Yule T D, Mahi-Brown C A, Tung K S
Department of Pathology, Washington University School of Medicine, St. Louis, Missouri 63110.
J Reprod Immunol. 1990 Aug;18(1):89-103. doi: 10.1016/0165-0378(90)90026-3.
The present data on testicular autoimmune disease suggest that CD4+ helper type T cells are responsible for adoptive transfer of murine experimental autoimmune orchitis (EAO). In passive EAO, the earliest lymphoid cell infiltration is confined to terminal segments of seminiferous tubules. Both orchitis and vasitis develop. In active EAO, any location in the testis is affected, frequently involving subcapsular seminiferous tubules. The location of maximum histopathology in passive EAO coincides with the site in the normal testis that expresses maximal Ia. Demonstration of IgG in the testis after immunization with testicular antigens or after transfer of sera from orchiectomized mice immunized with testis shows that autoantigens are present on the germ cells outside the Sertoli cell barrier, suggesting the existence of dynamic protective mechanisms against immune responses to the non-sequestered autoimmunogenic germ cells in normal individuals.
目前关于睾丸自身免疫性疾病的数据表明,CD4 +辅助性T细胞负责小鼠实验性自身免疫性睾丸炎(EAO)的过继转移。在被动性EAO中,最早的淋巴细胞浸润局限于曲细精管的终末段。睾丸炎和输精管炎都会发生。在主动性EAO中,睾丸的任何部位都会受到影响,经常累及被膜下的曲细精管。被动性EAO中最大组织病理学变化的位置与正常睾丸中表达最大量Ia的部位一致。在用睾丸抗原免疫后或在用睾丸免疫的去势小鼠的血清转移后,在睾丸中检测到IgG,这表明自身抗原存在于支持细胞屏障外的生殖细胞上,提示正常个体中存在针对未隔离的自身免疫原性生殖细胞免疫反应的动态保护机制。