Treatment of Systemic Sclerosis Associated Interstitial Lung Disease

Systemic sclerosis (SSc) is a systemic connective tissue disorder characterized by progressive skin and visceral organ fibrosis, vasculopathy, and immune dysregulation. Interstitial lung disease (ILD) is a common manifestation and major contributor to morbidity and mortality. Immunosuppression is us...

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Main Authors: Iris Yan Ki Tang, So Ho
Format: Article
Language:English
Published: World Scientific Publishing 2020-12-01
Series:Journal of Clinical Rheumatology and Immunology
Subjects:
Online Access:http://www.worldscientific.com/doi/epdf/10.1142/S2661341720300050
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author Iris Yan Ki Tang
So Ho
author_facet Iris Yan Ki Tang
So Ho
author_sort Iris Yan Ki Tang
collection DOAJ
description Systemic sclerosis (SSc) is a systemic connective tissue disorder characterized by progressive skin and visceral organ fibrosis, vasculopathy, and immune dysregulation. Interstitial lung disease (ILD) is a common manifestation and major contributor to morbidity and mortality. Immunosuppression is usually indicated for extensive or progressive SSc-ILD. Recently, antifibrotic and biological therapies have been shown to be efficacious in treating SSc-ILD in various studies. In this article, we will descriptively review the latest evidence on the treatment of SSc-ILD.
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spelling doaj.art-b59b1b8ec9854e33b2fb3c827031598b2022-12-21T22:44:09ZengWorld Scientific PublishingJournal of Clinical Rheumatology and Immunology2661-34172661-34252020-12-01202566410.1142/S266134172030005010.1142/S2661341720300050Treatment of Systemic Sclerosis Associated Interstitial Lung DiseaseIris Yan Ki Tang0So Ho1Department of Medicine and Geriatrics, Kwong Wah Hospital, Hong KongDepartment of Medicine and Therapeutics, The Chinese University of Hong Kong, Hong KongSystemic sclerosis (SSc) is a systemic connective tissue disorder characterized by progressive skin and visceral organ fibrosis, vasculopathy, and immune dysregulation. Interstitial lung disease (ILD) is a common manifestation and major contributor to morbidity and mortality. Immunosuppression is usually indicated for extensive or progressive SSc-ILD. Recently, antifibrotic and biological therapies have been shown to be efficacious in treating SSc-ILD in various studies. In this article, we will descriptively review the latest evidence on the treatment of SSc-ILD.http://www.worldscientific.com/doi/epdf/10.1142/S2661341720300050systemic sclerosissclerodermainterstitial lung diseasepulmonary fibrosislung disease
spellingShingle Iris Yan Ki Tang
So Ho
Treatment of Systemic Sclerosis Associated Interstitial Lung Disease
Journal of Clinical Rheumatology and Immunology
systemic sclerosis
scleroderma
interstitial lung disease
pulmonary fibrosis
lung disease
title Treatment of Systemic Sclerosis Associated Interstitial Lung Disease
title_full Treatment of Systemic Sclerosis Associated Interstitial Lung Disease
title_fullStr Treatment of Systemic Sclerosis Associated Interstitial Lung Disease
title_full_unstemmed Treatment of Systemic Sclerosis Associated Interstitial Lung Disease
title_short Treatment of Systemic Sclerosis Associated Interstitial Lung Disease
title_sort treatment of systemic sclerosis associated interstitial lung disease
topic systemic sclerosis
scleroderma
interstitial lung disease
pulmonary fibrosis
lung disease
url http://www.worldscientific.com/doi/epdf/10.1142/S2661341720300050
work_keys_str_mv AT irisyankitang treatmentofsystemicsclerosisassociatedinterstitiallungdisease
AT soho treatmentofsystemicsclerosisassociatedinterstitiallungdisease