Research Article | Open Access
Azim Hossain, Jason M. God, Faisal F. Y. Radwan, Shereen Amria, Dan Zhao, Jennifer R. Bethard, Azizul Haque, "HLA Class II Defects in Burkitt Lymphoma: Bryostatin-1-Induced 17 kDa Protein Restores CD4+ T-Cell Recognition", Journal of Immunology Research, vol. 2011, Article ID 780839, 10 pages, 2011. https://doi.org/10.1155/2011/780839
HLA Class II Defects in Burkitt Lymphoma: Bryostatin-1-Induced 17 kDa Protein Restores CD4+ T-Cell Recognition
While the defects in HLA class I-mediated Ag presentation by Burkitt lymphoma (BL) have been well documented, CD4+ T-cells are also poorly stimulated by HLA class II Ag presentation, and the reasons underlying this defect(s) have not yet been fully resolved. Here, we show that BL cells are deficient in their ability to optimally stimulate CD4+ T cells via the HLA class II pathway. The observed defect was not associated with low levels of BL-expressed costimulatory molecules, as addition of external co-stimulation failed to result in BL-mediated CD4+ T-cell activation. We further demonstrate that BL cells express the components of the class II pathway, and the defect was not caused by faulty Ag/class II interaction, because antigenic peptides bound with measurable affinity to BL-associated class II molecules. Treatment of BL with broystatin-1, a potent modulator of protein kinase C, led to significant improvement of functional class II Ag presentation in BL. The restoration of immune recognition appeared to be linked with an increased expression of a 17 kDa peptidylprolyl-like protein. These results demonstrate the presence of a specific defect in HLA class II-mediated Ag presentation in BL and reveal that treatment with bryostatin-1 could lead to enhanced immunogenicity.
Burkitt lymphoma (BL) is an aggressive non-Hodgkin’s B-cell malignancy, occurring most frequently as endemic BL in children living in areas of high malarial prevalence . This malignancy may also be found in other parts of the world as sporadic BL and accounts for 1-2% of all lymphomas in Western countries . The clinical manifestations of BL are variable, with tumors of the jaw characteristically seen in endemic BL and tumors in the gut associated with sporadic BL [2–4]. BL has one of the fastest doubling times among human malignancies and is frequently associated with immune deficiency .
In addition to its strong association with malaria, BL has a high correlation with Epstein-Barr Virus (EBV). EBV infection, however, is not requisite for the development of BL, and the degree of association with EBV varies based on the type of BL. EBV infection occurs in >90% of endemic BL cases, 10–15% of sporadic BL, and 40% of human immunodeficiency virus (HIV) associated BL . While the exact role that EBV plays in the development of BL remains largely unknown, it is understood that EBV gene products may be involved in the transformation of BL cells and their decreased immunogenicity. Additional evidence for EBV having a role in development of BL stems from EBV’s link to various other lymphoid malignancies including Hodgkin’s lymphoma, transplant-related B-cell lymphomas, T-cell lymphomas, adult T-cell leukemia, and natural killer cell leukemia [5–8]. While BL has varying associations with malaria and EBV and in some cases is not associated with either, the one feature shared by all BLs is overexpression of the oncogenic transcription factor c-myc, which has a gene network comprising up to 15% of all known genes . This abnormality results from the translocation of the MYC gene to an immunoglobulin locus leading to its constitutive activation [10–12].
BL is known to be deficient in HLA class I-mediated antigen (Ag) presentation to CD8+ T lymphocytes [13–15]. However, the role of HLA class II-mediated Ag presentation in generating an immune response to BL has not been fully elucidated. The class I defect has been well studied and is understood to result from the weak immunogenicity of EBV nuclear Ag 1 (EBNA1), which is poorly processed and presented through the class I pathway [16–18]. Another EBV gene product, gp42, has a role in mediating virus binding through interaction with HLA class II and it has been speculated to block the interaction between class II and the T-cell receptor [19, 20]. Although HLA class I-mediated activation of CD8+ T cells leads to Ag-specific lysis of tumor cells, an HLA class II response is vital for the generation of sustained immune responses . Our laboratory has previously shown that B-cell lymphomas are deficient in HLA class II-mediated Ag presentation , and in this study we explore the role of B-cell-associated molecules in restoration of CD4+ T-cell recognition of BL cells.
The study presented here suggests that multiple defects may contribute to BL’s inability to efficiently present Ag via HLA class II molecules. We confirm expression of a transfected HLA class II allele in both BL cells and EBV-immortalized B-lymphoblastoid cells (B-LCL), and demonstrate that the transfected HLA class II efficiently binds exogenously delivered Ag to form class II peptide complexes. However, while B-LCL were capable of CD4+ T-cell stimulation, BL cells were deficient in their ability to do so, and addition of external co-stimulation was insufficient to overcome this defect. In addition, treatment of BL cells with bryostatin-1 partially restored class II-mediated Ag presentation. This restoration was linked to the upregulation of a 17 kDa protein in bryostatin-treated BL which was expressed at low levels in untreated BL but highly expressed in B-LCL, suggesting that this protein may play a role in enhancing class II-mediated Ag presentation. In other studies, bryostatin-1 has been shown to increase HLA class II expression in dendritic cells and in a colorectal carcinoma cell line, but its effect on HLA class II expression and Ag presentation in lymphoid malignancies has not previously been evaluated [23, 24]. On the whole, these results suggest that BL possesses multiple defects which lead to an impaired ability to stimulate CD4+ T cells through HLA class II Ag presentation. These defects may provide the opportunity to develop novel immunotherapies leading to more targeted treatment of BL and other lymphoid malignancies. This study also provides a rationale for the further evaluation of bryostatin-1 as a therapeutic treatment of lymphoid malignancies.
2. Materials and Methods
2.1. Cell Lines
Human BL cell lines, Nalm-6, Ramos, and Ous, were maintained in complete RPMI-1640 supplemented with 10% fetal bovine serum (Invitrogen, Carlsbad, CA), 50 U/mL penicillin 50 μg/mL streptomycin, and 1% L-glutamine (Mediatech, Manassas, VA). The Ous cell line was a gift from Dr. Christian Munz (Rockefeller University). The human B-lymphoblastoid cell lines (B-LCL) 6.16 and Frev were maintained in IMDM supplemented with 10% bovine growth serum (Hyclone, Logan, UT), 50 U/mL penicillin 50 μg/mL streptomycin, and 1% L-glutamine (Mediatech). Nalm-6, Ramos, and 6.16 cells were retrovirally transfected for constitutive expression of HLA-DR4 (DRB1*0401) with linked drug selection markers for hygromycin and histidinol resistance to generate Nalm-6.DR4, Ramos.DR4, and 6.16.DR4 [22, 25]. Frev did not require transfection of the class II allele as it constitutively expresses HLA-DR4. Surface HLA-DR4 expression in the transfectants was confirmed by flow cytometric analysis using the DR4-specific mAb, 359-F10 [22, 26, 27]. 6.16.DR4 cells were further transfected with DMα and DMβ for constitutive expression of HLA-DM molecules to generate 6.16.DR4.DM . The expression of HLA-DM on 6.16.DR4.DM cells was confirmed by western blotting. T-cell hybridomas 2.18a and 1.21 recognize Ig κ residues 188–203 and 145–159, respectively, and were generated by immunization of DR4-transgenic mice as described [25, 28]. The T-cell hybridoma 17.9 (generously provided by D. Zaller, Merck Research Laboratories, Rahway, NJ) responds to human serum albumin (HSA) residue 64–76 K . These T cell hybridomas are less dependent on costimulatory signals for their stimulation. Cells were cultured in RPMI 1640 with 10% FBS, 50 U/mL penicillin, 50 μg/mL streptomycin, and 50 μM β-mercaptoethanol (Invitrogen).
2.2. Antigens, Peptides, and Other Reagents
Human serum albumin (HSA) and human IgG kappa (IgG κ) were purchased from Sigma (St. Louis, MO). peptide (sequence: VKLVNEVTEFAKTK) human IgG immunodominant peptide (κI; sequence: KHKVYACEVTHQGLSS), and subdominant peptide (κII; sequence: KVQWKVDNALQSGNS) were produced using Fmoc technology and an Applied Biosystems Synthesizer as described, dissolved in PBS, and stored at −20°C until used [25, 29, 30]. Reverse phase HPLC purification and mass spectrometry were used to analyze the peptide and showed a peptide purity >99%. Bryostatin-1 was purchased from Sigma.
2.3. Antigen Presentation Assays
B-LCL and BL were incubated with 0 μM, 5 μM, 10 μM, or 20 μM HSA Ag or HSA synthetic peptide for 3–24 h at 37°C in the appropriate cell culture media to determine optimal antigen concentrations to use in antigen presentation assays [22, 25]. Following titration, the same assays were carried out using only the optimal concentration of each antigen. Cells were then washed and co-cultured with the T-cell hybridoma 17.9 for 24 h at 37°C. In parallel assays, 2.18a and 1.21 were stimulated with anti-CD3/CD28 prior to co-culture with Nalm-6.DR4, Ramos.DR4, or 6.16.DR4.DM which had been incubated with κI or κII . Following co-culture, T cell production of IL-2 was quantitated by ELISA . Assays were repeated in triplicate with standard error for triplicate samples within a single experiment being reported.
2.4. Western Blotting
Western blot analysis was performed on whole cell lysates of Frev, Nalm-6.DR4, 6.16.DR4.DM, and Ramos.DR4. Expression of HLA class II, Ii, and HLA-DM was analyzed as described previously [32, 33]. Densitometry was performed using a ChemiDoc XRS station (Bio-Rad) where the protein bands were analyzed using the Quantity One 4.6.3 software (Bio-Rad). Relative protein expression levels were stated as a ratio of specific proteins expressed/β-actin for each sample. Data are representative of at least three separate experiments.
2.5. IL-2 ELISA
IL-2 levels in Ag presentation assay supernatant were quantitated by ELISA. A 96-well ELISA plate was coated overnight at 4°C with purified rat anti-mouse IL-2 (Sigma). The plate was then washed and blocked with 2% BSA at RT for 30 m. After washing, standards and samples were plated in appropriate wells and incubated at RT for 2 h. A standard curve was generated using recombinant IL-2 purchased from R&D (Minneapolis, MN). The plate was washed, and biotinylated rat anti-mouse IL-2 (Sigma) was added and incubated at RT for 1 h. Following washing, avidin peroxidase (Pierce, Rockford, IL) was added to each well and incubated at RT for 30 m. The plate was washed, and PNPP substrate (Thermo Scientific, Rockford, IL) was added to each well and incubated at RT. Readings were taken every 30 m at 405 nm. IL-2 levels in sample wells are expressed in pg/mL, calculated from the standard curve. Assays were repeated in triplicate and expressed as mean IL-2 ± SEM.
2.6. Peptide Binding Assays
Nalm-6.DR4, Ramos.DR4, 6.16.DR4.DM, and Frev cells were fixed in 1% paraformaldehyde and then incubated overnight with 0 μM, 10 μM, or 20 μM biotinylated HSA peptide (b-HSA) in 150 mM CPB (pH 7.4), washed with PBS, and lysed on ice for 20 min with 50 mM Tris buffer (pH 8) containing 0.15 M NaCl and 0.5% IGEPAL CA 630 (Sigma) as described [30, 34]. Cell supernatants were added to plates (Costar, Cambridge, MA) previously coated overnight with the anti-human class II antibody 37.1 (kindly provided by L. Wicker, Merck Research Lab, Rahway, NJ). The captured class II-peptide complexes were detected with europium-labeled streptavidin (Pharmacia Fine Chemicals, Piscataway, NJ) using a fluorescence plate reader (Delfia, Wallac, Turku, Finland). The number of total DR molecules within B-LCL/BL cells was quantitated as described .
2.7. Bryostatin-1 Treatment of BL Cells
Nalm-6.DR4 and Ramos.DR4 were treated with 0, 20, or 40 nM of bryostatin-1 for overnight. Following incubation, untreated and bryostatin-treated cells were used in Ag presentation assays with HSA peptide followed by ELISA IL-2 quantitation as already described. In separate assays, Ramos.DR4 were treated with 40 nM bryostatin overnight and then fixed in 1% paraformaldehyde for 5 min. Following fixation, the cells were washed and incubated with 0 μM, 10 μM, or 40 μM of b-HSA for 3 h at 37°C with shaking. The cells were then washed and lysed in Hanks Balanced Salt Solution with 1% Triton-X-100 and protease inhibitors (PMSF and TLCK). The lysate was added to wells of a 96-well plate precoated with the anti-HLA class II antibody, 37.1. Captured class II peptide complexes were detected using streptavidin peroxidase and BD OptEIA TMB substrate reagents (BD, San Diego, CA). The reaction was stopped using 1 M phosphoric acid and the resulting absorbance was read at 450 nM.
Additionally, surface protein expression in 6.16.DR4.DM, untreated Nalm-6.DR4, and bryostatin-treated Nalm-6.DR4 was evaluated by SDS-PAGE protein separation. Nalm-6.DR4 cells were treated overnight with 40 nM of bryostatin-1. Following incubation, 6.16.DR4.DM, untreated Nalm-6.DR4, and bryostatin-treated Nalm-6.DR4 were washed in citrate phosphate buffer (CPB) to elute cell surface proteins. The resulting eluate was then subjected to SDS-PAGE. A 17 kDa band was excised from these gels and analyzed by MALDI TOF-TOF mass spectrometry. Proteins in CPB eluate from 6.16.DR4.DM were separated by electrophoresis on large, nonreducing gels. The 17 kDa band was excised and the protein was extracted by sonication in PBS on ice. Ramos.DR4 cells were incubated with the HSA peptide in the 17 kDa extract for use in Ag presentation assays as described. T cell production of IL-2 was quantitated .
2.8. Protein Extraction and Digestion
CPB eluate was obtained from 6.16.DR4.DM, untreated Nalm-6.DR4, and bryostatin-treated Nalm-6.DR4 as described previously . Extracts were concentrated, and protein concentrations were measured, then run on a non-reducing gel, and stained with Coomassie blue. Gel plugs were excised and placed in an eppendorf tube. Each plug was washed with 50 mM ammonium bicarbonate for 10 minutes. Next, the plugs were destained using 25 mM ammonium bicarbonate in 50% acetonitrile for 15 minutes. The plugs were dehydrated with 100% acetonitrile for 15 minutes and dried in a speedvac. Each gel plug was covered with Proteomics Grade Trypsin (Sigma) and incubated at 37°C overnight. The supernatant was collected in a clean dry eppendorf tube. Peptides were further extracted with 1 wash of 25 mM ammonium bicarbonate for 20 minutes and three washes of 5% formic acid, 50% acetonitrile for 20 minutes each. The supernatent was collected and pooled after each wash then dried down in a speedvac to ~1 uL. Prior to analysis, the samples were reconstituted with 10 uL of 0.1% trifluoroacetic acid. Samples were then concentrated with a C18 Ziptip (Millipore) and eluted with 0.1% TFA, 50% acetonitrile, and 7.0 mg/mL α-cyano-4-hydroxycinnamic acid directly onto the MALDI target.
2.9. Mass Spectrometric Analysis (MALDI TOF/TOF)
After the spots were dried completely, the plate was loaded into the Applied Biosystems 4800 Proteomics Analyzer. An external calibration was performed prior to analyzing samples utilizing the manufacturer’s standards and protocols. Samples were analyzed in batch mode using 2000 laser shots per spectrum. First, peptide mass maps were acquired over the m/z range of 800–3500 in reflectron mode with a delayed extraction time optimized for m/z 2000 by averaging 2000 scans to locate peaks of peptide origin. The next batch run performed MS-MS analyses to obtain sequence data on the 20 most abundant peaks from the MS analysis. Upon completion of the batch processing, the data was exported into the GPS Explorer data processing system for interpretation and identification. The MASCOT database-searching algorithm analyzed the data and summarized the results in report format. Database searches were performed using 2 missed cleavages and one differential modification of methionine oxidation. The top 20 matches were reviewed prior to assigning confident protein identifications.
3.1. BL Cells Display Decreased HLA Class II-Mediated CD4+ T-Cell Stimulation
Although BL and B-LCL both express surface HLA class II, we transfected these cell lines to express a common class II allele so that we might obtain a more direct comparison of class II-mediated Ag presentation between the two cell types. Retroviral gene transfections of a DR4 allele, HLA DRB1*0401, were carried out on our BL (Nalm-6 and Ramos) and B-LCL (6.16) cell lines. Flow cytometric analysis confirmed transfection and expression of this allele in all three cell lines (data not shown). 6.16.DR4 cells were additionally transfected with HLA-DM to generate 6.16.DR4.DM cells expressing similar levels of HLA-DM when compared to Nalm-6.DR4 and Ramos.DR4 . Transfectants were then sorted, matched for surface DR4 expression, and incubated, along with Ous and Frev, in culture media with either HSA antigen or HSA peptide. Following incubation, cells were washed and co-cultured with the T-cell hybridoma, 17.9, for 24 h at 37°C. Culture supernatant was collected and assayed by ELISA for IL-2 levels. The results of these assays demonstrate that Nalm-6.DR4, Ramos.DR4, and Ous were deficient in their ability to stimulate IL-2 production in 17.9 by class II-mediated presentation of HSA epitope or HSA synthetic peptide (Figures 1(a)–1(d)). The B-LCL lines 6.16.DR4.DM and Frev, however, stimulated production of high levels of IL-2 (Figures 1(a)–1(d)). Supplemental Figure 1 (see Supplemental material available online at doi:10.1155/2011/585893) shows the results of whole HSA and HSA peptide titration with Nalm-6.DR4, Ramos.DR4 and 6.16.DR4.DM. Nalm-6.DR4 and Ramos.DR4 fail to stimulate IL-2 production at all concentrations of whole HSA or HSA peptide, while 6.16.DR4.DM shows a dose-dependent increase in levels of IL-2 production. These results suggest that BL cells possess a defect(s) in the presentation of Ag to CD4+ T cells in the context of HLA class II.
3.2. BL and B-LCL Express Similar Levels of HLA Class II Pathway Components
Western blot analysis was performed on Nalm-6.DR4, Ramos.DR4, 6.16.DR4.DM, and Frev for expression of HLA class II, Ii, and HLA-DM. Data from these analyses revealed that both BL and B-LCL expressed detectable levels of these immune components (Figure 2(a)). As a wild type B-LCL, Frev expresses higher levels of class II pathway components than Nalm-6.DR4, Ramos.DR4, and 6.16.DR4.DM, as analyzed by densitometry and corrected for actin loading controls (Figure 2(b)). These data suggest that the observed defect in class II-mediated Ag presentation by BL is not the result of a defect in the HLA class II processing and presentation pathway.
3.3. Addition of External Co-Stimulation Is Insufficient to Overcome the BL-Associated Defect in Class II-Mediated Ag Presentation
It has previously been reported that BL cells are deficient in expression of co-stimulatory molecules (CD80/86). In order to determine if this was the cause of the defect in class II-mediated Ag presentation by BL, Ag presentation assays were performed in the presence of external co-stimulatory signals as described. In this assay, T-cell hybridomas were treated with anti-CD3/CD28 plus cross-linked IgG and co-cultured with the BL cells that were preincubated with HSA peptide. The addition of external co-stimulation had little to no effect on class II Ag presentation by BL (Figure 3). While 6.16.DR4.DM stimulated high levels of IL-2 production in T cells with or without external co-stimulation, Nalm-6.DR4 and Ramos.DR4 showed no significant increase in stimulation of IL-2 production in T cells with external co-stimulation.
3.4. HSA Peptide Binds with Similar Affinity to HLA Class II on BL and B-LCL
The next step in evaluating the BL-related defect in HLA class II Ag presentation was to assess the binding efficiency of HSA peptide to BL-expressed surface DR4. Nalm-6.DR4, Ramos.DR4, 6.16.DR4.DM, and Frev were incubated with various concentrations of b-HSA at pH 7.4. Class II peptide complexes were then detected in an ELISA format using europium-labeled streptavidin. Data showed a dose-dependent response with each cell line binding b-HSA peptide with a similar, measurable affinity (Figure 4). These results suggest that BL’s reduced capacity to present Ag via HLA class II is not a result of impaired peptide binding to HLA class II molecules.
3.5. Bryostatin Treatment of BL Increases Peptide Binding to HLA Class II and Restores Class II Ag Presentation and CD4+ T-Cell Recognition
Previous studies on bryostatin-1 have shown that it causes upregulation of HLA class II molecules in the professional Ag presenting dendritic cells and leads to increased T-cell stimulation by these cells . Based on this finding, we sought to determine if bryostatin-1 treatment would impact Ag presentation by BL. Nalm-6.DR4 and Ramos.DR4 cells were treated with bryostatin-1 overnight and then used in Ag presentation assays with HSA as already described. Untreated BL cells showed similarly low levels of T-cell stimulation, whereas cells treated with bryostatin-1 at 20–40 nM restored Ag presentation and T-cell stimulation (Figure 5(a)). Ramos.DR4 cells were treated with bryostatin-1 overnight, and peptide binding to HLA class II was measured as already described. Ramos.DR4 treated with 40 nM bryostatin-1 showed significantly higher levels of peptide binding at both 10 μM and 40 μM b-HSA (Figure 5(b)).
(a) peptide presentation
(b) HLA-DR4- peptide binding
3.6. Bryostatin Treatment Upregulates Expression of an Immunostimulatory 17 kDa Protein in BL
To determine the nature of the class II presentation restoration in BL following bryostatin-1 treatment, protein expression patterns in CPB eluates from Nalm-6.DR4 and 6.16.DR4.DM were analyzed by gel electrophoresis (non-reducing gel) and coomassie blue staining. This study showed that a 17 kDa protein was consistently expressed at low levels in BL cells (Nalm-6.DR4) but high levels in B-LCL (6.16.DR4.DM) cells (Figure 6(a)). Following overnight treatment of BL cells with bryostatin-1, expression of this 17 kDa protein was restored to levels comparable to 6.16.DR4.DM cells (Figure 6(a)). This protein band was then cut from the gel and analyzed by MALDI TOF/TOF mass spectrometry, revealing a peptidylprolyl-like protein (accession number: 89058151). To further analyze the function of this 17 kDa protein, CPB eluates from 6.16.DR4.DM cells or bryostatin-1-treated BL cells were separated on a large non-reducing gel, the band corresponding to 17 kDa protein was excised, and the protein was extracted by sonication in PBS on ice. Ramos.DR4 cells were then incubated with HSA peptide (10 μM) in the presence of this extract, followed by washing and co-culture with 17.9 T cells. ELISA IL-2 quantitation of the assay supernatant showed a significant increase in the stimulation of IL-2 production by Ramos.DR4 cells incubated with HSA in the presence of the 17 kDa extract (Figure 6(b)). These results suggest that bryostatin-1 treatment upregulates expression of a 17 kDa protein in BL, and this protein has an immunostimulatory function.
BL possesses a well-known defect in HLA class I-mediated Ag presentation, resulting from the poor immunogenicity of the EBNA1 protein. EBNA1 possesses an internal Gly-Ala repeat that impairs its proteasomal processing, leading to weak stimulation of CD8+ T cells . This defect, although well studied, addresses only one aspect of the immune response to BL. Less is known about the role of HLA class II-mediated immune responses to this malignancy. Studies have generally focused on CD8+ T-cell responses due to their ability to directly kill target cells, but CD4+ T-cell responses mediated by class II are needed for lasting immune responses and memory [36, 37].
In this study, we have shown that although BLs express measurable class II proteins on their cell surface, they were unable to stimulate CD4+ T cells through presentation of HSA peptide or epitope. We demonstrate further that when incubated in buffer at pH 5.5, BL cells regain class II-mediated Ag presentation capacity. Treatment of BL with bryostatin-1 led to restoration of class II presentation and CD4+ T-cell stimulation. This restoration was due, in part, to the upregulation of a 17 kDa, immunostimulatory, peptidylprolyl-like protein which is normally expressed at very low levels in BL, but highly expressed in B-LCL.
The efficiency of class II-mediated Ag presentation to CD4+ T cells may be partially affected by the expression levels of components in the class II pathway: Ii (invariant chain), HLA-DM and HLA-DO [26, 33, 38]. However, we did not observe any significant differences in the expression levels of these pathway components between two BL and two B-LCL cell lines, ruling this out as contributing to the observed defect in BL. CD4+ T cell activation is also dependent on signals delivered by the co-stimulatory molecules, CD80/86, expressed by B cells, yet BLs are known to express lower levels of these molecules . It is plausible that the BL-associated class II defect was a result of insufficient co-stimulation. External co-stimulation may be provided to T cells in the form of anti-CD28, which serves as a surrogate for CD80/86. While our T-cell hybridomas do not require co-stimulation, we still evaluated whether the decreased expression of co-stimulatory molecules contributed to the BL defect. However, even under these conditions, BL cells were unable to stimulate activation of CD4+ T cells. We gleaned further evidence that co-stimulation is not the cause the BL-associated class II defect from assays demonstrating that cross-linking IgM on BL cells failed to result in CD4+ T-cell stimulation (data not shown).
The presentation of Ag via HLA is central to the immune system’s ability to detect pathogens and transformed cells and mount immune responses to these cells. Efficient Ag presentation is dependent on efficient binding of peptides to HLA. While co-stimulation was not the cause of BL’s inability to present Ag through class II, the possibility existed that BL-expressed class II was not able to bind Ag efficiently, thus preventing T-cell stimulation. Binding assays, however, demonstrated that BL and B-LCL both bound peptide with a similar, measurable affinity.
Bryostatin-1, a potent modulator of protein kinase C, has previously been shown to stimulate upregulation of HLA class II in colorectal cell lines and dendritic cells and to enhance Ag presentation in dendritic cells [23, 24]. To date, however, its effect on HLA class II expression and Ag presentation in lymphoid malignancies has not been evaluated. Based on this information, we sought to determine if treatment with bryostatin-1 was sufficient to enable restoration of class II-mediated Ag presentation to BL. We found that the BL cell lines Nalm-6.DR4 and Ramos.DR4 did indeed regain HLA class II Ag presentation capacity following treatment with bryostatin-1. Our assays with Ramos.DR4 cells demonstrated that restoration of HLA class II Ag presentation could partially be due to increased peptide binding by HLA class II following treatment with bryostatin-1. Additionally, protein expression analysis following bryostatin-1 treatment showed a marked increase in a 17 kDa peptidylprolyl-like protein in Nalm-6.DR4, which was expressed at very low levels in untreated Nalm-6.DR4 and expressed at high levels in 6.16.DR4.DM. This protein, when extracted and used in Ag presentation assays, enhanced class II-mediated Ag presentation in 6.16.DR4.DM cells. Thus, bryostatin-induced restoration of class II Ag presentation in BL cells was mediated by an increased expression of a peptidylprolyl-like protein.
BL is a rapidly growing malignancy and thus requires aggressive chemotherapy to control its spread. Currently used chemotherapy regimens have achieved high cure rates in both adults and children, but treatment-associated toxicities are problematic. This issue is of particular concern for elderly and HIV-infected patients who show inferior responses and reduced tolerance of treatment-associated toxicities . Treatment success has improved with the use of anti-CD20 monoclonal antibody, rituximab . However, toxicities remain problematic, and the use of an immunosuppressive in HIV-infected patients is a subject of ongoing debate [42, 43]. While current treatments for BL have shown overall success, there is obvious room for improvement in the treatment of elderly and HIV-infected patients. Our future studies will continue to evaluate the role of bryostatin-1 in restoring class II-mediated Ag presentation in BL and determine the immunostimulatory role of the peptidylprolyl-like protein. A better understanding of these factors may lead to development of novel immunotherapies which could augment, lessen, or eliminate the need for toxic chemotherapies.
Azim Hossain and Jason M. God contributed equally to this paper.
We thank Dr. Janice Blum (Indiana University School of Medicine) for providing cell lines and reagents, and Dr. Daniel Knapp (Department of Pharmacology) for mass spectrometry facility and technical assistance. This work was supported by grants from the National Institutes of Health (5R01CA129560 and CA129560-S1) to A. Haque. The research presented in this article was also supported in part by the Tissue Biorepository and Flow Cytometry Shared Resource as part of the Hollings Cancer Center at the Medical University of South Carolina which is funded by a Cancer Center Support Grant P30 CA138313.
Supplemental Figure 1 shows the results of whole HSA and HSA peptide titration with Nalm-6.DR4, Ramos.DR4 and 6.16.DR4.DM cells. BL cell lines Nalm 6.DR4 and Ramos.DR4 fail to stimulate IL-2 production at concentrations 5, 10 and 20 µM of whole HSA or HSA peptide, while the B-LCL 6.16.DR4.DM line shows a dose-dependent increase in levels of IL-2 production. These results suggest that BL cells possess a defect(s) in the presentation of Ag(s) to stimulate CD4+ T cells via HLA class II molecules, and this defect in Ag presentation is not dependent on antigen concentration.
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