Coronavirus disease 2019 (COVID-19) has rapidly evolved into a global pandemic. A total of 1578 patients admitted into a newly built hospital specialized for
COVID-19 treatment in Wuhan, China, were enrolled. Clinical features and the levels of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2)
immunoglobulin (Ig)M and
IgG were analyzed. In total, 1532 patients (97.2%) were identified as laboratory-confirmed cases. Seventy-seven patients were identified as asymptomatic carriers (n = 64) or SARS-CoV-2
RNA positive before symptom onset (n = 13). The positive rates of SARS-CoV-2
IgM and
IgG were 80.4% and 96.8%, respectively. The median of
IgM and
IgG titers were 37.0A U/ml (interquartile range [IQR]: 13.4-81.1 AU/ml) and 156.9 AU/ml (IQR: 102.8-183.3 AU/ml), respectively. The
IgM and
IgG levels of asymptomatic patients (median titers, 8.3 AU/ml and 100.3 AU/ml) were much lower than those in symptomatic patients (median titers, 38.0 AU/ml and 158.2 AU/ml). A much lower
IgG level was observed in
critically ill patients 42-60 days after symptom onset. There were 153 patients with
viral RNA shedding after
IgG detection. These patients had a higher proportion of
critical illness during hospitalization (p < .001) and a longer
hospital stay (p < .001) compared to patients with viral clearance after
IgG detection.
Coronary heart disease (odds ratio [OR], 1.89 [95% confidence interval [CI], 1.11-3.24]; p = .020), and
intensive care unit admission (OR, 2.47 [95% CI, 1.31-4.66]; p = .005) were independent risk factors associated with
viral RNA shedding after
IgG detection. Symptomatic patients produced more
antibodies than asymptomatic patients. The patients who had SARS-CoV-2
RNA shedding after developing
IgG were more likely to be sicker patients.