Husebye Eystein S, Løvås Kristian
Section of Endocrinology, Institute of Medicine, University of Bergen, Bergen, Norway.
Endocrinol Metab Clin North Am. 2009 Jun;38(2):389-405, ix. doi: 10.1016/j.ecl.2009.01.010.
Autoimmune Addison's disease and autoimmune ovarian insufficiency are caused by selective targeting by T and B lymphocytes to the steroidogenic apparatus in these organs. Autoantibodies toward 21-hydroxylase are a clinically useful marker for autoimmune Addison's disease. Autoantibodies to 21-hydroxylase are found in premature ovarian insufficiency, but others also can be present, notably antibodies against side-chain cleavage enzyme. The autoimmune response primarily targets the theca cells, yielding elevated concentrations of inhibin, which is emerging as a useful diagnostic marker for autoimmune etiology of ovarian insufficiency. Little is known about its immunogenetics, but in contrast to Addison's disease, several experimental models of autoimmune premature ovarian insufficiency are available for study.
自身免疫性艾迪生病和自身免疫性卵巢功能不全是由T淋巴细胞和B淋巴细胞选择性靶向这些器官中的类固醇生成装置所致。针对21-羟化酶的自身抗体是自身免疫性艾迪生病的一种临床有用标志物。在卵巢早衰患者中可发现针对21-羟化酶的自身抗体,但也可能存在其他自身抗体,尤其是针对侧链裂解酶的抗体。自身免疫反应主要靶向卵泡膜细胞,导致抑制素浓度升高,抑制素正逐渐成为卵巢功能不全自身免疫病因的一种有用诊断标志物。关于其免疫遗传学知之甚少,但与艾迪生病不同,有几种自身免疫性卵巢早衰的实验模型可供研究。