key: cord-0909615-fmkfo5ju
authors: Meng, Qing-Bin; Peng, Jing-Jing; Wei, Xin; Yang, Jia-Yao; Li, Peng-Cheng; Qu, Zi-Wei; Xiong, Yong-Fen; Wu, Guang-Jiang; Hu, Zhi-Min; Yu, Jian-Chun; Su, Wen
title: Clinical application of combined detection of SARS-CoV-2-specific antibody and nucleic acid
date: 2020-10-06
journal: World J Clin Cases
DOI: 10.12998/wjcc.v8.i19.4360
sha: f6341835cca53515941bc02c35712d33f938bfeb
doc_id: 909615
cord_uid: fmkfo5ju

BACKGROUND: The global outbreak of human severe acute respiratory syndrome coronavirus (SARS-CoV)-2 infection represents an urgent need for readily available, accurate and rapid diagnostic tests. Nucleic acid testing of respiratory tract specimens for SARS-CoV-2 is the current gold standard for diagnosis of coronavirus disease 2019 (COVID-19). However, the diagnostic accuracy of reverse transcription polymerase chain reaction (RT-PCR) tests for detecting SARS-CoV-2 nucleic acid may be lower than optimal. The detection of SARS-CoV-2-specific antibodies should be used as a serological non-invasive tool for the diagnosis and management of SARS-CoV-2 infection. AIM: To investigate the diagnostic value of SARS-CoV-2 IgM/IgG and nucleic acid detection in COVID-19. METHODS: We retrospectively analyzed 652 suspected COVID-19 patients, and 206 non-COVID-19 patients in Wuhan Integrated TCM and Western Medicine Hospital. Data on SARS-CoV-2 nucleic acid tests and serum antibody tests were collected to investigate the diagnostic value of nucleic acid RT-PCR test kits and immunoglobulin (Ig)M/IgG antibody test kits. The χ2 test was used to compare differences between categorical variables. A 95% confidence interval (CI) was provided by the Wilson score method. All analyses were performed with IBM SPSS Statistics version 22.0 (IBM Corp., Armonk, NY, United States). RESULTS: Of the 652 suspected COVID-19 patients, 237 (36.3%) had positive nucleic acid tests, 311 (47.7%) were positive for IgM, and 592 (90.8%) were positive for IgG. There was a significant difference in the positive detection rate between the IgM and IgG test groups (P < 0.001). Using the RT-PCR results as a reference, the specificity, sensitivity, and accuracy of IgM/IgG combined tests for SARS-CoV-2 infection were 98.5%, 95.8%, and 97.1%, respectively. Of the 415 suspected COVID-19 patients with negative nucleic acid test results, 366 had positive IgM/IgG tests with a positive detection rate of 88.2%. CONCLUSION: Our data indicate that serological IgM/IgG antibody combined test had high sensitivity and specificity for the diagnosis of SARS-CoV-2 infection, and can be used in combination with RT-PCR for the diagnosis of SARS-CoV-2 infection.

Coronavirus disease 2019 (COVID-19) was first reported in Wuhan, Hubei Province, China and has spread worldwide [1, 2] . COVID-19 is a highly transmissible disease caused by severe acute respiratory syndrome coronavirus (SARS-CoV)-2, which was also named 2019 novel coronavirus (2019-nCoV) [2, 3] . As of April 19, 2020, 2160207 confirmed COVID-19 cases were reported worldwide, causing 146088 deaths [4] . The World Health Organization (WHO) declared COVID-19 a global pandemic on March 11, 2020 [5, 6] . The global outbreak of human SARS-CoV-2 infection has highlighted the necessity for readily available, accurate and rapid diagnostic tests.

Nucleic acid testing or genetic sequencing of respiratory tract specimens for SARS-CoV-2 is the current gold standard for the diagnosis of COVID-19 [7] [8] [9] . However, according to recent evidence, the diagnostic accuracy of reverse transcription polymerase chain reaction (RT-PCR) tests for detecting SARS-CoV-2 nucleic acid may be lower than optimal. Liu et al [10] analyzed the RT-PCR results of throat swab samples from 4880 cases of suspected SARS-CoV-2 infection, and found that only 38.42% were positive. Another important concern is the number of false-negative RT-PCR results for COVID-19 [11] . RT-PCR has some other limitations, including potential biological safety hazards due to handling of patient samples and long waiting time for results.

Given the limitations of the currently used nucleic acid detection for diagnosis of COVID-19, clinical laboratories should apply sensitive and accurate assays such as immunological detection kits that target viral antigens or antibodies for diagnosing SARS-CoV-2 infection as quickly as possible [12] . Therefore, SARS-CoV-2 serum IgM and IgG antibody positivity was added to the diagnostic criteria in the Novel Coronavirus Pneumonia Diagnosis and Treatment Guidelines (Trial Version 7) [13] . Dong et al [14] reported a COVID-19 case without detectable virus in oropharyngeal specimens and suggested testing for serum IgM and IgG antibodies to SARS-CoV-2 as an alternative for diagnosis. Li et al [15] demonstrated a rapid and simple point-of-care lateral flow immunoassay that can detect SARS-CoV-2 IgM and IgG antibodies in the blood of patients at different stages of infection. The overall testing sensitivity was 88.66% and specificity was 90.63%. However, there is limited clinical information on the SARS-CoV-2 antibody test (colloidal gold).

In the present study, we collected clinical data from 652 suspected COVID-19 patients and 206 non-COVID-19 patients to investigate the diagnostic value of SARS-CoV-2 IgM/IgG antibody test kits with colloidal gold immunoassays and nucleic acid RT-PCR test kits.

The study was conducted in accordance with the Declaration of Helsinki and was approved by the Ethics Committee of Wuhan Integrated TCM and Western Medicine Hospital, Huazhong University of Science and Technology (No.

[2020]8). The requirement for written informed consent was waived given the context of emerging infectious diseases.

From January 4 to April 5, 2020, data on 1876 consecutive patients who underwent SARS-CoV-2 nucleic acid tests and chest computed tomography were retrospectively collected in Wuhan Integrated TCM and Western Medicine Hospital. A total of 1018 patients were excluded because they did not have SARS-CoV-2 IgM/IgG antibody tests. We included 652 suspected COVID-19 patients and 206 non-COVID-19 patients ( Figure 1 ). RT-PCR, SARS-CoV-2 IgM/IgG antibody tests, and pulmonary imaging features were extracted from patients' electronic medical records in our hospital information system. The patients were clinically diagnosed with COVID-19 according October to the Diagnosis and Treatment Protocol for Novel Coronavirus Pneumonia (Trial Version 7) [13] . Suspected COVID-19 patients met the following criteria: Clear history of epidemiological contact, typical clinical symptoms and pulmonary imaging features.

The SARS-CoV-2 Antibody Test Kit (catalog No. 20203400177, colloidal gold) was obtained from Innovita (Tangshan) Biotechnology Co., Ltd. (Tangshan, China), with the recombinant SARS-CoV-2 antigen coated on the surface of the colloid gold particles. The SARS-CoV-2 nucleic acid detection kit (catalog No. 20203400057, fluorescent PCR) was purchased from Shanghai Zhijiang Biotechnology Co., Ltd.

(Shanghai, China) [16] .

Peripheral blood (4 mL) was collected from each patient with a yellow top collection tube and sent to the laboratory for serum SARS-CoV-2 IgM/IgG antibody test. Detection of serum IgM/IgG antibody was performed using the SARS-CoV-2 Antibody Test Kit (colloidal gold). The presence of two purple bands (M and C) indicated the presence of SARS-CoV-2 IgM antibodies. The presence of two purple bands (G and C) indicated the presence of SARS-CoV-2 IgG antibodies. For negative results, only one purple band appeared at the control line (C). If the control line (C) failed to appear, regardless of whether the G/M line was visible, the test was invalid.

Fluorescent PCR for SARS-CoV-2 nucleic acid detection: Pharyngeal swabs were used to collect secretions from the lateral and posterior pharyngeal walls and placed in sterile tubes (containing 1 mL sterile normal saline). Fluorescence PCR was performed using the SARS-CoV-2 Nucleic Acid Detection Kit. The results were divided into positive and negative according to the manufacturer's protocol.

The statistical methods used in this study were reviewed by Guang-Jiang Wu from Beijing Shijitan Hospital, Capital Medical University. Categorical variables were displayed as counts and percentages. Continuous variables were presented as median (interquartile range; IQR). The χ 2 test was used to compare differences between categorical variables. The specificity, sensitivity, positive predictive value (PPV) and negative predictive value (NPV) of the SARS-CoV-2 Antibody Test Kit (colloidal gold) were calculated according to the following formulas. Specificity positive); NPV (%) = 100 × [true negative/(true negative + false negative)]; and Accuracy (%) = 100 × (true positive + true negative)/( true positive + false positive + true negative + false negative). A 95% confidence interval (CI) was provided by the Wilson score method. All P values were two-sided, and P < 0.05 was considered statistically significant. All analyses were performed with IBM SPSS Statistics version 22.0 (IBM Corp., Armonk, NY, United States).

Of the 652 suspected COVID-19 patients, 237 had positive and 415 had negative SARS-CoV-2 nucleic acid tests with a positive detection rate of 36.3% (95%CI: 32.6%-40.1%); therefore, 237 patients were confirmed to have COVID-19 by the SARS-CoV-2 nucleic acid RT-PCR test.

The median time from illness onset to IgM/IgG antibody tests was 34 d (IQR 28-39 d).

A representative photograph of SARS-CoV-2 IgM and IgG antibody tests is shown in Figure 2 . Figure 2A shows detection of IgM in low concentration (Score 1) and IgG in high concentration (Score 2); Figure 2B shows IgG only in high concentration (Score 2); Figure 2C shows both IgM and IgG in high concentration (Score 2); and Figure 2D shows no IgM and IgG (Score 0). Score ≥ 1 was defined as positive.

Of 206 non-COVID-19 patients, one was positive for IgM antibody against SARS-CoV-2, and two were positive for IgG antibody against SARS-CoV-2. Of the 652 suspected COVID-19 patients, 311 were positive for SARS-CoV-2-specific IgM antibody with a positive detection rate of 47.7% (95%CI: 43.9%-51.5%); 592 patients were positive for SARS-CoV-2-specific IgG antibody with a positive detection rate of 90.8% (95CI: 88.6%-93.0%); and 593 patients were positive for SARS-CoV-2-specific IgM and/or IgG antibody combined tests with a positive detection rate of 91.0% (95%CI: 88.7%-93.2%). There was a significant difference regarding the positive detection rate between the IgM and IgG test groups (P < 0.001) ( Table 1) .

Of the 237 patients who were positive for SARS-CoV-2 nucleic acid tests, 109 were positive for IgM, 227 patients were positive for IgG, and 227 patients were positive for IgM and/or IgG. Using the RT-PCR results as a reference, the specificity, sensitivity, and accuracy of SARS-CoV-2-specific IgM, IgG and IgM/IgG combined tests for detecting SARS-CoV-2 infection are shown in Table 2 .

Receiver operating characteristic curve analysis showed that the area under the curve of IgM tests, IgG tests and IgM/IgG combined tests for diagnosing COVID-19 were 0.728 (95%CI: 0.681-0.775), 0.978 (95%CI: 0.963-0.993) and 0.978 (95%CI: 0.963-0.993) (Figure 3 ).

Of the 415 suspected COVID-19 patients who were negative for SARS-CoV-2 nucleic acid tests, 366 patients were positive for SARS-CoV-2-specific IgM and/or IgG antibody tests with a positive detection rate of 88.2% (95%CI: 85.1-91.3%).

In the current retrospective study, we included 652 suspected COVID-19 patients with a clear history of epidemiological contact, typical clinical symptoms and pulmonary imaging features, to investigate the positive detection rate of nucleic acid and antibody tests. The results showed that of 652 patients, 237 (36.3%) were confirmed to have COVID-19 by the SARS-CoV-2 nucleic acid test, 311 (47.7%) were positive for SARS-CoV-2-specific IgM antibodies, 592 (90.8%) were positive for SARS-CoV-2-specific IgG antibodies, and 593 (91.0%) were positive for SARS-CoV-2 specific IgM and/or IgG antibodies. We included 237 confirmed COVID-19 patients with positive SARS-CoV-2 nucleic acid tests and 206 confirmed non-COVID-19 patients to evaluate the performance of the SARS-CoV-2-specific IgM and IgG antibody test kit.

Liu et al [10] reported that the positive rate of RT-PCR detection of SARS-CoV-2 infection was 38.4% (1875/4880) and an increased positive percentage was found in male and older patients. Ai et al [17] reported that 59% (601/1014) of patients had positive SARS-CoV-2 RT-PCR results. In the current study, the positive percentage of Table 1 Severe acute respiratory syndrome coronavirus immunoglobulin M and immunoglobulin G antibody detection result, n (%) SARS-CoV-2 RT-PCR tests was lower than that of previous studies. According to the Novel Coronavirus Pneumonia Diagnosis and Treatment Guidelines, SARS-CoV-2 nucleic acid test by RT-PCR assay on respiratory tract specimens plays an important role in the etiological diagnosis of SARS-CoV-2 infection and discharge evaluation [13] . However, the accuracy of the laboratory diagnosis of COVID-19 using RT-PCR is affected by many potential factors, including preanalytical problems such as improper collection, storage and transport of swabs; sample contamination and testing patients receiving antiretroviral therapy; as well as analytical problems such as active viral recombination, use of inadequately validated assays, instrument malfunctioning, along with other specific technical issues [9] . Therefore, it is necessary to develop a more sensitive, accurate and simple detection method for the diagnosis of SARS-CoV-2 infection. Dong et al [14] reported that COVID-19 was confirmed with positive IgM and positive IgG antibodies tests against SARS-CoV-2. As recently reported, a rapid IgM/IgG October 6, 2020 Volume 8 Issue 19 combined antibody test was used for the diagnosis of SARS-CoV-2 infection, showing 88.66% sensitivity and 90.63% specificity [15] . In the current study, we found that the specificity, sensitivity, and accuracy of IgM and/or IgG antibody combined detection for the diagnosis of SARS-CoV-2 infection were 98.5% (203/206), 95.8% (227/237), and 97.1% (430/443), respectively. Of the 415 suspected COVID-19 patients who were negative for SARS-CoV-2 nucleic acid tests, 88.2% (366) of patients were positive for SARS-CoV-2 specific IgM and/or IgG antibody tests. Therefore, 366 patients were considered to have COVID-19 with SARS-CoV-2 IgM and/or IgG antibody tests. All the results confirmed that IgM and/or IgG antibody tests can be used as an effective method for serological diagnosis of SARS-CoV-2 infection. According to the Diagnosis and Treatment Protocol for Novel Coronavirus Pneumonia (Trial Version 7), double positive results of IgM and IgG antibody tests can be used as serological evidence for the diagnosis of SARS-CoV-2 infection [13] . However, the fact that IgM testing may be negative in convalescent patients with COVID-19 is not surprising considering the probable kinetics of SARS-CoV-2-specific IgM antibody [18] [19] [20] . Therefore, IgM and/or IgG positivity should be used as serological evidence for the diagnosis of SARS-CoV-2 infection.

There were several notable limitations in the present study. Firstly, the main weaknesses were its single center retrospective nature and small sample size. Secondly, due to the retrospective nature of the study, most patients did not complete the dynamic monitoring of SARS-CoV-2-specific IgM and IgG by the end of the study. Thirdly, the median time from symptom onset to the IgM and IgG test was long due to late availability of the SARS-CoV-2-specific IgM and IgG test kits. October 

In summary, this retrospective study indicated that serum specific IgM and IgG antibody combined test has high sensitivity, specificity and accuracy for the diagnosis of SARS-CoV-2 infection. Our data indicate that the antibody-based test can be used as a detection tool in combination with RT-PCR in the diagnosis of SARS-CoV-2 infection in epidemic areas. 

According to recent evidence, the diagnostic accuracy of reverse transcription polymerase chain reaction (RT-PCR) tests for detecting SARS-CoV-2 nucleic acid may be lower than optimal. Given the limitations of RT-PCR tests for the diagnosis of COVID-19, clinical laboratories should apply sensitive and accurate assays such as immunological detection kits that target viral antigens or antibodies for diagnosing SARS-CoV-2 infection as quickly as possible. We are very interested in this issue and hope that we can present a new antibody test adopted in our hospital.

The objectives were to report the diagnostic value of SARS-CoV-2 IgM/IgG and nucleic acid detection in COVID-19.

We retrospectively analyzed data on 652 suspected COVID-19 patients, and 206 non-COVID-19 patients in Wuhan Integrated TCM and Western Medicine Hospital. RT-PCR, SARS-CoV-2 IgM/IgG antibody tests, and pulmonary imaging features were extracted from patients' electronic medical records in our hospital information system. The specificity, sensitivity, PPV and NPV of the SARS-CoV-2 Antibody Test Kit were calculated. A 95% confidence interval (CI) was provided by the Wilson score method. All analyses were performed with IBM SPSS Statistics version 22.0 (IBM Corp., Armonk, NY, United States), and two-tailed P values less than 0.05 were considered to be statistically significant.

Of the 652 suspected COVID-19 patients, 237 (36.3%) patients were confirmed to have COVID-19 by the SARS-CoV-2 nucleic acid RT-PCR test. Using RT-PCR results as a reference, the specificity, sensitivity, and accuracy of the SARS-CoV-2-specific IgM/IgG combined tests for detecting SARS-CoV-2 infection were 98.5%, 95.8%, and 97.1%, respectively. Of the 415 suspected COVID-19 patients who were negative for the SARS-CoV-2 nucleic acid tests, 366 patients were positive for the SARS-CoV-2specific IgM and/or IgG antibody tests with a positive detection rate of 88.2%.

Our data indicate that the serological IgM/IgG antibody combined test had high specificity, sensitivity, and accuracy for the diagnosis of SARS-CoV-2 infection, and can be used in combination with RT-PCR for the diagnosis of SARS-CoV-2 infection.

For COVID-19 patients, it is worth further completing the dynamic monitoring of SARS-CoV-2-specific IgM and IgG.

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The authors thank Professor Ling-Qian Chang (Beijing Advanced Innovation Center for Biomedical Engineering, School of Biological Science and Medical Engineering, Beihang University), Associate Professor Feng Chen (College of Materials Science and Engineering, Zhejiang University of Technology) and Jie Qiao (Hubei College of Traditional Chinese Medicine, Wuhan, Hubei Province, China) for their guidance in study design and interpretation of results, and review of the manuscript.

 Volume 8  Issue 19