http://orcid.org/0000-0002-8070-9727
Figures
Abstract
Acute lymphoblastic leukemia (ALL) is the most common cancer in children around the globe. Mexico City has one of the highest incidence rates of childhood leukemia worldwide with 49.5 cases per million children under the age of 15 which is similar to that reported for Hispanic populations living in the United States. In addition, it has been noted a dismal prognosis in Mexican and Hispanic ALL pediatric population. Although ALL, like cancer in general, has its origins in endogenous, exogenous, and genetic factors, several studies have shown that the immune system also plays a deterministic role in cancer development. Among various elements of the immune system, T lymphocytes and NK cells seem to dominate the immune response against leukemia. The aim of the present study was to perform a phenotypic and functional characterization of NK cells in ALL Mexican children at the moment of diagnosis and before treatment initiation. A case-control study was conducted by the Mexican Interinstitutional Group for the Identification of the Causes of Childhood Leukemia (MIGICCL). 41 cases were incident ALL children younger than 17 years old and residents of Mexico City. 14 controls were children without leukemia, matched by age and sex with cases. NK cell function was evaluated by degranulation assays towards K562 cells and SLAM-associated protein (SAP) expression was measured by intracellular staining. All assays were performed using peripheral blood mononuclear cells from controls and patients. The results indicate that NK mediated cytotoxicity, measured by CD107a degranulation assays in response to K562 cells, was reduced in ALL patients compared to controls. Interestingly, an impaired NK cell killing of target cells was not equally distributed among ALL patients. In contrast to patients classified as high-risk, standard-risk patients did not display a significant reduction in NK cell-mediated cytotoxicity. Moreover, patients presenting a leukocyte count ≥ 50,000xmm3 displayed a reduction in NK-cell mediated cytotoxicity and a reduction in SAP expression, indicating a positive correlation between a reduced SAP expression and an impaired NK cell-mediated citotoxicity. In the present study it was observed that unlike patients with standard-risk, NK cells from children presenting high-risk ALL, harbor an impaired cytotoxicity towards K562 at diagnosis. In addition, NK cell function was observed to be compromised in patients with a leukocyte count ≥50,000xmm3, where also it was noticed a decreased expression of SAP compared to patients with a leukocyte count <50,000xmm3. These data indicate NK cell-mediated cytotoxicity is not equally affected in ALL patients, nevertheless a positive correlation between low SAP expression and decreased NK cell-mediated cytotoxicity was observed in ALL patients with a leukocyte count ≥50,000xmm3. Finally, an abnormal NK cell-mediated cytotoxicity may represent a prognostic factor for high-risk acute lymphoblastic leukemia.
Citation: Valenzuela-Vazquez L, Núñez-Enríquez JC, Sánchez-Herrera J, Jiménez-Hernández E, Martín-Trejo JA, Espinoza-Hernández LE, et al. (2020) Functional characterization of NK cells in Mexican pediatric patients with acute lymphoblastic leukemia: Report from the Mexican Interinstitutional Group for the Identification of the Causes of Childhood Leukemia. PLoS ONE 15(1): e0227314. https://doi.org/10.1371/journal.pone.0227314
Editor: Francesco Bertolini, European Institute of Oncology, ITALY
Received: July 22, 2019; Accepted: December 16, 2019; Published: January 17, 2020
Copyright: © 2020 Valenzuela-Vazquez et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Data Availability: All relevant data are within the manuscript.
Funding: This work was supported by the Consejo Nacional de Ciencia y Tecnologia [grant numbers SALUD‐2010‐1‐141026, FIS/IMSS/PROT/895, PDCPN2013‐01‐215726, FIS/IMSS/PROT/1364, SALUD 2015‐1‐262190, FIS/IMSS/PROT/1533, CB‐2015‐1‐258042, FIS/IMSS/PROT/1548, and FONCICYT/37/2018, FIS/IMSS/PROT/1782]; and by the Instituto Mexicano del Seguro Social [grant numbers FIS/IMSS/PROT/PRIO/11/017, FIS/IMSS/PROT/G12/1134, FIS/IMSS/PROT/G11/951, FIS/IMSS/PROT/PRIO/14/031, FIS/IMSS/PROT/MD13/1254, FIS/IMSS/PROT/PRIO/15/048, FIS/IMSS/PROT/MD15/1504, FIS/IMSS/PROT/G15/1477]. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
Introduction
Acute lymphoblastic leukemia (ALL) is the most common cancer during childhood. Different clinical, immunophenotypic and molecular subtypes have been described for the disease [1]. In contrast to other cancers, ALL has reached cure rates around 90% in developed countries as a result of the improvement in chemotherapy treatments based on a prognostic stratification. Among prognostic features, the age and white blood cell count (WBC) are the most consistently used across chemotherapy protocols [2].
Mexico City has one of the highest incidence rates of childhood leukemia worldwide with 49.5 cases per million children under the age of 15, which is similar to that reported for Hispanic populations living in the United States [3–5]. In addition, the Hispanic population not only has the highest incidence rates in ALL, but also one of the lowest survival rates within the United States, so that the ethnic and racial disparities are also considered as important factors that influence both the incidence and the efficacy of the treatment for this cancer [6]. In previous studies, it has been reported that there are differences in the clinical characteristics at diagnosis of Mexican patients with ALL in comparison to children from other populations where survival rates are better. For instance, almost 50% of ALL Mexican children are classified as having high risk of relapse according to the National Cancer Institute (NCI) criteria based on patient´s age and WBC count at diagnosis, whereas in developed countries, only one third of patients are classified as having a high risk of relapse using the same criteria [7, 8].
Furthermore, despite the use of the same chemotherapy regimens, in the last years it has been reported an upward trend since the incidence, relapses and mortality rates for Mexican children with ALL occur at a frequency of three times higher in comparison to that reported for children from developed countries [7]. Therefore, the identification of novel risk factors associated with ALL and the development of new therapeutic targets become extremely necessary for high risk populations.
As other cancers, ALL seems to be originated by multifactorial causes including both genetic and environmental. In the last decade, immune response has been demonstrated to play an essential role in the recognition and killing of cancer cells [9]. T lymphocytes along NK cells are immune cells that seem to dominate the immune response against leukemia [10]. Consequently, the important role of NK cells has been clearly demonstrated in the treatment of high risk leukemia [11]. Additional evidence has arisen from studies conducted in high-risk pediatric ALL patients undergoing hematopoietic stem cell transplantation (HSCT), showing the importance of selecting donors with allogenic NK cells to successfully cure patients [12, 13]. In contrast, an impaired NK cell-mediated cytotoxicity and/or abnormal expression of surface receptors has been observed in patients suffering from leukemia [14–16]. Notwithstanding, the studies have been conducted mostly in patients with chronic or myeloid leukemias [17–19]. A previous study has reported that peripheral blood NK cells from B-ALL patients have a compromised cytotoxicity towards K562 and autologous blasts. In addition, cell surface expression of NKp46 and NKG2A were altered in NK cells from B-ALL patients regarding age-matched healthy controls [20]. In the same study, Rouce and collaborators showed that after leukemia remission, NK cell-mediated cytotoxicity is recovered towards K562 but no towards autologous blast, indicating that blast undergo successful immune editing resulting in the selection of blast that avoid NK cell effector responses [20]. A recent investigation has suggested that a low NK cell production in bone marrow from patients suffering from ALL may contribute in disease progression. Moreover, an increase in the percentages of NK cells expressing class I restricted T-cell associated molecule (CRTAM) may be also associated with suppressor properties favoring malignant progression [21].
NK cells play an essential role in killing unwanted cells such as cancer and virus-infected cells. Unlike T and B lymphocytes, whereas antigen receptors dominate effector functions, NK cells express various germ-line encoding receptors that either activate or inhibit NK cell-mediated lysis of target cells [22]. A delicate balance between the signals emanating from activation and inhibition receptors dictate the outcome [23]. A major group of receptors influencing NK cell effector functions are those belonging to Killer cell immunoglobulin-like receptors (KIR) family. By recognizing MHC-I molecules on target cells, members of this family can either activate or inhibit NK cell function. Interestingly, an important association between a particular KIR genotype and an increased risk of leukemia has been reported [24]. Moreover, this association was more pronounced in Hispanic patients. Besides surface receptors, NK cells express an important number of signaling proteins including adapters and enzymes. Whereas genetic evidence has shown redundancy in signaling proteins governing NK cell-mediated effector functions [25], recent studies have led us to appreciate a unique role for a family of adapter proteins named signaling lymphocytic activation molecule (SLAM)-associated protein (SAP)-related adaptors [26, 27]. The SAP family of adapters are signaling proteins that play an essential role in dictate NK cell responsiveness [28, 29]. This family is composed by three members named SAP, EAT-2 (Ewing’s sarcoma-associated transcript 2) and ERT (EAT-2-related transducer, only in mouse). By mean of their SH2 domains, members of this family are able to interact with the immunoreceptor tyrosine-based switch motif (ITSMs) domains presents in the cytoplasmic region of the SLAM family of receptors [30]. Mouse models have shown that NK cells from mice lacking either SAP o simultaneously SAP, EAT-2 and ERT are unresponsive towards hematopoietic target cells whereas maintain responsiveness towards non-hematopoietic target cells [26]. These studies indicate the important role of SAP family proteins in governing NK cell-mediated cytotoxicity towards hematopoietic cells including malignancies. At present is unknown whether an altered expression of members of the SAP family in NK cells is associated with NK cell dysfunction favoring the emergence of hematological malignancies.
The aim of the present study was to perform a phenotypic, based on SAP expression, and a functional characterization, based on lysis of K562, of NK cells from children with high incidence for ALL at the moment of diagnosis and before treatment initiation.
Material and methods
Patients
The Mexican Inter-Institutional Group for identifying childhood leukemia causes (MIGICCL) conducted a case-control study. 41 cases were patients aged under 17 years diagnosed with ALL between July 1, 2016 and January 31, 2017, and treated in Mexico City public hospitals. Diagnosis of ALL was based on the morphologic and immunophenotypic features of leukemic cells. Peripheral blood samples (2–3 ml) from patients were obtained at the moment of diagnosis and before treatment initiation. 14 healthy controls were selected from the same health institution that referred the children with leukemia. The controls were children without leukemia matched with cases regarding age and sex. Children with the following diagnoses were not invited to participate: neoplasms, hematological diseases, allergies, infections, and congenital malformations. The main diagnoses of the controls were open fractures, hernias, orchidopexy, tonsillectomy, and other benign surgical diseases. Blood samples from the control group were taken at the time the patient was punctured before starting anesthesia and the surgical procedure.
Clinical data collection and risk classification
Information regarding gender; age at diagnosis; white blood cell count (WBC); immunophenotype; dates of ALL diagnosis, treatment initiation, last visit, death, relapse, was collected from the patients’ clinical charts.
Risk classification at the moment of diagnosis was based on the National Cancer Institute [31] risk criteria. Patients between 1 and 10 years old and a leukocyte count <50 x 109/L were classified as NCI standard-risk whereas those aged ≥10 years or a leukocyte count ≥50 x 109/L were classified as NCI high-risk. All patients were treated according to the chemotherapy protocol used in the hospital where they received medical care.
Approval by National Scientific Research and Ethics Committee was obtained with the number R-2016-785-042. Furthermore, written informed consent was obtained from child´s parents and assent from patients ≥8 years of age.
NK cell phenotyping
Peripheral blood mononuclear cells (PBMC) were isolated using Ficoll density separation (GE healthcare, Life Systems). For the evaluation of intracellular expression of SAP in NK cells, the PBMCs were stained with the following panel of fluorochrome-conjugated monoclonal Abs directed against cell surface markers: CD3 FITC (Biolegend, clone OKT3), CD56 APC (Biolegend, clone 5.1H11). Then, cells were fixed and permeabilized using Cytofix/Cytoperm Kit (BD Bioscience) and finally stained using the murine PE conjugated monoclonal antibody directed against human SAP (Thermo Scietific, clone XLP 1D12). An isotype control was used for every staining. Flow cytometric data were acquired on FACSCanto II (BD bioscience) and analyses with the use of FlowJo 7.6.5 software (Tree Star, Ashland, OR). Gates were set to exclude CD3+lymphocytes. Thereafter, NK cells were defined by the expression of CD56. The MFI SAP expression in NK cells was determined by using isotype control. SAP expression was analyzed in 18 B-ALL patients and 14 age-matched healthy controls.
NK cell degranulation assays
NK cell degranulation assays were performed as previously described [32–34]. Briefly, PBMCs (1x106/ml) were incubated with K562 cells (2x106/ml) in a total volume of 200 ul in a 96 well plate. After 4 hours of incubation at 37°C, cells were recovered and stained using following antobodies: anti-CD3 FITC, anti-CD56 APC, and anti-CD107 PE (Biolegend, clone H4A3). GolgiStop was not included in these assays. Cells were acquired on FACSCanto II (BD bioscience) and analyses with the use of FlowJo 7.6.5 software (Tree Star, Ashland, OR). Gates were set to exclude CD3+ lymphocytes. Thereafter, the percentage of cells positive for CD107a was obtained after gating in CD3-CD56+ lymphocytes. The basal percentages for CD107a were obtained from PBMCs incubated alone. Degranulation was represented as ΔCD107a, which is the difference between the percentage of NK cells expressing surface CD107a after K562 stimulation and the percentage of NK cells expressing surface CD107a after incubation with medium alone. NK cell degranulation assays were performed in 41 acute leukemia patients and 14 age-matched healthy controls.
Statistical analysis
Statistical analyses were performed by using SPSS IBM (Statistical Package for the Social Sciences, Inc., Version 21, Chicago, IL, USA). U-Mann Whitney Test was used to compare differences regarding phenotypic and functional features between cases and controls and disease subtypes and clinical subgroups (high vs. standard risk, WBC <50,000 and ≥50,000).
Results
Study population
Samples of 41 patients with ALL were included in the present analysis. The median age of patients was 11 years (range: 2–16 years). Of these, 35 corresponded to B-ALL, and 6 to T-ALL. There was a slight predominance of males (53.6%; n = 22). According to NCI risk classification criteria, 27 patients (65.8%) were high-risk patients. NK cell degranulation analysis was performed in a total of 41 ALL patients, whereas the assays for SAP expression and NK cell degranulation on same sample was possible to be conducted only in 18 patients. All data were compared with age-matched controls.
Abnormal NK cell percentages in pediatric ALL patients
It has been reported that patients suffering from leukemia have abnormal percentages and absolute numbers of NK cells at moment of diagnosis [35, 36]. Therefore, we decide to evaluate the percentages of NK cells in pediatric patients suffering from ALL. In our study, at moment of diagnosis, we found a significant difference in the percentages of NK cells in ALL patients compared to age-matched controls as previously reported (Fig 1A and 1B). Moreover, a significant difference was also observed in pre-B-ALL patients compared to T-ALL patients, where those with T-ALL displayed the lowest percentages (Fig 1C). Interestingly, when ALL patients were stratified according to age as risk factor, the percentages of NK cells in ALL patients between 1 and 9 years of age were significantly lower compared to ALL patients aged 10 years or older (Fig 1D). These data suggest that the percentages of peripheral blood NK cells are lower in ALL patients.
A) Gating strategy to obtain NK cell percentages and representative FACS plots. NK cells from pediatric patients or healthy controls were defined by gating on the CD3-CD56+ lymphocyte fraction of PBMCs. B) The Percentages of NK cells in the lymphocyte gates were analyzed in 41 patients with ALL at moment of diagnosis compared to 14 healthy age-matched controls. C) Percentages of NK cells were analyzed according to immunophenotype in 30 pre-B-ALL patients and 6 T-All patients. D) Percentages of NK cells were analyzed according to age in 30 pre-B-ALL patients compared to 14 age-matched controls. Error bars denote standard error of the mean between individuals within group. P values report significance according to U-Mann Whitney Test one-tail. All data were acquired on FACSCanto II (BD bioscience) and analyses with the use of FlowJo 7.6.5 software (Tree Star, Ashland, OR).
NK cell-mediated cytotoxicity is impaired in patients with ALL
An impaired NK cell effector functions has been associated with a higher incidence of cancer including hematological malignancies [37, 38]. There are few studies assessing the functional competence of NK cells in pediatric patients with ALL. The observation by Rouce and collaborators has provided information on the state of NK cell responsiveness at moment of diagnosis and remission [20]. However, none study has provided information on whether NK cell-mediated cytotoxicity results equally affected taking in consideration important prognostic features and risk factors. Our data showed, as evidenced by degranulation assays using K562 as target cells, that peripheral blood NK cells from ALL patients have an impaired NK cell cytotoxicity compared to age matched-controls (Fig 2A and 2B). The impaired NK cell-mediated lysis of K562 was more significantly affected in those patients suffering from T-ALL compared to B-ALL (Fig 2C). Interestingly, those pediatric ALL patients with ages above 10 years showed a significant lower NK cell degranulation compared to patients with ages between 1- and 9-year-old (Fig 2D). Moreover, in those patients stratified into a high-risk population, the NK cell degranulation was significantly reduced compared to standard-risk population to compared to age-matched controls (Fig 2E). Interestingly, NK cell cytotoxicity was compromised in those B-ALL patients with WBC over 50,000xmm3 compared to B-ALL patients with WBC below 50,000xmm3 (Fig 2F). These data suggest that NK cell cytotoxicity is not equally affected in all pediatric patients suffering with ALL.
A) Representative FACS plots depict NK cell response (CD107a degranulation) against K562 cells. B) NK cell degranulation assays were performed in 41 acute leukemia patients and 14 healthy age-matched controls. C) NK cell degranulation assays were performed in 30 pre-B-ALL, 6 T-ALL patients and 14 age-matched controls. D) NK cell degranulation was analyzed according to age in 30 pre-B-ALL patients and 14 age-matched controls. E) NK cell degranulation was analyzed according to high risk or standard risk in 30 pre-B-ALL patients and 14 age-matched controls. F) NK cell degranulation was analyzed according to WBC in 30 pre-B-ALL patients and 14 age-matched controls. Degranulation was represented as ΔCD107a, which is the difference between the percentage of NK cells expressing surface CD107a after K562 stimulation and the percentage of NK cells expressing surface CD107a after incubation with medium alone. Error bars denote standard error of the mean between individuals within group. P values report significance according to U-Mann Whitney Test one-tail.
SAP expression in NK cells from B-ALL patients is partially reduced
SAP has been reported to be critical in regulating NK cell responsiveness towards hematopoietic cells [26, 29]. Various mouse models indicate that NK cells lacking SAP expression loss the ability to kill hematopoietic cells whereas retain their competence to eliminate non-hematopoietic cells. In humans, SAP deficiency as consequence of deleterious mutations in SH2D1A results in an immunodeficiency characterized by an abnormal susceptibility to EBV infections. As consequence, lymphoproliferative disorders are observed in these patients probably caused by inability of NK cells to properly eliminate transformed cells and/or antigen presenting cells. Despite the importance of SAP in regulating NK cells effector functions, no other human pathology has been associated with SAP abnormal expression or function. As SAP plays a critical role in regulate NK cell responsiveness towards hematopoietic cells, we decided to evaluate whether SAP expression is abnormal in NK cells from patients suffering ALL leukemia at moment of diagnosis. Our data indicate that there is not a significant difference in the frequencies of NK cells expressing SAP between B-ALL patients and age-matched controls (Fig 3A and 3B). Moreover, the frequencies of NK cells expressing SAP remain normal when patients were stratified according to various prognostic features and risk factors (Fig 3C–3E). Although we did observe a significant difference only in patients with standard-risk compared to healthy controls, we did not observe any difference when healthy donors were compared to those ALL patients in high-risk group. These results suggest that the frequencies of NK cells expressing SAP remain unaffected in patients with B-ALL.
A) Representative FACS plots depict frequencies of SAP+ NK cells. B) Frequencies of CD3-CD56+ cells expressing SAP were analyzed in 18 pre-B-ALL patients compared to 14 age-matched controls. C) Frequencies of CD3-CD56+ cells expressing SAP were analyzed according to risk factor in 18 pre-B-ALL patients and 14 age-matched controls. D) Frequencies of CD3-CD56+ cells expressing SAP were analyzed according to age in 18 pre-B-ALL patients and 14 age-matched controls. E) Frequencies of CD3-CD56+ cells expressing SAP were analyzed according to WBC in 18 pre-B-ALL patients and 14 age-matched controls. Error bars denote standard error of the mean between individuals within group. P values report significance according to U-Mann Whitney Test one-tail.
In addition to frequencies of NK cells expressing SAP, we decide to evaluate the mean fluorescence intensity (MFI) of SAP in NK cells. We did not find a significant difference in SAP expression in NK cells from healthy controls and pre-B ALL patients (Fig 4A and 4B) Moreover, when patients were stratified according to other prognostic factors (age or risk factor) none difference was found between patients and age-matched healthy controls (Fig 4C and 4D). In contrast, we found that NK cells from patients with WBC over 50,000xmm3 express less SAP compared to patients with WBC below 50,000xmm3 (Fig 4E).
A) Representative FACS histogram depict MFI of SAP+ NK cells. B) SAP fold MFI for CD3-CD56+ cells was analyzed in 18 pre-B-ALL patients regarding 14 age-matched controls. C) SAP fold MFI for CD3-CD56+ cells was analyzed according to risk factor in 18 pre-B-ALL patients and 14 age-matched controls. D) SAP fold MFI for CD3-CD56+ cells was analyzed according to age of 18 pre-B-ALL patients and 14 age-matched controls. E) SAP fold MFI for CD3-CD56+ cells was analyzed according to WBC in 18 pre-B-ALL patients. Error bars denote standard error of the mean between individuals within group. P values report significance according to U-Mann Whitney Test one-tail.
A positive correlation between SAP expression and a reduced NK cell cytotoxicity is revealed in B-ALL patients with WBC over 50,000xmm3
A reduction or absence of SAP expression results in a significant reduction in the ability of NK cells to kill malignant hematopoietic cells as evidenced in NK cells from patients with XLP1 [29, 39, 40]. Therefore, we determined whether a reduction in the expression of SAP observed in those patients with WBC over 50,000 correlates with an impaired NK cell-mediated cytotoxicity. By using a lineal regression analysis, our data demonstrated a positive correlation between a low expression of SAP and a reduced NK cell cytotoxicity in pediatric patients suffering from B-ALL (Fig 5).
A positive correlation study was applied to 18 pre-B-ALL patients, where was possible to determine both NK cell-mediated cytotoxicity and SAP analysis expression. The R2- and P values are indicated.
Discussion
Acute lymphoblastic leukemia represents the most common and lethal cancer during childhood [41, 42]. Whereas genetic and environmental factors are important factors that predispose the outcome, immune cells are now being recognized as determinants in the development of leukemia and other cancers. Among immune cells, NK cells play an important role in recognizing and killing leukemia cells [22, 38]. In consequence, NK cell-based immunotherapies have proven to be successful in the treatment of high-risk leukemia [38, 43]. However, it is also noticed that not all leukemias, either myeloid or lymphoid, are equally susceptible to these cell-based therapy regimens. Therefore, a phenotypic and functional characterization of NK cells under specific leukemia scenarios become essential in order to understand the particularities related to NK cells and different kinds of leukemia.
In this work, we presented a phenotypical and functional characterization of peripheral blood NK cells from pediatric patients suffering from ALL at moment of diagnosis. As shown by previous studies, we did observe a significant difference in the percentages of peripheral blood NK cells from patients at moment of diagnosis compared to healthy age-matched controls [35, 36]. This was also true when NK cell percentages were analyzed taking into consideration prognostic features such as WBC and whether leukemia was from T or B cell-type. Notably, a significant reduction in percentages of NK cells was also noticed when patients were stratified according to age, whereby those aged between 1 to 9 years display lower percentages of NK cells compared to patients aged 10 years old and above. As far as we know, our study is the first study conducted in patients from Mexico City, which have one of the highest risk factors for developing ALL worldwide.
Similar to results obtained by Rouce and colleagues, NK cell-mediated cytotoxicity towards K562 cells was reduced in peripheral blood NK cells from ALL leukemia patients compared to age-matches controls. This impaired NK cell-mediated cytotoxicity was observed in patients with both B-ALL and T-ALL. Interestingly, when NK cell-mediated lysis towards K562 was analyzed taking into consideration different prognostic features, an impaired NK cell-mediated cytotoxicity was observed only in patients classified as high- but not as low-risk compared to age-matched healthy controls. Interestingly, a lower NK cell-mediated cytotoxicity was also noticed in ALL patients aged over 10 years old and above compared to both healthy controls of same age, and to ALL patients aged between 1–9 years old. In contrast, ALL patients in the 1-9-year cohort did not display a lower NK cell-mediated cytotoxicity compared to age-matched healthy controls. Finally, an impaired NK cell-mediated cytotoxicity was also observed in those B-ALL patients with WBC over 50,000xmm3 compared to B-ALL patients with WBC below 50,000xmm3. These data suggest that an abnormal NK cell effector function is not necessarily equally observed in all pediatric B-ALL patients and that there are other factors that may contribute to determine whether the NK cell-mediated cytotoxicity will result impaired or not. According to our data, the WBC and patients age, resulted to be the major factors that were associated with an abnormal NK cell-mediated cytotoxicity. Interestingly, both WBC over 50,000xmm3 and age, are two reliable prognostic factors used to determine the risk factor and the probability of remission [2, 44]. Based on these findings, our study suggest that an impaired NK cell mediated cytotoxicity can also emerge as a possible prognostic factor for high risk pediatric patients suffering from B-ALL, complementing observations made by Agnieszka et al [45].
Minimal residual disease (MDR) has recently been describe as a reliable factor to determine risk factor and the probability of remission for ALL patients. In our study, we lack any information regarding the status for MRD in our patients, however it will be interesting to evaluate in further studies a possible association between an abnormal NK cell-mediated cytotoxicity and MRD. In addition, in only 17.7% of ALL patients from Mexico City, the four most common gene rearrangements have been detected [14, 46], making difficult to address how NK cell function may be affected by such genetic alterations in patients with ALL. With no doubt, this remain an interesting issue to be addressed in future studies.
The finding that those patients with WBC over 50,000xmm3 displayed a reduced NK cell lysis towards K562 at moment of diagnosis, suggest an important association between a compromised NK cell effector function and high probability of re-incidence of the disease. However, at this point, it is not clear why not all B-ALL patients displayed a significant reduction in the ability of NK cells to kill target cells and further studies will be necessary to address this issue.
SAP family adapters play an essential role in regulate NK cells lysis towards hematopoietic cells. Individuals carrying missense mutations in the gene encoding for SAP, develop a lymphoproliferative syndrome as consequence of an abnormal susceptibility of EBV infections [47, 48] and very often, these individuals develop lymphoma. Besides XLP-1, there are no other evidences where an abnormal SAP expression or function is associated with a human pathology. As far as we know, our study is the first evidence that in those pediatric B-ALL patients with WBC over 50,000xmm3, the NK cells display a partial decrease in SAP expression regarding those patients with WBC below 50,000xmm3. Moreover, by using a lineal regression analysis, our data demonstrated a positive correlation between a low expression of SAP and a reduced NK cell cytotoxicity in pediatric patients suffering from B-ALL. Therefore, our data suggest that a partial decrease in SAP expression may contribute with an impaired NK cell-mediated cytotoxicity observed in B-ALL patients. Our study also provide evidence that an abnormal NK cell phenotype and function are not equally displayed in pediatric patients suffering from B-ALL. These data suggest that there are unidentified factors that might contribute to influence NK cell biology in patients with leukemia. In contrast, NK cell mediated-cytotoxicity and SAP expression become important variables that might be useful to determine the patient outcome.
Conclusions
In the present study it was observed that NK cells from children with ALL harbor an impaired cytotoxicity towards K562 at moment of diagnosis. A more detailed analysis taking into consideration prognostic features and risk factor, revealed that NK cell phenotype and function are not equally affected in all B-ALL patients. Moreover, NK cell-mediated cytotoxicity was compromised in those patients with a leukocyte count ≥50,000xmm3 where also it was found a decreased expression of SAP regarding patients with a leukocyte count < 50,000xmm3. These data suggest a positive correlation between low SAP expression and decreased NK cell-mediated cytotoxicity in pediatric patients suffering from ALL.
References
- 1. Greaves M. A causal mechanism for childhood acute lymphoblastic leukaemia. Nat Rev Cancer. 2018;18(8):471–84. Epub 2018/05/23. pmid:29784935.
- 2. Friedmann AM, Weinstein HJ. The role of prognostic features in the treatment of childhood acute lymphoblastic leukemia. Oncologist. 2000;5(4):321–8. Epub 2000/08/31. pmid:10965000.
- 3. Carroll WL, Bhojwani D, Min DJ, Raetz E, Relling M, Davies S, et al. Pediatric acute lymphoblastic leukemia. Hematology Am Soc Hematol Educ Program. 2003:102–31. Epub 2003/11/25. pmid:14633779.
- 4. Perez-Saldivar ML, Fajardo-Gutierrez A, Bernaldez-Rios R, Martinez-Avalos A, Medina-Sanson A, Espinosa-Hernandez L, et al. Childhood acute leukemias are frequent in Mexico City: descriptive epidemiology. BMC Cancer. 2011;11:355. Epub 2011/08/19. pmid:21846410
- 5. Wilkinson JD, Gonzalez A, Wohler-Torres B, Fleming LE, MacKinnon J, Trapido E, et al. Cancer incidence among Hispanic children in the United States. Rev Panam Salud Publica. 2005;18(1):5–13. Epub 2005/08/18. pmid:16105320.
- 6. Abrahao R, Lichtensztajn DY, Ribeiro RC, Marina NM, Keogh RH, Marcos-Gragera R, et al. Racial/ethnic and socioeconomic disparities in survival among children with acute lymphoblastic leukemia in California, 1988–2011: A population-based observational study. Pediatr Blood Cancer. 2015;62(10):1819–25. Epub 2015/04/22. pmid:25894846.
- 7. Nunez-Enriquez JC, Barcenas-Lopez DA, Hidalgo-Miranda A, Jimenez-Hernandez E, Bekker-Mendez VC, Flores-Lujano J, et al. Gene Expression Profiling of Acute Lymphoblastic Leukemia in Children with Very Early Relapse. Arch Med Res. 2016;47(8):644–55. Epub 2017/05/10. pmid:28476192.
- 8. Inaba H, Greaves M, Mullighan CG. Acute lymphoblastic leukaemia. Lancet. 2013;381(9881):1943–55. Epub 2013/03/26. pmid:23523389
- 9. Palucka AK, Coussens LM. The Basis of Oncoimmunology. Cell. 2016;164(6):1233–47. Epub 2016/03/12. pmid:26967289
- 10. Chiossone L, Dumas PY, Vienne M, Vivier E. Natural killer cells and other innate lymphoid cells in cancer. Nat Rev Immunol. 2018;18(11):671–88. Epub 2018/09/14. pmid:30209347.
- 11. Locatelli F, Pende D, Mingari MC, Bertaina A, Falco M, Moretta A, et al. Cellular and molecular basis of haploidentical hematopoietic stem cell transplantation in the successful treatment of high-risk leukemias: role of alloreactive NK cells. Front Immunol. 2013;4:15. Epub 2013/02/05. pmid:23378843
- 12. Locatelli F, Pende D, Maccario R, Mingari MC, Moretta A, Moretta L. Haploidentical hemopoietic stem cell transplantation for the treatment of high-risk leukemias: how NK cells make the difference. Clin Immunol. 2009;133(2):171–8. Epub 2009/06/02. pmid:19481979.
- 13. Pende D, Marcenaro S, Falco M, Martini S, Bernardo ME, Montagna D, et al. Anti-leukemia activity of alloreactive NK cells in KIR ligand-mismatched haploidentical HSCT for pediatric patients: evaluation of the functional role of activating KIR and redefinition of inhibitory KIR specificity. Blood. 2009;113(13):3119–29. Epub 2008/10/24. pmid:18945967.
- 14. Maki G, Hayes GM, Naji A, Tyler T, Carosella ED, Rouas-Freiss N, et al. NK resistance of tumor cells from multiple myeloma and chronic lymphocytic leukemia patients: implication of HLA-G. Leukemia. 2008;22(5):998–1006. Epub 2008/02/22. pmid:18288133.
- 15. Fauriat C, Just-Landi S, Mallet F, Arnoulet C, Sainty D, Olive D, et al. Deficient expression of NCR in NK cells from acute myeloid leukemia: Evolution during leukemia treatment and impact of leukemia cells in NCRdull phenotype induction. Blood. 2007;109(1):323–30. Epub 2006/08/31. pmid:16940427.
- 16. Sanchez-Correa B, Morgado S, Gayoso I, Bergua JM, Casado JG, Arcos MJ, et al. Human NK cells in acute myeloid leukaemia patients: analysis of NK cell-activating receptors and their ligands. Cancer Immunol Immunother. 2011;60(8):1195–205. Epub 2011/06/07. pmid:21644031.
- 17. Chang MC, Cheng HI, Hsu K, Hsu YN, Kao CW, Chang YF, et al. NKG2A Down-Regulation by Dasatinib Enhances Natural Killer Cytotoxicity and Accelerates Effective Treatment Responses in Patients With Chronic Myeloid Leukemia. Front Immunol. 2018;9:3152. Epub 2019/02/02. pmid:30705677
- 18. Tsirogianni M, Grigoriou E, Kapsimalli V, Dagla K, Stamouli M, Gkirkas K, et al. Natural killer cell cytotoxicity is a predictor of outcome for patients with high risk myelodysplastic syndrome and oligoblastic acute myeloid leukemia treated with azacytidine. Leuk Lymphoma. 2019:1–7. Epub 2019/04/06. pmid:30947589.
- 19. Diermayr S, Himmelreich H, Durovic B, Mathys-Schneeberger A, Siegler U, Langenkamp U, et al. NKG2D ligand expression in AML increases in response to HDAC inhibitor valproic acid and contributes to allorecognition by NK-cell lines with single KIR-HLA class I specificities. Blood. 2008;111(3):1428–36. Epub 2007/11/13. pmid:17993609.
- 20. Rouce RH, Shaim H, Sekine T, Weber G, Ballard B, Ku S, et al. The TGF-beta/SMAD pathway is an important mechanism for NK cell immune evasion in childhood B-acute lymphoblastic leukemia. Leukemia. 2016;30(4):800–11. Epub 2015/12/02. pmid:26621337
- 21. Ramirez-Ramirez D, Padilla-Castaneda S, Galan-Enriquez CS, Vadillo E, Prieto-Chavez JL, Jimenez-Hernandez E, et al. CRTAM(+) NK cells endowed with suppressor properties arise in leukemic bone marrow. J Leukoc Biol. 2019;105(5):999–1013. Epub 2019/02/23. pmid:30791148.
- 22. Moretta L, Pietra G, Montaldo E, Vacca P, Pende D, Falco M, et al. Human NK cells: from surface receptors to the therapy of leukemias and solid tumors. Front Immunol. 2014;5:87. Epub 2014/03/19. pmid:24639677
- 23. Long EO, Kim HS, Liu D, Peterson ME, Rajagopalan S. Controlling natural killer cell responses: integration of signals for activation and inhibition. Annu Rev Immunol. 2013;31:227–58. Epub 2013/03/23. pmid:23516982
- 24. de Smith AJ, Walsh KM, Ladner MB, Zhang S, Xiao C, Cohen F, et al. The role of KIR genes and their cognate HLA class I ligands in childhood acute lymphoblastic leukemia. Blood. 2014;123(16):2497–503. Epub 2014/02/13. pmid:24518758
- 25. Lanier LL. NK cell recognition. Annu Rev Immunol. 2005;23:225–74. Epub 2005/03/18. pmid:15771571.
- 26. Dong Z, Cruz-Munoz ME, Zhong MC, Chen R, Latour S, Veillette A. Essential function for SAP family adaptors in the surveillance of hematopoietic cells by natural killer cells. Nat Immunol. 2009;10(9):973–80. Epub 2009/08/04. pmid:19648922.
- 27. Dong Z, Veillette A. How do SAP family deficiencies compromise immunity? Trends Immunol. 2010;31(8):295–302. Epub 2010/07/24. pmid:20650688.
- 28. Veillette A. NK cell regulation by SLAM family receptors and SAP-related adapters. Immunol Rev. 2006;214:22–34. Epub 2006/11/15. pmid:17100873.
- 29. Wu N, Zhong MC, Roncagalli R, Perez-Quintero LA, Guo H, Zhang Z, et al. A hematopoietic cell-driven mechanism involving SLAMF6 receptor, SAP adaptors and SHP-1 phosphatase regulates NK cell education. Nat Immunol. 2016;17(4):387–96. Epub 2016/02/16. pmid:26878112.
- 30. Latour S, Veillette A. The SAP family of adaptors in immune regulation. Semin Immunol. 2004;16(6):409–19. Epub 2004/11/16. pmid:15541655.
- 31. Francis SS, Wallace AD, Wendt GA, Li L, Liu F, Riley LW, et al. In utero cytomegalovirus infection and development of childhood acute lymphoblastic leukemia. Blood. 2017;129(12):1680–4. Epub 2016/12/17. pmid:27979823
- 32. Marcenaro S, Gallo F, Martini S, Santoro A, Griffiths GM, Arico M, et al. Analysis of natural killer-cell function in familial hemophagocytic lymphohistiocytosis (FHL): defective CD107a surface expression heralds Munc13-4 defect and discriminates between genetic subtypes of the disease. Blood. 2006;108(7):2316–23. Epub 2006/06/17. pmid:16778144.
- 33. Bryceson YT, Fauriat C, Nunes JM, Wood SM, Bjorkstrom NK, Long EO, et al. Functional analysis of human NK cells by flow cytometry. Methods Mol Biol. 2010;612:335–52. Epub 2009/12/25. pmid:20033652
- 34. Bryceson YT, Pende D, Maul-Pavicic A, Gilmour KC, Ufheil H, Vraetz T, et al. A prospective evaluation of degranulation assays in the rapid diagnosis of familial hemophagocytic syndromes. Blood. 2012;119(12):2754–63. Epub 2012/02/02. pmid:22294731.
- 35. Aggarwal N, Swerdlow SH, TenEyck SP, Boyiadzis M, Felgar RE. Natural killer cell (NK) subsets and NK-like T-cell populations in acute myeloid leukemias and myelodysplastic syndromes. Cytometry B Clin Cytom. 2016;90(4):349–57. Epub 2015/12/10. pmid:26648320.
- 36. Parrado A, Casares S, Rodriguez-Fernandez JM. Natural killer cytotoxicity and lymphocyte subpopulations in patients with acute leukemia. Leuk Res. 1994;18(3):191–7. Epub 1994/03/01. pmid:7511191.
- 37. Finn OJ. Immuno-oncology: understanding the function and dysfunction of the immune system in cancer. Ann Oncol. 2012;23 Suppl 8:viii6–9. Epub 2012/08/29. pmid:22918931
- 38. Baier C, Fino A, Sanchez C, Farnault L, Rihet P, Kahn-Perles B, et al. Natural killer cells modulation in hematological malignancies. Front Immunol. 2013;4:459. Epub 2014/01/07. pmid:24391641
- 39. Coffey AJ, Brooksbank RA, Brandau O, Oohashi T, Howell GR, Bye JM, et al. Host response to EBV infection in X-linked lymphoproliferative disease results from mutations in an SH2-domain encoding gene. Nat Genet. 1998;20(2):129–35. Epub 1998/10/15. pmid:9771704.
- 40. Sayos J, Wu C, Morra M, Wang N, Zhang X, Allen D, et al. The X-linked lymphoproliferative-disease gene product SAP regulates signals induced through the co-receptor SLAM. Nature. 1998;395(6701):462–9. Epub 1998/10/17. pmid:9774102.
- 41. Smith MA, Seibel NL, Altekruse SF, Ries LA, Melbert DL, O’Leary M, et al. Outcomes for children and adolescents with cancer: challenges for the twenty-first century. J Clin Oncol. 2010;28(15):2625–34. Epub 2010/04/21. pmid:20404250
- 42. Linabery AM, Ross JA. Trends in childhood cancer incidence in the U.S. (1992–2004). Cancer. 2008;112(2):416–32. Epub 2007/12/13. pmid:18074355.
- 43. Cruz-Munoz ME, Valenzuela-Vazquez L, Sanchez-Herrera J, Santa-Olalla Tapia J. From the "missing self" hypothesis to adaptive NK cells: Insights of NK cell-mediated effector functions in immune surveillance. J Leukoc Biol. 2019;105(5):955–71. Epub 2019/03/09. pmid:30848847.
- 44. Stary J, Zimmermann M, Campbell M, Castillo L, Dibar E, Donska S, et al. Intensive chemotherapy for childhood acute lymphoblastic leukemia: results of the randomized intercontinental trial ALL IC-BFM 2002. J Clin Oncol. 2014;32(3):174–84. Epub 2013/12/18. pmid:24344215.
- 45. Mizia-Malarz A, Sobol-Milejska G. NK Cells as Possible Prognostic Factor in Childhood Acute Lymphoblastic Leukemia. Dis Markers. 2019;2019:3596983. Epub 2019/02/06. pmid:30719179
- 46. Bekker-Mendez VC, Miranda-Peralta E, Nunez-Enriquez JC, Olarte-Carrillo I, Guerra-Castillo FX, Pompa-Mera EN, et al. Prevalence of gene rearrangements in Mexican children with acute lymphoblastic leukemia: a population study-report from the Mexican Interinstitutional Group for the identification of the causes of childhood leukemia. Biomed Res Int. 2014;2014:210560. Epub 2015/02/19. pmid:25692130
- 47. Schuster V, Kreth HW. X-linked lymphoproliferative disease is caused by deficiency of a novel SH2 domain-containing signal transduction adaptor protein. Immunol Rev. 2000;178:21–8. Epub 2001/02/24. pmid:11213803.
- 48. Pachlopnik Schmid J, Canioni D, Moshous D, Touzot F, Mahlaoui N, Hauck F, et al. Clinical similarities and differences of patients with X-linked lymphoproliferative syndrome type 1 (XLP-1/SAP deficiency) versus type 2 (XLP-2/XIAP deficiency). Blood. 2011;117(5):1522–9. Epub 2010/12/02. pmid:21119115.