key: cord-1035941-sk9iilum
authors: Kong, Wen-Hua; Zhao, Rong; Zhou, Jun-Bo; Wang, Fang; Kong, De-Guang; Sun, Jian-Bin; Ruan, Qiong-Fang; Liu, Man-Qing
title: Serologic Response to SARS-CoV-2 in COVID-19 Patients with Different Severity
date: 2020-07-23
journal: Virol Sin
DOI: 10.1007/s12250-020-00270-x
sha: 8e64233f3ce51851740af4bce0fbefdbde0b8194
doc_id: 1035941
cord_uid: sk9iilum

The immense patient number caused by coronavirus disease 2019 (COVID-19) global pandemic brings the urge for more knowledge about its immunological features, including the profile of basic immune parameters. In this study, eighty-eight reported COVID-19 patients in Wuhan were recruited from January to February, 2020, including 32 severe/critical cases and 56 mild/moderate cases. Their mean age was 56.43 years (range 17–83) and gender ratio (male/female) was 43:45. We tested SARS-CoV-2 RNA with commercial kits, investigated the level of serologic IgM and IgG antibodies against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) using magnetic particle chemiluminescence immunoassays, and compared the results of serologic tests and nucleic acid test (NAT). Among 88 patients, 95.45% were confirmed as positive by the combination of NAT and antibody test, which was significantly higher (P < 0.001) than by single nucleic acid test (73.86%) or serologic test (65.91%). Then the correlation between temporal profile and the level of antibody response was analyzed. It showed that seroconversion started on day 5 after disease onset and IgG level was rose earlier than IgM. Comparison between patients with different disease severity suggested early seroconversion and high antibody titer were linked with less severe clinical symptoms. These results supported the combination of serologic testing and NAT in routine COVID-19 diagnosis and provided evidence on the temporal profile of antibody response in patients with different disease severity.

The outbreak of novel coronavirus disease 2019 has become a global pandemic and caused over 2 million infections by April 15th, 2020 (WHO 2020). According to the Chinese Centers for Disease Prevention and Control (CDC) report, among 72,314 COVID-19 cases in China's mainland most of cases (81%) presented only mild illness or moderate pneumonia, yet 14% developed severe symptoms such as dyspnea, high respiratory frequency and low blood oxygen saturation, and another 5% were in critical conditions like respiratory failure, septic shock, and multiple organ dysfunction/failure (Epidemiology Working Group for NCIP Epidemic Response and Chinese CDC, 2020; Wu and McGoogan 2020) . The global case-fatality rate (CFR) of COVID-19 was 6.4% as of April 15, 2020 (WHO 2020 ), yet the CFR could be even elevated among severe/critical cases, elder population, and patients with preexisting comorbidity Chen et al. 2020; Wu and McGoogan 2020) . The reported CFR in ICU cases ranged from 22.72% to 38.5% Huang et al. 2020; Richardson et al. 2020) .

It is believed that early adaptive immune response plays an important role in eliminating the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), while the inflammation driven by elevated innate immune response is a major cause of life-threatening respiratory disorders in severe COVID-19 cases Thevarajan et al. 2020 (Lauer et al. 2020; Long et al. 2020; Thevarajan et al. 2020; Xiang et al. 2020; Zhang et al. 2020; Zhao et al. 2020a, b) , which confirmed the emergence of IgM, IgG and neutralizing antibodies against SARS-CoV-2 and suggested the application of serologic test in COVID-19 diagnosis (Long et al. 2020; Zhang et al. 2020) . However, some reports about the temporal profile of SARS-CoV-2 antibodies were mutually contradictory (Thevarajan et al. 2020; Xiang et al. 2020; Zhao et al. 2020a ) and the immune responses of patients with different demographic and clinical features remain unclear. In this study, we, compared the results of serologic tests and nucleic acid test (NAT) from a group of COVID-19 patients in Wuhan, and analyzed the serologic IgM and IgG antibody level of patients with different disease severity.

In this study, we included confirmed patients with both throat swab and blood sample delivered to the Wuhan CDC laboratory before March 1st, 2020. 

The nucleic acid was extracted from 200 lL of throat swab medium using a GeneRotex automated nucleic acid extraction system (Tianlong, Xi'an, China). Due to medical resource limitations, two commercial quantitative PCR (qPCR) kits were employed in the detection of SARS-CoV-2 RNA. One of the assays (Daan Gene, Guangzhou, China) was used from January to early February, targeting at SARS-CoV-2 ORF1ab and N gene, with a limit of detection (LoD) of 500 copies/mL. The other assay (BGI, Shenzhen, China) which was used after February 5th targeted at ORF1ab fragment only and its LoD was 100 copies/mL. The cutoff cycle-threshold (Ct) was 40 for both kits. Both assays were approved by the National Medical Products Administration (NMPA) of China and had been established in our laboratory.

The levels of SARS-CoV-2-binding IgM and IgG antibodies were assessed using semi-quantitative magnetic particle chemiluminescence immunoassays (M-CLIAs) on an Axceed 260 automated magnetic analyzer (Bioscience, Chongqing, China) (Loeffelholz and Tang 2020), as described by Long et al.(2020) . Both IgM and IgG assays had received NMPA approvals with registration numbers of 20203400182 and 20203400183, respectively. The sensitivity and specificity of the IgM assay in pre-marketing clinical evaluation were 88.30% and 99.50%, while those of the IgG assay were 87.25% and 99.25%. Fifteen microliter of serum was diluted for 50 times before being used in each test.

Procedures and cut-off value set-up were performed following the manufacturers' instructions. Antibody levels were presented as the measured chemiluminescence values divided by the cutoff (S/Co) (Long et al. 2020 ).

Statistical analyses were performed with Prism 8.0 (Graph-Pad, San Diego, USA). Categorical variables were compared using Chi square test. For continuous variables, t test or Mann-Whitney U test were employed after their normality determined by Kolmogorov-Smirnov test. A P-value of less than 0.05 was considered statistically significant.

A total of 88 COVID-19 patients from eleven designated hospitals were included in this study, of whom 43 were male and 45 were female. Their mean age was 56.43 years old (range 17-83) and the median interval between initial symptom onset and sample collection was 11 days (range 1-37). Thirty-two patients (36.4%) had severe/critical illnesses and required oxygen supplementation or higher life support, while the other 56 patients had mild or moderate symptoms (Table 1) . qPCR test confirmed 65 SARS-CoV-2 infected cases among 88 participants (73.86%). No significant difference was observed between the positive rates of two qPCR kits (37/53 versus 28/35, v 2 = 1.133, P = 0.287). On the other hand, the positive rates of serum IgM and IgG antibody against SARS-CoV-2 were 32.95% (29/88) and 65.91% (58/88), respectively (Table 2) . Altogether, 84 COVID-19 cases (95.45%) were identified among all patients by the combination of NAT and antibody test, which was significantly more than single NAT (v 2 = 15.793, P \ 0.001) or serologic test (v 2 = 24.643, P \ 0.001). The consistency rate between results of antibody test and NAT was 48.86% [(39 ? 4)/88].

Notably, all the patients that were positive for SARS-CoV-2 IgM were also positive for SARS-CoV-2 IgG. The earliest seroconversion of IgG antibody was observed 5 days after the disease onset, and that time interval of IgM antibody was 8 days (Fig. 1) . For 51 patients with sample collected at 10 days or later after symptom onset, the seroconversion rate was 47.06% for IgM (24/51) and 82.35% for IgG (42/51). Both antibodies were detectable in samples collected over 30 days after onset.

When comparing patients with mild/moderate symptoms and patients with severe/critical diseases, no obvious difference was found between their gender ratios (P = 0.136), age composition (P = 0.571) and NAT positive rates (P = 0.748), but the mild/moderate group had later sampling time and higher antibody positive rates than the severe/critical group (Table 1) . When comparing to the severe/critical cases with the same sampling time, mild/moderate cases presented higher seroconversion rate and higher antibody titer for both IgM and IgG antibodies (Fig. 2) . Similar analysis was performed on cases of different genders and in different age groups, but no significant difference was observed between their antibody levels and temporal profiles (Fig. 3 ).

Although NAT has been regarded as the gold standard of COVID-19 laboratory diagnosis, it is not suitable for low viral load patients and its accuracy is largely depended on the sampling procedure . It makes serologic test a valuable compliment for clinical diagnosis as well as providing information about the disease dynamic. In this study, two NMPA approved M-CLIA kits were used to detect the level of SARS-CoV-2 IgM and IgG antibodies in the serum of COVID-19 patients. In addition to the 65 COVID-19 patients identified by NAT, the antibody tests identified another 19 SARS-CoV-2 infected patients among the 88-person cohort, which diminished the need of multiple sampling and significantly improved the diagnostic accuracy. Meanwhile, the relatively low consistency between NAT and antibody test results also indicated those Temporal profile of serum antibody is vital for the interpretation of serologic test result and evaluating the immune protection situation of subject. In this study, level of serum antibody against SARS-CoV-2 started to rise since day 5 after disease onset and remained high in samples collected 1 month after onset. IgG level was rose earlier than IgM, just like in several other studies (Thevarajan et al. 2020; Zhang et al. 2020) , but it could be related to the unbalanced sensitivity of IgM and IgG assays, since earlier IgM seroconversion has also been reported Zhao et al. 2020a) . The validation and standardization of SARS-CoV-2 serologic assays in large clinical cohort is crucial for enabling uniform assessment of immunogenicity and efficacy (Okba et al. 2020) .

We further looked into the possible correlates of serum antibody level with demographic features, including gender, age and disease severity. Our results suggested early seroconversion and high antibody titer were likely linked with less severe clinical symptoms. The finding is in consistent with earlier observations of recovered patients Thevarajan et al. 2020 ) and the 'twophase immune response' theory in which early adaptive immune response plays protective role in the course of COVID-19 , but opposite to a previous study which reported positive correlation between clinical severity and antibody titer (Zhao et al. 2020a ). Such conflicted data warrant further study of the immunological characteristics of COVID-19 patients with different disease severity.

There are several limitations in this study. First, only one blood sample was collected from each patient, causing a delay between the reported seroconversion time and the actual seroconversion time. Second, two different NAT assays were exploited in the detection of SARS-CoV-2 RNA due to the urgent procurement in the outbreak, which leaded to a potential difference in test sensitivity. Finally, participants' comorbid conditions were not included in the analysis, because we did not have access to the clinical information of participants.

In summary, this study supported the combination of serologic testing and NAT in routine COVID-19 diagnosis and provided evidence on the temporal profile of antibody response against SARS-CoV-2 in patients with different disease severity. More insights about the immunological features of COVID-19 patients are important for disease prognosis prediction and vaccine development.

Animal and Human Rights Statement All procedures performed in studies involving human participants were in accordance with the ethical standards of the institutional and with 1964 Helsinki declaration and later amendments or comparable ethical standards. This study was reviewed and approved by the Ethics Committee of Wuhan Centers for Disease Prevention and Control. Since samples were collected with medical necessity and in accordance to the government guidance, written informed consent was waived. Fig. 3 Comparison of serologic test results between COVID-19 patients of different genders and age groups. A The serologic test results of males (black dots) and females (grey dots) were compared. Every dot represented one patient and the vertical axis reported the S/Co values of SARS-CoV-2 IgM and IgG antibody tests. B The serologic test results of \ 60 years group (black dots) and C 60 years group (grey dots) were compared. Every dot represented one patient and the vertical axis reported the S/Co values of SARS-CoV-2 IgM and IgG antibody tests. The dash line represented the threshold of each test.

The early phase of the COVID-19 outbreak in

Epidemiological and clinical characteristics of 99 cases of 2019 novel coronavirus pneumonia in Wuhan, China: a descriptive study

Characterization of anti-viral immunity in recovered individuals infected by SARS-CoV-2

Chinese Center for Disease Control and Prevention (2020) The epidemiological characteristics of an outbreak of 2019 novel coronavirus diseases (COVID-19) in China

Baseline characteristics and outcomes of 1591 patients infected with SARS-CoV-2 admitted to ICUs of the Lombardy region

The incubation period of coronavirus disease 2019 (COVID-19) from publicly reported confirmed cases: estimation and application

Laboratory diagnosis of emerging human coronavirus infections-the state of the art

The diagnosis and treatment plan of the novel coronavirus-infected pneumonia, 3rd edn National Health Commission of the People's Republic of China (2020b) The prevention and control plan of new coronavirus pneumonia

Association of public health interventions with the epidemiology of the COVID-19 outbreak in Wuhan

Zanos TP (2020) Presenting characteristics, comorbidities, and outcomes among 5700 patients hospitalized with COVID-19 in the New York city area

COVID-19 infection: the perspectives on immune responses. Version 2

Breadth of concomitant immune responses prior to patient recovery: a case report of non-severe COVID-19

Temporal profiles of viral load in posterior oropharyngeal saliva samples and serum antibody responses during infection by SARS-CoV-2: an observational cohort study

World Health Organization (2020) Coronavirus disease 2019 (Covid-19) situation reports

Characteristics of and important lessons from the coronavirus disease 2019 (COVID-19) outbreak in China: summary of a report of 72 314 cases from the Chinese Center for Disease Control and Prevention

Neutralizing antibody responses to SARS-CoV-2 in a COVID-19 recovered patient cohort and their implications

Antibody detection and dynamic characteristics in patients with COVID-19

Molecular and serological investigation of 2019-nCoV infected patients: implication of multiple shedding routes

Antibody responses to SARS-CoV-2 in patients of novel coronavirus disease 2019

Serological diagnostic kit of SARS-CoV-2 antibodies using CHO-expressed full-length SARS-CoV-2 S1 proteins

Acknowledgements The work was supported by the Emergency Scientific Research Project for COVID-19 from Wuhan City (Grant No. 2020020101010008).

Author Contributions WHK and MQL designed the study. WHK, RZ, JBZ, DGK, JS, QR, and MQL collected samples and clinical information and analyzed data. WHK, RZ and MQL analyzed and interpreted the data. WHK and MQL wrote and revised the manuscript. MQL finalized the manuscript. All authors had full access to the final version of the report and agreed to the submission.

Conflict of interest The authors declare that they have no conflict of interest.