# The diagnostic and immunomodulatory role of IL-37 in pediatric sepsis

**Authors:** Jin Ma, Yanling Zhang, Changrui Sun, Hao Yang, Zhixin Song, Feiqi Huang, Chunxiang Wu

PMC · DOI: 10.3389/fimmu.2026.1765956 · Frontiers in Immunology · 2026-02-12

## TL;DR

This study shows that IL-37 is elevated in children with sepsis and may help diagnose and treat the condition by reducing inflammation and altering immune cells.

## Contribution

The study identifies IL-37 as a potential diagnostic biomarker and therapeutic target for pediatric sepsis.

## Key findings

- Serum IL-37 levels were significantly higher in pediatric sepsis patients compared to non-septic patients and healthy controls.
- Recombinant IL-37 reduced systemic inflammation and improved survival in a murine sepsis model.
- IL-37 neutralization increased CD4+ T cells and NKT cells in septic PBMCs.

## Abstract

Sepsis arises from a dysregulated host inflammatory response to infection. The levels and pathogenic role of interleukin-37 (IL-37) in pediatric sepsis remain to be fully elucidated.

Serum IL-37 concentrations were measured in two independent cohorts of pediatric patients with sepsis from Chongqing (discovery cohort, n=40) and Sichuan (validation cohort, n=105). The immunomodulatory effects of IL-37 were systematically investigated through: 1) a murine sepsis model (cecal ligation and puncture), and 2) ex vivo experiments using peripheral blood mononuclear cells (PBMCs) from patients under standardized culture conditions.

Admission serum IL-37 levels were significantly higher in pediatric patients with sepsis compared to non-septic patients and healthy controls. To assess its diagnostic potential, ROC curve analyses were performed, yielding areas under the curve (AUC) of 0.76 [P<0.0001; 95% confidence interval (95% CI), 0.66 - 0.85] and 0.77 [P<0.0001; 95% CI, 0.71 - 0.84] from the two medical centers. In septic mice, therapeutic administration of recombinant IL-37 significantly attenuated systemic inflammation (reduced IL-6, CXCL-1, CCL-2; increased IL-10), decreased the proportion of M1 macrophages without altering total macrophage counts in peritoneal lavage fluids (PLF), and improved survival rates. In vitro, IL-37 neutralization with a specific antibody in septic PBMCs increased the percentages of CD4+ T cells and NKT cells.

This study identifies elevated IL-37 as a potential diagnostic biomarker for pediatric sepsis and demonstrates its role in modulating hyperinflammation and immune cell differentiation. IL-37 represents a promising therapeutic target for pediatric sepsis.

## Linked entities

- **Genes:** IL37 (interleukin 37) [NCBI Gene 27178]
- **Proteins:** IL37 (interleukin 37), IL6 (interleukin 6), CXCL1 (C-X-C motif chemokine ligand 1), CCL2 (C-C motif chemokine ligand 2), IL10 (interleukin 10)
- **Species:** Mus musculus (taxon 10090)

## Full-text entities

- **Genes:** Notch1 (notch 1) [NCBI Gene 18128] {aka 9930111A19Rik, Mis6, N1, Tan1, lin-12}, Fcgr3 (Fc receptor, IgG, low affinity III) [NCBI Gene 14131] {aka CD16}, IL2 (interleukin 2) [NCBI Gene 3558] {aka IL-2, TCGF, lymphokine}, Ptprc (protein tyrosine phosphatase receptor type C) [NCBI Gene 19264] {aka B220, CD45R, Cd45, L-CA, Ly-5, Lyt-4}, CD19 (CD19 molecule) [NCBI Gene 930] {aka B4, CVID3}, Tslp (thymic stromal lymphopoietin) [NCBI Gene 53603], CD4 (CD4 molecule) [NCBI Gene 920] {aka CD4mut, IMD79, Leu-3, OKT4D, T4}, IL4 (interleukin 4) [NCBI Gene 3565] {aka BCGF-1, BCGF1, BSF-1, BSF1, IL-4}, IFNG (interferon gamma) [NCBI Gene 3458] {aka IFG, IFI, IMD69}, Camp (cathelicidin antimicrobial peptide) [NCBI Gene 12796] {aka CAP18, CLP, Cnlp, Cramp, FALL39, MCLP}, Ecd (ecdysoneless cell cycle regulator) [NCBI Gene 70601] {aka 5730461K03Rik, Hsgt1}, Cd3e (CD3 antigen, epsilon polypeptide) [NCBI Gene 12501] {aka CD3, CD3epsilon, T3e}, IL37 (interleukin 37) [NCBI Gene 27178] {aka FIL1, FIL1(ZETA), FIL1Z, IL-1F7, IL-1H, IL-1H4}, CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, MERTK (MER proto-oncogene, tyrosine kinase) [NCBI Gene 10461] {aka MER, RP38, Tyro12, c-Eyk, c-mer}, Il10 (interleukin 10) [NCBI Gene 16153] {aka CSIF, If2a, Il-10}, Cxcl1 (C-X-C motif chemokine ligand 1) [NCBI Gene 14825] {aka Fsp, Gro1, KC, Mgsa, N51, Scyb1}, TGFB1 (transforming growth factor beta 1) [NCBI Gene 7040] {aka CAEND1, CED, DPD1, IBDIMDE, LAP, TGF-beta1}, Cd19 (CD19 antigen) [NCBI Gene 12478], CD8A (CD8 subunit alpha) [NCBI Gene 925] {aka CD8, CD8alpha, IMD116, Leu2, p32}, Mrc1 (mannose receptor, C type 1) [NCBI Gene 17533] {aka CD206, MR}, Ncam1 (neural cell adhesion molecule 1) [NCBI Gene 17967] {aka CD56, E-NCAM, NCAM-1, Ncam}, Itgam (integrin alpha M) [NCBI Gene 16409] {aka CD11b/CD18, CR3, CR3A, Cd11b, F730045J24Rik, Ly-40}, NFKB1 (nuclear factor kappa B subunit 1) [NCBI Gene 4790] {aka CVID12, EBP-1, KBF1, NF-kB, NF-kB1, NF-kappa-B1}, Ly6 (lymphocyte antigen 6 complex) [NCBI Gene 17062] {aka Ala-1, DAG, H9/25, Ly-27, Ly-6, Ly27}, IL18R1 (interleukin 18 receptor 1) [NCBI Gene 8809] {aka CD218a, CDw218a, IL-18R, IL-18R-alpha, IL-18Ralpha, IL-1Rrp}, Il6 (interleukin 6) [NCBI Gene 16193] {aka Il-6}, IL1RAPL1 (interleukin 1 receptor accessory protein like 1) [NCBI Gene 11141] {aka IL-1-RAPL-1, IL-1RAPL-1, IL1R8, IL1RAPL, IL1RAPL-1, MRX10}, Cd4 (CD4 antigen) [NCBI Gene 12504] {aka L3T4, Ly-4}, PTEN (phosphatase and tensin homolog) [NCBI Gene 5728] {aka 10q23del, BZS, CWS1, DEC, GLM2, MHAM}, CALCA (calcitonin related polypeptide alpha) [NCBI Gene 796] {aka CALC1, CGRP, CGRP-I, CGRP-alpha, CGRP1, CT}, IL10 (interleukin 10) [NCBI Gene 3586] {aka CSIF, GVHDS, IL-10, IL10A, TGIF}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, CXCL1 (C-X-C motif chemokine ligand 1) [NCBI Gene 2919] {aka FSP, GRO1, GROa, MGSA, MGSA-a, NAP-3}, Cd86 (CD86 antigen) [NCBI Gene 12524] {aka B7, B7-2, B7.2, B70, CLS1, Cd28l2}, Ccl2 (C-C motif chemokine ligand 2) [NCBI Gene 20296] {aka HC11, JE, MCAF, MCP-1, MCP1, SMC-CF}, Ly6g (lymphocyte antigen 6 family member G) [NCBI Gene 546644] {aka Gr-1, Gr1, Ly-6G}, Nfkb1 (nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105) [NCBI Gene 18033] {aka NF-KB1, NF-kappaB, NF-kappaB1, p105, p50, p50/p105}, SPATA2 (spermatogenesis associated 2) [NCBI Gene 9825] {aka PD1, PPP1R145, tamo}, IL1A (interleukin 1 alpha) [NCBI Gene 3552] {aka IL-1 alpha, IL-1A, IL1, IL1-ALPHA, IL1F1}, Apc (APC, WNT signaling pathway regulator) [NCBI Gene 11789] {aka CC1, Min, mAPC}, CCL2 (C-C motif chemokine ligand 2) [NCBI Gene 6347] {aka GDCF-2, HC11, HSMCR30, MCAF, MCP-1, MCP1}
- **Diseases:** organ damage (MESH:D000092124), inflammatory bowel disease (MESH:D015212), bacterial (MESH:D001424), Sepsis (MESH:D018805), tissue injury (MESH:D017695), septic (MESH:D001170), immune dysregulation (OMIM:614878), HIV infection (MESH:D015658), dislocation (MESH:D004204), Septic Shock (MESH:D012772), deaths (MESH:D003643), inflammatory bone disorders (MESH:D001847), PLF (MESH:D010538), colitis (MESH:D003092), cardiovascular, coagulation (MESH:D001778), infected (MESH:D007239), organ dysfunction (MESH:D009102), analgesia (MESH:D000699), bacteria (MESH:C000719206), damage to the respiratory (MESH:D012140), shock (MESH:D012769), Inflammation (MESH:D007249), periodontitis (MESH:D010518), allergic contact dermatitis (MESH:D017449), gouty arthritis (MESH:D015210), malignant tumors (MESH:D009369)
- **Chemicals:** lipid (MESH:D008055), CO2 (MESH:D002245), Gibco 1640 medium (-), Giemsa (MESH:D001399), xylazine (MESH:D014991)
- **Species:** Homo sapiens (human, species) [taxon 9606], Bacteria Latreille et al. 1825 (Bacteria stick insect, genus) [taxon 629395], Mus musculus (house mouse, species) [taxon 10090]
- **Cell lines:** PLF — Cirrhinus mrigala (Mrigala), Spontaneously immortalized cell line (CVCL_A2ZP), /6 — Homo sapiens (Human), Tongue squamous cell carcinoma, Cancer cell line (CVCL_5985)

## Full text

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## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12937001/full.md

## References

48 references — full list in the complete paper: https://tomesphere.com/paper/PMC12937001/full.md

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Source: https://tomesphere.com/paper/PMC12937001