Paola Cagnati
University of Genoa
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Publication
Featured researches published by Paola Cagnati.
The American Journal of Medicine | 2012
Giuseppe Murdaca; Paola Cagnati; Rossella Gulli; Francesca Spanò; Francesco Puppo; Corradino Campisi; Francesco Boccardo
Lymphedema is a chronic, progressive, and often debilitating condition. Primary lymphedema is a lymphatic malformation developing during the later stage of lymphangiogenesis. Secondary lymphedema is the result of obstruction or disruption of the lymphatic system, which can occur as a consequence of tumors, surgery, trauma, infection, inflammation, and radiation therapy. In this review, we report an update upon the diagnostic approach and the medical and surgical therapy for both primary and secondary lymphedema.
Expert Opinion on Drug Safety | 2012
Giuseppe Murdaca; Barbara Maria Colombo; Paola Cagnati; Rossella Gulli; Francesca Spanò; Francesco Puppo
The ongoing progresses in the knowledge of the pathogenic mechanisms of various immune-mediated and inflammatory diseases as well as the availability of innovative biotechnological approaches have led to the development of new drugs that add to conventional treatments. Among these, tumor necrosis factor (TNF)-α inhibitors, that is, infliximab, adalimumab, etanercept, golimumab and certolizumab pegol, are now available for clinical use. This editorial discusses the recent indications of TNF-α inhibitors, the pretreatment considerations, the reported adverse events and, finally, the recommendations for its use in pregnancy.
American Journal of Clinical Dermatology | 2010
Giuseppe Murdaca; Barbara Maria Colombo; Gianfranco Barabino; Matteo Caiti; Paola Cagnati; Francesco Puppo
Granuloma annulare (GA) is a chronic inflammatory disease of unknown etiology characterized by the development of plaques preferentially localized to the distal extremities. Spontaneous remission and relapses are quite common and the course of GA is not easy to predict. Moreover, most therapeutic regimens have been used anecdotally and with variable success. We report the case of a 62-year-old White female patient affected by disseminated GA unsuccessfully treated with psoralen plus UVA photochemotherapy, prednisone, and cyclosporine (ciclosporin) who responded to the anti-tumor necrosis factor-a monoclonal antibody infliximab administered intravenously at a dosage of 5 mg/kg at weeks 0, 2, and 6 and thereafter at monthly intervals for 10 additional months. Most of the GA lesions improved within 8 weeks and then slowly resolved within 10 months of treatment. We suggest that infliximab may be proposed as an additional therapeutic option in the treatment of recalcitrant forms of disseminated GA.
Clinical Immunology | 2009
Giuseppe Murdaca; Paola Contini; Maurizio Setti; Paola Cagnati; Francesca Lantieri; Francesco Indiveri; Francesco Puppo
We have reported that serum level of soluble HLA-A, -B, -C (sHLA-A,-B,-C) antigens is elevated in HIV-infected subjects and decreases after antiretroviral therapy (HAART). In this study, we measured the levels of soluble HLA-G (sHLA-G) antigens in a cohort of HIV-infected patients before and during HAART. sHLA-G and sHLA-A, -B, -C levels were significantly elevated in HIV-infected subjects as compared with controls before antiretroviral treatment and significantly decreased after 36 months of HAART. sHLA-G levels were correlated with sHLA-A, -B, -C levels, the decrease of plasma HIV-RNA level, the increase of CD4+ T-lymphocyte number and the decrease of CD8+ T-lymphocyte number. These results suggest that the measurement of sHLA-G and sHLA-A, -B, -C antigen serum levels might represent a useful surrogate marker to monitor virological response and immune reconstitution in HIV-positive subjects undergoing HAART treatment.
Redox Report | 2013
Giuseppe Murdaca; Francesca Spanò; Paola Cagnati; Francesco Puppo
Abstract Objectives During the last decade many new biological immune modulators have entered the market as new therapeutic principles. Tumor necrosis factor (TNF)-α is a pro-inflammatory cytokine known to a have a key role in the pathogenic mechanisms of various immune-mediated or inflammatory diseases. However, TNF-α also plays a key role in endothelial dysfunction and, thus, in the development and progression of atherosclerosis. What, then, is the potential therapeutic role of TNF-α inhibitors? Methods We analysed the current literature concerning the administration of TNF-α inhibitors and their potential benefits upon endothelial function. Results TNF-α inhibitors decrease the serum levels of inflammatory markers such as TNF-α itself, CRP, IL-6, and increased the tissue expression of endothelial NO synthase and the vasodilatory response to bradykinin. Discussion TNF-α inhibitors may change the progression of endothelial dysfunction and, thus, slow down the atherosclerotic process.
Allergy | 2008
G. Ciprandi; Barbara Maria Colombo; Paola Contini; Paola Cagnati; Angela Pistorio; Francesco Puppo; Giuseppe Murdaca
Background: Allergic rhinitis (AR) is characterized by Th2‐polarized immune response. Soluble HLA (sHLA) molecules play an immunomodulatory activity. So far, however, no study investigated them in AR.
Human Immunology | 2011
Giuseppe Murdaca; Paola Contini; Maurizio Setti; Paola Cagnati; Francesca Spanò; Francesca Lantieri; Francesco Puppo
We have previously reported that the serum levels of soluble human leukocyte antigen (HLA)-A, -B, -C, and -G antigens are elevated in human immunodeficiency virus (HIV)-infected subjects and decrease after antiretroviral therapy. In this study, we measured soluble HLA-G serum levels in patients with acquired immune deficiency syndrome (AIDS) affected by different AIDS-defining conditions before and during antiretroviral therapy and correlated them with virologic and immunologic parameters of response to treatment. Soluble HLA-G levels were significantly higher in AIDS patients before treatment as compared with healthy controls and significantly decreased after 36 months of therapy. The decrease of soluble HLA-G correlated with the decrease of plasma HIV-RNA level and CD8(+) T-lymphocytes number and with the increase of CD4(+) T-lymphocytes number. Soluble HLA-G levels were significantly higher in patients with opportunistic infections and Kaposis sarcoma compared with patients with the wasting syndrome. These data suggest that infections and neoplasms may trigger the shedding of soluble HLA-G molecules, and confirm that the level of soluble HLA-G in serum might represent a surrogate marker to monitor virologic response and immune reconstitution in HIV-positive individuals.
The Journal of Rheumatology | 2008
Giuseppe Murdaca; Paola Cagnati; Rossella Gulli; Matteo Caiti; Francesco Boccardo; Corradino Campisi; Francesco Puppo
To the Editor: Antiphospholipid syndrome (APS) is characterized by a state of hypercoagulability potentially resulting in thrombosis of all segments of the vascular bed1,2, fetal loss, and moderate thrombocytopenia3,4. APS is associated with elevated titers of antiphospholipid antibodies (aPL) and/or lupus anticoagulant (LAC)5,6. Gastrointestinal manifestations are rarely observed (about 1.5% of patients) and intestinal infarction, resulting from mesenteric vessel thrombosis, has been infrequently reported3. The presentation may be acute (acute abdomen), often preceded by intestinal angina1. Rarely, thrombosis of large vessels (aorta and inferior vena cava) has also been reported in association with aPL7. We describe a case of recurrent ...
Atherosclerosis | 2012
Giuseppe Murdaca; Barbara Maria Colombo; Paola Cagnati; Rossella Gulli; Francesca Spanò; Francesco Puppo
Human Immunology | 2007
Giuseppe Murdaca; Paola Contini; Maurizio Setti; Paola Cagnati; Roberto Villa; Francesca Lantieri; Francesco Indiveri; Francesco Puppo