Laskin C A, Haddad G, Soloninka C A
J Immunol. 1986 Sep 15;137(6):1867-73.
Murine lupus is characterized by the production of numerous autoantibodies and immune complex glomerulonephritis. Anti-DNA antibodies are the hallmark of this disorder and may be associated pathogenetically with the glomerulonephritis. The cellular mechanisms underlying the regulation of the production of anti-DNA antibodies may prove to be the fundamental abnormalities responsible for the lupus syndrome seen in these mice. By using a system of spontaneous anti-DNA antibody production in vitro, we have determined that such production is characteristic of autoimmune NZB and MRL-lpr/lpr mice but not of the nonautoimmune control strains. Additional examination of the cellular mechanisms involved in the regulation of this response in NZB mice revealed: 1) this response is markedly T cell dependent, 2) NZB T cells are essential for maximal production of this autoantibody, and 3) NZB T cells actively interfere with normal immune regulatory mechanisms that lead to the production of anti-DNA antibodies spontaneously in vitro by nonautoimmune syngeneic B lymphocytes. Although these studies of anti-DNA antibody production in vitro disagree with previous work by others they successfully reproduce the results obtained earlier in experiments performed in vivo.
小鼠狼疮的特征是产生大量自身抗体和免疫复合物性肾小球肾炎。抗DNA抗体是这种疾病的标志,并且在发病机制上可能与肾小球肾炎相关。抗DNA抗体产生调节的细胞机制可能被证明是这些小鼠中出现的狼疮综合征的根本异常原因。通过使用体外自发产生抗DNA抗体的系统,我们已经确定这种产生是自身免疫性NZB和MRL-lpr/lpr小鼠的特征,而非自身免疫对照品系则不具有。对NZB小鼠中参与这种反应调节的细胞机制的进一步研究揭示:1)这种反应明显依赖T细胞,2)NZB T细胞对于这种自身抗体的最大产生至关重要,3)NZB T细胞积极干扰正常的免疫调节机制,这些机制会导致非自身免疫性同基因B淋巴细胞在体外自发产生抗DNA抗体。尽管这些体外抗DNA抗体产生的研究与其他人先前的工作不一致,但它们成功地重现了早期体内实验获得的结果。