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[阻断抑制性杀伤细胞免疫球蛋白样受体对人自然杀伤细胞体外细胞毒活性的影响]

[Effects of blocking inhibitory KIR receptors on cytotoxic activity of human NK cells in vitro].

作者信息

Wu Gong-qiang, Zhao Yan-min, Huang He, Lai Xiao-yu

机构信息

Institute of Hematology, The First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.

出版信息

Zhejiang Da Xue Xue Bao Yi Xue Ban. 2011 Sep;40(5):475-81. doi: 10.3785/j.issn.1008-9292.2011.05.003.

Abstract

OBJECTIVE

To investigate the effect of blocking the inhibitory receptors KIR2DL1 and KIR2DL2/2DL3 with monoclonal antibody on cytotoxic activity of human NK cells.

METHODS

Human peripheral blood NK cells were isolated by Rosettesep NK sorting kit. The cytotoxic activity of NK cells against human leukemia NB4, K-562, Raji cells and allogeneic mature or dendritic cells (DCs) was detected before or after KIR2DL1 and KIR2DL2/2DL3 were blocked. The effect of NK cells on T lymphocyte proliferation was detected by mixed lymphocyte reaction and TGF-β1 concentration in culture supernatant was measured.

RESULTS

The cytotoxicity of NK cells to NB4 cells was augmented with increasing concentration of the antibody. Combination of both antibodies enhanced killing activity of NK cells. NK cells had strong cytotoxicity to K-562 cells, but were not enhanced by the blockade of inhibitory receptors. The cytotoxicity to Raji cells was not evidently augmented. The cytotoxicity of NK cells to mature DC was enhanced remarkably with the increase of concentration of the antibodies (2.20% ±1.10% compared with 37.59% ±5.06%, P<0.05). In mixed lymphocyte reaction, the blockade of two antibodies enhanced the inhibition effect of NK cells on T cell proliferation (77.85% ± 8.31% compared with 43.05% ± 5.95%, P<0.05) and the content of TGF-β1 in the supernatant was increased.

CONCLUSION

The cytotoxic effects of human NK cells against target cells were significantly enhanced with the blockade of inhibitory KIR receptor; and the cytokine TGF-β1 secreted by NK cells further inhibits T cells proliferation.

摘要

目的

研究用单克隆抗体阻断抑制性受体KIR2DL1和KIR2DL2/2DL3对人自然杀伤(NK)细胞细胞毒活性的影响。

方法

采用Rosettesep NK分选试剂盒分离人外周血NK细胞。在阻断KIR2DL1和KIR2DL2/2DL3前后,检测NK细胞对人白血病NB4、K-562、Raji细胞以及同种异体成熟细胞或树突状细胞(DCs)的细胞毒活性。通过混合淋巴细胞反应检测NK细胞对T淋巴细胞增殖的影响,并测定培养上清液中转化生长因子-β1(TGF-β1)的浓度。

结果

随着抗体浓度增加,NK细胞对NB4细胞的细胞毒性增强。两种抗体联合使用可增强NK细胞的杀伤活性。NK细胞对K-562细胞具有较强的细胞毒性,但抑制性受体的阻断未增强其毒性。对Raji细胞的细胞毒性未明显增强。随着抗体浓度增加,NK细胞对成熟DC的细胞毒性显著增强(2.20%±1.10%与37.59%±5.06%相比,P<0.05)。在混合淋巴细胞反应中,两种抗体的阻断增强了NK细胞对T细胞增殖的抑制作用(77.85%±8.31%与43.05%±5.95%相比,P<0.05),且上清液中TGF-β1的含量增加。

结论

阻断抑制性KIR受体可显著增强人NK细胞对靶细胞的细胞毒作用;NK细胞分泌的细胞因子TGF-β1可进一步抑制T细胞增殖。

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