Fingeroth J D, Weis J J, Tedder T F, Strominger J L, Biro P A, Fearon D T
Proc Natl Acad Sci U S A. 1984 Jul;81(14):4510-4. doi: 10.1073/pnas.81.14.4510.
Identity of the Epstein-Barr virus (EBV) receptor with the complement receptor type 2 (CR2) was established in three sets of experiments using the monoclonal antibodies, HB-5 and anti-B2, which recognize a Mr 145,000 B-lymphocyte membrane protein that is CR2. First, the rank order for binding of fluoresceinated EBV to four lymphoblastoid cell lines (SB, JY, Raji, and Molt-4) was identical to the rank order for binding of HB-5 and anti-B2 by analytical flow cytometry. Second, pretreatment of cells with HB-5 followed by treatment with goat F(ab')2 fragments to mouse IgG blocked binding of fluoresceinated EBV on SB, a B-lymphoblastoid cell line. Virus attachment was not inhibited by HB-5 alone, second antibody alone, rabbit anti-C3b receptor, or UPC10 (an irrelevant monoclonal antibody). Third, transfer of CR2 from SB to protein A-bearing Staphylococcus aureus particles, to which HB-5 had been absorbed, conferred on them the specific ability to bind 125I-labeled EBV. We conclude that CR2 is the EBV receptor of human B lymphocytes.
在三组实验中,利用单克隆抗体HB - 5和抗B2确定了爱泼斯坦 - 巴尔病毒(EBV)受体与2型补体受体(CR2)的同一性,这两种抗体识别一种分子量为145,000的B淋巴细胞膜蛋白,即CR2。首先,通过分析流式细胞术,荧光素标记的EBV与四种淋巴母细胞系(SB、JY、Raji和Molt - 4)结合的排序与HB - 5和抗B2结合的排序相同。其次,先用HB - 5处理细胞,再用山羊抗小鼠IgG的F(ab')2片段处理,可阻断荧光素标记的EBV与B淋巴母细胞系SB的结合。单独的HB - 5、单独的二抗、兔抗C3b受体或UPC10(一种无关的单克隆抗体)均不抑制病毒附着。第三,将CR2从SB转移到已吸附HB - 5的带有蛋白A的金黄色葡萄球菌颗粒上,赋予它们结合125I标记的EBV的特定能力。我们得出结论,CR2是人B淋巴细胞的EBV受体。