Back to Search
Start Over
Quantitative Antibody Levels Against SARS-CoV-2 Spike Protein in COVID-19 and Multisystem Inflammatory Syndrome in Children
- Source :
- Viral Immunology. 35:681-689
- Publication Year :
- 2022
- Publisher :
- Mary Ann Liebert Inc, 2022.
-
Abstract
- The majority of children with coronavirus diseases 2019 (COVID-19) are asymptomatic or develop mild symptoms, and a small number of patients require hospitalization. Multisystem inflammatory syndrome in children (MIS-C) is one of the most severe clinical courses of COVID-19 and is suggested to be a hyperinflammatory condition. This study aimed to compare quantitative antibody levels against SARS-CoV-2 spike protein in children with COVID-19 and MIS-C. Blood samples from 75 patients [n?=?36 (48%) with mild/asymptomatic (group 1), n?=?22 (29.3%) with moderate-to-severe SARS-CoV-2 infection (group 2) and n?=?17 (22.6%) patients with MIS-C (group 3)] were analyzed 3 months after COVID-19. The majority of the children with asymptomatic/mild COVID-19 symptoms (80.6%), moderate/severe disease (90.9%), and MIS-C (82.4%) had detectable IgG antibodies to SARS-CoV-2 spike protein (p?=?0.567). The mean antibody value against SARS-CoV-2 spike protein was 321.9?±?411.6 in group 1, 274?±?261 in group 2, and 220?±?299 in group 3, respectively (p?>?0.05). Patients diagnosed with COVID-19 (asymptomatic/mild+moderate/severe) and those with MIS-C were also compared; the antibody positivity rates [COVID-19 group: 85.5%, MIS-C group: 82.4%, (p?=?0.833)] and mean antibody values [COVID-19 group: 303.9?±?360.3, MIS-C group: 220?±?299, (p?>?0.05)] were similar in both groups. In conclusion, the majority of children with COVID-19 and MIS-C developed a detectable antibody level against SARS-CoV-2 spike protein 3 months after COVID-19. Quantitative antibody levels were similar in both asymptomatic/mild disease, moderate/severe disease, and MIS-C group. Long-term studies evaluating antibody responses in children with COVID-19 and MIS-C are needed for more accurate vaccine schedules.
Details
- ISSN :
- 15578976 and 08828245
- Volume :
- 35
- Database :
- OpenAIRE
- Journal :
- Viral Immunology
- Accession number :
- edsair.doi.dedup.....0b1a7d56f514a46edf679046c9100dd9
- Full Text :
- https://doi.org/10.1089/vim.2022.0089