Abstract
Advances in cellular and spatial profiling technologies have rapidly expanded the understanding of fibroblast heterogeneity within the target tissues of disease. In 2025, there has been a shift towards a consensus definition of shared cross-tissue fibroblast states and a greater understanding of their molecular drivers and disease-relevant effector functions.
| Original language | English |
|---|---|
| Number of pages | 3 |
| Journal | Nature Reviews Rheumatology |
| DOIs | |
| Publication status | E-pub ahead of print - 19 Dec 2025 |
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