Publications by authors named "D Biondini"

Article Synopsis
  • Recent studies indicate that B cells and autoantibodies are found in idiopathic pulmonary fibrosis (IPF), suggesting the existence of tertiary lymphoid structures (TLS), which are typically not identified in IPF's histological features.
  • The research examines TLS quantity, size, and activation in lung samples from IPF patients at various stages, linking these characteristics to clinical outcomes and disease progression.
  • Results show that the presence and activation of TLS are higher in IPF cases compared to controls, with significant differences noted between rapid and slow progressors, implying that B-cell activity and TLS may influence the disease's mechanism and severity.
View Article and Find Full Text PDF

Depending on local cues, macrophages can polarize into classically activated (M1) or alternatively activated (M2) phenotypes. This study investigates the impact of polarized macrophage-derived Extracellular Vesicles (EVs) (M1 and M2) and their cargo of miRNA-19a-3p and miRNA-425-5p on TGF-β production in lung fibroblasts. EVs were isolated from supernatants of M0, M1, and M2 macrophages and quantified using nanoscale flow cytometry prior to fibroblast stimulation.

View Article and Find Full Text PDF

Background: The family of Suppressor of Cytokine Signaling (SOCS) acts as a controller of the duration and intensity of cytokine function by negatively regulating the JAK-STAT signaling pathway. SOCS' role in inflammatory diseases in animal models is well demonstrated. However, its role in the development of human disease is still under investigation.

View Article and Find Full Text PDF

Solitary fibrous tumors (SFTs) are rare mesenchymal neoplasms constituting less than 2% of all soft tissue tumors. They typically originate in the thoracic cavity, mainly in the pleura, but can also occur in other various sites such as lung parenchyma, pericardium, and bronchus. In this study, a 49-year-old non-smoking female with a history of allergies presented to our pulmonary clinic with a chronic cough.

View Article and Find Full Text PDF

The term pulmonary hypertension (PH) refers to different conditions, all characterized by increased pressure and resistance in the pulmonary arterial bed. PH has a wide range of causes (essentially, cardiovascular, pulmonary, or connective tissue disorders); however, idiopathic (i.e.

View Article and Find Full Text PDF