Ohashi Y, So S K, Minasi P N, Tabbara K F
Invest Ophthalmol Vis Sci. 1985 Feb;26(2):214-9.
New Zealand Black and White F1 hybrid mice (NZB/W mice) spontaneously develop an autoimmune disease which provides us with a suitable animal model for Sjögren's syndrome. With increasing age, these mice develop foci of mononuclear cell infiltration in the lacrimal and salivary glands, which closely resemble the lesions seen in patients with Sjögren's syndrome. We studied the cell-mediated and antibody-mediated immune responses of NZB/W mice to lacrimal gland cells. Lacrimal gland acinar cells were isolated from 2-month-old NZB/W or BALB/c mice for the target of 51Cr-release assay. There was no statistically significant difference in the spleen cell-mediated cytotoxicity to lacrimal gland cells among NZB/W mice of different ages (2, 5, and 8 months old). With increasing age, on the other hand, we found a statistically significant increase in the titers of autoantibodies to lacrimal gland cells in NZB/W mice, while aged BALB/c mice did not develop such antibodies. Fractionation of pooled positive sera by gel filtration revealed that this cytotoxic activity was mostly recovered in the IgM fraction. The tissue absorption study showed that these antibodies cross-reacted with salivary gland and kidney.
新西兰黑白F1杂交小鼠(NZB/W小鼠)会自发患上一种自身免疫性疾病,这为我们提供了一种合适的干燥综合征动物模型。随着年龄增长,这些小鼠的泪腺和唾液腺会出现单核细胞浸润灶,这与干燥综合征患者所见的病变非常相似。我们研究了NZB/W小鼠对泪腺细胞的细胞介导免疫反应和抗体介导免疫反应。从2个月大的NZB/W或BALB/c小鼠中分离泪腺腺泡细胞,作为51Cr释放试验的靶细胞。不同年龄(2、5和8个月大)的NZB/W小鼠的脾细胞对泪腺细胞的细胞毒性在统计学上没有显著差异。另一方面,随着年龄增长,我们发现NZB/W小鼠中针对泪腺细胞的自身抗体滴度在统计学上显著增加,而老年BALB/c小鼠则未产生此类抗体。通过凝胶过滤对混合阳性血清进行分离显示,这种细胞毒性活性大多在IgM组分中恢复。组织吸收研究表明,这些抗体与唾液腺和肾脏发生交叉反应。