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Monovalent SARS-CoV-2 mRNA Vaccine Does not Boost Omicron-Specific Immune Response in Diabetic and Control Pediatric
Alan Sariol1, Molly A Vickers1, Shannon M Christensen2
1Department of Microbiology and Immunology, University of Iowa, Iowa City, Iowa, USA.
Insights
Children with type 1 diabetes (T1D) mount robust immune responses to COVID-19 vaccines, comparable to healthy peers. However, a booster dose unexpectedly failed to significantly increase neutralizing antibodies against Omicron variants in T1D children.
Area of Science:
- Immunology
- Pediatrics
- Endocrinology
Background:
- Limited data exists on SARS-CoV-2 vaccine immunogenicity in pediatric populations, especially those with type 1 diabetes (T1D).
- Children with T1D are at higher risk for severe infections, underscoring the need to understand their vaccine responses.
Purpose of the Study:
- To investigate the immunogenicity of COVID-19 mRNA vaccines in children with T1D compared to non-diabetic controls.
- To assess the impact of a third vaccine dose on antibody and T cell responses against SARS-CoV-2 variants.
Main Methods:
- Comparative study of 35 children with T1D and 23 controls receiving COVID-19 mRNA vaccines.
- Measurement of SARS-CoV-2 neutralizing antibody titers and spike protein-specific T cell responses.
- Analysis of responses after primary vaccination series and after a third booster dose.
Main Results:
- Children with T1D exhibited comparable neutralizing antibody titers and T cell responses to controls after initial vaccination.
- A third booster dose increased neutralizing antibody titers against ancestral SARS-CoV-2 strains.
- Unexpectedly, the booster dose did not significantly enhance neutralizing antibody titers against Omicron variants in T1D children, unlike in adults.
Conclusions:
- COVID-19 mRNA vaccines elicit comparable immune responses in children with T1D and healthy children.
- Booster doses are effective against ancestral strains but show limited enhancement against Omicron variants in T1D pediatric populations.
- Further research is needed to optimize vaccination strategies for children with T1D against emerging SARS-CoV-2 variants.
Abstract:
While the immunogenicity of SARS-CoV-2 vaccines has been well described in adults, pediatric populations have been less studied. In particular, children with type 1 diabetes are generally at elevated risk for more severe disease after infections, but are understudied in terms of COVID-19 and SARS-CoV-2 vaccine responses. We investigated the immunogenicity of COVID-19 mRNA vaccinations in 35 children with type 1 diabetes (T1D) and 23 controls and found that these children develop levels of SARS-CoV-2 neutralizing antibody titers and spike protein-specific T cells comparable to nondiabetic children. However, in comparing the neutralizing antibody responses in children who received 2 doses of mRNA vaccines (24 T1D; 14 controls) with those who received a third, booster dose (11 T1D; 9 controls), we found that the booster dose increased neutralizing antibody titers against ancestral SARS-CoV-2 strains but, unexpectedly, not Omicron lineage variants. In contrast, boosting enhanced Omicron variant neutralizing antibody titers in adults.
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