CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Spatial immunoprofiling of retroperitoneal leiomyosarcomas reveals intratumoral heterogeneity in immune cell infiltration, checkpoint molecule expression, and tertiary lymphoid structures.
Spatial immunoprofiling of retroperitoneal leiomyosarcomas reveals intratumoral heterogeneity in immune cell infiltration, checkpoint molecule expression, and tertiary lymphoid structures.
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这些发现突出了显著的瘤内异质性,这可能导致了 ICI 治疗反应的差异。由于免疫检查点分子表达影响治疗资格,可能需要从不同肿瘤区域进行多次活检,以准确评估免疫浸润并指导治疗决策。
平滑肌肉瘤(LMS)是一种罕见的侵袭性癌症,转移阶段的治疗选择有限。对免疫检查点抑制剂(ICIs)的反应不一致,可能是由于肿瘤内异质性,这种异质性在腹膜后LMS等大肿瘤中更为明显。
本研究通过分析不同肿瘤区域中的免疫细胞、三级淋巴结构(TLSs)、检查点分子和细胞因子分泌,探讨了四个大型未治疗LMS肿瘤(每个肿瘤十个样本)的异质性。
免疫组分中观察到显著的区域依赖性差异,TLS仅存在于肿瘤边缘,且在同一肿瘤的不同样本中表现不一致。程序性细胞死亡1(PD-1)和程序性死亡配体1(PD-L1)的表达水平在单个肿瘤内存在差异,并在特定区域发现了共同的免疫模式,包括吲哚胺2,3-双加氧酶1升高、特定巨噬细胞亚群缺失,以及器官邻近边缘处PD-1和淋巴细胞活化基因3(LAG-3)表达降低。抗LAG-3阻断以区域特异性方式改变了细胞因子和检查点分子水平。
This study examined heterogeneity in four large treatment-naive LMS tumours (ten samples per tumour) by analysing immune cells, tertiary lymphoid structures (TLSs), checkpoint molecules, and cytokine secretion across different tumour regions.
Significant region-dependent differences were observed in immune components, with TLSs present only at tumour margins and inconsistently across samples from the same tumour. Expression levels of programmed cell death 1 (PD-1) and programmed death ligand 1 (PD-L1) varied within individual tumours, and shared immune patterns were identified in specific regions, including elevated indoleamine 2,3-dioxygenase 1, absence of a particular macrophage subpopulation, and reduced PD-1 and lymphocyte activation gene 3 (LAG-3) expression at organ-adjacent margins. Anti-LAG-3 blockade altered cytokine and checkpoint molecule levels in a region-specific manner.
These findings highlight substantial intratumoral heterogeneity, which may contribute to the variable response to ICI therapy. As immune checkpoint molecule expression influences treatment eligibility, multiple biopsies from different tumour regions may be necessary to assess immune infiltration accurately and guide therapy decisions.
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