Bernabeu C, Finlay D, van de Rijn M, Maziarz R T, Biro P A, Spits H, de Vries J, Terhorst C P
J Immunol. 1983 Oct;131(4):2032-7.
Genes coding for the heavy chain of the class I antigens HLA-A2 or HLA-B7 of the human major histocompatibility complex have been introduced into mouse LtK- cells by cotransfection with the herpes simplex virus thymidine kinase gene. HAT-resistant colonies were isolated expressing either HLA-A2 or HLA-B7 as monitored by indirect immunofluorescence. Immunoprecipitation analysis of both antigens by either sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE) or isoelectric focusing (IEF) showed that they were identical to the HLA-A2 and HLA-B7 expressed in the human lymphoblastoid cell line JY (homozygous HLA-A2, HLA-B7). However, human cytotoxic T lymphocytes (CTL) generated against JY and CTL clones specific for HLA-A2 or HLA-B7 were unable to recognize the transfectants as targets. These results indicate that the human HLA-A2 (or B7) complexed with the murine beta 2-microglobulin could be an inappropriate target structure for the CTL. However, because the transfectants are not killed by human CTL even in the presence of lectins, it is suggested that other molecules that are not able to overcome the human-mouse species barrier may be involved in the killing mechanism.
编码人类主要组织相容性复合体I类抗原HLA - A2或HLA - B7重链的基因,已通过与单纯疱疹病毒胸苷激酶基因共转染的方式导入小鼠LtK - 细胞。通过间接免疫荧光监测,分离出表达HLA - A2或HLA - B7的抗HAT菌落。通过十二烷基硫酸钠聚丙烯酰胺凝胶电泳(SDS - PAGE)或等电聚焦(IEF)对两种抗原进行免疫沉淀分析,结果表明它们与人类淋巴母细胞系JY(纯合HLA - A2,HLA - B7)中表达的HLA - A2和HLA - B7相同。然而,针对JY产生的人类细胞毒性T淋巴细胞(CTL)以及针对HLA - A2或HLA - B7的CTL克隆,均无法将转染细胞识别为靶细胞。这些结果表明,与小鼠β2 - 微球蛋白复合的人类HLA - A2(或B7)可能是CTL不合适的靶结构。然而,由于即使在存在凝集素的情况下,转染细胞也不会被人类CTL杀死,因此有人提出,在杀伤机制中可能涉及其他无法跨越人鼠种属屏障的分子。