Hypertrophic scar after
burn injury is a significant problem. Previous studies have examined the roles for
decorin, interleukin-1β, and transforming growth factor-β1 in
hypertrophic scar formation locally, but few have considered their systemic influence. The authors conducted a pilot study to examine whether serum levels of these molecules could predict
hypertrophic scar formation. Serum levels were measured using
enzyme-linked
immunosorbent assay, and
hypertrophic scar formation determined from chart reviews. Peripheral blood mononuclear cells and fibroblasts were stimulated with
decorin, interleukin-1β, and transforming growth factor-β1, and expression of profibrotic molecules examined using flow cytometry, immunofluorescence microscopy, quantitative polymerase chain reaction, and mass spectrometry. Multiple linear regression analysis suggested early serum levels of
decorin and interleukin-1β, and late serum levels of transforming growth factor-β1 were predictive of
hypertrophic scar formation.
Decorin up-regulated the expression of
toll-like receptor 4 and C-X-C receptor 4 in peripheral blood mononuclear cells, and interleukin-1β up-regulated fibroblast production of C-X-C
ligand 12. Transforming growth factor-β1 up-regulated, and interleukin-1β down-regulated, the production of profibrotic
cytokines,
collagen, and myofibroblast differentiation. The model predicting
hypertrophic scar formation is supported by clinical results and limited in vitro experiments.