Stead Family Department of Pediatrics, Carver College of Medicine, University of Iowa, Iowa City, IA 52242, USA.
Immunology Graduate Program, University of Iowa, Iowa City, IA 52242, USA.
Int J Mol Sci. 2020 Dec 13;21(24):9478. doi: 10.3390/ijms21249478.
Sjögren syndrome (SS) is an immunologically complex, chronic autoimmune disease targeting lacrimal and salivary glands. Nonobese diabetic (NOD) mice spontaneously develop inflammation of lacrimal and salivary glands with histopathological features similar to SS in humans including focal lymphocytic infiltrates in the affected glands. The innate immune signals driving lymphocytic infiltration of these glands are not well-defined. Here we evaluate the role of Toll-like receptor (TLR) 7 in the development of SS-like manifestations in NOD mice. We created a knockout NOD mouse strain and performed histological and gene expression studies to characterize the effects of TLR7 on autoimmunity development. TLR7 was required for male-specific lacrimal gland inflammation but not for female-specific salivary gland inflammation. Moreover, TLR7 was required for type 1 diabetes development in male but not female NOD mice. RNA sequencing demonstrated that TLR7 was associated with a type I interferon (IFN) response and a type I IFN-independent B cell response in the lacrimal glands. Together these studies identify a previously unappreciated pathogenic role for TLR7 in lacrimal gland autoimmunity and T1D development in male NOD mice adding to the growing body of evidence supporting sex differences in mechanisms of autoimmune disease in NOD mice.
干燥综合征(SS)是一种免疫复杂的慢性自身免疫性疾病,以泪腺和唾液腺为靶器官。非肥胖型糖尿病(NOD)小鼠自发发生泪腺和唾液腺炎症,其组织病理学特征与人 SS 相似,包括受影响腺体的局灶性淋巴细胞浸润。目前尚不清楚驱动这些腺体淋巴细胞浸润的先天免疫信号。在这里,我们评估了 Toll 样受体(TLR)7 在 NOD 小鼠发生 SS 样表现中的作用。我们创建了 TLR7 敲除 NOD 小鼠品系,并进行了组织学和基因表达研究,以表征 TLR7 对自身免疫发展的影响。TLR7 是男性特异性泪腺炎症所必需的,但不是女性特异性唾液腺炎症所必需的。此外,TLR7 是男性 NOD 小鼠而非女性 NOD 小鼠发生 1 型糖尿病所必需的。RNA 测序表明,TLR7 与泪腺中的 I 型干扰素(IFN)反应和 I 型 IFN 非依赖性 B 细胞反应有关。这些研究共同确定了 TLR7 在男性 NOD 小鼠的泪腺自身免疫和 T1D 发展中的先前未被认识到的致病作用,这增加了越来越多的证据支持 NOD 小鼠自身免疫疾病机制中的性别差异。