IL-3 驱动的 T 细胞-嗜碱性粒细胞串联增强了抗肿瘤免疫力。

IF 8.1 1区 医学 Q1 IMMUNOLOGY
Jian Wei, Colleen L Mayberry, Xiaoting Lv, Fangyan Hu, Taushif Khan, Natalie A Logan, John J Wilson, John D Sears, Damien Chaussabel, Chih-Hao Chang
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引用次数: 0

摘要

细胞毒性T淋巴细胞(CTL)在抗癌过程中发挥着关键作用,但它们的功效往往受到免疫抑制性肿瘤微环境的阻碍,从而导致衰竭。本研究探讨了白细胞介素(IL)-3 在通过 CTL 调节抗肿瘤免疫中的作用。瘤内 CTL 的 IL-3 产量会逐渐下降,这与细胞毒性功能受损有关。通过腹腔注射重组IL-3、表达IL-3的肿瘤细胞或IL-3设计的CD8+T细胞来增强IL-3的补充,可在提高CTL活性的同时保护患者免受肿瘤进展的影响。CTL 对这种疗效至关重要,因为 IL-3 对 Rag1 基因敲除小鼠或 CD8+ T 细胞耗竭后的肿瘤生长没有影响。CTL衍生的IL-3不是直接发挥作用,而是对嗜碱性粒细胞施加影响,协同放大CTL内的抗肿瘤免疫力。引入 IL-3 激活的嗜碱性粒细胞可延缓肿瘤进展,而嗜碱性粒细胞耗竭则会降低补充 IL-3 的效果。此外,IL-3 还能促使嗜碱性粒细胞产生 IL-4,从而提高 CTL IFN-γ 的产生和活力。值得注意的是,嗜碱性粒细胞产生的IL-4的重要性从IL-4基因敲除的肿瘤小鼠缺乏IL-3补充剂的益处中可见一斑。总之,这项研究揭示了IL-3介导的CTL-嗜碱性粒细胞在调节抗肿瘤免疫中的串联作用,并为利用IL-3维持作为优化和增强癌症免疫疗法的一种有前途的方法提供了前景。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
IL3-Driven T Cell-Basophil Crosstalk Enhances Antitumor Immunity.

Cytotoxic T lymphocytes (CTL) are pivotal in combating cancer, yet their efficacy is often hindered by the immunosuppressive tumor microenvironment, resulting in CTL exhaustion. This study investigates the role of interleukin-3 (IL3) in orchestrating antitumor immunity through CTL modulation. We found that intratumoral CTLs exhibited a progressive decline in IL3 production, which was correlated with impaired cytotoxic function. Augmenting IL3 supplementation, through intraperitoneal administration of recombinant IL3, IL3-expressing tumor cells, or IL3-engineered CD8+ T cells, conferred protection against tumor progression, concomitant with increased CTL activity. CTLs were critical for this therapeutic efficacy as IL3 demonstrated no impact on tumor growth in Rag1 knockout mice or following CD8+ T-cell depletion. Rather than acting directly, CTL-derived IL3 exerted its influence on basophils, concomitantly amplifying antitumor immunity within CTLs. Introducing IL3-activated basophils retarded tumor progression, whereas basophil depletion diminished the effectiveness of IL3 supplementation. Furthermore, IL3 prompted basophils to produce IL4, which subsequently elevated CTL IFNγ production and viability. Further, the importance of basophil-derived IL4 was evident from the absence of benefits of IL3 supplementation in IL4 knockout tumor-bearing mice. Overall, this research has unveiled a role for IL3-mediated CTL-basophil cross-talk in regulating antitumor immunity and suggests harnessing IL3 sustenance as a promising approach for optimizing and enhancing cancer immunotherapy. See related Spotlight, p. 798.

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来源期刊
Cancer immunology research
Cancer immunology research ONCOLOGY-IMMUNOLOGY
CiteScore
15.60
自引率
1.00%
发文量
260
期刊介绍: Cancer Immunology Research publishes exceptional original articles showcasing significant breakthroughs across the spectrum of cancer immunology. From fundamental inquiries into host-tumor interactions to developmental therapeutics, early translational studies, and comprehensive analyses of late-stage clinical trials, the journal provides a comprehensive view of the discipline. In addition to original research, the journal features reviews and opinion pieces of broad significance, fostering cross-disciplinary collaboration within the cancer research community. Serving as a premier resource for immunology knowledge in cancer research, the journal drives deeper insights into the host-tumor relationship, potent cancer treatments, and enhanced clinical outcomes. Key areas of interest include endogenous antitumor immunity, tumor-promoting inflammation, cancer antigens, vaccines, antibodies, cellular therapy, cytokines, immune regulation, immune suppression, immunomodulatory effects of cancer treatment, emerging technologies, and insightful clinical investigations with immunological implications.
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