Literature DB >> 16344498

Serum levels of monocyte chemotactic protein-3/CCL7 are raised in patients with systemic sclerosis: association with extent of skin sclerosis and severity of pulmonary fibrosis.

K Yanaba1, K Komura, M Kodera, T Matsushita, M Hasegawa, K Takehara, S Sato.   

Abstract

OBJECTIVE: To determine serum levels of monocyte chemotactic protein-3 (MCP-3) and its clinical associations in patients with systemic sclerosis (SSc).
METHODS: Serum MCP-3 levels from 69 patients with SSc were examined by ELISA.
RESULTS: Serum MCP-3 levels were raised in patients with SSc (n = 69) compared with healthy controls (n = 28). Patients with diffuse cutaneous SSc (n = 36) had higher levels of serum MCP-3 than those with limited cutaneous SSc (n = 33). Patients with raised MCP-3 levels had pulmonary fibrosis and decreased vital capacity (VC) more often than those with normal MCP-3 levels. MCP-3 levels correlated positively with the extent of skin fibrosis, and inversely with %VC and carbon monoxide transfer factor (Tlco) in patients with SSc.
CONCLUSION: MCP-3 levels were increased in patients with SSc, and correlated with the extent of skin sclerosis and the severity of pulmonary fibrosis. These results suggest that MCP-3 may have a role in the development of fibrosis in SSc.

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Year:  2006        PMID: 16344498      PMCID: PMC1797996          DOI: 10.1136/ard.2005.040782

Source DB:  PubMed          Journal:  Ann Rheum Dis        ISSN: 0003-4967            Impact factor:   19.103


  15 in total

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2.  Scleroderma (systemic sclerosis): classification, subsets and pathogenesis.

Authors:  E C LeRoy; C Black; R Fleischmajer; S Jablonska; T Krieg; T A Medsger; N Rowell; F Wollheim
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Authors:  M Hasegawa; S Sato; K Takehara
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Authors: 
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Authors:  R M Silver; K S Miller; M B Kinsella; E A Smith; S I Schabel
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10.  Localization of collagen mRNA in normal and scleroderma skin by in-situ hybridization.

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Review 5.  The role of inflammation in the pathogenesis of idiopathic pulmonary fibrosis.

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6.  Serum cytokines and their predictive value in pulmonary involvement of systemic sclerosis.

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7.  Multiplex cytokine analysis of dermal interstitial blister fluid defines local disease mechanisms in systemic sclerosis.

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8.  Pathogenesis of systemic sclerosis associated interstitial lung disease.

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9.  Enhanced chemokine-receptor expression, function, and signaling in healthy African American and scleroderma-patient monocytes are regulated by caveolin-1.

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10.  Distal Lung Microenvironment Triggers Release of Mediators Recognized as Potential Systemic Biomarkers for Idiopathic Pulmonary Fibrosis.

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  10 in total

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