Results 31 to 40 of about 178,684 (248)

Emerging Role of Dipeptidyl Peptidase-4 in Autoimmune Disease

open access: yesFrontiers in Immunology, 2022
Dipeptidyl-peptidase IV (DPP4), originally identified as an aminopeptidase in 1960s, is an ubiquitously expressed protease presented as either a membrane-bound or soluble form.
Jie Huang   +7 more
doaj   +1 more source

Canakinumab for the treatment of autoinflammatory very early onset- inflammatory bowel disease

open access: yesFrontiers in Immunology, 2022
IntroductionTherapeutic options are critically needed for children with refractory very early onset inflammatory bowel disease (VEO-IBD). Our aim was to evaluate clinical response to canakinumab, an anti-IL-1β monoclonal antibody, in patients with VEO ...
Eliana Shaul   +13 more
doaj   +1 more source

Systemic autoinflammatory disorders

open access: yesClinical and Experimental Pediatrics, 2023
Inflammation is a physiologic defense mechanism against an out-side attack. Usually, it resolves after the removal of noxious causes, but systemic autoinflammatory disorders (SAIDs) have recurrent or repeated acute inflammation through uncontrolled gene function, which can present as gain-of-function or loss-of-function of a gene during inflammation ...
openaire   +3 more sources

Severe osteoarticular involvement in isotretinoin-triggered acne fulminans: two cases successfully treated with anakinra. [PDF]

open access: yes, 2017
Acne fulminans (AF) is a severe form of inflammatory and ulcerated acne associated with fever, malaise, joint swellings and polyarthralgia.1 Osteoarticular lesions are often described and can be radiologically indistinguishable from those observed in
Barbareschi   +9 more
core   +1 more source

The autoinflammatory diseases

open access: yesSwiss Medical Weekly, 2012
The monogenic autoinflammatory syndromes are conditions caused by mutations of genes coding for proteins that play a pivotal role in the regulation of the inflammatory response. Due to their genetic nature, most of these disorders have an early onset.
S Federici, R Caorsi, M Gattorno
openaire   +4 more sources

Autoimmunity, Autoinflammation, and Infection in Uveitis [PDF]

open access: yes, 2018
Funding/Support: No funding or grant support. Financial Disclosures: John V. Forrester has received an honorarium for lecturing from Janssen (London, UK). Lucia Kuffova has undertaken consultancy work for Abbvie (London, UK). Andrew D.
Dick, Andrew D.   +2 more
core   +4 more sources

HLA Class I or Class II and Disease Association: Catch the Difference if You Can [PDF]

open access: yes, 2017
The association of autoimmune diseases with HLA has been known for many decades. To date, however, the underlying mechanisms have not been fully understood. The recently introduced genome-wide association studies (GWAS) have suggested that several genes
Fiorillo, Mt   +3 more
core   +7 more sources

Spectrum of Genetic Autoinflammatory Diseases Presenting with Cutaneous Symptoms

open access: yesActa Dermato-Venereologica, 2020
Autoinflammatory diseases comprise a group of chronic disabling entities characterized by inflammation without the presence of infectious agents, auto-antibodies or antigen-specific T-cells. Many autoinflammatory diseases are caused by monogenic defects,
Hanna Bonnekoh   +5 more
doaj   +1 more source

Vasculitis associated with adenosine deaminase 2 deficiency: at the crossroads between Behçet’s disease and autoinflammation. A viewpoint

open access: yesReumatismo, 2023
Adenosine deaminase 2 deficiency (DADA2) is a rare monogenic vasculopathy caused by loss-of-function homozygous or compound heterozygous mutations in ADA2, formerly CECR1 (cat eye syndrome chromosome region 1) gene.
A. Colangelo   +5 more
doaj   +1 more source

Could pentraxin-3 be a new marker for subclinical inflammation in familial Mediterranean fever? [PDF]

open access: yes, 2015
Not ...
Evrengül, Harun   +3 more
core   +1 more source

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