Latent Membrane Protein LMP2A Impairs Recognition of EBV-Infected Cells by CD8+ T Cells
Epstein-Barr virus (EBV) is carried by most humans. It can cause several types of cancer. In healthy infected people, EBV persists for life in a "latent" state in white blood cells called B cells. For infected persons to remain healthy, it is crucial that they harbor CD8-positive "killer" T cells that recognize and destroy precancerous EBV-infected cells. However, this protection is imperfect, because the virus is not eliminated from the body, and the danger of EBV-associated cancer remains. How does the virus counteract CD8+ T cell control? Here we study the effects of latent membrane protein 2A (LMP2A), which is an important viral molecule because it is present in several types of EBV-associated cancers, and in latently infected cells in healthy people. We show that LMP2A counteracts the recognition of EBV-infected B cells by antiviral killer cells. We found a number of mechanisms that are relevant to this effect. Notably, LMP2A disturbs expression of molecules on B cells that interact with NKG2D, a molecule on the surface of CD8+ T cells that aids their activation. In this way, LMP2A weakens important immune responses against EBV. Similar mechanisms may operate in different types of LMP2A-expressing cancers caused by EBV.
Published in the journal:
. PLoS Pathog 11(6): e32767. doi:10.1371/journal.ppat.1004906
Category:
Research Article
doi:
https://doi.org/10.1371/journal.ppat.1004906
Summary
Epstein-Barr virus (EBV) is carried by most humans. It can cause several types of cancer. In healthy infected people, EBV persists for life in a "latent" state in white blood cells called B cells. For infected persons to remain healthy, it is crucial that they harbor CD8-positive "killer" T cells that recognize and destroy precancerous EBV-infected cells. However, this protection is imperfect, because the virus is not eliminated from the body, and the danger of EBV-associated cancer remains. How does the virus counteract CD8+ T cell control? Here we study the effects of latent membrane protein 2A (LMP2A), which is an important viral molecule because it is present in several types of EBV-associated cancers, and in latently infected cells in healthy people. We show that LMP2A counteracts the recognition of EBV-infected B cells by antiviral killer cells. We found a number of mechanisms that are relevant to this effect. Notably, LMP2A disturbs expression of molecules on B cells that interact with NKG2D, a molecule on the surface of CD8+ T cells that aids their activation. In this way, LMP2A weakens important immune responses against EBV. Similar mechanisms may operate in different types of LMP2A-expressing cancers caused by EBV.
Introduction
Epstein-Barr virus (EBV), which belongs to the human herpesvirus family, is a persistent virus carried by more than 90% of the adult population worldwide. EBV has a preferential B cell tropism, and latently infected B cells constitute the viral reservoir in healthy carriers [1]. Acute infection can lead to infectious mononucleosis (IM), a self-limiting lymphoproliferative disease characterized by expansion of EBV-infected B cells and virus-specific CD8+ T cells [2]. EBV is an oncovirus, and can contribute to the development of various cancers, such as Burkitt lymphoma, nasopharyngeal carcinoma and Hodgkin lymphoma [3,4]. In healthy carriers, EBV infection is under control of a diverse repertoire of antigen-specific T cells, and an important role is played by CD8+ T cells that recognize viral protein-derived peptides presented by MHC class I molecules [2]. In contrast, immunosuppressed patients who lack EBV-specific T cell responses, such as patients after transplantation, are prone to developing EBV-associated lymphoproliferative disease. This condition can be treated or prevented by transfer of EBV-specific T cells [5–7].
In immunocompetent EBV carriers, a majority of EBV-infected B cells in peripheral blood carry EBV without expressing any viral protein, a state that is called "true latency" or "latency 0" [4,8]. Thus, such latently infected B cells are invisible to EBV-specific T cells.
In contrast, during lytic EBV replication many viral proteins are expressed [9,10]. In this situation, the virus would be particularly vulnerable to immune control. Thus, EBV has evolved a number of proteins expressed in the lytic cycle that interfere with the display of viral antigens to CD8+ T cells. These proteins include BNLF2a, which inhibits the transporter of antigen processing [11], BILF1, which induces MHC class I internalization and degradation [12], and BGLF5, which inhibits cellular protein biosynthesis [13].
In proliferating infected B cells, EBV installs another program of gene expression, the "growth" or "latency III" program. This type of latency is found in in vitro EBV-induced lymphoblastoid cell lines (LCLs), in post-transplant lymphoproliferative diseases [14], as well as in EBV-infected B cells in lymphoid organs during primary and persistent EBV infection, where this program is thought to lead to amplification of EBV load through proliferation of infected cells [4,8]. Several immunogenic EBV antigens, the latent membrane proteins (LMP1, LMP2A, LMP2B) and the Epstein-Barr nuclear antigens (EBNA1, -2, -3A, -3B, -3C, -LP), are expressed in latency III EBV-infected B cells [9,10]. How do B cells expressing the EBV "growth program" manage to escape from recognition and elimination by virus-specific T cells? Previous studies on immunoevasion in EBV latency have focused on the nuclear protein EBNA1 or the latent membrane protein LMP1. EBNA1 interferes with its own presentation to CD8+ T cells through its glycine-alanine repeat domain [15,16], which reduces processing by the proteasome [17] and interferes in cis with EBNA1 translation [18–20]. As a result, presentation of EBNA1 epitopes on MHC class I to T cells is reduced. Likewise, LMP1 interferes in cis with presentation of its own epitopes [21]. Although several other viral proteins are expressed in the EBV growth program, it has remained unknown whether presentation to T cells of epitopes from these proteins may be suppressed by viral mechanisms.
The EBV latent protein LMP2A is a regular constituent of the EBV growth program, and is also expressed in a variety of EBV-associated cancers [9,10]. LMP2A has various functions in infected cells. Reminiscent of the accessory subunits of the B-cell receptor, the N-terminal cytoplasmic domain of LMP2A activates protein tyrosine kinases and induces downstream pathways of B cell activation [22,23]. Accordingly, LMP2A can stand in for deficient B-cell receptor signaling in mouse or human models, ensuring B cell survival [24,25]. In EBV-infected B cells, however, LMP2A counteracts lytic EBV reactivation triggered by cross-linking of the B-cell receptor [26–28]. No consensus has been reached yet on the importance of LMP2A in B cell proliferation and transformation [25,29–35].
Given these complexities, we hypothesized that LMP2A may have other functions that are not cell-intrinsic or directly related to virus replication, but related to immune control. This possibility was already suggested by the observation that LMP2A modulates signalling of type I/II interferon receptors in epithelial cells [36], that the presence of LMP2A alters the expression of several immune-related genes [37], and that LMP2A increases expression of the cytokine interleukin-10 (IL-10) [38], which may exert immunomodulatory functions. In this study, we investigated the influence of LMP2A in recognition of infected cells by immune effector cells. We show that LMP2A reduces recognition of infected B cells by EBV-specific CD8+ T cells, and we describe several mechanisms that may contribute to this effect.
Results
We established EBV-transformed B cell lines (lymphoblastoid cell lines, LCLs) with an EBV deleted for LMP2A [25]. This virus is deleted for the promoter and the first exon of LMP2A on a background of EBV strain B95.8. Expression of LMP2B is still possible in this mutant. In line with previous findings [25,29], we found that the LMP2A-deficient virus (ΔLMP2A) had reduced efficiency of B cell transformation. To facilitate the establishment of LMP2A-deficient LCLs, we infected primary B cells with mutant EBV on a layer of murine fibroblasts overexpressing human CD40 ligand (CD40L). Infection with recombinant EBV 2089 [39] that contains the complete B95.8 EBV genome (here denoted "wild-type", WT), which is parental to the ΔLMP2A construct, was carried out in parallel under the same conditions. Outgrowing B cell cultures were expanded and maintained in the absence of CD40L stimulators. Under these conditions, WT and ΔLMP2A LCLs could be established with similar efficiency, and expanded in parallel using the same procedures. A closer analysis of established WT and ΔLMP2A LCLs showed that the rate of apoptosis was the same, but proliferation was somewhat slower in ΔLMP2A LCLs (S1 Fig). Thus, LMP2A increased the efficiency of EBV transformation in vitro, but was not essential for the proliferation of established LCLs.
We analyzed the reactivity of EBV-specific CD8+ T cells to ΔLMP2A and WT LCLs (Fig 1). We found that CD8+ T cell clones specific for epitopes from all latent antigens tested (EBNA1, EBNA3A, LMP2) showed a higher IFN-γ release in response to ΔLMP2A LCLs than to WT LCLs (Fig 1A and 1C). CD8+ T cells specific for the LMP2 epitope CLG recognized ΔLMP2A LCLs, because the CLG peptide is derived from a transmembrane region that is shared between LMP2A and LMP2B. CD8+ T cell clones specific for lytic-cycle antigens (BRLF1, BZLF1) showed weak recognition of both types of LCLs, and therefore differences in recognition could not be detected (Fig 1B). Thus, LMP2A interferes with CD8+ T cell recognition of EBV latent antigens.
To confirm that these differences in T cell recognition were caused by LMP2A and not some other unrecognized deviations between the two EBV constructs, we tested the effect of LMP2A on CD8+ T cell recognition in isolation, in the absence of an EBV genome (Fig 1D). Co-transfection of LMP2A reduced CD8+ T cell recognition of 293T kidney cells transfected with the HCMV antigen pp65. This experiment showed that the effect of LMP2A on T cell recognition was not limited to the context of the EBV genome.
In the early stages of infection, there are differences in EBV gene transcription in B cells carrying LMP2A-negative EBV as opposed to LMP2A-positive EBV [35]. Thus, we investigated whether the observed differences in T cell recognition of ΔLMP2A and WT LCLs were related to differential expression of EBV antigens. Average transcript levels of several EBV latent antigens (EBNA1, EBNA3A, LMP2) appeared to be increased in ΔLMP2A LCLs (Fig 2A). However, this difference reached p < 0.05 only for EBNA1. No difference between WT and ΔLMP2A LCLs was seen for median expression of the lytic-cycle genes BZLF1 and gp350. Thus, LMP2A may downmodulate the expression of some latent antigens in EBV-infected B cells, in particular EBNA1. This may contribute to the reduced presentation of these antigens to CD8+ T cells by WT LCLs.
LMP1 is an EBV protein that may alter CD8+ T cell recognition of infected cells, in particular by inducing MHC I pathway components through NF-κB, but also by inducing immunomodulatory genes [21,40]. We found that expression of LMP1 at the protein level was somewhat reduced in ΔLMP2A LCLs (Fig 2B). This argued against a possible role of LMP1 in contributing to increased recognition of ΔLMP2A LCLs by upregulating MHC I presentation.
Next, we investigated whether LMP2A modulated the reactivity of CD8+ T cells to EBV-infected B cells by mechanisms other than altering the availability of EBV antigens. We loaded WT and ΔLMP2A LCLs exogenously with peptides CRV and VLE, derived from the human cytomegalovirus (HCMV) protein IE-1, and we analyzed LCL recognition by HCMV-specific CD8+ T cell clones (Fig 3). Peptide-loaded ΔLMP2A LCLs were more strongly recognized by these CD8+ T cells than peptide-loaded WT LCLs, resulting in higher IFN-γ release. We also investigated direct killing by cytotoxic CD8+ T cells, but did not observe differences in killing of WT and ΔLMP2A LCLs loaded with HCMV peptides (S2 Fig). The reasons for differential regulation of IFN-γ secretion and direct cytotoxicity in this setting remain to be elucidated.
Because the intracellular antigen processing machinery was bypassed in these peptide-loading experiments, LMP2A appears to act on CD8+ T cells through mechanisms other than regulation of EBV antigens or of intracellular processing pathways. Therefore, we studied the effect of LMP2A on cell surface-residing or secreted factors relevant for CD8+ T cell recognition.
It was recently shown that LMP2A increases IL-10 production in infected B cells [38]. The possibility of a similar effect in our system was intriguing, because cellular IL-10 and its viral homolog reduce the antiviral activity of different types of immune effector cells [41–43]. In accordance with Incrocci and colleagues [38], we found that WT LCLs released higher amounts of IL-10 than LCLs lacking LMP2A (Fig 4A). These levels of secreted IL-10 were not mirrored by transcription levels for human IL-10 (Fig 4B), which suggested an effect of LMP2A on post-transcriptional regulation of IL-10 [44]. In contrast to cellular IL-10, transcription of viral IL-10 was very low in each type of LCL (Fig 4B), in accordance with its description as a lytic-cycle gene [45]. To determine whether differences in IL-10 release could directly influence T cell reactivity to LCLs, we used specific antibodies to block IL-10 receptor on CD8+ T cells (Fig 4C and 4E), or to neutralize IL-10 in the supernatant (Fig 4D and 4F). In each case, recognition of WT or ΔLMP2A LCLs was not altered. Thus, modulation of IL-10 secretion by LMP2A did not directly affect the ability of CD8+ T cells to recognize infected B cells. This experiment did not rule out indirect effects of secreted IL-10, which may act back on the LCLs over time in culture and modulate their immunogenicity.
We continued by analyzing ΔLMP2A and WT LCLs for cell surface molecules involved in the interaction between CD8+ T cells and LCLs. First, we determined the levels of total MHC-I and individual MHC-I allotypes (Fig 5). MHC-I was marginally increased in LCLs deleted for LMP2A as compared with WT LCLs (p = 0.0046). A similar tendency was observed for some of the individual MHC-I allotypes, but did not reach p < 0.05.
Next, we examined whether expression of selected costimulatory and immunomodulatory molecules on the surface of LCLs was altered in the absence of LMP2A (Fig 6). We found strong differences in expression for some of these molecules. The coinhibitory B7 family molecule PD-L1 (B7-H1) was (somewhat unexpectedly) induced in ΔLMP2A LCLs, whereas the costimulatory B7 molecule CD86 was equally expressed on ΔLMP2A and WT LCLs. CD11a, the α chain of the integrin LFA-1 that plays important roles in the immunological synapse, was strongly downregulated in the absence of LMP2A, whereas ICAM-1 (CD54), its counterpart, was expressed equally in the presence or absence of LMP2A. So far, these alterations were not obviously connected with the increased susceptibility of ΔLMP2A cells to CD8+ T cell recognition.
Recent reports suggested that EBV infection induces ligands of the coactivatory receptor NKG2D, a molecule expressed on T and NK cells [46–49]. However, a comprehensive analysis of NKG2D ligands on LCLs has not previously been performed. Our analyses by flow cytometry showed that EBV infection induced the expression of three NKG2D ligands (MICA, MICB and ULBP4) on LCLs (Fig 6). These molecules were not expressed on primary B cells. Markedly higher levels of MICA and ULBP4 were detected on ΔLMP2A LCLs as compared to WT LCLs, whereas MICB levels did not differ (Fig 6). We could not detect expression of the other five NKG2D ligands (ULBP1, 2, 3, 5, 6) on the surface of WT or ΔLMP2A LCLs with available monoclonal antibodies, but this does not rule out that these molecules may as well be modulated by LMP2A. Our results suggested a possible contribution of NKG2D ligands to differential recognition of LCLs by CD8+ T cells.
We tested the functional relevance of differential NKG2D ligand expression for CD8+ T cell recognition. An analysis of NKG2D levels on several CD8+ T cell clones showed that all were positive for NKG2D (Fig 7A). Differences in NKG2D expression levels were not correlated with antigen specificity. When we blocked NKG2D on EBV-specific CD8+ T cells with a specific antibody, IFN-γ release after contact with LCLs was reduced (Fig 7B–7D). A reduction in the reactivity of CD8+ T cells to both WT and mutant LCLs was observed after blocking, but reduction was even slightly stronger for ΔLMP2A LCLs than for WT LCLs (Fig 7C and 7D). Likewise, blocking NKG2D on HCMV-specific CD8+ T cell clones led to reduced recognition of peptide-loaded LCLs (Fig 7E). Thus, NKG2D ligands on LCLs contribute to their recognition by CD8+ T cells irrespective of antigen specificity. LMP2A reduces CD8+ T cell recognition of EBV-infected B cells by reducing the expression of NKG2D ligands.
Since expression of PD-L1, a ligand of the immunomodulatory receptor PD-1 on T cells, was increased on ΔLMP2A LCLs (Fig 6), the question emerged whether PD-L1 may counteract T cell recognition of ΔLMP2A LCLs. In this case, even greater differences in T cell recognition of ΔLMP2A LCLs as opposed to WT LCLs might be revealed by masking the effects of PD-L1. Since it was reported that stimulation of PD-L1 on LCLs induces their apoptosis in a T-cell-independent manner [50], we used a PD-1-blocking antibody, EH12.2H7, that was described to interfere with T-cell-inhibitory interactions of PD-L1 and PD-1 [51]. Thus, we tested blocking antibodies to NKG2D and PD-1 in T cell recognition assays. Interestingly, blockade of PD-1 did not increase T cell recognition of ΔLMP2A LCLs, but reduced it, although less so than blockade of NKG2D (Fig 8). Addition of PD-1 antibody to NKG2D antibody did not further modify recognition of ΔLMP2A LCLs, although recognition of WT LCLs was additively reduced by the two antibodies. We conclude that the increased amounts of PD-L1 on ΔLMP2A LCLs did not counteract T cell recognition and resulting IFN-γ production.
Discussion
In this report, we show that LMP2A interferes with CD8+ T cell recognition of latently infected B cells, and identify several mechanisms that may contribute to this interference. First, we found that LMP2A decreased mRNA expression levels of EBV latent antigens targeted by CD8+ T cells, in particular EBNA1. Second, LMP2A downregulated MHC class I, although to a limited extent. Third, two ligands of the coactivatory receptor NKG2D were strongly upregulated in LMP2A-deficient LCLs, and blocking of NKG2D reduced T cell recognition of infected cells. We conclude that LMP2A hampers CD8+ T cell recognition of infected cells through different mechanisms including regulation of NKG2D ligands.
A basis for the present work was the efficient generation of ΔLMP2A LCLs. The importance of LMP2A for human B cell transformation by EBV has been controversial: some studies did not identify a role of LMP2A [30–34], but others reported that LMP2A increases B cell proliferation and transformation [25,29,35]. In our experience, LMP2A is important for establishment of EBV latent infection in vitro, as we found it difficult to establish ΔLMP2A LCLs under standard conditions. However, when we supplemented a strong CD40 stimulus for the first days after infection [52,53], ΔLMP2A LCLs and WT LCLs could be generated with similar yield, and ΔLMP2A LCLs could then be maintained autonomously. This finding confirmed that LMP2A is not essential for maintenance and proliferation of established LCLs, as long as the B cell receptor is expressed [25].
Another important function of LMP2A is its role in "stabilizing latency", i.e. prevention of lytic-cycle induction. A complex picture has emerged, in which LMP2A interferes with lytic induction after exogenous B-cell receptor stimulation [26–28,30,54], but induces basal levels of lytic gene expression in the absence of such a stimulus [55]. In accordance with earlier results [35], we found that baseline lytic gene expression was low both in WT and ΔLMP2A, and therefore was without consequence for recognition by T cells [2,56]. Thus, the "latency-stabilizing" function of LMP2A does not appear to be relevant for T cell recognition of B cells that express the growth program in the absence of exogenous triggers. It remains to be investigated whether the immunomodulatory functions of LMP2A extend to cells in lytic cycle.
Two EBV latent proteins, EBNA1 and LMP1, were previously shown to modulate antigen presentation to CD8+ T cells. EBNA1 does not affect presentation of other antigens, but specifically interferes in cis with its own presentation by blocking its own proteasomal processing [17] and modulating its translation [19,20], both through its glycine-alanine-rich domain. LMP1 is a strong inducer of MHC I presentation through activation of the NF-κB pathway [21,57], but contains a structural element that acts in cis to protect epitopes derived from its own sequence from efficient presentation [21]. LMP1 is also unusual in that peptides derived from secreted LMP1 were shown to interfere with T cell activation [58]. However, this requires amounts of LMP1 that are much higher than those secreted by EBV-infected cells [58]. To our knowledge, it has remained untested whether EBV latent antigens more generally affect recognition by and activation of CD8+ T cells.
Suggestions regarding a role of LMP2A in T immune modulation emerged from comprehensive microarray-based analyses of LMP2A-mediated changes to the transcriptome of mouse and human B cells [37]. Interestingly, transcription of genes in the inflammation/immunity category, including interferon-regulating factors, was repressed by LMP2A in human LCLs, whereas no such genes were induced [37]. Among genes of direct relevance for the B-cell—T-cell interface, CD86 was induced and LFA-1 was repressed by LMP2A in BJAB cells, but no differential expression of these genes was found in LCLs with or without LMP2A [37]. These findings highlight that the effects of LMP2A depend on the cellular context, and that T-cell-modulatory functions of LMP2A in more restricted modes of EBV latency may hypothetically be even stronger than in the LCL system studied here. For example, the ability of LMP2A to interfere with signaling through interferon receptors [36] may further contribute to LMP2A-mediated evasion from T cell recognition.
Our data demonstrated that LMP2A markedly reduced the reactivity of EBV-specific CD8+ T cells against LCLs. This was true for all latent EBV antigens investigated (LMP2, EBNA1, EBNA3A). The epitopes we analyzed are processed by different pathways for their presentation: CLG and FLY are TAP-independent epitopes, with FLY being immunoproteasome-dependent [59,60], while RPP and HPV are TAP-dependent [61]. A reduction of CD8+ T cell reactivity was also observed on LCLs loaded with exogenous peptides from a different pathogen, which makes it clear that LMP2A does not exclusively affect intracellular mechanisms of antigen provision and presentation. Reduced CD8+ T cell reactivity in the presence of LMP2A was observed in the context of all HLA allotypes that were studied: HLA A*0201, B*0702, and B*3501 for intracellularly processed EBV epitopes, HLA A*0201 and C*0702 for exogenously loaded HCMV epitopes. Thus, our data indicate that LMP2A affects CD8+ T cell reactivity regardless of the identity of the peptide presented, the mechanism of processing, or the presenting HLA molecule.
However, our results also suggested an antigen-specific aspect to the immunomodulatory effects of LMP2A, because we found a trend toward elevated expression of several latent genes in the absence of LMP2A. This is in line with the idea that LMP2A may mediate global B-cell transcription factor regulation to reduce expression of EBV latency proteins [62,63]. This was not true for LMP1, however, whose protein expression in the absence of LMP2A was reduced. Our findings are in line with similar tendencies in EBV latent gene expression in the first seven days after B cell infection with EBV ΔLMP2A [35]. It is intriguing that EBNA1 was the EBV latent antigen whose mRNA expression was most clearly reduced by LMP2A, since both antigens are part of the restricted EBV gene expression spectrum in latency II EBV malignancies such as nasopharyngeal carcinoma and Hodgkin lymphoma [64,65]. If LMP2A interferes with presentation of EBNA1-derived and other peptides also in latency II type cancers, this will have important implications for their immune surveillance.
Among immunomodulatory cytokines, IL-10 was a particularly interesting candidate in our context, because it is constitutively produced at high levels by EBV-transformed B cells [66,67], and a recent report showed that LMP2A increased IL-10 production in Burkitt lymphoma cell lines [38]. Moreover, EBV encodes a viral homologue of human IL-10 [68]. Both human and viral IL-10 were suggested early on to interfere with cellular immune responses to EBV [41,69], but it may be difficult to distinguish an immunomodulatory function of cellular or viral IL-10 from their function as growth factors for EBV-infected B cells [66,70,71]. vIL-10 contributes to downregulation of the transporter of antigen processing 1 (TAP1) and MHC-I in the early phase of B cell infection [43], but recognition of early-infected B cells by EBV-specific CD8+ T cells was not increased in the absence of vIL-10 [42]. Our data showed that LCLs lacking LMP2A released lower amounts of IL-10 compared to WT LCLs, but reactivity of CD8+ T cell clones was not altered by neutralization of IL-10 or blocking of the IL-10 receptor. However, a more indirect role of IL-10 remains possible. Therefore, LCL-secreted IL-10 may act back on the LCLs over time, and thus downregulate MHC-I or other relevant molecules [43,72] in WT LCLs more strongly than in ΔLMP2A LCLs.
PD-1 is an immunomodulatory receptor found on activated T cells, on exhausted virus-specific T cells in chronic infection, but also on functional EBV-specific effector memory T cells in latent infection [73]. Blocking of the interaction between PD-1 and its ligand, PD-L1, may restore antiviral T cell function [74]. Somewhat counter-intuitively, we found PD-L1 to be downregulated in LCLs in the presence of LMP2A. When we blocked PD-1 on CD8+ T cells, we did not observe increased reactivity to LCLs, but rather a reduction in reactivity. The possibility remains that PD-L1 on EBV-infected B cells exerts a more long-term influence on shaping specific CD8+ T cell repertoires and functions that was not tested in our experiments.
NKG2D is an agonistic receptor on T and NK cells and recognizes a number of ligands that are upregulated on target cells in conditions such as malignant transformation, viral infection or heat shock [75]. Increased expression of some NKG2D ligands after EBV infection was described [46–48,76], but a comprehensive analysis of NKG2D ligands on LCLs has been lacking. Our analysis of the eight known NKG2D ligands showed that EBV infection induced the expression of three of them (MICA, MICB, and ULBP4), and that induction of MICA and ULBP4 was even more increased in the absence of LMP2A. In addition, we demonstrated that blocking of NKG2D on CD8+ T cells distinctly affected the recognition of LCLs by these effector cells. A recent study has shown that in patients with genetic deficiencies in the magnesium transporter MAGT1, who are particularly susceptible to EBV infection and EBV+ lymphomas, NKG2D plays an important role in the control of EBV infection by NK and CD8+ T cells [46]. A role for NKG2D in control of EBV-associated cancer has been further illustrated in a mouse model of LMP1-induced cancer that could be therapeutically targeted through NKG2D [76]. Targeting of the NKG2D ligand MICB by an EBV-encoded miRNA may decrease susceptibility of EBV-infected B cells to lysis by NK cells [77]. Thus, NKG2D ligands represent important coagonists for EBV-specific adaptive and innate immunity, and it appears an efficient strategy for the virus to blunt cellular immune responses by decreasing surface expression of NKG2D ligands through the action of LMP2A.
Taken together, we describe here a functional immunomodulatory effect for the EBV protein LMP2A, and show that LMP2A mediates partial escape of infected B cells from recognition by CD8+ T cells. Several immunoevasive mechanisms are driven by LMP2A in EBV-infected B cells. Thus, it will be urgent to determine the role played by LMP2A in evasion from T and NK cell recognition in other modes of EBV infection, and in different types of EBV-associated lymphoproliferative and malignant diseases.
Materials and Methods
Ethics statement
Mononuclear cells were isolated from standard blood donations by anonymous healthy adult donors purchased in the form of buffy coats from the Institute for Transfusion Medicine, University of Ulm, Germany, or from voluntary healthy adult blood donors providing written informed consent. The institutional review board (Ethikkommission, Klinikum der Universität München, Grosshadern, Munich, Germany) approved this procedure. All work was conducted according to the principles expressed in the Helsinki Declaration.
Virus production
Virus-producing cell lines for recombinant EBV 2089 (EBV WT), derived from EBV strain B95.8 [39], and its ΔLMP2A-deleted derivative EBV 2525 [25] were provided by Wolfgang Hammerschmidt [25,39]. In 293HEK-derived EBV producer cell lines, which stably carry the EBV genome in an episomal form, the viral lytic cycle was induced by transient transfection of expression plasmids coding for transcription factor BZLF1 and glycoprotein gp110/BALF4 [78]. EBV-containing supernatant was harvested three days later, centrifuged to reduce cellular debris, filtered (0.8 μM), and stored at 4°C. Titer of infectious virus was determined by infecting Raji cells for three days and quantifying GFP-positive cells as described [78]. Infection of B cells was performed at 0.1 virus units per cell.
B cells and LCLs
Standard cell culture medium was RPMI 1640 with 10% foetal bovine serum, 100 U/ml penicillin, 100 μg/ml streptomycin (all from Invitrogen), and 100nM sodium selenite (ICN). Stimulator cell line LL8 was generated by stable transfection of L929 mouse fibroblasts with an expression plasmid for human CD40 ligand carrying a G418-selectable marker, followed by two rounds of single-cell cloning under selection. We found this stimulator cell line to be functionally analogous to the one described earlier [53,79]. Lymphoblastoid cell lines were established from primary B cells purified from freshly isolated PBMCs. Untouched B cells were negatively isolated using Human B Cell Isolation Kit II (Miltenyi Biotec, Bergisch Gladbach, Germany). Enrichment of B cells was verified by flow cytometry (anti-CD19 clone HIB19; anti-CD3 clone HIT3a, Biolegend), and was in the range of 95–98%. B cells were plated at 1×105 cells/well in 24-well plates on an adherent cell layer of irradiated (180 Gy) CD40 ligand-expressing LL8 cells in standard medium supplemented with 1 mg/mL cyclosporine A (Novartis). B cells were infected with 0.1 virus units per cell. Half of the culture supernatant was exchanged at day 1 post infection. Outgrowing cultures were transferred after 1–2 weeks to a fresh plate, and further cultivated autonomously in the absence of LL8 cells. Presence of mutant EBV and absence of endogenous EBV wild type was confirmed by PCR every few weeks with primers L2BRC (5'-GCTTCCTCGTGCTTTACGGTATC-3') and L2BRD (5'-AAGAACTTTGACCTGTTGTCCCTG-3') for amplification of a product bridging the LMP2A deletion, primers L2INA (5'-CATTGCGGGTGGATAGCCTC-3') and L2BRD for amplification of the deleted sequence. Proliferating EBV-infected LCLs were analyzed and used in T cell assays between 1.5 and 4 months after infection.
DNA transfection
DNA transfection experiments were performed with 293T human embryonic kidney cells with a plasmid expressing HCMV pp65 fused to a destabilized green fluorescent protein (GFP) under the HCMV immediate-early promoter (provided by Manuel Albanese and Wolfgang Hammerschmidt) (pp65-GFP). A plasmid expressing full-length LMP2A under the control of the SV40 early promoter (pSV-LMP2A) and the corresponding control (pSV) were used for co-transfection. The pp65-GFP plasmid and pSV plasmids were used at a 1:10 ratio. One day before transfection, 293T cells were plated in 24-well plates (1×105 cells/well). Transfection was performed with a mix of 1.17 μl of Metafectene Pro (Biontex) and 390 ng of plasmid DNA in a volume of 100 μl of OptiMEM (Gibco) for each well, according to the manufacturer's protocol. Two days after transfection, cells were used for T cell assays and assessment of transfection efficiency by FACS. About 40–50% of cells were GFP-positive.
T cell clones
To identify EBV-positive donors among anonymously purchased buffy coats, serum-containing cell-free supernatant was tested for IgG specific for EBV EBNA1 and VCA by a rapid immunofiltration assay (RDT EBV IgG Assay, Bio-Rad). EBV-specific T cells were directly isolated from PBMCs of EBV-seropositive, HLA-typed donors after stimulation with a matched peptide and IFN-γ secretion assay (Miltenyi Biotec). For single T cell cloning, isolated IFN-γ-secreting cells were seeded into round-bottom 96-well plates at 0.7 or 2.5 cells per well in 200 μl of medium supplemented with 1000 U/mL rIL-2, 1×105/mL irradiated (50 Gy) HLA-matched LCLs, and 1.5×106/mL of a mixture of irradiated (50 Gy) allogeneic PBMCs from at least three different donors. Outgrowing T cell clones were expanded in round-bottom 96-well plates by restimulating every 2 weeks under the same conditions. The specificity of the T cell clones was determined by IFN-γ ELISA with individual antigenic peptides (see below), and by staining with HLA-peptide pentamers (Proimmune, Oxford, UK). The T cell clones were specific for the following epitope peptides, abbreviated by their first three amino acids in one-letter code: CLG (CLGGLLTMV, LMP2, A*0201) [80], YVL (YVLDHLIVV, BRLF1 A*0201) [81], FLY (FLYALALLL, LMP2, A*0201) [60,82], RPP (RPPIFIRRL, EBNA3A, B*0702) [83], RAK (RAKFKQLL, BZLF1, B*0801) [84], HPV (HPVGEADYFEY, EBNA1, B*3501) [85]. HCMV-specific CD8+ T cells clones specific for NLV (NLVPMVATV, pp65, A*0201) [86], CRV (CRVLCCYVL, IE-1, C*0702) [87] and VLE (VLEETSVML, IE-1, A*0201) [88] were obtained as described [87].
Flow cytometry
Flow cytometric analysis was performed with a BD FACS Calibur or a BD LSR Fortessa machine. Analysis of WT and mutant LCLs lacking LMP2A established from the same donor was always conducted in parallel and for at least one WT line and one ΔLMP2A line. Generally, 1–1.5×105 cells were stained in a V-bottom 96-well plate at 4°C for 20 minutes in a volume of 20 μl, washed twice in 200 μl of buffer (PBS + 2% FCS), resuspended in buffer, and analyzed immediately. When unlabeled antibodies were included in the staining that required counterstaining with labeled anti-Ig antibodies, two to three rounds of staining and washing were performed as necessary. Antibodies anti-MICA (clone 159227, unlabeled), anti-MICB (clone 236511, unlabeled), and anti-ULBP1 (clone 170818, unlabeled) were from R&D Systems and were counterstained with anti-IgG-APC (clone Poly4053) from Biolegend. Anti-ULBP2/-5/-6 (clone 165903, PE-labeled) and anti-ULBP3 (clone 166510, PE-labeled), were from R&D Systems; anti-ULBP4 (6E6, unlabeled) was from Santa Cruz; anti-CD11a (clone G43-25B, PE-labeled) was from BD Bioscience; anti-CD48 (clone 5F4, PE-labeled), anti-PD-L1 (clone 29E.2A3, APC-labeled), anti-CD86 (clone IT2.2, APC-labeled), anti-ICAM-1 (clone HCD54, APC-labeled), anti-HLA-ABC (clone W6/32, APC-labeled), and anti-HLA-A2 (clone BB7.2, PE-labeled) were from Biolegend; and anti-HLA-B7 (clone BB7.1) was from Millipore. Antibody anti-HLA-A3 (clone 4i87, IgM, USB) was counterstained with anti-IgM-PE (clone RMM-1; BioLegend). A hybridoma producing the HLA-C/HLA-E-specific antibody DT9 (IgG2b) was kindly provided by Véronique Braud, Nice, France [89], and counterstained with anti-mouse IgG-APC (clone Poly4053) from Biolegend. HLA-Bw6 was stained with a PE-labeled human antibody (REA143, 130-099-843) from Miltenyi Biotec. Isotype controls were IgG2A (clone 133304) and IgG2B (clone 133303) from R&D Systems; IgG1 (clone MOPC-21), IgG2A (clone MOPC-173), and IgG2B (clone MG2b-57) from Biolegend.
T cells were stained with antibodies anti-NKG2D (1D11, APC-labelled), anti-CD8 (RPA-T8, Pacific Blue- or FITC-labelled), anti-CD3 (HIT3a, PE-Cy5-labelled) from BioLegend.
Combined analysis of proliferation and apoptosis of LCLs was performed using CellTrace Violet (Life Technologies), AnnexinV-Cy5 conjugate (ApoScreen, Southern Biotech), and propidium iodide (PI, Life Technologies). One million cells was stained with 1 μl of CellTrace Violet in 1 ml PBS, washed, cultivated in 3 ml of full medium in a 12 well plate at 1x106 cells/well, and incubated for 4 days. Cells were harvested, counted, and 2.5×105 cells were stained in 200 μl buffer with 2 μl of AnnexinV-Cy5 and propidium iodide at 1 μg/ml, before proceeding to flow cytometric analysis.
T cell effector assays
For IFN-γ ELISA, effector cells (2.5×104 cells/well) and target cells (5×104 cells/well) were co-cultivated in 200 μl/well in a V-bottom 96-well plate at 37°C and 5% CO2. For IL-10 ELISA, LCLs were plated at 5×105 cells/ml in a 12-well or V-bottom 96-well plate and incubated at 37°C and 5% CO2. Supernatants were harvested after 16–18 hours. ELISA was performed according to the manufacturer's instructions (Mabtech, Nacka, Sweden). Blocking by specific purified antibodies was performed where indicated. Antibody was added to the effector cells (anti-NKG2D, anti-IL10R) or to the target cells (anti-IL10) at a pre-established concentration and incubated for 1 hour at 37°C prior to the addition of the target or effector cells, respectively. We used antibodies to IL-10 and IL-10R that were previously shown to neutralize activity at the same or lower concentrations [90–92]. Antibodies used for blocking, and matched isotype controls, were all low-endotoxin, azide-free (LEAF) and purchased from Biolegend: anti-NKG2D (clone 1D11, used at 50 μg/ml) with isotype (mouse IgG1, clone MOPC-21), anti-IL10R (clone 3F9, used at 20 μg/ml) with isotype (rat IgG2a, clone RTK2758), anti-IL10 (clone JES3-9D7, used at 20 μg/ml) with isotype (rat IgG1, clone RTK2071), anti-PD-1 (clone EH12.2H7, used at 10 μg/ml) with isotype (mouse IgG1, clone MOPC-21). Investigation of the recognition by CD8+ T cell clones of WT and ΔLMP2A LCLs established from the same donor was always performed in parallel and for at least one WT line and one ΔLMP2A line. Statistical analysis was performed with GraphPad Prism software.
The cytotoxic reactivity of CD8+ T cell clones against target cells was measured by calcein-release assay. Target cells (4×105) were labeled with 1 μg/ml in 500 μl medium. After incubation for 1 hour at 37°C cells were washed 3 times with sterile PBS, and 5×103 target cells/well were plated in a V-bottom 96-well plate (final volume 200 μl/well). For each target cell type, spontaneous release (no effector cells, 0% lysis) and maximal release (addition of 0.5% of triton-X 100, 100% lysis) was determined. Effector cells were co-incubated with target cells for 3 hours at a 2:1 ratio. Afterwards, 100 μl of supernatant were collected and transferred to a fresh flat-bottom 96-well plate and fluorescence intensity at 485/535 nm was measured in an Infinite F200 PRO fluorometer (Tecan). RPMI without phenol red was used to reduce background fluorescence.
Quantitative RT-PCR
Total RNA was extracted from LCLs with the RNeasy Mini Kit, and cDNA synthesis was performed with the QuantiTect kit, both from Qiagen, Hilden, Germany. Quantitative PCR was performed on a LightCycler 480 (Roche, Basel, Switzerland) using the SYBR Green LC480 Mix. Primers were as follows: human IL-10 (forward: 5'-GCAGGTGAAGAATGCCTTTA-3', reverse: 5'-CCCTGATGTCTCAGTTTCGT-3'), BZLF1 unspliced (forward: 5'-GCACATCTGCTTCAACAGGA-3', reverse: 5'-CCAAACATAAATGCCCCATC–3'), EBNA1 (forward: 5'-CGCAAGGAATATCAGGGATG-3', reverse: 5'-TCTCTCCTAGGCCATTTCCA-3'), gp350 (forward: 5'- TTGTGAAATTTCGCCATCCT-3', reverse: 5'-CAAAACCCCGTGTACCTG-3'). Primers specific for BCRF1 (vIL-10), EBNA3A, LMP2AB, and GUSB were described before [42]. Specific mRNA expression was standardized to the housekeeping gene β-glucuronidase (GUSB) [91,93]. WT and ΔLMP2A LCLs simultaneously established from the same donor were always analyzed in parallel.
Analysis of protein levels
Cells were incubated for 15 min on ice with lysis buffer (50 mM Tris/HCl pH 7.4, 150 mM NaCl, 1% NP40, 0.5% DOC, 0.1% SDS) together with protease inhibitor (completeMini, Roche). Protein concentration was determined with the Bio-Rad Protein Assay. Proteins were separated on an 8% SDS-PAGE gel and transferred to a nitrocellulose membrane by semi-dry blotting. Blots were probed with antibodies specific for LMP1 (1G6, provided by Elisabeth Kremmer, 1:25 dilution) [94] and GAPDH (1A7, 1:10 dilution). Blots were further probed with secondary antibodies conjugated to horseradish peroxidase, and immunoreactive proteins were detected by incubation with chemoluminescence substrate (0.1M Tris/HCl, pH 8.8, 200 mM p-Coumaric Acid in DMSO, 1.25 mM Luminol in DMSO) and exposure of CEA RP NEW films (Agfa HealthCare, Belgium).
Supporting Information
Zdroje
1. Thorley-Lawson DA, Hawkins JB, Tracy SI, Shapiro M (2013) The pathogenesis of Epstein-Barr virus persistent infection. Curr Opin Virol 3: 227–232. doi: 10.1016/j.coviro.2013.04.005 23683686
2. Hislop AD, Taylor GS, Sauce D, Rickinson AB (2007) Cellular responses to viral infection in humans: lessons from Epstein-Barr virus. Annu Rev Immunol 25: 587–617. 17378764
3. Rickinson AB (2014) Co-infections, inflammation and oncogenesis: Future directions for EBV research. Semin Cancer Biol
4. Young LS, Rickinson AB (2004) Epstein-Barr virus: 40 years on. Nat Rev Cancer 4: 757–768. 15510157
5. Moosmann A, Bigalke I, Tischer J, Schirrmann L, Kasten J et al. (2010) Effective and long-term control of EBV PTLD after transfer of peptide-selected T cells. Blood 115: 2960–2970. doi: 10.1182/blood-2009-08-236356 20103780
6. Moosmann A, Hammerschmidt W, Kolb HJ (2012) Virus-specific T cells for therapy—approaches, problems, solutions. Eur J Cell Biol 91: 97–101. doi: 10.1016/j.ejcb.2011.04.001 21640430
7. Rooney CM, Smith CA, Ng CY, Loftin SK, Sixbey JW et al. (1998) Infusion of cytotoxic T cells for the prevention and treatment of Epstein-Barr virus-induced lymphoma in allogeneic transplant recipients. Blood 92: 1549–1555. 9716582
8. Hochberg D, Middeldorp JM, Catalina M, Sullivan JL, Luzuriaga K et al. (2004) Demonstration of the Burkitt's lymphoma Epstein-Barr virus phenotype in dividing latently infected memory cells in vivo. Proc Natl Acad Sci U S A 101: 239–244. 14688409
9. Kuppers R (2003) B cells under influence: transformation of B cells by Epstein-Barr virus. Nat Rev Immunol 3: 801–812. 14523386
10. Thorley-Lawson DA, Gross A (2004) Persistence of the Epstein-Barr virus and the origins of associated lymphomas. N Engl J Med 350: 1328–1337. 15044644
11. Hislop AD, Ressing ME, van Leeuwen D, Pudney VA, Horst D et al. (2007) A CD8+ T cell immune evasion protein specific to Epstein-Barr virus and its close relatives in Old World primates. J Exp Med 204: 1863–1873. 17620360
12. Zuo J, Currin A, Griffin BD, Shannon-Lowe C, Thomas WA et al. (2009) The Epstein-Barr virus G-protein-coupled receptor contributes to immune evasion by targeting MHC class I molecules for degradation. PLoS Pathog 5: e1000255. doi: 10.1371/journal.ppat.1000255 19119421
13. Zuo J, Thomas W, van Leeuwen D, Middeldorp JM, Wiertz EJ et al. (2008) The DNase of gammaherpesviruses impairs recognition by virus-specific CD8+ T cells through an additional host shutoff function. J Virol 82: 2385–2393. 18094150
14. Brink AA, Dukers DF, van den Brule AJ, Oudejans JJ, Middeldorp JM et al. (1997) Presence of Epstein-Barr virus latency type III at the single cell level in post-transplantation lymphoproliferative disorders and AIDS related lymphomas. J Clin Pathol 50: 911–918. 9462239
15. Blake N, Lee S, Redchenko I, Thomas W, Steven N et al. (1997) Human CD8+ T cell responses to EBV EBNA1: HLA class I presentation of the (Gly-Ala)-containing protein requires exogenous processing. Immunity 7: 791–802. 9430224
16. Levitskaya J, Coram M, Levitsky V, Imreh S, Steigerwald-Mullen PM et al. (1995) Inhibition of antigen processing by the internal repeat region of the Epstein-Barr virus nuclear antigen-1. Nature 375: 685–688. 7540727
17. Levitskaya J, Sharipo A, Leonchiks A, Ciechanover A, Masucci MG (1997) Inhibition of ubiquitin/proteasome-dependent protein degradation by the Gly-Ala repeat domain of the Epstein-Barr virus nuclear antigen 1. Proc Natl Acad Sci U S A 94: 12616–12621. 9356498
18. Apcher S, Komarova A, Daskalogianni C, Yin Y, Malbert-Colas L et al. (2009) mRNA translation regulation by the Gly-Ala repeat of Epstein-Barr virus nuclear antigen 1. J Virol 83: 1289–1298. doi: 10.1128/JVI.01369-08 19019958
19. Tellam J, Smith C, Rist M, Webb N, Cooper L et al. (2008) Regulation of protein translation through mRNA structure influences MHC class I loading and T cell recognition. Proc Natl Acad Sci U S A 105: 9319–9324. doi: 10.1073/pnas.0801968105 18591662
20. Yin Y, Manoury B, Fahraeus R (2003) Self-inhibition of synthesis and antigen presentation by Epstein-Barr virus-encoded EBNA1. Science 301: 1371–1374. 12958359
21. Smith C, Wakisaka N, Crough T, Peet J, Yoshizaki T et al. (2009) Discerning regulation of cis- and trans-presentation of CD8+ T-cell epitopes by EBV-encoded oncogene LMP-1 through self-aggregation. Blood 113: 6148–6152. doi: 10.1182/blood-2009-02-203687 19372256
22. Alber G, Kim KM, Weiser P, Riesterer C, Carsetti R et al. (1993) Molecular mimicry of the antigen receptor signalling motif by transmembrane proteins of the Epstein-Barr virus and the bovine leukaemia virus. Curr Biol 3: 333–339. 15335726
23. Beaufils P, Choquet D, Mamoun RZ, Malissen B (1993) The (YXXL/I)2 signalling motif found in the cytoplasmic segments of the bovine leukaemia virus envelope protein and Epstein-Barr virus latent membrane protein 2A can elicit early and late lymphocyte activation events. EMBO J 12: 5105–5112. 8262054
24. Caldwell RG, Wilson JB, Anderson SJ, Longnecker R (1998) Epstein-Barr virus LMP2A drives B cell development and survival in the absence of normal B cell receptor signals. Immunity 9: 405–411. 9768760
25. Mancao C, Hammerschmidt W (2007) Epstein-Barr virus latent membrane protein 2A is a B-cell receptor mimic and essential for B-cell survival. Blood 110: 3715–3721. 17682125
26. Miller CL, Burkhardt AL, Lee JH, Stealey B, Longnecker R et al. (1995) Integral membrane protein 2 of Epstein-Barr virus regulates reactivation from latency through dominant negative effects on protein-tyrosine kinases. Immunity 2: 155–166. 7895172
27. Miller CL, Lee JH, Kieff E, Burkhardt AL, Bolen JB et al. (1994) Epstein-Barr virus protein LMP2A regulates reactivation from latency by negatively regulating tyrosine kinases involved in sIg-mediated signal transduction. Infect Agents Dis 3: 128–136. 7812651
28. Miller CL, Lee JH, Kieff E, Longnecker R (1994) An integral membrane protein (LMP2) blocks reactivation of Epstein-Barr virus from latency following surface immunoglobulin crosslinking. Proc Natl Acad Sci U S A 91: 772–776. 8290598
29. Brielmeier M, Mautner J, Laux G, Hammerschmidt W (1996) The latent membrane protein 2 gene of Epstein-Barr virus is important for efficient B cell immortalization. J Gen Virol 77: 2807–2818. 8922475
30. Konishi K, Maruo S, Kato H, Takada K (2001) Role of Epstein-Barr virus-encoded latent membrane protein 2A on virus-induced immortalization and virus activation. J Gen Virol 82: 1451–1456. 11369890
31. Longnecker R, Miller CL, Miao XQ, Marchini A, Kieff E (1992) The only domain which distinguishes Epstein-Barr virus latent membrane protein 2A (LMP2A) from LMP2B is dispensable for lymphocyte infection and growth transformation in vitro; LMP2A is therefore nonessential. J Virol 66: 6461–6469. 1328675
32. Longnecker R, Miller CL, Miao XQ, Tomkinson B, Kieff E (1993) The last seven transmembrane and carboxy-terminal cytoplasmic domains of Epstein-Barr virus latent membrane protein 2 (LMP2) are dispensable for lymphocyte infection and growth transformation in vitro. J Virol 67: 2006–2013. 8383224
33. Longnecker R, Miller CL, Tomkinson B, Miao XQ, Kieff E (1993) Deletion of DNA encoding the first five transmembrane domains of Epstein-Barr virus latent membrane proteins 2A and 2B. J Virol 67: 5068–5074. 8392630
34. Speck P, Kline KA, Cheresh P, Longnecker R (1999) Epstein-Barr virus lacking latent membrane protein 2 immortalizes B cells with efficiency indistinguishable from that of wild-type virus. J Gen Virol 80: 2193–2203. 10466819
35. Wasil LR, Tomaszewski MJ, Hoji A, Rowe DT (2013) The effect of Epstein-Barr virus Latent Membrane Protein 2 expression on the kinetics of early B cell infection. PLoS ONE 8: e54010. doi: 10.1371/journal.pone.0054010 23308294
36. Shah KM, Stewart SE, Wei W, Woodman CB, O'Neil JD et al. (2009) The EBV-encoded latent membrane proteins, LMP2A and LMP2B, limit the actions of interferon by targeting interferon receptors for degradation. Oncogene 28: 3903–3914. doi: 10.1038/onc.2009.249 19718044
37. Portis T, Dyck P, Longnecker R (2003) Epstein-Barr Virus (EBV) LMP2A induces alterations in gene transcription similar to those observed in Reed-Sternberg cells of Hodgkin lymphoma. Blood 102: 4166–4178. 12907455
38. Incrocci R, McCormack M, Swanson-Mungerson M (2013) Epstein-Barr virus LMP2A increases IL-10 production in mitogen-stimulated primary B-cells and B-cell lymphomas. J Gen Virol 94: 1127–1133. doi: 10.1099/vir.0.049221-0 23303827
39. Delecluse HJ, Hilsendegen T, Pich D, Zeidler R, Hammerschmidt W (1998) Propagation and recovery of intact, infectious Epstein-Barr virus from prokaryotic to human cells. Proc Natl Acad Sci U S A 95: 8245–8250. 9653172
40. Middeldorp JM, Pegtel DM (2008) Multiple roles of LMP1 in Epstein-Barr virus induced immune escape. Semin Cancer Biol 18: 388–396. doi: 10.1016/j.semcancer.2008.10.004 19013244
41. Bejarano MT, Masucci MG (1998) Interleukin-10 abrogates the inhibition of Epstein-Barr virus-induced B-cell transformation by memory T-cell responses. Blood 92: 4256–4262. 9834231
42. Jochum S, Moosmann A, Lang S, Hammerschmidt W, Zeidler R (2012) The EBV immunoevasins vIL-10 and BNLF2a protect newly infected B cells from immune recognition and elimination. PLoS Pathog 8: e1002704. doi: 10.1371/journal.ppat.1002704 22615564
43. Zeidler R, Eissner G, Meissner P, Uebel S, Tampe R et al. (1997) Downregulation of TAP1 in B lymphocytes by cellular and Epstein-Barr virus-encoded interleukin-10. Blood 90: 2390–2397. 9310490
44. Ng TH, Britton GJ, Hill EV, Verhagen J, Burton BR et al. (2013) Regulation of adaptive immunity; the role of interleukin-10. Front Immunol 4: 129. doi: 10.3389/fimmu.2013.00129 23755052
45. Stewart JP, Behm FG, Arrand JR, Rooney CM (1994) Differential expression of viral and human interleukin-10 (IL-10) by primary B cell tumors and B cell lines. Virology 200: 724–732. 8178456
46. Chaigne-Delalande B, Li FY, O'Connor GM, Lukacs MJ, Jiang P et al. (2013) Mg2+ regulates cytotoxic functions of NK and CD8 T cells in chronic EBV infection through NKG2D. Science 341: 186–191. doi: 10.1126/science.1240094 23846901
47. Kong Y, Cao W, Xi X, Ma C, Cui L et al. (2009) The NKG2D ligand ULBP4 binds to TCRgamma9/delta2 and induces cytotoxicity to tumor cells through both TCRgammadelta and NKG2D. Blood 114: 310–317. doi: 10.1182/blood-2008-12-196287 19436053
48. Pappworth IY, Wang EC, Rowe M (2007) The switch from latent to productive infection in Epstein-Barr virus-infected B cells is associated with sensitization to NK cell killing. J Virol 81: 474–482. 17079298
49. Wiesmayr S, Webber SA, Macedo C, Popescu I, Smith L et al. (2012) Decreased NKp46 and NKG2D and elevated PD-1 are associated with altered NK-cell function in pediatric transplant patients with PTLD. Eur J Immunol 42: 541–550. doi: 10.1002/eji.201141832 22105417
50. Kim YS, Park GB, Lee HK, Song H, Choi IH et al. (2008) Cross-linking of B7-H1 on EBV-transformed B cells induces apoptosis through reactive oxygen species production, JNK signaling activation, and fasL expression. J Immunol 181: 6158–6169. 18941206
51. Haile ST, Dalal SP, Clements V, Tamada K, Ostrand-Rosenberg S (2013) Soluble CD80 restores T cell activation and overcomes tumor cell programmed death ligand 1-mediated immune suppression. J Immunol 191: 2829–2836. doi: 10.4049/jimmunol.1202777 23918985
52. Ruprecht CR, Lanzavecchia A (2006) Toll-like receptor stimulation as a third signal required for activation of human naive B cells. Eur J Immunol 36: 810–816. 16541472
53. Wiesner M, Zentz C, Mayr C, Wimmer R, Hammerschmidt W et al. (2008) Conditional immortalization of human B cells by CD40 ligation. PLoS ONE 3: e1464. doi: 10.1371/journal.pone.0001464 18213373
54. Merchant M, Swart R, Katzman RB, Ikeda M, Ikeda A et al. (2001) The effects of the Epstein-Barr virus latent membrane protein 2A on B cell function. Int Rev Immunol 20: 805–835. 11913951
55. Schaadt E, Baier B, Mautner J, Bornkamm GW, Adler B (2005) Epstein-Barr virus latent membrane protein 2A mimics B-cell receptor-dependent virus reactivation. J Gen Virol 86: 551–559. 15722514
56. Pudney VA, Leese AM, Rickinson AB, Hislop AD (2005) CD8+ immunodominance among Epstein-Barr virus lytic cycle antigens directly reflects the efficiency of antigen presentation in lytically infected cells. J Exp Med 201: 349–360. 15684323
57. Rowe M, Khanna R, Jacob CA, Argaet V, Kelly A et al. (1995) Restoration of endogenous antigen processing in Burkitt's lymphoma cells by Epstein-Barr virus latent membrane protein-1: coordinate up-regulation of peptide transporters and HLA-class I antigen expression. Eur J Immunol 25: 1374–1384. 7774641
58. Dukers DF, Meij P, Vervoort MB, Vos W, Scheper RJ et al. (2000) Direct immunosuppressive effects of EBV-encoded latent membrane protein 1. J Immunol 165: 663–670. 10878338
59. Lautscham G, Mayrhofer S, Taylor G, Haigh T, Leese A et al. (2001) Processing of a multiple membrane spanning Epstein-Barr virus protein for CD8(+) T cell recognition reveals a proteasome-dependent, transporter associated with antigen processing-independent pathway. J Exp Med 194: 1053–1068. 11602636
60. Lautscham G, Haigh T, Mayrhofer S, Taylor G, Croom-Carter D et al. (2003) Identification of a TAP-independent, immunoproteasome-dependent CD8+ T-cell epitope in Epstein-Barr virus latent membrane protein 2. J Virol 77: 2757–2761. 12552018
61. Tellam J, Connolly G, Green KJ, Miles JJ, Moss DJ et al. (2004) Endogenous presentation of CD8+ T cell epitopes from Epstein-Barr virus-encoded nuclear antigen 1. J Exp Med 199: 1421–1431. 15148340
62. Portis T, Longnecker R (2003) Epstein-Barr virus LMP2A interferes with global transcription factor regulation when expressed during B-lymphocyte development. J Virol 77: 105–114. 12477815
63. Portis T, Ikeda M, Longnecker R (2004) Epstein-Barr virus LMP2A: regulating cellular ubiquitination processes for maintenance of viral latency? Trends Immunol 25: 422–426. 15275641
64. Bell AI, Groves K, Kelly GL, Croom-Carter D, Hui E et al. (2006) Analysis of Epstein-Barr virus latent gene expression in endemic Burkitt's lymphoma and nasopharyngeal carcinoma tumour cells by using quantitative real-time PCR assays. J Gen Virol 87: 2885–2890. 16963746
65. Kuppers R (2009) The biology of Hodgkin's lymphoma. Nat Rev Cancer 9: 15–27. doi: 10.1038/nrc2542 19078975
66. Burdin N, Peronne C, Banchereau J, Rousset F (1993) Epstein-Barr virus transformation induces B lymphocytes to produce human interleukin 10. J Exp Med 177: 295–304. 8381152
67. Finke J, Ternes P, Lange W, Mertelsmann R, Dolken G (1993) Expression of interleukin 10 in B lymphocytes of different origin. Leukemia 7: 1852–1857. 7694007
68. Hsu DH, de Waal Malefyt R, Fiorentino DF, Dang MN, Vieira P et al. (1990) Expression of interleukin-10 activity by Epstein-Barr virus protein BCRF1. Science 250: 830–832. 2173142
69. Swaminathan S, Hesselton R, Sullivan J, Kieff E (1993) Epstein-Barr virus recombinants with specifically mutated BCRF1 genes. J Virol 67: 7406–7413. 7693971
70. Beatty PR, Krams SM, Martinez OM (1997) Involvement of IL-10 in the autonomous growth of EBV-transformed B cell lines. J Immunol 158: 4045–4051. 9126962
71. Miyazaki I, Cheung RK, Dosch HM (1993) Viral interleukin 10 is critical for the induction of B cell growth transformation by Epstein-Barr virus. J Exp Med 178: 439–447. 8393476
72. Salek-Ardakani S, Arrand JR, Mackett M (2002) Epstein-Barr virus encoded interleukin-10 inhibits HLA-class I, ICAM-1, and B7 expression on human monocytes: implications for immune evasion by EBV. Virology 304: 342–351. 12504574
73. Duraiswamy J, Ibegbu CC, Masopust D, Miller JD, Araki K et al. (2011) Phenotype, function, and gene expression profiles of programmed death-1(hi) CD8 T cells in healthy human adults. J Immunol 186: 4200–4212. doi: 10.4049/jimmunol.1001783 21383243
74. Barber DL, Wherry EJ, Masopust D, Zhu B, Allison JP et al. (2006) Restoring function in exhausted CD8 T cells during chronic viral infection. Nature 439: 682–687. 16382236
75. Gonzalez S, Lopez-Soto A, Suarez-Alvarez B, Lopez-Vazquez A, Lopez-Larrea C (2008) NKG2D ligands: key targets of the immune response. Trends Immunol 29: 397–403. doi: 10.1016/j.it.2008.04.007 18602338
76. Zhang B, Kracker S, Yasuda T, Casola S, Vanneman M et al. (2012) Immune surveillance and therapy of lymphomas driven by Epstein-Barr virus protein LMP1 in a mouse model. Cell 148: 739–751. doi: 10.1016/j.cell.2011.12.031 22341446
77. Nachmani D, Stern-Ginossar N, Sarid R, Mandelboim O (2009) Diverse herpesvirus microRNAs target the stress-induced immune ligand MICB to escape recognition by natural killer cells. Cell Host Microbe 5: 376–385. doi: 10.1016/j.chom.2009.03.003 19380116
78. Altmann M, Hammerschmidt W (2005) Epstein-Barr virus provides a new paradigm: a requirement for the immediate inhibition of apoptosis. PLoS Biol 3: e404. 16277553
79. Garrone P, Neidhardt EM, Garcia E, Galibert L, van Kooten C et al. (1995) Fas ligation induces apoptosis of CD40-activated human B lymphocytes. J Exp Med 182: 1265–1273. 7595197
80. Lee SP, Thomas WA, Murray RJ, Khanim F, Kaur S et al. (1993) HLA A2.1-restricted cytotoxic T cells recognizing a range of Epstein-Barr virus isolates through a defined epitope in latent membrane protein LMP2. J Virol 67: 7428–7435. 7693972
81. Saulquin X, Ibisch C, Peyrat MA, Scotet E, Hourmant M et al. (2000) A global appraisal of immunodominant CD8 T cell responses to Epstein-Barr virus and cytomegalovirus by bulk screening. Eur J Immunol 30: 2531–2539. 11009086
82. Meij P, Leen A, Rickinson AB, Verkoeijen S, Vervoort MB et al. (2002) Identification and prevalence of CD8(+) T-cell responses directed against Epstein-Barr virus-encoded latent membrane protein 1 and latent membrane protein 2. Int J Cancer 99: 93–99. 11948498
83. Hill A, Worth A, Elliott T, Rowland-Jones S, Brooks J et al. (1995) Characterization of two Epstein-Barr virus epitopes restricted by HLA-B7. Eur J Immunol 25: 18–24. 7531143
84. Bogedain C, Wolf H, Modrow S, Stuber G, Jilg W (1995) Specific cytotoxic T lymphocytes recognize the immediate-early transactivator Zta of Epstein-Barr virus. J Virol 69: 4872–4879. 7609055
85. Rickinson AB, Moss DJ (1997) Human cytotoxic T lymphocyte responses to Epstein-Barr virus infection. Annu Rev Immunol 15: 405–431. 9143694
86. Diamond DJ, York J, Sun JY, Wright CL, Forman SJ (1997) Development of a candidate HLA A*0201 restricted peptide-based vaccine against human cytomegalovirus infection. Blood 90: 1751–1767. 9292508
87. Ameres S, Mautner J, Schlott F, Neuenhahn M, Busch DH et al. (2013) Presentation of an immunodominant immediate-early CD8+ T cell epitope resists human cytomegalovirus immunoevasion. PLoS Pathog 9: e1003383. doi: 10.1371/journal.ppat.1003383 23717207
88. Khan N, Cobbold M, Keenan R, Moss PA (2002) Comparative analysis of CD8+ T cell responses against human cytomegalovirus proteins pp65 and immediate early 1 shows similarities in precursor frequency, oligoclonality, and phenotype. J Infect Dis 185: 1025–1034. 11930311
89. Braud VM, Allan DS, Wilson D, McMichael AJ (1998) TAP- and tapasin-dependent HLA-E surface expression correlates with the binding of an MHC class I leader peptide. Curr Biol 8: 1–10. 9427624
90. Akdis CA, Blesken T, Akdis M, Wuthrich B, Blaser K (1998) Role of interleukin 10 in specific immunotherapy. J Clin Invest 102: 98–106. 9649562
91. Iskra S, Kalla M, Delecluse HJ, Hammerschmidt W, Moosmann A (2010) Toll-like receptor agonists synergistically increase proliferation and activation of B cells by Epstein-Barr virus. J Virol 84: 3612–3623. doi: 10.1128/JVI.01400-09 20089650
92. Liu Y, de Waal Malefyt R, Briere F, Parham C, Bridon JM et al. (1997) The EBV IL-10 homologue is a selective agonist with impaired binding to the IL-10 receptor. J Immunol 158: 604–613. 8992974
93. de Brouwer AP, van Bokhoven H, Kremer H (2006) Comparison of 12 reference genes for normalization of gene expression levels in Epstein-Barr virus-transformed lymphoblastoid cell lines and fibroblasts. Mol Diagn Ther 10: 197–204. 16771605
94. Nicholls J, Hahn P, Kremmer E, Frohlich T, Arnold GJ et al. (2004) Detection of wild type and deleted latent membrane protein 1 (LMP1) of Epstein-Barr virus in clinical biopsy material. J Virol Methods 116: 79–88. 14715310
Štítky
Hygiena a epidemiologie Infekční lékařství LaboratořČlánek vyšel v časopise
PLOS Pathogens
2015 Číslo 6
- Jak souvisí postcovidový syndrom s poškozením mozku?
- Měli bychom postcovidový syndrom léčit antidepresivy?
- Farmakovigilanční studie perorálních antivirotik indikovaných v léčbě COVID-19
- 10 bodů k očkování proti COVID-19: stanovisko České společnosti alergologie a klinické imunologie ČLS JEP
Nejčtenější v tomto čísle
- HIV Latency Is Established Directly and Early in Both Resting and Activated Primary CD4 T Cells
- A 21st Century Perspective of Poliovirus Replication
- Adenovirus Tales: From the Cell Surface to the Nuclear Pore Complex
- Battling Phages: How Bacteria Defend against Viral Attack