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Article

Experimental models for the autoimmune and inflammatory blistering disease, Bullous pemphigoid.

Archives of dermatological research - 1 Nov 2007

Leighty Lisa, Li Ning, Diaz Luis A, Liu Zhi

Abstract excerpt

Bullous pemphigoid (BP) is a subepidermal skin blistering disease characterized immunohistologically by dermal-epidermal junction (DEJ) separation, an inflammatory cell infiltrate in the upper dermis, and autoantibodies targeted toward the hemidesmosomal proteins BP230 and BP180. Development of a...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

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Identifiers

PMID: 17879094
DOI: 10.1007/s00403-007-0790-5
PMCID: PMC2064945

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-17879094-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

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Experimental models for the autoimmune and inflammatory blistering disease, Bullous pemphigoid.PMID 17879094Read ↗

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Deletion of the major bullous pemphigoid epitope region of collagen XVII induces blistering, autoimmunization, and itching in mice.Semantic proximity Read ↗

The role of antibody class and target on subepidermal blistering disease phenotype and management.Semantic proximity Read ↗

Bullous Pemphigoid: Trigger and Predisposing Factors.Semantic proximity Read ↗

Autoreactive T and B cells from bullous pemphigoid (BP) patients recognize epitopes clustered in distinct regions of BP180 and BP230.Semantic proximity Read ↗

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