|Home | About | Journals | Submit | Contact Us | Français|
Class II MHC proteins bind peptides and present them to CD4+ T cells as part of the immune system's surveillance of bodily tissues for foreign and pathogenic material. Antigen processing and presentation pathways have been characterized in detail in normal cells, but there is little known about the actual viral peptides that are presented to CD4+ T cells that signal infection. In this study, two-dimensional LC-MS/MS was used to identify vaccinia virus-derived peptides among the hundreds to thousands of peptide antigens bound to the human class II MHC protein HLA-DR1 on the surface of vaccinia virus-infected cells. The peptides, derived from the I6L, D6R, and A10L viral proteins, were 15 residues in length, bound efficiently to HLA-DR1 as synthetic peptides, and were recognized by vaccinia-specific CD4+ T cells obtained from an immunized donor.
The eradication of smallpox in 1980 is considered to be one of the most important achievements in public health. Although variola virus, the causative agent of smallpox, is found only in a few high security laboratories at the present time, the possible development of variola as a bioweapon 1, 2 and the emergence of related viruses such as monkeypox 3 have renewed interest in immunization against smallpox and other poxvirus infections. Central to the success of the eradication campaign was the use of vaccinia virus as a vaccine for this disease. However serious side effects with the current vaccine limit its use as a preventive tool 4. Identification of vaccinia-derived epitopes presented by MHC molecules to virus-specific T cells capable of generating immune responses comparable to those elicited by the attenuated virus but without severe side effects is a major goal in the development of a new generation of safer smallpox vaccines. For poxvirus such as smallpox and vaccinia, CD4+ T cell epitopes, which are presented by class II MHC proteins, are of particular interest because of their role in development of protective antibody responses induced by vaccination 5.
Only recently have CD4+ T cell epitopes been identified for vaccinia virus 6-10. Classically, T-cell epitopes are defined by screening of sets of partially overlapping synthetic peptides covering the entire sequence of known antigenic proteins, or covering the entire protein component of a genome if no protein antigens are known. Candidate epitopes are tested for immunogenicity using blood samples from immunized or exposed donors. For a large-genome virus like vaccinia, which encodes over 230 open reading frames, such screening is extremely labor-intensive and requires large numbers of synthetic peptides and blood samples. Recent approaches to identification of CD4+ T-cell epitopes from vaccinia have emphasized development of high-throughput screening methodology 7, 9 and computational prediction of MHC binding affinity 8, 10 to winnow the number of candidate peptides prior to screening. In all of these studies T cells were used to distinguish epitope from non-epitope sequences. This limits the identification of T cell epitopes to those detected by the particular T cell lines used, for which the specificity is dictated by the method used to elicit the line and individual-to-individual differences in immune responses. In addition, impaired antigen presentation in vaccinia infected cells has been reported 11, 12 and appears to be at the level of peptide loading into MHC class II molecules. Direct characterization of peptides bound to class II MHC molecules in infected cells provides information about vaccinia T cell epitopes complementary to that obtained from cellular studies, and could provide insights into vaccinia effects on antigen presenting pathways.
Mass spectometry has proven effective in the identification of endogenous “self”-peptides presented by a normal uninfected cell 13-16, and the spectrum of naturally processed self peptides has been characterized for many MHC II proteins (for examples, see entries in the Syfpeithi (www.syfpeithi.de) 17 and IEDB (www.immunepitope.org) 18 databases). Peptides derived from viral proteins are expected to be present at low abundance among the total pool of MHC-bound peptides, but recent advances in mass spectrometry instrumentation and associated computational methods have allowed extension of these techniques to characterization of peptide antigens derived from infectious agents. The combination of reverse phase liquid chromatography, T cell screening of chromatographic fractions, and tandem mass spectrometry has been used to characterize several naturally processed MHC class I-restricted CD8+ T cell epitopes, derived from hepatitis B virus 19, Epstein-Barr virus, 20, 21 and Borna disease virus, one of the few experimental infectious models in rats 22. Far fewer naturally-processed pathogen-derived epitopes have been characterized for MHC class II proteins 23. Two groups have identified MHC class II-bound peptides derived from the transforming viruses used to immortalize the cell lines under study, Epstein-Barr virus 24, 25 and chicken syncytial virus 26 but it is not known whether such peptides are recognized by pathogen-specific T cells. The Mayo Vaccine Research Group has reported an increasing number of HLA-DR3-restricted T cell epitopes originating from measles virus 27-29. Finally, four HLA-DR1-associated peptide epitopes originating from Neisseria meningitides bacteria have been identified using a stable isotope tagging approach 30. In this work, we report identification by liquid chromatography and tandem mass spectrometry of three naturally-processed CD4+ T-cell epitopes derived from vaccinia virus. The peptides were sequenced directly after elution from DR1 isolated from infected cells, without the need for pre-screening chromatographic fractions using T cell lines. Each of the identified peptides binds to DR1, and was recognized by CD4+ T cells from a vaccinated donor.
The MVA strain of vaccinia virus 31, 32 and an established DR1+ human B lymphoblastoid cell line (LG2, IMGT entry HC10984 33) were used in this study. Cells were infected with live vaccinia virus at a multiplicity of infection (MOI) of approximately 1 and incubated at 37° C and 5% CO2. Uninfected (control) and vaccinia-infected cells were harvested at various times post-infection (1−22 hrs). Equal-sized batches (1 × 109) cells were collected by centrifugation (1500g, RT, 10 min), washed in phosphate-buffered saline, and used for isolation of HLA-DR1 molecules and HLA-DR1 - bound peptides as described below.
The fraction of LG2 cells infected with vaccinia virus was determined by Flow cytometry using purified anti-E3L monoclonal antibody (Tw2.3), a gift of J.W. Yewdell (National Institute of Allergy and Infectious Diseases, Bethesda, MD). The vaccinia E3L protein is a late viral protein that can be detected in infected cells after fixation and permeabilization 34. At each time point a small aliquot of cells was treated with Cytofix/cytoperm solutions (BD Biosciences), as described by the manufacturer, and divided into fractions for staining with 10 μg/ml of anti-E3L monoclonal antibody (TW2.3), anti-DR1 monoclonal antibody (LB3.1), or an isotype-matched control antibody. Following incubation on ice for 40 min, unbound antibody was removed by three washes with cytoperm buffer. Cell fractions were then incubated with anti-mouse IgG (H+L)-FITC labeled (Jackson ImmunoResearch) in cytoperm buffer. After washing with cytoperm, cells were fixed with 1% paraformaldehyde in PBS and loaded into a FACSCalibur instrument (BDBiosciences) equipped with CellQuest Sofware. The obtained dataset was analyzed with FlowJo7.2 (Tree Start Inc).
The procedure used for isolation of detergent-solubilized MHC class II proteins from human B cell lines was modified from the one originally described by Gorga et al 35. Immunoaffinity columns were constructed using protein A-Sepharose (Repligen Corporation, Needham, MA) covalently coupled to a purified HLA-DR1-specific mAb (LB3.1, IgG2b). Briefly, anti-HLA-DR1 mAb (2 mg/ml) was added to 5 ml of protein A-Sepharose beads and mixed by rocking for 1 h. Following incubation, the beads were washed with 200mM sodium borate (pH 9.0) and resuspended in 10 ml of borate buffer containing 400mM freshly-dissolved dimethyl pimelimidate dihydrochloride (DMP). The coupling reaction was allowed to proceed for 30 minutes, followed by sequential washing with (i) 200mM ethanolamine (pH 8.0), (ii) 200mM borate (pH 9.0), (iii) phosphate-buffered saline (PBS) with 0.02% sodium azide (PBSZ), and finally (iv) 50mM CAPS, (pH 11.5) before equilibration and storage in PBSZ.
Uninfected and vaccinia-infected B cells (109/preparation) were resuspended in 10ml of ice-cold lysis buffer (50mM Tris-HCl, 150mM NaCl, pH 8.0) containing “complete” protease inhibitor tablets (Roche Diagnostics GmbH, Mannheim, Germany). The cells were lysed using a polytron homogenizer, and the mixture was centrifuged at 6,000g, 4° C for 10 min to remove unlysed cells, nuclei and cell debris. The supernatant was reserved and the pellet was resuspended, homogenized, and centrifuged again. This procedure was repeated until the lysate was no longer turbid. The combined supernatants were spun at 75,000g for 1 h at 4° C to pellet the membrane fractions. Pelleted membranes were solubilized in 25 ml of ice-cold lysis buffer containing 5% β-octylglucoside (Sigma-Aldrich Corp., St. Louis, MO) and mixed slowly overnight to promote solubilization. After centrifugation of the solubilized membranes at 75,000g for an additional hour, the MHC-class II peptide complexes were isolated by immunoaffinity chromatography using HLA-DR1-specific mAb (LB3.1) coupled to protein A-Sepharose. Briefly, a chain of affinity columns (uncoupled Protein A sepharose, human IgG-Protein A sepharose, HLA-A2-specific BB7.2-Protein A sepharose and HLA-DR1-specific LB3.1-Protein A sepharose) were washed with PBS and equilibrated in lysis buffer, the sample was loaded, and the columns were washed with 5 column volumes of lysis buffer containing 5% β-octylglucoside and 10 column volumes of lysis buffer containing 1% β-octylglucoside. The columns were separated, and HLA- DR1 molecules were eluted from LB3.1-Protein A Sepharose with 5 column volumes of 50mM CAPS (pH 11.5). Eluates were immediately neutralized with 300mM NaH2PO4 (pH 6.0), and concentrated by ultrafiltration (Amicon Ultracel-10 membrane, Millipore, Billerica, MA) approximately 20 fold. Buffer exchange, to PBS, was performed to remove any remaining detergent.
HLA-DR1, pre-loaded with influenza hemagglutinin (HA) fragment 306−318 (PKYVKQNTLKLAT), was used as an internal standard (1μg) corresponding to ~1% of the total amount of HLA-DR1 level, of purified recombinant HLA-DR1 in complex with HA peptide was added to the infected and control sample lysates before immunoaffinity purification.
Peptides were released by acid elution following a procedure originally developed by Demotz et al 36. Acetic acid (14% final concentration) was added to immunoaffinity-purified HLA-DR1 to dissociate any bound peptides. The mixture, in a total volume of 2 ml, was incubated at 65° C for 10 min to promote full peptide dissociation. Released peptides were concentrated by another ultrafiltration step (Centricon YM-10 membrane, Millipore, Billerica, MA), and were further vacuum-concentrated in a Speed-Vac (Savant Industries) before storage at −20° C.
HLA class II-eluted peptides were desalted and fractionated into 12 fractions per sample using a 1 mm i.d. (inner diameter) by 10 mm long reversed phase cartridge (Peptide Micro Trap; Michrom BioResources, Inc., Auburn, CA). The solvent system was composed of 0.01% trifluoroacetic acid in water (A) and 0.01% trifluoroacetic acid in acetonitrile (B). The sample was introduced into the column for 15 min using solvent A, after that flow was reversed and the cartridge was washed with 2% B in A for 5 minutes. Then the gradient of 2−60% B in 30 min, 60−100% B in 15 min at flow rate 0.2 ml/min was programmed. The gradient was followed by 10 minutes wash using solvent B only. The collected fractions (5 minutes, 1ml each; 12 per sample) were vacuum-concentrated to a final volume of ~10 μl.
The eluted peptide fractions were diluted with acetonitrile/formic acid to produce final concentrations of 2% acetonitrile and 2% formic acid and were analyzed by microcapillary LC-MS/MS using a Finnigan LTQ linear quadrupole ion trap mass spectrometry system (ThermoFisher, MA). Peptides were first trapped on a 300 μm i.d. × 5 mm, 5 μm, 100Å C-18 PepMap column (LC Packings, CA) at a flow rate of 35 μl/min in 2% acetonitrile, 0.1% formic acid. The flow through the trapping column was then reversed and reduced to 350 nl/min and directed onto the 75 μm i.d. × 100 mm PicoFrit capillary column (New Objective, MA). The solvent system was composed of 0.1% formic acid, 0.01% trifluoroacetic acid in 2% acetonitrile (A) and 0.1% formic, 0.01% trifluoroacetic acid in 90% acetonitrile (B). The elution gradient was programmed as follows: 2% B for 4 min, 2−17% B in 8 min, 17−40% B in 18 min, and 40−98% B in 4 min. The LTQ mass spectrometer was operated in data dependent mode with one full survey scan (m/z 400−2000), followed by product ion scans (relative CID energy 35) of 10 the most intense ions in the survey scan. The product ion scans were acquired with a 2.0 unit isolation width and normalized collision energy of 35.0. Ions selected for product ion scans were placed on an exclusion list for the following 30 sec. Sample ion spectra are shown in Supplemental Figure 1.
The product ion acquired spectra were searched against the combined human and vaccinia virus strain MVA subsets of the NCBI nr database (July 2006 release) using the SEQUEST (ThermoFinnigan, San Jose, CA; version 27, rev. 12) search engine. Search parameters were set as follows: precursor ion mass tolerance ±1.5Da, fragment ion mass tolerance ±0.5Da, no enzyme specificity, monoisotopic precursor mass, monoisotopic fragment ion mass, variable modification of methionine oxidation. Search results were imported into the Scaffold program (version Scaffold-01_06_06, Proteome Software Inc., Portland, OR) for subsequent X!Tandem (www.thegpm.org; version 2006.04.01.2) searching and probabilistic evaluation of search results. Search results were filtered using Sequest based thresholds at HUPO recommended confidence settings 37 (ΔCn>0.1; XCorr: 1+ > 1.5, 2+ > 2.3, 3+ > 2.5; Sp≥300) with a Scaffold peptide probability >80% and protein probability >50%. An additional search was carried out using these same parameters but instead performed against a database containing both forward and reverse human and vaccinia sequences. Of the 102 ions from the infected cell sample for which sequence identification could be made, only one (m/z=908.76) scored above these filter settings in a reverse database search. All vaccinia sequences identified were confirmed by comparison of the product ion spectra from the eluted samples and the product ion spectra obtained from the synthetic peptides.
Peptides I6L[338−352] sequence IYTYRIIKSSFPVPT, D6R[157−171] sequence KIPFLLLSGSPITNT, and A10L[293−307] sequence SMRYQSLIPRLVEFF from vaccinia virus, and the control Gag peptide from HIV Gag protein p24[33−44] sequence PEVIPMFSALSEGATP38 and HA[306−318] peptide PKYVKQNTLKLAT were synthesized using standard solid-phase Fmoc chemistry on a Symphony (Protein Technology Inc., Tucson, AZ) peptide synthesizer and purified by HPLC (Vydac-C18). The purity and homogeneity of each peptide was checked by high performance liquid chromatography and MALDI-TOF mass spectrometry.
For peptide binding experiments, recombinant HLA-DR1 protein was produced by expression of the extracellular domains of its α and β subunits in Escherichia coli, followed by isolation of inclusion bodies and refolding in vitro as described previously 39. Refolded HLA-DR1 was purified by immunoaffinity chromatography using the conformation-specific monoclonal antibody LB3.1, followed by gel filtration chromatography in phosphate-buffered saline, pH 6.8. The protein concentration was measured by UV absorbance at 280 nm, using ε280 of 54375 M−1 cm−1. A competition binding assay was used to determine the binding affinities of the synthetic peptides to HLA-DR1. Peptide-free HLA-DR1 (15nM) was mixed together with biotinylated influenza hemagglutinin HA[306−318] peptide probe (Habio, 15nM) and varying concentrations of unlabelled competitor peptide (10−10 - 10−5 M). The mixtures were incubated for 3 days at 37° C in 100mM sodium phosphate buffer at pH 5.5, containing protease inhibitors and 0.5 mg/ml β-octylglucoside, followed by detection of bound biotinylated peptide using an immunoassay that employs anti-DR1 capture antibody LB3.1 and alkaline phosphatase-labeled streptavidin. IC50 values were obtained by fitting a binding curve to the plots of absorbance versus concentration of competitor peptide.
The generation and characterization of vaccinia T cell lines (TCLs) used in this study have been described 10. Briefly, blood samples were obtained from a DR1 donor using sodium heparin as anticoagulant. This donor was immunized approximately 35 years before the first sample of blood was obtained. A second blood sample was obtained 13 days after re-immunization (2nd dose of the vaccine). Peripheral blood lymphocytes (PBMCs) were purified from blood samples by standard techniques using Ficoll-Hypaque (Pharmacia). After washing with PBS, cells were resuspended in cRPMI+10%HS (RPMI supplemented with 10% heat inactivated human AB+ serum, L-glutamine, penicillin streptomycin, non-essential amino acids, and sodium pyruvate) and adjusted to concentration of 2 million/ml. One million cells were then added per well into a 24 well tissue culture plate and volume adjusted to 1ml by addition of antigen. In the case of anti-vaccinia TCLs, we used a cell extract of CV-1 cells infected with the Dryvax strain of vaccinia virus as antigen. Vaccinia virus in the extract was inactivated by incubation at 60°C for 1 hr and concentration adjusted to 1.7×107 pfu/ml by dilution in cRPMI+10% HS. After three days of antigenic stimulation, 1ml of cRPMI+10% HS supplemented with 100 U/ml IL-2 were added per well. During the following 12 days, cells were fed with medium supplemented with IL-2 every three to four days. TCLs to peptide A10L were generated as described above from the same vaccinia-immunized donor and from a non-immunized donor using 10 μM of peptide instead of vaccinia virus for the in vitro expansion.
T cell responses were evaluated by IFN-γ ELISPOT according to the protocol described by the manufacturer (BD Biosciences). Briefly, ELISPOT plates were coated overnight with anti-human IFN-γ antibody and the following day washed three times with PBS and blocked with cRPMI + 10% HS for two hours. As antigen presenting cells, we used either (a) MVA-infected-LG2 B cells fixed for 10 min on ice with 1 % paraformaldehyde in PBS, washed twice with PBS and once with cRPMI + 10%HS, or (b) autologous PBMCs that were irradiated before use (4800 rads). LG2 cells were used at 5×104 cells/well and PBMCs at 1×105 cells/well. Synthetic peptides served as antigen in assays using PBMCs. T cells were added after washing twice in PBS and once in cRPMI + 10% HS. Fifty thousand T cells were added per well. ELISPOT plates were incubated for either 1 to 22 hours, when infected LG2 cells were used as APCs, or overnight (15 to 17 hours), when irradiated PBMCs were used as APCs. Following incubation, the plates were washed, incubated sequentially with biotinylated anti-IFN-γ, avidin-peroxidase, and finally in AEC substrate. The number of IFN-γ-secreting cells was determined using an ELISPOT analyzer equipped with ImmunoSpot 3.2 software (Cellular Technology Ltd, Cleveland, Ohio).
In order to increase the likelihood of isolating MHC-vaccinia peptide complexes among the pool of endogenous peptide complexes, we infected HLA-DR1 (DRB1*0101)-positive B-lymphoblastoid cell line LG2 with the attenuated vaccinia virus strain MVA (modified vaccinia Ankara) and followed the kinetics of the T-cell response from 1 to 22 hours post infection. We reasoned that T cell responses to virus-infected cells would correlate with the number or quantity of vaccinia peptides bound to MHC molecules. In this manner, T cells will be used as an indicator of antigen processing and presentation (Figure 1A). Lymphoblastoid cell lines, similar to the one we used in this study, are frequently used to study class II-restricted responses.
We found that T cell responses, measured as the number of IFN-γ secreting cells in an ELISPOT assay, increased over time with the maximum response at 22 hours, the last time point analyzed. To measure the fraction of cells infected under these conditions, we used flow cytometry to detect expression of the late vaccinia protein E3L in samples of permeabilized cells. Approximately 50% of the cells expressed vaccinia proteins at 22 hours post-infection (Figure 1B). Infected cells harvested at this time were used for isolation of MHC proteins and characterization of MHC-bound peptides. HLA-DR1 was isolated from infected and control non-infected LG2 cells by immunoaffinity chromatography of detergent-solubilized membrane fractions, following a conventional protocol 35 (see Methods for details). Approximately 0.6 mg of DR1 was recovered from 1 liter culture medium containing 109 cells. No significant difference in yield of HLA-DR1 was observed between the infected and control samples (not shown). Peptides were eluted under acid conditions as described 13, 40 and vacuum concentrated for further analysis.
The eluted peptides were desalted and fractioned into a total of 12 fractions per sample using an off-line Peptide Micro Trap reverse-phase HPLC trapping column (Michrom BioResources, Inc., Auburn, CA). Each fraction was analyzed separately by μLC-MS/MS (LTQ, ThermoFinnigan) and the resulting MS/MS spectra were searched for human and vaccinia peptides using the SEQUEST search engine (ThermoFisher). The spectra were searched against a library containing the NCBI non-redundant (nr) human database and all vaccinia (MVA) sequences, using Sequest XCorr-based thresholds at HUPO recommended filter settings (ΔCn>0.1; 1+ > 1.5, 2+ > 2.3, 3+ > 2.5) with Sp≥ 300 and Scaffold peptide probability at 80% or higher. These filter settings allowed for identification of an internal control peptide (influenza hemagglutinin (HA) fragment 306−318 PKYVKQNTLKLAT) in both infected and non-infected samples, while at the same time eliminated all vaccinia-derived false-positive sequences identified in non-infected sample. The internal standard was introduced in the form of purified HLA-DR1-HA peptide complexes at approximately 1% abundance to the mixture of MHC-peptide complexes purified from infected and control cells. The HA peptide sequence was identified by a SEQUEST search within Peptide Micro Trap fraction 9 (from both infected and control cells) with m/z 753.3 (+2) (data not shown).
One potential complication in the use of database-driven sequence identification rather than complete de novo sequencing based on fragmentation analysis is the possibility of misidentification of peptides due to statistical matching of incomplete fragmentation patterns 41. One proposed solution to this problem is the inclusion of randomized sequences in the database that can be used to evaluate the statistical frequency of such mismatches 42. A reverse database analysis of a subset of 102 peptide ions identified in fractions from the infected cells, only one was identified in a reverse database search using the same parameters, suggesting an approximate false-positive rate of ~1%. Overall, 165 individual DR1-bound peptides derived from 106 different human proteins were identified in fractions from the infected and non-infected control cells (see Supplement Table 1 and 2). In many cases, a particular peptide sequence was represented by several partially overlapping peptides in nested sets, as previously observed for naturally processed peptides bound to MHC class II proteins 13, 16, 43, a result of the differential processing of peptide termini extending out the ends of the MHC peptide class II binding groove. Peptide sequences derived from the MHC class II-associated invariant chain, the MHC class I protein HLA-A2, and the transferrin receptor have been observed previously in studies of endogenous peptides bound to HLA-DR1 isolated from B cell lines 13, 44. Sequences derived from annexin A2, MHC class II DR alpha, protective protein for beta-galactosidase, eukaryotic translation elongation factor 1, phosphoglycerate kinase, and cathepsin S have been observed previously in a study of endogenous peptides presented by DR1/DR12 heterozygous dendritic cells 45. The other sequences likely represent new endogenous peptide sequences. Most of the peptide sequences derived from human proteins were observed in both infected and control cells, but 44 peptides were observed only in the control cells, and 39 only in the infected cells. No significant differences in length, net charge, or average Kyte-Doolittle hydrophobicity values 46 were observed between the sets of peptides eluted from infected or control cells.
The SEQUEST search identified three peptides with sequences originating from vaccinia virus proteins (Table 1), present in the vaccinia-infected but not in non-infected cells that provided a control for false identification.
These vaccinia-derived peptides had SEQUEST XCorr scores significantly higher than the top match of the peptides eluted from non-infected cells, which could be considered as a relevant background level. These peptides originate from three different proteins: the telomere binding protein I6L (MVA067L), the early transcription factor VETF-1 aka D6R (MVA103R), and the major core protein A10L, precursor p4a of core protein 4a, (MVA121L). The first of these sequences is derived from the vaccinia virus telomere binding protein I6L and was found in Peptide Micro Trap fraction 5.
Figure 2A shows the CID product ion spectrum from precursor ion of m/z 892.93 (+2) that has been identified as IYTYRIIKSSFPVPT from vaccinia virus protein I6L (NCBI accession number gi|47088395) residues 338−352. To verify the identification of the m/z 892.93 (+2) as IYTYRIIKSSFPVPT, this sequence was chemically synthesized, purified, and subjected to the same MS/MS fragmentation (see Figure 2B). The naturally processed peptide obtained from the m/z 892.93 and the synthetic peptide IYTYRIIKSSFPVPT demonstrated an essentially identical product ion spectrum, clearly confirming the validity of the identification. The I6L residue 338−352 sequence identified here is highly conserved among poxvirus family members and within different vaccinia strains (see Table 2).
The second vaccinia virus derived peptide was found in fraction 8. The product ion spectrum (Figure 3A) obtained for a precursor ion m/z 801.10 (+2) has been identified as KIPFLLLSGSPITNT from the vaccinia virus early gene transcription factor (D6R or VETF-1; NCBI accession number gi|47088431) residues 157−171. A BLAST search done for this sequence shows that the identified peptide is highly conserved across number of other poxviruses as well as within vaccinia virus strains (Table 2).
MS/MS fragmentation pattern of synthetic KIPFLLLSGSPITNT peptide (Figure 3B) matches the spectrum of the naturally processed material confirming positive identification.
The third vaccinia peptide was found in fraction 9. Its precursor ion was m/z 944.00 (+2) and it was identified as SMRYQSLIPRLVEFF from vaccinia virus major core protein 4a (A10L; NCBI accession number gi|47088449) residues 293−307 (Figure 4A). The identified fragment appears to be conserved among poxvirus family members (see Table 2). In addition, the naturally processed peptide and the synthetic peptide SMRYQSLIPRLVEFF peptide exhibit nearly identical product ion spectra confirming the validity of the identification (Fig 4B).
Comparison of integrated peak intensities of the three vaccinia-derived peptides and the internal HA control peptide in experimental samples and in synthetic peptide mixtures suggests that the A10L and I6L peptides were present at ~1% or less of the total DR1-bound peptide pool, with the D10R peptide present at a substantially lower abundance. Additional viral peptides bound to DR1 on the surface of vaccinia-infected B cells might be present but below our level of detection.
Each of these peptides are encoded by a gene with a promoter sequence characteristic of late gene expression 47-49, and each is a component of the infectious viral particle 50. None of the proteins is known to be membrane associated, although I6L has been suggested to be important in encapsidation of the virus 51. How these proteins enter the MHC class II antigen loading process is not clear. It is possible that membrane-associated virions access the endo/lysosomal pathway through conventional endocytosis, or that autophagocytic pathways can access viral factories, the site of intensive vaccinia protein synthesis and viral assembly in infected cells 52.
Each of the eluted peptides was 15 residues long. In each case, the predicted DR1-binding 9-mer sequence (underlined in Table 2) was flanked by three residues on each side, consistent with the pattern observed for most naturally processed class II MHC antigens. The 15 residue length is somewhat shorter although not significantly different than the median eluted peptide length from either the infected or non-infected cells (18 residues), and within the range observed in a previous study for naturally processed measles peptides 29.
To evaluate the biological relevance of the naturally processed vaccinia-derived peptides, we characterized their affinity for HLA-DR1 and their recognition by human CD4+ T cells specific for vaccinia virus. The binding affinity of synthetic peptide to HLA-DR1 was studied using a competition ELISA-based assay (see Fig 5). Peptide binding IC50 values were 6.5 to 136 nM (Table 1), within the range of known antigenic peptides, and comparable to the tight-binding immunogenic HA peptide from influenza (IC50 = 35nM).
In order to demonstrate that the vaccinia-derived naturally-processed peptides eluted from infected cells in fact contain epitopes recognized by CD4+ T cells, we studied the IFN-γ response of T cells from a HLA-DR1 vaccinia-immunized donor to synthetic peptides representing these sequences by ELISPOT. This assay measures the frequency of T cells that respond to antigenic stimulation by secreting IFN-γ. As shown in Figure 6A, a vaccinia-specific T cell line generated many years after a single vaccinia immunization shows a weak response to D6R peptide. Responses to the remaining two peptides are in the same range that the background response. These findings suggest that the response to the D6R peptide is long lived and the corresponding T cells relatively abundant in this donor.
A second vaccinia immunization would be expected to increase the frequency of responding T cells, and we subsequently analyzed the response of T cells obtained 13 days after a booster immunization (figure 6B). We observed an improved response to the I6L peptide, but, somewhat contrary to our expectations, not to the D6R peptide. Thus, a T cell response to the I6L peptide also is induced by vaccination, but the responding cells either are short-lived or present at a lower abundance relative to those directed at the D6R peptide. The lack of recognition of the A10L peptide could indicate that T cells recognizing this peptide are absent, are present at a very low frequency, or do not expand well in vitro using the heat-inactivated vaccinia stimulation protocol employed in the generation of vaccinia-specific T cell lines. To explore these possibilities, we obtained blood from one immunized and one non-immunized DR1+ donors, and generated peptide-specific T cells lines by expansion with peptide A10L instead of heat-killed vaccinia virus. The fine specificity of the anti-peptide T cell lines was evaluated as before by IFN-γ ELSIPOT in antigen presenting cells pulsed with peptide A10L or a control peptide (Gag peptide). As shown in Figure 6C, responses to either Gag or A10L peptides in the T cell line generated from the non-immunized donor are in the same order of T cells from wells in which peptide was omitted suggesting a very low frequency of anti-peptide A10L T cells in the non-immunized donor. In contrast, responses to peptide A10L in the T cell line generated from the immunized donor were approximately three times higher than the ones observed in the control peptide or wells without peptide. Thus, the A10L peptide also is recognized by T cells of an immunized donor.
The first vaccinia-derived CD4+ T cell epitopes were reported in 2006 in a study of CD4+ and CD8+ T cell responses to overlapping peptide series covering the A29L, L1R, B5R, and A33R proteins 6. These proteins induce protective antibodies in animal models. However, the epitopes were not associated with a particular MHC protein. Very recently, four studies have reported identification of MHC-restricted CD4+ T cell epitopes in humans 7, 8, 10, and mice 9. These epitopes were identified by large-scale screening 7, 9 or bioinformatical 8, 10 approaches. In three of these studies 6, 7, 9, none of the epitopes identified here were observed. Two of the epitopes identified here, from the D1R and I6L epitopes, were identified in our previous study 10. The A10L epitope described here was not identified in any of the previous cell-based epitope screens, despite being present at relatively high abundance among the pool of DR1-bound peptides. The inability of previous approaches to identify this epitope may relate to differences in antigen processing pathways in infected as compared to non-infected cells, or to aspects of the generation of vaccinia-specific T cell lines, or to individual differences in anti-vaccinia immune responses. Since this epitope derives from an abundantly expressed viral core protein and the naturally processed MHC-bound peptide is present at high levels on the surface of vaccinia-infected cells, it would appear to be an attractive candidate for inclusion in a subunit vaccine.
In conclusion, we have directly identified from the pool of endogenous MHC-bound peptides by database analysis three vaccinia-derived peptides naturally processed in infected cells and loaded onto the class II MHC protein HLA-DR1. The findings were additionally validated using synthetic versions of the identified peptide sequences. In each case, the fragmentation spectra of the eluted peptides were essentially identical to those of the corresponding synthetic peptides, confirming their identification. These epitopes, conserved in the poxvirus family, are among the naturally processed and characterized CD4+ vaccinia epitopes, and could find use in the development of next-generation vaccines against smallpox and other poxvirus, and in the evaluation of T cell immunity induced by vaccine candidates.
I. Strug et al. "Vaccinia peptides eluted from HLA-DR1 isolated from virus-infected cells are recognized by CD4+ T cells from a vaccinated donor."
Supplementary Figure 1. Ion chromatograms.
Base peak (most abundant ion) and specific ion intensity plots for fractions containing (A) the highly abundant endogenous peptide derived from MHC class I (B) vaccinia peptide I6L [338-352], (C) vaccinia peptide A10L [393-307], and (D) the internal control HA peptide. No distinct peak in either base peak or specific ion plots was observed for the lower abundance vaccinia peptide D6R [157-171].
Supplementary Table I - Peptides from infected cells
Supplementary Table II - Peptides from control cells
The authors thank Loretta Lee for culture of LG2 cells and J.W. Yewdell for the anti-E3L monoclonal antibody Tw2.3. Core resources supported by the Diabetes Endocrinology Research Center grant DK32520 were used. This work was supported by NIH-U19-057319.