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Investigating the Seroconversion Patterns of Specific Antibodies Against Various Antigens of Sars-Cov-2 in Hospitalized Covid-19 Patients and Vaccinated Individuals Publisher



Matinfar S1 ; Mortezagholi S2 ; Amiri D1 ; Pashaiefar H3 ; Eskandarian M1 ; Ghadimi S4 ; Nazari MF4 ; Tavakoli S4 ; Valizadeh M4 ; Namaki S2 ; Tabarsi P4 ; Boutrabi M1 ; Shabani M2
Authors
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Authors Affiliations
  1. 1. Synapse IVD Accelerator, Tehran, Iran
  2. 2. Department of Immunology, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran
  3. 3. Hematology, Oncology and Stem Cell Transplantation Research Center, Tehran University of Medical Sciences, Tehran, Iran
  4. 4. Clinical Tuberculosis and Epidemiology Research Center, National Research Institute of Tuberculosis and Lung Diseases, Shahid Beheshti University of Medical Sciences, Tehran, Iran

Source: Archives of Clinical Infectious Diseases Published:2024


Abstract

Background: Inducing a humoral response to SARS-CoV-2 may partially control virus dissemination. However, there is a lack of consistency in the reported kinetics of IgM and IgG responses to SARS-CoV-2. Additionally, the humoral response to SARS-CoV-2 may differ from that elicited by vaccination. Therefore, we were motivated to evaluate the kinetics of antibodies against SARS-CoV-2 in both infected and vaccinated individuals. Objectives: This study aimed to investigate the seroconversion patterns of specific antibodies against various antigens of SARS-CoV-2 in hospitalized COVID-19 patients and vaccinated individuals, focusing specifically on comparing the humoral responses elicited by infection and vaccination. Methods: Serial blood and swab samples were collected from 134 COVID-19 patients at six time points following admission. Real-time RT-PCR specific for SARS-CoV-2, as well as anti-SARS-CoV-2 IgM and IgG, were tested using ELISA. Additionally, 141 serum samples were obtained from vaccinated individuals. Anti-SARS-CoV-2 spike and RBD IgGs, along with neutralizing antibodies (NAs), were assessed using ELISA in both the vaccinated group and 96 COVID-19 patients. Results: Anti-SARS-CoV-2 IgM was found positive in 23.3% of patients at 0-7 days after symptom onset, with seropositivity increasing to 71.7% at 15-21 days. Subsequently, IgM positivity gradually decreased to 62.7% at > 28 days post-symptom onset. Meanwhile, anti-SARS-CoV-2 IgG was positive in 28.3% of patients at 0-7 days, rising to 83.7% at 22-28 days after symptom onset, and remained constant thereafter. Anti-spike and RBD IgGs, along with NAs, were detected in 89.7%, 87.4%, and 87.9% of vaccinated individuals, respectively, and in 37.5%, 32.3%, and 32.3% of COVID-19 patients, respectively. There was a significant correlation between anti-spike IgG and anti-RBD IgG levels and NAs in both COVID-19-infected and vaccinated individuals. The mean concentrations of anti-spike and RBD IgGs were higher in vaccinated individuals with a history of COVID-19 infection compared to those without prior infection. Conclusions: The antibody profile for IgM and IgG against SARS-CoV-2 suggests that as time passes after the onset of disease symptoms, the seropositivity in COVID-19 patients increases. Furthermore, antibodies against SARS-CoV-2 are produced more efficiently through COVID-19 vaccination than natural infection. © 2024, Matinfar et al.