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通过肿瘤微环境重编程克服免疫耐药:新兴的免疫治疗策略与转化进展

英文原题:Overcoming immune resistance through tumor microenvironment reprogramming: Emerging immunotherapeutic strategies and translational advances.

查看英文原题

Overcoming immune resistance through tumor microenvironment reprogramming: Emerging immunotherapeutic strategies and translational advances.

PubMed 2026/08/06(内容时间) Biochem Pharmacol Q1 · IF 6.5(JCR 2025)

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中文摘要

乳腺、卵巢、宫颈和子宫内膜恶性肿瘤由于转移进展、免疫逃逸以及治疗反应持久性有限,仍然是癌症相关发病率和死亡率的主要原因。尽管免疫检查点抑制剂已改善了部分患者的结局,但其疗效常常受到深度免疫抑制性肿瘤微环境(TME)的限制。本综述总结了驱动这些恶性肿瘤免疫抵抗的分子机制,并重点介绍了提高免疫治疗疗效的新兴策略。本文在T细胞功能障碍和肿瘤免疫逃逸的背景下,讨论了经典和新兴免疫检查点的作用,包括程序性细胞死亡受体1(PD-1)、程序性细胞死亡配体1(PD-L1)、T细胞免疫球蛋白和黏蛋白结构域3(TIM-3)、细胞毒性T淋巴细胞相关蛋白4(CTLA-4)、淋巴细胞活化基因3(LAG-3)、具有Ig和ITIM结构域的T细胞免疫受体(TIGIT)、V域Ig抑制T细胞活化(VISTA)以及Siglec介导的糖免疫检查点。本文还考察了调节免疫细胞浸润的机制,包括趋化因子信号传导、基质重塑和细胞因子网络,探讨它们对TME内免疫排斥或免疫激活的贡献。

此外,本文评估了代谢重编程通路,包括乳酸蓄积、腺苷信号传导和色氨酸分解代谢,在抑制抗肿瘤免疫和促进肿瘤进展中的作用。本文还强调了表观遗传调控在恢复抗原呈递、干扰素信号传导和免疫反应性方面的治疗潜力。

最后,讨论了抗体-药物偶联物、癌症疫苗和过继性细胞疗法方面的进展,这些是有前景的策略,将靶向细胞毒性与免疫激活相结合。总体而言,这些见解支持生物标志物驱动的联合治疗,以克服免疫耐药并改善乳腺和妇科恶性肿瘤的持久临床结局。

展开英文摘要原文

Breast, ovarian, cervical, and endometrial malignancies remain major causes of cancer-related morbidity and mortality due to metastatic progression, immune evasion, and the limited durability of therapeutic responses. Although immune checkpoint inhibitors have improved outcomes in selected patients, their efficacy is frequently constrained by profoundly immunosuppressive tumor microenvironments (TMEs). This review summarizes the molecular mechanisms driving immune resistance across these malignancies and highlights emerging strategies to improve immunotherapeutic efficacy.

The roles of classical and emerging immune checkpoints, including Programmed cell death receptor 1 (PD-1), Programmed cell death-ligand 1 (PD-L1), T-cell immunoglobulin and mucin domain 3 (TIM-3), Cytotoxic T-lymphocyte-associated protein 4 (CTLA-4), Lymphocyte-activation gene 3 (LAG-3), T-cell immunoreceptor with Ig and ITIM domains (TIGIT), V-domain Ig suppressor of T-cell activation (VISTA), and Siglec-mediated glyco-checkpoints, are discussed in the context of T-cell dysfunction and tumor immune escape.

Mechanisms regulating immune cell infiltration, including chemokine signaling, stromal remodeling, and cytokine networks, are also examined for their contributions to immune exclusion or activation within the TME.

Furthermore, metabolic reprogramming pathways, including lactate accumulation, adenosine signaling, and tryptophan catabolism, are evaluated for their roles in suppressing antitumor immunity and promoting tumor progression. The therapeutic potential of epigenetic modulation to restore antigen presentation, interferon signaling, and immune responsiveness is also highlighted.

Finally, advances in antibody-drug conjugates, cancer vaccines, and adoptive cellular therapies are discussed as promising strategies that combine targeted cytotoxicity with immune activation.

Overall, these insights support biomarker-driven combination therapies to overcome immune resistance and improve durable clinical outcomes in breast and gynaecological malignancies.

论文信息

作者
Uttam V、Daffara S、Singh S、Kaur R、Sethi G、Jain A
第一作者单位
Non-coding RNA and Cancer Biology Lab, Department of Zoology, Central University of Punjab, Ghudda, 151401 Bathinda, Punjab, India.India
通讯作者单位
Non-coding RNA and Cancer Biology Lab, Department of Zoology, Central University of Punjab, Ghudda, 151401 Bathinda, Punjab, India. Electronic address: aklankjain@gmail.com.India
文献类型
综述
期刊
Biochemical pharmacology2026 Nov
原文标识
PubMed 42562333 · DOI 10.1016/j.bcp.2026.118331