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Pediatric T cell and B cell responses to SARS-CoV-2 infection
L. Benjamin Hills, … , Matthew S. Kelly, Shane Crotty
L. Benjamin Hills, … , Matthew S. Kelly, Shane Crotty
Published September 4, 2025
Citation Information: JCI Insight. 2025;10(20):e196032. https://doi.org/10.1172/jci.insight.196032.
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Clinical Research and Public Health Clinical Research Immunology Infectious disease

Pediatric T cell and B cell responses to SARS-CoV-2 infection

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Abstract

BACKGROUND Understanding age-associated differences in acute and memory adaptive immunity to SARS-CoV-2 and how they contribute to more favorable outcomes in children is critically important.METHODS We evaluated SARS-CoV-2–specific T cell, B cell, and antibody responses in 329 peripheral blood samples collected from nonhospitalized children, adolescents, and adults at 3 time points, including acute and memory time points.RESULTS Most children produced robust CD4+ T cell responses during infection and developed memory CD4+ T cells; however, young children less than 4 years old often had undetectable CD4+ T cell responses compared with older children and adults. Young children also generated reduced frequencies of memory B cells; despite this, they mounted substantial and durable neutralizing antibody responses. CD4+ T cell responses in children were biased toward non-spike epitopes, especially in asymptomatic cases. Memory B cells in children were preferentially classical memory or, paradoxically, CXCR3+.CONCLUSION These findings support the concept that the kinetics and composition of T and B cell responses shift across age groups and may be associated with milder COVID-19 outcomes in children.FUNDING NIH National Institute of Allergy and Infectious Diseases (NIAID) award AI142742, the Duke University School of Medicine, and grants from the Children’s Miracle Network Hospitals, the Translating Duke Health Children’s Health and Discovery Initiative, the NIH NIAID (R01-AI161008-02), and the Defense Advanced Research Projects Agency N66001-09-C-2082. NIH Career Development Awards (K23-AI135090 and K01-AI173398). NIH contract 75N93019C00065.

Authors

L. Benjamin Hills, Numana Bhat, Jillian H. Hurst, Amber Myers, Thomas W. Burke, Micah T. McClain, Elizabeth Petzold, Alexandre T. Rotta, Nicholas A. Turner, Alba Grifoni, Daniela Weiskopf, Yvonne Dogariu, Genevieve G. Fouda, Sallie R. Permar, Alessandro Sette, Christopher W. Woods, Matthew S. Kelly, Shane Crotty

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Figure 7

Antigen-specific B cell memory to SARS-CoV-2 infection in children and adults.

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Antigen-specific B cell memory to SARS-CoV-2 infection in children and a...
(A) Representative flow cytometry plots showing spike (left), RBD (middle), and nucleocapsid (right) probe binding BMem in children (n = 50) and adults (n = 12) at 6 months postinfection. (B) Frequencies of spike (left), RBD (middle), and nucleocapsid-binding (right) BMem shown as percentages of total B cells (CD19+CD20+). (C) Correlations of spike (left) and RBD-binding (right) BMem frequencies with age, in children (blue) and adults (black). (D) Relative frequencies of IgG, IgM, IgA, and other isotypes of BMem indicated as percentage of spike (left), nucleocapsid (middle), and total (right) BMem. Center lines in B represent the GeoMean. Center lines and error bars in D represent the mean ± SD. P values for B were calculated by Mann-Whitney test and for D by Mann-Whitney test with Holm-Šídák correction, indicated as *P < 0.05, **P < 0.01. r in C indicates Spearman correlation coefficient; r values in black indicate Spearman correlation coefficient for the combined pediatric and adult data; r values in blue indicate Spearman correlation coefficient for the pediatric data alone.

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