Identification of New Autoantigens for Primary Biliary Cirrhosis Using Human Proteome Microarrays*

Primary biliary cirrhosis (PBC) is a chronic cholestatic liver disease of unknown etiology and is considered to be an autoimmune disease. Autoantibodies are important tools for accurate diagnosis of PBC. Here, we employed serum profiling analysis using a human proteome microarray composed of about 17,000 full-length unique proteins and identified 23 proteins that correlated with PBC. To validate these results, we fabricated a PBC-focused microarray with 21 of these newly identified candidates and nine additional known PBC antigens. By screening the PBC microarrays with additional cohorts of 191 PBC patients and 321 controls (43 autoimmune hepatitis, 55 hepatitis B virus, 31 hepatitis C virus, 48 rheumatoid arthritis, 45 systematic lupus erythematosus, 49 systemic sclerosis, and 50 healthy), six proteins were confirmed as novel PBC autoantigens with high sensitivities and specificities, including hexokinase-1 (isoforms I and II), Kelch-like protein 7, Kelch-like protein 12, zinc finger and BTB domain-containing protein 2, and eukaryotic translation initiation factor 2C, subunit 1. To facilitate clinical diagnosis, we developed ELISA for Kelch-like protein 12 and zinc finger and BTB domain-containing protein 2 and tested large cohorts (297 PBC and 637 control sera) to confirm the sensitivities and specificities observed in the microarray-based assays. In conclusion, our research showed that a strategy using high content protein microarray combined with a smaller but more focused protein microarray can effectively identify and validate novel PBC-specific autoantigens and has the capacity to be translated to clinical diagnosis by means of an ELISA-based method.

The anti-nuclear antibodies (ANA) represent another type of important serum biomarkers for PBC diagnosis and have been reported to be achieving positive rates of 50 -70% (27)(28)(29)(30). Three major immunofluorescence patterns of ANA have been described for PBC, and some of their contributing autoantigens have also been identified. Nuclear envelope pattern (anti-nuclear envelope antibodies) refers to the anti-nuclear pore glycoprotein 210 (Gp210), anti-nuclear pore glycoprotein p62 (p62), and anti-lamin B receptor (LBR) antibodies (31); the multiple nuclear dot pattern associates with anti-nuclear body protein Sp140 and nuclear autoantigen Sp100 antibodies (32). Anti-centromere antibodies (ACA) mainly target CENP-B (33). Recent studies have shown that ANA, especially the anti-Gp210 antibody and the ACA, are correlated with severe disease course and poor prognosis of PBC (34 -36). The sensitivity of anti-Gp210 for PBC has been reported to be 20 -30% (31,37). However, similar to the AMA, ANA have been clinically detected in sera of patients with other autoimmune diseases and even in a remarkable proportion (1 of 20) of sera from healthy individuals (38). ACA are widely accepted as relatively specific biomarkers of limited cutaneous systemic sclerosis (SSc) (39) but again have been frequently detected in a number of other conditions, including primary Sjö gren's syndrome, systematic lupus erythematosus (SLE) (40,41), and rheumatoid arthritis (RA) (41), and occasionally detected in certain cancers, such as breast cancer (42) and non-Hodgkin's lymphoma (43). The diagnosis of PBC can be further complicated by the clinical and biochemical features of liver abnormalities shared by other autoimmune diseases, such as autoimmune hepatitis (AIH), SSc, RA, and SLE (44 -47). Although the detection of PBC-specific autoantibodies may help to distinguish PBC from other autoimmune diseases (37), the diagnostic role of PBC-specific ANA has not been fully developed (48). Therefore, the identification of new autoantibodies as noninvasive biomarkers remains a priority of PBC research (49).
The conventional methods to screen for novel autoantibodies in PBC patients are cumbersome and time-consuming (50). The recently developed functional protein microarrays were designed to survey thousands of potential antigens in a single experiment and have facilitated rapid and cost effective identification of novel biomarkers (51)(52)(53). Although human protein microarrays have become a robust tool for screening autoantibodies in sera from patients with various autoimmune diseases (52)(53)(54)(55)(56)(57)(58)(59)(60) and cancers (56,61), the major limitation is the comprehensiveness of these previously used human protein microarrays. Here, we employed a recently developed human proteome microarray with ϳ80% coverage of the human proteome to screen for novel PBC-specific biomarkers. The resulting PBC-associated candidate proteins were then used to construct a focused PBC microarray, for additional validation using a much larger cohort. Two of the validated autoantigens were further converted to the traditional ELISAbased assay to demonstrate their utility for clinical diagnosis.  (62). All PBC serum samples were tested for AMA detection by indirect immunofluorescence assay with Hep2 cells (Euroimmune, Lü beck, Germany) and for the AMA-M2 antibodies detection by the anti-M2-3E ELISA kit (Euroimmune). Furthermore, any PBC patient whose sera produced negative results for AMA and/or M2 were confirmed as having PBC by liver biopsy and meeting other criteria. Of the 191 PBC serum samples used for validation with PBC microarray, 167 were clinically characterized as AMA-positive and 163 as M2-positive. In addition, 66 and 44 PBC sera were characterized as anti-nuclear envelope antibody-and ACA-positive, respectively. The remaining 550 serum samples representing the various disease controls were diagnosed according to the respective general criteria used for each disease. The study was approved by the Ethics Committee of Peking Union Medical College Hospital.
Human Proteome Microarrays-The human proteome microarray used in the first phase of this study was composed of about 17,000 unique human full-length proteins and was constructed in Dr. Zhu's laboratory at Johns Hopkins University Medical School (63). This novel human proteome microarray contained 48 blocks arranged in a 25 ϫ 32 array layout. Each of the recombinant human proteins was printed in duplicate, as were the control probes (printing buffer, human IgG, etc.). All of the recombinant human proteins were generated by the Saccharomyces cerevisiae expression system and carried an N-terminal GST tag.
The quality of the microarray was measured by using mouse anti-GST monoclonal antibody and confirmed with Cy5-labeled antimouse IgG antibody. In brief, the microarray was first incubated with blocking buffer (3% BSA in 0.1% (v/v) PBS plus 0.1% (v/v) Tween 20) at 37°C for 1 h, after which 180 l of mouse anti-GST monoclonal antibody (1:1000 dilution; Beijing Protein Innovation Co. Ltd., Beijing, China) was added and further incubated under a glass coverslip (LifterSlip; Erie Science Company, Portsmouth, NH) at 37°C for 1 h. After washing three times with 1ϫ PBS plus Tween 20 by gentle shaking for 10 min each, the microarray was incubated with 180 l of Cy5-labeled goat anti-mouse IgG antibody (1:1000; Jackson Laboratory, Bar Harbor, ME) in the dark at 37°C for 1 h. Subsequently, the microarray was washed three times with 1ϫ PBS plus Tween 20 and then three times with double-distilled H 2 O. To fully remove the double-distilled H 2 O, the microarray was centrifuged for 5 min at 100 ϫ g in a 50-ml centrifuge tube. Finally, the microarray was scanned with the LuxScan TM 10K Microarray Scanner (BioCapital, Beijing, China), and the probe signals were acquired using GenePix Pro 6.0 software (Molecular Devices, Sunnyvale, CA). We considered the probes detectable when their signal to noise ratios for both duplicates were over 3. SPSS 17.0 software (Chicago, IL) was used to calculate the percentage of detectable probes and the coefficient factor of duplicate spots.
Sera Profiling Using the Human Proteome Microarrays-The procedure of sera assay was similar to that described above for the mouse anti-GST antibody assay, but with the following modifications. First, after blocking, the 1:1,000 diluted patient sera were incubated with the microarrays. Second, after washing away the sera, the 1:1,000 diluted Cy5-labeled goat anti-human IgG antibody was applied.
After the microarray was scanned and probes' signal intensities were acquired, positive calling in each microarray was conducted according to the procedure previously described by Hu et al. (64). PBC-specific autoantigen candidates were identified according to the following criteria: (a) Fisher's exact test on positive incidence showing statistical significance between PBC and control samples (p Ͻ 0.05) or (b) positive rate above 15% in PBC sera and 0% in controls.
Construction of the PBC Microarray-Twenty-one PBC-specific autoantigen candidates and nine other PBC-related antigens, which had been identified either in clinical use or by experimental studies reported in the literature, were prepared and printed on the PBCfocused microarray. All of the antigens were expressed and purified according to the method previously described (65). The recombinant proteins were eluted into protein microarray printing buffer (30% glycerol, 50 mM HEPES, pH 7.5, 100 mM NaCl, 1 mM Triton X-100, 30 mM reduced glutathione, and 1 mM DTT). The purified antigens, together with negative and positive controls (printing buffer, GST, human IgG, mouse IgG, and nucleoprotein of influenza) were printed in duplicate within 12 identical probe areas on each OPEpoxySlide TM (CapitalBio Corp., Beijing, China) to prepare the PBC-focused microarray. The printed low density protein microarrays were stored at 4°C under vacuum until use.
Sera Assay with PBC Microarray-The PBC microarrays were subjected to 191 PBC and 321 control sera. First, the arrays were warmed to room temperature (ϳ30 min) and then a 12-hole rubber gasket (CapitalBio Corp.) was applied to each array to form 12 individual chambers. The subsequent assay process was identical to that described for the human proteome microarray assay, with the exception of the volume of fluid for each chamber being 30 l. After incubation with the Cy5-labeled anti-human IgG, the rubber gaskets were removed carefully, and the wells were washed. The arrays were scanned by the LuxScan TM 10K microarray scanner using the same parameters for the larger array, and all of the signal intensities were acquired with the GenePix Pro 6.0 software. The serum samples with extremely high GST signal intensity (beyond the 99% spectrum of normal distribution) were considered to be GST-positive and were excluded from further analysis. The average signal intensity from healthy sera plus five times their standard deviations were set as the cutoff. The reproducibility of PBC-focused microarray was demonstrated by repeated hybridization experiments with randomly selected PBC (n ϭ 12) and control (n ϭ 12) sera, which resulted in a high correlation coefficient value (0.991) with p value equaled 0.000.
ELISA-The purified recombinant proteins were further verified prior to their use in validation analysis. Specifically, the ORF constructs of the newly identified antigens were verified by sequencing, and the identities of their protein products were confirmed by mass spectrometry. Then the verified recombinant proteins were coated onto 96-well plates at 4°C overnight. Nonspecific binding was blocked by incubating with 200 l of PBS plus Tween 20 containing 1% BSA/well at 4°C overnight. The following day, the wells were incubated with human sera (1:100) at 37°C for 1 h and then washed three times with 400 l/well of PBS plus Tween 20. Subsequently, 100 l of horseradish peroxidase-labeled mouse anti-human IgG monoclonal antibody (1:1,000; Beijing Protein Innovation Co. Ltd.) was added to each well. After three washes with 300 l/well of PBS plus Tween 20, 100 l of tetramethybenzidine substrate solution (Sigma-Aldrich) was added and incubated for 90 s at room temperature. The reaction was terminated by addition of 50 l of 2 N H 2 SO 4 /well, and immunoreactivity was measured by reading the A 450 . The sera with extremely high GST reactions (beyond the 99% spectrum of normal distribution) were considered GST-positive and were excluded from further analysis. We set A 450 Ͼ0.4 as the cutoff for positive hits.
Immunoblot Analysis-Two-hundred nanograms of hexokinase-1 (HK1) (isoform I, 128.5 kDa) was expressed by yeast with the GST-His 6 tag, 200 ng of KLHL7 (65 kDa) expressed by Escherichia coli with the His 6 tag, and 50 ng of GST-His 6 tag (26 kDa) were resolved by 12% SDS-PAGE at 20 mA until the smallest band of the prestained protein marker (7 kDa) (New England Biolabs, Ipswich, MA) reached the bottom of the gel. The separated proteins were electrotransferred onto polyvinylidene fluoride membranes (Millipore, Billerica, MA) at 350 mA for 1.5 h. After blocking nonspecific binding sites with 5% nonfat milk powder diluted in 1ϫ PBS plus Tween 20, the membranes were incubated with sera (1:400) or mouse anti-GST antibody (1:2,000) at 37°C for 1 h, followed by three washes with 1ϫ PBS plus Tween 20 for 10 min each. Then the membranes were incubated with horseradish peroxidase-conjugated anti-human IgG or anti-mouse IgG at 37°C for 1 h. After three washes with 1ϫ PBS plus Tween 20 for 10 min each, the immunoreactive bands were detected by the addition of enhanced chemiluminescence reagents (Beijing Applygen Ltd., Beijing, China) and were visualized by ImageQuant (GE Healthcare).
Statistics-All statistical analysis was performed with SPSS 17.0 software. p values were calculated by the chi-squared test or Fisher's exact test when suitable.

Identification of PBC-associated Autoantigens Using the
Human Proteome Microarrays-To globally identify the PBCassociated autoantigens, we employed the human proteome microarrays containing about 17,000 human proteins to perform serum profiling of samples collected from PBC patients and other liver diseases and healthy controls. Because the human proteins on the microarrays were expressed and purified from yeast as N-terminally tagged GST fusion proteins, the quality of the microarray was able to be evaluated by applying the anti-GST antibody. The assay indicated that 97.6% of the proteins were detectable by anti-GST signals, and the microarray had a high correlation coefficient (0.978) between duplicate spots, which suggested that it was of high quality (supplemental Fig. 1).
To identify novel biomarkers more efficiently, we employed a two-phase strategy, as previously described (52). Phase I included a prescreening with a small sample size on the high content proteome microarray, whereas phase II was a large scale validation on a smaller but more focused microarray. In Phase I, we selected 26 PBC patients and 20 control samples, with the latter including 5 AIH, 5 HBV, and 10 healthy samples. These serum samples were individually applied as probes to the human proteome microarrays, followed by detection of bound human autoantibodies using a Cy5-conjugated antihuman IgG antibody (Fig. 1).
To identify potential PBC-associated autoantigens, we used Genepix Pro 6.0 to acquire the resultant signal intensities of all protein spots in each assay and identified the positives within each microarray (see details under "Experimental Procedures"). The total number of positive hits on each microarray ranged from 70 to 709 for the PBC sera (347 Ϯ 191) and from 74 to 1,440 for the control sera (429 Ϯ 306). Using Fisher's exact test, we determined that seven proteins, including two members of the M2 autoantigen complex, BCOADC-E2 and PDC-E1␣, showed significant association with the PBC patients (p Ͻ 0.05). In addition, 16 other proteins, including another member of the M2 autoantigen complex, PDC-E1␤, were found to be positive in more than 15% of the PBC patient sera, whereas none of them were scored as positive in the control samples (supplemental Table 1).
Validation of PBC-associated Autoantigens with PBC Microarray-To validate the potential autoantigens identified on the comprehensive human proteome microarray, and to determine their respective sensitivities and specificities for PBC diagnosis, we purified 21 of the 23 candidates, along with the other three members of the M2 complex (PDC-E2, E3BP, and OGDC-E2) and six additional autoantigens previously re-ported in PBC-related studies (Gp210, p62, CENP-B, Sp100, Sp140, and LBR) (32, 35, 66 -69), to fabricate a PBC-focused microarray composed of 30 antigens. We then probed this new PBC-focused microarray with different cohorts of a much larger sample size, which included 191 PBC patients, 43 AIH patients, 55 HBV patients, 31 HCV patients, 48 RA patients, 45 SLE patients, 49 SSc patients, and 50 healthy controls (Fig. 2).
Using a z score of Ͼ5 (see "Experimental Procedures") as the cutoff value, we analyzed the positive rates of each antigen in different groups. We first examined the sensitivity of these 30 antigens by comparing the results from the 191 PBC and 50 healthy samples (Table I and supplemental Table 2). The positive rates for all 30 antigens in the healthy controls were Յ2%. In contrast, 13 of the PBC candidate proteins, six of which were newly identified, were scored as positive in at least 29 (Ͼ15%) of the PBC samples. At this cutoff, the difference of positive rates between the PBC patients and healthy controls for all 13 autoantigens were statistically significant (p Ͻ 0.05). Fig. 3 shows the box plot analysis of signal intensities from the 13 proteins to provide a more intuitive view.
Of the six known members of the M2 complex, BCOADC-E2, PDC-E2, and E3BP showed strong positive signals in PBC patient sera, producing positive rates of 62.3, 51.83, and 33.51%, respectively. The positive rates for the other three members, OGDC-E2, PDC-E1␣, and PDC-E1␤, were only 8.4, 9.4, and 12.6%, respectively. The positive rates of some of the M2 components (PDC-E2, OGDC-E2, and E3BP) were somewhat lower than previously reported (14), which could be because we only detected the presence of the IgG isotype, whereas the previous studies also measured other isotypes. When only one of the six M2 components was required to attain a positive score for PBC diagnosis, the positive rate increased to 82.2% (157 of 191) in PBC sera, similar to that of 84.8% (162 of 191), determined with a commercial anti-M2-3E kit (Euroimmun Corp.) that is commonly used in clinics. Detailed information for M2 detection in the 191 PBC sera by both methods is listed in supplemental Table 3. More importantly, the results of our microarray-based method were comparable with those obtained with the commercial kit at a 91.6% matched ratio. These results confirmed that our microarray system is reliable.
For the PBC antigens reported in the literature, CENP-B and Sp140 showed positive rates of 30.9 and 15.2% in our assays, respectively, similar to the previously reported rates of 26 -29% (35,36) and 15% (32), respectively. In addition, Gp210 and LBR showed strong positive rates in PBC patient sera, with positive ratios of 58.6 and 15.7%, respectively, whereas much lower positive rates of 22.3-44% (35, 67, 70 -73) and 1-9% (31,(73)(74)(75), respectively, were previously reported. It is plausible that the immunoblotting technique used in these previous reports was not as sensitive as the microarray-based assays used in this study.
More importantly, we were able to confirm six new antigens that showed rather high positive rates in PBC samples: HK1 isoform I (46.6%), HK1 isoform II (44.0%), Kelch-like protein 12 (KLHL12) (40.3%), Kelch-like protein 7 (KLHL7) (35.1%), zinc finger and BTB domain-containing protein 2 (ZBTB2) (16.8%), and eukaryotic translation initiation factor 2C, subunit 1 (EIF2C1) (15.2%). Because PBC is a liver-specific autoimmune disease and because other liver diseases tend to exhibit similar symptoms at the first clinical presentation (76), we next examined the specificity of these new PBC autoantigens among other types of liver diseases, including AIH and viral hepatitis. By comparing the results of PBC sera with those from sera of 43 AIH and 86 viral hepatitis (55 HBV and 31 HCV) (Table I), we found that all but EIF2C1 showed significantly reduced positive rates (p Ͻ 0.01) in the sera from AIH patients, as compared with the sera from PBC patients; similarly, all proteins showed significantly reduced positive rates (p Ͻ 0.001) in the sera from viral hepatitis patients. Therefore, the majority, if not all, of these newly identified autoantigens were highly specific for PBC.
The ability of the newly identified autoantigens to differentiate PBC from AIH prompted us to examine their abilities to differentiate PBC from other autoimmune diseases. We therefore surveyed their autoimmunity in 142 serum samples collected from systemic autoimmune disease patients, including 48 RA patients, 45 SLE patients, and 49 SSc patients (Table I).
As compared with the PBC results, all five antigens showed significantly reduced positive rates in both RA (p Ͻ 0.01) and SSc (p Ͻ 0.05) sera. Although to a lesser extent for SLE samples, the HK1 isoform I, KLHL12, and KLHL7 still showed significant differentiation power (p Ͻ 0.05). Therefore, these newly identified autoantigens have the potential to be used for distinguishing PBC from other autoimmune diseases.

Development of New Biomarkers for Clinical Diagnosis-
The ultimate application of novel biomarkers is for clinical diagnosis, preferably in the form of an ELISA, because it is still one of the most popular methods used in clinics. Because the sequences of isoforms I and II of HK1 are identical, except for a stretch of 21 amino acids at the N terminus, the two antigens performed similarly in sera detection assays; therefore, we selected only isoform I for further development as a biomarker. In addition, because EIF2C1 showed a similar positive ratio in SLE and PBC patients, we did not pursue further development of this potential biomarker. Thus, we only ap- plied HK1-isoform I, KLHL7, KLHL12, and ZBTB2 to an ELISA-based platform and tested them against 495 of the serum samples used in the PBC-focused microarray and 439 additional samples, for a total of 934 samples, 297 of which were PBC-diagnosed. OD distribution for KLHL12 and ZBTB2 were shown in Fig. 4. However, all tested samples showed similar OD values for HK1-isoform I and KLHL7 (data not shown).
Using an A 450 of Ͼ0.4 as the cutoff value, we analyzed the positive rates for each group and compared these results with those obtained using the microarray platform. The observed positive detection rates for KLHL12 and ZBTB2 ELISA were 29.6 and 11.2%, respectively, slightly lower than the rates obtained with the microarray platform, indicating that the latter is probably more sensitive (Table II).
KLHL7, KLHL12, and ZBTB2 are all nuclear proteins and share a BTB (for BR-C, ttk, and bab) or POZ (for pox virus and zinc finger) domain. The BTB/POZ motif is widely described as an evolutionarily conserved protein-protein interaction motif that has been found in species ranging from flies to mammals (90,91) and is often present at the N termini of zinc finger transcription factors. Previous studies have suggested that the BTB/POZ domain is required for interaction with cullin-3 and for the formation of the ubiquitin-protein E3 ligase complex, which could interact with the dishevelled homolog 3 protein DVL3 upon activation of the Wnt signaling pathway by WNT3A (92).
Besides the BTB domain, KLHL12 and KLHL7 also share six Kelch motif repeats (90,91). The Kelch motif generally contains 50 amino acids that form a four-stranded ␤-sheet "blade," whereas repeated Kelch motifs form a larger structure called a ␤-propeller that contains multiple potential protein-protein contact sites (93). KLHL12 and KLHL7 have been identified as autoantigens in Sjö gren's syndrome by means of SEREX technology and determined to have 23 and 17% sensitivities, respectively, but they have not been found in RA, SLE, or healthy subjects (94). In our test of large cohorts of patients with PBC or other types of autoimmune diseases, KLHL12 and KLHL7 were both identified as new biomarkers for PBC diagnosis and showed rather high sensitivities of 40.3 and 35.1%, respectively. Consistent with previous reports, only a few (2 of 48 RA and 2 of 45 SLE) or no (0 of 50 healthy) serum samples in this study were found to be serologically reactive to KLHL12 or KLHL7.
ZBTB2, a transcription factor of the POZ and Kruppel (better known as POK) subfamily, is characterized by four C2H2type zinc fingers. It has been demonstrated to function as a potential proto-oncogenic master control gene in the p53 pathway by directly interacting with the zinc finger domains of p53. In addition, ZBTB2 acts as a potent p21 transcription repressor, a function that requires its BTB domain for interactions with other co-repressors, such as BCoR, N-CoR, and SMRT (95). Although it has not been previously reported as an autoantigen for any autoimmune diseases, this study provides convincing evidence that ZBTB2 can serve as a useful PBC-specific autoantigen with 11.8% sensitivity and 99.7% specificity. The fact that the BTB domain of ZBTB2 is in common with those of KLHL7 and KLHL12 suggests that there might be a common epitope residing in the BTB HK1 is a member of the hexokinase family, which phosphorylates glucose to produce glucose-6-phosphate. The HK1 isoform I is localized to the outer mitochondrial membrane in tissues that are strictly dependent on glucose utilization for their physiologic functions, including the brain, erythrocytes, platelets, lymphocytes, and fibroblasts (96). In our microarraybased serum profiling assay, we found that two of the four AMA ϩ /M2 Ϫ sera were reactive to HK1. Because of its mitochondrial location, HK1 positivity may partially explain why some sera demonstrate AMA positivity and M2 negativity. Compared with isoform I, the HK1 isoform II lacks the N-terminal porin-binding domain, which is responsible for targeting the protein to the mitochondrial outer membrane; thus, isoform II is localized mainly in the cytosol (98). Because of the high sequence similarity shared between these two isoforms, it is expected that they are targeted by at least some of the same autoantibodies. Indeed, the signal intensities of these two isoforms were highly correlated. Additionally, the HK1 has been identified as an autoantigen associated with autistic children, and anti-HK1 autoantibodies were shown to impair growth and induce apoptosis in cultured human neuroblastoma cells (97). It would be interesting to determine whether HK1-positive patients also suffer from similar nervous system-associated impairments.
In addition, the eukaryotic translation initiation factor EIF2C1 was also identified as a new autoantigen that was recognized by 15.2% PBC sera. However, it was not specific for PBC, because 15.6% of SLE sera and 9.3% of AIH sera also showed positive immunoreactivity.
To begin to evaluate the potential clinical utility of our newly identified PBC autoantigens, we performed correlation analysis and found that most of the newly identified antigens did not significantly correlate with known antigens in PBC patients (supplemental Table 4). Then we calculated the diag-nosis sensitivity and specificity achieved with different combinations of the autoantigens. The diagnosis sensitivity of the six M2 components was improved from 82.2 to 92.2% when combined with the six newly identified autoantigens. When the above 12 antigens were combined with another six reported PBC-associated antigens, the sensitivity was further improved to 94.8%. However, the combinations did not improve specificity, which was decreased from 89.7 to 73.5 and 66.7%, respectively.
Currently, M2 autoantigen-based tests are the most frequently used method for PBC diagnosis. However, an M2negative result does not absolutely rule out PBC diagnosis, and these patients must undergo biopsy and careful analysis of many other clinical features to obtain an accurate diagnosis. Therefore, identification of novel biomarkers for M2-negative PBC patients will reduce the physical impact on these patients and associated costs of invasive testing and subjective evaluation. When we combined the newly identified antigen KLHL12 with Gp210, we could readily detect positive signals in 47.8% of M2-negative PBC patients with a specificity of 90.4%, similar to that of the M2-based diagnosis for PBC patients (89.7%).
In conclusion, we have identified six new autoantigens with at least 15% positivity in PBC serum samples by using a protein microarray-based approach. This two-phase strategy combines a proteome-wide screen for novel autoantigens followed by a stringent validation step using additional cohorts to ensure the success of identification of useful autoantigens for a particular disease. Successful application of these autoantigens in a clinic friendly ELISA suggests that these new autoantigens may serve as useful serological biomarkers for diagnosis of PBC, especially for M2-negative PBC patients.