Pemphigus vulgaris (PV) is an autoimmune bullous skin disease where tolerance to the
desmosomal protein desmoglein 3 (Dsg3), and perhaps additional epidermal targets, is lost …

Pemphigus vulgaris (PV) is an autoimmune disease characterized by the presence of IgG
autoantibodies against desmoglein-3. Despite the variety of findings, the chemokine and …

Bullous pemphigoid (BP) is the most common autoimmune bullous disease, characterized
by severe pruritus and skin blistering. The loss of tolerance against Collagen XVII, also …

Pemphigus represents a group of rare and severe autoimmune intra-epidermal blistering
diseases affecting the skin and mucous membranes. These painful and debilitating diseases …

The loss of balance between regulatory T (Treg) and T helper 17 (Th17) causes loss of
tolerance against desmoglein (Dsg)-3 leading to pemphigus vulgaris (PV), an autoimmune …

Pemphigus vulgaris (PV) is a blistering skin disorder mediated by autoantibodies targeting
the epidermal adhesion molecule desmoglein 3 (Dsg3). As Th2‐associated cytokines are …

Pemphigus is a complex dermatologic autoimmune bullous disease whose pathogenic
mechanism is not fully understood. Anti-desmoglein-1 (Dsg1) and anti-Dsg3 autoantibodies …

Background TH 2 cells were thought to be a pivotal factor for initiation of the autoimmune
blistering disease pemphigus. However, the role of other T-cell subsets in pemphigus …

Pemphigus is a rare and life-threatening group of blistering autoimmune diseases that
affects the skin and mucous membranes. There are two major subtypes of pemphigus …

Pemphigus vulgaris (PV) and bullous pemphigoid (BP) are two major subtypes of
autoimmune bullous diseases (AIBD), characterized by blisters and erosions of skin and/or …