Tumor-activated TCRγδ⁺ T cells from gastric cancer patients induce the antitumor immune response of TCRαβ⁺ T cells via their antigen-presenting cell-like effects.
Chaoming MaoXiao MouYuepeng ZhouGuoyue YuanChengcheng XuHongli LiuTingting ZhengJia TongShengjun WangDeyu ChenPublished in: Journal of immunology research (2014)
Human γδ T cells display the principal characteristics of professional antigen-presenting cells (APCs), in addition to playing a vital role in immunity through cytokine secretion and their cytotoxic activity. However, it is not clear whether γδ T cells perform APC-like functions under pathological conditions. In this study, we showed that, in contrast to peripheral-derived γδ T cells directly isolated from PBMCs of gastric cancer patients, tumor-activated γδ T cells not only killed tumor cells efficiently but also strongly induced primary CD4(+) and CD8(+) αβ T cells proliferation and differentiation. More importantly, they abrogated the immunosuppression induced by CD4(+)CD25(+) Treg cells and induced the cytotoxic function of CD8(+) αβ T cells from patients with gastric cancer. In conclusion, tumor-activated γδ T cells can induce adaptive immune responses through their APC-like functions, and these cells may be a potentially useful tool in the development of tumor vaccines and immunotherapy.
Keyphrases
- immune response
- induced apoptosis
- cell cycle arrest
- end stage renal disease
- signaling pathway
- chronic kidney disease
- magnetic resonance
- high glucose
- newly diagnosed
- regulatory t cells
- cell death
- oxidative stress
- diabetic rats
- dendritic cells
- case report
- computed tomography
- magnetic resonance imaging
- toll like receptor
- drug induced
- peritoneal dialysis
- mesenchymal stem cells
- prognostic factors
- cell therapy
- pi k akt
- stress induced