Fu Li, Feng Wei, Li Shou-Rou, Huang Bing-Yu
Department of Obstetrics and Gynecology, West China Second University Hospital, Sichuan University, Chengdu 610041, China.
J Reprod Immunol. 2007 Aug;75(1):40-7. doi: 10.1016/j.jri.2007.02.009. Epub 2007 Apr 6.
Experimental autoimmune ovarian disease (AOD) is a T cell-mediated chronic inflammatory disease that may lead to premature ovarian failure. Autoimmune disease can be suppressed by oral administration of autoantigens leading to tolerance. One of the major mechanisms of oral tolerance is induction of regulatory CD4+ T cells that can mediate active suppression by producing immunomodulatory cytokines. However, the role of oral tolerance as a treatment for experimental AOD has received little attention. Therefore, the purpose of this study was to examine the conditions necessary to produce oral tolerance in experimental AOD in B6AF1 female mice. In this study, mice received different doses of peptides of the mouse zona pellucida 3 (pZP3) via gastric intubation for 7 times. After 4 times of oral administration, AOD was induced by immunization with pZP3. The optimal tolerating regimen for oral administration of pZP3 in mice was 10 microg, which decreased morbidity of oophoritis compared to the control group. In this moderate-dose therapeutic group (MD), alterations in the estrous cycle were normalized and CD4+ T cells that were CD25+ increased while those that were CD25- decreased. The severity of autoimmune oophoritis and the titer of ZP autoantibodies were also significantly reduced. These findings suggest that oral administration of pZP3 may be successfully used as an oral tolerance strategy for suppression of AOD.
实验性自身免疫性卵巢疾病(AOD)是一种由T细胞介导的慢性炎症性疾病,可能导致卵巢早衰。自身免疫性疾病可通过口服自身抗原诱导耐受来抑制。口服耐受的主要机制之一是诱导调节性CD4+ T细胞,这些细胞可通过产生免疫调节细胞因子介导主动抑制。然而,口服耐受作为实验性AOD治疗方法的作用鲜受关注。因此,本研究的目的是探讨在B6AF1雌性小鼠实验性AOD中产生口服耐受所需的条件。在本研究中,小鼠通过胃插管接受不同剂量的小鼠透明带3(pZP3)肽,共7次。口服4次后,用pZP3免疫诱导AOD。小鼠口服pZP3的最佳耐受方案为10微克,与对照组相比,这降低了卵巢炎的发病率。在这个中等剂量治疗组(MD)中,动情周期的改变恢复正常,CD25+的CD4+ T细胞增加,而CD25-的CD4+ T细胞减少。自身免疫性卵巢炎的严重程度和ZP自身抗体的滴度也显著降低。这些发现表明,口服pZP3可能成功用作抑制AOD的口服耐受策略。