Results 31 to 40 of about 4,291 (203)

Deciphering the Contribution of BP230 Autoantibodies in Bullous Pemphigoid

open access: yesAntibodies, 2022
Bullous pemphigoid (BP) is a subepidermal autoimmune blistering disease predominantly affecting elderly patients and carries significant morbidity and mortality.
Connor Cole   +2 more
doaj   +1 more source

Bullous pemphigoid in infants: characteristics, diagnosis and treatment [PDF]

open access: yes, 2014
BACKGROUND: Bullous pemphigoid (BP) in infants is a rare but increasingly reported autoimmune blistering skin disease. Autoantibody reactivity is usually poorly characterized. Current guidelines do not address specific aspects of the infantile form of BP.
Agnes Schwieger-Briel   +8 more
core   +2 more sources

Dipeptidyl peptidase IV inhibitor-associated bullous pemphigoid: a recently recognized autoimmune blistering disease with unique clinical, immunological and genetic characteristics

open access: yesImmunological Medicine, 2019
Bullous pemphigoid (BP) is an organ-specific autoantibody-mediated autoimmune blistering skin disorder that tends to affect the elderly. Tense blister formation associated with itchy urticarial erythema is clinically observed in BP, and subepidermal ...
Wataru Nishie
doaj   +1 more source

Human eosinophils express the high affinity IgE receptor, FcεRI, in bullous pemphigoid.

open access: yesPLoS ONE, 2014
Bullous pemphigoid (BP) is an autoimmune blistering disease mediated by autoantibodies targeting BP180 (type XVII collagen). Patient sera and tissues typically have IgG and IgE autoantibodies and elevated eosinophil numbers. Although the pathogenicity of
Kelly N Messingham   +5 more
doaj   +1 more source

Significant Role of Collagen XVII And Integrin beta 4 in Migration and Invasion of The Less Aggressive Squamous Cell Carcinoma Cells [PDF]

open access: yes, 2017
Collagen XVII and integrin alpha 6 beta 4 have well-established roles as epithelial adhesion molecules. Their binding partner laminin 332 as well as integrin alpha 6 beta 4 are largely recognized to promote invasion and metastasis in various cancers, and
Franzke, Claus-Werner   +13 more
core   +9 more sources

Molecular architecture and function of the hemidesmosome [PDF]

open access: yes, 2015
Hemidesmosomes are multiprotein complexes that facilitate the stable adhesion of basal epithelial cells to the underlying basement membrane. The mechanical stability of hemidesmosomes relies on multiple interactions of a few protein components that form ...
Gerhard Wiche   +2 more
core   +3 more sources

Case Report: Prurigo nodularis-like linear IgA/IgG bullous dermatosis: a case report and literature review

open access: yesFrontiers in Immunology, 2023
Linear IgA/IgG bullous dermatosis (LAGBD) is a rare autoimmune subepidermal bullous disorder characterized by linear deposition of concurrent IgA and IgG autoantibodies along the basement membrane zone (BMZ). The clinical features of LAGBD can be diverse,
Yuxi Zhou   +7 more
doaj   +1 more source

Are Anti-BP180 IgG1 or IgG4 Autoantibodies Pathogenic? [PDF]

open access: yesJournal of Investigative Dermatology, 2002
Bullous pemphigoid (BP) is an acquired autoimmune skin disease characterized by autoantibodies against two hemidesmosomal antigens, BP230 (BPAG1) and BP180 (BPAG2) and subepidermal blisters (Stanley et al, 1981; Diaz et al, 1990; Stanley, 1999). In the skin lesions of these patients basal keratinocytes detach from the underlying dermis at the level of ...
openaire   +2 more sources

Case Report: The many faces of bullous pemphigoid

open access: yesFrontiers in Immunology, 2023
The pemphigoid group comprises a number of bullous skin diseases with autoantibodies against different constituents of the basement membrane zone that result in subepidermal detachment and clinically characteristic tense blisters, erosions, urticarial ...
Laura Rechtien   +9 more
doaj   +1 more source

Mixed muco-cutaneous pemphigoid: Clinical and immunological features of 15 cases

open access: yesFrontiers in Immunology, 2023
IntroductionWe describe a series of patients whose auto-immune bullous skin disease (AIBD) of the dermal-epidermal junction (DEJ) was characterized by clinical, immunological and ultrastructural features intermediate between bullous pemphigoid (BP) and ...
Raphaël Janela   +9 more
doaj   +1 more source

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