Hefeneider S H, Conlon P J, Dower S K, Henney C S, Gillis S
J Immunol. 1984 Apr;132(4):1863-8.
MRL/MP lpr-lpr (MRL-lpr) mice spontaneously develop an age-related disease characteristic of human systemic lupus erythematosus (SLE). Old MRL-lpr mice (4 mo of age) develop antibodies to nucleic acids, display immune complex glomerulonephritis, and have a massive T cell-associated lymphadenopathy. In concert with disease development is data showing an age-related loss of interleukin 2 (IL 2) production by mitogen-stimulated lymphoid cells from these mice. The loss of IL 2 production has been suggested to be involved in the onset and/or development of autoimmune disease seen in these animals. In this report, we examined the frequency of both IL 2 and colony-stimulating factor (CSF) producer T cells in the MRL-lpr mouse by using a limiting dilution analysis assay. Our results show that the number of IL 2 and CSF producer cells present in autoimmune animals is similar to the number found in normal control mice. In addition, IL 2 and CSF producer T cells from autoimmune MRL-lpr mice make similar levels of lymphokine activity, as do producer T cells from normal mice. Our data argue against the previously hypothesized role that a paucity of IL 2 production may be involved in the etiology of autoimmune disease.
MRL/MP lpr-lpr(MRL-lpr)小鼠会自发发展出一种具有人类系统性红斑狼疮(SLE)特征的与年龄相关的疾病。老年MRL-lpr小鼠(4月龄)会产生针对核酸的抗体,表现出免疫复合物性肾小球肾炎,并伴有大量与T细胞相关的淋巴结病。与疾病发展相一致的是,有数据表明这些小鼠经丝裂原刺激的淋巴细胞产生白细胞介素2(IL-2)的能力会随着年龄增长而丧失。IL-2产生能力的丧失被认为与这些动物中出现的自身免疫性疾病的发生和/或发展有关。在本报告中,我们通过使用有限稀释分析测定法检测了MRL-lpr小鼠中产生IL-2和集落刺激因子(CSF)的T细胞的频率。我们的结果表明,自身免疫动物中产生IL-2和CSF的细胞数量与正常对照小鼠中的数量相似。此外,来自自身免疫性MRL-lpr小鼠的产生IL-2和CSF的T细胞产生的淋巴因子活性水平与正常小鼠的产生细胞相似。我们的数据反驳了先前假设的观点,即IL-2产生不足可能参与自身免疫性疾病的病因。