小鼠白血病病毒抗体活性明显缺乏与(AKR×CBA)F1小鼠淋巴瘤发展的相关性

R.D. Barnes, Maureen Tuffrey, H.C. Holmes
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引用次数: 0

摘要

我们过去曾提出这样的假设,即AKR小鼠中病毒相关淋巴瘤的发展可能在某种程度上与小鼠白血病病毒(MuLV)抗体活性的发生有关。在这里,我们试图使用该实验室最近开发的125I蛋白A放射免疫分析法来检验这一假设。先前在天然来源的(AKR×CBA/H-T6Crc)F1中的发现证实了MuLV的存在,此外,其水平与AKR相当,甚至偶尔超过AKR。尽管如此,肿瘤在生命的第一年并不常见,此时无法检测到抗体活性。后来人们注意到淋巴瘤确实发生在F1,但发生在第二年。为了验证我们的假设,即肿瘤耐药性和抗体活性之间可能存在关联,在这一后期对这些杂交种进行了进一步的研究。此外,我们还检查了其他几组小鼠,在这些小鼠中,我们试图通过实验过早地诱导抗体活性。在这两种情况下,肿瘤发展与抗MuLV活性的存在之间没有明显的关系。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The apparent lack of association of antibody activity to murine leukemia virus and lymphoma development in (AKR × CBA) F1 mice

We have in the past proposed the hypothesis that virus-associated lymphoma development in AKR mice might be in some way related to the occurrence of antibody activity to murine leukemia virus (MuLV). Here we have attempted to test this hypothesis using the 125I-protein A radioimmunoassay recently developed in this laboratory. Previous findings in naturally derived (AKR × CBA/H-T6Crc) F1 confirmed the presence of MuLV, moreover, at levels comparable to or indeed occasionally in excess of, the AKR. Despite this, tumours were uncommon during the first year of life and no antibody activity could be detected at this time. It was later noted that lymphomas did occur in the F1 but in the second year. To test our hypothesis that there may be a possible association between tumour resistance and antibody activity, these hybrids have been investigated further during this later period.

In addition, we have examined other groups of mice in which we have attempted to prematurely induce antibody activity experimentally.

In both these situations there was no apparent relationship between tumour development and the presence of anti-MuLV activity.

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