Roloson G J, Haagensen D E, Chambers C A, Bolognesi D P
J Immunol. 1981 Jun;126(6):2328-31.
We have previously described a passive serum therapy system in which potent protection against challenge of syngeneic mice with large doses (10(4) X LD100) of AD755a tumor cells can be accomplished by administration of as little as 2 to 5 microliters/mouse of hyperimmune anti-tumor cell serum. The present results demonstrate that the efficacy of the serum protection effect is strain-dependent and is under the control of a single genetic locus, denoted ADP-1. Through a series of crosses between highly protected C57BL/6J and nonprotected BALB/cJ mice, the ADP-locus has been mapped to chromosome 2 [linkage group V], approximately 23 centimorgans toward te centromere from the locus controlling agouti coat color. Thus, the protection locus is not linked to either the H-2 region or to previously described loci regulating the replication and disease induction of type-C viruses closely related to the virus associated with the AD775a tumor. The possible functions of the ADP-1 locus are discussed and further aspects of this experimental model are described in the accompanying papers.
我们之前描述过一种被动血清疗法系统,在该系统中,通过给同基因小鼠每只注射低至2至5微升的超免疫抗肿瘤细胞血清,就能有效保护其免受大剂量(10⁴×LD100)AD755a肿瘤细胞的攻击。目前的结果表明,血清保护作用的功效具有品系依赖性,且受单个基因座控制,该基因座被命名为ADP-1。通过高度受保护的C57BL/6J小鼠和未受保护的BALB/cJ小鼠之间的一系列杂交,ADP基因座已被定位到2号染色体[连锁群V]上,距离控制刺鼠毛色的基因座约23厘摩,朝向着丝粒。因此,该保护基因座既不与H-2区域连锁,也不与先前描述的调控与AD775a肿瘤相关病毒密切相关的C型病毒复制和疾病诱导的基因座连锁。本文讨论了ADP-1基因座的可能功能,并在随附论文中描述了该实验模型的其他方面。