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通过阻断T细胞中的转化生长因子-β信号通路实现免疫介导的肿瘤根除。

Immune-mediated eradication of tumors through the blockade of transforming growth factor-beta signaling in T cells.

作者信息

Gorelik L, Flavell R A

机构信息

Section of Immunobiology, Yale University School of Medicine and Howard Hughes Medical Institute, New Haven, Connecticut, USA.

出版信息

Nat Med. 2001 Oct;7(10):1118-22. doi: 10.1038/nm1001-1118.

Abstract

Despite the existence of tumor-specific antigens and demonstrated presence of tumor-specific immune cells, the majority of tumors manage to avoid immune-mediated destruction. Various mechanisms have been suggested for tumor evasion from immune response. One such mechanism is thought to be mediated by transforming growth factor-beta (TGF-beta), an immunosuppressive cytokine found at the site of most tumors. We demonstrate here that T-cell-specific blockade of TGF-beta signaling allows the generation of an immune response capable of eradicating tumors in mice challenged with live tumor cells. In addition, we provide mechanisms through which abrogation of TGF-beta signaling leads to the enhancement of anti-tumor immunity. Our data indicate that T-cell-specific blockade of TGF-beta signaling has strong therapeutic potential to shift the balance of the immune response in favor of anti-tumor immunity.

摘要

尽管存在肿瘤特异性抗原且已证实存在肿瘤特异性免疫细胞,但大多数肿瘤仍能避免免疫介导的破坏。针对肿瘤逃避免疫反应的现象,人们提出了多种机制。其中一种机制被认为是由转化生长因子-β(TGF-β)介导的,TGF-β是一种在大多数肿瘤部位发现的免疫抑制细胞因子。我们在此证明,T细胞特异性阻断TGF-β信号传导能够产生一种免疫反应,该反应能够在受到活肿瘤细胞攻击的小鼠体内根除肿瘤。此外,我们还提供了TGF-β信号传导缺失导致抗肿瘤免疫力增强的机制。我们的数据表明,T细胞特异性阻断TGF-β信号传导具有强大的治疗潜力,可使免疫反应的平衡向有利于抗肿瘤免疫的方向转变。

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