在骨髓驱动的肿瘤免疫抑制中靶向 PI3K-gamma:临床前文献的系统回顾和荟萃分析。

IF 4.6 2区 医学 Q2 IMMUNOLOGY
Haonan Xu, Shannon Nicole Russell, Katherine Steiner, Eric O'Neill, Keaton Ian Jones
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引用次数: 0

摘要

肿瘤微环境(TME)中免疫细胞和基质细胞之间错综复杂的相互作用对肿瘤的进展产生了重大影响。髓系细胞,包括肿瘤相关巨噬细胞(TAMs)、中性粒细胞(TANs)和髓源抑制细胞(MDSCs),对肿瘤微环境中的免疫抑制做出了贡献(Nakamura 和 Smyth 在 Cell Mol Immunol 17(1):1-12 (2020). https://doi.org/10.1038/s41423-019-0306-1 ; DeNardo 和 Ruffell 在 Nat Rev Immunol 19(6):369-382 (2019). https://doi.org/10.1038/s41577-019-0127-6 )。这对依赖宿主免疫发挥作用的新型免疫疗法提出了巨大挑战。本系统综述探讨了抑制磷酸肌酸 3- 激酶γ(PI3Kγ)作为逆转实体瘤中髓系驱动的免疫抑制策略的临床前证据。2022 年 10 月 6 日,我们使用关键词和主题词检索了 EMBASE、MEDLINE 和 PubMed 数据库,以获取相关研究。这些研究以动物模型中的PI3Kγ抑制为重点,均符合预先确定的纳入和排除标准。提取的数据包括肿瘤生长动力学、生存终点和免疫反应,并进行了荟萃分析。研究遵循 PRISMA 和 MOOSE 指南。共有 36 项涉及 73 种动物模型的研究被纳入综述和荟萃分析。肿瘤模型包括乳腺癌、结直肠癌、肺癌、皮肤癌、胰腺癌、脑癌、肝癌、前列腺癌、头颈癌、软组织癌、胃癌和口腔癌。主要的PI3Kγ抑制剂是IPI-549和TG100-115,这两种抑制剂对γ异构体具有良好的特异性。81%的研究探讨了联合疗法,通常涉及化疗、放疗、免疫检查点抑制剂、生物制剂或疫苗。对肿瘤生长动力学的分析表明,PI3Kγ单药治疗的反应虽不尽相同,但具有统计学意义,而联合治疗组的肿瘤生长则持续降低。生存期分析表明,联合治疗可明显提高中位总生存期。这篇系统综述全面分析了在骨髓驱动的肿瘤免疫抑制中研究 PI3Kγ 抑制的临床前研究。已确定的研究强调了 PI3Kγ 抑制通过调节髓系细胞功能重塑 TME 的潜力。PI3Kγ抑制与其他治疗方式的结合显示出更强的抗肿瘤效果,表明这是一种克服免疫抑制的协同方法。这些发现支持了PI3Kγ靶向疗法的潜力,尤其是在联合疗法中的潜力,是未来在各种实体瘤类型中进行临床探索的一个很有前景的途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Targeting PI3K-gamma in myeloid driven tumour immune suppression: a systematic review and meta-analysis of the preclinical literature.

Targeting PI3K-gamma in myeloid driven tumour immune suppression: a systematic review and meta-analysis of the preclinical literature.

The intricate interplay between immune and stromal cells within the tumour microenvironment (TME) significantly influences tumour progression. Myeloid cells, including tumour-associated macrophages (TAMs), neutrophils (TANs), and myeloid-derived suppressor cells (MDSCs), contribute to immune suppression in the TME (Nakamura and Smyth in Cell Mol Immunol 17(1):1-12 (2020). https://doi.org/10.1038/s41423-019-0306-1 ; DeNardo and Ruffell in Nat Rev Immunol 19(6):369-382 (2019). https://doi.org/10.1038/s41577-019-0127-6 ). This poses a significant challenge for novel immunotherapeutics that rely on host immunity to exert their effect. This systematic review explores the preclinical evidence surrounding the inhibition of phosphoinositide 3-kinase gamma (PI3Kγ) as a strategy to reverse myeloid-driven immune suppression in solid tumours. EMBASE, MEDLINE, and PubMed databases were searched on 6 October 2022 using keyword and subject heading terms to capture relevant studies. The studies, focusing on PI3Kγ inhibition in animal models, were subjected to predefined inclusion and exclusion criteria. Extracted data included tumour growth kinetics, survival endpoints, and immunological responses which were meta-analysed. PRISMA and MOOSE guidelines were followed. A total of 36 studies covering 73 animal models were included in the review and meta-analysis. Tumour models covered breast, colorectal, lung, skin, pancreas, brain, liver, prostate, head and neck, soft tissue, gastric, and oral cancer. The predominant PI3Kγ inhibitors were IPI-549 and TG100-115, demonstrating favourable specificity for the gamma isoform. Combination therapies, often involving chemotherapy, radiotherapy, immune checkpoint inhibitors, biological agents, or vaccines, were explored in 81% of studies. Analysis of tumour growth kinetics revealed a statistically significant though heterogeneous response to PI3Kγ monotherapy, whereas the tumour growth in combination treated groups were more consistently reduced. Survival analysis showed a pronounced increase in median overall survival with combination therapy. This systematic review provides a comprehensive analysis of preclinical studies investigating PI3Kγ inhibition in myeloid-driven tumour immune suppression. The identified studies underscore the potential of PI3Kγ inhibition in reshaping the TME by modulating myeloid cell functions. The combination of PI3Kγ inhibition with other therapeutic modalities demonstrated enhanced antitumour effects, suggesting a synergistic approach to overcome immune suppression. These findings support the potential of PI3Kγ-targeted therapies, particularly in combination regimens, as a promising avenue for future clinical exploration in diverse solid tumour types.

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来源期刊
CiteScore
10.50
自引率
1.70%
发文量
207
审稿时长
1 months
期刊介绍: Cancer Immunology, Immunotherapy has the basic aim of keeping readers informed of the latest research results in the fields of oncology and immunology. As knowledge expands, the scope of the journal has broadened to include more of the progress being made in the areas of biology concerned with biological response modifiers. This helps keep readers up to date on the latest advances in our understanding of tumor-host interactions. The journal publishes short editorials including "position papers," general reviews, original articles, and short communications, providing a forum for the most current experimental and clinical advances in tumor immunology.
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