Mini Review ARTICLE
NK cells during dengue disease and their recognition of dengue virus-infected cells
- 1Department of Research in Virology and Biotechnology, Gorgas Memorial Institute for Health Studies, Panama City, Panama
- 2Institute for Scientific Research and Technology Services (INDICASAT-AIP), Panama City, Panama
- 3Department of Biotechnology, Acharya Nagarjuna University, Guntur, India
The innate immune response, in addition to the B- and T-cell response, plays a role in protection against dengue virus (DENV) infection and the degree of disease severity. Early activation of natural killer (NK) cells and type-I interferon-dependent immunity may be important in limiting viral replication during the early stages of DENV infection and thus reducing subsequent pathogenesis. NK cells may also produce cytokines that reduce inflammation and tissue injury. On the other hand, NK cells are also capable of inducing liver injury at early-time points of DENV infection. In vitro, NK cells can kill antibody-coated DENV-infected cells through antibody-dependent cell-mediated cytotoxicity. In addition, NK cells may directly recognize DENV-infected cells through their activating receptors, although the increase in HLA class I expression may allow infected cells to escape the NK response. Recently, genome-wide association studies have shown an association between MICB and MICA, which encode ligands of the activating NK receptor NKG2D, and dengue disease outcome. This review focuses on recognition of DENV-infected cells by NK cells and on the regulation of expression of NK cell ligands by DENV.
Dengue is a major public health problem in tropical and subtropical regions world wide and is caused by four serotypes of dengue virus (DENV-1, -2, -3, -4), a flavivirus transmitted to humans by Aedes mosquitoes (1). DENV infection can be asymptomatic or induce mild to severe disease, traditionally referred to as dengue hemorrhagic fever/dengue shock syndrome (DHF/DSS), which can lead to death (2). While there have been important advances in elucidating dengue pathogenesis, it is difficult to foretell if an acutely infected individual will develop the disease and to predict its severity; however, disease outcome appears to depend on the virus as well as on host genetics and prior immunity (3–5). For this reason, it is crucial to understand the immune response during DENV infection. Many studies have focused on the adaptive response, as antibodies and T cells play a crucial role in protection against infection, as well as in the pathogenesis of dengue disease (4–6). The innate immune response plays an intrinsic role at the level of the infected cell (7), but also recruits and activates innate immune cells that can eliminate the virus at early stages and induce the development of the adaptive response (8, 9). Indeed, the extent of DENV replication during the early period of infection correlates with dengue disease severity (10–14). Interstitial dendritic cells (DCs) are believed to constitute the first line of host defense against invading DENV at the anatomical sites where it replicates after the initial bite by infected mosquitoes (8). Type-I interferon-dependent immunity is known to play a critical role, and early activation of natural killer (NK) cells may also be important in limiting viral replication at the early stages of DENV infection (6, 8).
NK Cells in Viral Infections
Natural killer cells are innate lymphocytes specialized in defense against viral and intracellular bacterial infections and tumors (15). NK cells share some characteristics with the adaptive immune system and may possess specific memory features against some viruses and antigens (16). They can be rapidly recruited into infected organs and tissues by chemoattractant factors produced by virus-infected cells and activated resident macrophages and DCs, which are a major source of the interferon IFNα/β that induces NK cell proliferation and activation (17, 18). Reciprocally, NK cells can shape DCs activation and subsequently the adaptive response (17). Once activated, NK cells fight infection by producing chemokines and anti-viral cytokines, mainly IFNγ and MIP1-β, and by recognizing and eliminating infected cells by antibody-dependent cell-mediated cytotoxicity (ADCC) or by direct recognition through their activating receptors (15). NK cells have activating and inhibitory receptors that allow them to recognize stressed cells, tumors, and pathogen-infected cells and to differentiate them from healthy cells (15, 19). Most of the inhibitory receptors recognize classic and non-classic major histocompatibility complex class I (MHC I) molecules, and many viruses decrease the expression of MHC I molecules in infected cells to escape the CD8+ T-cell response, thereby becoming more vulnerable to NK cell recognition (19–21).
Virus-infected cells often induce or increase the expression of ligands at their surface, allowing for recognition by NK cell activating receptors, including NKG2D, DNAM-1, CD94-NKG2C; the NCR receptors NKp46, NKp30, NKp44; and others (19, 20, 22). The ligands include host stress-induced molecules and viral proteins (20). To date, the ligands for many of the activating receptors (for example the NCRs) are still unknown, and their expression has been detected indirectly by cell staining with recombinant receptors or by blocking of killing with receptor-specific antibodies. A better characterization of NK ligands is needed. NKG2D is the most well-characterized NK activating receptor, and ligand binding leads to target killing and cytokine production (22). NKG2D ligand expression is increased by “stress” conditions, including viral infections (22, 23). In humans, eight ligands have been described for NKG2D, including MICA, MICB, and ULBP1-6. In addition to expression of NKG2D ligands on the surface of infected cells, soluble isoforms can be released into the serum, although the physiological relevance of the soluble ligands is controversial (22, 24). These soluble forms have been described in cancer patients, as well as in HIV-1-infected patients without therapy (25, 26) suggesting that soluble NKG2D ligands might be released in other viral infections.
Role of NK Cells in Dengue Disease
Many studies suggest that NK cells play a role in the response against DENV infection, principally in the early infection stages by limiting DENV replication. A higher absolute number of NK cells was observed in patients with mild dengue fever (DF) compared with children who developed DHF (27–29). However, the percentage of NK cells and CD8+ T cells expressing CD69, a marker of activation, was higher early during infection of children who developed DHF (27, 30). Homchampa et al. found evidence of NK cell cytotoxicity against non-infected K562 target cells from children with acute dengue, and the cytolytic activity was increased on a per-cell basis in the early disease stages of dengue compared with healthy controls, and was even higher in the most severe form of the disease. It was suggested that this NK cell activity was associated with higher viremia in the more severe cases. Studies in adults showed that patients with mild disease had higher numbers of NK cells, with the majority of cells having increased expression of activation markers (CD69, CD38, and HLA-DR), adhesion molecules (CD11a and CD44) (Table 1), and markers of intracellular cytotoxic granules (TIA-1), in contrast to severe dengue where reduced NK cell numbers were observed (31). The authors suggest that higher NK cell percentages and activity might indicate a good prognosis of disease. In a genome-wide association study (GWAS), it was shown that the transcriptome of blood cells from children with DSS was characterized by decreased abundance of transcripts related to T and NK responses, probably not due to a difference in lymphocyte counts but to an impaired response (32). The differences observed in NK cell numbers and percentages in these studies may be explained by differences in age (children versus adults), ethnicity, time of infection, and the experimental methods to define NK cells and their activation. Nonetheless, all these observations point to the importance of NK cells and their activation during early DENV infection. The activation and phenotype of NK cells during dengue acute infection is further developed by Petitdemange et al., under the research topic “protective immune response to dengue virus infection and vaccines: perspectives from the field to the bench.”
Table 1. Summary of the published findings related to ligands for receptors on NK cells and dengue virus infection.
The protective role of NK cells in the response against DENV is supported in mice models of the disease. In immunocompetent A/J mice, the early activation of NK and B cells was associated with the control of the viral load and the prevention of disease (33, 34). In C57BL/6 mice, the recruitment of NK and NKT cells by mast cells to the site of infection was also crucial for viral clearance (35), underlining the importance of these cells during the host early response against DENV. The early recruitment of NK cells to the liver was induced in part by CXCL10 (IP-10), and in the liver NK cells produce effector molecules (perforin, granzyme A, and granzyme B) needed for viral clearance (36). On the other hand, NK cells appear to play not only a protective role in dengue disease, as it was shown that after intrahepatic infiltration, NK cells were responsible for cell death in the liver at the early phase of infection, whereas CD8+ T cells were responsible for damage later (37). The mechanism of this cell death has not been elucidated, but the authors suggested that NK cells were killing DENV-infected cells. It is possible that under some conditions, the elimination of DENV-infected cells by NK cells can be exacerbated in a way that the immune effector cells become responsible for organ injury. Similarly, NKT cells in some conditions can be detrimental during dengue pathogenesis, in part by inducing NK cells and neutrophils activation (38).
Natural killer cells may play an important role in early DENV infection in vivo also by producing together with γδ T cells, IL-22 and IL-17A, which may influence dengue disease outcome (39). NK, NKT, and T cells that can respond in a non-TcR-dependent fashion are a major source of IFNγ in immune responses induced by inactivated DENV (40); however, in this context, the frequency of IFNγ-producing cells observed was very low. Using C57BL/6 mice, a study confirmed the role of NK cells in the early IFNγ production induced by IL-12 and IL-18 in response to DENV, key for the control of viral load and DENV-2-associated disease severity and lethality (41).
Natural killer cells can mediate ADCC against DENV-infected cells (42, 43) and this mechanism may be important during secondary infections when antibodies to DENV are present. Indeed, ADCC activity in plasma obtained before secondary DENV-2 or DENV-3 infection correlated with serotype-specific neutralizing antibody titers, anti-DENV IgG1 levels, and a multitypic PRNT50 pattern (44). Interestingly, a higher level of ADCC activity measured before secondary DENV-3 infection was associated with lower subsequent viremia, which suggests a protective role for antibodies and NK cells; however, this association was not observed for secondary DENV-2 infection. In another study, ADCC was correlated with DENV surface antigen expression, suggesting recognition by anti-DENV antibodies (42), whose Fc region is then recognized by the activating low affinity CD16 (FcγRIII) receptor on NK cells (45).
Human NK cells (CD3−CD16+CD11b+ cells) can lyse DENV-infected cells to a greater level than uninfected cells even in the absence of antibodies, suggesting a mechanism of direct recognition as well (42, 43). These studies were performed using DENV-infected Raji cells as targets. The NK receptors and their ligands implicated in the direct recognition of DENV-infected cells have not been fully elucidated, indicating the need for future studies.
Expression of NK Cell Ligands during Dengue Disease
Viruses try to escape the immune response of the host. As NK cells are crucial players in the anti-viral response, many viruses induce the up-regulation of MHC I, which serve as ligands for NK inhibitory receptors, in order to dampen the NK cell response even if enhancing expression of MHC I might increase their recognition by CD8+ T cells (20). DENV and other flaviviruses induce the up-regulation of MHC I (46–51). Expression of flavivirus pr-M protein in hamster cells induced increased surface expression of MHC I, although the authors suggested this could be an incidental consequence of viral assembly rather than a specific mechanism of immune evasion (52). It has also been shown that human cell lines expressing the non-structural (NS) proteins of DENV up-regulate MHC I (HLA-A, -B, -C) expression at their surface by TAP-dependent and TAP-independent pathways (46). This resulted in a lower sensibility to lysis by NK cells, probably due to recognition by the corresponding inhibitory receptors (e.g., KIR2DL1 for HLA-C) and the inhibitory receptor LIR-1 that recognizes all MHC I proteins (Table 1). Further studies are needed to determine if MHC I up-regulation by DENV is the response to a particular viral protein, viral replication itself, or type-I IFNs induced by viral infection, and whether it plays a role in immune evasion of NK cells in vivo. Neurotropic flaviviruses, such as West Nile virus (WNV), can transiently activate and then suppress NK cell activity (53). Future studies are needed to determine if this happens during DENV infection by analyzing NK cell activity at different time points post-infection.
Even if DENV NS proteins induce MHC I up-regulation, NK cells can kill DENV-infected cells (28, 42, 43), suggesting that the signals for NK cell activation overcome the inhibitory signals. As described above, NK cells can kill DENV-infected cells by ADCC mediated by CD16 (42, 44) (Table 1), which is expressed on resting human NK cells and can induce a strong activating signal leading to cytolysis (20, 54). Interestingly, NK cells can also kill DENV-infected cells in the absence of antibodies (42), implicating a direct recognition by NK cell activating receptors. It has been reported that the activating receptor NKp44 can interact with the envelope protein (E) of DENV (55) (Table 1). NKp44 has also been implicated in killing WNV-infected cells after blocking the inhibitory receptor LIR-1 on NK cells, and this also induced IFNγ production. Further studies are necessary to determine if recognition of DENV-E by NKp44 on NK cells can induce a similar response against DENV-infected cells. NKp44 is expressed on activated, but not resting, NK cells (56) and can trigger NK cell killing of both tumor and virus-infected cells (57, 58).
Recently, a sequencing-based typing method and genotyping of asymptomatic DF and DHF patients in Cuba uncovered an association of certain alleles of the MICA and MICB genes (MICA*008 and MICB*008) with symptomatic DENV infection (59) (Table 1). The importance of MICB in dengue susceptibility was also indicated by GWAS with a large number of pediatric cases in Vietnam, where certain MICB and PLCE1 alleles showed a significant association with DSS (60). These results were confirmed by a study showing that MICB rs3132468 and PLCE1 risk genotypes were also associated with less severe clinical phenotypes of dengue in adults as well as with DENV infection in infants (61). This strongly suggests a role for this MICB variant in susceptibility to overall clinically apparent dengue disease. It still has not been determined whether the association between these NKG2D ligands and dengue clinical responses is directly due to the function of MICA/B molecules in dengue pathogenesis. Nonetheless, the importance of NKG2D ligands in the NK cell response against other viral infections (22) supports this hypothesis. Given the role of MICB in activation of NK, NKT, and CD8+ T cells through the NKG2D receptor, these findings support a central role for these cell types in shaping the outcome of DENV infection. It is plausible that the MICB risk-associated phenotype is associated with an impaired NK cell response, potentially resulting in a higher in vivo virus titer and an increased risk of developing both symptomatic and severe dengue. Furthermore, inefficient induction of cytokines secreted by NK cells might result in dysregulated T-cell responses that may also shape the clinical phenotype (62). NKG2D ligand (MICA/B) expression on DENV-infected cells may allow direct recognition by NK cells, which might be important for the early innate immune response against DENV infection, leading to either more effective control of viral infection or alternatively contributing to the disease pathology. The expression pattern of these NKG2D ligands in DENV-infected cells in vitro and in vivo needs to be determined. It is also necessary to determine if in acute viral infections such as DENV, the production of soluble NKG2D ligands can also be observed and if this impacts dengue clinical manifestations. Because ligands of other NK activating receptors, such as DNAM-1, can be induced by “stress” (23), further studies are needed to characterize all the NK receptor ligands induced during DENV infection, and the results may depend on the cell-type analyzed, as well as the DENV serotype. A complete characterization of DENV-infected cell recognition by NK cells (Figure 1) is crucial to better understanding the role of these cells in dengue disease.
Figure 1. Schematic model of NK cells interaction with DENV-infected cells. NK cells recognize infected cells through the interaction of their receptors with ligands on the infected cells, the outcome depends on the balance between activating or inhibitory signals. Once activated NK cells are capable of ADCC or direct cytotoxicity, and of producing cytokines, mainly IFNγ.
The innate immune response, and particularly type-I IFN and NK cells, plays a key role during the early infection events due to its ability to rapidly limit viral dissemination and to affect the antigen-specific, adaptive immune responses to effectively clear pathogens (8, 9). More studies in animal models and human populations will enable deciphering NK cell responses during DENV infection in vivo. Furthermore, in vitro experiments will also be needed to determine which NK receptors and ligands are implicated in DENV-infected cell recognition and NK cell-mediated killing and cytokine production. To date, only the up-regulation of MHC I and the induction of a putative NKp44 ligand (DENV-E protein) have been reported in DENV-infected cells. Are there other ligands that play a role in NK cell recognition induced during DENV infection? Genetic studies suggest an important role for the NKG2D ligands MICA and MICB; however, as yet no functional experiments have validated this hypothesis. There is still much to do to determine if ligands of other NK receptors, for example HLA-E for CD94/NKG2A-C and the ligands for the activating receptors 2B4 and DNAM-1, are induced or repressed during DENV infection, and whether this has an implication in the immune response to DENV and its clinical outcome. Finally, the characterization of NK receptor ligands and the NK cell phenotype in patients’ blood cells will provide insights into the NK cell subsets activated during dengue disease. It will also establish possible associations between NK cell activity or NK cell ligand expression and protection from disease and/or increased dengue severity. Whether DENV interferes with innate anti-viral immunity mediated by NK cells at early times of infection and whether DENV virulence might be associated with its ability to counter the host cell defenses are critical issues that remain to be elucidated.
Conflict of Interest Statement
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
The authors thank Eva Harris (University of California Berkeley) and Lewis Lanier (University of California San Francisco) for helpful comments and scientific discussion of the manuscript. The authors are supported by grants from Secretaría Nacional de Ciencia, Tecnología e Innovación, Panama (270-2013-288 to Davis Beltrán and 71-2012-4-CAP11-003 to Sandra López-Vergès).
2. Anon. Dengue: Guidelines for Diagnosis, Treatment, Prevention and Control. Geneva: World Health Organization and the Special Programme for Research and Training in Tropical diseases (2009). p. 25–8.
3. OhAinle M, Balmaseda A, Macalalad AR, Tellez Y, Zody MC, Saborío S, et al. Dynamics of dengue disease severity determined by the interplay between viral genetics and serotype-specific immunity. Sci Transl Med (2011) 3(114):114ra128. doi:10.1126/scitranslmed.3003084
9. Sun P, Kochel TJ. The battle between infection and host immune responses of dengue virus and its implication in dengue disease pathogenesis. ScientificWorldJournal (2013) 2013:843469. doi:10.1155/2013/843469
10. Durbin AP, Vargas MJ, Wanionek K, Hammond SN, Gordon A, Rocha C, et al. Phenotyping of peripheral blood mononuclear cells during acute dengue illness demonstrates infection and increased activation of monocytes in severe cases compared to classic dengue fever. Virology (2008) 376(2):429–35. doi:10.1016/j.virol.2008.03.028
11. Duyen HT, Ngoc TV, Hado T, Hang VT, Kieu NT, Young PR, et al. Kinetics of plasma viremia and soluble nonstructural protein 1 concentrations in dengue: differential effects according to serotype and immune status. J Infect Dis (2011) 203(9):1292–300. doi:10.1093/infdis/jir014
12. Libraty DH, Young PR, Pickering D, Endy TP, Kalayanarooj S, Green S, et al. High circulating levels of the dengue virus nonstructural protein NS1 early in dengue illness correlate with the development of dengue hemorrhagic fever. J Infect Dis (2002) 186(8):1165–8. doi:10.1086/343813
13. Srikiatkhachorn A, Wichit S, Gibbons RV, Green S, Libraty DH, Endy TP, et al. Dengue viral RNA levels in peripheral blood mononuclear cells are associated with disease severity and preexisting dengue immune status. PLoS One (2012) 7(12):e51335. doi:10.1371/journal.pone.0051335
14. Tricou V, Minh NN, Farrar J, Tran HT, Simmons CP. Kinetics of viremia and NS1 antigenemia are shaped by immune status and virus serotype in adults with dengue. PLoS Negl Trop Dis (2011) 5(9):e1309. doi:10.1371/journal.pntd.0001309
17. Della Chiesa M, Sivori S, Castriconi R, Marcenaro E, Moretta A. Pathogen-induced private conversations between natural killer and dendritic cells. Trends Microbiol (2005) 13(3):128–36. doi:10.1016/j.tim.2005.01.006
21. López-Botet M, Angulo A, Gumá M. Natural killer cell receptors for major histocompatibility complex class I and related molecules in cytomegalovirus infection. Tissue Antigens (2004) 63(3):195–203. doi:10.1111/j.1399-0039.2004.00210.x
23. Cerboni C, Fionda C, Soriani A, Zingoni A, Doria M, Cippitelli M, et al. The DNA damage response: a common pathway in the regulation of NKG2D and DNAM-1 ligand expression in normal, infected, and cancer cells. Front Immunol (2014) 4:508. doi:10.3389/fimmu.2013.00508
25. Matusali G, Tchidjou HK, Pontrelli G, Bernardi S, D’Ettorre G, Vullo V, et al. Soluble ligands for the NKG2D receptor are released during HIV-1 infection and impair NKG2D expression and cytotoxicity of NK cells. FASEB J (2013) 27(6):2440–50. doi:10.1096/fj.12-223057
26. Nolting A, Dugast AS, Rihn S, Luteijn R, Carrington MF, Kane K, et al. MHC class I chain-related protein A shedding in chronic HIV-1 infection is associated with profound NK cell dysfunction. Virology (2010) 406(1):12–20. doi:10.1016/j.virol.2010.05.014
27. Green S, Pichyangkul S, Vaughn DW, Kalayanarooj S, Nimmannitya S, Nisalak A, et al. Early CD69 expression on peripheral blood lymphocytes from children with dengue hemorrhagic fever. J Infect Dis (1999) 180(5):1429–35. doi:10.1016/j.jmb.2013.11.023
29. Wahid SF, Sanusi S, Zawawi MM, Ali RA. A comparison of the pattern of liver involvement in dengue hemorrhagic fever with classic dengue fever. Southeast Asian J Trop Med Public Health (2000) 31(2):259–63.
30. Chau TNB, Quyen NT, Thuy TT, Tuan NM, Hoang DM, Dung NT, et al. Dengue in Vietnamese infants – results of infection-enhancement assays correlate with age-related disease epidemiology, and cellular immune responses correlate with disease severity. J Infect Dis (2008) 198(4):516–24. doi:10.1086/590117
31. Azeredo EL, De Oliveira-Pinto LM, Zagne SM, Cerqueira DI, Nogueira RM, Kubelka CF. NK cells, displaying early activation, cytotoxicity and adhesion molecules, are associated with mild dengue disease. Clin Exp Immunol (2006) 143(2):345–56. doi:10.1111/j.1365-2249.2006.02996.x
32. Devignot S, Sapet C, Duong V, Bergon A, Rihet P, Ong S, et al. Genome-wide expression profiling deciphers host responses altered during dengue shock syndrome and reveals the role of innate immunity in severe dengue. PLoS One (2010) 5(7):e11671. doi:10.1371/journal.pone.0011671
33. Shresta S, Kyle JL, Robert Beatty P, Harris E. Early activation of natural killer and B cells in response to primary dengue virus infection in A/J mice. Virology (2004) 319(2):262–73. doi:10.1016/j.virol.2003.09.048
34. Shresta S, Sharar KL, Prigozhin DM, Snider HM, Beatty PR, Harris E. Critical roles for both STAT1-dependent and STAT1-independent pathways in the control of primary dengue virus infection in mice. J Immunol (2005) 175(6):3946–54. doi:10.4049/jimmunol.175.6.3946
35. St John AL, Rathore AP, Yap H, Ng ML, Metcalfe DD, Vasudevan SG, et al. Immune surveillance by mast cells during dengue infection promotes natural killer (NK) and NKT-cell recruitment and viral clearance. Proc Natl Acad Sci USA (2011) 108(22):9190–5. doi:10.1073/pnas.1105079108
36. Chen J-P, Lu HL, Lai SL, Campanella GS, Sung JM, Lu MY, et al. Dengue virus induces expression of CXC chemokine ligand 10/IFN-gamma-inducible protein 10, which competitively inhibits viral binding to cell surface heparan sulfate. J Immunol (2006) 177(5):3185–92. doi:10.4049/jimmunol.177.5.3185
37. Sung JM, Lee C-K, Wu-Hsieh BA. Intrahepatic infiltrating NK and CD8 T cells cause liver cell death in different phases of dengue virus infection. PLoS One (2012) 7(9):e46292. doi:10.1371/journal.pone.0046292
38. Renneson J, Guabiraba R, Maillet I, Marques RE, Ivanov S, Fontaine J, et al. A detrimental role for invariant natural killer T cells in the pathogenesis of experimental dengue virus infection. Am J Pathol (2011) 179(4):1872–83. doi:10.1016/j.ajpath.2011.06.023
39. Guabiraba R, Besnard AG, Marques RE, Maillet I, Fagundes CT, Conceição TM, et al. IL-22 modulates IL-17A production and controls inflammation and tissue damage in experimental dengue infection. Eur J Immunol (2013) 43(6):1529–44. doi:10.1002/eji.201243229
41. Fagundes CT, Costa VV, Cisalpino D, Amaral FA, Souza PR, Souza RS, et al. IFN-γ production depends on IL-12 and IL-18 combined action and mediates host resistance to dengue virus infection in a nitric oxide-dependent manner. PLoS Negl Trop Dis (2011) 5(12):e1449. doi:10.1371/journal.pntd.0001449
42. Kurane I, Hebblewaite D, Brandt WE, Ennis FA. Lysis of dengue virus-infected cells by natural cell-mediated cytotoxicity and antibody-dependent cell-mediated cytotoxicity. J Virol (1984) 52(1):223–30.
43. Kurane I, Hebblewaite D, Ennis FA. Characterization with monoclonal antibodies of human lymphocytes active in natural killing and antibody-dependent cell-mediated cytotoxicity of dengue virus-infected cells. Immunology (1986) 58(3):429–36.
44. Laoprasopwattana K, Libraty DH, Endy TP, Nisalak A, Chunsuttiwat S, Ennis FA, et al. Antibody-dependent cellular cytotoxicity mediated by plasma obtained before secondary dengue virus infections: potential involvement in early control of viral replication. J Infect Dis (2007) 195(8):1108–16. doi:10.1086/512860
45. Lanier LL, Kipps TJ, Phillips JH. Functional properties of a unique subset of cytotoxic CD3+ T lymphocytes that express Fc receptors for IgG (CD16/Leu-11 antigen). J Exp Med (1985) 162(6):2089–106. doi:10.1084/jem.162.6.2089
46. Hershkovitz O, Zilka A, Bar-Ilan A, Abutbul S, Davidson A, Mazzon M, et al. Dengue virus replicon expressing the nonstructural proteins suffices to enhance membrane expression of HLA class I and inhibit lysis by human NK cells. J Virol (2008) 82(15):7666–76. doi:10.1128/JVI.02274-07
47. Lobigs M, Blanden RV, Müllbacher A. Flavivirus-induced up-regulation of MHC class I antigens; implications for the induction of CD8+ T-cell-mediated autoimmunity. Immunol Rev (1996) 152:5–19. doi:10.1111/j.1600-065X.1996.tb00908.x
48. Lobigs M, Müllbacher A, Regner M. MHC class I up-regulation by flaviviruses: immune interaction with unknown advantage to host or pathogen. Immunol Cell Biol (2003) 81(3):217–23. doi:10.1046/j.1440-1711.2003.01161.x
49. Momburg F, Müllbacher A, Lobigs M. Modulation of transporter associated with antigen processing (tap) -mediated peptide import into the endoplasmic reticulum by flavivirus infection. J Virol (2001) 75(12):5663–71. doi:10.1128/JVI.75.12.5663-5671.2001
54. Bryceson YT, March ME, Ljunggren H-G, Long EO. Synergy among receptors on resting NK cells for the activation of natural cytotoxicity and cytokine secretion. Blood (2006) 107(1):159–66. doi:10.1182/blood-2005-04-1351
55. Hershkovitz O, Rosental B, Rosenberg LA, Navarro-Sanchez ME, Jivov S, Zilka A, et al. NKp44 receptor mediates interaction of the envelope glycoproteins from the West Nile and dengue viruses with NK cells. J Immunol (2009) 183(4):2610–21. doi:10.4049/jimmunol.0802806
56. Vitale M, Bottino C, Sivori S, Sanseverino L, Castriconi R, Marcenaro E, et al. NKp44, a novel triggering surface molecule specifically expressed by activated natural killer cells, is involved in non-major histocompatibility complex-restricted tumor cell lysis. J Exp Med (1998) 187(12):2065–72. doi:10.1084/jem.187.12.2065
58. Moretta A, Bottino C, Vitale M, Pende D, Cantoni C, Mingari MC, et al. Activating receptors and coreceptors involved in human natural killer cell-mediated cytolysis. Annu Rev Immunol (2001) 19:197–223. doi:10.1146/annurev.immunol.19.1.197
59. García G, del Puerto F, Pérez AB, Sierra B, Aguirre E, Kikuchi M, et al. Association of MICA and MICB alleles with symptomatic dengue infection. Hum Immunol (2011) 72(10):904–7. doi:10.1016/j.humimm.2011.06.010
60. Khor CC, Chau TN, Pang J, Davila S, Long HT, Ong RT, et al. Genome-wide association study identifies susceptibility loci for dengue shock syndrome at MICB and PLCE1. Nat Genet (2011) 43(11):1139–41. doi:10.1038/ng.960
61. Whitehorn J, Chau TN, Nguyet NM, Kien DT, Quyen NT, Trung DT, et al. Genetic variants of MICB and PLCE1 and associations with non-severe dengue. PLoS One (2013) 8(3):e59067. doi:10.1371/journal.pone.0059067
62. Lang PA, Lang KS, Xu HC, Grusdat M, Parish IA, Recher M, et al. Natural killer cell activation enhances immune pathology and promotes chronic infection by limiting CD8+ T-cell immunity. Proc Natl Acad Sci U S A (2012) 109(4):1210–5. doi:10.1073/pnas.1118834109
Keywords: dengue, NK cell, NK receptor, NK ligand, innate immune response
Citation: Beltrán D and López-Vergès S (2014) NK cells during dengue disease and their recognition of dengue virus-infected cells. Front. Immunol. 5:192. doi: 10.3389/fimmu.2014.00192
Received: 21 February 2014; Accepted: 18 April 2014;
Published online: 05 May 2014.
Edited by:Simona Zompi, University of California, Berkeley, USA
Reviewed by:Birgit Strobl, University of Veterinary Medicine Vienna, Austria
Alexis DeHaven Dunkle, Lawrence Livermore National Laboratory, USA
Copyright: © 2014 Beltrán and López-Vergès. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Sandra López-Vergès, Department of Research in Virology and Biotechnology, Gorgas Memorial Institute for Health Studies, Ave. Justo Arosemena and Calle No. 35, Panama City 0816-02593, Panama e-mail: firstname.lastname@example.org, email@example.com