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新型循环 NK 细胞亚群的特征描述与功能分析。

Characterization and functional analysis of novel circulating NK cell sub-populations.

机构信息

Division of Clinical Immunology, Department of Medical Technology.

Biomedical Technology Research Center, National Center for Genetic Engineering and Biotechnology, National Science and Technology Development Agency, at the Faculty of Associated Medical Sciences, Chiang Mai University, Chiang Mai, Thailand.

出版信息

Int Immunol. 2019 Jul 30;31(8):515-530. doi: 10.1093/intimm/dxz027.

Abstract

Natural killer (NK) cells are innate lymphoid cells having potent cytolytic function that provide host defense against microbial infections and tumors. Using our generated monoclonal antibody (mAb), named FE-1H10, new NK cell sub-populations in peripheral blood were identified. The molecules recognized by mAb FE-1H10 were expressed on a sub-population of CD3-CD56dim NK cells. The epitope recognized by mAb FE-1H10 was demonstrated to be N-glycan and proven to be different from CD57. Upon K562 stimulation, the CD56dimFE-1H10+ NK cell sub-population exhibited significantly lower cytolytic function with low ability to degranulate and release cytolytic granules compared to the CD56dimFE-1H10- NK cell sub-population. Moreover, the CD56dimFE-1H10+ NK cells produced less IFN-γ and TNF-α than the CD56dimFE-1H10- NK cells. We demonstrated here that mAb FE-1H10 could identify two sub-populations of circulating CD56dim NK cells with different functions. Our discovery of new sub-populations of NK cells improves our understanding of NK cell biology and may lead to the development of new approaches for NK cell therapy.

摘要

自然杀伤 (NK) 细胞是先天淋巴细胞,具有强大的细胞溶解功能,可提供宿主对微生物感染和肿瘤的防御。使用我们生成的单克隆抗体 (mAb),命名为 FE-1H10,鉴定了外周血中的新 NK 细胞亚群。mAb FE-1H10 识别的分子表达在 CD3-CD56dim NK 细胞的一个亚群上。mAb FE-1H10 识别的表位被证明是 N-糖基,并被证明与 CD57 不同。在 K562 刺激下,与 CD56dimFE-1H10- NK 细胞亚群相比,CD56dimFE-1H10+ NK 细胞亚群的细胞溶解功能明显降低,脱颗粒和释放细胞溶解颗粒的能力较低。此外,CD56dimFE-1H10+ NK 细胞产生的 IFN-γ 和 TNF-α 少于 CD56dimFE-1H10- NK 细胞。我们在这里证明,mAb FE-1H10 可以识别具有不同功能的两种循环 CD56dim NK 细胞亚群。我们对 NK 细胞亚群的新发现提高了我们对 NK 细胞生物学的理解,并可能为 NK 细胞治疗的新方法的发展提供依据。

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