Strategies for treating idiopathic pulmonary fibrosis

RM Du Bois - Nature reviews Drug discovery, 2010 - nature.com
Idiopathic pulmonary fibrosis (IPF) is the most common and most lethal diffuse fibrosing lung
disease, with a mortality rate that exceeds that of many cancers. Recently, there have been …

Relationship between cytokine profiles and clinical outcomes in patients with systemic sclerosis

J Baraut, L Michel, F Verrecchia, D Farge - Autoimmunity reviews, 2010 - Elsevier
Although the pathogenesis of systemic sclerosis (SSc) remains unknown, cytokine
production and release are key events in this autoimmune disease, characterized by T cell …

Experience with rituximab in scleroderma: results from a 1-year, proof-of-principle study

D Daoussis, SNC Liossis, AC Tsamandas… - …, 2010 - academic.oup.com
Objective. To assess the efficacy of rituximab (RTX) in SSc. Methods. Fourteen patients with
SSc were evaluated. Eight patients were randomized to receive two cycles of RTX at …

Marginal decline in forced vital capacity is associated with a poor outcome in idiopathic pulmonary fibrosis

CJ Zappala, PI Latsi, AG Nicholson… - European …, 2010 - Eur Respiratory Soc
In therapeutic studies in idiopathic pulmonary fibrosis (IPF), the low prevalence of significant
change in pulmonary functional tests (PFTs) has been a major constraint. The prognostic …

[HTML][HTML] Circulating monocytes from systemic sclerosis patients with interstitial lung disease show an enhanced profibrotic phenotype

SK Mathai, M Gulati, X Peng, TR Russell, AC Shaw… - Laboratory …, 2010 - Elsevier
Profibrotic cells derived from circulating CD14+ monocytes include fibrocytes and
alternatively activated macrophages. These cells are associated with interstitial lung disease …

Improved survival in systemic sclerosis is associated with better ascertainment of internal organ disease: a retrospective cohort study

SI Nihtyanova, EC Tang, JG Coghlan… - … Journal of Medicine, 2010 - academic.oup.com
Abstract Background: Systemic sclerosis (SSc) has high mortality and morbidity. Current
management focuses on early detection and treatment of organ-based manifestations. Aim …

Predictors of interstitial lung disease in early systemic sclerosis: a prospective longitudinal study of the GENISOS cohort

S Assassi, R Sharif, RE Lasky, TA McNearney… - Arthritis research & …, 2010 - Springer
Introduction The objective of the present study was to examine the association of baseline
demographic and clinical characteristics with sequentially obtained measurements of forced …

Cell adhesion molecules regulate fibrotic process via Th1/Th2/Th17 cell balance in a bleomycin-induced scleroderma model

A Yoshizaki, K Yanaba, Y Iwata, K Komura… - The Journal of …, 2010 - journals.aai.org
Mice sc injected with bleomycin, an experimental model for human systemic sclerosis,
develop skin and lung fibrosis, which is mediated by inflammatory cell infiltration. This …

[HTML][HTML] A computer-aided diagnosis system for quantitative scoring of extent of lung fibrosis in scleroderma patients

HJ Kim, DP Tashkin, P Clements, G Li… - Clinical and …, 2010 - ncbi.nlm.nih.gov
Objectives To evaluate an improved quantitative lung fibrosis score based on a computer-
aided diagnosis (CAD) system that classifies CT pixels with the visual semi-quantitative …

Treatment with rapamycin prevents fibrosis in tight‐skin and bleomycin‐induced mouse models of systemic sclerosis

A Yoshizaki, K Yanaba, A Yoshizaki… - Arthritis & …, 2010 - Wiley Online Library
Objective Rapamycin, a novel macrolide immunosuppressive drug, is increasingly used as
an agent for posttransplant immunosuppression and treatment of autoimmune disease. The …