Abstract

ObjectivesThis study aimed to determine the IgM and IgG responses against severe acute respiratory syndrome coronavirus (SARS‐CoV)‐2 in coronavirus disease 2019 (COVID‐19) patients with varying illness severities.MethodsIgM and IgG antibody levels were assessed via chemiluminescence immunoassay in 338 COVID‐19 patients.ResultsIgM levels increased during the first week after SARS‐CoV‐2 infection, peaked 2 weeks and then reduced to near‐background levels in most patients. IgG was detectable after 1 week and was maintained at a high level for a long period. The positive rates of IgM and/or IgG antibody detections were not significantly different among the mild, severe and critical disease groups. Severe and critical cases had higher IgM levels than mild cases, whereas the IgG level in critical cases was lower than those in both mild and severe cases. This might be because of the high disease activity and/or a compromised immune response in critical cases. The IgM antibody levels were slightly higher in deceased patients than recovered patients, but IgG levels in these groups did not significantly differ. A longitudinal detection of antibodies revealed that IgM levels decreased rapidly in recovered patients, whereas in deceased cases, either IgM levels remained high or both IgM and IgG were undetectable during the disease course.ConclusionQuantitative detection of IgM and IgG antibodies against SARS‐CoV‐2 quantitatively has potential significance for evaluating the severity and prognosis of COVID‐19.

Highlights

  • The novel coronavirus, severe acute respiratory syndrome coronavirus (SARS-CoV)-2, has been identified as the causative pathogen of coronavirus disease 2019 (COVID-19).[1,2,3,4] This disease has been called a public health emergency of international concern by the World Health Organization (WHO)

  • Clinical & Translational Immunology published by John Wiley & Sons Australia, Ltd on behalf of Australian and New Zealand Society for Immunology Inc

  • Similar serological responses have been observed in COVID-19 patients, and the dynamic pattern of these responses is consistent with acute viral infection.[14]

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Summary

Introduction

The novel coronavirus, severe acute respiratory syndrome coronavirus (SARS-CoV)-2, has been identified as the causative pathogen of coronavirus disease 2019 (COVID-19).[1,2,3,4] This disease has been called a public health emergency of international concern by the World Health Organization (WHO). Since December 2019, a serious outbreak of the disease has spread via human-to-human transmission from China to more than 200 countries and territories worldwide.[5,6] The numbers of infected cases and deaths associated with COVID-19 are still a 2020 The Authors. Clinical & Translational Immunology published by John Wiley & Sons Australia, Ltd on behalf of Australian and New Zealand Society for Immunology Inc. Detection of antibodies to SARS-CoV-2 increasing daily. As of 6 April 2020, SARS-CoV-2 has caused 1 210 956 confirmed cases and 67 594 deaths worldwide according to the WHO.[6]

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