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CD155 表达损害非小细胞肺癌抗 PD-1 治疗应答

英文原题:CD155 expression impairs anti-PD1 therapy response in non-small cell lung cancer.

查看英文原题

CD155 expression impairs anti-PD1 therapy response in non-small cell lung cancer.

PubMed 2022/06/11(内容时间) Clin Exp Immunol Q2 · IF 3.9(JCR 2025)

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中文摘要

CD155是肿瘤细胞表达的免疫检查点蛋白,可与其配体TIGIT相互作用;抑制这一通路为癌症治疗提供了新方向。目前尚不清楚CD155表达是否影响非小细胞肺癌(NSCLC)患者对抗PD-1治疗的应答。本观察性研究分析NSCLC患者CD155表达及其对PD-1抑制剂的治疗应答。研究回顾性采用免疫组化检测接受PD-1治疗的晚期NSCLC患者CD155表达和TIL(肿瘤浸润淋巴细胞)中的TIGIT。CD155阳性患者对PD-1治疗的应答显著差于CD155阴性患者[总体缓解率(ORR):25.6%对54.8%,P<0.01;无进展生存期中位数:5.1对7.1个月,风险比(HR)=2.322;95% CI 1.396–3.861,P=0.001]。这一影响在PD-L1阳性患者中更明显。PD-L1阳性肺腺癌(LUAC)和肺鳞癌(LUSC)患者中,CD155表达均与PD-1治疗应答较差相关;该关联见于一线PD-1治疗、后线PD-1治疗及PD-1联合治疗。

此外,TIGIT表达与PD-1治疗效果无关。本项初步研究提示,CD155表达会削弱PD-1治疗效果并增加疾病进展风险。CD155通路可能是有前景的免疫治疗靶点,同时靶向CD155/TIGIT和PD-1/PD-L1可能提高免疫治疗效果。

展开英文摘要原文

CD155 is an immune checkpoint protein expressed in tumor cells that interacts with its ligand TIGIT, and inhibition of this point presents a new and novel way for cancer therapy. At present, whether the expression of CD155 affects the response to anti( )-PD1 treatment in non-small cell lung cancer (NSCLC) patients is unclear. This observational study characterizes the expression of CD155 in NSCLC patients and its responses to PD1 inhibitors.

We retrospectively detected the expression of CD155 and tumor-infiltrated lymphocyte (TIL) TIGIT by immunohistochemistry in advanced NSCLC patients who had received PD1 therapy. The patients with CD155 positive had a significantly worse response to PD1 therapy compared with CD155-negative patients (ORR: 25. 6% vs 54. 8%, P < 0. 01; median PFS: 5. 1 vs 7. 1 months, HR = 2. 322; 95% CI 1. 396-3.

861, P = 0. 001). This effect is more prominent in PD-L1 positive patients. In PD-L1-positive patients, CD155 expression is associated with a poor response to PD1 therapy in both LUAC (lung adenocarcinoma) and LUSC (lung squamous cell carcinoma); meanwhile, the expression of CD155 was associated with a poor response to the first-line PD1 therapy, posterior-line PD1 therapy, and PD1 combination therapy.

Furthermore, the expression of TIGIT was not correlated with the therapeutic effect of PD1.

Our pilot study suggests that CD155 expression attenuates the therapeutic effect of PD1 therapy and is associated with a higher risk of progression. The CD155 pathway may be a promising immunotherapeutic target and simultaneously targeting CD155/TIGIT and PD1/PD-L1 can improve the effect of immunotherapy.

论文信息

作者
Jiang C、Qu X、Ma L、Yi L、Cheng X、Gao X、Wang J、Che N
单位
Department of Medical Oncology, Beijing Chest Hospital, Capital Medical University, Beijing Tuberculosis and Thoracic Tumor Research Institute, Beijing, China.China
文献类型
观察性研究
期刊
Clinical and experimental immunology2022 Jun 11
原文标识
PubMed 35262683 · DOI 10.1093/cei/uxac020