首页> 美国卫生研究院文献>Proceedings of the National Academy of Sciences of the United States of America >Antigen-stimulated CD4 T-cell expansion is inversely and log-linearly related to precursor number
【2h】

Antigen-stimulated CD4 T-cell expansion is inversely and log-linearly related to precursor number

机译:抗原刺激的CD4 T细胞扩增与前体数目成反比和对数线性关系

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。
获取外文期刊封面目录资料

摘要

Antigen-driven expansion of specific CD4 T cells diminishes, on a per cell basis, as infused cell number increases. There is a linear relation between log precursor number and log factor of expansion (FE), with a slope of ∼−0.5 over a range from 3 to 30,000 precursors. Cell number dependence of FE is observed at low precursor number, implying that the underlying process physiologically regulates antigen-driven T-cell expansion. FE of small numbers of transgenic precursors is not significantly affected by concomitant responses of large numbers of cells specific for different antigens. Increasing antigen amount or exogenous IL-2, IL-7, or IL-15 does not significantly affect FE, nor does FE depend on Fas, TNF-α receptor, cytotoxic T-lymphocyte antigen-4, IL-2, or IFN-γ. Small numbers of Foxp3-deficient T-cell receptor transgenic cells expand to a greater extent than do large numbers, implying that this effect is not mediated by regulatory T cells. Increasing dendritic cell number does result in larger FE, but the quantitative relation between FE and precursor number is not abrogated. Although not excluding competition for peptide/MHC complexes as an explanation, fall in FE with increasing precursor number could be explained by a negative feedback in which increasing numbers of responding cells in a cluster inhibit the expansion of cells of the same specificity within that cluster.
机译:抗原驱动的特定CD4 T细胞的扩增随输入细胞数的增加而逐个减少。对数前体数量与对数扩展因子(FE)之间存在线性关系,在3至30,000个前体范围内,斜率约为-0.5。在低前体数目下观察到FE的细胞数依赖性,这意味着潜在的过程在生理上调节抗原驱动的T细胞扩增。少量转基因前体的FE不会受到大量对不同抗原具有特异性的细胞的伴随反应的显着影响。抗原量增加或外源性IL-2,IL-7或IL-15不会显着影响FE,FE也不依赖于Fas,TNF-α受体,细胞毒性T淋巴细胞抗原4,IL-2或IFN- γ。少量的Foxp3缺陷型T细胞受体转基因细胞比大量的扩展程度更大,这表明这种作用不是由调节性T细胞介导的。树突状细胞数目的增加确实会导致较大的FE,但不会废除FE与前体数目之间的定量关系。尽管不排除对肽/ MHC复合物竞争的解释,但FE随前体数目增加而下降可通过负反馈来解释,其中簇中响应细胞数量的增加抑制了该簇中相同特异性细胞的扩增。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号