Lakow E, Tsoukas C D, Vaughan J H, Altman A, Carson D A
J Immunol. 1983 Jan;130(1):169-72.
A mutant of the Jurkat human T lymphoblastoid cell line deficient in hypoxanthine phosphoribosyltransferase, and resistant to ouabain, was fused with peripheral blood T lymphocytes primed in vitro with Epstein Barr virus- (EBV) transformed autologous B lymphocytes. After selection of somatic cell hybrids and cloning, hybridoma cell lines were obtained that reacted with autologous EBV-infected B lymphocytes, as detected by the release of interleukin 2 into the culture medium. The hybridomas did not react with i) EBV-uninfected autologous or allogeneic B lymphocytes, ii) three out of four allogeneic EBV-transformed cell lines, or iii) two established EBV-negative B cell lines. These functional hybridomas may ultimately prove useful in dissecting the means by which human T lymphocytes recognize and regulate EBV infection in vivo.
次黄嘌呤磷酸核糖基转移酶缺陷且对哇巴因耐药的人Jurkat T淋巴母细胞系突变体,与用爱泼斯坦-巴尔病毒(EBV)转化的自体B淋巴细胞体外致敏的外周血T淋巴细胞融合。在选择体细胞杂种并克隆后,获得了杂交瘤细胞系,通过向培养基中释放白细胞介素2检测到,这些细胞系与自体EBV感染的B淋巴细胞发生反应。这些杂交瘤不与以下细胞发生反应:i)未感染EBV的自体或同种异体B淋巴细胞;ii)四个同种异体EBV转化细胞系中的三个;或iii)两个已建立的EBV阴性B细胞系。这些功能性杂交瘤最终可能有助于剖析人类T淋巴细胞在体内识别和调节EBV感染的方式。