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克服异抗原免疫力,使免疫能力高的"NoGlow"小鼠能够进行细胞跟踪和基因调控
Timothy N Trotter1, Andrea Wilson2, Jason McBane1
1Department of Surgery, Duke University, Durham, North Carolina.
Cancer research communications
|April 9, 2024
概括
我们开发了NoGlow小鼠,表达非功能性外来蛋白质,防止免疫排斥,并使细胞跟踪和基因调节用于生物医学研究.
科学领域:
- 免疫学 免疫学 免疫学
- 遗传学 是一个遗传学.
- 生物医学研究生物医学研究
背景情况:
- 动物模型中的异生菌基因表达可以触发免疫反应,阻碍细胞跟踪和基因调节.
- 诱导耐受性或限制表达的现有方法有局限性,例如废除报告员实用性或次优耐受性.
研究的目的:
- 开发一种新的小鼠模型,克服对外基因的免疫反应,以可靠的细胞跟踪和基因调节.
- 验证该模型对研究中心和外围耐受性机制的实用性.
- 为了使瘤学,发育生物学和移植的体内研究.
主要方法:
- 开发了"NoGlow"小鼠与CRE介导的重组,以表达抗原完好但非功能形式的GFP,Luc和rtTA3.
- 利用特定组织的CREs来评估免疫耐受性的模型和基于性别的差异.
- 疫苗接种后评估背景光/发光和适应性免疫力对转基因异原抗原.
- 证明了三重转基因细胞的跟踪和四环素诱导基因调节.
主要成果:
- NoGlow小鼠没有可检测的背景光或发光.
- 在接种疫苗后观察到对编码的转基因异原抗原的有限适应性免疫力.
- NoGlow小鼠成功地跟踪并允许三重转基因细胞的基因调节,与转基因负对照不同.
- 该模型支持 de novo 转移从正统植入的瘤细胞,尽管高的异抗原表达.
结论:
- NoGlow小鼠模型通过克服对外基因的免疫排斥,为体内研究提供了关键资源.
- 这种模型可以实现可靠的细胞跟踪和四环素诱导基因调节.
- 在研究适应性免疫,转移,免疫治疗和耐受性方面,NoGlow小鼠非常有价值.
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