NKG2D公司
MHC I级
自然杀伤细胞
细胞
受体
免疫学
体外
主要组织相容性复合体
癌症研究
细胞生物学
生物
化学
抗原
细胞毒性T细胞
生物化学
作者
Masahisa Jinushi,Tetsuo Takehara,Tomohide Tatsumi,Naoki Hiramatsu,Ryotaro Sakamori,Shinjiro Yamaguchi,Norio Hayashi
标识
DOI:10.1016/j.jhep.2005.05.026
摘要
Background/Aims MHC class I-related chain A (MICA), a human ligand of natural killer (NK) cell stimulatory receptor NKG2D, is expressed in human hepatocellular carcinomas (HCC). Earlier research demonstrated that the soluble form of MICA (sMICA) is released from some types of tumors, but its presence and role in HCC was not determined. Methods Serum sMICA was studied in 26 patients with HCC. In vitro experiments were performed to examine the impact of sMICA on NK cell expression of NKG2D and subsequent dendritic cell (DC) activation. Results The levels of sMICA were frequently elevated in patients with advanced HCC. The elevation of sMICA was associated with down-regulated NKG2D expression and impaired activation of NK cells. In vitro experiments revealed that sMICA derived from advanced HCC was responsible for down-modulation of NKG2D expression and NK cell functions. NK cells upon stimulation of human hepatoma cells induced maturation of DC and enhanced the allostimulatory capacity of DC; maturation and activation of DC were completely abolished when NK cells were pre-treated with sMICA-containing serum. Conclusions sMICA is present in sera of patients with advanced HCC and may serve as a tumor evasion mechanism by negatively modulating both innate and adaptive immunity.
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