Snyder Jessica M, Treuting Piper M, Nagy Lee, Yam Cathy, Yi Jaehun, Brasfield Alicia, Nguyen Lisa Phuong Anh, Hajjar Adeline M
Department of Comparative Medicine, University of Washington, Seattle, Washington, United States of America; Comparative Pathology Program, University of Washington, Seattle, Washington, United States of America.
Department of Comparative Medicine, University of Washington, Seattle, Washington, United States of America.
PLoS One. 2014 Sep 17;9(9):e107257. doi: 10.1371/journal.pone.0107257. eCollection 2014.
A humanized TLR7/TLR8 transgenic mouse line was engineered for studies using TLR7/8 ligands as vaccine adjuvants. The mice developed a spontaneous immune-mediated phenotype prior to six months of age characterized by runting, lethargy, blepharitis, and corneal ulceration. Histological examination revealed a marked, multisystemic histiocytic infiltrate that effaced normal architecture. The histological changes were distinct from those previously reported in mouse models of systemic lupus erythematosus. When the mice were crossed with MyD88-/- mice, which prevented toll-like receptor signaling, the inflammatory phenotype resolved. Illness may be caused by constitutive activation of human TLR7 or TLR8 in the bacterial artificial chromosome positive mice as increased TLR7 and TLR8 expression or activation has previously been implicated in autoimmune disease.
构建了一种人源化TLR7/TLR8转基因小鼠品系,用于使用TLR7/8配体作为疫苗佐剂的研究。这些小鼠在6月龄前出现了一种自发的免疫介导表型,其特征为发育迟缓、嗜睡、睑缘炎和角膜溃疡。组织学检查显示有明显的多系统组织细胞浸润,破坏了正常结构。这些组织学变化与先前在系统性红斑狼疮小鼠模型中报道的不同。当这些小鼠与MyD88基因敲除小鼠杂交时,后者可阻止Toll样受体信号传导,炎症表型得以缓解。疾病可能是由细菌人工染色体阳性小鼠中人TLR7或TLR8的组成性激活引起的,因为先前已发现TLR7和TLR8表达或激活增加与自身免疫性疾病有关。