Anti-intercellular substance antibodies. Presence in serum samples of 14 patients without pemphigus
- 1 January 1983
- journal article
- research article
- Published by American Medical Association (AMA) in Archives of Dermatology
- Vol. 119 (1) , 17-21
- https://doi.org/10.1001/archderm.119.1.17
Abstract
Of 1500 patients whose serum samples were evaluated by indirect immunofluorescence microscopy, 14 had demonstrable titers of anti-intercellular substance (ICS) antibodies in the absence of clinical or histologic evidence of pemphigus. The anti-ICS antibodies were absorbed by A and B blood group antigens in 9 of the 14 patients. In 5 patients, the titers of anti-ICS antibodies were unchanged after absorption with blood substances. All 5 of these patients had cicatricial or bullous pemphigoid on clinical, histologic and immunopathologic examination. Clinical pemphigus did not develop in any of the 14 patients on follow-up examinations conducted for 3-18 mo. Anti-ICS antibodies may be produced in several clinical conditions in which there is damage to the epidermis. These anti-ICS antibodies may not have any pathogenetic activity in vivo, at least within the time limits defined by the follow-up examinations.This publication has 7 references indexed in Scilit:
- Detection of Pemphigoid Antigen, Pemphigus Antigen, and Keratin Filaments by Indirect Immunofluorescence in Cultured Human Epidermal CellsJournal of Investigative Dermatology, 1980
- Complement-fixing intercellular antibodies in a case of cicatricial pemphigoidArchives of Dermatology, 1980
- Coexistence of bullous pemphigoid and systemic lupus erythematosusArchives of Dermatology, 1978
- Pemphigus-like antibodies in bullous pemphigoidArchives of Dermatology, 1977
- Autoimmunity in concurrent myasthenia gravis and pemphigus erythematosusJAMA, 1968
- Autoantibodies in Pemphigus VulgarisJAMA, 1965
- Demonstration of Skin Antibodies in Sera of Pemphigus Vulgaris Patients by Indirect Immunofluorescent Staining.Experimental Biology and Medicine, 1964