Abstract

Numerous studies have suggested that the titers of antibodies against SARS-CoV-2 are associated with the COVID-19 severity, however, the types of antibodies associated with the disease maximum severity and the timing at which the associations are best observed, especially within one week after symptom onset, remain controversial. We attempted to elucidate the antibody responses against SARS-CoV-2 that are associated with the maximum severity of COVID-19 in the early phase of the disease, and to investigate whether antibody testing might contribute to prediction of the disease maximum severity in COVID-19 patients. We classified the patients into four groups according to the disease maximum severity (severity group 1 (did not require oxygen supplementation), severity group 2a (required oxygen supplementation at low flow rates), severity group 2b (required oxygen supplementation at relatively high flow rates), and severity group 3 (required mechanical ventilatory support)), and serially measured the titers of IgM, IgG, and IgA against the nucleocapsid protein, spike protein, and receptor-binding domain of SARS-CoV-2 until day 12 after symptom onset. The titers of all the measured antibody responses were higher in severity group 2b and 3, especially severity group 2b, as early as at one week after symptom onset. Addition of data obtained from antibody testing improved the ability of analysis models constructed using a machine learning technique to distinguish severity group 2b and 3 from severity group 1 and 2a. These models constructed with non-vaccinated COVID-19 patients could not be applied to the cases of breakthrough infections. These results suggest that antibody testing might help physicians identify non-vaccinated COVID-19 patients who are likely to require admission to an intensive care unit.

Highlights

  • Coronavirus disease 2019 (COVID-19), caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), exhibits a wide clinical spectrum, ranging from an asymptomatic state to severe disease requiring mechanical respiratory support

  • In regard to the kinetics of IgG, the titers of IgG(S1) and IgG(RBD) increased in a bell-shaped manner depending on the disease maximum severity from day 3 to day 6; the IgG(S1) and IgG (RBD) titers appeared to increase earlier in severity group 2b than in severity groups 1, 2a, and 3, while the time-course of increase of the IgG(N) titers appeared to be similar between severity groups 2b and 3 (Figures 2D–F)

  • In regard to the kinetics of IgA, the titers of IgA increased with increasing maximum severity of COVID-19, especially from day 3 to day 6, and no differences were observed in the pattern of increase of IgA(N), IgA(S1) and IgA(RBD) among the severity group (Figures 2G–I)

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Summary

Introduction

Coronavirus disease 2019 (COVID-19), caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), exhibits a wide clinical spectrum, ranging from an asymptomatic state to severe disease requiring mechanical respiratory support. Several demographic characteristics and clinical features, including laboratory data, have been reported to be associated with the severity of COVID-19, including male sex, advanced age, underlying hypertension, diabetes, and cardiovascular disease, positive smoking history [1, 2], and serum CRP and D-Dimer levels [3, 4]. In addition to the aforementioned parameters, the titers of antibodies against SARS-CoV-2 have been reported by several studies to be associated with the disease severity in COVID-19 patients. In general, studies have reported positive associations between SARS-CoV-2 antibody titers and the clinical disease severity and/or laboratory data such as the serum CRP, a few studies have denied the existence of a positive association between the antibody titers and the severity of COVID-19 [5,6,7]. Various antigens eliciting the antibody responses have been demonstrated to be associated with the disease severity, including antibodies elicited against the spike (S) protein and/or receptor-binding domain (RBD) in the S protein [12, 16, 19, 22, 29, 30, 32, 36], antibodies elicited against the nucleocapsid (N) protein [10, 11, 13, 23, 32, 33, 36], and antibodies against both the S and N proteins [14, 24]

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