Background
Severe acute respiratory syndrome (SARS), a newly emerging infectious disease, is caused by a SARS-associated coronavirus (SARS-CoV) [
1‐
3], which may originate from some wild animals [
4]. After its first occurrence, SARS rapidly spread around the world along international air-travel routes, reaching all five continents and resulting in several hundreds of deaths [
5]. The most recent epidemic of SARS occurred in Beijing and Anhui, China in April 2004 and originated from laboratory contamination (WHO update 7; see Further Information). Although the outbreaks seem to be over, SARS remains a safety concern because of the possible reintroduction of a SARS-like coronavirus (SL-CoV) into humans and the risk of an escape of SARS-CoV from laboratories [
6‐
8]. More importantly, a new recombinant virus derived from human [
9], swine and/or avian influenza virus, might re-emerge as a new SARS-CoV type, much like the recent emergence of a novel swine-origin influenza A (H1N1) in humans. Thus, it is essential to develop various and distinct strategies to combat this highly contagious disease.
The published literature reports that high titres of neutralizing antibodies and SARS-CoV-specific cytotoxic T lymphocyte (CTL) responses were detected in patients who had recovered from SARS [
10,
11], and the levels of those responses correlated well with disease outcome [
12]. Hence, both humoral and cellular immune responses appear to be crucial for the clearance of SARS-CoV infection. Immune responses can be raised directly against several of the SARS-CoV proteins [
13‐
15]. Targeting the spike (S) structural glycoprotein [
12,
16‐
18] in particular induces a robust immune response, suggesting it plays an important role in the systemic clearance of SARS-CoV [
10]. The viral surface S protein is involved in host cell receptor recognition, virus attachment and entry [
19]; adaptive evolution of S protein, thus, contributes to SARS-CoV overcoming the species barrier [
20]. Hence, many vaccines and therapeutics against SARS-CoV target the S protein [
19]. Considering that cytotoxic T-cell responses participate in the clearance of virus from recovered SARS patients and contribute to immunopathology in early stages of the disease [
21], one of the most attractive S protein-based strategies proposes eliciting a SARS-CoV CTL response to clear the infection. To this end, a detailed understanding of the S protein-mediated CTL response is essential.
Development of effective treatments and vaccines against SARS-CoV depends upon the underlying mechanisms of various immune effectors in protective immunity and identification of the protective antigens recognized by each. Epitopes are the basic antigenic elements of virus structural proteins, which functionally induce the host cell-mediated immune response. Identification of the CTL-specific epitopes of SARS-CoV proteins could provide the basis for the development of SARS immunity-based treatments and aid in the understanding of mechanisms underlying SARS-CoV pathogenesis.
HLA-A*0201 is expressed 39-46% of all major ethnicities [
22]. The identification of HLA-A*0201-restricted SARS-CoV/S CTL epitopes is an important contribution towards understanding the role of CTLs in SARS-CoV pathogenesis and protection. Currently, several CTL-specific SARS-CoV S protein epitopes have been identified in the context of HLA-A*0201, including S
411-420, S
787-795, S
978-986, S
1042-1050, S
1167-1175, S
1203-1211 and SSp-1 [
23‐
26], and the H2 complex, including S
366-374, S
436-443, S
525-532 and S
1031-1047[
18,
27]. It is likely that additional S protein CTL epitopes exist. S protein is relatively large in size and usage of different detection methods may result in the identification of novel S protein-derived epitopes. In turn, this data will provide advances towards understanding the mechanisms of SARS-CoV infection, and contribute to the development of future SARS-CoV infection intervention strategies.
In this study, we identified a novel SARS/S-specific, HLA-A*0201-restricted epitope that was conserved among SARS-CoV strains. Based on a binding affinity-based prediction and a proteosomal cleavage site prediction, we constructed a panel of potential HLA-A*0201-restricted CTL peptides from the S protein. Each candidate peptide was evaluated for its binding affinity to HLA-A*0201 molecules using the T2 cell-peptide binding test. We then evaluated the ability of HLA-A*0201 binding peptides to provoke CTL responses in peripheral blood lymphocytes (PBL). PBL preparations from major histocompatibility complex (MHC)-matched healthy donors or HLA-A2.1/Kb transgenic (Tg) mice, were incubated with dendritic cells (DCs) that had been pre-pulsed with the peptides of interest. We identified a novel SARS-CoV S protein-derived CTL epitope S(958-966)(VLNDILSRL) that was capable of priming the S protein-specific HLA-A2.1-restricted CTL response. The effective CTL response was evidenced by cell death of peptide-pulsed T2 and peptide-pulsed Jurkat-A2/Kb cells. The findings of this study should provide insight into the immunological characteristics of spike protein and provide an alternative strategy for the future development of SARS-CoV S protein CTL epitope-based vaccines.
Discussion
It is known that SARS-CoV can induce a strong specific CTL response in infected patients, besides high titres of neutralizing antibodies [
10,
11]. Furthermore, the CTL response levels correlate with disease outcome [
12], suggesting CTL response is crucial for the clearance of SARS-CoV. Among all the encoded proteins in the SARS-CoV genome, S protein is currently considered the most important target to prime the host immune response [
12,
16‐
18]. It has been reported that an inflammatory cell influx of airway macrophages and a massive release of cytokines occur during the peak of SARS infection [
30]. Thus, it is reasonable to investigate the underlying mechanism of specific CTL response induced by SARS-CoV S protein during SARS-CoV infection which may have a positive role in SARS-CoV clearance or a negative role in SARS-CoV immunopathogenesis.
In this study, we predicted and validated a novel CTL epitope of SARS-CoV S protein. We used two prediction systems to identify candidate CTL epitopes of S protein (i.e., HLA-A2-binding peptide prediction method combined with a proteosomal cleavage site prediction system) to improve prediction accuracy. The eight predicted peptides were then verified via MHC peptide binding assay (Table
1). Among the eight candidate peptides, Sp5, Sp6, Sp7 and Sp8 exhibited the highest capacity to induce more potent CTLs secreting IFN-γ and to lyse target cells from HLA-A*0201-matched healthy donor PBLs (Figure
2). Further
in vivo investigation showed that plasmid encoding the full-length SARS-CoV S gene elicited strong CTL response in HLA-A2.1/K
b transgenic mice. These CTLs could produce substantial amounts of IFN-γ and kill target cells in a peptide-specific and HLA-A*0201-restricted manner (Figure
3), suggesting the predicted candidate peptides were native epitopes, capable of priming CTL responses
in vivo. We found that candidate peptide Sp8 held the greatest ability to secrete IFN-γ and kill target cells
in vivo (Figure
3). Another candidate peptide, Sp7, failed to induce the most potent peptide specific CTLs in Tg mice (Figure
3), despite it having had the highest such ability in comparison to the rest of the
in vitro stimulation set (Figure
2), indicating the need for candidate peptides to be biofunctionally validated
in vivo.
To date, several CTL epitopes of SARS-CoV S protein have been identified in the context of HLA-A*0201, including S
411-420, S
787-795, S
978-986, S
1042-1050, S
1167-1175, S
1203-1211 and SSp-1 [
23‐
26], or of the H2 complex, including S
366-374, S
436-443, S
525-532 and S
1031-1047[
18,
27]. In this study, we predicted and validated a novel CTL epitope of SARS-CoV S protein, Sp8 (S
958, VLNDILSRL). This may be due to the unique predictive methods used in our study. We combined strategies for prediction (i.e., HLA-A2-binding peptide prediction method combined with a proteosomal cleavage site prediction system). Previous studies used single methods, such as HLA peptide binding prediction or overlapping peptide strategy [
18,
23‐
27], suggesting different prediction strategies might lead to different results. In any case, the predicted candidate peptides require additional validation methods to ensure accuracy.
In our study, we also determined that among the eight peptides we predicted, four could potent prime CTLs to produce significant IFN-γ and lyse target cells; although, Sp8 peptide exhibited the most potency for CTL priming. However, Zhou
et al. reported that they only found one predicted peptide that could stimulate IFN-γ secretion and target cell lysis [
26]. This may reflect the different stimulators used in these studies; Zhou used peptides to stimulate the effector cells directly while we used DCs loaded with the candidate peptides.
We argue for the use of DCs as stimulator cells in ex vivo study because DCs are the most potent APCs for priming T cells, and they not only present peptides to T cells but also provide many important co-stimulatory signals. Moreover, under in vivo conditions DCs present peptides to T cells in the context of MHC molecules. Thus, using DCs as ex vivo stimulator cells most closely mimics the in vivo context.
Methods
Sequence alignments
Nucleotide sequences of SARS-CoV strains were analyzed using BioEdit version 5.0.9 software suite. The corresponding amino acid sequences of S protein were then aligned with Clustal W
http://www.ebi.ac.uk/clustalw/. SARS-CoV strains used were as follows, with the nucleotide sequence GenBank accession numbers in parentheses: BJ01 (AY278488), BJ02 (AY278487), BJ03 (AY278490), CUHK-Su10 (AY282752), CUHK-W1 (AY278554), Frankfurt 1 (AY291315), GD01 (AY278489), HKU-39849 (AY278491), HSR 1 (AY323977), Sin2500 (AY283794), Sin2677 (AY283795), Sin2679 (AY283796), Sin2748 (AY283797), Sin2774 (AY283798), TOR2 (AY274119), TW1 (AY291451), TWC (AY321118) and Urbani (AY278741).
Peptides
To identify potential HLA-A*0201-binding peptides within the S protein of the SARS-CoV (BJ01) strain, a combination of two computer algorithms was utilized. The predictive algorithm, "ProPred1"[
31], is a matrix-based method that allows the prediction of MHC binding sites in an antigenic sequence for 47 MHC class-I alleles. We restricted our analysis to the HLA-A2 allele, since it is prevalent in a large percentage of all major ethnicities and it is the most extensively studied HLA class-I antigen [
22]. ProPred1 also allows the prediction of the standard proteasomal and immunoproteasomales cleavage sites in an antigenic sequence. The simultaneous prediction of MHC binding and proteasomal cleavage sites in an antigenic sequence leads to the identification of potential T-cell epitopes. The second algorithm, "SYFPEITHI", was developed by H. G. Rammensee
et al[
32], and ranks peptides according to a score that takes into account the presence of primary and secondary MHC-binding anchor residues. The 9 mer peptides with a score exceeding 24 were selected in "SYFPEITHI".
The amino acid sequence of SARS-CoV/S (BJ01) was analyzed on both of the computer programs for the existence of 9-amino acid peptides predicted to bind to HLA-A2. The candidates peptides were synthesized at SHENYOU Biotech (Shanghai, China) and purified by reverse phase HPLC to > 95%, as confirmed by mass spectrometry. The published HLA-A*0201-restricted peptide S
411-420 (KLPDDFMGCV) derived from the S protein of SARS-CoV [
26] was used as a positive control for HLA-A*0201-binding ability, and the HBcAg-derived H-2
b-restricted peptide HBcAg
(131-140) (AYRPPNAPIL) was used as a negative control. Lyophilized peptides were dissolved in PBS at a concentration of 1 mg/ml and stored in aliquots at -20°C.
Cells and Cell Culture
HLA-A2+ individuals were selected by flow cytometry screening using the anti-HLA-A2 monoclonal antibody BB7.2. Buffy coats from HLA-A2+ normal donors were purchased from Southwest Hospital (Third Military Medical University, Chongqing, China). PBL from an HLA-A2+ healthy donor were separated on Ficoll-Hypaque density gradients (TBD, Inc, Tianjin, China), washed three times in phosphate-buffered saline (PBS), resuspended in RPMI1640 medium (Gibco, BRL) supplemented with L-glutamine (10 mg/ml), penicillin (5 × 104U/L), streptomycin (50 mg/L) and 10% fetal calf serum (FCS), and plated in 6-well plates at 4 × 106 cells per well.
Human TAP-deficient T2 cell line and BB7.2 cell line producing mAb against HLA-A2 were purchased from American Type Culture Collection. T2 cell line was maintained in RPMI1640 medium supplemented with 20% fetal bovine serum and 100 μg/ml penicillin/streptomycin. BB7.2 cell line was maintained in DMEM containing 10% FCS, 4 μg/L glucose, penicillin (5 × 10
4U/L) and streptomycin (50 mg/L). Jurkat-A2/K
b cells, a generous gift from Dr. W. Martin Kast (the Norris Comprehensive Cancer Center, Los Angeles, CA) and Dr. Jehad Charo (the Max Delbruck Center for Medicine, Berlin, Germany), were transfected with the HLA chimeric molecule containing the α1 and α2 domains from human HLA-A*0201 and α3 from mouse H-2K
b, to serve as a model system of HLA restricted responses [
33]. The Jurkat-A2/K
b (J(A2/kb)) cell line was maintained in RPMI1640 medium (Gibco, BRL) plus 10% calf serum and supplemented with 4 μg/L glucose, penicillin (5 × 10
4 U/L) and streptomycin (50 mg/L). All cell lines mentioned above were kept at 37°C in a humidified atmosphere of 5% CO
2 in air.
Animals
HLA-A2.1/Kb transgenic (Tg) mice were purchased from the Jackson Laboratory (Bar harbor, ME). For experimental purposes, six to eight week-old mice were used. Cell surface HLA-A*0201 expression was assessed by flow cytometry using fluorescein isothiocyanate (FITC)-labeled HLA-A2-specific mAb BB7.2 (Sterotec Ltd, Oxford, UK). Mice were kept in SPF animal care facilities and all experiments were performed according to the guidelines in the Institutional Animal Committee of TMMU.
Binding assay of candidate peptides to HLA-A2
All candidate peptides were tested individually for their capacity to bind to HLA-A2 molecules on the surface of human TAP-deficient T2 cells [
28]. Briefly, T2 cells were incubated with 20 μg/ml candidate peptides and 3 μg/ml human β2-microglobulin (Sigma, St Louis, MO) in serum-free RPMI1640 for 18 hours at 37°C in a 5% CO
2 atmosphere. Expression of HLA-A*0201 on T2 cells was then determined by staining with FITC-conjugated anti-HLA-A2 mAb BB7.2 and data analyzed using a FACSCalibur flow cytometer (Becton Dickinson, Mountain View, CA) and CellQuest software (Becton Dickinson). The published peptide S
411-420 and HBcAg
(131-140) served as positive and negative control, respectively. The former is known to bind to HLA-A2 molecule with high affinity, the latter has been identified as mouse H2K
d epitope that has little binding affinity with HLA-A2 molecule. The fluorescence index (FI) was calculated as follows: FI = [(mean FITC fluorescence with the given peptide - mean FITC fluorescence without peptide)/(mean FITC fluorescence without peptide)]. Peptides with an FI more than 1 were regarded as high-affinity epitopes.
Generation of CTLs in healthy donors
Human peripheral blood monocyte-derived DCs were generated as described previously [
28] with minor modifications. Briefly, human PBLs were suspended in serum-free RPMI1640 and allowed to adhere to 6-well plates at a final concentration of 1 × 10
7 cells/3 ml/well and cultured in 5% CO2 at 37°C. After 2 hours, non-adherent cells were gently removed with warm medium. The resulting adherent cells were cultured in RPMI1640 medium supplemented with 10% FCS, 20 ng/ml recombinant human interleukin-4 (IL-4) (R&D Systems, Minneapolis, MN) and 800 U/ml recombinant human granulocyte-macrophage colony stimulating factor (GM-CSF; Sandoz, Basel, Switzerland) in 5% CO
2 at 37°C. Every two days, one-half of the medium was replaced by fresh medium containing double concentration of GM-CSF and IL-4 as indicated above. Cell suspensions were collected for analysis of surface phenotype at different stages of development. After five days of culture, DCs were harvested for subsequent experiments (90% pure as confirmed by analysis of relatively DC-specific phenotype and with a typical DC morphology). 10 ng/ml recombinant human tumor necrosis factor (TNF-α, Peprotech, Rocky Hill, NJ) was added to the medium to induce phenotypic and functional maturation. Then, 48 hours later, DCs were used to prime autologous PBLs as follows, DCs were pulsed with 20 μg/ml peptide in the presence of 3 μg/ml β2-microglobulin at 37°C for 5 hours and irradiated at 30 Gy before use. PBLs (2 × 10
6 cells/3 ml culture medium) were co-cultured with 2 × 10
5 peptide-pulsed irradiated autologous DCs in a 6-well plate in the presence of 10 ng/ml recombinant human interleukin-7 (IL-7; Peprotech). After 24 to 48 hours 20 IU/ml human interleukin-2 (IL-2, Sigma) was added to the culture medium. Lymphocytes were re-stimulated each week in the same manner. Three days after the second round of re-stimulation, induced cells were harvested and tested by cytokine determination and cytotoxicity assays.
Generation of CTLs in HLA-A2.1/Kb transgenic mice
A plasmid S/pVAX1 encoding SARS-CoV S protein was constructed and used to immunize the HLA-A2.1/K
b transgenic mice at a dose of 100 μg (in 100 μl of PBS) of plasmid S/pVAX1 by injection into tibialis anterior muscles. Mice were re-inoculated four times every seven days under the same conditions. In this study, bone marrow-derived DCs were generated from transgenic mice as previously described [
34,
35] with some modification. DCs were pulsed with 20 μg/ml peptide in the presence of 3 μg/ml β2-microglobulin at 37°C for 5 hours and irradiated at 30 Gy before use. Spleens were aseptically removed after the final scheduled immunization. Splenic single-cell suspensions were then harvested and cultured in 6-well plates at a density of 1 × 10
7 cells/3 ml/well, in the presence of 1 × 10
5 peptide-loaded irradiated syngeneic DCs. On day six of culture, induced cells were harvested and tested by cytokine determination and cytotoxicity assays.
Cytotoxicity assays
Cytotoxic activity of CTLs was determined in a standard 4-hour
51Cr release assay as previously described [
36] with some modification. In human cytotoxicity assays, DCs derived from a healthy HLA-A2
+ donor were incubated with each of candidate peptides and used to stimulate autologous healthy HLA-A2
+ donor PBLs. T2 cells loaded with the relevant peptides were used as target cells in cytotoxicity assays. As a positive control group, HLA-A2
+ PBLs were stimulated with S
411-420-pulsed autologous DCs. HLA-A2
+ PBLs stimulated with HBcAg
(131-140)-pulsed autologous DCs served as the negative control group. In DNA-immunized mice cytotoxicity assays, the target cells were the J(A2/kb) cells loaded with the candidate peptides, the positive control peptide S
411-420, the irrelevant peptides HBcAg
(131-140), and J(A2/kb) cells alone.
First, T2 cells and/or J(A2/kb) cells were loaded with 20 μg/ml peptides and 3 μg/ml human β2-microglobulins and incubated at 37°C for 2 hours. Then peptide-pulsed T2 cells and/or J(A2/kb) cells were labeled with 51Cr sodium chromate (Na51CrO4, Perkin-Elmer Life Science, Boston, MA) for 90 minutes at 37°C. 51Cr-labeled target cells were washed three times and mixed with graded doses of effectors in 96-well plates. After incubation at 37°C for 4 hours, a total of 100 μl supernatant was collected from each well and radioactivity was counted with a gamma counter. Each assay was performed in triplicate. Percent specific lysis was determined according to the following formula: percent specific lysis = [(mean experimental cpm - mean spontaneous cpm)/(mean maximum cpm - mean spontaneous cpm)] × 100%. Spontaneous and maximum releases were determined by incubating the labeled targets with medium alone or 1 M HCl, respectively. Spontaneous release was always < 15% of maximum release.
Enzyme-linked immunosorbent spot (ELISPOT) assay
ELISPOT assay was performed using a commercially available kit (U-CyTech, Netherlands) according to the manufacturer's instructions and published literature [
37] with some modification. Autologous DCs were pulsed with 20 μg/ml candidate peptides and used as stimulators for HLA-A2.1
+ PBLs from the immunized mice. Effector cells (1 × 10
5) and stimulator cells (1 × 10
5) were seeded into 96-well polyvinylidene fluoride (PVDF)-backed microplates pre-coated with anti-IFN-γ mAb. After incubation at 37°C for 48 hours, cells were removed and plates processed as described in the instruction. Resulting spots were counted with a stereomicroscope (Carl Zeiss, Thornwood, NY) under magnifications of ×20 to ×40. Only brown and/or blue colored spots with fuzzy borders were scored as spot-forming cells (SFCs). As a positive control, S
411-420-loaded DCs were used as stimulator cells. The HBcAg
(131-140)-loaded DCs, DCs alone, and medium were used as negative controls. Negative control values were always < 20 SFC per 10
6 input cells. Results were considered positive when at least 120 SFC/10
6 PBL were detected. Each assay was run in triplicate and results were representative of three experiments.
Acknowledgements
This work was supported by grants from the National Key Basic Research Program of China (2003CB514108, 2001CB510001), and the National Natural Science Foundation of China (NSFC, 30490240). We thank Dr W. Martin Kast (the Norris Comprehensive Cancer Center, Los Angeles, CA) and Dr. Jehad Charo (the Max-Delbruck-Center for Medicine, Berlin) for generously providing us with Jurkat-A2/Kb cell lines, respectively.
Authors' contributions
YL carried out the cell and animal manipulation, the CTL cytolysis assay. ZR carried out the immunoassays. LW participated in the design of the study and performed the statistical analysis. BN and YW conceived of the study, and participated in its design and coordination and helped to draft the manuscript. All authors read and approved the final manuscript.