Evaluation of MHC-II peptide binding prediction servers: applications for vaccine research
© Lin et al; licensee BioMed Central Ltd. 2008
Published: 12 December 2008
Initiation and regulation of immune responses in humans involves recognition of peptides presented by human leukocyte antigen class II (HLA-II) molecules. These peptides (HLA-II T-cell epitopes) are increasingly important as research targets for the development of vaccines and immunotherapies. HLA-II peptide binding studies involve multiple overlapping peptides spanning individual antigens, as well as complete viral proteomes. Antigen variation in pathogens and tumor antigens, and extensive polymorphism of HLA molecules increase the number of targets for screening studies. Experimental screening methods are expensive and time consuming and reagents are not readily available for many of the HLA class II molecules. Computational prediction methods complement experimental studies, minimize the number of validation experiments, and significantly speed up the epitope mapping process. We collected test data from four independent studies that involved 721 peptide binding assays. Full overlapping studies of four antigens identified binding affinity of 103 peptides to seven common HLA-DR molecules (DRB1*0101, 0301, 0401, 0701, 1101, 1301, and 1501). We used these data to analyze performance of 21 HLA-II binding prediction servers accessible through the WWW.
Because not all servers have predictors for all tested HLA-II molecules, we assessed a total of 113 predictors. The length of test peptides ranged from 15 to 19 amino acids. We tried three prediction strategies – the best 9-mer within the longer peptide, the average of best three 9-mer predictions, and the average of all 9-mer predictions within the longer peptide. The best strategy was the identification of a single best 9-mer within the longer peptide. Overall, measured by the receiver operating characteristic method (AROC), 17 predictors showed good (AROC > 0.8), 41 showed marginal (AROC > 0.7), and 55 showed poor performance (AROC < 0.7). Good performance predictors included HLA-DRB1*0101 (seven), 1101 (six), 0401 (three), and 0701 (one). The best individual predictor was NETMHCIIPAN, closely followed by PROPRED, IEDB (Consensus), and MULTIPRED (SVM). None of the individual predictors was shown to be suitable for prediction of promiscuous peptides. Current predictive capabilities allow prediction of only 50% of actual T-cell epitopes using practical thresholds.
The available HLA-II servers do not match prediction capabilities of HLA-I predictors. Currently available HLA-II prediction servers offer only a limited prediction accuracy and the development of improved predictors is needed for large-scale studies, such as proteome-wide epitope mapping. The requirements for accuracy of HLA-II binding predictions are stringent because of the substantial effect of false positives.
Vaccines are the most effective means for fighting against infectious diseases . They are emerging as promising therapies for cancer , allergy , and autoimmunity . The goal of vaccination is to induce immunity against pathogens and cancer cells by stimulating antigen-specific cytotoxic T lymphocytes (CTLs) or B cells. CTLs recognize peptide antigens presented by major histocompatibility complex class I (MHC-I) molecules on infected cells or cancer cells and kill them. B cells produce antibodies that specifically recognize pathogen- or cancer related molecules. Both these processes are initiated and regulated by T-helper (Th) cells that recognize antigenic peptides presented by MHC class II (MHC-II) molecules. MHC-II molecules present antigenic peptides internalized by professional antigen presenting cells, such as macrophages, dendritic cells, or T lymphocytes. A vaccine must at minimum contain two antigenic epitopes: one to induce specific B-cell or CTL responses and another to induce specific Th cells that regulate (initiate, enhance, or suppress) immune responses . Peptides presented by MHC-I molecules are mainly intracellular and those presented by MHC-II molecules originate mainly from or extracellular proteins. A distinct characteristic of MHC molecules of either class is a groove that binds peptides in a highly promiscuous manner.
The peptide-binding groove of a MHC molecule consists of a β-sheet and two α-helices. A peptide binds through a network of hydrogen bonds between its backbone and the binding groove, and through interactions between the peptide side chains and pockets inside the binding groove [6, 7]. Most MHC-I binding peptides are 8–11 amino acids long . MHC-II molecules bind nested sets of peptides most of which are 14–18 amino acids long , but some can extend beyond 30 amino acids. MHC-I molecules accommodate the whole length of the binding peptide inside their grooves that are closed . Binding grooves of a MHC-II molecules have open ends; they accommodate the 9-mer binding core of the peptides inside while peptide termini protrude outside of the grooves .
The ability of the immune system to respond to a particular antigen differs between individuals because they display different patterns of MHC genes. Human MHC molecules are known as human leukocyte antigens. Each human individual expresses up to six HLA-I molecules and up to a dozen HLA-II molecules. HLA genes show extensive polymorphism. As of August 2008, more than 3000 HLA alleles have been identified and sequenced including 2215 HLA-I and 986 HLA-II sequences . The diversity of HLA molecules increases the probability that any foreign antigen will contain HLA-binding peptides suitable as vaccine targets. The amino acids within the binding groove determine the specificity of peptide binding to a given HLA molecule. Across multiple HLA molecules, the polymorphic residues that form the binding groove determine the repertoire of binding peptides to a particular HLA molecule. Tens of thousands of allele-specific and promiscuous MHC binders and T-cell epitopes have been identified in humans and mice while smaller numbers have been identified in other model animals, such as monkeys and rats [11, 12].
Identification of HLA binding molecules is, therefore, important for both understanding the basing molecular function of the immune system and for vaccine development. However, systematic T-cell epitope mapping is costly and time-consuming because it involves synthesis and testing of overlapping peptides spanning the full length of target antigens. For short peptides such as tumor antigen surviving (BIRC5), that is 142 amino acids long, full overlapping studies of both HLA-I and -II binders were performed for several HLA molecules [13, 14]. However systematic studies are prohibitively expensive for studies of long antigens, such as autoantigen thyroglobulin (2768 amino acids long), where computational predictions were used to preselect suitable targets followed by experimental validation [15, 16]. This problem is particularly pronounced in the studies of whole pathogen proteomes, even in small viruses, such as influenza , or dengue .
Computational prediction of peptide binding to MHC molecules has been a topic of vigorous research and development activity [19–22]. Computational methods for prediction of HLA-I binding have reached a high level of sophistication and accuracy and represent significant research resources . Computational predictions of HLA-II binding were useful in the study of infectious disease [24, 25], cancer [26, 27], and autoimmunity [15, 16]. However, recent reports have indicated that computational predictions of HLA-II binding are of much lower accuracy than for their HLA-I counterparts [28, 29], and even that these predictions may cause more confusion than conclusion . The methods used for assessment of predictors of HLA-II binding have suffered from inadequately defined test sets and testing strategies. Several critical issues need to be addressed to rectify these failings.
Only a small fraction of peptides in a given pathogen or tumor-specific proteome are able to bind to a specific MHC molecule . Tens of thousands of protein variants have been characterized in viruses [17, 18]. Several hundred of tumor-related antigens and their variants have been reported [32, 33]. The extensive variability of target antigens significantly increases the number of testable targets, making each individual binding peptide a representative of a large family of individual peptide groups or families .
The comparison studies performed to date have been based on assessing predictive performance using pre-defined sets of peptides, rather than well-defined standardized full-overlapping studies of complete antigens. This introduces biases and the reported performances are likely to be overestimates.
HLA-II peptide binding is mediated through 9-mer binding core, but longer peptides are used for experimental measurement of binding. Hereby we predict one element (the 9-mer binding cores) and experimentally test with another element (15-mer, or longer peptides). This makes the improvement of false positive rate an important issue in prediction of HLA-II binding and it requires sophisticated statistical and machine learning approaches (see [28, 29, 34]).
Both ends of the peptide binding grooves in HLA-II molecules are open, allowing the peptides to be more variable in length (typically 14–18 amino acids) and flanking residues are known to selectively affect binding . This effect is not considered in most of the HLA-II prediction methods.
Some longer peptides bind MHC-II through multiple overlapping 9-mer registers [34, 35] adding further complexity to the selection of actual binding cores. The simpler question of identification of the location of 9-mer binding is extended to identification of multiple binding cores and their locations within the same peptide.
Experimental measurements of HLA-II binding shows variation depending on the conditions of the experiment, even for the control peptides.
Sufficient quantities of HLA-II binding data are available only for some HLA-DR molecules while, notwithstanding notable exceptions , HLA-DQ and -DP molecules have been understudied.
Presentation of HLA-II binding peptides depends on antigen processing steps including editing by HLA-DM and other accessory molecules. DM editing affects the density and preference for particular peptide species . These effects have not yet been included in the prediction approaches.
HLA-II binding predictions are thus more complex than HLA-I predictions [23, 37, 38]. Various prediction algorithms have been developed to facilitate the identification of HLA-II binding peptides within protein antigens. They made computational pre-screening of antigens for HLA-II epitopes a standard approach in epitope-mapping studies; more than twenty prediction servers have been developed to facilitate the identification of MHC-II binding peptides. The performance of six prediction methods has been compared in each of the three recent studies [28–30]. The overall conclusions of these studies were similar, indicating a relatively low prediction accuracy of HLA-II binding predictors. Large quantities of HLA-DR binding peptides with precise measurements have recently become available [28, 29], yet contemporary methods have shown little, if any, improvement when compared to the older TEPITOPE method.
This study extends the assessment of predictive power to include a much larger number of servers that predict HLA-II binding. This study was limited to seven common HLA-DR molecules that have sufficient amount and quality of peptide binding data. We compiled and established standardized test data sets that are more representative of the experimental reality, and defined a uniform scaling scheme to use data from different studies. Finally we assessed the practical applicability of HLA-II binding predictions to identification of HLA-II T-cell epitopes. Our study identified several key issues that need to be addressed for the development of improved prediction systems of HLA-II binding.
While not all the servers were designed specifically for peptide binding predictions, all of them have implemented modules for this step. Some servers also have advanced options, for example, MHCPred enables users to specify anchor positions. For this analysis we used the simplest prediction method available at each server. The numbers of the servers for individual HLA-DR alleles we studied were: HLA-DRB1*0101 – 19, HLA-DRB1*0301 – 15, HLA-DRB1*0401 – 20, HLA-DRB1*0701 – 16, HLA-DRB1*1101 – 17, HLA-DRB1*1301 – 9, and HLA-DRB1*1501 – 17.
Comparing the prediction performance across HLA-DR alleles, the best predictors are for HLA-DRB1*0101, where seven predictors showed good classification accuracy, while six DRB1*1101 predictors, three DRB1*0401 predictors, and only one DRB1*0701 predictor showed good classification accuracy. None of predictors for DRB1*0301, DRB1*1301, and DRB1*1501 showed good classification performance. Important to note, only four HLA-DRB1*0101 predictors have shown performance that approaches the value of AROC = 0.9 while other "good" predictors are close to the lower borderline leaving ample space for the improvement.
The best prediction server across all HLA molecules evaluated in this study is NETMHCIIPAN, closely followed by PROPRED, IEDB_SAT, and MULTI_SVM. The best predictors we recommend for each allele are marked by asterisks in Figure 1.
Prediction of promiscuous peptides
Prediction of T-cell epitopes
Prediction performance of selected representative servers at two scenarios: a) thresholds that correctly predict ~80% of T-cell epitopes; b) thresholds that correctly predict ~50% of T-cell epitopes.
TP (tumor epitopes)
a) 80% prediction
b) 50% prediction
To identify 80% of T cell epitopes, the threshold for each predictor had to be set low, which resulted in a large number of false positives. This problem was pronounced for predictors such as MHCPRED, MULTI_ANN and RANKPEP, since the number of false positives even exceeded that of true negatives. At this threshold, IEDB (consensus), MULTPRED (SVM), and PROPRED showed the best performance. On the other hand, the thresholds for predicting ~50% of known T cell epitopes were much more stringent, significantly lowering the rate of false positives relative to the 80% threshold. At this threshold, NetMHCIIpan, IEDB (consensus), and PROPRED showed the best performance
Conclusion and discussion
In this study we evaluated the performance of 21 prediction servers for HLA-II binding peptides. Seven DRB1*0101 predictors, six DRB1*1101 predictors, three DRB1*0401 predictors, and one DRB1*0701 predictor showed good performance in identification of binders and non-binders. None of predictors for DRB1*0301, DRB1*1301, and DRB1*1501 performed well, indicating that much room for improvement still exists for MHC-II prediction.
The results suggest that some of current predictors are useful for pre-screening Th epitopes, although a relatively large number of false positives (at lower thresholds) and false negatives (at higher thresholds) would also be produced. Predictions using lower thresholds are useful for screening true negatives, while predictions at higher thresholds help cheaply identify a subset of the T-cell epitopes. Unlike MHC-I predictions, we have no evidence that nonlinear methods would perform better than linear methods. One possible reason may be due to the fact that nonlinear methods, such as ANN or SVM, generally require relatively larger amount of data for model development than linear methods. However, the amount of high-quality binding data for MHC-II binding is still far from sufficient, which limits the capability of nonlinear methods to recognize characteristics underlying MHC-peptide interaction
In summary, the prediction accuracy of HLA-II binding peptides is inferior to that of HLA-I binding peptides. Several factors appear to account for this disparity. Insufficient or low-quality training data has been the problem for developers of prediction methods for HLA-II binding peptides. Another problem with HLA-II predictions is the difficulty in identifying 9-mer binding cores within longer peptides used for training as well as lack of consideration of the influence of flanking residues. Amino acids flanking the binding core, contribute to MHC-peptide interactions and also antigen processing preferences [34, 40]. Another reason of poor performance for MHC-II prediction is that the binding groove of HLA-II molecules is relatively permissive for peptide binding, which limits the stringency of specific binding motifs. We propose that with new large datasets available [29, 37, 41, 42] new methods that implement knowledge-based strategies and computational search techniques need to be developed. Examples showing various approaches that can improve HLA-binding prediction systems include the use of advanced search algorithms [28, 29, 43], advanced statistical and machine learning approaches [44–47], combination approaches [28, 38, 48, 49], novel scoring functions , and improved use of structural predictions [51, 52], or application of knowledge-based approaches [53–57]. Future HLA-DR prediction developments studies should, at minimum, use standardized data sets, provide improved definition of binding cores, minimize number of false positives, and consider the effects of flanking residues.
Results of this study will help researchers to determine the most appropriate servers for pre-screening of HLA class II binding peptides. In addition, this study has defined basic criteria for slection of predication thresholds for selection of peptides that are most likely to be potential HLA-II epitopes. On the other hand, it provides guidelines for testing and test data to server developers. This knowledge, together with standardized test data sets should empower them to produce better solutions and improve prediction performance. Normalization and standardization methods that we introduced in this study enable annotation and integration of heterogeneous data into a uniform format, which facilitates the development of advanced algorithms. Future advancement in high-throughput measurements of binding affinities is expected to significantly improve the prediction performance of MHC-II binding peptides.
Materials and methods
List of prediction servers of HLA class II binding peptides, their URLs (as of December 2007), and name abbreviations.
MHC Binder Prediction
Partial least square
Summary of the four testing protein antigens
Number of peptides
Length of peptides
Predictions and comparisons
Each protein sequence was submitted to the prediction servers and the results were recorded. Most servers predict binding affinities of 9-mer peptides while the experiments were conducted on longer peptides ranging from 15 aa to 19 aa. Three mapping methods were explored to map the 9-mer predictions to experimental results. First, the highest prediction score of the overlapping 9-mer peptides spanning the length of a longer peptide was used as the predicted binding of the longer peptide. Second, the average score of the overlapping 9-mers was used as the predicted binding. Finally, the average of the top three predicted 9-mer scores of the overlapping peptides was used as the prediction score.
Prediction accuracy is measured in terms of the area under the receiver operating characteristic curve (AROC) . The ROC curve is a plot of the true positive rate TP/(TP+FN) on the vertical axis vs. false positive rate FP/(TN+FP) on the horizontal axis for the full range of the decision thresholds. The values AROC ≥ 0.9 indicate excellent, 0.9 > AROC ≥ 0.8 good, 0.8 > AROC ≥ 0.7 marginal and 0.7 > AROC poor predictions .
In this study we defined promiscuous peptides as those peptides from the test set that bound four or more of the seven studied alleles. Binding was defined as half maximal inhibitory concentration (IC50) lower than 100 nM (for DRB1*0101, 0401, 0701, and 1501), or lower than 1000 nM (for DRB1*0301, 1101, and 1301).
where is the scaled score, y min is the minimum and y max is the maximum score. The experimental binding affinity was corrected for variation in binding affinity of control peptides between different experiments then scaled. All values are accessible at DFRMLI site.
This work was supported by the ImmunoGrid project, under EC contract FP6-2004-IST-4, No. 028069, and NIH grant U19 A157330.
This article has been published as part of BMC Bioinformatics Volume 9 Supplement 12, 2008: Asia Pacific Bioinformatics Network (APBioNet) Seventh International Conference on Bioinformatics (InCoB2008). The full contents of the supplement are available online at http://www.biomedcentral.com/1471-2105/9?issue=S12.
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