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Identification of immune‐associated signatures and potential therapeutic targets for pulmonary arterial hypertension

27 Sept 2023

Abstract excerpt

Pulmonary arterial hypertension (PAH) comprises a heterogeneous group of diseases with diverse aetiologies. It is characterized by increased pulmonary arterial pressure and right ventricular (RV) failure without specific drugs for treatment. Emerging evidence suggests that inflammation and autoimmune disorders are common features across all PAH phenotypes. This provides a novel idea to explore the characteristics...

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PMID: 37753829
DOI: 10.1111/jcmm.17962

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

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