Publications by authors named "Irene Gallais-Serezal"

Article Synopsis
  • Rituximab (RTX) is a key treatment for various autoimmune and chronic inflammatory diseases but increases the risk of severe infections and lowers vaccine effectiveness due to its impact on B cell responses.
  • During the COVID-19 pandemic, RTX-treated patients faced heightened disease severity, which led to delays or avoidance of RTX treatments to protect against SARS-CoV-2 infections.
  • A study of thirteen patients showed that while some had positive T cell responses post-vaccination, those recently treated with RTX had significantly lower antibody responses, suggesting a need for caution in timing vaccinations relative to RTX infusions to optimize immune protection.
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Article Synopsis
  • The study aimed to evaluate the experiences and perceptions of patients with atopic dermatitis (AD) regarding dupilumab treatment from January 2017 to December 2021.
  • A total of 82 patients participated, with 77 completing a questionnaire on their treatment experience, including satisfaction levels and injection methods.
  • The results indicated that dupilumab provided high patient satisfaction (mean score of 7.5) and a lower treatment burden, although 47% experienced a wearing-off of its beneficial effects.
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  • Relapses of psoriasis are linked to tissue-resident memory T cells that produce specific cytokines, which play a key role in maintaining inflammation in the skin.* -
  • Research using gas chromatography/mass spectrometry shows that the fatty acid composition of skin differs between healthy individuals and normal-looking skin in psoriasis patients, yet there’s no significant difference between nonlesional and resolved skin.* -
  • Higher levels of oleic acid in resolved skin correlate with a lower activation of IL-17 in T cells, suggesting that adjusting fatty acid levels could be a potential therapeutic strategy for managing inflammatory skin diseases.*
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Although retinoids are considered as the most effective treatment, management of dissecting cellulitis of the scalp (DCS) is often challenging. A multicentre retrospective study was conducted to evaluate the efficacy of anti-tumour necrosis factor (TNF) agents in treating DCS after failure of other conventional treatments. Twenty-six patients were included.

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Psoriasis (PsO) and psoriatic arthritis (PsA), together known as psoriatic disease (PsD), are immune-mediated diseases with a chronic and relapsing course that affect the skin, the joints or both. The pathophysiology of PsO is complex and involves abnormal expression of keratinocytes and infiltration of the skin with dendritic cells, macrophages, neutrophils and T lymphocytes. Around 30% of patients with PsO develop arthritis with axial and/or peripheral manifestations.

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Article Synopsis
  • Dissecting cellulitis of the scalp (DCS) is a rare and hard-to-treat inflammatory condition affecting the scalp, which is often resistant to standard therapies.
  • A study involving nine patients who had DCS and were treated with TNF inhibitors showed promising results, with significant reductions in symptoms and improvements in quality of life.
  • The findings suggest that TNF inhibitors can be effective in managing DCS for patients who do not respond to conventional treatments.
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Persistent and impaired inflammation impedes tissue healing and is a characteristic of chronic wounds. A better understanding of the mechanisms controlling wound inflammation is needed. In this study, we show that in human wound-edge keratinocytes, the expressions of microRNA (miR)-17, miR-18a, miR-19a, miR-19b, and miR-20a, which all belong to the miR-17∼92 cluster, are upregulated during wound repair.

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Psoriasis is an inflammatory disease that arises in genetically predisposed individuals. Chronic skin lesions that contain activated immune cells can persist for years. Systemic inhibition of TNF, IL-17 and IL-23 cytokines has revolutionized psoriasis care during the recent decades.

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The human skin hosts innumerable microorganisms and maintains homeostasis with the local immune system despite the challenges offered by environmental factors such as ultraviolet radiation (UVR). UVR causes cutaneous alterations such as acute (i.e.

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Venous ulcers are the most common type of human chronic nonhealing wounds and are stalled in a constant and excessive inflammatory state. The molecular mechanisms underlying the chronic wound inflammation remain elusive. Moreover, little is known about the role of regulatory RNAs, such as microRNAs, in the pathogenesis of venous ulcers.

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An increasing number of studies reveal the importance of long noncoding RNAs (lncRNAs) in gene expression control underlying many physiological and pathological processes. However, their role in skin wound healing remains poorly understood. Our study focused on a skin-specific lncRNA, LOC105372576, whose expression was increased during physiological wound healing.

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Background: Resident T cells are implicated in the maintenance and recurrence of psoriatic lesions. Whether skin that has not yet experienced psoriasis in patients with established disease harbors pathogenic T cells is less investigated.

Objective: We sought to analyze the composition of resident T cells and T cell-driven tissue responses in skin never affected by psoriasis from patients with mild disease.

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Psoriasis is driven by focal disruptions of the immune-homeostasis in human skin. Local relapse following cessation of therapy is common and unpredictable, which complicates clinical management of psoriasis. We have previously shown that pathogenic resident T cells accumulate in active and resolved psoriasis, but whether these cells drive psoriasiform tissue reactions is less clear.

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Tissue-resident memory T (Trm) cells form a heterogeneous population that provides localized protection against pathogens. Here, we identify CD49a as a marker that differentiates CD8 Trm cells on a compartmental and functional basis. In human skin epithelia, CD8CD49a Trm cells produced interferon-γ, whereas CD8CD49a Trm cells produced interleukin-17 (IL-17).

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Epidermal Langerhans cells (LCs) are spatially separated from dermal dendritic cells (DCs) in healthy human skin. In active psoriasis, maintained by local production of IL-23 and IL-17, inflammatory DCs infiltrate both skin compartments. Here we show that CCR2 epidermal DCs (eDCs) were confined to lesional psoriasis and phenotypically distinct from dermal DCs.

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Hereditary angioedema (HAE) is a rare genetic disorder that is primarily caused by a defect in the C1 inhibitor (C1-INH). The recurrent symptoms are subcutaneous edema and abdominal pain. Laryngeal edema, which can also occur, is life threatening if it goes untreated.

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