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CD8+ T细胞亚群的变化作为影响肺部癌症患者免疫衰老的证据:一项观察性病例对照研究。

Shifts in subsets of CD8+ T-cells as evidence of immunosenescence in patients with cancers affecting the lungs: an observational case-control study.

作者信息

Onyema Oscar Okwudiri, Decoster Lore, Njemini Rose, Forti Louis Nuvagah, Bautmans Ivan, De Waele Marc, Mets Tony

机构信息

Gerontology Department and Frailty in Aging Research (FRIA) Group, Faculty of Medicine and Pharmacy, Vrije Universiteit Brussel, Laarbeeklaan 103, B-1090, Brussel, Belgium.

Department of Medical Oncology, Oncologisch Centrum, Universitair Ziekenhuis Brussel & Vrije Universiteit Brussel, Laarbeeklaan 101, B-1090, Brussel, Belgium.

出版信息

BMC Cancer. 2015 Dec 28;15:1016. doi: 10.1186/s12885-015-2013-3.

Abstract

BACKGROUND

Shifts in CD8+ T-cell subsets that are hallmarks of immunosenescence are observed in ageing and in conditions of chronic immune stimulation. Presently, there is limited documentation of such changes in lung cancer and other malignancies affecting the lungs.

METHODS

Changes in CD8+ T-cell subsets, based on the expression of CD28 and CD57, were analysed in patients with various forms of cancer affecting the lungs, undergoing chemotherapy and in a control group over six months, using multi-colour flow cytometry.

RESULTS

The differences between patients and controls, and the changes in the frequency of CD8+ T-cell subpopulations among lung cancer patients corresponded to those seen in immunosenescence: lower CD8-/CD8+ ratio, lower proportions of CD28+CD57- cells consisting of naïve and central memory cells, and higher proportions of senescent-enriched CD28-CD57+ cells among the lung cancer patients, with the stage IV lung cancer patients showing the most pronounced changes. Also observed was a tendency of chemotherapy to induce the formation of CD28+CD57+ cells, which, in line with the capacity of chemotherapy to induce the formation of senescent cells, might provide more evidence supporting CD28+CD57+ cells as senescent cells.

CONCLUSION

Immunosenescence was present before the start of the treatment; it appeared to be pronounced in patients with advanced cases of malignancies affecting the lungs, and might not be averted by chemotherapy.

摘要

背景

在衰老过程以及慢性免疫刺激情况下,可观察到作为免疫衰老标志的CD8 + T细胞亚群发生变化。目前,关于肺癌及其他影响肺部的恶性肿瘤中此类变化的文献记载有限。

方法

采用多色流式细胞术,对接受化疗的各类肺部癌症患者以及一个对照组在六个月期间基于CD28和CD57表达的CD8 + T细胞亚群变化进行了分析。

结果

患者与对照组之间的差异,以及肺癌患者中CD8 + T细胞亚群频率的变化与免疫衰老中所见变化一致:肺癌患者的CD8 - /CD8 + 比率较低,由幼稚和中枢记忆细胞组成的CD28 + CD57 - 细胞比例较低,而富含衰老细胞的CD28 - CD57 + 细胞比例较高,其中IV期肺癌患者的变化最为明显。还观察到化疗有诱导CD28 + CD57 + 细胞形成的趋势,鉴于化疗诱导衰老细胞形成的能力,这可能为支持CD28 + CD57 + 细胞为衰老细胞提供更多证据。

结论

免疫衰老在治疗开始前就已存在;在影响肺部的晚期恶性肿瘤患者中似乎较为明显,且化疗可能无法避免。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae03/4692066/4ca8156bb56c/12885_2015_2013_Fig1_HTML.jpg

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