通过快速尸检确定肺腺癌中树突状细胞的空间分布和与 T 细胞的联系

IF 3.6 3区 医学 Q2 IMMUNOLOGY
Hilal Ozakinci, Xiaofei Song, Gina S Nazario, Thomas Lila, Benjamin Chen, Tyler Simpson, Jonathan V Nguyen, Carlos M Moran Segura, Zachary J Thompson, Ram Thapa, Trevor A Rose, Eric B Haura, Bruna Pellini, Xiaoqing Yu, Brian H Ruffell, Dung-Tsa Chen, Theresa A Boyle, Amer A Beg
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引用次数: 0

摘要

1型树突状细胞(cDC1)对CD8+ T细胞的活化至关重要,2型树突状细胞(cDC2)可调节CD4+ T细胞的反应,成熟的调节性树突状细胞可抑制肿瘤微环境(TME)中T细胞的反应。然而,我们对 cDC 在人类 TME 中的分布、cDC 在转移部位的流行以及 cDC 在早期和晚期疾病中的差异还缺乏清晰的认识。我们对 10 位肺腺癌患者的快速尸检标本进行了评估,通过使用 18 种标记物和 42 个肿瘤的多重免疫荧光检测 cDC 和免疫细胞。首先,我们发现T细胞、cDC1和cDC2局限于基质,而成熟的调节性DC则富集于肿瘤,这表明它们具有独特的定位特异性功能。其次,肺部和淋巴结肿瘤比肝脏肿瘤更富含T细胞和cDCs,凸显了转移部位TME的差异。第三,虽然 T 细胞和 cDC1 的比例在不同阶段没有差异,但晚期 cDC2 和巨噬细胞比例的增加表明不同阶段 T 细胞反应的调控可能存在差异。总之,这些发现为我们了解人类癌症中的 cDC 生物学提供了新的视角,可能具有重要的治疗意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Rapid Autopsy to Define Dendritic Cell Spatial Distribution and T Cell Association in Lung Adenocarcinoma.

Immunotherapy response is associated with the presence of conventional dendritic cells (cDCs). cDC type 1 (cDC1) is critically important for CD8+ T cell activation, cDC type 2 (cDC2) regulates CD4+ T cell responses, and mature regulatory cDCs may dampen T cell responses in the tumor microenvironment (TME). However, we lack a clear understanding of cDC distribution in the human TME, cDC prevalence in metastatic sites, and cDC differences in early- versus late-stage disease. Rapid autopsy specimens of 10 patients with lung adenocarcinoma were evaluated to detect cDCs and immune cells via multiplex immunofluorescence using 18 markers and 42 tumors. First, we found that T cells, cDC1, and cDC2 were confined to stroma, whereas mature regulatory DCs were enriched in tumor, suggesting unique localization-specific functions. Second, lung and lymph node tumors were more enriched in T cells and cDCs than liver tumors, underscoring differences in the TME of metastatic sites. Third, although the proportion of T cells and cDC1 did not differ in different stages, an increase in the proportion of cDC2 and macrophages in late stage suggests potential differences in regulation of T cell responses in different stages. Collectively, these findings provide new, to our knowledge, insights into cDC biology in human cancer that may have important therapeutic implications.

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来源期刊
Journal of immunology
Journal of immunology 医学-免疫学
CiteScore
8.20
自引率
2.30%
发文量
495
审稿时长
1 months
期刊介绍: The JI publishes novel, peer-reviewed findings in all areas of experimental immunology, including innate and adaptive immunity, inflammation, host defense, clinical immunology, autoimmunity and more. Special sections include Cutting Edge articles, Brief Reviews and Pillars of Immunology. The JI is published by The American Association of Immunologists (AAI)
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