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Dive into the research topics where M. C. Colanardi is active.

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Featured researches published by M. C. Colanardi.


Clinical & Experimental Allergy | 2004

Desloratadine in combination with montelukast in the treatment of chronic urticaria: a randomized, double‐blind, placebo‐controlled study

E. Nettis; M. C. Colanardi; M. T. Paradiso; A. Ferrannini

Background Chronic urticaria (CU) is a common skin condition. It is frequently a disabling disease due to the persistency of clinical symptoms, the unpredictable course and negative influence on the quality of life.


Contact Dermatitis | 2002

Occupational irritant and allergic contact dermatitis among healthcare workers

E. Nettis; M. C. Colanardi; Anna Lucia Soccio; A. Ferrannini; A. Tursi

Contact dermatitis is the most frequent occupational dermatosis and non‐specific irritants in addition to specific Type IV sensitization are involved. We reviewed our database for data from 1994 to 1998 and selected 360 consecutive patients working in healthcare environments and experiencing contact dermatitis at their hands, wrists and forearms. We found that allergic contact dermatitis and irritant contact dermatitis were considered to be work‐related in 16.5% (72/436) and 44.4% (194/436) of diagnoses, respectively. Occupational irritant contact dermatitis is due to exposure to a wide range of irritants in the workplace, such as soaps, solvents, cleansers and protective gloves, which conspire to remove the surface lipid layer and/or produce cellular damage. In this study the major relevant aetiological agents that induced occupational allergic contact dermatitis were: nickel sulphate (41 patch positivities), components of disinfectants [glutaraldehyde ( 5 ) and benzalkonium chloride ( 7 )] and rubber chemicals [thiuram mix ( 15 ), carba mix ( 9 ) and tetramethylthiuram monosulphide ( 6 )]. The best treatment for allergic contact dermatitis is to avoid those allergens causing the rash. Whenever this is not possible, contact with them needs to be reduced using properly selected protective gloves. Finally, subjects with atopic dermatitis should avoid ‘wet work’ and contact with irritants, because atopic dermatitis is significantly associated with irritant contact dermatitis.


Blood | 2008

Validation of PDGFRβ and c-Src tyrosine kinases as tumor/vessel targets in patients with multiple myeloma: preclinical efficacy of the novel, orally available inhibitor dasatinib

Addolorata Coluccia; Teresa Cirulli; Paola Neri; Domenica Mangieri; M. C. Colanardi; Antonio Gnoni; Nicola Di Renzo; Franco Dammacco; Pierfrancesco Tassone; Domenico Ribatti; Carlo Gambacorti-Passerini; Angelo Vacca

Inhibition of multiple myeloma (MM) plasma cells in their permissive bone marrow microenvironment represents an attractive strategy for blocking the tumor/vessel growth associated with the disease progression. However, target specificity is an essential aim of this approach. Here, we identified platelet-derived growth factor (PDGF)-receptor beta (PDGFRbeta) and pp60c-Src as shared constitutively activated tyrosine-kinases (TKs) in plasma cells and endothelial cells (ECs) isolated from MM patients (MMECs). Our cellular and molecular dissection showed that the PDGF-BB/PDGFRbeta kinase axis promoted MM tumor growth and vessel sprouting by activating ERK1/2, AKT, and the transcription of MMEC-released proangiogenic factors, such as vascular endothelial growth factor (VEGF) and interleukin-8 (IL-8). Interestingly, pp60c-Src TK-activity was selectively induced by VEGF in MM tumor and ECs, and the use of small-interfering (si)RNAs validated pp60c-Src as a key signaling effector of VEGF loop required for MMEC survival, migration, and angiogenesis. We also assessed the antitumor/vessel activity of dasatinib, a novel orally bioactive PDGFRbeta/Src TK-inhibitor that significantly delayed MM tumor growth and angiogenesis in vivo, showing a synergistic cytotoxicity with conventional and novel antimyeloma drugs (ie, melphalan, prednisone, bor-tezomib, and thalidomide). Overall data highlight the biologic and therapeutic relevance of the combined targeting of PDGFRbeta/c-Src TKs in MM, providing a framework for future clinical trials.


British Journal of Dermatology | 2007

Double-blind, placebo-controlled study of sublingual immunotherapy in patients with latex-induced urticaria: a 12-month study

E. Nettis; M. C. Colanardi; Anna Lucia Soccio; M. Marcandrea; L. Pinto; A. Ferrannini; A. Tursi; Angelo Vacca

Background  Natural rubber latex (NRL) allergy is a worldwide problem. Although prevention is sufficient to reduce sensitization, prolonged avoidance is needed to prevent resensitization or adverse reactions on re‐exposure.


British Journal of Dermatology | 2006

Levocetirizine in the treatment of chronic idiopathic urticaria: a randomized, double-blind, placebo-controlled study

E. Nettis; M. C. Colanardi; L. Barra; A. Ferrannini; Angelo Vacca; A. Tursi

Background  Chronic urticaria is a common skin condition. It is frequently a disabling disease because of the persistence of clinical symptoms, the unpredictable course and its negative influence on the quality of life.


British Journal of Dermatology | 2004

Sodium benzoate‐induced repeated episodes of acute urticaria/angio‐oedema: randomized controlled trial

E. Nettis; M. C. Colanardi; A. Ferrannini; A. Tursi

Background  Sodium benzoate (E 211) is widely used to delay yeast spoilage of acidic foods and beverages. Numerous cases of adverse reactions to benzoate have been recorded, but most of the studies that have been conducted lacked proper placebo controls or blinding.


British Journal of Dermatology | 2006

Desloratadine in combination with montelukast suppresses the dermographometer challenge test papule, and is effective in the treatment of delayed pressure urticaria: a randomized, double-blind, placebo-controlled study.

E. Nettis; M. C. Colanardi; Anna Lucia Soccio; A. Ferrannini; Angelo Vacca

Background  Delayed pressure urticaria (DPU) comes under the heading of physical urticaria. Characteristically itchy, tender or painful weals occur at sites of local pressure including the waistband, soles of the feet and palms of the hands. Lesion onset is typically 3–12 h after the application of pressure, and lesions may persist for more than 24 h. The treatment of DPU is often unsatisfactory.


Current Drug Targets - Immune, Endocrine & Metabolic Disorders | 2003

Drug-induced aseptic meningitis.

E. Nettis; Gianfranco Calogiuri; M. C. Colanardi; A. Ferrannini; A. Tursi

Aseptic meningitis is a rare but well-recognized complication of drug therapy. The clinical presentation of drug-induced aseptic meningitis (DIAM) is distinct. Symptoms typically include fever, neck stiffness, headache, confusion, nausea and vomiting. The major categories of causative agents are non-steroidal anti-inflammatory drugs, antimicrobials and also intravenous immunoglobulins, monoclonal antibodies and vaccines. These drugs most commonly implicated as causes of aseptic meningitis act more likely through an immunological mechanisms. However, the exact pathogenetic mechanism of DIAM is still unknown. The diagnosis of drug-induced aseptic meningitis is difficult and infectious etiologies must be excluded. In some cases the diagnosis has been confirmed by rechallenging the patient with the suspected agent. In this case, informed written consent is necessary and rechallenge must be medically supervised both to document the response and to offer medical care and advice, if required. The outcome of DIAM is generally good, usually without long term sequelae.


Allergy | 2003

Results of standard series patch testing in patients with occupational allergic contact dermatitis.

E. Nettis; M. Marcandrea; M. C. Colanardi; M. T. Paradiso; A. Ferrannini; A. Tursi

Background:  In the workplace, the skin is at high risk of exposure to chemicals and other contaminants, and occupational dermatitis is an important field of study.


Clinical & Experimental Allergy | 2003

Suspected tartrazine‐induced acute urticaria/angioedema is only rarely reproducible by oral rechallenge

E. Nettis; M. C. Colanardi; A. Ferrannini; A. Tursi

Background Tartrazine has been frequently linked to several diseases. However, a cause‐and‐effect role for tartrazine in these illnesses, especially in urticaria, has not always been established.

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