Peripheral Blood T Cells of Patients with IPAH Have a Reduced Cytokine-Producing Capacity

Pulmonary arterial hypertension (PAH) is rare disease that is categorized as idiopathic (IPAH) when no underlying cause can be identified. Lungs of most patients with IPAH contain increased numbers of T cells and dendritic cells (DCs), suggesting involvement of the immune system in its pathophysiolo...

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Detalles Bibliográficos
Autores principales: van Uden, Denise, Koudstaal, Thomas, van Hulst, Jennifer A. C., Vink, Madelief, van Nimwegen, Menno, van den Toorn, Leon M., Chandoesing, Prewesh P., van den Bosch, Annemien E., Kool, Mirjam, Hendriks, Rudi W., Boomars, Karin A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9224379/
https://www.ncbi.nlm.nih.gov/pubmed/35742956
http://dx.doi.org/10.3390/ijms23126508

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9224379/
https://www.ncbi.nlm.nih.gov/pubmed/35742956
http://dx.doi.org/10.3390/ijms23126508

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