Engineering the next generation of CAR-NK immunotherapies

Abstract

Over the past few years, cellular immunotherapy has emerged as a novel treatment option for certain forms of hematologic malignancies with multiple CAR-T therapies now routinely administered in the clinic. The limitations of generating an autologous cell product and the challenges of toxicity with CAR-T cells underscore the need to develop novel cell therapy products that are universal, safe, and potent. Natural killer (NK) cells are part of the innate immune system with unique advantages, including the potential for off-the-shelf therapy. A recent first-in-human trial of CD19-CAR-NK infusion in patients with relapsed/refractory lymphoid malignancies proved safe with promising clinical activity. Building on these encouraging clinical responses, research is now actively exploring ways to further enhance CAR-NK cell potency by prolonging in vivo persistence and overcoming mechanisms of functional exhaustion. Besides these strategies to modulate CAR-NK cell intrinsic properties, there are increasing efforts to translate the successes seen in hematologic malignancies to the solid tumor space. This review will provide an overview on current trends and evolving concepts to genetically engineer the next generation of CAR-NK therapies. Emphasis will be placed on innovative multiplexed engineering approaches including CRISPR/Cas9 to overcome CAR-NK functional exhaustion and reprogram immune cell metabolism for enhanced potency.

Introduction

Adoptive cellular immunotherapy has moved from the bench to the bedside and heralds a new, promising era in the treatment of hematologic malignancies, with multiple CD19-directed chimeric antigen receptor (CAR)-T therapies now available [1–6]. With the recent FDA approval of CAR-T cells targeting B cell maturation antigen (BCMA) in patients with relapsed/refractory (R/R) multiple myeloma [7, 8], the therapeutic scope of adoptive cellular therapeutics has been successfully expanded beyond CD19 positive lymphoid malignancies. While CAR-T cell products undoubtfully have improved clinical outcomes and provided new hope for patients with refractory and relapsed hematologic malignancies, nearly 5 years of real-world clinical experience since market approval of the first CAR T cell product have also led to a somewhat sobering experience for many in the field. Besides the cumbersome logistics associated with autologous cell manufacturing and high rates of cell therapy-related toxicities, the most pressing concern remains suboptimal long-term disease control. As the most recent results from the initial pivotal trials show, current generation CAR-T products still fail to deliver long-term responses for many patients, with a significant proportion of treated patients eventually relapsing and succumbing to their disease [9–11].

CAR constructs are generally composed of an extracellular synthetic receptor for antigen recognition, an extracellular hinge region, a transmembrane domain and one or multiple intracellular co-stimulatory domains. The CAR receptor typically is derived from a murine mAb in the form of a single-chain variable fragment (scFv) but can also be encoded to express a naturally occurring surface receptor with affinity for tumor-specific ligands. The latter approach has gained increased attention as it circumvents the alloreactive potential arising from the murine scFv origin which can lead to CAR immunogenicity and result in treatment failure [12]. Depending on the composition of the intracellular signaling domains, CAR constructs can be ascribed to certain generations. While first generation CAR constructs rely on a single intracellular signaling domain [13], second [14, 15] and third [16, 17] generation CAR molecules are designed for dramatically augmented intracellular effector signaling by carrying either one or multiple additional co-stimulatory endodomains, typically in the form of either CD28 or 4-1BB.

In recent years, CAR engineering of natural killer (NK) cells has gained considerable traction due to the unique biological properties of NK cells that make them highly attractive cells for cancer immunotherapy. NK cells are innate immune cells which mediate cytotoxicity against cancerous and virally infected cells through multiple mechanisms of action [18]. The traditional dogma, by which NK recognition of abnormal cells is primarily driven by loss of target MHC-I surface expression, has over time been expanded by a more subtle understanding of the complex integration of multiple stimuli from both activating and inhibitory receptors which collectively determine NK cell activation state and target engagement. NK cells, even when genetically engineered to express a CAR molecule, retain their intrinsic capacity to recognize tumor cells through their native receptors, thereby providing them with an additional layer of anti-tumor reactivity independent of CAR-redirected killing. Of note, NK cells do not rely on the T-cell receptor (TCR) for cytotoxic killing. This endows them with a more favorable safety profile compared to their T-cell contenders, which, in the allogeneic setting, need to be further genetically modified to circumvent graft versus host disease (GvHD).

CAR-NK cells can be generated from NK cells derived from a variety of different sources including cord blood (CB), peripheral blood cell (PB), NK cell lines as well as hematopoietic and induced pluripotent stem cells (iPSC). While each source of NK cell presents its unique advantages and challenges, these have been reviewed in detail previously [19, 20] and will not be the focus of this article.

A new horizon—translating CAR-NK immunotherapy into the clinic

Clinical application of CAR-engineered NK cells was first reported in 2018 by a group from mainland China. Using a third-generation CD33-directed CAR construct with CD28 and 4-1BB co-stimulatory domains to transduce NK-92-derived NK cells, the researchers were able to demonstrate in a phase 1 study (NCT02944162) the safe infusion of up to 5 × 10⁹ CAR-NK cells into three patients with R/R acute myeloid leukemia (AML). While the therapy proved safe and without any evidence of significant adverse events, no durable remissions were attained. The study’s negative results were attributed mainly to the limited in vivo persistence of irradiated NK-92 cells, with CAR-NK levels dropping below detection thresholds within 1 week after infusion [21]. Indeed, in vivo expansion and long-term persistence of CAR-engineered lymphocytes constitute the linchpin of cell-based therapies which, when achieved, provide a decisive edge over mAb therapies by contributing to durable clinical responses. NK cells physiologically have a life span of only 2 weeks [22] which requires any successful CAR-NK engineering approach to overcome this inherent biological boundary, to achieve sustained responses.

Our group successfully pioneered a novel cord-blood-derived CD19-directed CAR-NK product with constitutive IL-15 cytokine support (CD19-CD28-ζ-2A-iCasp9-IL15) for sustained in vivo persistence [23]. In an interim analysis of the first 11 patients with heavily pre-treated R/R lymphoid malignancies who were infused with this product, eight (73%) achieved clinically meaningful responses with seven (63%) achieving a complete remission (CR) (NCT03056339) [24]. The interim results demonstrated an excellent safety profile with no occurrences of cytokine release syndrome (CRS), neurological toxicities, or GvHD. Of note, CAR-NK cells were detected for up to 1 year after infusion with responders exhibiting significantly enhanced CAR-NK peak copy numbers compared to patients who did not have a response. While larger multicenter trials will eventually need to validate our encouraging findings and assess long-term response duration, the interim results clearly demonstrate the potential of CAR-NK therapy for patients with high-risk lymphoid malignancies.

Most recently, preliminary data from an ongoing phase 1 clinical trial (NCT04023071) investigating an induced pluripotent stem cell (iPSC)-derived NK cell product, FT516, have been reported. FT516 has been engineered to express a non-cleavable Fc receptor (CD16a) to specifically redirect NK cells using monoclonal antibodies and enhance antibody-dependent cellular cytotoxicity (ADCC) [25]. Among the 11 patients with R/R B-NHL who received the investigational cell therapy in combination with rituximab, eight patients achieved an objective response (73%), six patients (55%) attained a complete remission and no evidence of CRS, ICANS or GvHD was observed [26]. Longer follow-up data will need to address whether the observed responses are durable and infused NK cells persist over time.

Evolving clinical trials landscape for CAR-NK immunotherapy

The past few years have witnessed an unprecedented acceleration in the early phase clinical trial activity in CAR-NK immunotherapy with multiple CAR-modified NK cell products currently under clinical investigation. Across the trials landscape, investigators are testing CAR constructs against a multitude of target antigens, using different sources of NK cells and various modular CAR designs. Overall, there are two main trends to highlight. Most noticeably, there has been a shift in the scope of targeted disease. While most of the earlier trials focused on targeting hematologic malignancies, many of the more recent trials seek out to explore CAR-NK cell immunotherapy as a new means to combat solid tumors. Second, there is an increasing appreciation of more sophisticated construct designs, enabled by multiplexed gene editing approaches, to enhance NK cell potency and persistence. In this review we first will summarize the recent clinical trial activity, highlighting the most promising CAR-NK cell candidates currently in clinical testing. In the second part of this review, we will elaborate on some of the novel genetic engineering avenues pursued to devise the next generation of CAR-NK cell immunotherapies.

Table 1 provides a list of all currently registered CAR-NK cell trials. While most CAR-based therapeutic approaches deliberately set out to target an individual tumor surface antigen in a highly specific manner, a different strategy has been employed with the design of NKX101, a donor-derived CAR-modified NK cell product engineered to express a synthetic NKG2D activating receptor [27]. NKG2D, a germline-encoded NK cell receptor, interacts with a plethora of stress ligands expressed on abnormal cells and is considered one of the central activating receptors driving innate NK cell effector responses. NKX101 (NGD2D-OX40-CD3ζ-Il15) demonstrated promising anti-leukemic activity in vivo [27] and is currently being evaluated in a phase 1 trial in patients with R/R AML as well as those with high-risk myelodysplastic syndrome (NCT04623944).

Table 1.

Overview of current phase 1/2 trials evaluating CAR-NK immunotherapy

Antigen target	Disease focus	Construct design	NK cell origin	Identifier	Sponsor	Location	First posted	Status
CD19	R/R B-ALL	CAR.19-41BB-CD3ζ	Haplo-identical donor	NCT00995137	St Jude Children's Research Hospital, Memphis, TN	USA	2009	Completed; no updates reported since 2017
CD19	R/R B-NHL	CAR.19-41BB-CD3ζ	Haplo-identical donor	NCT01974479	National University Health System	Singapore	2013	Suspended for interim review
CD33	R/R AML	CAR.33-CD28-4-1BB-CD3ζ	NK-92 cell line	NCT02944162	PersonGen BioTherapeutics	China	2016	Unknown, candidate not listed on sponsor website
CD7	CD7+ R/R leukemia/ lymphoma	CAR.7-CD28-4-1BB-CD3ζ	NK-92 cell line	NCT02742727	PersonGen BioTherapeutics	China	2016	Unknown, candidate not listed on sponsor website
CD19	R/R CD19+ lymphoid malignancies	CAR.19-CD28-41BB-CD3ζ	NK-92 cell line	NCT02892695	PersonGen BioTherapeutics	China	2016	Unknown, candidate not listed on sponsor website
Muc1	Advanced solid tumors	Undisclosed	Undisclosed	NCT02839954	PersonGen BioTherapeutics	China	2016	Unknown, candidate not listed on sponsor website
CD19	R/R ALL, R/R CLL, R/R B-NHL	CAR.CD19-CD28-CD3ζ.iCasp9-IL15	Cord blood	NCT03056339	MD Anderson Cancer Center, Houston, TX	USA	2017	Phase 1 portion completed; Phase 2 recruiting
HER2	HER2+ recurrent glioblastoma	CAR.HER2. CD28.CD3ζ	NK-92 cell line	NCT03383978	Johann Wolfgang Goethe University Hospital	Germany	2017	Recruiting
PSMA	Castrate-resistant prostate cancer	Undisclosed	iPSC	NCT03692663	Allife Medical Science and Technology	China	2018	Not yet recruiting
Mesothelin	Ovarian cancer	Undisclosed	iPSC	NCT03692637	Allife Medical Science and Technology	China	2018	Not yet recruiting
NKG2D ligands	Advanced solid tumors	Undisclosed	Autologous + allogeneic NK cells not further specified	NCT03415100	The Third Affiliated Hospital of Guangzhou Medical University	China	2018	Unknown
CD22	R/R B-NHL	Undisclosed	iPSC	NCT03692767	Allife Medical Science and Technology	China	2018	Unknown
BCMA	R/R B-NHL	Undisclosed	iPSC	NCT03559764	Allife Medical Science and Technology	China	2018	Unknown
BCMA	R/R Multiple myeloma	Undisclosed	NK-92 cell line	NCT03940833	Asclepius Technology Company Group	China	2019	Recruiting
CD20 (CD16a + Rituximab)	R/R AML/B-NHL	hnCD16; full construct undisclosed	iPSC	NCT04023071	Fate Therapeutics	USA	2019	Recruiting
ROBO1	Advanced solid tumors; pancreatic cancer	Undisclosed	Undisclosed	NCT03940820; NCT03931720; NCT03941457	Asclepius Technology Company Group	China	2019	Recruiting
CD19/CD22	R/R B-NHL	Undisclosed	iPSC	NCT03824964	Allife Medical Science and Technology	China	2019	Unknown
CD19	R/R B-NHL	Undisclosed	iPSC	NCT03824951; NCT03690310	Allife Medical Science and Technology	China	2019	Unknown
NKG2D ligands	R/R AML/MDS	CAR.NKG2D-OX40-CD3ζ	Donor-derived	NCT04623944	Nkarta	USA	2020	Recruiting
CD19 (± Rituximab or Obinutuzumab)	R/R B-NHL	CAR.19-NKG2D-2B4-CD3ζ-IL15RF-hnCD16	iPSC	NCT04245722	Fate Therapeutics	USA	2020	Recruiting
CD276 (CD16a + Enoblituzumab)	Ovarian cancer	hnCD16; full construct undisclosed	iPSC	NCT04630769	Fate Therapeutics	USA	2020	Recruiting
PD-L1 (CD16a + Avelumab)	Advanced solid tumors	hnCD16; full construct undisclosed	iPSC	NCT04551885	Fate Therapeutics	USA	2020	Recruiting
CD38/SLAMF7 (CD16a + Daratumumab/ Elotuzumab)	R/R Multiple myeloma/AML	hnCD16A-Il-15RF-CD38-/-; full construct undisclosed	iPSC	NCT04614636	Fate Therapeutics	USA	2020	Recruiting
BCMA (± daratumumab)	R/R Multiple myeloma	Undisclosed	iPSC	Pending	Fate Therapeutics	USA	Pending	IND application allowed
NKG2D ligands; SARS-CoV-2 S protein	COVID-19	Cord blood	CAR.NKG2D-ACE2-GM-CSF.IL15; full construct undisclosed	NCT04324996	Chongqing Public Health Medical Center	China	2020	Recruiting
CD19	R/R B-NHL	Undisclosed	Undisclosed	NCT04639739	Xinqiao Hospital of Chongqing	China	2020	Not yet recruiting
PD-L1; PD-1 (CD16a + Pembrolizumab)	Gastro-esophageal junction (GEJ) Cancer; Advanced HNSCC	CAR.PD-L1-FcεRIγ; full construct undisclosed	haNK cell line (NK-92 cell line engineered to express high-affinity CD16 and endoplasmic reticulum-retained IL-2)	NCT04847466	National Cancer Institute	USA	2021	Not yet recruiting
CD19	R/R B-NHL	Undisclosed	Haplo-identical donor	NCT04887012	Second Affiliated Hospital, School of Medicine, Zhejiang University	China	2021	Recruiting
CD19	R/R B-NHL	Cord blood	CAR.19.IL15; full construct undisclosed	NCT04796675	Wuhan Union Hospital	China	2021	Recruiting

ALL, acute lymphoblastic leukemia; AML, acute myeloid leukemia; BCMA, B-cell maturation antigen; CAR, chimeric antigen receptor; CD38^-/-, CD38 knock-out; CLL, chronic lymphocytic leukemia; DLBCL, diffuse large B-cell lymphoma; GEJ, gastroesophageal junction cancer; hnCD16, high-affinity, non-cleavable CD16; HNSCC, head and neck squamous cell carcinoma; IL15RF, IL15 receptor fusion; iPSC, induced pluripotent stem cell; NHL, non-Hodgkin lymphoma; PD-1, programmed cell death protein 1; PD-L1, programmed death-ligand 1; PSMA, prostate specific membrane antigen; R/R, relapsed or refractory; SARS-CoV-2, severe acute respiratory syndrome coronavirus 2

Another CAR-NK candidate which expresses both non-cleavable CD16a and a CD19-directed CAR receptor (CAR.19-NKG2D-2B4-CD3ζ-IL15RF-hnCD16) is currently evaluated clinically in advanced B-NHL and CLL in combination with anti-CD20 agents (NCT04245722). While no interim reports have yet been reported, preclinical in vivo data suggest superior tumor cell clearance for the multiplexed CAR candidate versus primary CD19-CAR-T cells [28]. FT538, a further CAR-NK candidate in clinical testing, has been engineered to be resistant to anti-CD38-mediated fratricidal killing by means of double allelic knock-out of CD38 and is being investigated against R/R multiple myeloma in combination with Daratumumab (NCT04614636). In contrast to CD38 wild type therapeutics, CD38^−/− CAR-NK cells may provide a clinical edge as they could eventually move into earlier lines of myeloma therapy including daratumumab-naïve patients.

Other ongoing studies are evaluating CB-derived NK cells CD19 (NCT04796675) and SARS-CoV-2 (NCT04324996), and NK-92-derived CAR-NK cells across a broad spectrum of tumor antigens including CD7 (NCT02742727), CD19 (NCT02892695), BCMA (NCT03940833), HER2 (NCT03383978) and PD-L1 (NCT04847466). While none of these trials have reported interim results yet, it will be interesting to observe the efficacy of CAR-NK cells against non-lymphoid malignancies.

Building the next generation of CAR-NK therapies

While the first part of this review has focused on the ongoing clinical development of CAR-NK immunotherapy, the second part aims to shed light on the most recent preclinical efforts to overcome some of the shortcomings seen with the current generation cell therapies.

Cancer cells have evolved sophisticated immunosuppressive mechanisms to thwart the effects of infiltrating lymphocytes and evade tumor immune surveillance. While earlier research focused predominantly on cancer-intrinsic mechanisms of immune escape, there has been an increasing appreciation of immune cell specific factors which underpin the fundamental phenotypic reconfigurations which leave immune cells in a dysfunctional state of ineffective tumor control. Finding a way to make CAR-engineered NK cells more potent, without compromising their favorable safety profile, is critical for the next generation of cell therapies. Current CAR-NK therapy constraints revolve around three recurring themes. First, CAR-NK therapies have thus far only been successfully applied to a very narrow repertoire of cancer-specific antigens. Second, limited in vivo persistence and eventual immune cell exhaustion pose a significant hurdle for long-term efficacy. Lastly, impaired trafficking to tumor beds and the delicacies of maneuvering the hostile tumor microenvironment impede the effective interaction of NK cells and their adversaries, ultimately leading to tumor immune evasion.

In the following sections of this review, we will (i) provide an overview of the ongoing preclinical efforts to redirect CAR specificity to extend the therapeutic scope of CAR-NK therapies and (ii) discuss some of the most interesting concepts to genetically reprogram CAR-NK cells to overcome some of the longstanding hurdles outlined above. We will then highlight the emerging applications of CAR-NK immunotherapy beyond hematologic malignancies including against COVID-19 and solid tumors, and iii) end this synopsis with an outlook on how we perceive CAR-NK immunotherapy will impact the field of cellular therapy and hematology/oncology over the coming years.

Extending the therapeutic scope for CAR-NK immunotherapy in hematologic malignancies

Most of the initial work in CAR-NK cell-based immunotherapy has focused on a very limited set of target antigens, mainly in the liquid cancer sphere. This next section will focus on the quest to find suitable tumor antigens to address cancer entities beyond B lymphoid malignancies and broaden the therapeutic scope for CAR-NK cell immunotherapy.

Aggressive T-cell malignancies

Aggressive T-cell malignancies represent an area of high unmet medical need, with dismal clinical outcomes and very limited therapeutic options at hand. CAR-T-based approaches have proven inherently challenging as shared expression of surface antigens among CAR-engineered T cells and transformed T lymphoblasts poses the risk of fratricide, a phenomenon by which infused CAR-T cells start attacking themselves leading to their own elimination. Another reason for concern is rooted in the potential contamination of autologous T-cell products with malignant T cells during the manufacturing process. CAR-NK cells lack expression of T-cell markers and can be derived from allogeneic sources, providing a compelling edge in the treatment of T-cell malignancies.

One group tested NK-92-derived cells, transduced to express a third-generation CAR construct (CD28-4-1BB-CD3ζ) against the pan-T-cell antigen CD3 and achieved significantly reduced tumor burden and prolonged survival in a T-ALL mouse model [29]. Although not as broadly expressed as CD3, CD4 represents another potential antigen for T-cell-directed therapies. NK-92 cells transduced with a third-generation anti-CD4-CAR construct (4-1BB-CD28-CD3ζ), when tested against a xenograft mouse model of anaplastic large cell lymphoma (ALCL), resulted in significant tumor control and prolongation of survival [30]. CD5 has similarly been targeted with another group engineering NK-92 cells with a third-generation CD5-CAR construct (4-1BB-CD28-CD3ζ) which resulted in enhanced anti-tumor efficacy in a T-ALL mouse model. More recently, a group from Tianjin, China designed a second-generation CD5-directed CAR construct (2B4-CD3ζ) which showed specific cytotoxicity against primary T-cell lymphoma cells in vitro and improved survival in a T-ALL in vivo mouse model [31]. CD7, while non-essential for normal T-cell development and homeostasis, is found on the majority of T-ALL clones and provides another alluring target for CAR receptor design. You et al. were able to construct a third-generation CAR molecule (4-1BB-CD28-CD3ζ) based on a CD7 nanobody which elicited potent anti-lymphoma responses in a mouse model of aggressive T-cell leukemia without significant fratricide [32]. Clinically, CD7-CAR-NK cells are already under investigation against aggressive T-cell malignancies in a Chinese-led phase 1 trial (NCT02742727).

While fratricide and contamination are of lesser concern with NK cell-based products, prolonged T-cell aplasia due to inadvertent elimination of healthy T cells resulting in severe immunosuppression, continues to be a major obstacle to be resolved before T-cell-directed therapies become a viable option in the clinic [33].

One strategy to mitigate the adverse effects of long-term T-cell aplasia inherent to T-cell-directed CAR-modified immune cells is to restore the cytotoxic potential of non-engineered NK cells using bispecific engagers that specifically guide NK cells towards tumor cells and mediate NK activation through high-affinity binding of their CD16A receptor. Our group has reported on the first successful application of pre-complexed NK cells using the tetravalent bispecific CD16A:CD30 immune cell engager AMF13 to induce CAR-like responses against CD30 positive malignancies. In brief, cord-blood-derived NK cells were pre-conditioned with the cytokines IL-12, IL-15 and IL-18 and pre-complexed with AMF13. Pursuing this approach, we were able to demonstrate increases in the cytotoxic potential of AFM13-loaded NK cells in vitro. When tested in lymphoma-bearing mice, AFM13-complexed NK cells elicited markedly improved anti-tumor responses and significantly prolonged survival, while no significant adverse toxicities were observed [34]. This approach is currently being tested in the clinic (NCT04101331).

Acute myeloid leukemia

Engineering CAR constructs targeting AML has proven challenging with two obstacles standing out [35]. Shared antigen expression of leukemic blasts and hematopoietic progenitor cells, as is the case for CD123 and CD33, raises the potential threat of on-target off-tumor toxicities eliciting prolonged multi-lineage cytopenias. Clonal heterogeneity and varied antigen expression across different AML populations represent another challenge leaving single-antigen targeted approaches prone to disease relapse, particularly in the presence of distinct leukemia-initiating clones characterized by discordant antigen signatures compared to bulk leukemic cells [35]. Our group and others have devised CAR molecules targeting CD123 using both third-generation (CD28-4-1BB-CD3ζ) and fourth-generation (CD28-CD3ζ-IL15) construct designs, and provided encouraging evidence for anti-leukemia cytotoxicity in vitro including against primary AML blasts [36, 37]. More recently, a third-generation CAR construct targeting CD4 (CD28-4-1BB-CD3ζ) was shown to specifically eliminate primary CD4 positive AML blasts and suppress disease progression in a cell-line-derived xenograft mouse model [38]. An innovative approach using the novel site-directed gene-insertion CRISPaint technology (CRISPR-assisted insertion tagging) to engineer two third-generation CD33-directed CAR-NK candidates (CD4-4-1BB-CD3ζ and NKG2D-2B4-CD3ζ) has been reported to elicit anti-leukemic activity in vitro [39].

An ingenious strategy to generate logic-gated CAR-NK circuits to address the two longstanding challenges, heterogeneous and shared antigen expression, which have thus far held back the success of AML cellular therapeutics, was reported by Dr. Gary Lee’s group [40]. Guided by a data-driven bioinformatics approach to predict optimal antigen combinations, they devised logic-gated CD33-OR-FLT3-NOT-EMCN CAR-NK cells. These cells specifically target AML blasts and leukemia-initiating cells by recognizing both CD33 and FLT3, but are inhibited when encountering endomucin (EMCN) which is present on up to 70% of FLT3-expressing hematopoietic stem cells. When co-cultured with FLT3 + EMCN-AML blasts and healthy FLT3 + EMCN + hematopoietic progenitor cells, their investigational allogeneic CAR-NK candidate exhibited selective and differential killing of the targeted blasts while sparing the hematopoietic stem cell compartment [41, 42].

Multiple myeloma

Multiple myeloma cells express a number of NK activating ligands and hence should be uniquely positioned to be targeted harnessing the power of CAR-modified NK cells [43]. Reports of CAR-NK immunotherapy to combat multiple myeloma date back to 2014 with one group reporting on the in vitro efficacy of a CD138-directed CAR construct used to genetically modify NK-92MI cells. Another group endowed NK-92 cells with a CS1-targeted CAR receptor which prolonged survival in vivo in a xenograft mouse model [44, 45]. Early efforts to target plasma cell diseases using NK cells were, however, restrained by concerns over NK fratricide due to their shared expression of CS1 and CD38. Independent of this NK cell intrinsic constraint, the field has shifted its attention towards exploring novel antigens, including BCMA, with the potential to induce remissions in patients with previous exposure to anti-CD38 agents. Reinforcing this notion, a two second-generation NK-92MI-CAR candidates (4-1BB-CD3ζ) targeting either NKG2D or BCMA were reported to mediate potent anti-myeloma activity in vitro [46–48]. Another team similarly was able to observe in vitro anti-tumor efficacy using a backbone encoding for both non-cleavable CD16a and BCMA combined with double allelic CD38 knock-out, paving the way for future combination therapies with CD38-targeted agents [49].

The next frontier—multiplexed genetic editing

Rational construct design

Besides redirecting CAR-NK cells to different target antigens, more recently the research focus has increasingly shifted towards optimized construct design based on modular combinations of different transmembrane and intracellular costimulatory domains to enhance CAR-NK potency.

Empowered by the versatile genetic engineering capabilities available today, researchers are now set up to fine-tune CAR constructs to induce more potent anti-tumor responses, increase antigen affinity or prolong in vivo persistence. Multiple co-stimulatory elements have been investigated for their potential to mount more effective anti-tumor responses, including domains derived from the immunoglobulin superfamily (CD28, ICOS), the TNF receptor superfamily (4-1BB, CD27, OX40, and CD40) and others including CD40L and toll-like receptors (TLRs) [50]. Compared to some of the earlier CAR-NK constructs which were primarily based on co-stimulatory domains involved in T-cell activation, there has been an increasing appreciation for NK-specific signaling adaptors with DAP10, DAP12 and 2B4 taking on particularly prominent roles [51–53]. These intracellular signaling adaptors mediate NK cell activation upon association with their respective upstream receptors. In a preclinical study investigating a CD19-directed CAR-NK candidate, incorporation of DAP10, the physiological adaptor for NK activating receptor NKG2D, enhanced the anti-tumor potency over a construct using CD3ζ signaling alone. Similar observations have been reported by others with amplified anti-tumor potency by including DAP12 in a prostate stem cell antigen (PSCA)-targeted CAR construct [54] and another group employing a 2B4-enhanced signaling strategy in mesothelin-targeted iPSC-derived natural killer cells [55].

Armored CARs

Modifications to CAR construct design across the first three CAR generations rely on physiologically occurring immune cell receptor domains. Fourth-generation constructs, dubbed armored CARs, take a dramatically different approach by incorporating molecular payloads and thereby endowing the CAR-modified immune cells with additional features and functionality which cannot be found within any physiological immune cell receptor. This approach enables CAR constructs to be engineered to address some of the inherent biological limitations of cellular immunotherapy, thereby positioning CAR engineering in the center of the synthetic biology revolution (Fig. 1).

Fig. 1.

Evolution of CAR construct design. (1) First generation CAR molecules contain a synthetic extracellular receptor for target antigen recognition, a transmembrane domain and one intracellular signaling domain. (2,3) Second and third generation CAR constructs are endowed with one or more intracellular co-stimulatory domains for augmented signaling. (4) Fourth generation constructs, dubbed armored CARs, contain molecular payloads which endow CAR-engineered cells with additional features and functionality. (5) Multi-specific targeting refers to genetic engineering strategies which aim to simultaneously target multiple tumor antigens. (6) Logic-gated CAR molecules are engineered to express both an activating (aCAR) and inhibitory (iCAR) CAR receptor on their surface. The former recognizes tumor-specific epitopes and is able to initiate immune cell activation and target engagement. The latter detects epitopes exclusively present on healthy tissues and inhibits immune cell activation. By integrating both signals, logic-gated CAR-modified NK cells can differentially kill tumor cells while sparing healthy tissues with shared antigens. (7) Bispecific Killer engagers (BiKes) are bispecific antibodies with binding sites for both FcRγIII (CD16A) and a tumor-specific epitope. Acting as a molecular glue, BiKes can bind and bring NK cells in close proximity of tumor cells for specific target elimination in a CAR-like manner. aCAR, activating chimeric antigen receptor; GzmB, granzyme B; HSC, hematopoietic stem cell; iCAR, inhibitory chimeric antigen receptor; IFNγ, interferon gamma; Il-15, interleukin 15; mAb, monoclonal antibody; PFN, perforin; T-NHL, T non-Hodgkin lymphoma; TNFα, tumor-necrosis factor alpha. Image created in BioRender

Arguably the most pressing biological constraint is limited in vivo persistence in the absence of exogenous cytokine support. While the clinical administration of cytokines is feasible, it carries with it considerable safety concerns and might inadvertently stimulate immunosuppressive immune cell compartments [56]. To overcome these obstacles, our group demonstrated how constitutive transgenic IL-15 cytokine support enables sustained in vivo persistence and augmented anti-tumor efficacy in a CD19-targeted CAR-NK candidate in patients with lymphoid malignancies [23, 24]. Empowered by modern bi- and multicistronic vector platforms, fourth-generation constructs can contain more than one desirable genetic modification, an engineering approach referred to as multiplexed genetic engineering. In the case of our group’s CD19-redirected CAR-NK product, we additionally included a molecular safety switch using an inducible Caspase9 (iCasp9) which can be activated by administration of a small molecule dimerizing drug to eliminate all circulating adoptive NK cells, in the event of adverse toxicities [23, 24].

Genetic disruption of CAR-NK immune checkpoints

Despite the remarkable successes seen with the administration of adoptive NK cell-based therapy, immune cell exhaustion remains a therapeutic barrier and strategies to overcome this are warranted to enhance long-term in vivo anti-tumor efficacy. For building the next generation of CAR-NK therapies, basic research on fundamental NK cell biology has once again shifted to the center of attention and significant efforts are underway to identify negative regulators of NK cell immune function. Recent advances in the understanding of the transcriptional networks involved in immune cell exhaustion, in large extent driven by high-throughput single-cell-based studies, have helped establish distinct signatures of dysfunctional NK cells. Several distinct phenotypic changes have been proposed to delineate exhausted NK cell subsets with upregulation of PD-1, LAG-3, TIM-3 [57] as well as TIGIT and KLRG1 [58] among those markers that confer impaired cytotoxic potential and hence embody putative candidates for targeted genetic ablation.

While the emergence of highly customizable and powerful viral vector platforms to deliver CAR molecules into various immune cell subsets was a prerequisite to enable the extraordinary strides seen in cellular immunotherapy over the last decade, the increasing adoption of targeted genetic perturbations using CRISPR/Cas9-mediated gene editing has opened up entirely new routes for modulating the underlying immune cell biology. Multiplexed genetic engineering strategies in particular allow for further improvement of CAR-modified immune cells in a site-directed manner so as to disrupt molecular pathways that negatively impact immune cell function. Multiple groups, including our own, have embarked on this journey to engineer the next generation of CAR-NK immunotherapies with enhanced potency, increased in vivo persistence and resistance to mechanisms of functional exhaustion with the ultimate goal to upend the field of cell therapy as we know it today (Fig. 2).

Fig. 2.

Multiplexed engineering strategies for building the next-generation of CAR-NK immunotherapy. (1) Ectopic expression of chemokine receptors enhances NK trafficking and infiltration into tumor beds. (2) Genetic disruption of negative regulators of NK immune function can help overcome functional exhaustion. (3) Neutralizing scFvs can intercept extracellular GM-CSF which has been linked to CRS/ICANS. (4) Cytokine pre-conditioning using Il-12/15/18 induces formation of memory-like NK cells with enhanced potency. (5) Knock-out of both surface and intracellular molecules conditions NK cells for combination therapies by preventing fratricide (CD38 KO) or immunosuppression (GR KO). (6) Metabolic reprogramming aims to render NK cells resistant to mechanisms of functional exhaustion by intervening in metabolic pathways. (7) Targeted genetic ablation of inhibitory receptors can safeguard CAR-NK cells against the immunosuppressive tumor microenvironment. A2AR, adenosine A2A receptor; CRS, cytokine release syndrome; GM-CSF, granulocyte macrophage colony stimulating factor; GR, glucocorticoid receptor; ICANS, immune cell-associated neurotoxicity syndrome; Il-10/12/15/18, interleukin 10/12/15/18; IDO, indoleamine 2,3-dioxygenase; PGE2, prostaglandin E2; scFv, single-chain variable fragment; TGFβ, transforming-factor beta; TGFBR2, transforming-factor beta receptor 2. Image created in BioRender

Genetic targeting of inhibitory immune checkpoints has emerged as a tantalizing concept to disrupt negative regulators of CAR-NK function for enhanced anti-tumor control. While NK cell activation states are intricately controlled by the complex interplay of both activating and inhibitory surface receptors, checkpoint blockade aims to skew this equilibrium towards heightened anti-tumor immunity. Genetic deletion of NKG2A, one of the most prominent germline-encoded inhibitory NK cell receptors, has previously been linked to increased cytotoxic potential against tumors expressing its cognate ligand HLA-E [59]. Blockade of TIGIT, another inhibitory checkpoint essential for maintaining balanced immune responses, has similarly been shown to prevent NK cell exhaustion [60]. Our group successfully targeted the cytokine-inducible Src homology 2-containing (CIS) protein, a key cytokine checkpoint upstream of interleukin 15 signaling, and achieved enhanced metabolic fitness and effector function in armored cord-blood-derived CAR-NK cells [61]. Other groups are striving to translate the lessons learned in the context of T-cell immunobiology and are investigating the effects of PD-1/PD-L1 and CTLA-4 blockade on NK cells [62, 63].

Safeguarding against the immunosuppressive tumor microenvironment

Apart from NK-intrinsic immune checkpoints, there are several extrinsic factors arising from the hostile tumor microenvironment which collectively create a highly unfavorable milieu for infiltrating immune cells. A mix of nutrient deprivation, acidity and hypoxia deprives infiltrating effector cells their anti-tumor activity. Furthermore, tumor cells have evolved mechanisms to attract regulatory immune cell compartments such as regulatory B cells and regulatory T cells as well as myeloid-derived suppressor cells (MDSCs), tumor-associated macrophages (TAMs), platelets, fibroblasts and stromal cells which secrete immunosuppressive cytokines including transforming growth factor β1 (TGFβ), adenosine, indoleamine 2,3-dioxygenase (IDO) and prostaglandin E2 (PGE2), further obliterating any remnants of an effective anti-tumor response. One of these extracellular immunosuppressive metabolites, adenosine, has successfully been rendered ineffective by blocking the expression of A2A adenosine receptor (A2AR) on the surface of NK cells. A2AR-deficient NK cells exhibited enhanced tumor control in a xenograft mouse model of BRAF-mutated melanoma [64, 65]. Our group successfully rendered primary human NK cells resistant to the immunosuppressive transforming growth factor β1 (TGFβ) by targeted perturbation of the TGFBR2 gene using CRISPR/Cas9 editing [66]. Building on these observations, we were also able to demonstrate that disruption of TGFβ receptor signaling, both using small molecule inhibitors and genetic ablation, preserves NK cell function in a glioblastoma stem cell (GSC)-engrafted mouse model and prevents formation of a GSC-induced NK cell inhibitory phenotype [67].

Together these studies highlight how novel genetic engineering approaches can be employed to disarm the hostile tumor microenvironment by rendering CAR-modified immune cells resistant to some of the most notorious immunosuppressive mechanisms, a theme we project will continue to have important reverberations in the treatment of human cancers, particularly when targeting solid tumors.

Designing safe CAR-NK products for clinical use

While these new tools allow to introduce deliberate genetic interventions, opening up opportunities to extend the scope and potency of cellular immunotherapies, they pose a theoretical risk of non-specific off-target genetic lesions resulting in unintended adverse outcomes [68]. Hence, careful safety considerations are required, particularly when aiming to administer CRISPR/Cas9 gene-edited cell products in the clinic. Recent innovations, that include the transient delivery of high-fidelity Cas9 ribonucleoprotein complexes through electroporation, mitigate most of these undesired genomic alterations and powerful sequencing technologies [69–71] that are sensitive enough to detect even the rarest off-site lesions provide an additional safety margin for genetically engineered lymphocytes for clinical use.

Modulating CAR-NK metabolism

A growing body of work has established the crucial role of rapid metabolic reconfigurations required for NK cells to effectively mount anti-tumor responses [72, 73]. Targeting of immune-metabolic pathways, hence, has emerged as an intriguing concept to render NK cells more metabolically robust and preserve their functional capacity. In NK cells, IFNγ production has been shown to be dependent on glucose-driven oxidative phosphorylation [74]. Once activated, NK cells undergo substantial metabolic changes, thereby increasing the rates of glycolysis and oxidative phosphorylation (OXPHOS) to support the energy requirements to mount effective immune responses [75–77]. NK cell metabolic requirements are highly context-specific; hence, regulatory pathways altering the metabolic machinery and configuration need to be meticulously orchestrated to meet the dynamic energy and biosynthesis demands. Mammalian target of rapamycin complex 1 (mTORC1) plays a key role in regulating NK cell metabolism and facilitates both early NK cell development as well as activation-induced expression of nutrient transporters and glycolytic enzymes to support functional responses in mature NK cells. Indeed, our group and others have demonstrated that disruption of CISH signaling metabolically reprograms CAR-NK cells to maintain elevated mTORC1 and MYC activity, promoting in vivo persistence and enhanced anti-tumor activity [61, 78, 79].

At the transcriptional level, sterol regulatory element-binding protein (SREBP) and MYC have been identified as the two central regulatory elements orchestrating the metabolic adaptations which enable activated NK cells to effectively mount immune responses. MYC signaling serves to adapt the metabolic machinery to the specific requirements of NK cells by upregulating the expression of glucose transporters and glycolytic enzymes as well as increasing mitogenesis. Intracellular MYC levels are extremely short lived and tightly regulated by the dynamic interplay of MYC protein biosynthesis and proteasomal degradation. One mechanism by which intracellular MYC protein levels are maintained in check in NK cells is by glycogen synthase kinase 3 (GSK3)-mediated phosphorylation with subsequent ubiquitination and proteasomal degradation. In patients with AML, GSK3 expression has been shown to be upregulated and linked to impaired NK cell cytotoxicity that can be restored by genetic or pharmacologic GSK repression [80]. In line with these observations, pharmacologic inhibition of GSK3 has been found to stabilize MYC levels in NK cells, thereby increasing their anti-tumor potency [81].

Maintaining NK cell mitochondrial fitness for memory formation

Deriving implications from the dynamic interplay of metabolic programs that underpin immune cell differentiation and functional responses has become an imperative to guide future genetic engineering approaches for building the next generation of CAR-NK immunotherapies. NK cells have traditionally been ascribed to the innate immune system. However, recent studies have increasingly challenged this paradigm as a result of the discovery of cytokine-induced memory-like phenotypes [82]. Todd A. Fehninger and his group translated this approach to the clinic and demonstrated that preactivation of isolated NK cells with IL-12, IL-15 and IL-18 robustly induced formation of a memory-like NK cell phenotype with enhanced effector function against myeloid leukemic blasts [83, 84]. Building on their observations, the authors enrolled patients with AML in a phase 1 clinical trial (NCT01898793) evaluating the concept of interleukin-preactivated NK cells, and observed clinical responses in five out of nine (56%) evaluable patients including four complete remissions (44%). Transferring the knowledge acquired to CAR-engineered NK cells, the same group recently reported on the successful application of CD19-CAR-modified memory-like NK cells against a xenograft lymphoma mouse model [85]. Several groups are now investigating and analyzing the immunometabolic signatures underpinning this distinct memory-like NK phenotype [73]. Mitochondrial fitness, in particular, has come to the center of attention with growing evidence linking mitochondrial dysfunction to impaired NK cell immune responses, and strategies to promote mitochondrial health to improve NK cell function are already under way [34, 86, 87].

CAR-NK immunotherapy in solid tumors

Although cellular immunotherapy has opened promising avenues of treatment for hematologic malignancies, these successes have so far not been successfully transferred to the treatment of solid tumors. Besides the intrinsic challenges of CAR-NK immunotherapy such as limited in vivo persistence and functional exhaustion, solid tumors pose a unique set of obstacles for cell-based treatment strategies routed in their complex clonal heterogeneity, shared antigen expression with healthy tissues, and the inherently hostile immunosuppressive microenvironment. Furthermore, solid tumors have evolved mechanisms to downregulate activating NK cell ligands on their surface and can effectively impair trafficking of immune cells into tumor beds. Despite these challenges, there has been a growing interest in combatting solid tumors using cellular therapeutics in multiple, currently ongoing, early phase studies targeting a diverse range of antigens including HER2 (glioblastoma; NCT03383978), PSMA (prostate cancer; NCT03692663), mesothelin (ovarian cancer; NCT03692637), MUC1 (advanced solid tumors; NCT02839954), NKG2D (advanced solid tumors; NCT03415100) and ROBO1 (advanced solid tumors; NCT03940820 and pancreatic cancer; NCT03941457).

Gene engineering for improved CAR-NK trafficking

To achieve clinically meaningful anti-tumor responses and enable the widespread adoption of engineered cellular therapeutics for the treatment of solid tumors, the next generation of CAR-NK therapies will need to be engineered for enhanced migration into tumor beds and improved ability to penetrate the barriers imposed by solid tumors. Several groups are now working on genetic modifications of NK chemokine receptors to allow more efficient NK homing into tumor sites. In renal cell carcinoma, NK cells modified to express supraphysiological levels of CXCR2 exhibited improved trafficking to sites of disease manifestation [88]. Similarly, forced expression of chemokine receptor 4 (CXCR4) on EGFRvIII-directed CAR-NK cells led to improved survival in an animal model of glioblastoma [89]. Yu Yugan Ng and colleagues recently tested ectopic expression of CXCR1 in a CAR targeting NKG2D ligands, and were able to demonstrate improved immune cell infiltration and augmented anti-tumor efficacy in a mouse model of peritoneal ovarian cancer [90].

Whereas many hematologic malignancies are inherently mono- or oligoclonal diseases, solid tumors are characterized by complex clonal landscapes with a high degree of heterogeneity. Single antigen-directed cellular therapies face significant obstacles combatting heterogeneous tumors driven by multiple co-evolving clones, each with its distinct immune phenotype and antigen expression pattern. Cell-based therapies applied to combat solid tumors must also disentangle the intricacies of shared antigen expression between tumor and healthy tissues to avoid inadvertent on-target, off-tumor toxicities.

Dual and multi-specific targeting has emerged as a promising concept to mitigate the challenges imposed by heterogeneous and shared antigen expression. In the effort to devise therapies against highly refractory diseases such as glioblastoma, NK-92-derived natural killer cells have been equipped with a dual-specific CAR construct with specificity towards both wild type EGFR and EGFRvIII. When injected into two different xenograft models of GBM, the dual-targeting CAR-NK cells effectively negated tumor growth and improved survival independent of the EGRF mutation status [91]. In early 2021, Jeffrey Miller’s group presented their work on multi-specific off-the-shelf B7-H3-targeted iPSC-derived CAR-NK cells which can recognize a broad range of solid tumors. B7-H3 (CD276), a member of the B7 protein superfamily, is upregulated on a wide range of tumors, particularly in the metastatic setting and has been linked to poor prognosis [92]. In their study, the authors were able to detect strong cytotoxicity signals in vitro against ovarian, prostate, bone, and breast cancer cell lines. Despite its conspicuous appeal as pan-cancer antigen, recent reports of potential on-target off-tumor toxicities have surfaced which led to the temporary halt of an ongoing phase 1 clinical study evaluating a bispecific T cell engager targeting B7-H3 and CD3 [93]. Efforts to advance B7-H3-directed therapies into the clinic, hence, will need to proceed with prudence and carefully monitor any signals of emerging safety concerns.

Adoptive CAR-NK immunotherapy for the treatment of viral pathogens including COVID-19

Although most applications of CAR immunotherapy have thus far focused on addressing cancer, adoptive cell-based therapies have gained much notice as a powerful route to treat life-threatening treatment-refractory viral infections, particularly in highly vulnerable immunocompromised patient populations including those with primary immunodeficiencies and allogeneic stem cell recipients [94].

Virus-specific T cells (VST), both donor-derived and from third-party cell banks, continue to be explored in the treatment of several viral pathogens including cytomegalovirus, Epstein–Barr virus, adenovirus, HHV6, BK virus and JC virus [94–97]. Against the backdrop of the ongoing global COVID-19 pandemic, many groups have rushed to translate the learnings from virus-specific T cells to address SARS-CoV-2 infections using novel cellular based approaches. While the share of vaccinated people has in recent months risen markedly in most developed countries, there still is a strong unmet need for effective treatments for high-risk and immunocompromised patients who might not achieve sustained neutralizing antibody responses. Legitimate concerns about the eventual emergence of immune escape mutants including those which can evade current vaccination and treatment efforts, remain, and thus uphold the interest in adoptive cell-based approaches for the treatment of COVID-19.

Our group successfully expanded SARS-CoV-2-directed cytotoxic T cells (CTL) from the peripheral blood of recovered donors [98] and is currently leading a phase 1/2 trial to assess the feasibility, safety and efficacy of SARS-CoV-2 virus-specific T cells (VST) in patients with mild to moderate COVID-19 disease (NCT047422595). With increasing evidence supporting the use of corticosteroids to improve outcomes for patients with COVID-19, we furthermore propose a novel engineering strategy delete the gene encoding for the endogenous glucocorticoid receptor (NR3C1) of these donor-derived SARS-CoV-2-specific VSTs using CRISPR/Cas9 gene editing, thereby rendering the lymphocytes resistant to the immunosuppressive potential of corticosteroids [98].

Aside from isolating and expanding SARS-CoV-2-directed cytotoxic lymphocytes from recovered donors, several other groups have been exploring ways to specifically modify natural killer cells to recognize and kill SARS-CoV-2-infected host cells. In 2020, a group in mainland China evaluated a novel dual NKG2D-ACE2-engineered cord-blood-derived CAR-NK cell candidate in its ability to combat COVID-19 and is testing this approach in an ongoing clinical phase 1/2 trial (NCT04324996). Genetically equipped with constitutive Il-15 cytokine support and targeting both the highly conserved S protein of SARS-CoV-2 through expression of its natural receptor ACE2, as well as NKG2D ligands on infected cells by encoding for the multi-specific activating receptor NKG2D, their investigational CAR construct may be an interesting approach for the treatment of high-risk COVID-19 patients. Aiming to negate cytokine release syndrome and potential neurotoxicity, the construct has been designed to secrete a neutralizing scFv fragment against GM-CSF which has been implicated in the onset and progression of CRS and ICANS [99]. Very recently, Dongfang Liu’s group reported on the generation of NK-92 cell-line-derived CAR-NK cells targeting SARS-CoV-2 and its D614G mutant. Using the scFv fragment from SARS-CoV-2 neutralizing antibody S309, the authors were able to demonstrate improved in vitro cytotoxic activity against pseudotyped SARS-CoV-2 viral particles and pseudo-SARS-CoV-2 infected target cells compared to an earlier construct the group had previously reported on [100, 101].

In summary, these early reports on CAR-modified natural killer cells targeting SARS-CoV-2 illustrate the broad applicability and immense potential of CAR-NK immunotherapy even beyond cancer, and foreshadow an era of universal off-the-shelf immune cell-based strategies in the treatment of other severe and life-threatening diseases.

Stitching it all together—CAR-NK immunotherapy coming of age

Despite recent advances, fundamental questions regarding the clinical administration CAR-NK cell immunotherapy remain. These include optimal patient selection, as well as ideal therapeutic sequencing of CAR-NK immunotherapy in the context of other established treatment regimens including autologous and allogeneic stem cell transplantation for hematologic malignancies. Future studies will need to address how to best select high-risk patients for CAR-NK immunotherapy by identifying prognostic biomarkers and assessing the optimal sequencing of CAR-redirected NK therapies to feed into established treatment algorithms.

While the recent report of the first successful clinical application of CAR-NK-based cellular therapy against high-risk lymphoid malignancies represents a major milestone in the field of cancer immunotherapy [24], it only marks the beginning of an exponential wave of cellular engineering innovations in the upcoming years. Going forward, we project that while conventional, non-antigen-specific cell-based therapies in the form of autologous and allogeneic stem cell transplant will continue to play an important role in the management of high-risk patients with hematologic malignancies for the foreseeable future, it is likely that antigen-specific CAR-based therapies will, over time, move up to earlier lines of therapy. Allogeneic off-the-shelf CAR-NK cell-based therapies are especially poised to supplant long-held treatment paradigms due to their broad applicability in the allogeneic setting and their tremendous cost–benefit compared to autologous cell products. For solid tumors, first interim reports of the currently ongoing clinical trials are highly anticipated and will allow for a more robust perspective on how fast cellular immunotherapy can conquer this area of high unmet medical need. Encouragingly, research activity has been spurred in recent years, and many promising CAR-NK cell candidates leveraging highly innovative next-generation genetic engineering approaches are underway to address the unique challenges of solid tumors and expected to advance to clinical testing in the near term. Underpinning these developments is the ever-growing understanding of fundamental immune cell biology, increasingly driven by powerful multi-omics and high-dimensional single cell analyses, which in many ways continue to lay the groundwork for a burst of innovations in the near future. Turbocharged with the powerful advances in genetic engineering capabilities, these insights are poised to spur further therapeutic innovations and, over time, radically alter long-held treatment paradigms and dramatically improve clinical outcomes to the benefit of generations of patients to come.

Abbreviations

A2AR

A2A adenosine receptor

ACE2

Angiotensin-converting enzyme 2

ADCC

Antibody-dependent cellular cytotoxicity

ALCL

Anaplastic large cell lymphoma

AML

Acute myeloid leukemia

BCMA

B-cell maturation antigen

B-NHL

B-cell non-Hodgkin lymphoma

Breg

Regulatory B cell

CAR-NK

Chimeric antigen receptor-modified natural killer cell

CISH

Cytokine-inducible SH2-containing protein

COVID-19

Coronavirus disease 2019

CR

Complete remission

CRISPaint

CRISPR-assisted insertion tagging

CRISPR/Cas9

Clustered regularly interspaced short palindromic repeats/Caspase 9

CRS

Cytokine release syndrome

CTL

Cytotoxic T cells

CTLA-4

Cytotoxic T-lymphocyte-associated protein 4

CXCR1/2/4

Chemokine receptor 1 (CXCR1); chemokine receptor 2 (CXCR2); chemokine receptor 4 (CXCR4)

DAP10

DNAX-activating protein 10

DAP12

DNAX-activating protein 12

EGFR

Epidermal growth factor receptor

EGFRvIII

Epidermal growth factor receptor variant III

EMCN

Endomucin

FDA

U.S. Food and Drug Administration

FLT3

Fms-like tyrosine kinase 3

GBM

Glioblastoma

GSC

Glioblastoma stem cell

GSK3

Glycogen synthase kinase 3

GvHD

Graft versus host disease

HER2

Receptor tyrosine-protein kinase erbB-2

HHV6

Human herpesvirus 6

HLA

Human leukocyte antigen

HSC

Hematopoietic stem cell

ICANS

Immune cell-associated neurologic toxicity

iCasp9

Inducible caspase 9

IDO

Indoleamine 2,3-dioxygenase

IFNγ

Interferon gamma

Il-12/15/18

Interleukin 12/15/18

iPSC

Induced pluripotent stem cells

JC virus

Human polyomavirus 2

KLRG1

Killer cell lectin-like receptor subfamily G member 1

LAG-3

Lymphocyte-activation gene 3

mAb

Monoclonal antibody

MDACC

The University of Texas MD Anderson Cancer Center

MDSCs

Myeloid-derived suppressor cells

MHC-1

Major histocompatibility complex 1

mTORC1

Mammalian target of rapamycin complex 1

MUC1

Mucin 1

NIH

National Institutes of Health

NK

Natural killer cells

OXPHOS

Oxidative phosphorylation

PBMC

Peripheral blood mononuclear cells

PD-1

Programmed cell death protein 1

PD-L1

Programmed death-ligand 1

PGE2

Prostaglandin E2

PSCA

Prostate stem cell antigen

PSMA

Prostate-specific membrane antigen

R/R

Relapsed or refractory

ROBO1

Roundabout homolog 1

SARS-CoV-2

Severe acute respiratory syndrome coronavirus 2

scFv

Single-chain variable fragment

SREBP

Sterol regulatory element-binding protein

T-ALL

T-cell acute lymphoblastic leukemia

TAMs

Tumor-associated macrophages

TCR

T-cell receptor

TGFβ

Transforming growth factor beta 1

TGFBR2

Transforming growth factor beta receptor 2

TIGIT

T-cell immunoreceptor with Ig and ITIM domains

TIM-3

T-cell immunoglobulin and mucin-domain containing-3

TLR

Toll-like receptor

TNF

Tumor necrosis factor

T-NHL

T-cell non-Hodgkin lymphoma

Treg

Regulatory T cell

VST

Virus-specific T cell

WT

Wild type

Author contributions

AB and KR wrote and approved the review article.

Declarations

Conflict of interest

K.R., and The University of Texas MD Anderson Cancer Center have an institutional financial conflict of interest with Takeda Pharmaceutical for the licensing of the technology related to CAR-NK cell research. MD Anderson has implemented an Institutional Conflict of Interest Management and Monitoring Plan to manage and monitor the conflict of interest with respect to MDACC’s conduct of any other ongoing or future research related to this relationship. K.R., and The University of Texas MD Anderson Cancer Center have an institutional financial conflict of interest with Affimed GmbH. Because MD Anderson is committed to the protection of human subjects and the effective management of its financial conflicts of interest in relation to its research activities, MD Anderson is implementing an Institutional Conflict of Interest Management and Monitoring Plan to manage and monitor the conflict of interest with respect to MD Anderson’s conduct of any other ongoing or future research related to this relationship. K.R. participates on the Scientific Advisory Board for GemoAb, AvengeBio, Virogin, GSK, Caribou and Bayer.