Hepatitis D virus (HDV) infection is a major global health issue around the world. There are approximately 15–20 million individuals infected with HDV worldwide. HDV infection usually causes increased mortality compared with infection with hepatitis B virus (HBV) alone. However, testing for the detection of HDV is not widely available in Taiwan. Therefore, the General Biologicals Corporation (GB) HDV Ab kit was developed for detecting anti-HDV antibodies.
Methods
A total of 913 serum and 462 EDTA-treated plasma samples were obtained from HBsAg-positive individuals in three hospitals in Taiwan from June 2014 to November 2017. We used three commercially available ELISA kits, DiaPro HDV Ab, DiaSorin ETI-AB-DELTAK-2 and GB HDV Ab, which were utilized strictly according to the instructions of the manufacturers.
Results
A comparative study of the results from the GB HDV Ab kit and the other commercial ELISA kits (DiaPro and DiaSorin) was performed to determine their efficacy for anti-HDV detection. The results indicated that the sensitivity of the GB HDV Ab kit for serum and EDTA samples was 100% compared to that of the DiaPro and DiaSorin kits, whereas the specificity for serum and EDTA samples was 99.3 and 98.1%, respectively. In addition, the overall agreement of the results of the GB HDV Ab kit for the serum and EDTA samples was 99.3 and 98.3%, respectively. It is worth noting that the performance of the GB HDV Ab kit was not affected by interference from triglyceride, bilirubin, hemoglobin, or human anti-mouse antibody. The limit of detection of the GB HDV Ab kit is approximately 100-fold lower than that of the other two commercial kits.
Conclusions
The GB HDV Ab kit, which presented equivalent sensitivity and specificity compared to both certified anti-HDV kits, would be a suitable kit for HDV diagnosis in Taiwan.
Hinweise
Publisher’s Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Abkürzungen
BL
Bilirubin
CI
Confidence intervals
COI
Cut-off index
EDTA
Ethylenediaminetetraacetic acid
ELISA
Enzyme-linked immunosorbent assay
HAMA
Human anti-mouse antibody plasma
HB
Hemoglobin
HBsAg
Hepatitis B virus surface antigen
HDAg
Hepatitis D virus antigen
HBV
Hepatitis B virus
HDV
Hepatitis D virus
IRB
Institutional Review Board
KCGMH
Kaohsiung Chang Gung Memorial Hospital
LCGMH
Linkou Chang Gung Memorial Hospital
MAPC
Multi-analyte positive control
NHP
Normal human plasma
NTUH
National Taiwan University Hospital
OD
Optical Density
TG
Triglyceride
Background
Hepatitis D virus (HDV) is a small single-stranded circular RNA with a negative polarity of approximately 1700 bases that produces hepatitis D antigen (HDAg) [1, 2]. Its replication is dependent on the hepatitis B virus (HBV) surface antigen (HBsAg) [3]. Coinfection with HDV and HBV usually leads to acute fulminant hepatitis, while superinfection can cause more severe hepatitis or cirrhosis than infection with HBV alone [4‐6].
Previous epidemiological studies estimated that approximately 15–20 million people are infected with HDV worldwide [7]. However, these findings were challenged in 2018 by subsequent studies proposing that 48–74 million people were infected with HDV worldwide [8‐10]. Although these estimates are still debated due to a lack of regional estimates [11, 12], recent studies have also shown that HDV infection is still endemic in most low-income countries [10]. Highly affected areas were the Western and Central Africa [13, 14], the Amazon basin [15] and the Mediterranean basin [16]. In particular, ∼60% of HBsAg-positive subjects were coinfected with HDV in Mongolia [17]. In Taiwan, the prevalence of HDV was approximately 4.4% among people infected with HBV [18].
Anzeige
However, the exact number of HDV infections is underestimated due to several factors. The first factor is the lack of knowledge of the regional HDV prevalence in low-income countries. Another is the rare systematic detection of anti-HDV antibodies in HBsAg-positive individuals, and the last is technical issues with enzyme immunoassays (EIAs), such as laboratory developed test (LDT) with lower sensitivity and specificity. These factors might lead to misdiagnosis and/or underestimation of HDV infection. Therefore, it is urgently necessary to establish sensitive and specific tools for HDV detection.
According to its genetic diversity, HDV has been divided into eight major genotypes (HDV-1 to HDV-8) [19, 20]. Among them, HDV-1, HDV-2, and HDV-4 are commonly found in Taiwan [18, 21]. The anti-HDV antibody is a useful marker to determine the activity of HDV infection [22]. Until 2018, enzyme immunoassays (EIAs) were the only technology used to detect anti-HDV antibodies on the market. Recently, many enzyme-linked immunosorbent assay (ELISA) kits have been developed to measure anti-HDV antibodies, such as DiaPro HDV Ab (DiaPro) and DiaSorin ETI-AB-DELTAK-2 (DiaSorin) [23, 24]. However, these diagnostic reagents are not licensed in Taiwan, so it is difficult to use them routinely in Taiwan. To date, domestically produced HDV diagnostic kits are mainly intended for research use only and usually have low sensitivity and specificity values. We successfully established a direct sandwich ELISA method (GB HDV Ab) to detect anti-HDV antibodies in human serum or plasma with ethylenediaminetetraacetic acid (EDTA).
In this study, 1375 HBsAg-positive specimens were examined to assess the performance of the GB HDV Ab kit and to compare the data from this kit with those obtained by using the two most commonly available ELISA kits from DiaPro and DiaSorin.
Materials and methods
Serum and EDTA-treated plasma specimen collection
A total of 913 serum and 462 EDTA-treated plasma samples were obtained from HBsAg-positive individuals in three hospitals in Taiwan from June 2014 to November 2017. The three hospitals were Kaohsiung Chang Gung Memorial Hospital (KCGMH), Linkou Chang Gung Memorial Hospital (LCGMH) and National Taiwan University Hospital (NTUH).
Anzeige
Ethics
Ethical approval was obtained from the Institutional Review Board (IRB) of KCGMH (106-3378C), LCGMH (201700109B0) and NTUH (201612075DSB). Informed consent was sought and documented for all participants in this study.
Performance of ELISA kits
Three commercially available ELISA kits, DiaPro HDV Ab (CE 0318), DiaSorin ETI-AB-DELTAK-2 (CE 0459) and GB HDV Ab (TFDA No. 005807), were utilized strictly according to the instructions of the manufacturers, as detailed in Table 1. The kits used in this study have different detection methods and use different HRP conjugates. According to the manufacturer’s guidelines, the cutoff value for the GB HDV Ab kit is defined as the mean value for the negative control + 0.11, and the cutoff for the DiaSorin kit is set as (0.5 × mean negative control) + (0.5 × mean positive control); the cutoff for the DiaPro kit is determined according to (mean negative control + mean positive control)/5. The positive and negative controls that were used were supplied by the manufacturer. Optical density (OD) was measured by an EMax Plus microplate reader (Molecular Devices), and the results were expressed as the cut-off index (COI = sample signal/cut-off value). HDV detection was considered positive for a COI value ≥1. The performance of the kits was evaluated in terms of sensitivity, specificity, and overall agreement with the 95% confidence intervals (95% CI) according to the CLSI EP12-A guidelines [25]. Sensitivity was calculated as true positives/(true positives + false negatives) × 100; specificity was calculated as true negatives/(true negatives + false positives) × 100; the overall agreement was calculated as (true positives + true negatives)/(true positives + false negatives + false positives + true negatives) × 100.
Table 1
Comparison of the three ELISA kits used for HDV detection
GB HDV Ab
DiaPro HDV Ab
DiaSorin ETI-AB-DELTAK-2
Manufacturer
General Biological Corporation
DiaPro
DiaSorin
Certification
TFDA MHW Medical Device Manufacturing No. 005807
CE 0318
CE 0459
Sample (volume)
serum and EDTA-plasma(100 μl)
serum and EDTA-plasma
(100 μl)
serum only (50 μl)
Principle
direct sandwich assay
two-step competitive assay
simultaneous competitive assay
Adsorbed Antigen
recombinant HDV antigen
recombinant HDV antigen
recombinant HDV antigen
HRP Conjugate
HDV small antigen
polyclonal Ab against HDV
human anti-HD Fab
Incubation Time
105 min
(60, 30, 15 min)
140 min
(60, 60, 20 min)
210 min
(180, 30 min)
Incubation Temperature
37 °C
37 °C or room temperature
37 °C orroom temperature
Reader Wavelength
450 nm (reading)
650 nm (blanking, if possible)
450 nm (reading)
620–630 nm (blanking, if possible)
450 nm (reading)
630 nm (blanking)
Control Well(s)
6 (Blank*1, NC*3, PC*2)
7 (Blank*1, NC*3, CAL*2, PC*1)
6 (Blank*1, NC*3, PC*2)
Interference testing
Interference testing was performed according to the CLSI EP07-A2 guidelines [26]. Briefly, 200 mg/dl triglyceride (TG) from an in-house serum sample with a high triglyceride titer (~ 400 mg/dl) was used as the stock; 0.4 mg/dl bilirubin (BL), which was obtained from Sigma, 5.5 g/dl hemoglobin (HB), which was obtained from healthy donors, 17 ng/ml human anti-mouse antibody plasma (HAMA), which was obtained from Meridian Life Science, and a three-fold dilution of a multi-analyte positive control (MAPC), which was obtained from SeraCare (Accurun Series 2700) and contained anti-HIV-1/2, anti-HTLV-I/II, anti-HBc, anti-HCV, anti-CMV, anti-Treponema pallidum, and HBsAg, was spiked into the serum and EDTA-plasma from HDV-positive patients.
The detection limit of the ELISA kits
The detection limits of the three commercially available ELISA kits were determined by using decreasing concentrations of anti-HDV in normal human plasma (NHP) or guinea pig sera. Anti-HDV was obtained from two standard sensitivity panels, including ACCURUNⓇ 127 Anti-Hepatitis Delta Positive Control (CE-IVD) from SeraCare Life Sciences and polyclonal anti-HDV from guinea pig.
Statistical analysis
All calculations were performed using Microsoft Excel 2016. Statistical significance (P values < 0.05) was assessed by the two-tailed Student’s t-test. The sensitivity, specificity, and overall agreement with the 95% CI were estimated for each kit.
Results
In the current study, we developed a direct sandwich GB HDV Ab kit, which can detect total anti-HDV antibodies. We determined the detection limits of the GB HDV Ab kit and commercial ELISA kits. Anti-HDV antibodies from humans and guinea pigs were serially 2-fold diluted with normal human plasma (NHP). The results showed that the GB kit had superior analytical sensitivity compared to the DiaPro and DiaSorin kits. The detection limit of the GB HDV Ab kit for ACCURUN 127 was 211-fold, which was better than that of the DiaPro (25-fold) and DiaSorin (29-fold) kits; for polyclonal anti-HDV antibodies from guinea pig, the detection limit of the GB HDV Ab kit was 29-fold, which was better than that of the DiaPro (27-fold) and comparable to that of the DiaSorin (29-fold) kits (Fig. 1).
×
In the current study, a total of 913 serum specimens and 462 EDTA-treated plasma samples from HBV-infected individuals from three hospitals in Taiwan obtained from June 2014 to November 2017 were tested with commercially available HDV detection ELISA kits from GB, DiaPro and DiaSorin, and the results are summarized in Table 2. For serum samples, it was evident that the GB HDV Ab kit had a similar performance, for which the specificity was 97.3% and the sensitivity was 100% compared to the DiaPro kit. The overall agreement of the GB HDV Ab kit results for the serum samples was 97.6%. Moreover, the GB HDV Ab kit also had good performance for the EDTA-treated plasma samples, for which the specificity was 97.2% and the sensitivity was 100%. The overall agreement of the results for the GB HDV Ab kit was 97.4%. The data indicated that the GB kit had a very similar performance compared to that of the DiaPro kit. However, 22 serum samples and 12 EDTA-treated plasma samples showed inconsistent results between the GB and DiaPro kits. Therefore, we used a third commercial kit, the DiaSorin ELISA kit, to confirm the positive or negative results for these inconsistent samples. The results showed that 15 serum samples and 4 EDTA-treated plasma samples were HDV-positive samples, and the results for one sample for the DiaSorin kit were equivocal. The equivocal result was excluded from the calculations. By doing so, the specificity of the GB HDV Ab kit for the serum and EDTA samples was determined to be 99.3 and 98.1%, respectively (Table 3). The sensitivity of the GB HDV Ab kit for the serum and EDTA samples was 100%. The overall agreement of the results for the GB HDV Ab kit for the serum and EDTA samples was 99.3 and 98.3%, respectively. These results were comparable to those obtained with the commercial ELISA kits employed in this study.
Table 2
Performance of the GB kit compared to the DiaPro kit
DiaPro
Serum
Total no.
EDTA-treated plasma
Total no.
Positive
Negative
Positive
Negative
GB
Positive
86
22
108
26
12
38
Negative
0
805
805
0
424
424
Total no.
86
827
913
26
436
462
Sensitivity (%)
100.0 (95.7 ~ 100.0)
100.0 (87.1 ~ 100.0)
Specificity (%)
97.3 (96.0 ~ 98.2)
97.2 (95.3 ~ 98.4)
Overall Agreement (%)
97.6 (95.5 ~ 99.3)
97.4 (94.9 ~ 99.1)
Table 3
Performance of the GB kit compared to the DiaPro + DiaSorin kits
DiaPro + DiaSorin
Serum
Total no.
EDTA-treated plasma
Total no.
Positive
Negative
Positive
Negative
GB
Positive
101
6
107
30
8
38
Negative
0
805
805
0
424
424
Total no.
101
811
912
30
432
462
Sensitivity (%)
100.0 (96.3 ~ 100.0)
100.0 (88.7 ~ 100.0)
Specificity (%)
99.3 (98.4 ~ 99.7)
98.1 (96.4 ~ 99.1)
Overall Agreement (%)
99.3 (97.1 ~ 100.0)
98.3 (95.6 ~ 100.0)
In addition, we also analyzed the genotypes of 38 HDV-positive samples from patients with HBV infection using PCR and DNA sequencing. A prevalence of 18.4% for the HDV-1 genotype (n = 7), 65.8% for the HDV-2 genotype (n = 25) and 15.8% for the HDV-4 genotype (n = 6) was observed. All the samples were positive for HDV antibodies, as detected by the GB HDV Ab kit (Fig. 2). These data indicate that the GB HDV Ab kit was able to detect antibodies from specimens containing HDV-1, HDV-2 and HDV-4, which are commonly found in Taiwan.
×
Anzeige
To determine which analytes might interfere with the performance of the GB HDV Ab kit, interference assays were performed. Interference test samples were generated by spiking potential interfering materials into serum and EDTA-treated plasma containing anti-HDV plasma (ACCURUN 127) (Table 4). The results showed that none of the interfering materials in serum and none of the materials except TG, BL and HAMA in EDTA-treated plasma affected the performance of the GB HDV Ab kit (p < 0.05). However, HB and MAPC in EDTA-treated plasma might affect the values of the COI determined by the GB HDV Ab kit.
Table 4
Performance of the GB kit in the presence of interfering compounds
Specimen
Interfering compound
mean COI
±
std. Dev.
p-value
Serum
TG (−)
3.65
±
0.60
0.87
TG (+)
3.59
±
0.09
BL (−)
2.95
±
0.83
0.77
BL (+)
2.75
±
0.67
HB (−)
3.85
±
0.38
0.62
HB (+)
3.68
±
0.40
HAMA (−)
3.60
±
0.16
0.43
HAMA (+)
3.80
±
0.35
MAPC (−)
3.26
±
0.49
0.20
MAPC (+)
3.89
±
0.52
EDTA-treated plasma
TG (−)
4.09
±
0.60
0.24
TG (+)
3.57
±
0.23
BL (−)
3.65
±
0.84
0.48
BL (+)
3.24
±
0.39
HB (−)
4.59
±
0.26
0.03
HB (+)
3.90
±
0.26
HAMA (−)
4.67
±
0.27
0.23
HAMA (+)
4.43
±
0.11
MAPC (−)
4.09
±
0.09
0.01
MAPC (+)
5.02
±
0.30
TG triglyceride, BL bilirubin, HB hemoglobin, HAMA human anti-mouse antibody plasma, MAPC multi-analyte positive control (SeraCare Accurun Series 2700)
In addition, the detection ranges for the COI and OD values of the positive samples with serum and EDTA-treated plasma obtained with the GB HDV Ab kit were wider than those of the DiaPro kit (Fig. 3). These results indicated that the GB kit could detect lower levels of anti-HDV antibodies and also had a wider detection range for HDV antibodies without dilution.
×
Discussion
In this study, the performance of three commercial HDV ELISA kits (GB, DiaPro, and DiaSorin) was investigated for serum and EDTA-treated plasma. An important issue that was encountered was the discordance between the results of the GB and DiaPro kits. Therefore, another available kit, DiaSorin, was used to resolve this issue. Among 913 serum samples, 86 HDV-positive samples and 827 HDV-negative samples were determined by the DiaPro kit. On the other hand, 108 HDV-positive samples and 805 HDV-negative samples were determined by the GB HDV Ab kit. Therefore, the 22 inconsistent samples were reconfirmed with the DiaSorin kit, resulting in 15 HDV-positive samples, 6 HDV-negative samples, and one equivocal result. Then, we assumed that the real status of the 912 serum samples reflected 101 HDV-positive samples and 811 HDV-negative samples. By doing so, the overall sensitivity and specificity of the GB HDV Ab kit were shown to be 100 and 99.3%, whereas those of the DiaPro kit were shown to be 85.1 and 100%, respectively. The results for the serum samples indicated that the performance of the GB HDV Ab kit was better than that of the DiaPro kit. Among the 462 EDTA samples, 26 HDV-positive samples and 436 HDV-negative samples were determined by the DiaPro kit. However, 38 HDV-positive samples and 424 HDV-negative samples were determined by the GB HDV Ab kit. Therefore, the 12 inconsistent samples were also reconfirmed by using the DiaSorin kit, which resulted in 4 HDV-positive samples and 8 HDV-negative samples. Then, we assumed that the 462 EDTA samples included 30 HDV-positive samples and 432 HDV-negative samples. Therefore, the overall sensitivity and specificity of the GB HDV Ab kit were 100 and 98.1%, respectively, whereas those of the DiaPro were 86.7 and 100%, respectively. Therefore, the present study revealed the better performance of the GB HDV Ab kit in terms of specificity and sensitivity compared to that of the DiaPro kit. In addition, the detection limit of the GB HDV Ab kit was better than that of the DiaPro and DiaSorin (Fig. 1). Therefore, the 6 negative serum and 8 negative plasma samples by DiaSorin might contain lower concentration of anti-HDV antibodies and only could be determined by GB HDV Ab kit due to the lower detection limit of GB kit. Further study is needed to address these questions.
In addition, the ELISA assay is usually affected by binding to natural unknown proteins, such as human anti-animal antibodies [27]. Therefore, we also used interference assays to determine the performance of the GB HDV Ab kit in the presence of interfering materials. The kit performance did not significantly change in the presence of five different interfering materials in serum except for HB and MAPC, for which the results for EDTA-treated plasma showed statistically significant variation (p < 0.05). Although not yet understood, the slight background observed in EDTA-plasma with hemoglobin (HB) or MAPC might be due to unspecific binding of the antibodies. The results indicated that the GB HDV Ab kit is suitable for detecting anti-HDV antibodies in serum samples.
Anzeige
Conclusion
The GB HDV Ab kit can successfully detect anti-HDV antibodies from patients infected with HDV genotypes 1, 2 and 4, which are commonly found in Taiwan. The GB kit has higher sensitivity and specificity than commercial ELISA kits. In addition, the GB HDV Ab kit showed improved performance during interference testing of serum samples, a wider detection range and a lower detection limit than commercial kits. The results indicated that the GB HDV Ab kit might be suitable for screening patients infected with HDV.
Acknowledgments
We thank Dr. Chang-Lin Wu and Yen-Ting Lin at the General Biological Corporation for their excellent technical assistance and discussion.
Consent to publication
Not applicable.
Ethics approval and consent to participate
Ethical approval was obtained from the Institutional Review Board (IRB) of KCGMH (106-3378C), LCGMH (201700109B0) and NTUH (201612075DSB). Informed consent was sought and documented for all participants in this study.
Anzeige
Competing interests
Guan-Yu Lin, Yi-Le Wu, Cheng-Si Wang, Chia-Yun Ko and Po-Hsin Peng are employees of General Biologicals Corporation.
Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
Publisher’s Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.