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与树突状细胞共培养可促进γ/δT细胞增殖,但不增强其细胞毒性活性。

Coculture with dendritic cells promotes proliferation but not cytotoxic activity of gamma/delta T cells.

作者信息

von Lilienfeld-Toal M, Sievers E, Bodemüller V, Mihailescu C, Märten A, Gorschlüter M, Schmidt-Wolf I G H

机构信息

Department of Medicine, Bonn University, Germany.

出版信息

Immunol Lett. 2005 Jun 15;99(1):103-8. doi: 10.1016/j.imlet.2005.02.001. Epub 2005 Feb 23.

Abstract

T cells bearing the gamma9/delta2 T cell receptor (TCR) have recently raised interest as non-MHC restricted effector cells against multiple myeloma. They are described to be stimulated by phosphoantigens without the need of antigen presenting cells. However, in the past a positive effect of cells of the monocyte lineage on activation of gamma/delta T cells has been shown. Monocyte derived dendritic cells (DC) are professional antigen presenting cells widely investigated as stimulators of alpha/beta T cells. But only little is known about the interaction of gamma/delta T cells and monocyte derived DC. Here, we investigated the effect of coculture of mature DC unpulsed or pulsed with ibandronate on the proliferation and cytotoxic activity of isolated gamma/delta T cells. After coculturing monocyte derived DC with isolated gamma/delta T cells, proliferation of gamma/delta T cells was enhanced as determined by the (3)H thymidine uptake assay. Also, IFN-gamma secretion was increased after coculture with DC. As DC are well known to induce activation of alpha/beta T cells we investigated whether the cytotoxic activity of gamma/delta T cells could be increased by coculture with DC. We found no difference in cytotoxic activity of gamma/delta T cells alone or cocultured with unpulsed or pulsed mature DC. Also, sensitizing of myeloma cells by addition of ibandronate could not increase lysis by gamma/delta T cells. In conclusion, monocyte derived DC are capable of stimulating proliferation and secretion of IFN-gamma of gamma/delta T cells but do not exert an effect on cytotoxic activity of gamma/delta T cells against myeloma cells.

摘要

携带γ9/δ2 T细胞受体(TCR)的T细胞最近作为针对多发性骨髓瘤的非MHC限制性效应细胞引起了人们的关注。据描述,它们可被磷酸抗原刺激,而无需抗原呈递细胞。然而,过去已显示单核细胞系细胞对γ/δ T细胞的激活有积极作用。单核细胞衍生的树突状细胞(DC)是作为α/β T细胞刺激物而被广泛研究的专业抗原呈递细胞。但关于γ/δ T细胞与单核细胞衍生DC之间的相互作用却知之甚少。在此,我们研究了未用伊班膦酸钠脉冲或用伊班膦酸钠脉冲的成熟DC与分离的γ/δ T细胞共培养对其增殖和细胞毒性活性的影响。将单核细胞衍生的DC与分离的γ/δ T细胞共培养后,通过(3)H胸苷摄取试验测定,γ/δ T细胞的增殖增强。此外,与DC共培养后,IFN-γ分泌增加。由于众所周知DC可诱导α/β T细胞的激活,我们研究了γ/δ T细胞与DC共培养是否可增强其细胞毒性活性。我们发现单独的γ/δ T细胞或与未脉冲或脉冲的成熟DC共培养的γ/δ T细胞在细胞毒性活性上没有差异。此外,添加伊班膦酸钠使骨髓瘤细胞致敏也不能增加γ/δ T细胞的裂解作用。总之,单核细胞衍生的DC能够刺激γ/δ T细胞的增殖和IFN-γ分泌,但对γ/δ T细胞针对骨髓瘤细胞的细胞毒性活性没有影响。

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