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  1. Article

    Open Access

    Clinical features and potential markers of disease in idiopathic non-histaminergic angioedema, a real-life study

    Idiopathic non-histaminergic acquired angioedema (InH-AAE) is a rare disease, with unknown etiology and pathogenesis, characterized by recurrent clinical manifestations and resistance to antihistamines and cor...

    Ilaria Mormile, Maria Celeste Gigliotti, Anne Lise Ferrara in Immunologic Research (2024)

  2. Article

    Open Access

    Melanoma-derived soluble mediators modulate neutrophil biological properties and the release of neutrophil extracellular traps

    Polymorphonuclear neutrophils (PMNs) are the main effector cells in the inflammatory response. The significance of PMN infiltration in the tumor microenvironment remains unclear. Metastatic melanoma is the mos...

    Luca Modestino, Leonardo Cristinziano in Cancer Immunology, Immunotherapy (2023)

  3. Article

    Open Access

    Interplay between C1-inhibitor and group IIA secreted phospholipase A2 impairs their respective function

    High levels of human group IIA secreted phospholipase A2 (hGIIA) have been associated with various inflammatory disease conditions. We have recently shown that hGIIA activity and concentration are increased in th...

    Anne Lise Ferrara, Maria Bova, Angelica Petraroli, Daniela Marasco in Immunologic Research (2023)

  4. Article

    Open Access

    Vascular endothelial growth factors and angiopoietins as new players in mastocytosis

    Mastocytosis is a disorder characterized by the abnormal proliferation and/or accumulation of mast cells in different organs. More than 90% of patients with systemic mastocytosis have a gain-of-function mutati...

    Simone Marcella, Angelica Petraroli in Clinical and Experimental Medicine (2021)

  5. Article

    Open Access

    Pathways of Neutrophil Granulocyte Activation in Hereditary Angioedema with C1 Inhibitor Deficiency

    Hereditary angioedema (HAE) with C1-inhibitor deficiency belongs to bradykinin-mediated angioedemas. It is characterized by recurrent subcutaneous and/or submucosal swelling episodes (HAE attacks) and erythema...

    Erika Kajdácsi, Nóra Veszeli, Blanka Mező in Clinical Reviews in Allergy & Immunology (2021)

  6. Article

    Open Access

    Roles of Immune Cells in Hereditary Angioedema

    Hereditary angioedema (HAE) is a rare genetic disease, characterized by recurrent and unexpected potentially life-threatening mucosal swelling. HAE may be further classified into HAE with C1‐inhibitor deficien...

    Anne Lise Ferrara, Leonardo Cristinziano in Clinical Reviews in Allergy & Immunology (2021)

  7. Article

    Open Access

    Abstracts from the 10th C1-inhibitor deficiency workshop

    Alvin H. Schmaier, Marco Cicardi, Avner Reshef in Allergy, Asthma & Clinical Immunology (2017)