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1.
Int J Mol Sci ; 21(8)2020 Apr 22.
Article in English | MEDLINE | ID: mdl-32331328

ABSTRACT

Therapy of multiple sclerosis (MS) with disease-modifying agents such as natalizumab or fingolimod has been associated with the development of cutaneous melanoma. Here we briefly revise literature data and report of a case of a 48-year old woman who developed a melanoma and several atypical naevi after sub sequential treatment with natalizumab (1 year) and fingolimod (7 years). By immunohistochemistry we observed the presence of T cells and leukocyte infiltration as well as of vascular endothelial growth factor (VEGF)-A expression in the patient melanoma biopsy. Then, we analyzed proliferation, migration and VEGF-A expression in three melanoma cell lines and found out that both natalizumab and fingolimod inhibited tumor cell proliferation but promoted or blocked cell migration depending on the cell line examined. VEGF-A secretion was augmented in one melanoma cell line only after fingolimod treatment. In conclusion, our in vitro data do not support the hypothesis of a direct action of natalizumab or fingolimod on melanoma progression but acting on the tumor microenvironment these treatments could indirectly favor melanoma evolution.


Subject(s)
Antirheumatic Agents/therapeutic use , Melanoma/diagnosis , Melanoma/etiology , Multiple Sclerosis/complications , Multiple Sclerosis/therapy , Antirheumatic Agents/adverse effects , Biomarkers , Biopsy , Disease Susceptibility , Female , Fingolimod Hydrochloride/adverse effects , Fingolimod Hydrochloride/therapeutic use , Humans , Immunohistochemistry , Immunosuppressive Agents/adverse effects , Immunosuppressive Agents/therapeutic use , Melanoma/metabolism , Melanoma/therapy , Middle Aged , Multiple Sclerosis/diagnosis , Natalizumab/adverse effects , Natalizumab/therapeutic use , Skin Neoplasms/diagnosis , Skin Neoplasms/etiology , Skin Neoplasms/therapy , Vascular Endothelial Growth Factor A/metabolism , Melanoma, Cutaneous Malignant
2.
Exp Mol Pathol ; 112: 104331, 2020 02.
Article in English | MEDLINE | ID: mdl-31705881

ABSTRACT

BACKGROUND: Significant alterations of the cutaneous microbiota (CM) have been recently demonstrated in bullous pemphigoid (BP). Microbiome data of both oral cavity (OM) and gut (GM) from patients affected by bullous disease are not available yet and, further consistent studies focused on the role of such microbial populations are still missing. OBJECTIVE: Objective: In this pilot study we characterized and compared GM, OM and CM of patients affected by pemphigus vulgaris (PV) and BP to investigate a distinctive microbiome composition in this two rare dermatological disorders. METHODS: High-throughput sequencing of the V1-V3 hyper-variable regions of 16S rRNA was used to compare the bacterial community composition of stool, skin and oral mucosae swabs in a cohort of PV and BP patients. A dedicated bioinformatics software coupled with in-house pipeline was implemented to analyse and compare diseases dataset. RESULTS: GM samples of both PV and BP patients were principally characterized by Firmicutes and Bacteroidetes phyla. Interestingly, the Firmicutes phylum and Staphylococcus genus were mainly represented in cutaneous samples. The diversity of phyla in oral mucosae was higher than those of gut and skin samples and, Bacteroidetes phylum was significantly underrepresented in all PV samples. CONCLUSION: Firmicutes phylum and Staphilococcus genus were the most represented in OM and CM swabs of PV and BP microbial populations. Moreover, we argue the quantitative imbalance linked to the decrease of Bacteriodetes in the oral cavity of PV patients might be associated to disease typical fetor. To shed light on this peculiar feature further studies are still required.


Subject(s)
Gastrointestinal Microbiome/genetics , Pemphigoid, Bullous/genetics , Pemphigus/genetics , Skin/microbiology , Adult , Aged , Aged, 80 and over , Bacteroidetes/genetics , Bacteroidetes/isolation & purification , Female , Firmicutes/genetics , Firmicutes/isolation & purification , High-Throughput Nucleotide Sequencing , Humans , Male , Microbiota/genetics , Middle Aged , Mouth/metabolism , Mouth/microbiology , Pemphigoid, Bullous/microbiology , Pemphigoid, Bullous/pathology , Pemphigus/microbiology , Pemphigus/pathology , RNA, Ribosomal, 16S/genetics , Skin/metabolism
3.
G Ital Dermatol Venereol ; 152(2): 117-121, 2017 Apr.
Article in English | MEDLINE | ID: mdl-26632959

ABSTRACT

BACKGROUND: Lichen sclerosus et atrophicus (LSA) is an inflammatory, mucocutaneous disorder that affects male and especially female with a debilitating impact on the quality of life. Common localization is the anogenital area. If not treated LSA can leave scars, functional impairment and can evolve in squamous cell carcinoma. The first line of treatment is represented by topical, ultra-potent corticosteroids, but often patients are unresponsive; moreover this therapy is frequently associated to relapses of the disease after discontinuation. METHODS: In this prospective observational study, the efficacy of three different treatments - topical calcineurin inhibitors, avocado and soya beans extracts, and methyl aminolevulinate photodynamic therapy (MAL-PDT) - was evaluated, and an effort has been made to define a therapeutic algorithm according to the severity of the disease. RESULTS: Of the 150 patients who were referred to the outpatient clinic for a dermatological and gynecological visit, 33 met the inclusion criteria. Sixteen (88%) patients showed an improvement of the lesion and a reduction of the itch; 3 (16.7%) patients with sever itch and fissurated lesions were evaluated for the MAL-PDT therapy. A total of 9 patients, after accurate examination of the lesions, were treated with MAL-PDT. The totality of the patients experienced a resolution of the lesions. CONCLUSIONS: In the early stages the use of ASE can represent a valid alternative that is well tolerated by the patients reducing the itching, dryness and improving the mucosal texture. The use of MAL-PDT represents a valid treatment in the moderate-severe stages of LSA.


Subject(s)
Anus Diseases/drug therapy , Dermatologic Agents/administration & dosage , Lichen Sclerosus et Atrophicus/drug therapy , Photochemotherapy/methods , Adult , Aged , Aged, 80 and over , Algorithms , Aminolevulinic Acid/administration & dosage , Aminolevulinic Acid/analogs & derivatives , Anus Diseases/pathology , Calcineurin Inhibitors/administration & dosage , Female , Humans , Lichen Sclerosus et Atrophicus/pathology , Male , Middle Aged , Persea/chemistry , Photosensitizing Agents/administration & dosage , Plant Extracts/administration & dosage , Prospective Studies , Quality of Life , Severity of Illness Index , Glycine max/chemistry , Treatment Outcome
4.
J Int Med Res ; 44(1 suppl): 95-99, 2016 Sep.
Article in English | MEDLINE | ID: mdl-27683149

ABSTRACT

OBJECTIVE: To evaluate results of the 'pSORRIDI' experience (which is a prevention campaign to evaluate the prevalence of comorbidities, multidisciplinary needs and appropriateness of the therapeutic approach for comorbidities) in patients already being treated for psoriasis. METHODS: Telephone interviews were conducted in patients with psoriasis, who then underwent comprehensive evaluation and investigation of comorbidities. If necessary, patients were referred to specialist cardiology, endocrinology and/or rheumatology services. RESULTS: Overall, 72.0% (54/75) of patients required a multidisciplinary consultation. Among patients referred to cardiology, therapeutic adjustment was needed in 33.3% (five of 15) patients and a redefined diagnosis in 26.7% (four of 15) cases. Among patients undergoing endocrinology evaluations, therapeutic adjustment and a redefined diagnosis were needed in 61.1% (11/18) and 33.3% (six of 18) patients, respectively; for rheumatology evaluations, therapeutic adjustment and a redefined diagnosis were needed in 76.2% (16/21) and 19.0% (four of 21) of patients, respectively. CONCLUSIONS: Among patients with psoriasis, there may be a need for an improvement in the diagnosis of underlying comorbid conditions, and in disease management of both psoriasis and any comorbid conditions.

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