Th17/IL-17A axis is critical for pulmonary arterial hypertension (PAH) in systemic sclerosis (SSc): SSc patients with high levels of serum IL-17A exhibit reduced lung functions and increased prevalence of PAH-Reference-Cited by-同舟云学术

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Th17/IL-17A axis is critical for pulmonary arterial hypertension (PAH) in systemic sclerosis (SSc): SSc patients with high levels of serum IL-17A exhibit reduced lung functions and increased prevalence of PAH

Published:2024-04 Issue: Volume:176 Page:156534
ISSN:1043-4666
Container-title:Cytokine
language:en
Short-container-title:Cytokine

Author:

Seki Noriyasu,Tsujimoto Hideto,Tanemura Shuhei,Ishigaki Sho,Takei Hiroshi,Sugahara Kunio,Yoshimoto Keiko,Akiyama Mitsuhiro,Kaneko Yuko,Chiba Kenji,Takeuchi Tsutomu

Funder

Mitsubishi Tanabe Pharma Corporation

Publisher

Elsevier BV

Reference51 articles.

1. Update on the profile of the EUSTAR cohort: an analysis of the EULAR Scleroderma Trials and Research group database;Meier;Ann. Rheum. Dis.,2012

2. Systemic sclerosis: a prototypic multisystem fibrotic disorder;Varga;J. Clin. Invest.,2007

3. Prevalence and outcome in systemic sclerosis associated pulmonary arterial hypertension: application of a registry approach;Mukerjee;Ann. Rheum. Dis.,2003

4. Early detection of pulmonary arterial hypertension in systemic sclerosis: a French nationwide prospective multicenter study;Hachulla;Arthritis Rheum.,2005

5. Predictors of isolated pulmonary hypertension in patients with systemic sclerosis and limited cutaneous involvement;Steen;Arthritis Rheum.,2003

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