Monovalent SARS-CoV-2 mRNA Vaccine Does not Boost Omicron-Specific Immune Response in Diabetic and Control Pediatric Patients

Author:

Sariol Alan1,Vickers Molly A1,Christensen Shannon M2,Weiskopf Daniela3,Sette Alessandro3,Norris Andrew W24,Tansey Michael J24,Pinnaro Catherina T24,Perlman Stanley1ORCID

Affiliation:

1. Department of Microbiology and Immunology, University of Iowa , Iowa City, Iowa , USA

2. Department of Pediatrics-Endocrinology and Diabetes, University of Iowa , Iowa City, Iowa , USA

3. Center for Infectious Disease and Vaccine Research, La Jolla Institute for Immunology , La Jolla, California , USA

4. Fraternal Order of Eagles Diabetes Research Center, University of Iowa , Iowa City, Iowa , USA

Abstract

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.

Funder

National Institutes of Health

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Immunology and Allergy

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