Dilworth S M, Griffin B E
Proc Natl Acad Sci U S A. 1982 Feb;79(4):1059-63. doi: 10.1073/pnas.79.4.1059.
A method is described for the production of hybridoma cell lines secreting antibodies directed against the polyoma virus tumor antigens (T-Ags). Ten cloned lines have been established by this procedure and designated alpha Py Cl and C4, with activities against all three T-Ags; alpha Py LT1, -4 and -7, with activities against large T-Ag only; and alpha Py MT5, -7, -10, -13, and -16, with activities against middle T-Ag only. Some of the antibodies appear to react also with specific cellular protein. Data from studies on alpha Py MT7 point to the possible existence of more than one antigenic form of the viral middle T-Ag and, similarly, from studies on alpha Py LT7, to more than one form of large T-Ag. The approximate positions on the polyoma virus genome of the sequences encoding antigenic determinants have been mapped by using defined polyoma virus deletion mutants. The availability of these monoclonal antibodies allows the isolation of large amounts of viral T-Ags.
描述了一种生产分泌针对多瘤病毒肿瘤抗原(T抗原)的抗体的杂交瘤细胞系的方法。通过该程序已建立了10个克隆系,命名为αPy Cl和C4,对所有三种T抗原有活性;αPy LT1、-4和-7,仅对大T抗原有活性;以及αPy MT5、-7、-10、-13和-16,仅对中T抗原有活性。一些抗体似乎也与特定的细胞蛋白发生反应。对αPy MT7的研究数据表明,病毒中T抗原可能存在不止一种抗原形式,同样,对αPy LT7的研究表明,大T抗原也有不止一种形式。通过使用确定的多瘤病毒缺失突变体,已绘制出编码抗原决定簇的序列在多瘤病毒基因组上的大致位置。这些单克隆抗体的可用性使得能够大量分离病毒T抗原。