# The Microbial Profile of Keloid Tissue: A Potential Biomarker for Lesion Activity

**Authors:** Wenjie Xia, Sihui Wang, Yang Xu, Hui Hua, Rong Guo, Bingrong Zhou

PMC · DOI: 10.3390/biomedicines14020386 · Biomedicines · 2026-02-07

## TL;DR

This study explores how the microbial makeup of keloid tissue differs when the lesions are active versus inactive, suggesting potential biomarkers for monitoring keloid activity.

## Contribution

The study identifies distinct microbial profiles in active keloids, offering new insights into microbiome-based monitoring of lesion activity.

## Key findings

- Active keloids have higher levels of Acinetobacter and Pseudomonas compared to normal skin.
- Inactive keloids show no significant microbial differences from normal skin.
- Lipid-related pathways are altered in active lesions based on functional predictions.

## Abstract

Background: Keloids can extend beyond the boundaries of the original wound and often cause itching or pain. Although the skin microbiome is known to influence various skin conditions, it is still unclear how the microbiota inside keloid tissues differ between active and inactive stages. Methods: We enrolled 43 patients with active keloids and 20 patients with inactive lesions. Tissue samples were collected from keloids and from nearby normal skin. In active lesions, both the relatively unstable and stable regions were also sampled. Microbial composition and predicted functions were analyzed using 16S Ribosomal RNA (rRNA) sequencing and standard bioinformatic approaches. Results: Active keloids exhibited a distinct microbial profile compared to normal skin. Acinetobacter and Pseudomonas were more abundant in active lesions, while Cutibacterium was more common in normal skin. Functional prediction also indicated changes in lipid-related pathways in active lesions. In contrast, inactive keloids showed no significant differences from normal skin, and different regions within active lesions had similar microbial features. Conclusions: This study indicates that alterations in the microbiota are linked to the activity of keloids. Potential microbiome-based translational pathways should be explored for monitoring and managing keloid activity in the future.

## Full-text entities

- **Genes:** TGFB1 (transforming growth factor beta 1) [NCBI Gene 7040] {aka CAEND1, CED, DPD1, IBDIMDE, LAP, TGF-beta1}, CAT (catalase) [NCBI Gene 847], TAFAZZIN (tafazzin, phospholipid-lysophospholipid transacylase) [NCBI Gene 6901] {aka BTHS, CMD3A, EFE, EFE2, G4.5, LVNCX}, PTK2 (protein tyrosine kinase 2) [NCBI Gene 5747] {aka FADK, FADK 1, FAK, FAK1, FRNK, PPP1R71}, YAP1 (Yes1 associated transcriptional regulator) [NCBI Gene 10413] {aka COB1, YAP, YAP-1, YAP2, YAP65, YKI}, CXCL8 (C-X-C motif chemokine ligand 8) [NCBI Gene 3576] {aka GCP-1, GCP1, IL8, LECT, LUCT, LYNAP}
- **Diseases:** tumor (MESH:D009369), Keloid (MESH:D007627), infected (MESH:D007239), fibrosis (MESH:D005355), inflammation (MESH:D007249), injury to (MESH:D014947), fibrotic diseases (MESH:D004194), skin diseases (MESH:D012871), skin injury (MESH:D000069836), pain (MESH:D010146), infectious (MESH:D003141), itching (MESH:D011537)
- **Chemicals:** nitrogen (MESH:D009584), CTAB (MESH:D000077286), LA (MESH:D019787), iodophor (MESH:D007466), SDS (MESH:D012967), silver (MESH:D012834), agarose (MESH:D012685), lipid (MESH:D008055), LPS (MESH:D008070)
- **Species:** Cutibacterium (genus) [taxon 1912216], Bacteria Latreille et al. 1825 (Bacteria stick insect, genus) [taxon 629395], Staphylococcus (genus) [taxon 1279], Homo sapiens (human, species) [taxon 9606], Acinetobacter (genus) [taxon 469], Actinomycetota (actinobacteria, phylum) [taxon 201174], Peptoniphilus (genus) [taxon 162289], Bacillota (clostridial firmicutes, phylum) [taxon 1239], Pseudomonas (RNA similarity group I, genus) [taxon 286], Pseudomonadota (proteobacteria, phylum) [taxon 1224]

## Full text

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## Figures

10 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12938717/full.md

## References

37 references — full list in the complete paper: https://tomesphere.com/paper/PMC12938717/full.md

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Source: https://tomesphere.com/paper/PMC12938717