Your browser doesn't support javascript.
loading
A case of spontaneous autoimmune skin disease in a cynomolgus monkey (Macaca fascicularis).
Onishi, Shinichi; Nakagawa, Minto; Matsuo, Saori; Shinozuka, Junko; Hiramatsu, Mio; Isobe, Takehito; Watanabe, Toshihiko; Kato, Atsuhiko.
Affiliation
  • Onishi S; Translational Research Division, Chugai Pharmaceutical Co., Ltd., 1-135 Komakado, Gotemba, Shizuoka 412-8513, Japan.
  • Nakagawa M; Translational Research Division, Chugai Pharmaceutical Co., Ltd., 1-135 Komakado, Gotemba, Shizuoka 412-8513, Japan.
  • Matsuo S; Translational Research Division, Chugai Pharmaceutical Co., Ltd., 1-135 Komakado, Gotemba, Shizuoka 412-8513, Japan.
  • Shinozuka J; Translational Research Division, Chugai Pharmaceutical Co., Ltd., 1-135 Komakado, Gotemba, Shizuoka 412-8513, Japan.
  • Hiramatsu M; Chugai Research Institute for Medical Science, Inc., 1-135, Komakado, Gotemba, Shizuoka 412-8513, Japan.
  • Isobe T; Research Division, Chugai Pharmaceutical Co., Ltd., 1-135 Komakado, Gotemba, Shizuoka 412-8513, Japan.
  • Watanabe T; Research Division, Chugai Pharmaceutical Co., Ltd., 1-135 Komakado, Gotemba, Shizuoka 412-8513, Japan.
  • Kato A; Translational Research Division, Chugai Pharmaceutical Co., Ltd., 1-135 Komakado, Gotemba, Shizuoka 412-8513, Japan.
J Toxicol Pathol ; 35(1): 103-106, 2022 Jan.
Article de En | MEDLINE | ID: mdl-35221502
Pemphigus is an autoimmune blistering disease characterized by lesions on the skin and mucous membranes. To date, no spontaneous cases of this disease have been reported in cynomolgus monkeys. This report describes the histopathological characteristics of spontaneous pemphigus in a cynomolgus monkey. Macroscopically, redness and scaling with pruritus were observed on the skin of the entire body. Histopathologically, the epidermis showed intercellular edema, and eosinophils and mononuclear cells infiltrated the epidermis. There was no obvious acantholysis in the epidermis. The perivascular area showed edema, and eosinophils and mononuclear cells infiltrated the vessels in the dermis. Immunohistochemically, the intercellular area in the epidermis was positive for Immunoglobulin G and Complement component 3. Serologically, anti-desmoglein 1 and desmoglein 3 antibodies in the serum were negative. From these findings, this case was diagnosed as an autoimmune skin disease, suspected to be pemphigus, and concluded as lesions being similar to those in human "pemphigus herpetiformis".
Mots clés

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Langue: En Journal: J Toxicol Pathol Année: 2022 Type de document: Article Pays d'affiliation: Japon Pays de publication: Japon

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Langue: En Journal: J Toxicol Pathol Année: 2022 Type de document: Article Pays d'affiliation: Japon Pays de publication: Japon