Steinberg A D, Melez K A, Raveche E S, Reeves J P, Boegel W A, Smathers P A, Taurog J D, Weinlein L, Duvic M
Arthritis Rheum. 1979 Nov;22(11):1170-6. doi: 10.1002/art.1780221103.
Investigators from this laboratory have been studying sex hormones in normal and autoimmune mice for the past 10 years. We have found that immune responses to DNa are influenced by sex hormones. Androgens reduce and estrogens increase both spontaneous and immunization-induced antibodies to single-stranded DNA in NZB X NZW, NZB X C3H, NZB X CBA, NZB X DBA mice. Treatment of female NZB/W mice with testosterone or 5 alpha dihydrotestosterone retards the progress of autoimmunity. Castration is not necessary for this effect. In contrast, danazol has no favorable effect on the disease process. Estrogens cause a marked acceleration of autoimmunity and a reduction in thymus weight. During the course of these studies, we found that a number of problems or variables arise in studying sex hormone effects, including: 1) X-linked genes, 2) metabolism of testosterone to estrogens, 3) dose of hormone, 4) age at which administration is initiated, 5) differential effects of sex hormones on different autoantibodies and various immune responses.
在过去10年里,该实验室的研究人员一直在研究正常小鼠和自身免疫小鼠体内的性激素。我们发现,对DNA的免疫反应受性激素影响。在NZB×NZW、NZB×C3H、NZB×CBA、NZB×DBA小鼠中,雄激素会减少,而雌激素会增加针对单链DNA的自发抗体和免疫诱导抗体。用睾酮或5α-二氢睾酮治疗雌性NZB/W小鼠可延缓自身免疫的进展。阉割并非产生此效应所必需。相比之下,达那唑对疾病进程没有有利影响。雌激素会导致自身免疫明显加速和胸腺重量减轻。在这些研究过程中,我们发现,在研究性激素效应时会出现一些问题或变量,包括:1)X连锁基因,2)睾酮向雌激素的代谢,3)激素剂量,4)开始给药时的年龄,5)性激素对不同自身抗体和各种免疫反应的差异效应。