[Clinicopathological characteristics of the CD8+ T lymphocytes infiltration and its mechanism in distinct molecular subtype of medulloblastoma].

Q3 Medicine
北京大学学报(医学版) Pub Date : 2024-06-18
Xiaodong Chai, Ziwen Sun, Haishuang Li, Liangyi Zhu, Xiaodan Liu, Yantao Liu, Fei Pei, Qing Chang
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引用次数: 0

Abstract

Objective: To investigate the characteristics of the CD8+ T cells infiltration from the 4 subtypes in medulloblastoma (MB), to analyze the relationship between CD8+ T cells infiltration and prognosis, to study the function of C-X-C motif chemokine ligand 11 (CXCL11) and its receptor in CD8+ T cells infiltration into tumors and to explore the potential mechanism, and to provide the necessary clinicopathological basis for exploring the immunotherapy of MB.

Methods: In the study, 48 clinical MB samples (12 cases in each of 4 subtypes) were selected from the multiple medical center from 2012 to 2019. The transcriptomics analysis for the tumor of 48 clinical samples was conducted on the NanoString PanCancer IO360TM Panel (NanoString Technologies). Immunohistochemistry (IHC) staining of formalin-fixed, paraffin-embedded sections from MB was carried out using CD8 primary antibody to analyze diffe-rential quantities of CD8+ T cells in the MB four subtypes. Through bioinformatics analysis, the relationship between CD8+T cells infiltration and prognosis of the patients and the expression differences of various chemokines in the different subtypes of MB were investigated. The expression of CXCR3 receptor on the surface of CD8+T cells in MB was verified by double immunofluorescence staining, and the underlying molecular mechanism of CD8+T cells infiltration into the tumor was explored.

Results: The characteristic index of CD8+T cells in the WNT subtype of MB was relatively high, suggesting that the number of CD8+T cells in the WNT subtype was significantly higher than that in the other three subtypes, which was confirmed by CD8 immunohistochemical staining and Gene Expression Omnibus (GEO) database analysis by using R2 online data analysis platform. And the increase of CD8+T cells infiltration was positively correlated with the patient survival. The expression level of CXCL11 in the WNT subtype MB was significantly higher than that of the other three subtypes. Immunofluorescence staining showed the presence of CXCL11 receptor, CXCR3, on the surface of CD8+T cells, suggesting that the CD8+T cells might be attracted to the MB microenvironment by CXCL11 through CXCR3.

Conclusion: The CD8+T cells infiltrate more in the WNT subtype MB than other subtypes. The mechanism may be related to the activation of CXCL11-CXCR3 chemokine system, and the patients with more infiltration of CD8+T cells in tumor have better prognosis. This finding may provide the necessary clinicopathological basis for the regulatory mechanism of CD8+T cells infiltration in MB, and give a new potential therapeutic target for the future immunotherapy of MB.

[CD8+T淋巴细胞浸润的临床病理特征及其在不同分子亚型髓母细胞瘤中的作用机制]。
研究目的探讨髓母细胞瘤(MB)4种亚型CD8+T细胞浸润的特点,分析CD8+T细胞浸润与预后的关系,研究C-X-C motif趋化因子配体11(CXCL11)及其受体在CD8+T细胞浸润肿瘤中的作用及潜在机制,为探讨MB的免疫治疗提供必要的临床病理依据:该研究选取了2012年至2019年多医学中心的48例临床MB样本(4个亚型各12例)。采用NanoString PanCancer IO360TM Panel(NanoString Technologies)对48份临床样本的肿瘤进行转录组学分析。使用CD8一抗对福尔马林固定、石蜡包埋的MB切片进行免疫组化(IHC)染色,分析MB四种亚型中CD8+ T细胞数量的差异。通过生物信息学分析,研究了CD8+T细胞浸润与患者预后的关系以及各种趋化因子在MB不同亚型中的表达差异。通过双重免疫荧光染色验证了CD8+T细胞表面CXCR3受体在MB中的表达,并探讨了CD8+T细胞浸润肿瘤的分子机制:结果:WNT亚型MB中CD8+T细胞的特征指数相对较高,表明WNT亚型中CD8+T细胞的数量明显高于其他三个亚型,这一点通过CD8免疫组化染色和利用R2在线数据分析平台进行的Gene Expression Omnibus(GEO)数据库分析得到了证实。CD8+T细胞浸润的增加与患者的生存率呈正相关。CXCL11在WNT亚型MB中的表达水平明显高于其他三种亚型。免疫荧光染色显示,CD8+T细胞表面存在CXCL11受体CXCR3,表明CD8+T细胞可能被CXCL11通过CXCR3吸引到MB微环境中:结论:与其他亚型相比,CD8+T细胞在WNT亚型MB中的浸润更多。其机制可能与 CXCL11-CXCR3 趋化因子系统的激活有关,肿瘤中 CD8+T 细胞浸润较多的患者预后较好。这一发现可能为CD8+T细胞在MB中浸润的调控机制提供了必要的临床病理学依据,并为未来MB的免疫治疗提供了新的潜在治疗靶点。
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
北京大学学报(医学版)
北京大学学报(医学版) Medicine-Medicine (all)
CiteScore
0.80
自引率
0.00%
发文量
9815
期刊介绍: Beijing Da Xue Xue Bao Yi Xue Ban / Journal of Peking University (Health Sciences), established in 1959, is a national academic journal sponsored by Peking University, and its former name is Journal of Beijing Medical University. The coverage of the Journal includes basic medical sciences, clinical medicine, oral medicine, surgery, public health and epidemiology, pharmacology and pharmacy. Over the last few years, the Journal has published articles and reports covering major topics in the different special issues (e.g. research on disease genome, theory of drug withdrawal, mechanism and prevention of cardiovascular and cerebrovascular diseases, stomatology, orthopaedic, public health, urology and reproductive medicine). All the topics involve latest advances in medical sciences, hot topics in specific specialties, and prevention and treatment of major diseases. The Journal has been indexed and abstracted by PubMed Central (PMC), MEDLINE/PubMed, EBSCO, Embase, Scopus, Chemical Abstracts (CA), Western Pacific Region Index Medicus (WPR), JSTChina, and almost all the Chinese sciences and technical index systems, including Chinese Science and Technology Paper Citation Database (CSTPCD), Chinese Science Citation Database (CSCD), China BioMedical Bibliographic Database (CBM), CMCI, Chinese Biological Abstracts, China National Academic Magazine Data-Base (CNKI), Wanfang Data (ChinaInfo), etc.
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