Ni Yan Hong, Ding Liang, Zhang Dong Ya, Hou Ya Yi, Huang Xiaofeng, Hu Qingang
Nanjing Stomatological Hospital, Medical School and The State Key Laboratory of Pharmaceutical Biotechnology, Division of Immunology, Nanjing university, Nanjing, China.
Histopathology. 2015 Nov;67(5):730-9. doi: 10.1111/his.12703. Epub 2015 May 19.
Toll-like receptor (TLR)-7 agonists have been used in cancer immunotherapy, but tumour heterogeneity means that TLR-7 activity is variable in different components of the tumour microenvironment and the characteristics of TLR-7 in oral squamous cell carcinoma (OSCC) are unclear.
Twenty healthy oral tissues, 50 oral leukoplakia tissues and 166 retrospective primary OSCC samples were collected for immunohistochemical staining of TLR-7 and showed up-regulated expression during carcinogenesis. Moreover, patients with high expression of TLR-7 in tumour cells (TCs) had poor differentiation and prognosis. Interestingly, patients with high expression of TLR-7 in stroma fibroblast-like cells (FLCs) had low tumour stage, no lymph node metastasis (LNM) and better prognosis. Furthermore, Ki-67, CD3, CD4, CD8 and forkhead box protein 3 (FoxP3)(+) tumour-infiltrated lymphocytes were assessed and we found that TLR-7(high) TCs were infiltrated by fewer CD3(+) CD4(+) but more FoxP3(+) lymphocytes. Importantly, patients with TLR-7(low) TCs and TLR-7(high) FLCs had less FoxP3(+) lymphocyte infiltration and longer survival time than those with TLR-7(high) TCs/TLR-7(low) FLCs, although TLR-7 was not an independent prognostic factor for OSCC.
The low expression of TLR-7 in tumour and high expression of TLR-7 in stroma predict a good clinical outcome for OSCC patients, and stroma FLCs might be amenable to immunotherapy by a TLR-7 agonist.
Toll样受体(TLR)-7激动剂已用于癌症免疫治疗,但肿瘤异质性意味着TLR-7活性在肿瘤微环境的不同成分中存在差异,且口腔鳞状细胞癌(OSCC)中TLR-7的特征尚不清楚。
收集20例健康口腔组织、50例口腔白斑组织和166例回顾性原发性OSCC样本进行TLR-7免疫组化染色,结果显示其在癌变过程中表达上调。此外,肿瘤细胞(TCs)中TLR-7高表达的患者分化差且预后不良。有趣的是,基质成纤维细胞样细胞(FLCs)中TLR-7高表达的患者肿瘤分期低、无淋巴结转移(LNM)且预后较好。此外,对Ki-67、CD3、CD4、CD8和叉头框蛋白3(FoxP3)(+)肿瘤浸润淋巴细胞进行评估,我们发现TLR-7(高)TCs被较少的CD3(+)CD4(+)淋巴细胞浸润,但被较多的FoxP3(+)淋巴细胞浸润。重要的是,TLR-7(低)TCs和TLR-7(高)FLCs的患者比TLR-7(高)TCs/TLR-7(低)FLCs的患者FoxP3(+)淋巴细胞浸润更少且生存时间更长,尽管TLR-7不是OSCC的独立预后因素。
肿瘤中TLR-7低表达和基质中TLR-7高表达预示着OSCC患者良好的临床结局,且基质FLCs可能适合用TLR-7激动剂进行免疫治疗。