Aguilera S, Ivanyi J
Eur J Immunol. 1978 Jun;8(6):446-51. doi: 10.1002/eji.1830080614.
Chicken IgM antibodies raised against sheep erythrocytes (SE) reacted with a heterophile carbohydrate antigen designated as "HC". This antigen was visualized by SE rosette formation with antibody-sensitized and formaldehyde-fixed target cells. Cells from eight lymphoblastoid lines and ten lines of diverse histogenetic origin all expressed HC on their surface to a greater or lesser degree when grown in fetal calf serum (FCS). Lymphoblastoid cell lines, HSB2 and Namalva, lost most of their HC antigen after three cell divisions when grown in medium which contained normal human serum (NHS) instead of FCS. The acquired origin of HC was demonstrated by the conversion of HSB2-HC- into HSB2-HC+ cells after incubation in the presence of FCS or fetuin for 18 h at 37 degrees C. The acquisition of HC antigen depended on the concentration of fetuin as well as the time and temperature of incubation. The presence of NHS in the culture medium reduced the degree of HC incorporation. The level of HC expressed on the cell surface was reduced by treating HSB2 cells with sodium periodate but not by proteolytic enzymes. Competitive inhibition with hog blood group substance and sheep IgG suggested similar specificity of HC on target cells which had been sensitized with either fetuin or sheep IgM (Eur. J. Immunol. 1977.7:204). The avidity of chicken antibodies to HC in either of these systems was several orders of magnitude lower than the binding to SE.
针对绵羊红细胞(SE)产生的鸡IgM抗体与一种被称为“HC”的嗜异性碳水化合物抗原发生反应。这种抗原通过与抗体致敏且经甲醛固定的靶细胞形成SE玫瑰花结来显现。当在胎牛血清(FCS)中生长时,来自8个淋巴母细胞系和10个不同组织发生学来源的细胞系的细胞表面均或多或少地表达HC。当在含有正常人血清(NHS)而非FCS的培养基中生长时,淋巴母细胞系HSB2和Namalva在三次细胞分裂后失去了大部分HC抗原。在37℃下于FCS或胎球蛋白存在的情况下孵育18小时后,HSB2 - HC - 细胞转变为HSB2 - HC + 细胞,从而证明了HC的后天来源。HC抗原的获得取决于胎球蛋白的浓度以及孵育的时间和温度。培养基中NHS的存在降低了HC掺入的程度。用高碘酸钠处理HSB2细胞可降低细胞表面表达的HC水平,但用蛋白水解酶处理则无此效果。用猪血型物质和绵羊IgG进行的竞争性抑制表明,在用胎球蛋白或绵羊IgM致敏的靶细胞上,HC具有相似的特异性(《欧洲免疫学杂志》1977年第7卷:204页)。在这两种系统中,鸡抗体对HC的亲和力比与SE的结合低几个数量级。