Results 81 to 90 of about 8,038 (216)

SP0119 The evolving role of mepolizumab in egpa [PDF]

open access: yesAnnals of the Rheumatic Diseases, 2018
There is overwhelming evidence that eosinophiles play a key role in the pathogenesis of EGPA. Il-5 is the central cytokine for eosinophil maturation, eosinophil release from the bone marrow and eosinophil survival. Mepolizumab is an antibody neutralising IL-5, which proved efficient in the hypereosinophilic syndrome and eosinophilc asthma, amongst ...
openaire   +1 more source

Blood Leukocyte Characterisation in Eosinophilic Granulomatosis with Polyangiitis (EGPA)

open access: yes
Introduction: Eosinophilic Granulomatosis with Polyangiitis (EGPA) is a rare, autoimmune condition, preceded by asthma and/or chronic rhinosinusitis symptoms, later developing blood and tissue eosinophilia, along with vasculitis and granuloma formation ...
Rebecca B. Dale (22309928)
core   +1 more source

Recalcitrant steroid-resistant EGPA with multisystem involvement

open access: yes, 2017
Eosinophilic granulomatosis with polyangiitis (EGPA) is a multisystem disorder classically characterized by sequential histopathologic and clinical disease phases. An eosinophilic tissue infiltration phase typically precedes the development of a systemic 
Gerard Cox   +4 more
core   +1 more source

A role for IL-33–activated ILC2s in eosinophilic vasculitis

open access: yesJCI Insight, 2021
Eosinophilic granulomatosis with polyangiitis (EGPA) is a rare but serious disease with poorly understood mechanisms. Here, we report that patients with EGPA have elevated levels of TSLP, IL-25, and soluble ST2, which are well-characterized cytokine ...
Maya E. Kotas   +8 more
doaj   +1 more source

181. Tissue immunophenotyping of three refractory cases of EGPA using single cell RNA sequencing

open access: yes, 2022
Background: Eosinophilic granulomatosis with polyangiitis (EGPA) is a multisystem inflammatory disorder currently classified as an Antineutrophil Cytoplasmic Antibody (ANCA) associated vasculitis.
David Jayne1, Matthew Coates1
core   +1 more source

Case Report: Triple autoimmune overlap: rheumatoid arthritis, systemic lupus erythematosus, and hypereosinophilic asthma with systemic manifestations

open access: yesFrontiers in Immunology
BackgroundOverlap between rheumatoid arthritis (RA) and systemic lupus erythematosus (SLE) (“rhupus”) is recognized, but coexistence with a severe eosinophilic asthma syndrome is exceptionally rare. We describe a triple autoimmune overlap of RA, SLE, and
Ji Li   +7 more
doaj   +1 more source

Eosinophilic granulomatosis with polyangiitis (Churg-Strauss) (EGPA) Consensus Task Force recommendations for evaluation and management [PDF]

open access: yes, 2015
Objective To develop disease-specific recommendations for the diagnosis and management of eosinophilic granulomatosis with polyangiitis (Churg-Strauss syndrome) (EGPA).
Bottero, P.   +46 more
core   +1 more source

PO:36:244 | Early diagnosis in eosinophilic granulomatosis with polyangiitis: a multidisciplinary approach

open access: yesReumatismo
Background. Early diagnosis of Eosinophilic Granulomatosis with Polyangiitis (EGPA) remains one of the major unmet needs in clinical practice due to the non-specific nature of prodromal symptoms and the lack of specific biomarkers, particularly in ...
Società Italiana di Reumatologia
doaj  

Eosinophilic Granulomatosis with Polyangiitis (EGPA)

open access: yesActa Medica, 2021
Abdurrahman Tufan, Hazan Karadeniz
openaire   +2 more sources

A new cytological approach to improve the final diagnosis of Eosinophilic Granulomatosis with Polyangiitis (EGPA)

open access: yes, 2017
Introduction: Eosinophilic granulomatosis with polyangiitis (EGPA) is an uncommon systemic necrotizing vasculitis that affects small to medium sized vessels and is associated with severe asthma, allergic rhinitis, nasal polyposis and blood and tissue ...
AGOSTINI, CARLO   +9 more
core   +1 more source

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