人性化鼠标
发病机制
甲状腺炎
免疫学
医学
免疫系统
自身免疫性疾病
疾病
自身免疫性甲状腺炎
自身免疫
遗传模型
基因检测
甲状腺
动物模型
桥本病
多系统疾病
免疫
人类疾病
基因
遗传倾向
计算生物学
模式生物
自身抗体
生物信息学
临床疾病
作者
Aizhan Kozhakhmetova,Mihaela Stefan-Lifshitz,Olga Meshcheryakova,Yaron Tomer
出处
期刊:Genes
[Multidisciplinary Digital Publishing Institute]
日期:2026-01-31
卷期号:17 (2): 170-170
标识
DOI:10.3390/genes17020170
摘要
BACKGROUND: Experimental autoimmune thyroiditis is an important animal model for studying Hashimoto's thyroiditis. Our aim was to develop the model using CBA/J-DR3 mice expressing human HLA-DR3, which is associated with autoimmune thyroiditis in humans, to better simulate human autoimmune thyroiditis. Such a humanized model can be used to test specific antigen therapies for autoimmune thyroiditis. METHODS: CBA/J-DR3 mice were produced by back-crossing B6-DR3 mice to the CBA/J background. Female CBA/J-DR3 mice were immunized with human thyroglobulin (Tg) in complete Freund's adjuvant on days 0 and 7. On day 21, mice were sacrificed, blood collected, spleen and thyroid harvested for analysis. Splenocytes were analyzed for T cell responses to Tg and its major T-cell epitope in human autoimmune thyroiditis, Tg.2098. Serum anti-thyroglobulin antibodies were measured by ELISA, and thyroid-stimulating hormone was measured using the Luminex assay. Thyroid histology and immunohistochemistry were examined. RESULTS: < 0.0001). T cells demonstrated higher reactivity to thyroid antigens by enhanced production of pro-inflammatory cytokines. Thyroid immunohistochemistry revealed mild CD3-positive T-cell infiltration. CONCLUSIONS: This novel humanized CBA/J-DR3 mouse model of Hashimoto's thyroiditis demonstrates key features of human autoimmune thyroiditis. The HLA-DR3 background and the immune response to Tg and Tg.2098 enhance translational relevance, making this a valuable model for studying thyroid disease pathogenesis and testing targeted immune-modifying therapies.
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