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1.
Infect Dis Rep ; 13(1): 23-25, 2021 Jan 01.
Article in English | MEDLINE | ID: mdl-33401389

ABSTRACT

The main localization of SARS-CoV-2 infection is the respiratory tract. Digestive and otorhinolaryngological localizations are also reported. More recently, dermatological manifestations have been reported during Coronavirus disease-19 (COVID-19). We report a case of a labial angioedema in a patient with confirmed COVID-19.

2.
Acta Derm Venereol ; 99(12): 1143-1147, 2019 Nov 01.
Article in English | MEDLINE | ID: mdl-31449317

ABSTRACT

Exosomes are involved in modulating the immune system and mediating communication between cells. The aim of this study was to investigate the involvement of exosomes in psoriasis. Exosomes from patients with psoriasis were analysed by nanoparticle tracking analysis and protein expression was analysed by western blotting. The concentration of HSP70 was determined by an enzyme-linked immunosorbent assay, and concentrations of interleukin (IL)-1ß, IL-2, IL-6, IL-10, IL-17A and tumour necrosis factor alpha (TNF-α) were determined by flow cytometry. Based on the severity of psoriasis, evaluated by body surface area (≤ 10% vs. > 10%), 2 groups of patients were compared (49 with mild psoriasis and 71 with moderate-to-severe psoriasis). The number (2.52×1011 ± 2.29×1010 vs. 1.79×1011 ± 1.93×1010, p = 0.19) and size (94.44 ± 22.00 nm vs. 96.87 ± 28.30 nm, p = 0.72) of exosomes and the concentration of HSP70 in the exosomes were not significantly different in the 2 groups of patients. IL-17A exosome levels were significantly higher in patients with moderate-to-severe psoriasis compared with those with mild psoriasis (p = 0.02). There were no significant differences in levels of TNF-α, IL-1, IL-2, IL-6 and IL-10. This study shows, for the first time, the presence of circulating exosomes in patients with psoriasis. These data confirm the involvement of circulating exosomes in psoriasis, in particular in moderate-to-severe psoriasis, through IL-17A-producing exosomes.


Subject(s)
Exosomes/metabolism , Interleukin-17/blood , Psoriasis/blood , Adolescent , Adult , Aged , Aged, 80 and over , Biomarkers/blood , Exosomes/immunology , Female , Humans , Male , Middle Aged , Prospective Studies , Psoriasis/diagnosis , Psoriasis/immunology , Severity of Illness Index , Up-Regulation , Young Adult
3.
Presse Med ; 46(9): 808-817, 2017 Sep.
Article in French | MEDLINE | ID: mdl-28683958

ABSTRACT

Monoclonal antibodies targeted against the immune checkpoint molecules CTLA-4 and PD-1 have recently obtained approval for the treatment of metastatic melanoma and advanced/refractory non small-cell lung cancers and metastatic renal cancer. Besides their efficacy profile, these immune targeted agents also generate immune-related adverse events that may be life threatening if not anticipated and managed appropriately. This new family of dysimmune toxicities remains largely unknown to the broad oncology community. We propose here some practical guidelines for the oncologist to help in the clinical care of patients under immune checkpoint molecules.


Subject(s)
Antibodies, Monoclonal/adverse effects , Antibodies, Monoclonal/therapeutic use , CTLA-4 Antigen/antagonists & inhibitors , Carcinoma, Non-Small-Cell Lung/drug therapy , Carcinoma, Non-Small-Cell Lung/genetics , Carcinoma, Renal Cell/drug therapy , Carcinoma, Renal Cell/genetics , Genes, cdc/drug effects , Immunotoxins/adverse effects , Immunotoxins/therapeutic use , Kidney Neoplasms/drug therapy , Kidney Neoplasms/genetics , Lung Neoplasms/drug therapy , Lung Neoplasms/genetics , Melanoma/drug therapy , Melanoma/genetics , Programmed Cell Death 1 Receptor/antagonists & inhibitors , Skin Neoplasms/drug therapy , Skin Neoplasms/genetics , CTLA-4 Antigen/genetics , Carcinoma, Non-Small-Cell Lung/pathology , Carcinoma, Renal Cell/pathology , Guideline Adherence , Kidney Neoplasms/pathology , Lung Neoplasms/pathology , Neoplasm Metastasis , Programmed Cell Death 1 Receptor/genetics , Skin Neoplasms/pathology
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