Institute for Research and Innovation in Health (i3S), University of Porto, Porto, Portugal.
Institute of Biomedical Sciences Abel Salazar (ICBAS), University of Porto, Porto, Portugal.
Cancer Immunol Res. 2020 Nov;8(11):1407-1425. doi: 10.1158/2326-6066.CIR-20-0264. Epub 2020 Sep 15.
Tumor growth is accompanied with dramatic changes in the cellular glycome, such as the aberrant expression of complex branched N-glycans. However, the role of this protumoral N-glycan in immune evasion and whether its removal contributes to enhancement of immune recognition and to unleashing an antitumor immune response remain elusive. We demonstrated that branched N-glycans are used by colorectal cancer cells to escape immune recognition, instructing the creation of immunosuppressive networks through inhibition of IFNγ. The removal of this "glycan-mask" exposed immunogenic mannose glycans that potentiated immune recognition by DC-SIGN-expressing immune cells, resulting in an effective antitumor immune response. We revealed a glycoimmune checkpoint in colorectal cancer, highlighting the therapeutic efficacy of its deglycosylation to potentiate immune recognition and, thus, improving cancer immunotherapy.
肿瘤生长伴随着细胞糖组的显著变化,例如异常表达复杂的分支 N-聚糖。然而,这种原肿瘤 N-聚糖在免疫逃避中的作用,以及它的去除是否有助于增强免疫识别并引发抗肿瘤免疫反应,仍然难以捉摸。我们证明,结直肠癌细胞利用分支 N-聚糖逃避免疫识别,通过抑制 IFNγ 来指示免疫抑制网络的建立。去除这种“聚糖掩蔽物”暴露出免疫原性甘露糖聚糖,增强了表达 DC-SIGN 的免疫细胞的免疫识别,从而产生有效的抗肿瘤免疫反应。我们在结直肠癌中揭示了一个糖免疫检查点,强调了其去糖基化以增强免疫识别的治疗效果,从而改善癌症免疫治疗。