# Age-related immune response disparities between adults and children with severe COVID-19: a case–control study in China

**Authors:** Hongliang Chen, Yuan Li, Liping Yuan, Fen Liu, Qian Sun, Qingkai Luo, Yefei Lei, Yinglan Hou, Jiayan Li, Liang Cai, Shixing Tang

PMC · DOI: 10.3389/fmicb.2025.1525051 · 2025-02-04

## TL;DR

This study compares immune responses in adults and children with severe COVID-19 in China, finding significant differences that could inform treatment approaches.

## Contribution

The study identifies age-related disparities in immune responses and cytokine profiles in severe COVID-19 patients using a case–control design with propensity score matching.

## Key findings

- Adults with severe COVID-19 showed lymphocyte exhaustion, elevated NEU/LYM ratio, and cytokine storm markers like IL-6 and TNF-α.
- Children exhibited distinct systemic immune responses compared to adults, suggesting different disease mechanisms.
- Propensity score matching helped mitigate confounding factors, revealing clear immune response disparities between age groups.

## Abstract

Elucidation of immune response differences is critical for uncovering underlying mechanisms and developing potential intervention measures among adults and children with COVID-19.

In this retrospective study, we analyzed serum biochemical markers and cytokine profiles among adults and children with COVID-19 in the First People’s Hospital of Chenzhou in Hunan, China from 1 December 2022 to 13 February 2023. A case–control study was conducted using propensity score matching (PSM) to mitigate possible confounding factors.

The significant differences observed included lymphocyte exhaustion, an increased neutrophil-to-lymphocyte (NEU/LYM) ratio, high levels of C-reactive protein (CRP), and a cytokine storm, characterized by high levels of Th1 proinflammatory cytokines, including interleukin 1β (IL-1β), IL-6, IL-8, interferon type I (IFN-γ), and tumor necrosis factor (TNF-α) in the lung among severe adult COVID-19 patients. Additionally, systemic immune responses were observed in children with COVID-19.

Significant differences in immune responses between adults and children with COVID-19 highlight the different mechanisms and potential intervention measures of COVID-19.

## Linked entities

- **Proteins:** IL1B (interleukin 1 beta), IL6 (interleukin 6), CXCL8 (C-X-C motif chemokine ligand 8), IFNG (interferon gamma), TNF (tumor necrosis factor)
- **Diseases:** COVID-19 (MONDO:0100096)

## Full-text entities

- **Genes:** IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}, CXCL8 (C-X-C motif chemokine ligand 8) [NCBI Gene 3576] {aka GCP-1, GCP1, IL8, LECT, LUCT, LYNAP}, IFNG (interferon gamma) [NCBI Gene 3458] {aka IFG, IFI, IMD69}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, IL1B (interleukin 1 beta) [NCBI Gene 3553] {aka IL-1, IL1-BETA, IL1F2, IL1beta}
- **Diseases:** COVID-19 (MESH:D000086382)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11832681/full.md

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Source: https://tomesphere.com/paper/PMC11832681