纵向血浆代谢组学指导食管鳞状细胞癌化疗免疫治疗的动态风险评估与饮食调节
Longitudinal Plasma Metabolomics Guides Dynamic Risk Assessment and Dietary Modulation for Esophageal Squamous Cell Cancer Chemoimmunotherapy.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Survival benefit and spatial properties of tertiary lymphoid structures in esophageal squamous cell carcinoma with neoadjuvant therapies.
Survival benefit and spatial properties of tertiary lymphoid structures in esophageal squamous cell carcinoma with neoadjuvant therapies.
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三级淋巴结构(TLSs)与接受单纯手术(SA)的食管鳞状细胞癌(ESCC)患者的生存相关。然而,其在新辅助治疗中的临床相关性仍知之甚少。
在此,我们首先研究了359例接受新辅助化疗(NCT)、新辅助免疫治疗(NCI)、新辅助放化疗(NCRT)或SA的ESCC患者中TLSs的存在、成熟度和空间分布。
我们发现成熟TLS(MTLS)是ESCC的独立预后因素。NCI组未成熟TLS病例最少。NCRT组MTLSs最少。MTLSs主要位于间质和正常区域;这些MTLSs与新辅助治疗结局呈正相关。在四组中,NCI组TLSs周围150 μm范围内的T细胞最多。大多数T细胞分散至距TLSs超过150 μm处,而B细胞仍集中在TLSs内。与SA组相比,先天性淋巴细胞和滤泡树突状细胞在NCRT和NCI组中的浸润及其与生存的关联有所不同。新型PD-L1联合阳性评分NCPS与MTLSs和新辅助治疗疗效呈正相关。ScRNA-seq分析显示,TLS+肿瘤具有增多的浆细胞、B细胞、Th17、Tfh和Th1,以及升高的耗竭CD8+ T细胞,后者高表达检查点分子和颗粒酶。
总之,MTLSs有利于接受多种新辅助治疗的ESCC患者的治疗结局。MTLSs的空间分布与新辅助治疗所改变的多区域免疫状态相关。
Tertiary lymphoid structures (TLSs) were associated with survival in esophageal squamous cell carcinoma (ESCC) undergoing surgery alone (SA).
However, their clinical relevance in neoadjuvant therapies remains less known.
Here, we firstly investigated the presence, maturation and spatial distribution of TLSs in 359 ESCC patients receiving neoadjuvant chemotherapy (NCT), neoadjuvant immunotherapy (NCI), neoadjuvant chemoradiotherapy (NCRT) or SA.
We found mature TLS (MTLS) was an independent prognostic factor in ESCC. NCI group had the lowest immature TLS cases. NCRT group had the lowest MTLSs. MTLSs mostly located in stromal and normal compartments; these MTLSs were positively correlated with neoadjuvant therapy outcomes. NCI group displayed the highest T cells within 150 μm proximity of TLSs among the four groups. Most T cells were dispersed up to more than 150 μm from TLSs, while B cells remained concentrated within TLSs. Innate lymphoid cells and follicular dendritic cells infiltrated and connected with survival differently in NCRT and NCI groups compared with SA group.
The novel PD-L1 combined positive score, NCPS, was positively connected with MTLSs and neoadjuvant therapy efficacy. ScRNA-seq analysis revealed TLS+ tumors had increased plasma cells, B cells, Th17, Tfh and Th1, and elevated exhausted CD8 + T cells that highly expressed checkpoint molecules and granzymes. Conclusively, MTLSs favored treatment outcome in ESCC patients receiving multiple neoadjuvant therapies. The spatial distribution of MTLSs was associated with multiregional immune status modified by the neoadjuvant therapies.
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