γδ T 细胞调节小细胞肺癌中的抗肿瘤免疫
γδ T cells modulate anti-tumor immunity in small cell lung cancer.
我们的发现表明,活化的γδ T细胞可能是SCLC治疗的有价值靶点。
英文原题:TCF1+CD4+ T cells and microglia co-orchestrate tertiary lymphoid structures to enhance prognosis and immunotherapy in non-small cell lung cancer with brain metastases.
TCF1+CD4+ T cells and microglia co-orchestrate tertiary lymphoid structures to enhance prognosis and immunotherapy in non-small cell lung cancer with brain metastases.
这些发现凸显了TLS作为NSCLC-BM患者预后生物标志物和潜在治疗靶点的重要性。
非小细胞肺癌脑转移(NSCLC-BM)预后不良,仅少数患者对免疫检查点抑制剂(ICIs)有应答。三级淋巴结构(TLSs)已在多种肿瘤中与预后及免疫治疗应答相关。鉴于脑转移独特的免疫环境,NSCLC-BM中的TLSs可能表现出不同的特征。然而,这些颅内TLSs的功能和形成机制仍未被充分了解。
我们回顾性分析了120例切除的NSCLC-BM样本。使用H&E和多色免疫组织化学(mIHC)评估了NSCLC-BM中TLS特征和功能状态的异质性。评估了与OS和iPFS的关联,并开发了包含TLS评分的列线图。利用公共scRNA-seq数据集和mIHC探索了TLS形成的潜在机制,并在LC-BrM小鼠模型中进行了体内功能验证。
TLS主要为瘤内和未成熟状态。瘤内TLS评分升高独立预测延长的OS和iPFS,并预测术后ICIs获益。TLS丰富的肿瘤表现出CD8+ T细胞、FOXP3-CD4+ T细胞和B细胞增加。在机制上,TCF1+CD4+ T细胞和小胶质细胞共定位于TLS内,并可能通过LTβ/LTβR信号促进其形成。同时,基质CXCL12被进一步鉴定为这些细胞的关键趋化因子,并与ICI治疗的良好结局相关。在功能上,rmCXCL12和抗PD-1的联合以LTβR依赖的方式促进TLS形成和颅内肿瘤控制。
BACKGROUND: Non-small cell lung cancer brain metastases (NSCLC-BM) confer a poor prognosis, with only a minority of patients responding to immune checkpoint inhibitors (ICIs). Tertiary lymphoid structures (TLSs) have been linked to prognosis and response to immunotherapy across various tumours. Given the unique immune environment of brain metastases, TLSs within NSCLC-BM might exhibit distinct characteristics. Nevertheless, the function and formation mechanisms of these intracranial TLSs remain inadequately understood. METHODS: We retrospectively analysed 120 resected NSCLC-BM samples. Heterogeneity of TLS characteristics and functional states in NSCLC-BM was assessed using H&E and multiplex immunohistochemistry (mIHC). Associations with OS and iPFS were evaluated, and a nomogram incorporating TLS score was developed. Potential mechanisms underlying TLS formation were explored using public scRNA-seq datasets and mIHC, and were functionally validated in vivo in the LC-BrM mouse model. FINDINGS: TLSs were primarily intratumoral and immature. Elevated intratumoral TLS scores independently predicted prolonged OS and iPFS, and predicted benefit from postoperative ICIs. TLS-rich tumours exhibited increased CD8+ T cells, FOXP3-CD4+ T cells, and B cells. Mechanistically, TCF1+CD4+ T cells and microglia co-localised within TLSs and might facilitate their formation via LTβ/LTβR signalling. Meanwhile, stromal CXCL12 was further identified as a crucial chemoattractant for these cells and correlated with favourable outcomes of ICI therapy. Functionally, the combination of rmCXCL12 and anti-PD-1 promotes TLS formation and intracranial tumour control in an LTβR-dependent manner. INTERPRETATION: These findings highlight the significance of TLSs as prognostic biomarkers and potential therapeutic targets in patients with NSCLC-BM. FUNDING: This work was supported by the Natural Science Foundation of China (82573031); the CQMU Program for Youth Innovation in Future Medicine (W0172); the Postdoctoral Fellowship Program of the China Postdoctoral Science Foundation (GZC20233356).
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