Abstract

The virological meaning of the different patterns of serology in COVID-19 has been little examined in clinical settings. Asymptomatic subjects with IgM-spike (S) and IgG-nucleocapsid (N) determinations by chemiluminescence were studied for SARS-CoV-2 shedding in respiratory secretions by transcription-mediated amplification (TMA). In subjects showing IgM-S positive and IgG-N negative, IgG-S was determined by lateral flow assay. A total of 712 individuals were tested: 30.0% presented IgM-S(+)/IgG-N(−), 25.8% had IgM-S(+)/IgG-N(+) and 44.2% had IgM-S(−)/IgG-N(+); the proportion with TMA(+) were comparable in these three groups: 12.1, 8.7 and 10.5%, respectively. In individuals with IgM-S(+)/IgG-N(−), IgG-S(+) was detected in 66.5%. The frequency of IgM-S(+)/IgG-S(−) in the total population was 10.0%, of whom 24.1% had TMA(+); the chances for TMA(+) in subjects with an IgM-S(+) alone pattern were 2.4%. Targeting of the same SARS-CoV-2 antigen seems to be better for the characterization of IgM/IgG patterns of response. IgM-S(+) alone reactivity is rare, and a small proportion is associated with viral shedding.

Highlights

  • Direct diagnosis of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is today based on antigen and molecular tests [1]

  • Serology tests for viral infections mostly inform of past or chronic infection, detection of IgM reactivity with negative IgG sets an indication to discard active infection [10,11]

  • Our analyses have shown that the chances of detecting SARS-CoV-2 shedding are low (12%) in individuals with an IgM positive alone response

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Summary

Introduction

Direct diagnosis of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is today based on antigen and molecular tests [1]. Serological studies may help with indicating or monitoring the efficacy of a SARS-CoV-2 vaccine [9]. The IgM and IgG responses have been used to determine the different phases of viral infections, namely acute, convalescent or chronic. The SARS-CoV-2 nucleocapsid (N) and spike (S) proteins have different kinetics, as anti-N antibodies decline earlier than anti-S [14,15,16,17]. Little is known about the correlation between the kinetics of IgM and IgG and SARS-CoV-2 shedding in respiratory secretions. We have evaluated the virological correlates, as the presence of SARS-CoV-2 RNA in nasal and pharyngeal swabs, in patients with the three possible IgM and IgG patterns

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