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循环 Hsp70 水平升高和 CD94+/CD69+ NK 细胞患病率增加可预测晚期非小细胞肺癌

英文原题:Elevated Levels of Circulating Hsp70 and an Increased Prevalence of CD94+/CD69+ NK Cells Is Predictive for Advanced Stage Non-Small Cell Lung Cancer.

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Elevated Levels of Circulating Hsp70 and an Increased Prevalence of CD94+/CD69+ NK Cells Is Predictive for Advanced Stage Non-Small Cell Lung Cancer.

PubMed 2022/11/21(内容时间) Cancers (Basel) Q2 · IF 4.8(JCR 2025)

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中文摘要

非小细胞肺癌(NSCLC)是全球第二常见诊断的肿瘤。尽管包括放化疗和免疫检查点抑制剂阻断在内的多模式治疗已取得临床进展,晚期NSCLC患者的总生存期仍然很差,不足16个月。已充分证实,包括NSCLC在内的许多侵袭性肿瘤实体在胞质中过表达主要应激诱导型热休克蛋白70(Hsp70),以肿瘤特异性方式将其呈递于质膜上,并将Hsp70释放入循环。尽管高Hsp70水平与肿瘤侵袭性和治疗耐药相关,但膜结合型Hsp70可作为肿瘤特异性抗原,被Hsp70致敏的自然杀伤(NK)细胞识别,这些细胞表达C型凝集素受体CD94,后者是活化性受体复合物CD94/NKG2C的组成部分。

因此,我们研究了循环Hsp70水平以及外周血淋巴细胞亚群组成的变化,作为NSCLC中晚期国际抗癌联盟(UICC)分期的潜在生物标志物。正如预期,与健康对照相比,NSCLC患者的循环Hsp70水平显著更高;与UICC I期患者相比,晚期UICC分期患者的循环Hsp70水平也显著更高。吸烟状态对循环Hsp70水平无显著影响。与此同时,CD4+辅助性T细胞的比例较健康对照和I期肿瘤患者更低,而CD8+细胞毒性T细胞的比例则逐渐升高。CD3-/CD56+、CD3-/NKp30、CD3-/NKp46+和CD3-/NKG2D+ NK细胞的患病率在疾病IV/IIIB期高于IIIA期,但与健康个体相比无统计学差异。

然而,与I期和健康对照相比,表达CD94和活化/耗竭标志物CD69的NK细胞比例在较高肿瘤分期中显著增加。我们推测,尽管循环Hsp70水平升高可能促进晚期NSCLC患者中CD94+ NK细胞的患病率,但由于CD4+ T辅助细胞来源的促炎细胞因子支持不足,这些NK细胞的细胞溶解活性也未能控制肿瘤生长。这一假设得到了以下比较性多重细胞因子分析的支持:在肺癌患者中,CD4+ T细胞比例低、NK细胞比例高且Hsp70水平高的患者,与CD4+ T细胞比例高但IL-2、IL-4、IL-6、IFN-γ、颗粒酶B水平较低的患者相比。

展开英文摘要原文

Non-small cell lung cancer (NSCLC) is the second most frequently diagnosed tumor worldwide. Despite the clinical progress which has been achieved by multimodal therapies, including radiochemotherapy, and immune checkpoint inhibitor blockade, the overall survival of patients with advanced-stage NSCLC remains poor, with less than 16 months.

It is well established that many aggressive tumor entities, including NSCLC, overexpress the major stress-inducible heat shock protein 70 (Hsp70) in the cytosol, present it on the plasma membrane in a tumor-specific manner, and release Hsp70 into circulation. Although high Hsp70 levels are associated with tumor aggressiveness and therapy resistance, membrane-bound Hsp70 can serve as a tumor-specific antigen for Hsp70-primed natural killer (NK) cells, expressing the C-type lectin receptor CD94, which is part of the activator receptor complex CD94/NKG2C.

Therefore, we investigated circulating Hsp70 levels and changes in the composition of peripheral blood lymphocyte subsets as potential biomarkers for the advanced Union for International Cancer Control (UICC) stages in NSCLC. As expected, circulating Hsp70 levels were significantly higher in NSCLC patients compared to the healthy controls, as well as in patients with advanced UICC stages compared to those in UICC stage I.

Smoking status did not influence the circulating Hsp70 levels significantly. Concomitantly, the proportions of CD4+ T helper cells were lower compared to the healthy controls and stage I tumor patients, whereas that of CD8+ cytotoxic T cells was progressively higher. The prevalence of CD3-/CD56+, CD3-/NKp30, CD3-/NKp46+, and CD3-/NKG2D+ NK cells was higher in stage IV/IIIB of the disease than in stage IIIA but were not statistically different from that in healthy individuals.

However, the proportion of NK cells expressing CD94 and the activation/exhaustion marker CD69 significantly increased in higher tumor stages compared with stage I and the healthy controls.

We speculate that although elevated circulating Hsp70 levels might promote the prevalence of CD94+ NK cells in patients with advanced-stage NSCLC, the cytolytic activity of these NK cells also failed to control tumor growth due to insufficient support by pro-inflammatory cytokines from CD4+ T helper cells.

This hypothesis is supported by a comparative multiplex cytokine analysis of the blood in lung cancer patients with a low proportion of CD4+ T cells, a high proportion of NK cells, and high Hsp70 levels versus patients with a high proportion of CD4+ T cells exhibiting lower IL-2, IL-4, IL-6, IFN-γ, granzyme B levels.

论文信息

作者
Seier S、Bashiri Dezfouli A、Lennartz P、Pockley AG、Klein H、Multhoff G
单位
Department of Radiation Oncology, Central Institute for Translational Cancer Research Technische Universität München (TranslaTUM), Klinikum Rechts der Isar, 81675 Munich, Germany.Germany
期刊
Cancers2022 Nov 21
原文标识
PubMed 36428793 · DOI 10.3390/cancers14225701