Research Article

Cross-Talk with Myeloid Accessory Cells Regulates Human Natural Killer Cell Interferon-γ Responses to Malaria

  • Kirsty C Newman equal contributor,

    equal contributor Contributed equally to this work with: Kirsty C Newman, Daniel S Korbel

    Affiliation: Department of Infectious and Tropical Diseases, London School of Hygiene and Tropical Medicine, London, United Kingdom

  • Daniel S Korbel equal contributor,

    equal contributor Contributed equally to this work with: Kirsty C Newman, Daniel S Korbel

    Affiliation: Department of Infectious and Tropical Diseases, London School of Hygiene and Tropical Medicine, London, United Kingdom

  • Julius C Hafalla,

    Affiliation: Department of Infectious and Tropical Diseases, London School of Hygiene and Tropical Medicine, London, United Kingdom

  • Eleanor M Riley mail

    To whom correspondence should be addressed. E-mail:

    Affiliation: Department of Infectious and Tropical Diseases, London School of Hygiene and Tropical Medicine, London, United Kingdom

  • Published: December 08, 2006
  • DOI: 10.1371/journal.ppat.0020118


Data from a variety of experimental models suggest that natural killer (NK) cells require signals from accessory cells in order to respond optimally to pathogens, but the precise identity of the cells able to provide such signals depends upon the nature of the infectious organism. Here we show that the ability of human NK cells to produce interferon-γ in response to stimulation by Plasmodium falciparum–infected red blood cells (iRBCs) is strictly dependent upon multiple, contact-dependent and cytokine-mediated signals derived from both monocytes and myeloid dendritic cells (mDCs). Contrary to some previous reports, we find that both monocytes and mDCs express an activated phenotype following short-term incubation with iRBCs and secrete pro-inflammatory cytokines. The magnitude of the NK cell response (and of the KIR CD56bright NK cell population in particular) is tightly correlated with resting levels of accessory cell maturation, indicating that heterogeneity of the NK response to malaria is a reflection of deep-rooted heterogeneity in the human innate immune system. Moreover, we show that NK cells are required to maintain the maturation status of resting mDCs and monocytes, providing additional evidence for reciprocal regulation of NK cells and accessory cells. However, NK cell–derived signals are not required for activation of accessory cells by either iRBCs or bacterial lipolysaccharide. Together, these data suggest that there may be differences in the sequence of events required for activation of NK cells by non-viral pathogens compared to the classical model of NK activation by virus-infected or major histocompatibility complex–deficient cells. These findings have far-reaching implications for the study of immunity to infection in human populations.


The outcome of infection is determined both by the ability to limit the initial phase of pathogen colonisation and by the ability to mount an effective adaptive immune response. Both of these processes are influenced by innate immune responses, of which a crucial component can be the ability of natural killer (NK) cells to secrete pro-inflammatory cytokines. Studies in both humans and mice indicate that the magnitude of the early (innate) interferon (IFN)–γ response is a crucial determinant of the outcome of malaria infection. In this study, Newman et al. show that activation of human NK cells by Plasmodium falciparum–infected red blood cells to produce IFN-γ is strictly dependent upon, and regulated by, contact-mediated and soluble (cytokine) signals from two accessory cell populations (myeloid dendritic cells and monocytes). Furthermore, the magnitude of the human NK cell IFN-γ response to P. falciparum–infected red blood cells is highly correlated with levels of expression of co-stimulatory molecules on resting accessory cells. These findings suggest that it might be possible to predict the magnitude of the innate cytokine response, and possibly even susceptibility to malarial disease, from the phenotype of resting monocytes. In addition, these data contribute to the development of a new model of NK activation by non-viral pathogens in which activation of accessory cells precedes, rather than follows, NK activation.


After years of neglect, in which the adaptive immune response to malaria was investigated in great depth with a view to rational development of antimalarial vaccines, the innate immune response to malaria has recently come under scrutiny. In part, this is driven by the realisation that innate immune responses initiate and mould the subsequent adaptive response and that understanding the innate immune response may aid the design of novel adjuvants and novel vaccine delivery systems. Furthermore, data from experiments in rodents and from clinical studies indicate that innate immune responses play a crucial role in controlling malaria infections [1] and can significantly alter the outcome of infection, especially in non-immune individuals. The key element in the cell-mediated effector response to malaria is the rapid induction of interferon (IFN)–γ [26]. We have shown that human natural killer (NK) cells can be an important early source of IFN-γ after exposure of leukocytes to Plasmodium falciparum–infected red blood cells (iRBCs) [79], although this response is extremely heterogeneous [8,9].

Emerging data suggest that signals from accessory cells such as macrophages, monocytes, and dendritic cells (DCs) are absolutely required for optimal NK cell responses to many infectious agents [1012]. Consistent with this, we have previously demonstrated that cloned NK cells are unable to respond to iRBCs in the absence of autologous peripheral blood mononuclear cells (PBMCs) [8]. However, an essential role for accessory cells in promoting robust pro-inflammatory responses to malaria is somewhat controversial given previous observations suggesting that accessory cell function is seriously impaired by exposure to malarial parasite ligands. For example, following exposure to iRBCs, both human DCs and monocytes secrete the immunosuppressive cytokine interleukin-10 (IL-10) [13,14], have an impaired ability to mature in response to lipopolysaccharides (LPS) and other ligands [13,1517], and are unable to present antigen to T cells [13]. Moreover, DCs from children with acute malaria infection have reduced human leukocyte antigen (HLA)–DR expression [18].

Here we have assessed the precise contribution of various subsets of accessory cells to NK cell activation by iRBCs. We demonstrate that cells of the myeloid lineage are not only activated by iRBCs, but also play a crucial role in controlling the magnitude of the early burst of NK cell–derived IFN-γ via both cytokine- and contact-dependent signals. Furthermore, we provide evidence that reciprocal interactions between NK cells and myeloid accessory cells regulate levels of activation of both cell populations, with major implications for the ability of the innate immune system to recognise and respond to infection.

Materials and Methods

Blood Donors

Adult blood donors were recruited at the London School of Hygiene and Tropical Medicine through an anonymous blood donation system. All donors were malaria naïve and healthy and gave fully informed consent for their blood to be used in this study. Ethical approval was given by the London School of Hygiene and Tropical Medicine Ethics Committee, application number 805. As we have previously shown that NK cells from only some donors make a strong IFN-γ response to iRBCs [79], cells from known high-responding donors were used for the majority of experiments described here.

P. falciparum Culture and Antigen Preparation

P. falciparum parasites (strain 3D7) were grown in ORh− human erythrocytes (National Blood Service, in RPMI 1640 (Gibco,​geid=11040) supplemented with 25 mM HEPES (Sigma-Aldrich,, 28 mM sodium bicarbonate (BDH,, 20 μg/l hypoxanthine (Sigma-Aldrich), and 10% normal human AB serum (National Blood Service). Cultures were gassed with 3% O2, 4% CO2, and 93% N2 and incubated at 37 °C. The culture medium was changed daily and the parasitaemia was determined by examination of Giemsa-stained thin blood smears. Parasite cultures were routinely shown by PCR (Stratagene, to be free from Mycoplasma contamination. Mature schizonts were harvested from cultures of 5%–8% parasitaemia by centrifugation through a 60% Percoll gradient (Sigma-Aldrich).

PBMC Preparation and Culture

Venous blood was collected into sodium heparin (10 IU/ml blood; CP Pharmaceuticals, and PBMCs were isolated by Histopaque 1077 (Sigma-Aldrich) density gradient centrifugation as described previously [9]. Cells were resuspended at a concentration of 106 cells/ml and cultured in flat-bottomed 24-well plates for 24 h. Schizont-infected (iRBCs) or uninfected red blood cells (uRBCs) were added at a ratio of three red blood cells per mononuclear cell.

Cell Surface and Intracellular Staining for Flow Cytometry

Surface and intracellular staining was performed as described previously [9]. The antibodies used were anti-CD3 PerCP, IgG1 PerCP, and anti-HLA-DR PerCP (all from BD Biosciences,; anti-CD11c AlexaFluor-647, IgG1 AlexaFluor-647, anti-CD56 AlexaFluor-647, IgG2a AlexaFluor-647, anti-IFN-γ FITC, anti-CD14 FITC, IgG1 FITC, anti-CD40 R-PE, anti-CD69 R-PE, IgG2a R-PE, anti-CD80 R-PE-Cy5, and IgG1 R-PE-Cy5 (all from Serotec, Flow cytometric analyses were performed using a Becton Dickinson FACSCalibur flow cytometer (BD Biosciences) and FlowJo analysis software (TreeStar,

NK Cell Purification

CD56+ CD3 NK cells were enriched from PBMCs by magnetic cell separation (NK Cell Enrichment kit; StemCell Technologies, according to the manufacturer's instructions and using LS separation columns (Miltenyi Biotec, B cells, T cells, monocytes, and erythrocytes were retained in the column, and the effluent containing unlabelled NK cells was collected. NK cells were counted, tested for viability by trypan blue exclusion, and routinely checked by flow cytometry for a purity of greater than 95%.

Depletion of Accessory Cells or NK Cells

PBMCs were depleted of different populations using monoclonal mouse antibodies to human HLA-DR (Scottish Antibody Production Unit, United Kingdom), CD14 (Serotec), or BDCA-4 (Miltenyi Biotec), and goat anti-mouse IgG MicroBeads (Miltenyi Biotec); CD19 MicroBeads (Miltenyi Biotec); biotinylated CD1c (BDCA-1) antibody and anti-biotin MicroBeads (Miltenyi Biotec); or CD56 positive selection kit (StemCell Technologies).

Transwell Cultures

PBMCs (1 × 106) in a volume of 800 μl of complete medium were placed in a tissue culture well. Purified NK cells (1 × 105) in a volume of 200 μl were placed in a Transwell with a 0.4-μm microporous polycarbonate membrane (Corning, and lowered into the culture well so that all cells were submerged in culture medium. iRBCs (3 × 106, bottom well, or 0.5 × 106, top well) were added as indicated. Plates were cultured for 24 h, and NK cells from the top well and/or PBMCs from the bottom well were harvested, stained, and analysed by flow cytometry as previously described.

Recombinant Cytokines and LPS

In all experiments a combination of human recombinant IL-12 (Peprotech, and human recombinant IL-18 (MBL International,, each at 0.1 μg/106 cells, was used as a positive control. Bioactive human recombinant transforming growth factor (TGF)–β (R&D Systems, was used at the concentrations indicated. LPS purified from Escherichia coli (Sigma-Aldrich) were used at a concentration of 1 μg/106 cells.

Cytokine Blocking

The following neutralising antibodies were used to block cytokines or their respective receptors: polyclonal rabbit anti-human IL-2 (Serotec), polyclonal rabbit anti-human IL-15 (Biosource,, monoclonal mouse anti-human IFN-α/β receptor chain 2 (Chemicon,, and polyclonal chicken anti-TGF-β (R&D Systems). The antibodies or their respective isotype-matched controls were added to PBMC cultures prior to the addition of iRBCs and at the concentrations indicated.

Quantification of Cytokine mRNA by Real-Time Quantitative PCR

For each donor, 107 PBMCs were cultured for 24 h in the presence or absence of 3 × 107 iRBCs. Non-adherent cells were discarded and adherent cells harvested after 15 min incubation on ice followed by scraping. Total RNA was isolated (RNeasy Micro kit; Qiagen, and cDNA was produced using oligo(dT)12–18mer primers and SuperScript III reverse transcriptase (Invitrogen, according to the manufacturer's instructions.



The concentration of total (bioactive and latent) and spontaneously bioactive TGF-β in culture supernatants was assessed using the Human TGF-β 1 DuoSet system (R&D Systems) according to the manufacturer's instructions.

Luminex Bead-Based Cytokine Quantification

Multiplex quantification of cytokine concentrations in tissue culture supernatants was performed using the Luminex 100 system (Luminex, with Bio-Plex upgrade (Bio-Rad Laboratories, Levels of IL-2, IL-10, and IL-12p70 were determined using the Beadlyte Human Multi-Cytokine Detection System 3 (Upstate, according to the manufacturer's instructions. Data analysis was performed using the Bio-Plex Manager software (Bio-Rad).

Statistical Analysis

All statistical analyses were performed using Prism 4 software (GraphPad Software, All r2 values given refer to a second-order polynomial fit of data shown. If data are plotted using log scale, analysis was carried out using log values. All t tests carried out were two-tailed paired t tests with 95% confidence intervals. Comparisons were made between actual data even where log axes have been used to plot data.


Optimal NK Cell Response to iRBCs Is Accessory Cell–Dependent

We have previously shown that cloned NK cell lines are unable to respond to iRBCs in the absence of accessory cells that are present among PBMCs [8]. To confirm and extend this observation, NK cells were purified from PBMCs of seven different donors by magnetic cell sorting (MACS) and stimulated for 24 h with IL-12 and IL-18, uRBCs, or iRBCs or left unstimulated and analysed for surface expression of CD3, CD56, CD69, and intracellular IFN-γ; unsorted PBMCs from the same donors were stimulated and analysed in an equivalent fashion (Figure 1). In PBMC cultures, as expected, IFN-γ+ (CD3 CD56+) NK cells were detected in both cytokine-stimulated and iRBC-stimulated cultures but not in unstimulated or uRBC-stimulated cultures (Figure 1A). We deliberately selected donors who were known, from previous studies, to be relatively high responders in this assay; nevertheless, the magnitude of the IFN-γ response to iRBCs varied between donors, with between 5% and 50% of NK cells making IFN-γ in response to iRBCs after 24 h (Figure 1C). In complete contrast, although purified NK cells made IFN-γ in response to cytokine stimulation (Figure 1B), no IFN-γ was produced by purified NK cells in response to iRBCs (Figure 1B and 1C).


Figure 1. NK Cells Do Not Respond to iRBCs in the Absence of Accessory Cells

PBMCs or MACS-purified NK cells from malaria-naïve donors were cultured alone or with IL-12 and IL-18, uRBCs, or live iRBCs for 24 h. Intracellular IFN-γ and surface expression of CD69 on CD3 CD56+ NK cells were analysed by flow cytometry.

(A and B) Representative example of NK responses to uRBCs, IL-12 and IL-18, and iRBCs in PBMCs (A) and purified NK cells (B). FACS plots are gated on CD3 CD56+ lymphocytes. Percentages indicate the proportion of CD3 CD56+ NK cells in each gate; data are based on the collection of 100,000 total events.

(C and D) Comparison of NK responses to iRBCs in PBMCs and in purified NK cells. (C) NK cell IFN-γ production for six donors. (D) CD69 surface expression levels for seven donors. **, p < 0.01; ***, p < 0.001; p-values are for paired t tests comparing stimulated and unstimulated NK cells from the same donor, or PBMCs and pure NK cells from the same donor.

(E) MACS-purified, CTG-labelled NK cells were added to autologous PBMCs. IFN-γ production in CTG+ (MACS-purified) and CTG (“untouched”) NK cells was assessed by flow cytometry after 24 h of stimulation with iRBCs. A representative example of the software gating strategy to analyse IFN-γ responses of CTG-labelled NK cells is shown. FACS plots were gated on CD3 CD56+ NK cells within the lymphocyte population (first panel), and NK cells were analysed for CTG staining (second panel). CTG+ CD3 CD56+ NK cells (third panel) or CTG CD3 CD56+ NK cells (fourth panel) were selected and analysed for intracellular IFN-γ production. Numbers indicate the proportion of IFN-γ+ NK cells.


We have shown that up-regulation of surface CD69 expression is a marker of partial (early) activation of NK cells [9], and thus, as expected, up-regulation of CD69 was consistently seen on NK cells within the iRBC-stimulated PBMC population (Figure 1D). Surface CD69 expression tended to be higher on unstimulated purified NK cells than on unstimulated NK cells within PBMCs, presumably because of partial activation during cell separation. However, CD69 surface expression was not significantly up-regulated on purified NK cells after stimulation with iRBCs, and NK CD69 expression was significantly higher among iRBC-stimulated PBMC NK cells than among purified NK cells (Figure 1D).

Importantly, the inability of purified NK cells to respond to iRBCs is not an artefact of the NK cell purification process as MACS-purified NK cells labelled with CellTracker Green (CTG) and added back to autologous PBMC cultures respond as well to iRBC stimulation as do “untouched” NK cells within PBMCs (Figure 1E).

Thus, these data indicate that accessory cells within PBMCs are required for both IFN-γ and CD69 expression among iRBC-stimulated NK cells.

Depletion of CD1c+ and CD14+ Accessory Cells Inhibits the NK Cell Response

To identify the accessory cell population(s) required for NK cell activation by iRBCs, PBMCs of known high-responding donors were depleted (by MACS) of cells expressing specific cell surface markers prior to incubation with iRBCs (Figure 2). PBMCs of all the donors tested in these experiments responded to iRBC stimulation, with 5%–40% of all NK cells producing IFN-γ after 24 h. Depletion of accessory cell populations did not affect the ability of NK cells to produce IFN-γ following stimulation with positive control stimuli (IL-12 and IL-18; Figure S1). Depletion of HLA-DR+ cells completely abolished the NK cell IFN-γ response to iRBCs in all donors, but depletion of BDCA-4+ plasmacytoid DCs (pDCs) had no consistent effect on the NK IFN-γ response. Likewise, depletion of CD19+ B cells did not reduce the NK cell IFN-γ response. However, depleting PBMCs of either CD1c+ myeloid DCs (mDCs) or CD14+ monocytes significantly reduced NK cell IFN-γ responses (monocytes, paired t test, t = 3.63, p = 0.036; mDCs, paired t test, t = 3.82, p = 0.032). In the one donor where depletion using either CD14 or CD1c did not substantially reduce the IFN-γ response (relative response, monocyte-depleted = 0.84, mDC-depleted = 0.90), a double depletion using both antibodies together was performed. In this case the IFN-γ response was substantially reduced (relative response = 0.32).


Figure 2. HLA-DR+ Accessory Cells Provide Activating Signals to NK Cells

PBMCs from malaria-naïve donors were depleted of different populations of accessory cells, and NK cell responses to iRBCs were analysed after 24 h of co-culture.

(A) Representative example of NK cell IFN-γ responses in undepleted PBMCs (top left), PBMCs depleted of all HLA-DR+ antigen-presenting cells (APC) (top right), CD14+ monocyte–depleted PBMCs (middle left), CD19+ B cell–depleted PBMCs (middle right), CD1c+ mDC–depleted PBMCs (bottom left), and BDCA-4+ pDC–depleted PBMCs (bottom right). FACS plots are gated on CD3 CD56+ lymphocytes. Percentages indicate the proportion of CD3 CD56+ NK cells that were positive for IFN-γ; data are based on the collection of 100,000 total events.

(B) NK cell IFN-γ production after depletion of different antigen-presenting cell populations. Percentage of IFN-γ NK cells relative to the response in undepleted PBMCs is shown; each spot represents data for a different donor. *, p < 0.05; ***, p < 0.0001; p–values are for paired t tests of the difference between depleted and undepleted cells:


These data indicate that the NK cell response to iRBCs is not dependent on a single population of accessory cells; rather, both mDCs and monocytes can provide activating signals for NK cells, and, in most donors, optimal NK activation requires both of these cell types to be present.

Monocytes and mDCs Are Activated by iRBCs

Given the numerous published reports indicating that monocyte and DC function is inhibited by exposure to iRBCs [13,14], it was important to determine whether the accessory cells required for NK cell activation were themselves activated by exposure to iRBCs. PBMCs from ten different donors were therefore stimulated with uRBCs, iRBCs, or E. coli LPS (or left unstimulated, growth medium alone [gm]) for 24 h, and then mDC and monocyte populations were analysed for expression of the activation markers CD40, HLA-DR, and CD80 (Figure 3; isotype control data to exclude non-specific binding of labelled antibodies by activated accessory cells are shown in Figure S2).


Figure 3. Accessory Cells Are Activated by iRBCs

PBMCs from ten malaria-naïve donors were cultured with live iRBCs or E. coli LPS for 24 h or left unstimulated. Surface expression of HLA-DR, CD40, and CD80 on accessory cells was analysed by flow cytometry.

Accessory cells were defined as HLA-DR+ CD11c+ cells (A, left), and CD14+ monocytes and CD14 mDCs were selected for further analysis (A, right). Representative examples of surface expression levels of CD40, HLA-DR, and CD80 on HLA-DR+ CD11c+ CD14+ monocytes (B) and HLA-DR+ CD11c+ CD14 mDCs (C) are shown. Data are based on the collection of 100,000 total events. Results for all ten donors are summarised in (D). *, p < 0.05; **, p < 0.01; ***, p < 0.001; p-values are for paired t tests comparing stimulated and unstimulated cells from the same donor.


Significant up-regulation of CD40, CD80, and HLA-DR was observed on monocytes from all donors following 24 h incubation with iRBCs (CD40, mean fold increase of median fluorescence intensity [MFI] = 6.3, paired t test, t = 3.59, p = 0.006; HLA-DR, mean fold increase of MFI = 1.7, paired t test, t = 3.42, p = 0.008; CD80, mean fold increase of MFI = 3.0, paired t test, t = 7.56, p < 0.0001). Activation of mDCs was also observed, with significant up-regulation of CD40 and HLA-DR expression (CD40, mean fold increase of MFI = 2.3, paired t test, t = 3.60, p = 0.006; HLA-DR, mean fold increase of MFI = 2.4, paired t test, t = 3.16, p = 0.012). There was, however, no significant change in expression of CD80 on mDCs after 24 h co-incubation with iRBCs (mean fold increase of MFI = 1.3, paired t test, t = 2.04, p = 0.072).

These data indicate that both mDCs and monocytes are activated after 24 h co-incubation with iRBCs but that the nature of activation differs between the two accessory cell populations. Up-regulation of CD40 is more pronounced in monocytes and up-regulation of HLA-DR is more pronounced in mDCs, whilst up-regulation of CD80 occurs exclusively in monocytes.

Accessory Cells Express Both Pro- and Anti-Inflammatory Cytokines in Response to Activation by iRBCs

To characterise further the activation of accessory cells by iRBCs, we analysed the cytokine response profile after culturing PBMCs for 24 h with iRBCs by quantitative real-time PCR analysis of adherent cells and by Luminex cytokine bead array analysis of culture supernatants (Figure 4).


Figure 4. Accessory Cell–Derived Cytokines Are Upregulated in Response to iRBCs

(A and B) PBMCs from four donors were stimulated with iRBCs for 24 h, and the amount of IFN-α, IL-2, IL-12, IL-15, IL-18, IL-23, IFN-γ, and IL-10 mRNA in adherent cells was determined by real-time quantitative PCR. The resting levels relative to the amount of β-actin mRNA are shown in (A). The fold up-regulation in response to iRBC stimulation is shown in (B).

(C) Cytokine levels in tissue culture supernatants were determined for eight donors in a bead-based cytokine quantification assay. Levels of IL-2 (left), IL-10 (middle), and IL-12 (right) for no stimulation (gm), uRBC stimulation, and iRBC stimulation are shown (arithmetic mean plus standard error of the mean).


Unstimulated adherent cells expressed detectable levels of mRNA for IL-15, IL-18, and, at somewhat lower levels, IL-10, IL-12, and IL-23, indicating either constitutive expression of these cytokines or their induction during the cell separation process. Levels of IFN-α, IL-2, and IFN-γ mRNA were below the limits of detection of the assay (Figure 4A). However, after iRBC stimulation there was very marked up-regulation of mRNA for IFN-α and IL-2 and, to a somewhat lesser extent, for IL-10 and IFN-γ but not for IL-12, IL-15, IL-18, or IL-23 (Figure 4B). Taken together, these data indicate constitutive or induced expression of IL-12, IL-15, IL-18, IL-23, IFN-α, IL-2, IL-10, and IFN-γ by adherent mononuclear cells stimulated with iRBCs. Production of IL-2, IL-10, and IL-12 in response to iRBC stimulation was confirmed at the protein level (Figure 4C); the discrepancy between mRNA and protein levels for IL-12 is most likely explained by the timing of the assays (all of which were conducted after 24 h).

Type 1 IFN and IL-2, but Not IL-15, Are Required for NK Cell Activation by iRBCs whilst TGF-β Suppresses This Response

NK cell activation by pathogens is typically dependent on accessory cell–secreted cytokines [1922], and we have shown that IL-12 and, to a somewhat lesser extent, IL-18 are required for optimal NK responses to iRBCs [7,8]. To determine whether other accessory cell–derived cytokines are also required for NK activation, the response to iRBCs was analysed in the presence or absence of neutralising antibodies to individual cytokines or their receptors. Of particular interest were those cytokines that we had found (as described above) to be specifically and strongly upregulated by iRBCs, namely IFN-α and IL-2. Also, since TGF-β has recently been reported to be a powerful inhibitor of NK cell activation [23], and since we have shown that induction of TGF-β in vivo in both human and rodent malaria infections is associated with lack of early IFN-γ responses [24,25], it was of considerable interest to determine whether TGF-β might regulate the NK cell IFN-γ response to iRBCs in our in vitro assay system where platelets and mononuclear cells provide an abundant source of latent TGF-β. Representative fluorescence activated cell sorting (FACS) plots showing the effect of blocking cytokines on IFN-γ response to iRBCs are shown in Figure S3.

In the presence of a blocking antibody to the IFN-α/β receptor, there is a significant and dose-dependent inhibition of the NK cell IFN-γ response to iRBCs (highest antibody dose, paired t test, t = 6.42, p = 0.023) (Figure 5A) and a similar, but less marked, reduction in CD69 expression (highest antibody dose, paired t test, t = 5.26, p = 0.034) (Figure S4). Similarly, neutralisation of IL-2 markedly inhibited NK cell IFN-γ responses in a dose-dependent manner (highest antibody dose, paired t test, t = 8.79, p = 0.001) (Figure 5B), and CD69 surface expression was also reduced, but to a lesser degree (highest antibody dose, paired t test, t = 4.43, p = 0.021) (Figure S4). On the other hand, neutralisation of IL-15 had only a minimal effect on NK cell IFN-γ responses (highest antibody dose, paired t test, t = 1.83, p = 0.209) (Figure 5C) or CD69 expression (highest antibody dose, paired t test, t = 3.36, p = 0.078) (Figure S4).


Figure 5. The NK Cell Response to iRBCs Is Controlled by Type 1 IFN, IL-2, and TGF-β

PBMCs from malaria-naïve donors were stimulated for 24 h with iRBCs in the presence of increasing concentrations of neutralising antibodies to (A) the IFN-α/β receptor, (B) IL-2, (C) IL-15, or (D) TGF-β. Percentages of IFN-γ NK cells relative to those observed with the respective concentration of isotype-matched control antibodies are shown. Only donors known to make a strong IFN-γ response to iRBCs were used; baseline percentages of NK cells that were IFN-γ+ after iRBC stimulation ranged from 5% to 40% for the donors shown here.


When PBMCs were incubated with iRBCs for 24 h in the presence or absence of increasing doses of neutralising antibody to TGF-β, there was a highly consistent, dose-dependent increase in the proportion of NK cells synthesising IFN-γ, with up to a 3-fold increase in IFN-γ+ NK cells in the presence of 100 μg/ml antibody (paired t test, t = 7.98, p = 0.004) (Figure 5D) and a slight, but statistically significant, increase in CD69 expression (highest antibody dose, paired t test, t = 4.00, p = 0.028) (Figure S4). Conversely, addition of recombinant human TGF-β led to a very marked, dose-dependent suppression of the NK cell IFN-γ response to iRBCs (highest dose, 1 ng/ml; paired t test, t = 12.8, p = 0.001; unpublished data).

Optimal NK Cell Response to iRBCs Requires Contact between NK Cells and Accessory Cells

For some microbial stimuli it has been reported that optimal NK cell activation requires contact with accessory cells [12,22,26,27]. We thus sought to determine whether such contact-dependent signals were also required for NK activation by iRBCs. Purified NK cells (in the upper chamber of a Transwell culture system) were separated from PBMCs (in the lower chamber) by a microporous membrane (0.4-μm diameter), which allowed diffusion of small molecules including cytokines, but not migration of leukocytes, iRBCs, or extracellular malarial merozoites. When a soluble positive control stimulus (phytohaemagglutinin) was added to the lower well, NK cells in the inner (top) well responded normally, indicating that diffusion of soluble signals was not impeded (Figure S5). When iRBCs were added to the lower chamber, NK cells within the PBMC population synthesised IFN-γ (Figure 6A, PBMC control) and upregulated CD69 (Figure 6B, PBMC control). However, addition of iRBCs to the upper well, the lower well, or both the upper and lower wells together was insufficient to induce optimal IFN-γ production among the NK cells in the upper well, suggesting that contact-mediated interactions between NK cells and iRBCs and/or between accessory cells and iRBCs are insufficient for full NK activation and that direct cell–cell contact between the NK cells and the accessory cells is required.


Figure 6. Contact between NK Cells and Accessory Cells Is Necessary for an Optimal Response to iRBCs

Purified NK cells and autologous PBMCs were co-cultured in Transwell plates, separated by a microporous membrane. The presence of iRBCs in the respective compartments, purified NK cells in the top well and PBMCs in the bottom well are indicated in the key to the figure. Intracellular production of IFN-γ (A) and surface expression levels of CD69 (B) on NK cells in the top well were analysed by flow cytometry. The black bars represent NK cell responses for PBMCs stimulated with iRBCs. All other bars represent values for purified NK cells (upper well). Percentages indicate the proportion of CD3 CD56+ NK cells that were positive for IFN-γ; data are based on the collection of 100,000 total events.


Contact between NK cells and accessory cells was also required for optimal up-regulation of CD69, although partial up-regulation of CD69 was observed in some cases when purified NK cells were in contact with iRBCs and/or when accessory cells were in contact with iRBCs. The up-regulation of CD69 by purified NK cells in the Transwell system (Figure 6), but not in regular cultures of purified NK cells (Figure 1), is presumably due to the presence of soluble, cytokine-mediated signals derived from PBMCs in the lower well.

NK Cell–Derived Signals Maintain the Maturation Status of Accessory Cells but Are Not Required for Accessory Cell Responses to iRBCs or LPS

In recent years it has become apparent that interactions between NK cells and DCs can be bidirectional. NK cells, especially those activated by prior exposure to IL-2, enhance DC maturation, inflammatory cytokine secretion, and antigen presentation in allogeneic situations and when exposed to virus-infected cells [2830]. On the other hand, the degree of reciprocity between NK cells and monocytes, and the potential for NK cells to augment accessory cell responses to non-viral pathogens, has not to our knowledge been investigated. We therefore examined whether the interactions that we had observed to be crucial for the activation of NK cells by iRBCs led to reciprocal activation of either monocytes or mDCs.

Whole PBMCs or PBMCs depleted of NK cells were cultured for 24 h without stimulation (gm) or with LPS or iRBCs. After 24 h, cells were stained for HLA-DR, CD14, either CD40 or CD80, and either CD11c or CD11b (Figure 7A). Both mDCs and monocytes expressed significantly lower levels of activation markers when cultured (without additional stimulation) in the absence of NK cells (Figure 7B–7D), confirming a previous report of a role for NK cells in promoting DC maturation [29] and extending this observation to monocytes. On the other hand, when cells were cultured with either LPS or iRBCs, there was no significant effect of the presence or absence of NK cells on expression levels of any of the activation markers in either mDCs or monocytes (Figure 7B–7D). Thus, while NK cells play a role in maturation of both monocytes and mDCs in resting conditions, the response of either of these cell types to LPS or iRBC stimulation is largely NK cell–independent. These data suggest that, at this early time point, the major inducers of myeloid cell activation are the pathogens themselves, rather than NK-derived IFN-γ.


Figure 7. NK Cells Are Required to Maintain Maturation Status of Accessory Cells

Whole PBMCs (closed circles) or NK cell–depleted PBMCs (open circles) were cultured alone or with E. coli LPS or iRBCs for 24 h. The MFIs of CD40, HLA-DR, and CD80 surface staining on (A) monocytes and (B) mDCs were determined by flow cytometric analysis. *, p < 0.05; p-values are for paired t tests comparing whole PBMCs with NK cell–depleted PBMCs from the same donor.


Degree of Monocyte Activation Correlates with Magnitude of NK Cell IFN-γ Response

We have previously shown that human NK cell responses to iRBCs are heterogeneous [8,9]. Here, we noticed a considerable degree of heterogeneity of accessory cell surface marker expression (Figure 3D) and of cytokine production (Figure 4) among donors, in terms of both resting levels and responses to iRBCs. Given the absolute dependence of the NK cell response to iRBCs on accessory cells, we sought to determine whether heterogeneity of NK cell responses correlated with heterogeneity of accessory cell responses. Since NK cell IFN-γ responses can vary between CD56bright and CD56dim NK cells—presumably because of differential expression of NK cell receptors including the killer cell immunoglobulin-like receptors (KIRs), which are expressed by CD56dim but not CD56bright NK cells—we analysed the correlation between accessory cell and NK cell responses for both of these NK cell populations.

Highly significant correlations were observed between iRBC-induced concentrations of IL-12 (Figure 8A) and IL-2 (Figure 8B) and the magnitude of the NK cell IFN-γ response. A particularly close correlation was observed between IL-12 concentrations and the proportion of IFN-γ+ CD56bright (KIR) cells, whilst, for several donors (see arrows in Figure 8), a significant discrepancy was seen in the response of the CD56dim population. Somewhat surprisingly, there was no correlation between iRBC-induced up-regulation of HLA-DR, CD40, or CD80 on either monocytes or mDCs and NK IFN-γ production (unpublished data). However, resting levels of expression of both CD40 and HLA-DR were tightly correlated with the NK cell IFN-γ response (Figure 8C and 8D). For resting levels of CD40 expression there was again a much closer correlation with the IFN-γ response of CD56bright NK cells than with that of CD56dim NK cells. One plausible interpretation of these data is that the NK cell IFN-γ response is very sensitive to accessory cell CD40 expression and IL-12 production, but that in CD56dim cells this response is moderated by KIR/major histocompatibility complex (MHC) class I–mediated signals.


Figure 8. NK Cell IFN-γ Response to iRBCs Correlates with Accessory Cell Activation

NK cell IFN-γ responses in PBMCs from eight malaria-naïve donors were analysed after 24 h of co-culture with iRBCs. The concentration in tissue culture supernatants of IL-12p70 and IL-2 was determined in a bead-based cytokine assay, and that of bioactive TGF-β by ELISA. The fluorescence intensities of CD40 and HLA-DR surface staining on CD14+ monocytes and the percentage of IFN-γ+ CD56+ NK cells were determined by flow cytometric analysis. Shown are the percentages of IFN-γ+ CD56bright NK cells (black squares) and IFN-γ+ CD56dim NK cells (grey triangles), along with the correlation of the percentage of IFN-γ+ CD56bright NK cells (black line) with the concentration of IL-12p70 and IL-2 in culture supernatants (A and B), with the MFI of CD40 and HLA-DR on resting monocytes (C and D), and with the up-regulation of bioactive TGF-β in culture supernatants (E). The correlation of TGF-β in culture supernatants with IFN-γ+ CD56dim NK cells is also shown (E, grey line). Correlation coefficients are indicated for CD56bright (upper values) and CD56dim (lower values). Correlations were calculated using a second-order polynomial fit algorithm. Black arrows indicate examples of donors where IFN-γ response is highly suppressed in the CD56dim NK cells. Flow cytometric data are based on the collection of 100,000 total events.


Our observation that TGF-β is able to markedly suppress NK cell IFN-γ responses (Figure 5) led us to consider whether the heterogeneity of NK cell responses was due to differential production and/or activation of TGF-β. There was no consistent increase or decrease in the concentration of bioactive TGF-β in the supernatants of iRBC-stimulated PBMCs; a modest increase in bioactive TGF-β concentration was observed for two donors, but these were, in fact, the donors with the highest NK cell IFN-γ responses to iRBCs, suggesting that suppression by TGF-β does not explain the heterogeneity of NK cell IFN-γ response. Rather, regulation of bioactive TGF-β appears to be positively correlated with NK cell IFN-γ expression (Figure 8E), and furthermore, the correlation with CD56dim NK cells was higher than that with CD56bright NK cells. This suggests that TGF-β is not causal in NK cell activation, but rather that the total amount of IFN-γ produced determines the amount of TGF-β. Thus, activation may lead to induction of negative feedback mechanisms in order to prevent excessive pro-inflammatory responses.


By carefully dissecting the requirements for activation of human NK cells by iRBCs, we have revealed that the early NK cell–derived IFN-γ response is absolutely dependent upon contact with, and cytokine production by, accessory cells. We have identified the requisite accessory cells as monocytes and mDCs and have shown that both cell types become highly activated during the first 24 h of exposure to iRBCs. Furthermore, we have demonstrated that whilst NK cells provide essential signals that maintain the maturation status of resting monocytes and mDCs, NK cells are not required for these same cells to respond fully to iRBCs. Finally, we have shown that the capacity of NK cells to secrete IFN-γ is highly correlated with both the resting phenotype of the accessory cells and the concentration of iRBC-induced monokines. Thus, functional heterogeneity of monocytes and mDCs among human populations appears to play a crucial role in determining the magnitude of the innate immune response to iRBCs.

A wealth of evidence suggests that, after interaction with malarial parasites, both monocytes and mDCs secrete immunosuppressive cytokines and have an impaired ability to respond to a variety of stimulatory ligands [1317,31]. These data have led some to conclude that monocyte and DC function is universally impaired by contact with malarial parasites and that this underlies an apparent suppression of immune responses seen during malaria infections. However, there have been several reports of activation of monocytes and DCs by Plasmodium-derived ligands [3234]. Studies of rodent malaria infections have begun to resolve this debate, showing that in the first 24 h of infection, splenic DCs are activated, secrete pro-inflammatory cytokines including IL-12 and tumour necrosis factor-α, and present antigen to T cells, but that they subsequently become refractory to re-stimulation and secrete anti-inflammatory cytokines such as IL-10 [35]. This sequence of events allows infection to be controlled whilst simultaneously avoiding immune-mediated pathology [25]. Here we show that human monocytes and mDCs are highly activated after 24 h of co-incubation with iRBCs. The myeloid cell response occurred in the presence or absence of NK cells, indicating that direct interaction with parasites—as opposed to NK-derived IFN-γ—drives the initial activation of these cells. Furthermore, this activation initiates and regulates the crucial early burst of IFN-γ from NK cells. However, our observation that NK activation goes hand in hand with IL-10 and TGF-β production, and that TGF-β can suppress NK IFN-γ production, is consistent with the notion that pro-inflammatory responses to malaria are carefully regulated by homeostatic mechanisms to prevent immune-mediated pathology.

Our observations regarding the accessory cell requirements for NK cell activation by malaria parasites are in partial agreement with a previous report invoking a role for monocytes in this response [36]; however, we show that mDCs play an equally important role. The fact that NK activation is suboptimal but not absent in the presence of only one or the other accessory cell population suggests that although there is some redundancy in their roles, they also provide complementary signals. Our data are consistent with reports of leukocyte activation by malarial glycosylphosphatidylinositol signalling through toll-like receptor (TLR) 2 and TLR4 [37], which are both expressed on monocytes and mDCs but not pDCs [38,39], although a role for other receptors cannot be ruled out. The reported activation of pDCs by a malarial hemozoin–TLR9 pathway [40,41] does not appear to be required for NK IFN-γ production, consistent with previous reports that NK cytotoxic activity but not IFN-γ secretion is dependent on pDC-derived signals [42,43]. In fact, depletion of pDCs increased the IFN-γ response of NK cells in two out of three donors, suggesting that pDCs may have a net anti-inflammatory effect in this system, perhaps mediated by either IL-10 or TGF-β. Further experiments are required to test this possibility.

The data presented here reveal that accessory cell–dependent activation of NK cells by iRBCs is multifactorial and, as in other systems, involves multiple cytokines (IL-2, IL-12, IL-18, and IFN-α) [4446] as well as direct contact between NK cells and accessory cells [12,22,26,27]. Whether accessory cells are the source of IL-2, as recently reported for human pDCs and mDCs [47], is not clear, and we cannot rule out that IL-2 is produced by a small contaminating population of rapidly responding T cells. Contact-dependent signals might include CD40–CD40L signalling [12], delivery of IL-12 from mDCs via an immune synapse [48], or binding of MHC–peptide complexes by activating KIR [49]. We believe that indirect, accessory cell–mediated signals are likely to be the major mechanism of NK cell activation by iRBCs, but we cannot rule out that the NK cell receives additional signals via direct interaction with iRBCs. Stable contacts between iRBCs and NK cells have been reported by ourselves and by others [9,36], and we have observed reorganisation of the actin cytoskeleton at the point of iRBC–NK contact [9]; the functional consequence of these interactions are, however, not yet fully understood.

Our observation that NK cells are not required for optimal activation of monocytes and mDCs by pathogen-derived ligands (iRBCs and LPS) runs somewhat counter to previous reports that NK cells augment DC maturation, cytokine secretion, and antigen presentation [2830]. One plausible explanation for this discrepancy is that the sequence of events leading to activation of NK cells and accessory cells depends on the nature of the stimulus. In the case of virally infected or neoplastic cells, altered expression of MHC or MHC-like ligands on the target cell will lead to direct activation of NK cells either through engagement of natural cytotoxicity receptors or changes in the balance of activating and inhibitory signals delivered by KIR receptors (reviewed in [50]). In this case, amplification of the innate response and induction of adaptive immunity would be facilitated if NK cells were able to provide activating signals to DCs and other antigen-presenting cells, which are much less sensitive to changes in MHC expression. On the other hand, in the case of bacterial and protozoal pathogens, which do not grossly alter MHC class I expression or induce MHC-related stress ligands on host cells, direct activation of NK cells is unlikely. Rather, DCs and monocytes are likely to be directly activated by binding of pathogen-associated molecular patterns to TLRs and other pattern recognition receptors and may not require additional signals from NK cells.

Given the importance of the innate response to malaria in determining the outcome of disease (reviewed in [1]), dissecting the basis for the heterogeneity of the human NK cell response to iRBCs could be crucial in understanding disease susceptibility. The close correlations shown here between accessory cell maturation, accessory cell responses to iRBCs, and induction of IFN-γ production by NK cells suggest that heterogeneity of NK cell responses to iRBCs [8,9] is a reflection of deeply rooted heterogeneity of innate responses within the human population. Ongoing studies of the immunogenetics of susceptibility to human malaria should begin to identify the underlying basis for this heterogeneity, but linking genotype to immunological phenotype may not be straightforward. Multiple genes, including various IFN regulatory factor proteins and components of the colony stimulating factor 1 signalling pathway, influence the maturation status of accessory cells [5153]. Moreover, the much stronger correlation of accessory cell status with activation of CD56bright (KIR) NK cells than with activation of CD56dim (KIR+) NK cells suggests that NK cell activation by pathogen-induced accessory cell signals may be modulated by NK cell receptor expression. Since KIR genes, along with MHC genes, are some of the most highly polymorphic loci in the human genome [54], dissecting the genetic basis of diversity in the human innate response is a daunting task. Nevertheless, as CD56dim cells are the major population of NK cells in peripheral blood and spleen [55], our data suggest that NK cell receptor expression is likely to have a significant influence on overall NK cell responsiveness and thus potentially affect the severity of malarial disease and other systemic infections. Despite the difficulties associated with carrying them out, population-based studies of disease risk and diversity in innate response genes could have far-reaching implications, and we have recently begun such studies in malaria-endemic populations. Since the antigen-presenting and co-stimulatory functions of accessory cells are pivotal for induction of adaptive immunity, and the magnitude of the early IFN-γ response affects adaptive responses [56], heterogeneity of expression of CD40, HLA-DR, and NK cell IFN-γ is likely to have a profound impact on the generation of acquired immune responses.

Supporting Information

Figure S1. Depletion of HLA-DR-Positive Cells Does Not Affect the Ability of NK Cells to Produce IFN-γ following Stimulation with IL-12 and IL-18

(A) Representative example of NK cell response to IL-12 and IL-18 when cultured in the context of whole PBMCs or PBMCs depleted of HLA-DR-positive cells.

(B) Data from five donors showing proportion of NK cells positive for intracellular IFN-γ following stimulation with IL-12 and IL-18 in the context of whole PBMCs or PBMCs depleted of HLA-DR-positive cells. There was no significant difference between responses (paired t test, t = 1.43, p = 0.226).


(1.3 MB TIF)

Figure S2. Staining with Isotype-Matched Control Antibodies Is Not Affected by Stimulation of Accessory Cells

Representative histograms showing staining of monocytes with (A) IgG1 and (B) IgG2a antibodies following culture of PBMCs with no stimulation (gm), LPS, or iRBCs. (C) Pooled data for monocytes stained for IgG1 following culture with indicated stimuli. (D) Pooled data for monocytes stained for IgG2a following culture with indicated stimuli. No significant increase in staining intensity of either antibody was observed after stimulation with E. coli LPS or iRBCs.


(385 KB TIF)

Figure S3. Effect of Blocking Antibodies on the NK Cell Response to iRBCs

Representative FACS plots showing the effect on the NK cell response to iRBCs of blocking with monoclonal antibodies of the following specificities: (A) anti-IL-2, (B) anti-TGF-β, and (C) anti-IFN-α receptor.


(1.4 MB TIF)

Figure S4. Up-Regulation of CD69 on NK Cells in Response to iRBCs Is Controlled by Type 1 IFN, IL-2, and TGF-β

PBMCs from malaria-naïve donors were stimulated for 24 h with iRBCs in the presence of increasing concentrations of neutralising antibodies to (A) the IFN-α/β receptor, (B) IL-2, (C) IL-15, or (D) TGF-β. MFI of CD69 on NK cells relative to that observed with the equivalent concentration of isotype-matched control antibody is shown.


(826 KB TIF)

Figure S5. Diffusion of Soluble Factors through Transwell Membrane

(A) Experimental setup. PBMCs were added to both the inner and outer compartments of a Transwell. Phytohaemagglutinin (PHA) (a mitogen) was added to the outer compartment, and the cells were cultured for 24 h at 37 °C. Cells were aspirated and stained for the surface markers CD56 and CD3 and intracellular IFN-γ.

(B) Proportion of IFN-γ+ NK cells amongst PBMCs from outer and inner compartments following 24 h culture (six donors). There is no significant difference in the response of cells aspirated from the outer or inner well (paired t test, t = 1.08, p = 0.331).


(275 KB TIF)

Accession Numbers

Online database accession and ID numbers for genes and proteins mentioned throughout this article can be found in Table 1.


Table 1.

Accession Numbers for Genes and Proteins



We would like to thank the London School of Hygiene and Tropical Medicine blood donors for their participation in this study; Carolynne Stanley, Elizabeth King, and Nikki D'Arcy for excellent technical assistance; and Simona Zompi for stimulating discussions.

Author Contributions

KCN, DSK, and EMR conceived and designed the experiments. KCN, DSK, and JCH performed the experiments. KCN, DSK, and EMR analyzed the data and wrote the paper.


  1. 1. Stevenson M, Riley E (2004) Innate immunity to malaria. Nat Rev Immunol 4: 169–180.
  2. 2. De Souza JB, Williamson KH, Otani T, Playfair JH (1997) Early gamma interferon responses in lethal and nonlethal murine blood-stage malaria. Infect Immun 65: 1593–1598.
  3. 3. Su Z, Stevenson MM (2000) Central role of endogenous gamma interferon in protective immunity against blood-stage Plasmodium chabaudi AS infection. Infect Immun 68: 4399–4406.
  4. 4. Meding SJ, Cheng SC, Simon-Haarhaus B, Langhorne J (1990) Role of gamma interferon during infection with Plasmodium chabaudi chabaudi. Infect Immun 58: 3671–3678.
  5. 5. Luty AJ, Lell B, Schmidt-Ott R, Lehman LG, Luckner D, et al. (1999) Interferon-gamma responses are associated with resistance to reinfection with Plasmodium falciparum in young African children. J Infect Dis 179: 980–988.
  6. 6. Dodoo D, Omer FM, Todd J, Akanmori BD, Koram KA, et al. (2002) Absolute levels and ratios of proinflammatory and anti-inflammatory cytokine production in vitro predict clinical immunity to Plasmodium falciparum malaria. J Infect Dis 185: 971–979.
  7. 7. Artavanis-Tsakonas K, Riley E (2002) Innate immune response to malaria: Rapid induction of IFN-gamma from human NK cells by live Plasmodium falciparum-infected erythrocytes. J Immunol 169: 2956–2963.
  8. 8. Artavanis-Tsakonas K, Eleme K, McQueen K, Cheng N, Parham P, et al. (2003) Activation of a subset of human NK cells upon contact with Plasmodium falciparum-infected erythrocytes. J Immunol 171: 5396–5405.
  9. 9. Korbel DS, Newman KC, Almeida CR, Davis DM, Riley EM (2005) Heterogeneous human NK cell responses to Plasmodium falciparum-infected erythrocytes. J Immunol 175: 7466–7473.
  10. 10. Krug A, French AR, Barchet W, Fischer JA, Dzionek A, et al. (2004) TLR9-dependent recognition of MCMV by IPC and DC generates coordinated cytokine responses that activate antiviral NK cell function. Immunity 21: 107–119.
  11. 11. Cleveland MG, Gorham JD, Murphy TL, Tuomanen E, Murphy KM (1996) Lipoteichoic acid preparations of gram-positive bacteria induce interleukin-12 through a CD14-dependent pathway. Infect Immun 64: 1906–1912.
  12. 12. Atochina O, Harn D (2005) LNFPIII/LeX-stimulated macrophages activate natural killer cells via CD40-CD40L interaction. Clin Diagn Lab Immunol 12: 1041–1049.
  13. 13. Urban BC, Willcox N, Roberts DJ (2001) A role for CD36 in the regulation of dendritic cell function. Proc Natl Acad Sci U S A 98: 8750–8755.
  14. 14. Deshpande P, Shastry P (2004) Modulation of cytokine profiles by malaria pigment—Hemozoin: Role of IL-10 in suppression of proliferative responses of mitogen stimulated human PBMC. Cytokine 28: 205–213.
  15. 15. Berry A, Chene G, Benoit-Vical F, Lepert JC, Bernad J, et al. (2005) Ex vivo and in vitro impairment of CD36 expression and tumor necrosis factor-alpha production in human monocytes in response to Plasmodium falciparum-parasitized erythrocytes. J Parasitol 91: 316–322.
  16. 16. Skorokhod OA, Alessio M, Mordmuller B, Arese P, Schwarzer E (2004) Hemozoin (malarial pigment) inhibits differentiation and maturation of human monocyte-derived dendritic cells: A peroxisome proliferator-activated receptor-gamma-mediated effect. J Immunol 173: 4066–4074.
  17. 17. Urban BC, Ferguson DJ, Pain A, Willcox N, Plebanski M, et al. (1999) Plasmodium falciparum-infected erythrocytes modulate the maturation of dendritic cells. Nature 400: 73–77.
  18. 18. Urban BC, Mwangi T, Ross A, Kinyanjui S, Mosobo M, et al. (2001) Peripheral blood dendritic cells in children with acute Plasmodium falciparum malaria. Blood 98: 2859–2861.
  19. 19. Gazzinelli RT, Denkers EY, Sher A (1993) Host resistance to Toxoplasma gondii: Model for studying the selective induction of cell-mediated immunity by intracellular parasites. Infect Agents Dis 2: 139–149.
  20. 20. Hunter CA, Slifer T, Araujo F (1996) Interleukin-12-mediated resistance to Trypanosoma cruzi is dependent on tumor necrosis factor alpha and gamma interferon. Infect Immun 64: 2381–2386.
  21. 21. Rottenberg M, Cardoni RL, Andersson R, Segura EL, Orn A (1988) Role of T helper/inducer cells as well as natural killer cells in resistance to Trypanosoma cruzi infection. Scand J Immunol 28: 573–582.
  22. 22. Siren J, Sareneva T, Pirhonen J, Strengell M, Veckman V, et al. (2004) Cytokine and contact-dependent activation of natural killer cells by influenza A or Sendai virus-infected macrophages. J Gen Virol 85: 2357–2364.
  23. 23. Laouar Y, Sutterwala F, Gorelik L, Flavell R (2005) Transforming growth factor-beta controls T helper type 1 cell development through regulation of natural killer cell interferon-gamma. Nat Immunol 6: 600–607.
  24. 24. Walther M, Tongren J, Andrews L, Korbel D, King E, et al. (2005) Upregulation of TGF-beta, FOXP3, and CD4(+)CD25(+) regulatory T cells correlates with more rapid parasite growth in human malaria infection. Immunity 23: 287–296.
  25. 25. Omer F, de Souza JB, Riley E (2003) Differential induction of TGF-beta regulates proinflammatory cytokine production and determines the outcome of lethal and nonlethal Plasmodium yoelii infections. J Immunol 171: 5430–5436.
  26. 26. Cardillo F, Voltarelli JC, Reed SG, Silva JS (1996) Regulation of Trypanosoma cruzi infection in mice by gamma interferon and interleukin 10: Role of NK cells. Infect Immun 64: 128–134.
  27. 27. Kamath AT, Sheasby CE, Tough DF (2005) Dendritic cells and NK cells stimulate bystander T cell activation in response to TLR agonists through secretion of IFN-alpha beta and IFN-gamma. J Immunol 174: 767–776.
  28. 28. Gerosa F, Baldani-Guerra B, Nisii C, Marchesini V, Carra G, et al. (2002) Reciprocal activating interaction between natural killer cells and dendritic cells. J Exp Med 195: 327–333.
  29. 29. Vitale M, Della Chiesa M, Carlomagno S, Pende D, Arico M, et al. (2005) NK-dependent DC maturation is mediated by TNFalpha and IFNgamma released upon engagement of the NKp30 triggering receptor. Blood 106: 566–571.
  30. 30. Piccioli D, Sbrana S, Melandri E, Valiante NM (2002) Contact-dependent stimulation and inhibition of dendritic cells by natural killer cells. J Exp Med 195: 335–341.
  31. 31. Schwarzer E, Arese P (1996) Phagocytosis of malarial pigment hemozoin inhibits NADPH-oxidase activity in human monocyte-derived macrophages. Biochim Biophys Acta 1316: 169–175.
  32. 32. Ndungu FM, Sanni L, Urban B, Stephens R, Newbold CI, et al. (2006) CD4 T cells from malaria-nonexposed individuals respond to the CD36-binding domain of Plasmodium falciparum erythrocyte membrane protein-1 via an MHC class II-TCR-independent pathway. J Immunol 176: 5504–5512.
  33. 33. Pais TF, Chatterjee S (2005) Brain macrophage activation in murine cerebral malaria precedes accumulation of leukocytes and CD8+ T cell proliferation. J Neuroimmunol 163: 73–83.
  34. 34. Prato M, Giribaldi G, Polimeni M, Gallo V, Arese P (2005) Phagocytosis of hemozoin enhances matrix metalloproteinase-9 activity and TNF-alpha production in human monocytes: Role of matrix metalloproteinases in the pathogenesis of falciparum malaria. J Immunol 175: 6436–6442.
  35. 35. Perry JA, Olver CS, Burnett RC, Avery AC (2005) Cutting edge: The acquisition of TLR tolerance during malaria infection impacts T cell activation. J Immunol 174: 5921–5925.
  36. 36. Baratin M, Roetynck S, Lepolard C, Falk C, Sawadogo S, et al. (2005) Natural killer cell and macrophage cooperation in MyD88-dependent innate responses to Plasmodium falciparum. Proc Natl Acad Sci U S A 102: 14747–14752.
  37. 37. Krishnegowda G, Hajjar AM, Zhu J, Douglass EJ, Uematsu S, et al. (2005) Induction of proinflammatory responses in macrophages by the glycosylphosphatidylinositols of Plasmodium falciparum: Cell signaling receptors, glycosylphosphatidylinositol (GPI) structural requirement, and regulation of GPI activity. J Biol Chem 280: 8606–8616.
  38. 38. Kadowaki N, Ho S, Antonenko S, Malefyt RW, Kastelein RA, et al. (2001) Subsets of human dendritic cell precursors express different toll-like receptors and respond to different microbial antigens. J Exp Med 194: 863–869.
  39. 39. Muzio M, Bosisio D, Polentarutti N, D'Amico G, Stoppacciaro A, et al. (2000) Differential expression and regulation of toll-like receptors (TLR) in human leukocytes: Selective expression of TLR3 in dendritic cells. J Immunol 164: 5998–6004.
  40. 40. Pichyangkul S, Yongvanitchit K, Kum-arb U, Hemmi H, Akira S, et al. (2004) Malaria blood stage parasites activate human plasmacytoid dendritic cells and murine dendritic cells through a Toll-like receptor 9-dependent pathway. J Immunol 172: 4926–4933.
  41. 41. Coban C, Ishii K, Kawai T, Hemmi H, Sato S, et al. (2005) Toll-like receptor 9 mediates innate immune activation by the malaria pigment hemozoin. J Exp Med 201: 19–25.
  42. 42. Romagnani C, Della Chiesa M, Kohler S, Moewes B, Radbruch A, et al. (2005) Activation of human NK cells by plasmacytoid dendritic cells and its modulation by CD4+ T helper cells and CD4+ CD25hi T regulatory cells. Eur J Immunol 35: 2452–2458.
  43. 43. Gerosa F, Gobbi A, Zorzi P, Burg S, Briere F, et al. (2005) The reciprocal interaction of NK cells with plasmacytoid or myeloid dendritic cells profoundly affects innate resistance functions. J Immunol 174: 727–734.
  44. 44. Biron CA, Nguyen KB, Pien GC, Cousens LP, Salazar-Mather TP (1999) Natural killer cells in antiviral defense: Function and regulation by innate cytokines. Annu Rev Immunol 17: 189–220.
  45. 45. Matikainen S, Paananen A, Miettinen M, Kurimoto M, Timonen T, et al. (2001) IFN-alpha and IL-18 synergistically enhance IFN-gamma production in human NK cells: Differential regulation of Stat4 activation and IFN-gamma gene expression by IFN-alpha and IL-12. Eur J Immunol 31: 2236–2245.
  46. 46. Naume B, Espevik T (1994) Immunoregulatory effects of cytokines on natural killer cells. Scand J Immunol 40: 128–134.
  47. 47. Feau S, Facchinetti V, Granucci F, Citterio S, Jarrossay D, et al. (2005) Dendritic cell-derived IL-2 production is regulated by IL-15 in humans and in mice. Blood 105: 697–702.
  48. 48. Borg C, Jalil A, Laderach D, Maruyama K, Wakasugi H, et al. (2004) NK cell activation by dendritic cells (DCs) requires the formation of a synapse leading to IL-12 polarization in DCs. Blood 104: 3267–3275.
  49. 49. Stewart CA, Laugier-Anfossi F, Vely F, Saulquin X, Riedmuller J, et al. (2005) Recognition of peptide-MHC class I complexes by activating killer immunoglobulin-like receptors. Proc Natl Acad Sci U S A 102: 13224–13229.
  50. 50. O'Connor GM, Hart OM, Gardiner CM (2006) Putting the natural killer cell in its place. Immunology 117: 1–10.
  51. 51. Dey A, She H, Kim L, Boruch A, Guris DL, et al. (2000) Colony-stimulating factor-1 receptor utilizes multiple signaling pathways to induce cyclin D2 expression. Mol Biol Cell 11: 3835–3848.
  52. 52. Zhang DE, Hetherington CJ, Meyers S, Rhoades KL, Larson CJ, et al. (1996) CCAAT enhancer-binding protein (C/EBP) and AML1 (CBF alpha2) synergistically activate the macrophage colony-stimulating factor receptor promoter. Mol Cell Biol 16: 1231–1240.
  53. 53. Tamura T, Nagamura-Inoue T, Shmeltzer Z, Kuwata T, Ozato K (2000) ICSBP directs bipotential myeloid progenitor cells to differentiate into mature macrophages. Immunity 13: 155–165.
  54. 54. Norman PJ, Parham P (2005) Complex interactions: The immunogenetics of human leukocyte antigen and killer cell immunoglobulin-like receptors. Semin Hematol 42: 65–75.
  55. 55. Ferlazzo G, Münz C (2004) NK cell compartments and their activation by dendritic cells. J Immunol 172: 1333–1339.
  56. 56. Mitchell AJ, Hansen AM, Hee L, Ball HJ, Potter SM, et al. (2005) Early cytokine production is associated with protection from murine cerebral malaria. Infect Immun 73: 5645–5653.