Impairment of natural killer cell and dendritic cell functions by the soluble form of MHC class I-related chain A in advanced human hepatocellular carcinomas

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
出处
期刊:Journal of Hepatology [Elsevier BV]
卷期号:43 (6): 1013-1020 被引量:216
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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