Skin involvement in scleroderma-where histological and clinical scores meet

Objectives. A clinico-pathological study in diffuse systemic sclerosis (SSc) patients was performed to analyse whether the skin histological organization and the pro-fibrotic signals elicited by TGF-β in fibroblasts vary according to the modified Rodnan skin score (mRSS). Methods. Twenty-seven SSc p...

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Veröffentlicht in:Rheumatology 2007-05, Vol.46 (5), p.833-841
Hauptverfasser: Verrecchia, F., Laboureau, J., Verola, O., Roos, N., Porcher, R., Bruneval, P., Ertault, M., Tiev, K., Michel, L., Mauviel, A., Farge, D.
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Sprache:eng
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Zusammenfassung:Objectives. A clinico-pathological study in diffuse systemic sclerosis (SSc) patients was performed to analyse whether the skin histological organization and the pro-fibrotic signals elicited by TGF-β in fibroblasts vary according to the modified Rodnan skin score (mRSS). Methods. Twenty-seven SSc patients underwent 45 skin biopsies with simultaneous measure of mRSS before or after treatment by immunosuppressive drugs, with or without autologous peripheral haematopoietic stem cell transplantation (HSCT). Results. Double-blind optic microscopy analysis of the biopsies standard extracellular matrix stains allowed to define three histological subgroups: 6 with grade 1 weak fibrosis, 30 with grade 2 moderate fibrosis and 9 with grade 3 severe fibrosis. A significant (P < 0.0001) was identified between the grades of fibrosis and the mRSS. In skin fibroblast cultures, Smad3 phosphorylation levels, as well as mRNA steady-state levels of two transforming growth factor (TGF)-β/Smad3 targets, COL1A2 and PAI-1, increased in parallel with the mRSS. When compared with pre-transplant values the degree of fibrosis observed after HSCT in the papillary and in the reticular dermis decreased in parallel with the fall in mRSS (n = 5 consecutive patients with repeated biopsies). Conclusions. The histological extent of skin fibrosis correlates closely with the mRSS. Both parameters appeared to regress after HSCT. The extent of TGF-β signalling activation in SSc skin fibroblasts appears to parallel the severity of disease.
ISSN:1462-0324
1462-0332
1460-2172
DOI:10.1093/rheumatology/kel451