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Updated: Jul 15, 2025

Noninvasive Sampling of Mucosal Lining Fluid for the Quantification of In Vivo Upper Airway Immune-mediator Levels
Published on: August 7, 2017
Multi-omics analysis of mucosal and systemic immunity to SARS-CoV-2 after birth
Florian Wimmers1, Allison R Burrell2, Yupeng Feng3
1Department of Molecular Medicine, Interfaculty Institute for Biochemistry, University of Tuebingen, 72076 Tuebingen, Baden-Wuerttemberg, Germany; DFG Cluster of Excellence 2180 "Image-guided and Functional Instructed Tumor Therapy" (iFIT), University of Tuebingen, 72076 Tuebingen, Baden-Wuerttemberg, Germany; German Consortium for Translational Cancer Research (DKTK), German Cancer Research Center (DKFZ), 69120 Heidelberg, Baden-Wuerttemberg, Germany.
Insights
Infants develop lasting immunity to SARS-CoV-2, unlike adults. Their robust mucosal and blood immune responses, including high antibody titers, persist for at least 300 days post-infection.
Area of Science:
- Immunology
- Virology
- Pediatrics
Background:
- Infant immunity to severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is not well understood.
- Understanding infant immune responses is crucial for public health strategies.
Purpose of the Study:
- To longitudinally analyze the dynamics of SARS-CoV-2 immunity in infants and young children.
- To compare immune responses to Omicron and non-Omicron variants in this age group.
Main Methods:
- Multi-omics analysis of blood and nasal swabs from infants before, during, and after SARS-CoV-2 infection.
- Longitudinal sampling over up to 300 days.
- Single-cell multi-omics to analyze gene expression in myeloid cells.
Main Results:
- Infants exhibited robust and durable antibody titers, with no decay observed up to 300 days.
- A strong mucosal immune response was characterized by inflammatory cytokines, interferon (IFN) α, and T helper (Th) 17 and neutrophil markers (interleukin [IL]-17, IL-8, and CXCL1).
- Blood immune responses showed innate cell activation, chemokines, and IFNα, correlating with viral load and interferon-stimulated genes (ISGs).
Conclusions:
- Infants mount a unique and durable immune response to SARS-CoV-2 infection.
- The findings provide insights into early-life immunity dynamics following viral infections.
- This study offers a snapshot of infant immunity during the initial weeks and months of life.
Abstract:
The dynamics of immunity to infection in infants remain obscure. Here, we used a multi-omics approach to perform a longitudinal analysis of immunity to severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) in infants and young children by analyzing blood samples and weekly nasal swabs collected before, during, and after infection with Omicron and non-Omicron variants. Infection stimulated robust antibody titers that, unlike in adults, showed no sign of decay for up to 300 days. Infants mounted a robust mucosal immune response characterized by inflammatory cytokines, interferon (IFN) α, and T helper (Th) 17 and neutrophil markers (interleukin [IL]-17, IL-8, and CXCL1). The immune response in blood was characterized by upregulation of activation markers on innate cells, no inflammatory cytokines, but several chemokines and IFNα. The latter correlated with viral load and expression of interferon-stimulated genes (ISGs) in myeloid cells measured by single-cell multi-omics. Together, these data provide a snapshot of immunity to infection during the initial weeks and months of life.
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