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首页> 外文期刊>Journal for ImmunoTherapy of Cancer >P03.03?Organization, function and gene expression of tertiary lymphoid structures in PDAC resembles lymphoid follicles in secondary lymphoid organs
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P03.03?Organization, function and gene expression of tertiary lymphoid structures in PDAC resembles lymphoid follicles in secondary lymphoid organs

机译:p03.03?PDAC中三级淋巴结结构的组织,功能和基因表达在次级淋巴器官中类似淋巴卵泡

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Background Secondary lymphoid organs (SLO) are involved in induction and enhancement of anti-tumor immune responses on different tumor entities. Recent evidence suggests that anti-tumor immune responses may also be induced or enhanced in the tumor microenvironment in so called tertiary lymphoid structures (TLS). It is assumed that TLS represent a hotspot for T cell priming, B cell activation, and differentiation, leading to cellular and humoral anti-tumor immune response. Methods FFPE-slides of 120 primary pancreatic ductal adenocarcinoma (PDAC) patients were immunohistochemically (IHC) stained for CD20, CD3, CD8 and HLA-ABC to analyze spatial distribution of tumor-infiltrating lymphocytes. 5-color immunofluorescence staining was performed to further investigate structural components of TLS in comparison to lymphoid follicles in SLOs. Microscope-based laser microdissection and Nanostring-base RNA expression analysis were used to compare gene expression in PDAC, TLS, SLOs and normal pancreatic tissue. Results TLS were frequently detected in PDAC and were mainly localized along the invasive tumor margin. In less than 10% of the cases TLS were infiltrating the tumors. Interestingly, 20% of the patients had no TLS. Results of TLS will be correlated with clinical parameters, Immunoscore and immune escape mechanisms. 5-color Immunofluorescence staining revealed similar organization and function of TLS and SLO. Finally, gene expression analyzed by Nanostring revealed largely overlapping expression patterns in TLS and SLO. Conclusions The results clearly demonstrate close similarities between SLO and TLS in terms of composition, distribution and gene expression Patterns. Disclosure Information M. Thelen: None. M.A. García-Márquez: None. T. Nestler: None. S. Wagener-Ryczek: None. J. Lehmann: None. E. Staib: None. F. Popp: None. F. Gebauer: None. P. Lohneis: None. M. Odenthal: None. S. Merkelbach-Bruse: None. C. Bruns: None. K. Wennhold: None. M. von Bergwelt-Baildon: None. H.A. Schl??er: None.
机译:背景技术次级淋巴器官(SLO)参与诱导和增强不同肿瘤实体的抗肿瘤免疫应答。最近的证据表明,在所谓的三级淋巴结结构(TLS)中,也可以在肿瘤微环境中诱导或增强抗肿瘤免疫应答。假设TLS代表T细胞引发,B细胞活化和分化的热点,导致细胞和体液抗肿瘤免疫反应。方法对120个初级胰腺导管腺癌(PDAC)患者的FFPE-载玻片是免疫组织化学(IHC)染色CD20,CD3,CD8和HLA-ABC,分析肿瘤浸润淋巴细胞的空间分布。进行5型彩色免疫荧光染色,以进一步研究TLS的结构组分与乳糜瓶中的淋巴卵泡相比。基于显微镜的激光微生物和纳米杆基RNA表达分析用于比较PDAC,TLS,SLO和正常胰腺组织中的基因表达。结果在PDAC中经常检测到TLS,主要是沿着侵入性肿瘤裕度定位的。在不到10%的病例中,TLS渗透肿瘤。有趣的是,20%的患者没有TLS。 TLS的结果将与临床参数,免疫审查和免疫逃逸机制相关联。 5型彩色免疫荧光染色揭示了TLS和SLO的类似组织和功能。最后,通过纳米分析分析的基因表达在TLS和SLO中显示出很大的重叠表达模式。结论结果清楚地展示了在组成,分布和基因表达模式方面的SLO和TL之间的密切相似性。披露信息M. Thelen:无。 m.a.garcía-márquez:没有。 T.雀巢:没有。 S. Wagener-Ryczek:没有。 J. Lehmann:没有。 E. staib:没有。 F. POPP:无。 F. Gebauer:没有。 P. lohneis:没有。 M. Odenthal:没有。 S.Merkelbach-Buxuse:没有。 C. Bruns:没有。 K. Wennhold:没有。 M. von Bergwelt-Baildon:没有。哈。 schl ??呃:没有。

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