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.

Nziza et al. profile anti-SARS-CoV-2 antibody responses in infants and toddlers after mRNA vaccination and demonstrate a strong functional activation of humoral immunity in this age group when compared with adults and naturally infected children.

Details

Title
Humoral profiles of toddlers and young children following SARS-CoV-2 mRNA vaccination
Author
Nziza, Nadège 1 ; Deng, Yixiang 2 ; Wood, Lianna 3   VIAFID ORCID Logo  ; Dhanoa, Navneet 4   VIAFID ORCID Logo  ; Dulit-Greenberg, Naomi 4 ; Chen, Tina 1   VIAFID ORCID Logo  ; Kane, Abigail S. 5 ; Swank, Zoe 6 ; Davis, Jameson P. 7   VIAFID ORCID Logo  ; Demokritou, Melina 4 ; Chitnis, Anagha P. 7 ; Fasano, Alessio 8   VIAFID ORCID Logo  ; Edlow, Andrea G. 9   VIAFID ORCID Logo  ; Jain, Nitya 8 ; Horwitz, Bruce H. 10   VIAFID ORCID Logo  ; McNamara, Ryan P. 1 ; Walt, David R. 6   VIAFID ORCID Logo  ; Lauffenburger, Douglas A. 11   VIAFID ORCID Logo  ; Julg, Boris 12   VIAFID ORCID Logo  ; Shreffler, Wayne G. 13   VIAFID ORCID Logo  ; Alter, Galit 12 ; Yonker, Lael M. 8   VIAFID ORCID Logo 

 Ragon Institute of MGH, MIT, and Harvard, Cambridge, USA (GRID:grid.461656.6) (ISNI:0000 0004 0489 3491) 
 Ragon Institute of MGH, MIT, and Harvard, Cambridge, USA (GRID:grid.461656.6) (ISNI:0000 0004 0489 3491); Massachusetts Institute of Technology, Department of Biological Engineering, Cambridge, USA (GRID:grid.116068.8) (ISNI:0000 0001 2341 2786) 
 Ragon Institute of MGH, MIT, and Harvard, Cambridge, USA (GRID:grid.461656.6) (ISNI:0000 0004 0489 3491); Boston Children’s Hospital, Department of Pediatric Gastroenterology, Boston, USA (GRID:grid.2515.3) (ISNI:0000 0004 0378 8438) 
 Massachusetts General Hospital, Department of Pediatrics, Boston, USA (GRID:grid.32224.35) (ISNI:0000 0004 0386 9924) 
 Massachusetts General Hospital, Department of Pediatrics, Boston, USA (GRID:grid.32224.35) (ISNI:0000 0004 0386 9924); Massachusetts General Hospital, Mucosal Immunology and Biology Research Center, Boston, USA (GRID:grid.32224.35) (ISNI:0000 0004 0386 9924) 
 Harvard Medical School, Boston, USA (GRID:grid.38142.3c) (ISNI:000000041936754X); Brigham and Women’s Hospital, Department of Pathology, Boston, USA (GRID:grid.62560.37) (ISNI:0000 0004 0378 8294) 
 Massachusetts General Hospital, Mucosal Immunology and Biology Research Center, Boston, USA (GRID:grid.32224.35) (ISNI:0000 0004 0386 9924) 
 Massachusetts General Hospital, Department of Pediatrics, Boston, USA (GRID:grid.32224.35) (ISNI:0000 0004 0386 9924); Massachusetts General Hospital, Mucosal Immunology and Biology Research Center, Boston, USA (GRID:grid.32224.35) (ISNI:0000 0004 0386 9924); Harvard Medical School, Boston, USA (GRID:grid.38142.3c) (ISNI:000000041936754X) 
 Harvard Medical School, Boston, USA (GRID:grid.38142.3c) (ISNI:000000041936754X); Massachusetts General Hospital, Department of Obstetrics and Gynecology, Division of Maternal-Fetal Medicine, Boston, USA (GRID:grid.32224.35) (ISNI:0000 0004 0386 9924); Massachusetts General Hospital, Vincent Center for Reproductive Biology, Boston, USA (GRID:grid.32224.35) (ISNI:0000 0004 0386 9924) 
10  Harvard Medical School, Boston, USA (GRID:grid.38142.3c) (ISNI:000000041936754X); Boston Children’s Hospital, Department of Emergency Medicine, Boston, USA (GRID:grid.2515.3) (ISNI:0000 0004 0378 8438) 
11  Massachusetts Institute of Technology, Department of Biological Engineering, Cambridge, USA (GRID:grid.116068.8) (ISNI:0000 0001 2341 2786) 
12  Ragon Institute of MGH, MIT, and Harvard, Cambridge, USA (GRID:grid.461656.6) (ISNI:0000 0004 0489 3491); Harvard Medical School, Boston, USA (GRID:grid.38142.3c) (ISNI:000000041936754X) 
13  Massachusetts General Hospital, Department of Pediatrics, Boston, USA (GRID:grid.32224.35) (ISNI:0000 0004 0386 9924); Harvard Medical School, Boston, USA (GRID:grid.38142.3c) (ISNI:000000041936754X) 
Pages
905
Publication year
2024
Publication date
2024
Publisher
Nature Publishing Group
e-ISSN
20411723
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
2919970917
Copyright
© The Author(s) 2024. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.