Loading…

Serologic responses to COVID-19 vaccination in children with history of multisystem inflammatory syndrome (MIS-C)

Understanding the serological responses to COVID-19 vaccination in children with history of MIS-C could inform vaccination recommendations. We prospectively enrolled seven children hospitalized with MIS-C and measured SARS-CoV-2 binding IgG antibodies to spike protein variants longitudinally pre- an...

Full description

Saved in:
Bibliographic Details
Published in:Vaccine 2023-04, Vol.41 (17), p.2743-2748
Main Authors: Perez, Maria A., Hsiao, Hui-Mien, Chen, Xuemin, Kunkel, Amber, Baida, Nadine, Hussaini, Laila, Lu, Austin T., Kao, Carol M., Laham, Federico R., Hunstad, David A., Beltran, Yajira, Hammett, Teresa A., Godfred-Cato, Shana, Chahroudi, Ann, Anderson, Evan J., Belay, Ermias, Rostad, Christina A.
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:Understanding the serological responses to COVID-19 vaccination in children with history of MIS-C could inform vaccination recommendations. We prospectively enrolled seven children hospitalized with MIS-C and measured SARS-CoV-2 binding IgG antibodies to spike protein variants longitudinally pre- and post-Pfizer-BioNTech BNT162b2 primary series COVID-19 vaccination. We found that SARS-CoV-2 variant cross-reactive IgG antibodies variably waned following acute MIS-C, but were significantly boosted with vaccination and maintained for up to 3 months. We then compared post-vaccination binding, pseudovirus neutralizing, and functional antibody-dependent cell-mediated cytotoxicity (ADCC) titers to the reference strain (Wuhan-hu-1) and Omicron variant (B.1.1.529) among previously healthy children (n = 16) and children with history of MIS-C (n = 7) or COVID-19 (n = 8). Despite the breadth of binding antibodies elicited by vaccination in all three groups, pseudovirus neutralizing and ADCC titers were significantly reduced to the Omicron variant.
ISSN:0264-410X
1873-2518
DOI:10.1016/j.vaccine.2023.03.021