Sutton L N, Mason D Y, Redman C W
Nuffield Department of Obstetrics and Gynaecology, John Radcliffe Hospital, Headington, Oxford, England.
Clin Exp Immunol. 1989 Dec;78(3):437-43.
Human fetal macrophages expressing class II major histocompatibility complex (MHC) antigens have been isolated from the stroma of the chorionic plate of term placentas, using enzymatic digestion procedures, and enriched by Percoll density centrifugation. These cells are adherent, phagocytic and express Fc receptors for IgG. By rosetting with bovine erythrocytes coated with IgG, they can be enriched to 77-95% purity. Placental macrophages isolated in this way stimulate the proliferation of lymphocytes from unrelated donors in mixed-cell cultures, and act as accessory cells in oxidative mitogenesis. In a family study, placental macrophages stimulated proliferation of maternal and paternal lymphocytes but there was no evidence for either priming to, or suppression by, the fetal cells when the responses of lymphocytes from the mother and her HLA identical twin were compared. The possibility that these cells can protect the fetus from infection and/or stimulate the production of maternal anti-fetal HLA-antibodies is discussed.
利用酶消化程序,从足月胎盘绒毛板基质中分离出表达II类主要组织相容性复合体(MHC)抗原的人胎儿巨噬细胞,并通过Percoll密度离心法进行富集。这些细胞具有黏附性、吞噬性,并表达IgG的Fc受体。通过与包被IgG的牛红细胞进行花环试验,可将它们富集至纯度为77%-95%。以这种方式分离的胎盘巨噬细胞在混合细胞培养中刺激无关供体淋巴细胞的增殖,并在氧化有丝分裂中充当辅助细胞。在一项家族研究中,胎盘巨噬细胞刺激了母方和父方淋巴细胞的增殖,但当比较母亲及其HLA同卵双胞胎的淋巴细胞反应时,没有证据表明胎儿细胞对其有启动作用或抑制作用。本文讨论了这些细胞保护胎儿免受感染和/或刺激母体产生抗胎儿HLA抗体的可能性。