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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 5

SARS-CoV-2–specific CD4+ T cell cytokine secretion in children.

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SARS-CoV-2–specific CD4+ T cell cytokine secretion in children.
(A) Spik...
(A) Spike- and non-spike-specific CD4+ T cell secreted cytokine responses. In the uninfected group, blue circles represent pediatric samples, and white circles represent adult samples. (B) Paired spike- and non-spike-specific IFN-γ secretion; children n: Un = 6, Acute = 24, 2m = 24; adults n: Un = 6, Acute = 6, 2m = 6. (C) Correlation between secreted cytokine measured by cytokine bead array and the frequency of TH subset determined by hybrid AIM assay. Indicated populations shown as percentage of OX40+CD40L+CD4+ for children and adults in aggregate. Solid black line in A and B indicates the lower LOD; dashed black line indicates the LOQ; dashed red line indicates the median of all DMSO-negative controls. Uninfected participants are indicated as Un; 2-month and 6-month time points as 2m and 6m. AIM+ in C denotes the frequencies of OX40+CD40L+ cells as percentage of CD4+ T cells. P values for A were calculated by Kruskal-Wallis test with Dunn’s correction, and for B by Wilcoxon’s test with Holm-Šídák correction and are indicated as *P < 0.05, **P < 0.01, ***P < 0.001, ****P < 0.0001. r in C indicates Spearman correlation coefficient.

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