Revealing the effect of X-ray or proton brain irradiation on systemic inflammation and leukocyte subpopulation interplay in rodents.

IF 3.6 3区 医学 Q3 CELL BIOLOGY Journal of Leukocyte Biology Pub Date : 2024-07-02 DOI:10.1093/jleuko/qiae156
Thao-Nguyen Pham, Julie Coupey, Marc Rousseau, Juliette Thariat, Samuel Valable
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Abstract

The absolute lymphocyte count (ALC), lymphocyte-to-monocyte ratio (LMR), and neutrophil-to-lymphocyte ratio (NLR) offer convenient means to assess systemic inflammation post-cancer treatment, which influences treatment outcomes. Understanding these biomarker variations and leukocyte subpopulation interplay is crucial for optimizing radiotherapy. Herein, leukocyte subpopulations (T-CD4+, T-CD8+, B-cells, NK-cells, neutrophils, monocytes) during and after brain irradiation (using X-rays or Protons) in tumor-free mice were used to compute ALC, LMR, and NLR, on which radiation parameter influence was assessed by principal component analysis (PCA). NLR kinetics were further examined using modeling. Leukocyte subpopulations interplays and their response to radiation parameters were examined using PCA and correlation analysis. Under X-rays, ALC and LMR decreased, with ALC recovered to baseline after irradiation, but not LMR. Both X-rays and protons increased the NLR during irradiation, recovering in protons but not X-rays. Both irradiation volume and dose rate had a pronounced effect on the NLR. Leukocyte subpopulation interplay was observed under X-rays and protons, normalizing in the proton group by day 28. Lymphopenia was observed in all lymphocyte subpopulations under X-ray irradiation but not protons. The recovery patterns varied among the subpopulations. Neutrophil counts increased during irradiation, with the recovery of protons, but not X-rays, by day 28. Interplays between NK-cells and myeloid subpopulations were evident under X-rays but not protons. Importantly, no interplay was detected between myeloid cells and T/B-cells, indicating that LMR and NLR variations were primarily due to independent responses to brain irradiation. A tumor-free experimental mouse model was used to study the effects of brain radiotherapy on systemic immunity. When administering fractionated irradiation with a total dose of 20 Gy using a vertical beam to either the whole brain or hemi-brain, proton irradiation had fewer adverse impacts on the immune system compared to X-rays in tumor-free rodents.

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揭示 X 射线或质子脑辐照对啮齿动物全身炎症和白细胞亚群相互作用的影响
淋巴细胞绝对计数(ALC)、淋巴细胞与单核细胞比值(LMR)和中性粒细胞与淋巴细胞比值(NLR)为评估癌症治疗后的全身炎症提供了便捷的方法,而炎症会影响治疗效果。了解这些生物标志物的变化和白细胞亚群的相互作用对优化放疗至关重要。在此,我们利用无肿瘤小鼠脑部照射(使用X射线或质子)期间和之后的白细胞亚群(T-CD4+、T-CD8+、B细胞、NK细胞、中性粒细胞、单核细胞)计算ALC、LMR和NLR,并通过主成分分析(PCA)评估辐射参数对其的影响。通过建模进一步研究了 NLR 动力学。白细胞亚群之间的相互作用及其对辐射参数的反应是通过 PCA 和相关分析进行检验的。在X射线照射下,ALC和LMR下降,照射后ALC恢复到基线,但LMR没有恢复到基线。在辐照期间,X射线和质子都会增加NLR,质子会恢复,但X射线不会。辐照量和剂量率对 NLR 都有明显的影响。在 X 射线和质子照射下观察到白细胞亚群相互作用,质子组在第 28 天时恢复正常。在 X 射线照射下,所有淋巴细胞亚群都出现了淋巴细胞减少症,而质子则没有。不同亚群的恢复模式各不相同。中性粒细胞计数在辐照期间增加,质子组在第 28 天前恢复,而 X 射线组则没有。在 X 射线照射下,NK 细胞和骨髓亚群之间的相互作用很明显,但质子则不明显。重要的是,髓系细胞和T/B细胞之间没有发现相互作用,这表明LMR和NLR的变化主要是由于对脑辐照的独立反应。研究人员利用无肿瘤实验小鼠模型来研究脑放射治疗对全身免疫的影响。在对全脑或半脑进行总剂量为20Gy的垂直射线分次照射时,质子照射与X射线相比对无肿瘤啮齿类动物免疫系统的不良影响较小。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Leukocyte Biology
Journal of Leukocyte Biology 医学-免疫学
CiteScore
11.50
自引率
0.00%
发文量
358
审稿时长
2 months
期刊介绍: JLB is a peer-reviewed, academic journal published by the Society for Leukocyte Biology for its members and the community of immunobiologists. The journal publishes papers devoted to the exploration of the cellular and molecular biology of granulocytes, mononuclear phagocytes, lymphocytes, NK cells, and other cells involved in host physiology and defense/resistance against disease. Since all cells in the body can directly or indirectly contribute to the maintenance of the integrity of the organism and restoration of homeostasis through repair, JLB also considers articles involving epithelial, endothelial, fibroblastic, neural, and other somatic cell types participating in host defense. Studies covering pathophysiology, cell development, differentiation and trafficking; fundamental, translational and clinical immunology, inflammation, extracellular mediators and effector molecules; receptors, signal transduction and genes are considered relevant. Research articles and reviews that provide a novel understanding in any of these fields are given priority as well as technical advances related to leukocyte research methods.
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