Mini Review ARTICLE
The More, The Better: “Do the Right Thing” For Natural Killer Immunotherapy in Acute Myeloid Leukemia
- Department of Experimental, Diagnostic and Specialty Medicine, Institute of Hematology L. and A. Seràgnoli, S. Orsola-Malpighi Hospital, University of Bologna, Bologna, Italy
Natural killer (NK) cells are circulating CD3− lymphocytes, which express CD56 or CD16 and an array of inhibitory receptors, called killer-immunoglobulin-like receptors (KIRs). Alloreactive KIR-ligand mismatched NK cells crucially mediate the innate immune response and have a well-recognized antitumor activity. Adoptive immunotherapy with alloreactive NK cells determined promising clinical results in terms of response in acute myeloid leukemia (AML) patients and several data demonstrated that response can be influenced by the composition of NK graft. Several data show that there is a correlation between NK alloreactivity and clinical outcome: in a cohort of AML patients who received NK infusion with active disease, more alloreactive NK cell clones were found in the donor repertoire of responders than in non-responders. These findings demonstrate that the frequency of alloreactive NK cell clones influence clinical response in AML patients undergoing NK cell immunotherapy. In this work, we will review the most recent preclinical and clinical data about the impact of alloreactive NK cells features other than frequency of alloreactive clones and cytokine network status on their anti-leukemic activity. A better knowledge of these aspects is critical to maximize the effects of this therapy in AML patients.
In the last years, major advances have been achieved in the understanding of acute myeloid leukemia (AML) biology (1). However, these preclinical results have weakly impacted on the clinical outcome of AML patients, whose prognosis is overall largely unsatisfactory (1–4). A significant improvement in AML outcome is provided by allogeneic stem cell transplantation (SCT), where alloreactive T cells and natural killer (NK) cells mediate the graft-versus-leukemia (GvL) effect, contributing to leukemia eradication and relapse prevention. However, for many patients, the cellular immunotherapy within SCT is hampered by the high risk of treatment-related morbidity and mortality. To expand the option of cellular immunotherapy besides the SCT setting, adoptive transfer of effector immune cells is a promising approach (5, 6).
Natural killer cells are circulating CD3− lymphocytes, which express CD56 or CD16. They account for 5–15% of circulating lymphocytes in humans and can be categorized into subpopulations with different maturation status and functional specificities. CD56loCD16+ NK cells with high cytotoxic potential are predominant in human blood, while the immunomodulatory CD56hiCD16− subset is more predominant in lymph nodes (7). NK cells mediate innate immune response and cancer immunological control independently from major histocompatibility complex (MHC)-based antigen recognition (8). A net effect between inhibitory receptors, such as killer-Immunoglobulin-like receptors (KIRs) and C-type lectin receptor (NKG2A), and activating receptors, including natural cytotoxic receptors (NCR), NKp46, NKp30, NKp44, and NKG2D, drives NK cell cytotoxic activity (9–11). Inhibitory KIRs are the most clinically relevant and interact with self and not self-HLA class I ligands (HLA-Bw4, HLA-C1, and HLA-C2) (12). During their maturation process, NK cells acquire cytolytic activity by upregulating cytotoxic receptors and expressing perforin under the stimulation of the T-cell derived cytokine interleukin (IL)-2. The subsequent “licensing” or “education” process is crucial for acquiring self-tolerance, avoiding NK-mediated self-damage (13). Several cytokines, such as interferon (IFN)-γ, tumor necrosis factor (TNF)-α, granulocyte-macrophage colony-stimulating factor (GM-CSF), and chemokines, such as CCL3, CCL4, and CCL5, are produced by stimulated NK cells, which, then, acquire the capacity of killing target cells, including tumor cells, through the perforin/granzyme pathway (14). As for AML, the first evidence of NK-mediated anti-leukemia effect was reported in the haploidentical T-cell depleted SCT setting, where it was demonstrated that a KIR-ligand mismatch between donor and recipient protects patients from leukemia relapse (15, 16).
NK Immunotherapy for AML: The State-of-Art of Clinical Trials
Acute myeloid leukemia cells are more sensitive to NK-mediated cytotoxicity than solid tumors (7). For this reason, several groups have been prompted to exploit in AML the potential of NK cell adoptive immunotherapy (17). High risk patients with myeloid malignancies were safely infused with highly purified NK cells to consolidate engraftment after haploidentical SCT (18), thus providing the rationale for exploring this strategy as a means of increasing GvL without concurrent GVHD effects (19). Besides the transplantation setting, adoptive immunotherapy with haploidentical NK cells in AML was exploited in adults and in childhood patients (20–23). Altogether, these studies demonstrated that NK cell-based adoptive immunotherapy is safe and feasible in AML patients. Of note, donor NK cells expanded after infusion and were in vivo alloreactive against recipient’s leukemic cells with some promising clinical responses. To increase the number of NK cells to be infused, ex vivo NK cell expansion is under preclinical and early clinical investigation. Co-culture of NK cells with feeder cells plus cytokines is effective in generating large number of NK cells with high antitumor effect and long survival (24). Clinically, expanded NK cells have proven to be safe and feasible (25). Very recently, a first-in-man study investigated the role of memory-like NK cells, obtained after in vitro differentiation from human NK cells with IL-12, IL-15, and IL-18 (26).
In Search for Biomarkers Predictive of Response to NK Immunotherapy for AML
Within clinical trials, “biology-driven approaches” have the potential to identify an array of biomarkers, which may be used to predict clinical response to NK immunotherapy and/or to guide clinical decision process. Some of these biomarkers may derive from the donor repertoire, whereas some others are related to host modifications after NK cell infusion (Figure 1).
Figure 1. Leukemia-cell intrinsic and extrinsic factors influencing natural killer (NK) cell function. NK cells are able to recognize acute myeloid leukemia (AML) blasts in a major histocompatibility complex-unrestricted manner inducing cell lysis through perforin/granzyme pathway. Within tumor microenvironment, regulatory T lymphocytes and MSCs play a role in inhibiting NK cell-mediated proliferation and cytotoxic function via the production of soluble factors, such as interleukin (IL)-10, transforming growth factor (TGF)-β, and indoleamine 2,3-dioxygenase (IDO), thus resulting in the downregulation of activating receptors (NKp30, NK944, and NKG2D) and in the upregulation of inhibitory receptors. Similar evasion mechanisms have been described as a consequence of a direct effect from AML cells on NK cells.
The NK cells cytolytic activity is regulated by inhibitory KIRs, which mediate self-tolerance by engaging HLA class I antigens. Four different inhibitory KIRs seem to be primarily involved in inducing NK alloreactivity because of a stronger recognition of HLA class I ligands: KIR2DL2/2DL3 recognize HLA-C1 ligands (HLA-Cw), KIR3DL1 recognizes Bw4 haplotypes, and KIR3DL2 targets HLA-A3 and HLA-A11 ligands. NK alloreactivity can be predicted according to four models. The “missing-self” or “KIR-ligand mismatch” or “ligand incompability model” is based on the absence in the recipient of inhibitory HLA-I molecules that are present in the donor. According to the “receptor–ligand” model, donor NK cells are activated through inhibitory KIRs, which do not bind their HLA ligands in the recipient. The “missing-ligand” model predicts alloreactivity when at least one HLA-ligand is missing. The last of the models mentioned above states that activating KIRs on donor cells are needed in order to achieve NK cell alloreactivity (27). In haploidentical SCT, KIR-L mismatch dramatically impacts on the efficacy of NK cells in enhancing anti-leukemia effect (15, 16, 23). Whether these findings may be directly translated into the immunotherapy field has not been fully elucidated. In their pioneering study of adoptive NK immunotherapy, Miller et al. showed that KIR-L mismatch between donor and recipient had a predictive value in terms of clinical response (20). These data have not been confirmed in the subsequent study on a wider number of patients (28). Moreover, KIR-L mismatch between recipient and donor was not enough to translate into a significant clinical benefit for previously selected KIR-L-mismatched donor–recipient pairs (20). These results may indicate that a deeper characterization of KIR–KIR-L interaction is probably needed in the setting of NK immunotherapy. Donors with group B KIR haplotypes have been shown to improve survival of AML patients undergoing unrelated SCT (29). Very recently, based on specific HLA/KIR subtype combinations, a predictive algorithm for donor selection has been developed in a cohort of 1,328 patients with AML who received HLA-matched SCT transplant (30). Then, the selection of donors with favorable KIR genes of the B haplotype and/or with specific HLA/KIR subtype combinations may be used to increase the potential benefit of KIR–KIR-L mismatch between donor and recipient.
Host Regulatory T Cells
Regulatory T lymphocytes (Tregs) are distinct CD4, CD25, and Foxp3 positive immunosuppressive lymphocytes, which induce tolerance by inhibiting immune responses, including NK cell-mediated cytotoxicity. During the development of malignancies, Tregs proliferate under the stimulation of transforming growth factor (TGF)-β secreted by myeloid dendritic cells (DCs) and accumulate in blood, draining lymph nodes, and tumor microenvironment (14). Many studies demonstrated that Tregs are able to influence NK cell activity (14, 28, 31). In particular, NK cell inhibition induced by Tregs is mediated by soluble and Tregs-bound TGF-β, both resulting in downregulating of NKG2D on NK cells (14). Accordingly, in mice Treg depletion with anti-CD25 monoclonal antibody abrogated tumor growth and allowed the proliferation of NK cells (32). The influence of Tregs in NK adoptive immunotherapy has been recently addressed by Miller et al. in a large group of patients infused with NK cells. In this study, 57 patients with relapsed or refractory AML who received lymphodepleting chemotherapy with fludarabine and cyclophosphamide followed by NK cell infusion were analyzed. Patients were divided into three subgroups on the basis of the methods of NK cell product preparation: cohort 1 received NK cells after CD3 depletion alone, cohort 2 received NK cells after CD3 depletion followed by CD56 positive selection, and cohort 3 received NK cells after a single-step CD3/CD19 depletion. Patients included in Cohort 3 received the highest NK cell dose and after NK infusion were treated with IL-2 diphteria toxin (IL-2DT), a cytotoxic fusion protein able to selectively deplete high affinity IL-2 receptors (CD25)-expressing cells, including Tregs. A clear association between NK expansion and clinical responses was documented and such correlation was partly dependent on host Tregs. These data suggest that Tregs frequency in patients infused with NK cells may be a biomarker predictive of NK cell expansion and activity and may have clinical implications for the choice and schedule of cytokine-based therapy after NK cell infusion. In particular, the potent effect of IL-2, commonly used in NK-based immunotherapy protocols, on NK cell expansion and activity may be counterbalanced by its detrimental proliferative activity on Tregs. Clinical trials, including post-infusion administration of cytokines, such as IL-15, with no proliferative effect on Tregs are highly warranted.
Leukemia-Cell Intrinsic and Extrinsic Factors
A large body of evidence support the interplay between AML cells and the different cell components of the immune system (33). Some reports indicate that NK cells may be defective in AML patients (34, 35). In particular, a deficient expression of NCRs in NK cells from AML patients and during leukemia evolution has been observed (36). Conversely, NK cells with an activated phenotype from AML patients are cytotoxic against primary AML cells (37). Leukemia-induced phenotypic and functional NK cell abnormalities have been described in AML patients and are predictive of remission-induction after chemotherapy (38). Soluble factors, including IL-10, TGF-β, or indoleamine 2,3-dioxygenase (IDO), have been correlated with AML-mediated impairment of NK function (39). Sera collected from human AML patients contain microvescicles enriched in TGF-β, which mediates the inhibition of NK cell activity (40). In support of a pathogenetic role of these mechanisms during AML development, the defects of NK cells were restored in patients achieving complete remission after chemotherapy (38, 40). Moreover, the expression by AML cells of the immunosuppressive surface proteins CD200 (41) and CD137 (42) has a direct suppressive effect on NK cell activity, thus contributing to leukemia escape from NK-mediated control. The role of leukemic bone marrow (BM) microenvironment is critical in mediating immunotolerance (43–45). An increasing body of evidence has shown that immune effector cells are dysfunctional as a consequence of inhibitory signals deriving from a wide variety of immune cell components of tumor microenvironment, such as tolerogenic DCs, macrophages, and myeloid-derived suppressor cells (MDSCs). In solid tumors, these immunosuppressive cell subsets are expanded in patients and their presence in the tumor microenvironment correlates with worse prognosis and a dysfunctional activity of NK cells (46–48). In AML, the role of these immunosuppressive cells is not well-understood yet, whereas the activity of mesenchymal stromal cells (MSCs) on NK cells in BM leukemic microenvironment has been widely investigated. In particular, MSCs can negatively interfere with the function of NK cells by reducing their cytotoxic activity and cytokine production (49). Similar to the effects derived from AML cells, MSC-driven impairment of NK cell function was related to a downregulation of the activating NK receptors NKp30, NKp44, and NKG2D and mediated by IDO and prostaglandin E2. Whether these evasion mechanisms by AML cells and by other cell components of leukemic BM niche may be active during adoptive NK cell transfer has not been specifically addressed within clinical trials. Future immunotherapy trials are expected to take into accounts some of these parameters, which may be correlated with response to NK immunotherapy.
NK Immunotherapy in AML: The Question of Dose
In SCT and cell therapy, how many cells should be infused to achieve a therapeutic effect represents a common and crucial question. Many efforts have been made, for example, to identify the minimum and optimal number of hematopoietic CD34+ stem/progenitor cells capable of a durable engraftment in autologous SCT (50) or, in the setting of allogeneic SCT, the dose of CD3+ T cells to be used as donor lymphocytes infusions (DLI) for relapsing leukemia (51, 52). For NK immunotherapy, whether the dose of infused NK cells really impacts on the clinical response is still a matter of debate. Although infused NK cells may eradicate AML cells in virtue of several factors other than their dose, preclinical studies have demonstrated that NK cell cytotoxicity is directly correlated to the ratio between NK and target cells (53–55). Then, to infuse an adequate number of NK cells is likely to be clinically relevant. Since NK cells account for only a small portion of circulating lymphocytes, several groups are exploring the option of increasing the number of infused NK cells by ex vivo expanding cytotoxic NK cells and different NK cell production protocols are under investigation (56). An overview of these strategies is out of the focus of the current review. Indeed, we consider a preliminary and fundamental step to address the question of the minimum number of effective NK cells to be infused as a means of adoptive immunotherapy. Under this viewpoint, there is no consensus on the parameters to be used for enumerating functionally active NK cells among infused cells, which increases variability among clinical studies and makes the comparison of clinical results extremely difficult, if not impossible (57). In a pediatric cohort of AML patients undergoing NK cell infusion as part of their post-remission strategy, mainly because of body weight discrepancy between donor and recipient, high numbers of total CD56+CD3− NK cells/kg were infused (21). Of note, CD56+CD3− NK cells were highly purified and the amount of contaminating cells, other than NK cells, was minimal. Interestingly, the clinical results were remarkable with 100% of patients achieving durable response. In our recent report on a group of elderly AML patients, who were infused with the same highly purified NK cell population as the pediatric study, a trend for better outcome in those patients who received higher numbers of NK cells was shown (23). In the largest study by Miller et al. (28), comparing the clinical results of 57 patients undergoing infusion of NK cells, total NK cell dose resulted as being not correlated with clinical response. Notably, in this study (28), three different methods for NK cell manufacturing were used and only in a minority of patients NK cells were highly purified as the studies above. Moreover, cell dose was not correlated with in vivo expansion and clinical response when purified NK cells were in vitro primed with IL-12, IL-15, and IL-18 (26). Although not conclusive, the results from these studies may suggest that the optimal NK cell dose may differ depending on the cell manufacturing system and that, in case CD56+CD3− NK cells are highly purified and not manipulated, the simple count of total infused NK cells may be used as a useful parameter to predict clinical response.
The possibility of infusing a number of functionally active NK cells is likely to have greater impact on the efficacy of NK infusion than simply enumerating the number of total NK cells. Indeed, in our cohort of elderly AML patients, a better response was observed when at least 2 × 105 functionally alloreactive donor NK cells/kg were infused (Figure 2). Our results indicate a highly predictive threshold of NK cells to be defined at the functional level (“functional dose”). Although such dose may be used to guide NK cell processing, the feasibility of such approach, which is based on a laborious and time-consuming alloreactive NK cell cloning, represents a major concern. Then, a major achievement will be to identify a functional dose of NK cells, predictive of response to NK cell infusion, by using alternative methods and tools. By moving from the results in the transplant setting (17), a new and predictive-of-response expression platform to be used in donor selection is likely to be a concrete possibility. The development of novel anti-KIR monoclonal antibodies that can distinguish inhibitory versus activating KIRs allows to identify alloreactive NK subpopulations in the majority of individuals at the phenotypical level. Although these new methods and tools require formal clinical testing and validation in large cohorts of patients undergoing NK immunotherapy, we may expect that the “functional dose” of NK cells to be infused will be identified without standard and cumbersome functional studies of NK cell cloning (58–60). Such approach will, then, allow to dissect donor NK cell repertoire at baseline, thus leading to definitively address the question of the correlation between NK cell dose and clinical response.
Figure 2. The “functional dose” of infused alloreactive natural killer (NK) cells is highly predictive of response in acute myeloid leukemia (AML) patients. A cohort of elderly AML patients in first complete remission received highly purified NK cells after lymphodepleting fludarabine and cyclophosphamide to prevent disease relapse. A better response in leukemia control was observed when at least 2 × 105 functionally alloreactive donor NK cells/kg were infused. Such threshold has been chosen as a “functional cell dose” to be used to select donor(s) and guide NK cell processing.
Although several clinical reports have clearly paved the way for exploiting NK cell-based adoptive immunotherapy for AML patients, several crucial issues remain to be established and settled. In particular, the founding question of the therapeutic dose of infused NK cells potentially exerting in vivo anti-leukemia effect is still unanswered. Preliminary data from recent studies have shed light on this point, although the great heterogeneity of clinical strategies, which include freshly isolated versus expanded, non-manipulated versus cytokine-primed NK cells, makes the comparison among trials extremely difficult. Advancements of diagnostic tools, coupled with a “biology-driven” approach, are expected to provide an array of biomarkers, which may help in selecting the best donor for the best patient, thus making NK immunotherapy really beneficial for a specific subset of AML patients.
SP wrote and revised the final manuscript; ML and DO provided figures and revised the final manuscript; VS, MC, DF, and GC contributed to manuscript preparation and editing; AC contributed to manuscript writing and final revision.
Conflict of Interest Statement
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
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Keywords: natural killer cells, acute myeloid leukemia, immunotherapy, biomarkers, cell dose
Citation: Parisi S, Lecciso M, Ocadlikova D, Salvestrini V, Ciciarello M, Forte D, Corradi G, Cavo M and Curti A (2017) The More, The Better: “Do the Right Thing” For Natural Killer Immunotherapy in Acute Myeloid Leukemia. Front. Immunol. 8:1330. doi: 10.3389/fimmu.2017.01330
Received: 18 August 2017; Accepted: 29 September 2017;
Published: 19 October 2017
Edited by:Katy Rezvani, University of Texas MD Anderson Cancer Center, United States
Reviewed by:Amorette Barber, Longwood University, United States
Aparna Rao, University of Pittsburgh, United States
Copyright: © 2017 Parisi, Lecciso, Ocadlikova, Salvestrini, Ciciarello, Forte, Corradi, Cavo and Curti. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Sarah Parisi, firstname.lastname@example.org