NK Cell Activation in Human Hantavirus Infection Explained by Virus-Induced IL-15/IL15Rα Expression

Summary

Hantaviruses cause severe clinical infections with up to 50% case-fatality rates. The diseases represent an important global health problem as no vaccine or specific treatment is available. The most prominent hallmark in patients is strong immune activation, reflected as massive CD8 T and NK cell expansion, accompanied by severe vascular leakage. The mechanisms behind this massive immune activation are still not fully understood. Here, we first assessed the expression of several activation markers and receptors on NK cells derived from hantavirus-infected patients using flow cytometry. High NK cell activation was observed during the acute phase of clinical infection. To address possible underlying mechanisms explaining this NK cell activation, we established an in vitro hantavirus infection model using human primary endothelial cells, the natural in vivo targets of the virus. We demonstrate hantavirus-induced IL-15/IL-15Rα on infected endothelial cells, and show that this results in NK cell activation, similar to the profile found in hantavirus-infected patients. Interestingly, these activated NK cells were able to kill uninfected endothelial cells despite their normal expression of HLA class I. The present data add further insights into hantavirus-induced pathogenesis and suggest possible targets for future therapeutical interventions in these severe diseases.

Introduction

Pathogenic hantaviruses are zoonotic, rodent-borne, viruses that belong to the Bunyaviridae family. When infecting humans, they cause hemorrhagic fever with renal syndrome (HFRS) or hantavirus pulmonary syndrome (HPS; also called hantavirus cardio-pulmonary syndrome), two severe acute diseases with case-fatality rates of up to 10% for HFRS and 50% for HPS [1]. HFRS-causing hantaviruses are mainly represented by the prototypic Hantaan virus (HTNV), Puumala virus (PUUV), Dobrava virus, and Seoul virus, whereas HPS-causing viruses include Andes virus, Sin Nombre virus, and related viruses [1].

Hantaviruses can infect several different types of cells, but endothelial and epithelial cells are the primary target cells for hantaviruses in humans [1]. Hantavirus infection of these cells is not cytopathogenic [2]. A common hallmark of HFRS/HPS is, as in other hemorrhagic fevers, increased immune activation and vascular permeability [1]. In the context of immune activation, HFRS and HPS patients have recently been shown to display strong cytotoxic lymphocyte expansions including both NK and CD8 T cells [3]–[6]. Patients also display increased infiltration of immune cells in infected organs, as well as elevated serum levels of, e.g., granzyme B, perforin, and TNF [7]–[10]. However, no overt damage in patients' infected endothelial cells has been observed [11]. Providing some insights into these findings, we recently found hantavirus-infected endothelial cells to be protected from cytotoxic lymphocyte-mediated killing, at least partly, through inhibition of granzyme B and caspase 3 mediated by the hantavirus nucleocapsid protein [12].

NK cells are an important part of the early host defense against virus infections. For instance, humans with specific NK cell-deficiencies often suffer from life threatening virus infections [13]–[15]. The anti-viral response of NK cells includes direct killing of virus-infected cells, mainly mediated through the release of perforin and granzymes, as well as production of pro-inflammatory cytokines including IFN-γ and TNF (reviewed in [13]). These NK cell responses are regulated through a finely tuned balance of signals derived from activating, e.g., NKG2D, and inhibitory NK cell receptors, e.g., killer cell Ig-like receptors (KIRs) and NKG2A/CD94 (reviewed in [16]–[18]). To ensure normal NK cell tolerance to self, and to prevent autoreactivity, most cells in the body express HLA class I ligands for NK cell inhibitory receptors. The expression of KIR and NKG2A inhibitory receptors that recognize self-HLA class I ligands is also needed for NK cells to acquire full functionality, a process referred to as NK cell education, arming, or licensing [19]–[21].

NK cells can be activated by virus-induced cytokines [22]. The principal cytokines involved in NK cell activation are type I interferons (IFN-α/β) as well as IL-12, IL-15, and IL-18 (reviewed in [23]). IL-15 is a pleiotropic cytokine that shares the IL-2 receptor (IL-2R) β and γ chains with IL-2, but has a unique high-affinity IL-15 receptor α chain (IL-15Rα) [24], [25]. IL-15 and IL-15Rα mRNA are abundantly expressed by various immune cell types including monocytes and dendritic cells (DCs), but they can also be expressed in various tissues, e.g., lung, heart, and kidney [24]–[26]. Expression of IL-15 and IL-15Rα is tightly controlled at multiple levels, involving transcription, translation, and intracellular trafficking [27], [28]. Unlike other cytokines, IL-15 is rarely secreted: instead, it is loaded onto IL-15Rα expressed on the same cell and then trans-presented to bystander cells expressing the IL-2Rβ and γ chains [29]. IL-15/IL-15Rα complexes presented to NK cells are essential for NK cell development, differentiation, and survival, and also stimulate NK cell effector functions [30], [31].

The recent observation of a long-term, persistent elevation in NK cell numbers in HFRS patients [3] posed a number of questions that formed the basis for the present study. In particular, (i) how is it associated to states of NK cell activation, (ii) which underlying mechanisms drive the strong NK cell response, and (iii) what potential effects could these NK cells have in hantavirus-infected patients? Here, we first analyzed NK cells in HFRS patients, showing a robust activation of CD56^dim NK cells during acute hantavirus infection. This finding prompted us to search for hantavirus-induced mechanism(s) underlying this NK cell activation. Strikingly, in vitro studies revealed marked hantavirus-induced IL-15 and IL-15Rα expression on the cell surface of infected endothelial and epithelial cells, and a distinct activation of CD56^dim NK cells mediated by trans-presented IL-15. The strength of this NK cell response was such that it led to killing of uninfected endothelial cells despite expression of normal HLA class I levels, while infected cells gained HLA class I expression and resistance to NK cell-mediated apoptosis induction. In summary, these results provide a potential mechanism behind the massive NK cell activation and proliferation observed in clinical HFRS. The consequences of this NK cell activation and proliferation are discussed in the context of human hantavirus immunopathogenesis and implications for future therapeutic strategies.

Results

CD56^dim NK cells are highly activated in HFRS patients

Following our previous observation of elevated NK cell numbers in PUUV-infected HFRS patients [3], we here first sought to characterize the activation status of these NK cells. Peripheral blood mononuclear cells (PBMCs) from 16 Swedish HFRS patients were sampled at the time of hospitalization and during the convalescence phase at day 60. For 8 patients, additional samples were available, consecutively collected for a period of up to 450 days (Figure 1A). CD56^bright and CD56^dim NK cells, the latter constituting the major part of peripheral NK cells [32], were analyzed by flow cytometry for expression of the early activation marker CD69, levels of various activating NK cell receptors, and cytotoxic effector molecules. CD56^dim NK cells were shown to express significantly elevated levels of CD69 during acute HFRS with up to 70% of the total CD56^dim NK cell population expressing CD69. CD56^bright NK cells exhibited some, but clearly lower, levels of activation (Figure 1B, Figure S1A). Percentages of CD69-positive CD56^dim NK cells subsequently declined over time (Figure 1C, Figure S1B). During the acute phase of HFRS, CD56^dim NK cells also expressed significantly higher levels of the activating NK cell receptors NKG2D and 2B4, and the natural cytotoxicity receptors NKp30 and NKp46 (Figure 1D and E), whereas the expression of other activating receptors including DNAM-1, CD161, and CD16 were not changed over time. In accordance with the relatively lower CD69 induction seen in CD56^bright NK cells (Figure 1B, Figure S1A), no marked increase in expression of NK cell activating receptors were observed on these cells (Figure 1D and E). Intracellular levels of the cytotoxic effector molecules granzyme B and perforin were elevated during the acute phase in both, CD56^dim and CD56^bright, NK cell subsets, although expression levels in the CD56^dim subset were clearly higher than in the CD56^bright NK cells (Figure 1F and G). In summary, cytotoxic CD56^dim NK cells were highly activated during the acute phase of clinical HFRS.

Cell-cell contact with hantavirus-infected endothelial cells results in CD56^dim NK cell activation

To approach possible mechanisms behind CD56^dim NK cell activation in hantavirus-infected patients, we exposed resting primary NK cells from healthy individuals to HTNV and assessed if the virus itself could provoke activation of NK cells. No evidence of hantavirus-replication was observed in HTNV-exposed NK cells, and no CD69 expression was induced on NK cells after exposure to the virus (Figure 2A and B). These findings suggest that NK cells do not respond to direct exposure to hantavirus.

Next, we investigated if NK cells were affected by HTNV-infected primary endothelial and renal epithelial cells, both target cells of hantavirus replication during acute infection in humans. Indeed, CD56^dim NK cells co-incubated with HTNV-infected cells acquired an activated phenotype, as reflected by an increase in expression of the activation markers CD69 and CD38 (Figure 2C–F). Activation of CD56^bright NK cell was also observed, but to a lower degree when compared to CD56^dim NK cells (Figure S2 A and B). No CD56^dim NK cell activation was apparent when NK cells and hantavirus-infected cells were separated by transwells (Figure 2D and F), suggesting that CD56^dim NK cell activation mediated by hantavirus-infected cells is largely dependent on direct cell-cell contact. Taken together, these results show that HTNV-infected cells can activate NK cells, in particular the CD56^dim NK cell subset, in a cell-cell contact-dependent manner.

Increased expression of IL-15 and IL-15Rα on hantavirus-infected endothelial and epithelial cells leads to CD56^dim NK cell activation

Following the results presented above, we sought to identify the mechanism underlying the cell-cell contact-dependent hantavirus-mediated CD56^dim NK cell activation. Virus-induced NK cell activation can be mediated by the induction of ligands for various NK cell activating receptors on infected cells. As previously shown for endothelial cells [3], the expression of ligands for the activating NK cell receptors NKG2D and DNAM-1 was not changed by HTNV-infection of renal epithelial cells in vitro (Figure S3). These findings shifted our focus to the possible involvement of other molecules likely being responsible for hantavirus-mediated activation of NK cells.

In this context, attention was drawn towards IL-15. IL-15 is essential for NK cell activation, and its expression can be modulated by virus infection of non-immune cells [33], [34]. Strikingly, HTNV-infection was found to up-regulate the expression of IL-15 and IL-15Rα mRNA in both endothelial and epithelial cells (Figure 3A and B). A two-fold increase in IL-15 and ten-fold increase in IL-15Rα mRNA levels were observed 24 h and 48 h, respectively, after HTNV-infection, and IL-15 and IL-15Rα mRNA levels remained at elevated levels until at least 96 h post infection (Figure 3A and B). Since IL-15 expression is subject to complex post-transcriptional control, we assessed the levels of IL-15 and IL-15Rα proteins in infected compared to uninfected cells. HTNV-infection caused elevated levels of total IL-15 and IL-15Rα protein in endothelial cells (Figure 3C and D) and increased cell surface expression of IL-15 and IL-15Rα on infected endothelial and epithelial cells, respectively (Figure 3E–H).

To test if virus-induced IL-15, trans-presented by IL-15Rα, was responsible for hantavirus-mediated CD56^dim NK cell activation, an anti-IL-15 neutralizing antibody was added to infected endothelial and epithelial cells to block IL-15 trans-presentation to NK cells. NK cells were co-incubated with hantavirus-infected cells, treated with anti-IL-15 antibody or the respective isotype control, and then assessed for activation, mirrored as CD69 up-regulation using flow cytometry. When this was done, fewer NK cells expressed CD69, and CD69 expression-levels (MFI) were lower on the NK cells expressing CD69 (Figure 3I–L). This results strongly suggest trans-presented IL-15 as a key molecule in inducing CD56^dim NK cell activation upon interaction with hantavirus-infected cells.

To address the possibility that CD56^dim NK cells, activated by hantavirus-infected cells trans-presenting IL-15, gained increased functional capacity, we quantified effector responses against NK cell-sensitive K562 cells. CD56^dim NK cells showed significantly increased degranulation, IFN-γ-, and TNF-responses towards K562 cells after pre-stimulation with HTNV-infected cells compared to pre-stimulation with uninfected cells (Figure 4A–C). The elevated levels of CD56^dim NK cells degranulation against K562 cells after pre-stimulation with HTNV-infected cells was also associated with an increased specific lysis of K562 cells (Figure 4D). Together, these results identify increased IL-15 and IL-15Rα surface expression on hantavirus-infected endothelial and epithelial cells as important factors for CD56^dim NK cell activation and effector functions including cytokine production and cytotoxicity.

Hantavirus-infected endothelial cells as targets for CD56^dim NK cells

Since HTNV-infected endothelial and epithelial cells induced CD56^dim NK cell activation and increased their capacity to respond towards K562 target cells, we next sought to assess consequences of interactions between activated NK cells and HTNV-infected endothelial cells. NK cells pre-activated with exogenous IL-15 or IFN-α readily responded to uninfected endothelial cells (Figure 5A). Comparably, responses were weaker towards HTNV-infected endothelial cells (Figure 5A). Similar results were obtained with uninfected and HTNV-infected epithelial cells (Figure S4). As previously reported [3], [35], HTNV-infection of endothelial cells increases their HLA class I expression (Figure 5B). This increase may, at least in part, contribute to weaker effector responses of activated NK cells towards HTNV-infected target cells. Corroborating the latter conclusion, blocking of HLA class I on the infected endothelial cells augmented the functional response of CD56^dim NK cells to a level comparable to the response towards HLA class I-blocked uninfected endothelial cells (Figure 5C and D). These results indicate that NK cells are affected by HTNV-infected cells in two contrasting ways: CD56^dim NK cells pre-stimulated by HTNV-infected cells are activated with increased cytotoxic potential towards NK cell-sensitive target cells, whereas effector responses against the infected endothelial and epithelial cells themselves are reduced compared to responses towards the uninfected endothelial and epithelial cells.

CD56^dim NK cells activated by hantavirus-infected endothelial cells kill uninfected endothelial cells

To finally analyze if NK cell activation mediated by surface-expressed IL-15 on HTNV-infected cells enables them to kill infected or uninfected endothelial cells, we stimulated resting NK cells by incubating them with uninfected and HTNV-infected endothelial cells, respectively. Subsequently, these NK cells were transferred to cultures with uninfected or HTNV-infected cells followed by analysis of NK cell degranulation and NK cell-mediated apoptosis of the target cells (see Figure 6A for experimental outline). CD56^dim NK cells pre-stimulated with HTNV-infected endothelial cells degranulated when subsequently co-incubated with uninfected control cells but not with infected cells (Figure 6B and C). Similar results were obtained using primary epithelial cells (Figure S5). Blocking of IL-15 on the infected cells during the pre-stimulation step diminished the following NK cell degranulation against uninfected cells (Figure 6D), showing that HTNV-activated IL-15 expression on infected cells is important for the ability of NK cells to later respond to uninfected endothelial cells. Interestingly, an increased level of apoptosis (Figure 6E and F) and specific lysis (Figure 6G) followed the exposure of uninfected cells to NK cells pre-stimulated with infected cells, suggesting that hantavirus infection may cause NK cell killing of uninfected endothelial cells. Together, these results show that CD56^dim NK cells, activated by surface-expressed IL-15 and IL-15Rα on hantavirus-infected cells, overcome HLA class I-mediated self-tolerance and can kill uninfected endothelial cells, whereas HTNV-infected cells are protected from lysis.

Discussion

We here show that CD56^dim NK cells from peripheral blood of hantavirus-infected patients are highly activated in the acute phase of HFRS, as manifested by increased expression of specific activation markers, activating NK cell receptors, and cytotoxic effector molecules. Further studies revealed that CD56^dim NK cells, predominantly, can get activated by hantavirus-infected endothelial and epithelial cells, and that these hantavirus-activated NK cells mirrored the NK cell activation profile observed in HFRS patients. IL-15/IL-15Rα cell surface expression on hantavirus-infected endothelial cells was identified as a key factor behind this NK cell activation. Interestingly, infected cells were not killed by NK cells, likely due to increased expression of HLA class I in combination with an inhibition of apoptosis induction in infected cells [12]. The observation that infected cells are not readily killed by NK cells may contribute to the sustained NK cell response observed in clinical HFRS.

In the present study, we observed a relatively stronger activation of CD56^dim than of CD56^bright NK cells in clinical HFRS. This in contrast to, e.g., acute HCV infection, where it has been shown that both NK cell subsets, CD56^dim and CD56^bright, are activated [36]. This suggests that different viruses may activate specific subsets of NK cells differently. CD56^dim NK cells are more prone towards cytotoxicity and respond preferentially to receptor-mediated activation following recognition of target cells, whereas CD56^bright NK cells respond primarily to cytokine stimulation by proliferating and producing pro-inflammatory cytokines [37]. Therefore, one could speculate that target cell-dependent activation dominates the shaping of the NK cell response in clinical HFRS. This presumption is supported by our findings that, in vitro, hantavirus-infected cells are able to activate NK cells, that this activation is contact-dependent, and that it predominantly affects the CD56^dim NK cells (Figure 2 and S2). We identified hantavirus-induced IL-15/IL-15Rα surface expression as one key factor for this NK cell activation (Figure 3). We did not observe infection-dependent changes for known NKG2D and DNAM-1 ligands on infected endothelial and epithelial cells. However, we have previously shown increased expression of the adhesion molecule ICAM-1, a ligand for LFA-1, and HLA-E, a ligand for the activating NKG2C/CD94 NK cell receptor, on HTNV-infected endothelial cells [3]. These ligands might, together with HTNV-induced IL-15, contribute to the activation and proliferation of NK cells observed in HFRS patients.

Corroborating the present findings, levels of IL-15 have been shown to be elevated in sera from patients during acute HFRS infection [3] and in Sin Nombre virus-infected monkeys [38], and an association between IL-15 serum levels and NK cell activation has been reported for other infectious diseases such as acute dengue virus infection [39]. IL-15 can induce increased expression of activating receptors, e.g., NKG2D, NKp30 and NKp46 ([40] and our unpublished observations), suggesting additional cytokine-driven NK cell activation during HFRS. The relatively reduced CD56^bright NK cell activation in HFRS patients despite elevated cytokine serum levels might be explained with the specific recruitment of activated CD56^bright NK cells to tissue, as suggested for acute influenza virus infection [41]. Corroborating this, no increase in peripheral blood CD56^bright NK cell numbers was seen during acute PUUV-infection [3]. Further, IL-15 presented on HTNV-infected endothelial cells might enhance transmigration of NK cells into infected tissue as shown for T cell recruitment into rheumatoid synovial tissue mediated by IL-15 expression on activated endothelial cells [42]. This is supported by findings of elevated numbers of activated T cells and NK cells in endobronchial mucosal biopsies and bronchial lavage fluid from HFRS patients [7].

Hantaviruses cause systemic viremia. We did not detect hantavirus replication in NK cells, and no effect on NK cell activation was observed after exposure of NK cells to hantavirus particles in vitro. Together, this indicates that direct infection of NK cells is not needed for NK cell activation in HFRS. Although initially identified as cells capable of reacting spontaneously against transformed cells, it has become apparent that NK cells, in order to perform their optimal effector functions, also undergo a process of priming [43]. During virus infection this can be achieved via DC-presented IL-15/IL-15Rα, an interaction described as the regulatory synapse [44]. DC-mediated NK cell activation enhances NK cell cytotoxicity and cytokine production although activated mature DCs are protected against these NK cell effector functions through high levels of HLA class I [45], [46]. We here show that hantavirus-infected endothelial cells, expressing IL-15/IL-15Rα, stimulate NK cells in a manner reminiscent of this DC-NK cell interaction. The infected endothelial cells are, similar to mature DCs, protected against NK cell attack via elevated HLA class I expression and, as previously reported, further protected against cytotoxic lymphocyte-mediated killing by inhibition of granzyme B and caspase 3 activity [12]. As endothelial cells are in direct contact with blood-derived NK cells, it is tempting to speculate that the endothelial cells, when infected with hantavirus, induce activation of CD56^dim NK cells, the dominant NK cell subset in blood. The role of DCs and other accessory cells in NK cell activation during HFRS remains to be investigated. For Lassa virus, an Arenavirus that also causes hemorrhagic fever, infected macrophages, but not DCs, are the main NK cell priming cells in vitro [47]. As infection and activation of DCs with hantavirus has been shown in vitro [35], it will be of interest to dissect the NK-DC interaction, and possible consequences of this, following hantavirus infection.

Educated NK cells express HLA class I-specific receptors that inhibit NK cell effector functions assuring tolerance to self [19]–[21]. We here show that stimulation of resting NK cells through contact with HTNV-infected endothelial cells can break this NK cell tolerance to self, thereby allowing NK cells to kill uninfected endothelial cells despite their normal HLA class I expression (Figure 6). A more detailed characterization of the HTNV-activated responding NK cells revealed that all CD56^dim NK cell subsets, irrespective of their expression of inhibitory HLA class I-specific receptors, were able to degranulate against uninfected cells with comparable strength. The detailed mechanism allowing the NK cells to overcome HLA class I-mediated inhibition remains to be elucidated, but in line with the rheostat model, suggesting that NK cells constantly adapt to their MHC class I environment [48], one could speculate that NK cells adjust to the increased HLA class I expression on HTNV-infected cells, thereby setting a new activation threshold. The lower, but normal, expression of HLA class I on the uninfected cells together with the preserved expression of NKG2D and DNAM-1 ligands potentially triggers NK cell attack and killing. NK cell-mediated killing of autologous non-transformed cells has been shown for immature DCs after priming of NK cells with mature DCs [45], [46], [49].

Whereas NK cells often are crucial for viral elimination, inappropriate NK cell responses can be detrimental and part of virus-associated pathological effects [50], [51]. Endothelial cell destruction, possibly leading to increased vascular permeability, might occur in HFRS patients, as elevated levels of caspase-cleaved cytokeratin-18, a marker of endothelial/epithelial apoptotic cell death, and of cell-free DNA and lactate dehydrogenase have been documented in HFRS patients, indicating increased cell death [52], [53]. Involvement of cytotoxic immune cells in this destruction is indicated by the increased serum levels of perforin and granzyme B found in HFRS patients [8], which is in line with our observation of increased granzyme B and perforin levels in NK cells during the acute phase of HFRS (Figure 1). However, the findings presented here, showing that hantavirus-infected cells inhibit NK cell responses through elevated HLA class I expression, together with our previous study demonstrating the inhibition of granzyme B and caspase 3 activity in infected cells via the hantavirus nucleocapsid protein [12], argue against direct NK cell-mediated killing of hantavirus-infected endothelial cells as a mechanism behind the increased vascular leakage in HFRS. This is corroborated through a study showing no overt damage of hantavirus-infected endothelial cells in deceased patients [11]. A possible alternative mechanism contributing to the increased vascular permeability in HFRS patients is suggested by our demonstration that NK cells, after activation through hantavirus-infected endothelial cells, killed uninfected endothelial cells in vitro. NK cell-mediated killing of autologous, bystander CD4 T cells involved in pathologic effects has been suggested during HIV infection [54].

HPS is a severe clinical condition with mortality rates of 30–50% that currently stands with no specific treatment. Previous efforts to treat HPS-patients with antiviral drugs or corticosteroids have not been successful and currently, symptomatic treatment with veno-arterial extracorporeal membrane oxygenation offers the best change for survival when more conventional intensive care therapies have failed [55]. In this regard, it is interesting to note that blocking the effects of IL-15 has been suggested as therapy in other situations where IL-15 is thought to drive the pathology as shown for various autoimmune diseases including rheumatoid arthritis and multiple sclerosis, but also the rare lymphoproliferative T-cell large granular lymphocytic leukemia [56]–[58]. The safety of an humanized anti-IL-2/IL-15Rβ-chain antibody was successfully tested in a phase I clinical trial, supporting the evaluation of this treatment in other IL-15-driven disorders [59]. Thus, it is tempting to speculate that blockade of IL-15 might represent a novel therapeutic target in HPS with the aim to reduce the rapid-onset hyperinflammatory condition these patients present with.

In summary, the present data add further insights into hantavirus-induced pathogenesis by revealing a possible connection between hantavirus-induced IL-15/IL-15Rα expression on infected endothelial cells and the massive NK cell activation observed in HFRS patients. Thus, targeting IL-15 might be useful in the attempt to design specific treatment strategies for this severe disease.

Materials and Methods

Blood samples and cells

Blood samples from healthy donors were collected after written informed consent and with the approval from the Regional Ethical Review Board of the Karolinska Institutet, Stockholm, Sweden. PBMC were isolated by density centrifugation (Ficoll-Hypaque; GE Healthcare) followed by negative NK cell isolation (Miltenyi) yielding >98% pure NK cells. PBMC from HFRS patients were collected in CPT tubes (BD Biosciences) after informed consent and approval by the Regional Ethical Review Board of Umeå University, Umeå, Sweden. Acute hantavirus infection was verified from patient plasma as previously described [60]. K562 cells (ATCC CCL-243) were grown in complete RPMI 1640 medium (10% FBS, L-glutamine, penicillin, and streptomycin). Primary human endothelial cells (HUVEC) and renal epithelial cells (Lonza) were grown according to the manufacturer's instructions using EGM-2 BulletKit and REGM BulletKit, respectively.

HTNV-infection of endothelial/epithelial cells

Prior to infection, cells were seeded in cell culture plates and grown without supplementing the medium with hydrocortisone, until 90% confluency. Propagation and titration of HTNV strain 76–118 was performed on Vero E6 cells as previously described [61]. Cells were infected with MOI 1, resulting in infection rates between 60–80% 72 hours post infection [3].

Flow cytometry and antibodies

The following monoclonal Abs were used, clone names and conjugates are given within parentheses: pan HLA class I-A647 (W6/32, A647) (Serotech). HLA-E (3D12, PE), IL-15Rα (eBioJM7A4, PE), and CD155 (2H7CD155, PE), (all eBioscience). IL-15 (34559, PE), MICA (159227, APC), MICB (236511, APC), ULBP1 (170818, unconjugated), ULBP2 (165903, unconjugated), ULBP3 (166510, unconjugated), ULBP4 (unconjugated) (all R&D). CD107a (H4A3, PE and FITC), IFN-γ (25723.11, FITC), granzyme B (GB11, AF647), perforin (δG9, FITC), CD14 (MφP9, APC-Cy7 and V500), CD19 (HIB19, APC-Cy7 and V500), CD16 (3G8, Pacific Blue), CD56 (B159, PE-Cy7), CD69 (FN50, APC and APC-Cy7), DNAM-1 (Dx11, FITC), NKG2D (1D11, PE), and CD112 (R2.525, PE) (all BD Biosciences). TNF-α (MAb11, Pacific blue), CD107a (H4A3, Brilliant Violet 421), CD56 (HCD56, Brilliant Violet 711), and CD38 (HIT2, AF700), (all BioLegend). NKG2A (Z199, APC), CD56 (NHK-1, ECD), CD69 (TP1.55.3, ECD), CD3 (UCHT1, PE-Cy5), 2B4 (C1.7, PE), NKp30 (Z25, PE and APC), and NKp46 (BAB281, PE), (all Beckman Coulter). CD3 (UCHT1, Cascade Yellow), (DakoCytomation). Unconjugated antibodies were detected using an anti-IgG secondary antibody (X56, APC, BD Biosciences). Live/Dead Aqua (Invitrogen) was used to exclude dead cells. Briefly, cells were stained for 20 min at 4°C in FACS buffer (PBS 2% FBS, 2mM EDTA) and fixed in 1% PFA. For intracellular staining, cells were stained for surface markers and then fixed and permeabilized using the Cytofix/Cytoperm kit (BD Biosciences). Samples were acquired on a CyAn ADP instrument (Beckman Coulter) or a LSRFortessa (BD Biosciences) and analyzed using FlowJo software version 9.7.6 (Tree Star Inc).

Functional NK cell assays

Prior to use in functional assays, isolated primary NK cells were pre-stimulated with IL-15 (20 ng/ml, R&D) or IFN-α (500 U/ml) overnight, or co-incubated with uninfected or HTNV-infected endothelial and epithelial cells at an effector/target ratio of 1∶1 at 37°C in complete RPMI medium. In some experiments IL-15 surface-expression on HTNV-infected endothelial cells was blocked using a neutralizing IL-15 mAb (R&D, clone 34593). For determination of NK cell effector functions, NK cells were incubated with respective target cells at an effector/target ratio of 1∶1 for 6 hours in the presence of anti-CD107a (H4A3, FITC, BD Biosciences). Brefeldin A and monensin (BD Biosciences) were added for the last 5 hours of the assay. If indicated, HLA class I was blocked on the endothelial cells using a combination of A6–136 hybridoma (kindly provided by Dr D Pende, Istituto Nazionale per la Ricerca sul Cancro, Genoa, Italy) and Dx17 mAbs (BD Biosciences) for 30 minutes at room temperature. Cytotoxicity assays were performed by labelling K562 and endothelial cells with CFSE (Invitrogen) and co-culturing these cells with NK cells, pre-stimulated as described above, at the indicated effector/target ratios for 4 hours. Cells were subsequently stained with Live/Dead Fixable Dead cell stain (Invitrogen). Cytotoxicity was calculated as followed: (% dead target cells in co-culture with NK cells−% dead target cells alone)/(100%−% dead target cells alone).

TUNEL assay

Apoptosis was assessed 5 h after transfer of NK cells to endothelial cells grown on glass slides with TUNEL staining. TUNEL assay (Roche) was performed as previously described [62]. After TUNEL reaction, cells were subjected to staining with anti-nucleocapsid protein mAb, followed by FITC-conjugated goat anti-mouse IgG (Sigma-Aldrich). Nuclei were counter stained with DAPI (Sigma-Aldrich).

Quantitative RT-PCR

Total RNA was isolated using TriPure Isolation Reagent (Roche Applied Science) and treated with Turbo DNA-free (Ambion) to remove any contaminating DNA. cDNA synthesis was performed using Superscript™ III Reverse Transcriptase, random primers, and RNAseOUT™ Recombinant Ribonuclease Inhibitor (Life Technologies). Total RNA was measured with TaqMan Gene Expression Assay for human IL-15, IL-15Rα and β-actin (all Life Technologies). The quantitative real-time PCR was performed using ABI7900 HT Fast sequence detection system (Life Technologies). Data were analysed with SDS software version 2.3. Data were normalized to β-actin and presented as the change in induction relative to that of uninfected cells.

Statistical methods

For comparison of matched groups the paired t-test (normally distributed data) was performed using GraphPad Prism software version 5.0 (GraphPad Software Inc.). Asterisks denote statistical significance (_* p<0.05, _** p<0.01, _*** p<0.001).

Ethics statement

Blood samples from healthy donors were collected after written informed consent and with the approval from the Regional Ethical Review Board of the Karolinska Institutet, Stockholm, Sweden.

Supporting Information

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