Abstract

The CovILD study is a prospective, multicenter, observational cohort study to systematically follow up patients after coronavirus disease-2019 (COVID-19). We extensively evaluated 145 COVID-19 patients at 3 follow-up visits scheduled for 60, 100, and 180 days after initial confirmed diagnosis based on typical symptoms and a positive reverse transcription-polymerase chain reaction (RT-PCR) for severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2). We employed comprehensive pulmonary function and laboratory tests, including serum concentrations of IgG against the viral spike (S) glycoprotein, and compared the results to clinical data and chest computed tomography (CT). We found that at the 60 day follow-up, 131 of 145 (90.3%) participants displayed S-specific serum IgG levels above the cut-off threshold. Notably, the highly elevated IgG levels against S glycoprotein positively correlated with biomarkers of immune activation and negatively correlated with pulmonary function and the extent of pulmonary CT abnormalities. Based on the association between serum S glycoprotein-specific IgG and clinical outcome, we generated an S-specific IgG-based recovery score that, when applied in the early convalescent phase, accurately predicted delayed pulmonary recovery after COVID-19. Therefore, we propose that S-specific IgG levels serve as a useful immunological surrogate marker for identifying at-risk individuals with persistent pulmonary injury who may require intensive follow-up care after COVID-19.

Highlights

  • The CovILD study is a prospective, multicenter, observational cohort study to systematically follow up patients after coronavirus disease-2019 (COVID-19)

  • We found that patients with impaired lung function, including measurements of forced expiratory volume in 1 s (FEV1; cut-off 80% of the calculated normal value), forced vital capacity (FVC; cut-off 80% of normal), FEV1/FVC or total lung capacity (TLC; cut-off 80% of normal), as well as a reduction of the diffusion capacity for carbon monoxide (DLCO) below normal levels and hypoxia, were related to increased S-specific IgG levels at the 60-day follow-up (Fig. 4)

  • SARS-CoV-2 causes a spectrum of manifestations that range from subclinical to severe and life-threatening infections

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Summary

Introduction

The CovILD study is a prospective, multicenter, observational cohort study to systematically follow up patients after coronavirus disease-2019 (COVID-19). Host–pathogen interplay occurring in the acute phase of SARS-CoV-2 infection is a major dictating factor in the disease course of COVID-19 This interplay is shaped by local and systemic immune responses against SARS-CoV-2, the spreading of virus in the respiratory tract, and by immune- and pathogen-mediated effects on pulmonary and other systems of the host o­ rganism[4,5]. Whereas pathogen-specific T cell responses are laborious to assess in a routine diagnostic setting, B cell-mediated immunity can be more tracked by the quantitative measurement of antibody ­levels[12]. Found a p­ ositive[17,32–34] or unclear ­association[35] between serum concentrations of IgG antibodies against SARS-CoV-2 and COVID-19 disease severity. The effects of SARS-CoV-2-specific IgG concentrations on the clinical course of COVID-19 remain controversial

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