule (either a chemical compound or a mAb) could be used as an antidote if CAR-T cells are overactivated.

2.1.1. Suicide Gene Switch

To date, two suicide genes have been integrated into CAR-T cells and tested in the clinic: the gene coding for herpes simplex virus thymidine kinase (HSV-TK) and the gene coding for inducible caspase-9 (iCasp9).
HSV-TK is a conventional method that has been used in the laboratory and in the clinic to induce T cell death (by administration of ganciclovir (GCV)) following the emergence of severe graft-versus-host disease (GvHD) associated with the therapeutic infusion of donor lymphocytes after allogeneic BMT. It is the suicide gene that has been most extensively tested in humans, and is known to be safe and effective [26]. Thus, in order to avoid the overactivation of CAR-T cells, HSV-TK has been incorporated into the CAR. Ganciclovir treatment leads to the formation of a toxic molecule [27,28] and the activation of caspase-8’s apoptotic function, with the induction of ligand-independent CD95 (Fas) aggregation and expression of Fas-associated protein with a death domain [29]. Although this strategy presents several advantages, it also has several limitations: (i) the induction of immunoreactivity against genetically modified cells [30], and (ii) a slow response (up to several days), due to the latency of genome incorporation. In fact, HSV-TK is a cell-cycle-dependent suicide gene, so GCV-based inhibition of HSV-TK-expressing T lymphocytes requires cell proliferation [31]. For these reasons, HSV-TK is not a good candidate for safer CAR-T cell therapy.
Similarly, iCasp9 is a safe, effective apoptosis system [32] used initially to prevent GvHD in patients having undergone hematopoietic stem cell transplantation (HSCT). Its use has now been broadened to CAR-T cell therapy. In this novel model, the suicide gene incorporates the intracellular part of the human caspase 9 protein, which is merged to a drug-binding domain comprising of an FK50-binding protein. The latter has a high affinity for a chemical inducer of dimerization (CID, a small molecule called AP1903) that can be intravenously administered in the event of adverse effects (such as life-threatening CRS) following CAR-T cell administration. Once the CID has been injected, it induces cross-linking of iCasp9’s drug-binding domain. In turn, dimerization activates the caspase and induces the apoptosis of the modified CAR-T cells [33] (Figure 4).
In vitro and in vivo experiments show that with a dose of 10 nM AP1903, the iCasp9 suicide gene can kill ~99% of T cells [34]. Lymphocytes that have integrated the iCasp9 gene have certain advantages over those having integrated the HSV-TK suicide gene, such as rapid activation (and therefore rapid cell death) and the humanized nature of the iCasp9 system (reducing the immunogenic risk).
Hoyos et al. were the first to perform a preclinical study of second-generation CD19-targeted CAR-T cells that co-expressed IL-15 and iCasp9. The researchers found that iCasp9-IL15-CD19 CAR-T cells were successfully eliminated within 72 h of AP1903 administration [35]. In another preclinical study of the therapeutic effect of iCasp9-CD20CAR-Δ19 T cells directed against multiple CD20+ tumor cell lines, mice were injected with the CD20+ Raji tumor cell line with firefly luciferase expression in order to noninvasively quantify tumor progression over time. By the end of the 90-day observation period, 69% of the CAR-T cell-treated mice were still alive and showed no firefly luciferase bioluminescence. The long-term complete remission rate was 68% in the cell-treated group and 0% in the control group. Moreover, 90% of the CAR-T cells were eradicated 24 h after the administration of 20 nM AP1903, and 98% were eradicated 72 h after [36]. Many other preclinical studies have also shown promising results for the iCasp9 safety switch in B cell lymphoid malignancies with iCasp9-CD20CAR-ΔNGFR T cells [37], in acute myelogenous leukemia (AML) with iCasp9-CD33CAR-Δ19 cells [38], and in chronic myeloid leukemia (CML) with iCasp9-IL1RAPCAR-Δ19 cells [39] (Table 2).
Based on these encouraging results, Phase I efficacy and safety trials of the iCasp9/AP1903 CAR-T technology have been initiated in several indications: diffuse intrinsic pontine glioma (DIPG), spinal diffuse midline glioma (DMG), relapsed/refractory neuroblastoma, refractory/metastatic sarcoma, relapsed/refractory acute lymphoblastic leukemia (ALL), relapsed/refractory B-cell lymphoma, and other solid cancers (Table 3).
While waiting for the results of these clinical trials to be published, it would be useful to better understand the positive clinical results obtained with iCasp9 as a safety switch strategy for patients undergoing allogeneic HSCT. In a Phase I clinical study (NCT00710892), five pediatric patients (aged between 3 and 17 years) with relapsed acute leukemia underwent allogeneic HSCT. Four of the five patients developed cutaneous GvHD within 14 to 42 days of the first T lymphocyte infusion. They were treated with a single dose of the CID AP1903. This eradicated 90% of the genetically modified T cells within 30 min. Even though this example is not related to CAR-T cell therapy, it illustrates the power of the iCasp9 tool in the treatment of GvHD and prevention of its recurrence [34]. Many other similar clinical trials (e.g., ACTRN12614000290695, NCT01494103) have also showed good efficacy, which makes us optimistic about the clinical prospects for iCasp9 CAR-T cells.

2.1.2. Elimination Markers

In the event of uncontrolled toxicity, genetically engineered CAR-T cells can also be eliminated by using clinically approved mAbs to target a co-expressed, truncated cell-surface protein. The underlying elimination mechanisms in CAR-T cell depletion are antibody-dependent cellular cytotoxicity (ADCC) and complement-dependent cytotoxicity. The truncated protein may be a cluster of differentiation (CD)-type polypeptide or a small epitope peptide recognized by a mAb [23]. The two commonly used truncated proteins are CD20 (recognized by the anti-CD20 mAb rituximab) [40,41], and the truncated human epidermal growth factor receptor polypeptide (huEGFRt, recognized by the anti-EGFR mAb cetuximab) [42,43]. Along with the CD20-rituximab and huEGFRt-cetuximab elimination switches, Kieback et al. suggested introducing a 10 amino-acid tag derived from the c-Myc protein into the recombinant antigen receptor, to enable in vivo elimination of the engineered T cells by administration of an anti-Myc mAb [44]. Despite the preclinical effectiveness of this strategy, the absence of a clinically approved antibody specific for c-Myc makes it ineligible for clinical trials.
Retroviral transfer of human CD20 as an elimination marker for CAR-T cell therapy has proven to be efficacious in many preclinical studies: rituximab ensured the depletion of 86% to 97% of CD20-expressing lymphocytes [40,45,46]. Furthermore, the binding between CD20 and CD34 in a highly compact epitope (RQR8, developed by Philip et al.,) expressed at the CAR-T cell surface marked an important step forward. RQR8 has a dual role by acting simultaneously as a selection marker when CD34 is targeted with an anti-CD34 mAb (QBEnd/10) and as a suicide molecule when CD20 is targeted with rituximab. This epitope was engineered to match the Miltenyi CliniMACS system, and represented a breakthrough in terms of safety and the cost of generating clinical-grade CAR-T cells [47]. Although the preclinical studies are encouraging, this technology has not yet entered clinical development. In fact, rituximab’s mechanism of action means that it eliminates not only malignant B cells expressing CD20 but also normal B cells, which in turn interferes with the reconstitution of the B cell compartment after the injection of the CD20-elimination-marker-expressing CAR-T cells. These limitations might explain why this approach has not yet been trialed in the clinic. In contrast, the huEGFRt-cetuximab suicide switch (which also had good preclinical results [42,48]) has entered clinical trials. The mechanisms of action of the above-mentioned OFF-switch strategies are illustrated in Figure 5.
A study by Wang et al. showed that more than 50% of huEGFRt+ CAR-T cells were eliminated in vitro within an hour of cetuximab administration, and that these lymphocytes were depleted in NOD/scid mice after 4 to 6 days of daily intraperitoneal injection of 1 mg cetuximab [42]. Even though this approach to eradicating T cells may not be fast enough to reverse toxic effects in patients, huEGFRt+ CAR-T cells (approved under BB-IND-15829) are now being evaluated in many Phase I clinical trials targeting different types of cancer: relapsed/refractory CLL, NHL, ALL, multiple myeloma (MM), recurrent/refractory solid tumors, recurrent/refractory central nervous system (CNS) tumors, relapsed/refractory AML, persistent/recurrent blastic plasmacytoid dendritic cell neoplasm (BPDCN), and recurrent/refractory neuroblastoma. The corresponding clinical trials are summarized in Table 4. Given that no results have yet been published, it is too early to accurately predict whether this encouraging safety strategy will give good results in humans.

2.1.3. SMASh CARs

Another approach to protein elimination is small-molecule-assisted shutoff (SMASh). This strategy (developed by Chung et al.) provides reversible control of CAR production by incorporating a self-cleaving degradation moiety regulated by a protease/protease inhibitor pair. The CAR is bound to a drug-sensitive viral protease and a degron (a protein destabilization element) at the C-terminal end of the CAR. This construct is also known as a switch-off CAR (SWIFF-CAR) [49]. Juillerat et al. used the HCV NS3 protease and its inhibitor asunaprevir (ASN) to integrate this OFF-switch into CAR-T cells. In vitro and in the absence of ASN, the degron is cut off from the CAR and thus exposes the antigen-targeting scFv at the CAR-T cell surface. When ASN is added to the medium, HCV NS3-catalyzed cleavage of the degron is inhibited. This allows the CAR to be degraded by the T-cell’s proteolytic pathways (Figure 6). Using the small molecule ASN, the integration of a protease-based shut-off system into CAR-T cells can inhibit the latter’s action within 48 h [50].
In contrast to the two above-mentioned approaches, the switch-off CAR system is particular in that it can shut down the genetically engineered lymphocytes’ cytolytic properties without depleting the cells. In order to translate this OFF-switch system into the clinic and to determine its feasibility and utility in humans, intricate in vivo preclinical experiments are essential for evaluating basic properties like the relationship between the sparing of normal tissue and tumor control, switch-off triggering, engraftment, and proliferation [50]. Even though the clinical management of toxicity using suicide and elimination gene systems requires a direct response, non-lethal switch-off systems with slower off-kinetics might be a good substitute pending the results of more extensive studies. Their reversible, continuous control and cost-effectiveness are attractive features [51,52].

2.1.4. The TKI-Based OFF-Switch

Dasatinib is a selective BCR/ABL family tyrosine kinase inhibitor (TKI) that suppresses the activity of the uncontrolled tyrosine kinase ABL [53,54]. It also blocks the LCK kinase, which is primarily expressed in T cells. Hence, after having screened a panel of TKIs, Mestermann et al. suggested using dasatinib as a pharmacological OFF-switch for CAR-T cells. In Mestermann et al.’s subsequent co-culture study, CD4+ and CD8+ CD19 CAR-T cells were turned off by dasatinib in a dose-dependent manner. A Western blot analysis confirmed that the dasatinib prevented the phosphorylation of CD3ζ and zeta-chain-associated protein kinase 70 (ZAP70), which have key roles in the TCR signaling pathway and in the induction of NFAT—an important transcription factor in activated CAR-T cells (Figure 7). After a 2-h incubation, removal of the drug, and a 7-h latency period, the treated CAR-T cells recover their antitumor activity at much the same level as untreated CAR-T cells [55,56].
With the aim of examining dasatinib’s effectiveness and fast response in preventing life-threatening CRS, the groups led by Hudecek and Sadelain set up a murine preclinical model [55,57]. SCID/beige mice injected with Raji lymphoma cells were treated with CD19 CAR-T cells, which led to acute (and in some cases fatal) CRS during the first 48 h. Dasatinib administration resulted in a significant decrease (relative to control mice) in levels of interleukin-2 (IL-2), interferon gamma (IFNγ), tumor necrosis factor alfa (TNF-α) and granulocyte-macrophage colony-stimulating factor (GM-CSF) 3 h after CAR-T cell infusion. Forty-eight hours later, 70% of the TKI-treated mice and 25% of the control mice were still alive. The efficacy of reversible dasatinib-mediated control over CAR-T cell function was independent of the CAR’s target antigen (CD19, ROR1 or SLAMF7) and the costimulatory domain (CD28 or 4-1BB). All these encouraging results showed that in contrast to suicide and elimination gene systems, dasatinib is a potentially reversible pharmacological OFF/ON safety switch that can prevent fatal CRS without eradicating therapeutic CAR-T cells [55,58]. Further in vivo studies of this system are needed to confirm the functional control of CAR-T cells in a clinical setting.

2.2. CAR-T Cells with an ON-Switch

Another way to overcome potential toxicity is to develop therapeutic lymphocytes expressing an “ON-switch”. Instead of eliminating overreacting CAR-T cells that cause life-threatening conditions, the use of an activating “switch-on” molecule enables the precise remote control of these cells in terms of timing, site of action, and dosage. Wu et al. developed an inducible system in which the antigen-binding and intracellular signaling components cannot connect without the presence of an injectable small heterodimerizing molecule. This agent enables the in vivo activation of ON-switch CAR-T cells and controls the timing and the location of transgene expression—thus improving their safety profile. If serious adverse reaction occurs, the small molecule can be immediately discontinued and the expression of the specific CAR on T lymphocytes will return to baseline levels within a few hours or days, without the need to kill the cells [59].

2.2.1. The Tetracycline-On System

Many preclinical studies have provided evidence of the potential advantages of the tetracycline-on (Tet-On) system [60]. This inducible gene expression system for mammalian cells is based on a reverse Tet transactivator (rtTA) fusion protein, which is responsible for the activation of the CAR gene promoter in the presence of doxycycline (Dox). The rtTA is composed of a doxycycline-binding Tet-repressor mutant protein and a C-terminal activator domain from the herpes simplex virus VP16 protein [61,62]. The first Tet-On systems needed two separate vectors: the first one held the rtTA gene and the second contained an inducible promoter for the desired gene. However, an all-in-one, third-generation Tet-inducible vector was recently proposed as an easier-to-use alternative for gene therapy [63].
For instance, Zhang et al. developed CD147 CAR-T cells with a tetracycline-controlled transcriptional activation system for the treatment of hepatocellular carcinoma. The researchers showed that CAR expression and function can be monitored with the Tet-On inducible gene system by Dox administration both in vitro and in vivo. The Tet-CD147 CAR’s expression level was highest 24 h after Dox administration and returned to basal values within 48 h of Dox removal from the culture medium. Nude mice bearing subcutaneous Huh-7 cells xenografts were then used to further evaluate the anti-tumor effect of Tet-CD147 CAR-T cells. The in vivo data showed that tumor volume and weight were lower in mice injected with (Dox+) Tet-CD147 CAR-T cells than in mice injected with (Dox−) Tet-CD147 CAR-T cells or peripheral blood mononuclear cells [64]. The Tet-On system has been tested in other inducible CAR-T cells, proving that this approach to controlling CAR -mediated activity has a better safety profile than conventional CAR-T cells but still has a powerful anti-tumor effect on B-cell malignancies (Tet-CD19 CAR-T cells) [65], and Tet-CD38 CAR-T cells for the treatment of MM [66]. Even though the aforementioned system is a promising toxicity-management strategy, further research is required to limit the adverse effects associated with the inducer; in fact, excessive exposure to Dox might accentuate the risk of antibiotic resistance in patients [67]. Clearly, the ideal solution would involve an alternative, non-antibiotic inducer molecule.

2.2.2. Switchable Adaptor CARs

The concept of adaptor CARs was introduced in 2006 by Clemenceau et al. These molecular safety switches were designed to improve the flexibility, tumor specificity, and controllability of conventional CAR-T cells [68]. To this end, the tumor-targeting and signaling parts of the conventional CARs were separated. The resulting binary system comprised an adaptor CAR and various tumor-specific soluble adaptor molecules. Even though the CAR’s extracellular domain is connected to a binding partner that is inserted into the adaptor molecule (rather than a tumor-associated antigen), the adaptor CAR’s main structure is still analogous to a conventional CAR. In turn, the dual-function adaptor molecule connects the tumor and the CAR-T cell and thus enhances tumor specificity. Hence, the antitumor response is much the same as that induced by traditional CAR-T cells. This novel adaptability provides new options for solving the main problems posed by conventional CAR-T cell therapy, such as antigen-negative relapse. Indeed, a single adaptor CAR can activate engineered T cells against any type of target antigens. This strategy enables the production of universal CAR-T cells directed against a variety of TAAs, which eliminates the need for costly and arduous work developing new CARs and genetically modified T cells. Furthermore, the power and number of active CAR-T cells can be managed by controlling the concentration of the administered adaptor molecules. CAR-T cells which are not triggered by an adaptor molecule are silenced (i.e., they lack the ability to identify and kill the target cell). In due course, inactive cells will be eliminated by the body. Various researchers have designed ten or so diverse adaptor CAR platforms that can be further divided into three main categories: Tag-specific adaptor CARs, bispecific antibody (bsAb)-binding adaptor CARs, and constant fragment (Fc)-binding adaptor CARs (Figure 8). The first of these classes is the most developed and so we shall focus here on the corresponding clinical trials. For more information on the different categories of CAR, adaptor molecules, designs, side effects, and perspectives, see [69].
As mentioned above, Clémenceau et al. were the first to develop an adaptor CAR composed of the ECD of CD16 and the FcγRI receptor’s intracellular-signaling domain. It was well known that CD16 interacts with the Fc portion of immunoglobulin G (IgGs) [68]. These results encouraged other researchers to use this platform and develop first-generation CD16 CARs [70]. However, the first-generation CAR-T cells containing only the CD3ζ intracellular-signaling domain failed to trigger an efficient antitumor effect [71]; hence, the integration of costimulatory molecules like 4-1BB gave rise to second-generation CD16 CARs [72,73]. Activation of these CAR-T cells, requires the administration of tumor-specific mAbs (such as rituximab, cetuximab or trastuzumab) whose antigen binding fragment (Fab) can bind to the TAA and whose Fc part can bind to the CD16 CAR [68,72,73]. Moreover, Caratelli et al. suggested the use of the ECD from CD32A; CD16 binds to IgG2 with low affinity, whereas CD32A can bind to IgG1 and IgG2 [74]. One of the strengths of Fc-binding adaptor CAR-T cells is the broad range of mAbs able to mediate ADCC, which facilitates target switching during treatment. The mechanism of action of this ON-switch strategy is illustrated in Figure 8.
This new approach has been extensively tested in the clinic. The first adaptor CARs to enter clinical trials were ACTR087 (CD16-BB/ζ) and ACTR707 (CD16-28). Various mAbs were used to bridge the extracellular portion of the CD16 CARs to the antigen expressed on cancer cells: rituximab, trastuzumab, and the humanized non-fucosylated IgG1 mAb targeting B-cell maturation antigen (SEA-BCMA) for the treatment of CD20-positive B cell lymphoma, HER2-positive solid tumors, and BCMA-positive MM, respectively (Table 5).
A preliminary report on the Phase I ACTR087/rituximab clinical trial (NCT03189836) showed two complete responses and one partial response out of six evaluable patients with rituximab-resistant NHL treated with the low dose of 0.5 × 106 ACTR T cells/kg, together with the anti-CD20 mAb rituximab. No adverse events were reported at this concentration. However, serious adverse events were noted for patients receiving a higher dose (1.5 × 106/kg) of ACTR T cells. Two of nine evaluable patients died from severe CRS or neurotoxicity, which was (in some cases) considered to be related to ACTR087. As a consequence, the FDA placed a clinical hold on the trial [75]. After the clinical trial had resumed, it was again placed on hold because of grade 3 neurotoxicity, cytomegalovirus (CMV) infection, and grade 4 respiratory distress [76]. Furthermore, a dose-escalation Phase I clinical trial (NCT03680560) of the efficacy of ACTR707 CAR-T cells/kg with trastuzumab has been conducted and completed in patients with HER2-positive advanced cancers. In contrast to other ACTR707-based clinical studies, no adverse events or toxicities were reported [77]. The reasons behind these observed differences require further investigation.
Another category of switchable CAR is the tag-specific adaptor CAR. It is composed of an ECD that can identify and target an attached tag for tumor-specific adaptor molecules. This tag can be enzymatic, chemical, or genetic. Many subcategories have already been developed, including biotin-binding immune receptors [78], α-fluorescein isothiocyanate (α-FITC) CARs [79], UniCARs [80], α-peptide-neoepitope (PNE) CARs [81,82,83], split, universal, and programmable CARs [84], and a SpyCatcher CAR [85]. As with Fc-binding adaptor CARs, promising preclinical results have led to two Phase I clinical trial approvals. The first (ongoing) trial (NCT04230265) examines the effect of UniCAR-28/ζ (UniCAR02) T cells) administrated with CD123 transmembrane domains (TMs) in patients with CD123-positive hematologic and lymphatic cancers. The second trial has not started yet but will investigate the activity of a combination of α-PNE CAR-T cells (CLBR001) and a CD19 Fab switch (SWI019) in patients with relapsed/refractory B cell cancers [86]. Furthermore, α-FITC CARs with EC17 (folate-FITC) are advancing towards clinical development in an indication of osteosarcoma [69].
The third and final category corresponds to bsAb-binding adaptor CARs, which are able to simultaneously target two different antigens. This dual-targeting CAR-T cell strategy enables the use of a single type of genetically modified T cells with several bispecific adaptors designed to kill a wide variety of antigenically different solid tumors [87,88,89]. From 2014 onwards, scientific discoveries enabled the elaboration of three subcategories: bsAb-binding immune receptors (BsAb-IRs) [89], synthetic agonistic receptors (SARs) [90], and “integrated modules optimize adoptive cell therapy” strategies [91] (Figure 8). The popularity of this strategy prompted good manufacturing practice (GMP) production of the bifunctional adaptor molecule CD19ECD-αCD20, which will be used to treat relapsed CD19-negative cancer patients having previously received CD19 CAR-T cells; the goal is to reactivate these persistent CAR-T cells [92].

2.3. Strategies for Eliminating On-Target Off-Tumor Toxicity

A novel strategy for preventing antigen escape (considered to be the major cause of resistance to cancer immunotherapy) is the multi-antigen-targeted CAR-T cell [93]. Various types have been developed: dual CAR-T cells, tandem CAR-T cells, trivalent CAR-T cells, and pooled CAR-T cells. The first type consists of combining two CARs that recognized different TAAs in a single CAR-T cell. The second type targets two TAAs with two distinct antigen-binding (scFv) domains linked in tandem to a single CAR. The third type contains three different CARs (recognizing three specific TAAs) in a single CAR-T cell. The last type is a combination of two CAR-T cell lines, each of which targets a specific TAA. Based on the signal transmission pattern, multi-antigen-targeted CAR-T cells have diverse logic-gate operations such as “AND”, “OR”, and “NOT” (Figure 9) [94].
Before we examine each strategy in detail, it is important to note that epitope selection is the most important determinant of therapeutic potential. As mentioned above, a valid TAA for CAR-T cells must meet rigorous criteria. However, neoantigens are considered to be the most attractive therapeutic targets in hematological and solid malignancies because (i) their expression is restricted to tumor cells that express the respective coding mutations and (ii) these antigens are recognized as non-self by the host immune system [95]. Most importantly, they meet the three main criteria for target selection in CAR-T cell therapy: coverage, stability, and specificity [93]. It is nevertheless difficult to find an ideal target for solid tumors due to inherent heterogeneity. This is why most of today’s targets cause significant off-target effects and limit the treatment’s intensity and effectiveness. Consequently, the treatment of solid tumors might require a combination of targets [93].

2.3.1. AND-Gate CAR-T Cells

In contrast to OR-gate CARs, AND-gate CARs (dual CAR-T cells or trivalent CAR-T cells) have two or more extracellular domains activated solely by dual or triple antigen binding (Figure 9a,b). This strategy has been successfully tested in preclinical models of breast and prostate cancer [96,97]. In Kloss et al.’s preclinical study, CAR-T cells targeting prostate stem cell antigen (PSCA) and prostate-specific membrane antigen (PSMA) were generated in order to test the antitumor activity and safety profile of this combinatorial strategy. In fact, PSCA and PSMA are promising TAAs for prostate cancer [98] but neither is restricted to prostate tissue: PSCA is expressed in prostate tumors but also in the bladder, kidney, and other organs [99], while PSMA is expressed in metastatic prostate cancer but also in type II astrocytes, the kidney, and other organs [100]. CAR-T cells that display both antigen specificities were able to eradicate PSCA+/PSMA+ tumors in mice and thus achieve long-term survival of all treated animals. However, PSCA−/PSMA+ and PSCA+/PSMA− tumors were not destroyed, which demonstrates that using an AND logic gate can enhance the specificity and safety of CAR-T cell therapy [96].
It is important to note that the partial signaling derived from a single CAR can be strong enough to generate off-target toxicity [101]. This is why a more sophisticated approach (based on synthetic Notch (SynNotch) receptors) has been elaborated (Figure 9a). SynNotch receptors comprise the main regulatory domain of the cell-cell stimulating receptor Notch. However, the extracellular recognition domain and the intracellular transcriptional domain are both synthetic. Once the specific antigen binds to the synNotch receptor, an orthogonal transcription factor is released. It enters the nucleus and leads to the expression of another functional CAR, which targets a different TAA. Hence, local action is provided by the engineered lymphocyte and the customized gene expression program [102].
Further investigations of the immunogenicity of nonhuman transcription factors are required [103]. Preclinical studies have shown that synNotch CAR activation was only effective in dual-positive tumors; however, this was proof that spatial control had been achieved [104,105]. To prove the concept whereby synNotch receptors can control the expression of CARs, Roybal et al. engineered CAR-T cells with a CD19 synNotch receptor and α-mesothelin (MSLN) CAR gene. It is only when the T cell is exposed to CD19 that α-MSLN is expressed. The engineered lymphocytes are ready to be activated if the two TAAs are present. In light of the success of this approach, another experiment has been conducted using human primary CD4+ T cells engineered with a GFP synNotch receptor in which the CD19 CAR gene was inserted and whose expression is controlled by the corresponding response elements. These CAR-T cells were activated only upon contact with target cells expressing both GFP and CD19 on their surface [105]. Concerning AND-gate trivalent CAR-T cells, Sukumaran et al. demonstrated how genetically modified T cells expressing PSCA, TGFβ, and IL4 CARs can improve efficacy and safety in a pancreatic cancer model. These triple-specificity lymphocytes can reduce on-target/off-tumor effects by concentrating all their power on the cancer site. The preclinical studies of AND-gate CAR-T cells are summarized in Table 6.

2.3.2. NOT-Gate CAR-T Cells

NOT-gate CAR-T cells (also referred to as inhibitory CAR (iCAR) T cells) contain both an activating receptor and an inhibitory receptor (Figure 9c). The interaction between the iCAR and its specific antigen induces an inhibitory signaling cascade and thus restrains T cell activity. This inhibitory receptor is engineered to target an antigen that is strongly expressed in healthy cells but almost absent in cancer cells—thus limiting the CAR-T cells’ access to tumor tissues. In a proof-of-concept study, Federov et al. developed an iCAR-T cell with two distinct receptors: a CD19 CAR linked to the CD28/CD3ζ signaling domain and a PSMA iCAR linked to an inhibitory intracellular domain derived either from programmed cell death-1 (PD-1) or cytotoxic T-lymphocyte-associated protein 4 (CTLA-4) antigens. The results proved the iCAR’s ability to exert negative control on T lymphocyte function when encountering cells co-expressing PSMA and CD19. In vitro PD-1-based iCAR-T cells were able to kill CD19+/PSMA- cells, since the absence of PSMA constitutes a “non-inhibitory” signal. In the presence of CD19+/PSMA+ cells, however, the cytotoxicity of iCAR-T cells was significantly reduced (by up to 95%). Cytokine secretion was also reduced (by up to 88%). In an in vivo mouse model, the data showed that PD-1-based iCAR-T cells (i) selectively inhibited the eradication of an “off-target” infused CD19+ B cell leukemia cell line (NALM/6) that expressed PSMA but (ii) efficiently killed “on-target” infused NALM/6 cells that did not express PSMA. Therefore, these NOT-gate CAR-T cells can distinguish between target and non-target cells in a heterogeneous population, both in vitro and in vivo [107]. Further research is needed to identify the most relevant combination of activating and inhibitory CARs and thus the ideal target antigens. In fact, identifying the right target for activating the iCAR is the major bottleneck in further development of iCAR-T cells.

2.3.3. OR-Gate CAR-T Cells

Even though OR-gate CAR-T cells were originally engineered to avoid tumor resistance (rather than toxicity), we decided to develop this approach in the most promising next-generation CAR-T cells. OR-gate CAR-T cells can be activated in the presence of one of the targeted TAAs. It is now possible to develop a pool of specific dual, trivalent and tandem CAR-T cells by using the OR logic gate (Figure 9c). Pooled CAR-T cells targeting HER2/IL-13Rα2 for glioblastoma (GBM) [108], CD19/CD123 for B-ALL [109], and EGFR/CD133 [110] have been tested in preclinical studies and showed some benefits as well as some disadvantages. Although these CAR-T cells showed greater levels of cytolysis and cytokine secretion than the individual CAR-T cell lines, they were less efficacious than dual and tandem CAR-T cells. Furthermore, when monospecific CD19 and CD20 CAR-T cells were co-incubated with wild-type Raji cells, CD20 CAR-T cells proliferated significantly less than CD19 CAR-T cells—indicating that the combination of two CAR-T cell lines can lead to growth competition. The results also showed that this combination therapy exerts important immune pressure on the cancer cells, which may cause simultaneous tumor antigen escape [111]. Many clinical trials of this new approach have been initiated. In a Phase I clinical study (NCT02465983), patients with pancreatic cancer received a combination of mesothelin CAR-T cells and CD19 CAR-T cells. According to the investigators, this would increase the persistence of mesothelin-specific CAR-T cells in the body via the elimination of B cells by CD19 CAR-T cells and thus the elimination of antibodies against the CARs. Two other Phase I clinical trials used pooled CAR-T cell products consisting of CD19 and CD20 CAR-T cells for diffuse large B cell lymphoma (DLBCL) (NCT02737085), and CD19 and CD22 CAR-T cells for B-cell hematologic malignancies (NCT02903810), in order to effectively control recurrence due to a CD19 escape mutation. The known disadvantages of pooled CAR-T cells highlight the advantages of bispecific CAR-T cells. When, in the aforementioned trial, dual CAR-T cells targeting HER2/IL-13Rα2 encountered one of the two antigens, the intensity of signal transduction (ZAP-70 phosphorylation) was equal to that of the standard CAR-T cell. However, the intensity was greater when the dual CAR-T cells encounter both antigens simultaneously [108].
Many preclinical studies of tandem CAR-T cells using the OR logic gate have highlighted (i) the latter’s efficacy when at least one of the two antigens is recognized, and (ii) synergistic antitumor activity when both antigens are encountered [111,112,113,114]. It is also noteworthy that CD19/CD22 tandem CAR-T cells induced minimal residual disease-negative remission in a 22-year old patient with relapsed and refractory B-ALL after haploidentical HSCT. This clinical case highlights the tandem CAR-T cells’ potential for inducing long-term remission in B-ALL patients [115]. Like dual CAR-T cells, trivalent CAR-T cells have also shown potential antitumor activity. In a preclinical study, trivalent CAR-T cells (targeting IL13Rα2, EphA2, and HER2) were tested in order to overcome the antigen pair diversity seen in GBM patients and thus the insufficient antigen coverage of dual CAR-T cells. This experiment demonstrated that targeting three antigens with a single CAR-T cell can surmount interpatient antigen variability better than a bivalent combination, and can kill almost 100% of GBM cancer cells [116]. There are several explanations for this enhanced anticancer efficiency, including amplified signaling, a wider variety of targeted antigens, and stronger immunological synapse formation. Despite the above-mentioned advantages, OR-gate CAR-T cells are unfortunately associated with more on-target/off-tumor toxicity than AND- and NOT-gate CAR-T cells are. The preclinical studies of OR-gate CAR-T cells are summarized in Table 7.

3. Conclusions

Genetically modified T cells with synthetic immune receptors are exceptionally efficacious in the precision treatment of hematological cancers. However, this new era in cancer immunotherapy has only just started, and one can already envision significant advances in safety and efficacy in the coming years. In fact, one of the biggest obstacles to the development of CAR-T cells strategies is the potential toxicity due to overactivation of the immune system or on-target/off-tumor activation. Here, we reviewed the various innovative strategies developed to overcome these hurdles. Although many CAR-T cells have been efficacious in preclinical studies, few have entered clinical development. As mentioned above, some of these strategies (suicide genes and elimination markers) are designed to eliminate CAR-T cells quickly when toxicities occur, which permanently deactivates the long-term anticancer effect. Other approaches (SMASh CARs, the TKI-based OFF-switch, the Tet-ON system and switchable adaptor CARs) are able to reversibly turn off the CAR-T cells’ activity without eliminating these expensive and life-saving cell drugs. However, some of these deactivating approaches may take time to work and thus may lead to critical situations. Even though further research on the safety of CAR-T cells is required, one can legitimately hope that next-generation CAR-T cells will be safer as well as more efficacious. Gaining a better understanding of the obstacles posed by tumor heterogeneity and the tumor microenvironment should enable researchers to develop more precise strategies for immunosuppression and supportive care. Greater knowledge would also allow the engineered T lymphocytes to bypass the tumor’s immunosuppressive mechanisms. Other bottlenecks that must not be neglected are the practical and financial aspects of GMP CAR-T cell production—especially since the clinical trial results suggest that CAR-T cells and other genetically modified immune cells (such as CAR-NK cells) will be treatment options for broad range of cancers. Lastly, the rapid success of this strategy in oncology might prompt developments in other fields of medicine, such as the treatment of autoimmune as well as infectious disease.

Author Contributions

Authors have contributed to the revision of the literature and writing of the review. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Conflicts of Interest

The authors have no conflict of interest to report.

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Figure 1. Structure of a chimeric antigen receptor (CAR)—a cell-surface receptor comprising an extracellular ligand binding domain (which recognizes a specific tumor-associated antigen (TAA)), a transmembrane (TM) domain, and an intracellular signaling domain. The latter consists of a T cell activation domain and one or more co-stimulatory domains (CD27, CD28, ICOS, 4-1BB, and/or OX40) (Adapted from Lee and Kim, 2019).
Figure 1. Structure of a chimeric antigen receptor (CAR)—a cell-surface receptor comprising an extracellular ligand binding domain (which recognizes a specific tumor-associated antigen (TAA)), a transmembrane (TM) domain, and an intracellular signaling domain. The latter consists of a T cell activation domain and one or more co-stimulatory domains (CD27, CD28, ICOS, 4-1BB, and/or OX40) (Adapted from Lee and Kim, 2019).
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Figure 2. General coding sequence for a CAR.
Figure 2. General coding sequence for a CAR.
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Figure 3. The four generations of CAR-T cells. First-generation CARs were composed of antibody single-chain variable fragments (scFvs) fused through a TM domain to the cytoplasmic tail of the TCR signaling component CD3ζ. Second-generation CARs had improved CAR-T cell proliferation and cytotoxicity, thanks to the addition of co-stimulatory signaling domains (such as CD27, CD28, CD134, and CD137). Third-generation CAR-T cells were generated by adding a second co-stimulatory signaling domain (such as OX-40, also known as CD134, or 4-1BB, also known as CD137) to second-generation constructs. Fourth-generation CAR-T cells, also known as “T cells redirected for universal cytokine-mediated killing” (TRUCKs) were then engineered to secrete transgenic cytokines (like interleukin-12) within the targeted cancer and thus attract more immune cells (such as natural killer (NK) cells and macrophages). (Adapted from Smith et al., 2016).
Figure 3. The four generations of CAR-T cells. First-generation CARs were composed of antibody single-chain variable fragments (scFvs) fused through a TM domain to the cytoplasmic tail of the TCR signaling component CD3ζ. Second-generation CARs had improved CAR-T cell proliferation and cytotoxicity, thanks to the addition of co-stimulatory signaling domains (such as CD27, CD28, CD134, and CD137). Third-generation CAR-T cells were generated by adding a second co-stimulatory signaling domain (such as OX-40, also known as CD134, or 4-1BB, also known as CD137) to second-generation constructs. Fourth-generation CAR-T cells, also known as “T cells redirected for universal cytokine-mediated killing” (TRUCKs) were then engineered to secrete transgenic cytokines (like interleukin-12) within the targeted cancer and thus attract more immune cells (such as natural killer (NK) cells and macrophages). (Adapted from Smith et al., 2016).
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Figure 4. Activation of iCasp9 induces the death of transduced cells. iCasp9 is synthetized in the transduced CAR-T cell as a homodimer. Administration of the chemical inducer of dimerization (CID) AP1903 causes iCasp9 dimerization and thus activation, which in turn triggers a signaling cascade leading to the apoptosis of the CAR-T cells (Adapted from Li and Zhao, 2017).
Figure 4. Activation of iCasp9 induces the death of transduced cells. iCasp9 is synthetized in the transduced CAR-T cell as a homodimer. Administration of the chemical inducer of dimerization (CID) AP1903 causes iCasp9 dimerization and thus activation, which in turn triggers a signaling cascade leading to the apoptosis of the CAR-T cells (Adapted from Li and Zhao, 2017).
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Figure 5. CAR T cells with an elimination marker. huEGFRt and CD20 have been tested as elimination marker systems co-delivered with CAR-T cells. The huEGFRt suicide molecule can be activated with an anti-EGFR cetuximab. In contrast, RQR8 (a 136-amino-acid marker with epitopes from CD34 and CD20) has a dual role, by acting simultaneously as a selection marker when CD34 is targeted with an anti-CD34 MAb (QBEnd/10) and as a suicide molecule when CD20 is targeted with rituximab (Adapted from Li and Zhao, 2017).
Figure 5. CAR T cells with an elimination marker. huEGFRt and CD20 have been tested as elimination marker systems co-delivered with CAR-T cells. The huEGFRt suicide molecule can be activated with an anti-EGFR cetuximab. In contrast, RQR8 (a 136-amino-acid marker with epitopes from CD34 and CD20) has a dual role, by acting simultaneously as a selection marker when CD34 is targeted with an anti-CD34 MAb (QBEnd/10) and as a suicide molecule when CD20 is targeted with rituximab (Adapted from Li and Zhao, 2017).
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Figure 6. Schematic representation of the SWIFF-CAR principle (Adapted from Juillerat et al., 2019).
Figure 6. Schematic representation of the SWIFF-CAR principle (Adapted from Juillerat et al., 2019).
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Figure 7. Schematic representation of the tyrosine kinase inhibitor (TKI)-based OFF-switch. The TKI dasatinib inhibits the phosphorylation of CD3ζ and ZAP70, which have a key role in the T-cell receptor (TCR) signaling pathway (Adapted from Wu et al., 2019).
Figure 7. Schematic representation of the tyrosine kinase inhibitor (TKI)-based OFF-switch. The TKI dasatinib inhibits the phosphorylation of CD3ζ and ZAP70, which have a key role in the T-cell receptor (TCR) signaling pathway (Adapted from Wu et al., 2019).
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Figure 8. Schematic representation of switchable adaptors. (1) Tag-specific adaptors CARs: (a) biotin-binding immune receptors (BBIRs), (b) split, universal, and programmable (SUPRA) CARs, (c) α-FITC CARs, (d) UniCARs, (e) α-peptide-neoepitope (α-PNE) CARs, (f) SpyCatcher, (g) fusion protein (FP) CARs, (2) bispecific antibody-binding (BsAb) adaptor CARs: (h) BsAb immune receptors (BsAb-IRs), (i) synthetic agonistic receptors (SARs), (3) Fc-binding CARs: (j) ADCC-mediating immune receptor (Adapted from Arndt et al., 2020).
Figure 8. Schematic representation of switchable adaptors. (1) Tag-specific adaptors CARs: (a) biotin-binding immune receptors (BBIRs), (b) split, universal, and programmable (SUPRA) CARs, (c) α-FITC CARs, (d) UniCARs, (e) α-peptide-neoepitope (α-PNE) CARs, (f) SpyCatcher, (g) fusion protein (FP) CARs, (2) bispecific antibody-binding (BsAb) adaptor CARs: (h) BsAb immune receptors (BsAb-IRs), (i) synthetic agonistic receptors (SARs), (3) Fc-binding CARs: (j) ADCC-mediating immune receptor (Adapted from Arndt et al., 2020).
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Figure 9. Combinatorial antigen targeting for solid tumors. (a) AND-gate CAR SynNotch (b) AND-gate/CAR Split, (c) NOT-gate CAR, and (d) OR-gate/tandem CAR (Adapted from Schmidts et al., 2018).
Figure 9. Combinatorial antigen targeting for solid tumors. (a) AND-gate CAR SynNotch (b) AND-gate/CAR Split, (c) NOT-gate CAR, and (d) OR-gate/tandem CAR (Adapted from Schmidts et al., 2018).
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Table
Table 1. Abbreviations.
Table 1. Abbreviations.
AbbreviationReferring toAbbreviationReferring to
ADCCAntibody-dependent cellular cytotoxicityHSV-TKHerpes simplex virus thymidine kinase gene
ALLAcute lymphoblastic leukemiaiCARInhibitory CAR
AMLAcute myelogenous leukemiaiCasp9Inducible caspase-9
ASNAsunaprevirIFNγInterferon gamma
BBIRBiotin-binding immune receptorIgGImmunoglobulin G
BMTBone marrow transplantationIL-2Interleukin-2
BPDCNBlastic plasmacytoid dendritic cell neoplasmITAMImmunoreceptor tyrosine-based motif
BsAbBispecific antibodymAbMonoclonal antibody
BsAb-IRBsAb immune receptorMSLNMesothelin
CAR-T cellChimeric antigen receptor T cellMHCMajor histocompatibility complex
CDCluster of differentiationNHLNon-Hodgkin’s lymphoma
CIDChemical induction of dimerizationNKNatural killer
CLLChronic lymphoblastic leukemiaPD-1Programmed cell death-1
CNSCentral nervous systemPNEPeptide neoepitope
CRSCytokine release syndromePSCAProstate stem cell antigen
CTLA-4Cytotoxic T-lymphocyte-associated protein 4PSMAProstate-specific membrane antigen
rtTAReverse Tet transactivator
DIPGDiffuse intrinsic pontine gliomaSARSynthetic agonistic receptor
DLBCLDiffuse large B cell lymphomaSWIFF-CARSwitch-off CAR
DMGDiffuse midline gliomaSMAShSmall-molecule-assisted shutoff
DoxDoxycyclineSUPRASplit, universal, and programmable
ECDExtracellular domainSynNotchSynthetic Notch
EGFREpidermal growth factor receptorTAATumor-associated antigen
FabFragment antigen bindingTCRT cell receptor
FDAFood and Drug AdministrationTetTetracycline
FITCFluorescein isothiocyanateTKITyrosine kinase inhibitor
GBMGlioblastomaTMTransmembrane
GCVGanciclovirTNF-αTumor necrosis factor alfa
GMPGood manufacturing practiceTRUCKT cells redirected for universal cytokine-mediated killing
GVHDGraft-versus-host diseaseTSATumor-specific antigen
HER2Human epidermal growth factor receptor-2ZAP70Zeta-chain-associated protein kinase 70
Table
Table 2. Summary of preclinical studies of iCasp9 T cells co-expressing different CARs.
Table 2. Summary of preclinical studies of iCasp9 T cells co-expressing different CARs.
CAR-T CellsCancer TypeTime after Suicide InductionPercentage of Eradicated CAR-T CellsReference
iCasp9-IL15-CD19CARB-cell malignancies24 h>95.0%[35]
iCasp9-CD20CAR-Δ19B-cell malignancies24 h
72 h		90.0%
98.0%		[36]
iCasp9-CD20CAR-ΔNCFRB-cell malignancies48 h>99.0%[37]
iCasp9-CD33CAR-Δ19AMLN/A76.4%[38]
iCasp9-IL1RAPCAR-Δ19CMLN/A87.0%[39]
Table
Table 3. Summary of clinical trials using iCasp9 CAR-T cells.
Table 3. Summary of clinical trials using iCasp9 CAR-T cells.
TargetCancer TypesNCT Number
GD2DIPG and DMGNCT04196413
Relapsed/refractory neuroblastomaNCT01822652
NCT03721068
NCT03373097
Refractory/metastatic GD2-positive sarcoma or neuroblastomaNCT01953900
NCT02107963
Solid cancersNCT02992210
CD19Relapsed/refractory ALLNCT03016377
NCT03594162
Relapsed/refractory B-cell lymphomaNCT03696784
NCT03579927
CD19 & CD22Relapsed/refractory B-cell lymphomaNCT03098355
CD30Relapsed/refractory CD30-positive lymphomasNCT02274584
MesothelinSolid cancersNCT02414269
Advanced breast cancerNCT02792114
Table
Table 4. Summary of clinical trials of huEGFRt+ CAR-T cells.
Table 4. Summary of clinical trials of huEGFRt+ CAR-T cells.
TargetCancer TypesNCT Number
CD19CLL, NHL and ALLNCT01865617
NCT03103971
NCT01815749
NCT03085173
NCT02146924
NCT02051257
NCT03579888
NCT02028455
NCT02746952
EGFRRecurrent/refractory solid tumorsNCT03618381
Recurrent or refractory pediatric CNS tumorsNCT03638167
HER2HER2-positive recurrent/refractory pediatric CNS tumorsNCT03500991
BCMAMMNCT03070327
CD22CD22+ leukemia and lymphomaNCT03244306
CD123CD123+ relapsed/refractory AML or persistent/recurrent BPDCNNCT03114670
NCT02159495
CD171Recurrent/refractory neuroblastoma or ganglioneuroblastomaNCT02311621
PD-1Recurrent glioblastoma multiformeNCT02937844
Table
Table 5. Summary of clinical trials using Fc-binding adaptor CARs.
Table 5. Summary of clinical trials using Fc-binding adaptor CARs.
CAR AdaptorAdaptor MoleculeCancer TypeNCT Number
CD16-BB/ζ
(ACTR087)		RituximabRefractory or relapsed
CD20-positive B cell lymphoma		NCT02776813
CD16-28
(ACTR707)		NCT03189836
ACTR087
ACTR707		TrastuzumabHER2-positive advanced solid tumor cancersNCT03680560
ACTR087
ACTR707		Rituximab
Trastuzumab
SEA-BCMA		B cell lymphoma
MM
HER2-positive solid tumor cancers		NCT02840110
ACTR087SEA-BCMARelapsed or refractory MMNCT03266692
Table
Table 6. Preclinical studies of AND-gate CAR-T cells.
Table 6. Preclinical studies of AND-gate CAR-T cells.
CAR-T Cell TypeTargetCancer TypesReference
Dual CAR-T cellPSMA/PSCAProstate cancer[96]
FRa/MSLNOvarian cancer[101]
CD19/GFPExperimental cancer[105]
CD19/MSLNExperimental cancer[105]
Trivalent CAR-T cellPSCA/TGFβ/IL4Pancreatic cancer[106]
Table
Table 7. Summary of preclinical studies of OR-gate CAR-T cells.
Table 7. Summary of preclinical studies of OR-gate CAR-T cells.
CAR-T Cell TypeTargetCancer TypeReference
Pooled CAR-T cellHER2/IL-13Rα2GMB[108]
CD19/CD123B-ALL[109]
CD19/CD20B-ALL[111]
EGFR/CD133Cholangiocarcinoma[110]
Dual CAR-T cellCD19/CD123B-ALL[109]
HER2/IL-13Rα2GMB[108]
Tandem CAR-T cellCD19/CD20B cell malignancies[111]
HER2/IL-13Rα2GMB[108]
CD20/HER2Experimental Cancer[114]
CD19/HER2Experimental Cancer[112]
Trivalent CAR-T cellHER2/IL13Rα2/EphA2GMB[116]
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Andrea, A.E.; Chiron, A.; Bessoles, S.; Hacein-Bey-Abina, S. Engineering Next-Generation CAR-T Cells for Better Toxicity Management. Int. J. Mol. Sci. 2020, 21, 8620. https://doi.org/10.3390/ijms21228620

AMA Style

Andrea AE, Chiron A, Bessoles S, Hacein-Bey-Abina S. Engineering Next-Generation CAR-T Cells for Better Toxicity Management. International Journal of Molecular Sciences. 2020; 21(22):8620. https://doi.org/10.3390/ijms21228620

Chicago/Turabian Style

Andrea, Alain E., Andrada Chiron, Stéphanie Bessoles, and Salima Hacein-Bey-Abina. 2020. "Engineering Next-Generation CAR-T Cells for Better Toxicity Management" International Journal of Molecular Sciences 21, no. 22: 8620. https://doi.org/10.3390/ijms21228620

APA Style

Andrea, A. E., Chiron, A., Bessoles, S., & Hacein-Bey-Abina, S. (2020). Engineering Next-Generation CAR-T Cells for Better Toxicity Management. International Journal of Molecular Sciences, 21(22), 8620. https://doi.org/10.3390/ijms21228620

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