Abstract | BACKGROUND: OBJECTIVE: We sought to evaluate the outcome of the use of IVIg in patients with autoimmune mucocutaneous blistering diseases refractory to conventional therapy or with contraindications for it. METHODS: RESULTS: Four (21%) of 19 cases presented a complete response (2 PV, 1 MMP and 1 epidermolysis bullosa acquisita). Five (26%) patients did not respond to the treatment (3 PV, 1 PF, 1 MMP). Ten patients (53%) had a partial response. LIMITATIONS: This was a retrospective noncontrolled study with a heterogeneous group of patients. CONCLUSION: The effectiveness of IVIg was inferior to that previously reported. This difference could be attributed to the preparations employed, the different severity of the disease, or individual responses in each patient dependent on Fc receptor gamma polymorphisms.
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Authors | Sonia Segura, Pilar Iranzo, Isabel Martínez-de Pablo, José Manuel Mascaró Jr, Mercè Alsina, Josep Herrero, Carmen Herrero |
Journal | Journal of the American Academy of Dermatology
(J Am Acad Dermatol)
Vol. 56
Issue 6
Pg. 960-7
(Jun 2007)
ISSN: 1097-6787 [Electronic] United States |
PMID | 17368865
(Publication Type: Journal Article)
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Chemical References |
- Immunoglobulins, Intravenous
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Topics |
- Adult
- Aged
- Autoimmune Diseases
(therapy)
- Epidermolysis Bullosa Acquisita
(therapy)
- Female
- Humans
- Immunoglobulins, Intravenous
(therapeutic use)
- Male
- Middle Aged
- Pemphigoid, Benign Mucous Membrane
(therapy)
- Pemphigus
(therapy)
- Remission Induction
- Retrospective Studies
- Skin Diseases, Vesiculobullous
(therapy)
- Treatment Outcome
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