首页> 美国卫生研究院文献>Oncotarget >Altered phenotypic and functional characteristics of CD3+CD56+ NKT-like cells in human gastric cancer
【2h】

Altered phenotypic and functional characteristics of CD3+CD56+ NKT-like cells in human gastric cancer

机译:人胃癌中CD3 + CD56 + NKT样细胞的表型和功能特性改变

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

CD3+CD56+ natural killer T (NKT)-like cells are a group of CD3+ T cells sharing characteristics of NK and T cells and constitute a major component of host anti-tumor immune response in human cancer. However, the nature, function and clinical relevance of CD3+CD56+ NKT-like cells in human gastric cancer (GC) remain unclear. In this study, we showed that the frequencies of CD3+CD56+NKT-like cells in GC tumors were significantly decreased and low levels of tumor-infiltrating CD3+CD56+ NKT-like cells were positively correlated with poor survival and disease progression. Most CD3+CD56+NKT-like cells in GC tumors were CD45RACD27+/− central/effector-memory cells with decreased activity and lower expression levels of CD69, NKG2D and DNAM-1 than those in non-tumor tissues. We further observed that tumor-infiltrating CD3+CD56+ NKT-like cells had impaired effector function as shown by decreased IFN-γ, TNF-α, granzyme B and Ki-67 expression. Moreover, in vitro studies showed that soluble factors released from GC tumors could induce the functional impairment of CD3+CD56+ NKT-like cells. Collectively, our data indicate that decreased tumor-infiltrating CD3+CD56+ NKT-like cells with impaired effector function are associated with tumor progression and poor survival of GC patients, which may contribute to immune escape of GC.
机译:CD3 + CD56 + 自然杀伤性T(NKT)样细胞是一组具有NK和T细胞特征的CD3 + T细胞。构成人类癌症中宿主抗肿瘤免疫反应的主要成分。然而,尚不清楚人类胃癌(GC)中CD3 + CD56 + NKT样细胞的性质,功能和临床意义。在这项研究中,我们表明,GC肿瘤中CD3 + CD56 + NKT样细胞的频率显着降低,且肿瘤浸润CD3 +的水平较低 CD56 + NKT样细胞与不良的生存和疾病进展呈正相关。 GC肿瘤中大多数CD3 + CD56 + NKT样细胞为CD45RA - CD27 +/- 中枢/效应子-记忆细胞的活性降低,CD69,NKG2D和DNAM-1的表达水平低于非肿瘤组织。我们进一步观察到肿瘤浸润的CD3 + CD56 + NKT样细胞的效应子功能受损,如IFN-γ,TNF-α,颗粒酶B和Ki- 67个表达式。此外,体外研究表明,GC肿瘤释放的可溶性因子可以诱导CD3 + CD56 + NKT样细胞的功能损伤。总体而言,我们的数据表明,效应子功能受损的肿瘤浸润性CD3 + CD56 + NKT样细胞减少与肿瘤进展和GC患者生存不良有关,这可能与有助于GC的免疫逃逸。

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