1. Humoral profiles of toddlers and young children following SARS-CoV-2 mRNA vaccination
- Author
-
Nadège Nziza, Yixiang Deng, Lianna Wood, Navneet Dhanoa, Naomi Dulit-Greenberg, Tina Chen, Abigail S. Kane, Zoe Swank, Jameson P. Davis, Melina Demokritou, Anagha P. Chitnis, Alessio Fasano, Andrea G. Edlow, Nitya Jain, Bruce H. Horwitz, Ryan P. McNamara, David R. Walt, Douglas A. Lauffenburger, Boris Julg, Wayne G. Shreffler, Galit Alter, and Lael M. Yonker
- Subjects
Science - Abstract
Abstract Although young children generally experience mild symptoms following infection with SARS-CoV-2, severe acute and long-term complications can occur. SARS-CoV-2 mRNA vaccines elicit robust immunoglobulin profiles in children ages 5 years and older, and in adults, corresponding with substantial protection against hospitalizations and severe disease. Whether similar immune responses and humoral protection can be observed in vaccinated infants and young children, who have a developing and vulnerable immune system, remains poorly understood. To study the impact of mRNA vaccination on the humoral immunity of infant, we use a system serology approach to comprehensively profile antibody responses in a cohort of children ages 6 months to 5 years who were vaccinated with the mRNA-1273 COVID-19 vaccine (25 μg). Responses are compared with vaccinated adults (100 μg), in addition to naturally infected toddlers and young children. Despite their lower vaccine dose, vaccinated toddlers elicit a functional antibody response as strong as adults, with higher antibody-dependent phagocytosis compared to adults, without report of side effects. Moreover, mRNA vaccination is associated with a higher IgG3-dependent humoral profile against SARS-CoV-2 compared to natural infection, supporting that mRNA vaccination is effective at eliciting a robust antibody response in toddlers and young children.
- Published
- 2024
- Full Text
- View/download PDF