Giuseppina D'Ascenzo
University of Siena
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Featured researches published by Giuseppina D'Ascenzo.
British Journal of Haematology | 2005
Pietro Rubegni; A. Cuccia; Paolo Sbano; G. Cevenini; Maria Rosaria Carcagnì; Giuseppina D'Ascenzo; G. De Aloe; Stefano Guidi; P. Guglielmetti; G. Marotta; Francesco Lauria; Alberto Bosi; Michele Fimiani
Recent studies suggest that extracorporeal photochemotherapy (ECP) may be beneficial in patients with steroid‐refractory chronic graft‐versus‐host disease (cGvHD). However, it is not yet clear whether certain conditions, such as age, mode of onset of cGvHD etc., influence clinical response and whether certain affected organs are more sensitive to ECP than others. We analysed the main clinical and laboratory parameters related to evolution of the disease in 32 steroid‐refractory cGvHD patients, to identify any useful response predictors to ECP. ECP affected the course of the disease positively in 78% (25/32) of our cases.
British Journal of Dermatology | 1997
Clelia Miracco; Pietro Rubegni; G. De Aloe; Giuseppina D'Ascenzo; C. Mazzatenta; M.M. de Santi; Michele Fimiani
Extracorporeal photochemotherapy (ExP) is a well‐tolerated new form of chemoimmunotherapy, which is considered to be effective for cutaneous T‐cell lymphoma (CTCL) and the treatment of choice for Sézary syndrome. Improvements have also been seen in patients with non‐erythrodermic mycosis fungoides (MF) in the early stages, even when tumour cells are not detectable in the peripheral blood. In this study, we used ExP as a monotherapy in seven patients who had early stage (Ib) MF, and who were no longer responsive to or had contraindications for other therapies. We observed a clinical improvement in the disease after 12 months of treatment: one patient showed a complete response, five a partial response, and one remained stable. In each patient we compared skin biopsies of large plaque lesions before and after the treatment. We undertook a histological evaluation of the infiltrate. The lymphoid cell proliferation and death rates were quantified using the following parameters: lymphoid cell density (LCD), Ki67+ lymphoid cell nuclei percentage (Ki67+ Lcn percentage), and apoptotic index (AI). Significant decreases in the lymphoid cell infiltrate and in cell proliferation, and a significant increase in AI were observed after therapy. The mean LCD decreased from 187 ± 33 to 34 ± 17·7, Ki67+ Lcn mean percentage decreased from 16·9 ± 3·9 to 4·9 ± 2·4, and the AI mean value increased from 0·05 ± 0·03 to 2·41 ± 1·54. Our results suggest a role for apoptosis in the improvement of the skin lesions and are in line with some reports on the mode of action of ExP. Although the way in which ExP works needs to be clarified further, it does seem to stimulate a CD8+ cell‐mediated anticlonotypic activity against circulating pathogenic clones. Furthermore, a release of tumour necrosis factor α (TNF‐α) by circulating monocytes has been demonstrated after ExP. Both are known to induce cell death by apoptosis.
Journal of The European Academy of Dermatology and Venereology | 2003
Clara Romano; Pietro Rubegni; G. De Aloe; E. Stanghellini; Giuseppina D'Ascenzo; Lucio Andreassi; Michele Fimiani
Background Eosinophilic fasciitis (EF) is a rare connective tissue disorder characterized clinically by symmetrical swelling, induration and thickening of the skin and histologically by thickening of the fascia with chronic inflammatory infiltrate containing eosinophils. The disease is classified in the spectrum morphea/systemic sclerosis and treated with systemic steroids and other immunosuppressant drugs.
International Journal of Immunopathology and Pharmacology | 2007
Pietro Rubegni; Paolo Sbano; G. Cevenini; M.G. Perari; G. Marotta; Massimiliano Risulo; Maria Rosaria Carcagnì; Giuseppina D'Ascenzo; G. De Aloe; Michele Fimiani
Extracorporeal photochemotherapy (ECP) has been used successfully for the treatment of chronic Graft versus Host Disease (cGvHD). However, the mechanism by which ECP exerts its protective effects remains elusive. Some recent observations have suggested a possible role of certain subsets of T lymphocytes with immunosuppressive properties (T-regulatory cells) that coexpress CD4 and high levels of the interleukin-2 receptor chain: CD4+CD25+ T lymphocytes. We studied whether ECP affects the percentage of these cells in the peripheral blood of patients with cGvHD. The study population consisted of 14 patients with cGvHD refractory to systemic steroids. On enrolment in each cycle of ECP, patients underwent clinical examination, blood chemistry analysis and other instrumental procedures to document and assess involvement of the various organs and systems. For cytofluorimetric identification and phenotyping of CD4+CD25+ T lymphocytes, peripheral blood samples were collected in EDTA anticoagulant before ECP, after 48 hours, and after 6 and 12 months from the start of treatment. The 14 patients in this study received a total of more than 300 cycles of ECP, with only minor side effects. The clinical outcome was negative in 2 patients and positive in 12 patients. Within-subject analysis indicated that the percentage of CD4+CD25+ T lymphocytes before ECP and after 12 months of treatment was significantly increased. Our study confirms that changes in the percentage of CD4+CD25+ T cells induced by ECP could be a central aspect in the cascade of immune events leading to the immunological and clinical effects of this treatment in patients with cGvHD.
Journal Der Deutschen Dermatologischen Gesellschaft | 2008
Maria Rosaria Carcagnì; Giovambattista De Aloe; Giuseppina D'Ascenzo; Pietro Rubegni; Michele Fimiani
Graft‐versus‐host disease (GvHD) is a common and often serious complication of hematopoietic stem cell transplantation. There are two major forms of GvHD: an acute form which develops in the first 100days after HSCT, and a chronic form which develops later. Chronic GvHD is a multiorgan syndrome with many features of autoimmune diseases, such as sclerodermatous skin changes, cholestasis, pulmonary fibrosis, xerostomia, oral ulcerations, myositis and fasci‐itis. Unlike acute GvHD which is characterized by acute alloreactivity,the etiology of chronic GvHD is controversial and is believed to be either an extension of acute GvHD and/or a result of dysfunctional immune reconstitution with generation of autoantibodies and autoreactive T‐cell clones. GvHD is usually treated with corticosteroids and other immunosuppressants which do not always succeed in arresting its evolution. Extracorporeal photochemotherapy has been used in patients with both acute and chronic GvHD.
British Journal of Dermatology | 2013
Pietro Rubegni; L. Feci; Sara Poggiali; G. Marotta; Giuseppina D'Ascenzo; F. Murdaca; Michele Fimiani
Extracorporeal photopheresis (ECP) has been used successfully to treat severe steroid‐refractory acute and chronic graft‐versus‐host disease (aGVHD, cGVHD) since the late 1990s.
Archives of Dermatological Research | 1997
Michele Fimiani; Pietro Rubegni; Maria Laura Flori; C. Mazzatenta; Giuseppina D'Ascenzo; Lucio Andreassi
Journal of The American Academy of Dermatology | 1994
Michele Fimiani; Pietro Rubegni; Giuseppina D'Ascenzo; Lucio Andreassi
International Journal of Immunopathology and Pharmacology | 2006
M. Di Renzo; Anna Laura Pasqui; Pietro Rubegni; Giuseppina D'Ascenzo; G. De Aloe; A. Auteri; Michele Fimiani
Journal Der Deutschen Dermatologischen Gesellschaft | 2008
Maria Rosaria Carcagnì; Giovambattista De Aloe; Giuseppina D'Ascenzo; Pietro Rubegni; Michele Fimiani