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套细胞淋巴瘤细胞与淋巴瘤相关巨噬细胞之间的对话是依鲁替尼耐药的基础。

Dialog between mantle cell lymphoma cells and lymphoma-associated macrophages underlies ibrutinib resistance.

作者信息

Sun Xiaoqing, Wang Caiqin, Cao Jianghua, Li Jing, Ma Gang, Wu Xianqiu, Sun Peng, Wang Yu, Huang Jiajia, Peter Gale Robert, Li Zhiming

机构信息

Department of Intensive Care Medicine (ICU), State Key Laboratory of Oncology in South China, Guangdong Provincial Clinical Research Center for Cancer, Sun Yat-sen University Cancer Center, Guangzhou 510060, P.R.China.

Department of Lymphoma and Hematology, the Afliated Cancer Hospital of Xiangya School of Medicine, Central South University, Hunan Cancer Hospital, Changsha 410013, Hunan, P.R.China.

出版信息

J Adv Res. 2025 Jul;73:631-644. doi: 10.1016/j.jare.2024.08.023. Epub 2024 Aug 19.

Abstract

INTRODUCTION

Patients with mantle cell lymphoma (MCL) frequently develop resistance to ibrutinib. Lymphoma-associated macrophages (LAMs) may play a causal role in this resistance but remain underexplored in current literature.

OBJECTIVES

To elucidate the role of LAMs in mediating ibrutinib resistance in MCL.

METHODS

We investigated macrophage polarization through multiparameter flow cytometry (MPFC) using antibodies against CD206 and CD86 in blood and tissue samples from patients with MCL, both resistant and sensitive to ibrutinib. Subsequently, we developed an in vitro co-culture model utilizing MCL cell lines to identify cytokines associated with ibrutinib resistance and macrophage M2 polarization. The mechanisms underlying resistance were examined using MPFC, RNA sequencing, and Western blot analysis. Additionally, we assessed whether SB225002, a CXCR2 inhibitor, could reverse ibrutinib resistance through CCK-8 and caspase-3 assays, as well as in a mouse xenograft model involving an ibrutinib-resistant MCL cell line.

RESULTS

In patients exhibiting ibrutinib resistance, the ratio of M2 to M1 LAMs was significantly higher compared to sensitive patients. In co-cultures of LAMs and MCL cells, the percentage of M2 macrophages, the IC50 value for ibrutinib, and the concentrations of IL-8 and CXCL5 were significantly elevated. Mechanistically, CXCL5 secreted by LAMs interacted with the CXCR2 on MCL cells, leading to the activation of the Akt, p38, and STAT3 signaling pathways in the presence of ibrutinib; this activity was diminished upon blockade of the CXCL5/CXCR2 axis. The combination of SB225002 and ibrutinib significantly enhanced MCL cell apoptosis, suppressed lymphoma growth in the xenograft model, and reprogrammed macrophage phenotype compared to treatment with ibrutinib alone.

CONCLUSION

Our data indicate that M2-polarized LAMs are associated with ibrutinib resistance in a model of MCL, and that a CXCR2 inhibitor can reverse this resistance. These findings suggest a potential new therapeutic strategy.

摘要

引言

套细胞淋巴瘤(MCL)患者常对依鲁替尼产生耐药性。淋巴瘤相关巨噬细胞(LAMs)可能在这种耐药性中起因果作用,但在当前文献中仍未得到充分研究。

目的

阐明LAMs在介导MCL对依鲁替尼耐药中的作用。

方法

我们使用抗CD206和CD86抗体,通过多参数流式细胞术(MPFC)研究了MCL患者(包括对依鲁替尼耐药和敏感的患者)血液和组织样本中的巨噬细胞极化情况。随后,我们利用MCL细胞系建立了体外共培养模型,以鉴定与依鲁替尼耐药和巨噬细胞M2极化相关的细胞因子。使用MPFC、RNA测序和蛋白质印迹分析研究了耐药的潜在机制。此外,我们通过CCK-8和caspase-3检测以及在涉及依鲁替尼耐药MCL细胞系的小鼠异种移植模型中评估了CXCR2抑制剂SB225002是否可以逆转依鲁替尼耐药性。

结果

与敏感患者相比,表现出依鲁替尼耐药的患者中M2与M1 LAMs的比例显著更高。在LAMs与MCL细胞的共培养中,M2巨噬细胞的百分比、依鲁替尼的IC50值以及IL-8和CXCL5的浓度均显著升高。从机制上讲,LAMs分泌的CXCL5与MCL细胞上的CXCR2相互作用,导致在存在依鲁替尼的情况下Akt、p38和STAT3信号通路的激活;当CXCL5/CXCR2轴被阻断时,这种活性减弱。与单独使用依鲁替尼治疗相比,SB225002和依鲁替尼的联合使用显著增强了MCL细胞凋亡,抑制了异种移植模型中的淋巴瘤生长,并重新编程了巨噬细胞表型。

结论

我们的数据表明,在MCL模型中,M2极化的LAMs与依鲁替尼耐药相关,并且CXCR2抑制剂可以逆转这种耐药性。这些发现提示了一种潜在的新治疗策略。

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