Oksenberg J R, Mor-Yosef S, Ezra Y, Brauthbar C
J Reprod Immunol. 1987 Apr;10(4):309-18. doi: 10.1016/0165-0378(87)90033-7.
Antigen presenting cells were isolated from early human decidua or peripheral blood by elution with EDTA of cells that after Ficoll-Paque separation bear receptors for, and have bound to, fibronectin. Decidual antigen presenting cells (DAPCs) co-cultured with TNP-modified autologous T cells induced the development of cytotoxic anti-TNP T lymphocytes with an efficiency comparable to that of peripheral blood antigen presenting cells (PAPCs). Treatment with anti HLA-class II antibody plus complement and UV radiation resulted in substantial inhibition of the accessory cell function. The T cell mediated lysis of TNP-modified targets is restricted by the major histocompatibility complex. Our results show that HLA-class I molecules are the most prominent restriction elements. The relevance of these data to the immunological mechanisms operating at the feto-maternal interface is discussed.
通过用乙二胺四乙酸(EDTA)洗脱在经菲可-泛影葡胺(Ficoll-Paque)分离后带有纤连蛋白受体并已结合纤连蛋白的细胞,从早期人蜕膜或外周血中分离出抗原呈递细胞。与经三硝基苯(TNP)修饰的自体T细胞共培养的蜕膜抗原呈递细胞(DAPC)诱导细胞毒性抗TNP T淋巴细胞的发育,其效率与外周血抗原呈递细胞(PAPC)相当。用抗HLA-II类抗体加补体以及紫外线辐射处理导致辅助细胞功能受到显著抑制。T细胞介导的对经TNP修饰靶标的裂解受主要组织相容性复合体限制。我们的结果表明,HLA-I类分子是最主要的限制元件。讨论了这些数据与在母胎界面起作用的免疫机制的相关性。