2023
DOI: 10.3389/fimmu.2023.1214011
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Case Report: Biological treatment of epidermolysis bullosa acquisita: report on four cases and literature review

Abstract: Epidermolysis bullosa acquisita (EBA) is a chronic, recurrent autoimmune subepidermal bullous disease characterized by the presence of autoantibodies targeting type VII collagen -- basement membrane zone antigen. Standard therapy for EBA includes a combination of systemic corticosteroids and dapsone; however, severe cases may require advanced treatment. The current article reports on four EBA cases in which biologics: infliximab, rituximab (Rtx), and intravenous immunoglobulin (IVIG) were applied. All patients… Show more

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Cited by 4 publications
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“…Epidermolysis bullosa acquisita (EBA) pertains to the category of AIBD, representing a rare disease distinguished by a heterogeneous clinical manifestation and the occurrence of autoantibodies directed against collagen VII. Conventional therapeutic interventions involve the administration of glucocorticosteroids (GCS) and dapsone (DP); however, in instances of heightened severity, more sophisticated treatment modalities may be employed [4][5][6].…”
Section: Introductionmentioning
confidence: 99%
“…Epidermolysis bullosa acquisita (EBA) pertains to the category of AIBD, representing a rare disease distinguished by a heterogeneous clinical manifestation and the occurrence of autoantibodies directed against collagen VII. Conventional therapeutic interventions involve the administration of glucocorticosteroids (GCS) and dapsone (DP); however, in instances of heightened severity, more sophisticated treatment modalities may be employed [4][5][6].…”
Section: Introductionmentioning
confidence: 99%