Hirschberg H
Hum Immunol. 1981 May;2(3):235-46. doi: 10.1016/0198-8859(81)90015-x.
Endothelial cells (EC) separated from the umbilical vein were shown to be free of contaminating monocytes. EC could replace peripheral blood-derived macrophages as antigen-presenting cells for in vivo sensitized T cells towards a variety of viral antigens. The T-cell--CE-antigen response was also specificity inhibited by anti-HLA-DR antisera. T cells primed by antigen together with autologous macrophages could be restimulated by antigen pulsed HLA-D/DR identical EC in an antigen specific secondary response, indicating a similar mechanism for antigen presentation by EC or macrophages.
从脐静脉分离出的内皮细胞(EC)被证明没有单核细胞污染。内皮细胞可以替代外周血来源的巨噬细胞,作为体内针对多种病毒抗原致敏的T细胞的抗原呈递细胞。T细胞与内皮细胞抗原的反应也受到抗HLA-DR抗血清的特异性抑制。在抗原特异性二次反应中,由抗原与自体巨噬细胞一起致敏的T细胞可以被脉冲了抗原的HLA-D/DR相同的内皮细胞再次刺激,这表明内皮细胞或巨噬细胞的抗原呈递机制相似。