肿瘤细胞治疗研究
英文原题:Targeting the Tumor Microenvironment in Triple-Negative Breast Cancer: Emerging Roles of Monoclonal Antibodies and Immune Modulation.
Targeting the Tumor Microenvironment in Triple-Negative Breast Cancer: Emerging Roles of Monoclonal Antibodies and Immune Modulation.
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三阴性乳腺癌(TNBC)是一种侵袭性强且临床治疗具有挑战性的乳腺癌亚型,其特征为雌激素受体、孕激素受体和HER2表达缺失。这种分子表型限制了靶向治疗的可及性,并导致早期复发率高、治疗耐药和临床结局差。越来越多的证据表明,肿瘤微环境(TME)是TNBC进展、免疫逃逸和治疗耐药的核心驱动因素。TME包含由免疫细胞和基质细胞、细胞外基质成分及可溶性介质组成的复杂动态网络,共同塑造肿瘤行为并影响治疗反应。
值得注意的是,TNBC常表现出免疫活跃的微环境,以高水平的TIL(肿瘤浸润淋巴细胞)和免疫检查点表达为标志,为基于免疫的治疗策略提供了窗口。本叙述性综述总结了目前关于TNBC肿瘤微环境细胞、分子和结构特征的认识,特别关注由肿瘤相关巨噬细胞、髓源性抑制细胞、癌相关成纤维细胞和功能失调T细胞介导的免疫抑制机制。
我们描述了单克隆抗体的临床开发及治疗影响,包括免疫检查点抑制剂和抗体-药物偶联物。此外,我们讨论了旨在调节TME以增强单克隆抗体疗效的策略,包括免疫细胞重编程、细胞外基质重塑、细胞因子/趋化因子阻断以及联合治疗策略。
最后,我们强调生物标志物驱动的患者分层和个性化治疗策略的作用,探讨TME靶向药物开发中当前的挑战和未来方向。总之,这些见解凸显了整合免疫调节和基于单克隆抗体的疗法以改善TNBC患者预后的潜力。
Triple-negative breast cancer (TNBC) is an aggressive and clinically challenging subtype of breast cancer characterized by the absence of estrogen receptor, progesterone receptor, and HER2 expression. This molecular phenotype narrows the availability of targeted therapies and contributes to high rates of early relapse, therapeutic resistance, and poor clinical outcomes.
Mounting evidence pinpoints the tumor microenvironment (TME) as a central driver of TNBC progression, immune evasion, and resistance to treatment. The TME encompasses a complex and dynamic network of immune and stromal cells, extracellular matrix components, and soluble mediators that collectively shape tumor behavior and influence therapeutic response.
Notably, TNBC often displays an immunologically active microenvironment, marked by high levels of tumor-infiltrating lymphocytes and immune checkpoint expression, opening a window for immune-based therapeutic strategies. This narrative review summarizes current knowledge on the cellular, molecular, and structural features of the TNBC tumor microenvironment, with particular focus on immunosuppressive mechanisms mediated by tumor-associated macrophages, myeloid-derived suppressor cells, cancer-associated fibroblasts, and dysfunctional T cells.
We describe the clinical development and therapeutic impact of monoclonal antibodies, including immune checkpoint inhibitors and antibody-drug conjugates.
Additionally, we discuss strategies aimed at modulating the TME to enhance monoclonal antibody efficacy, including immune cell reprogramming, extracellular matrix remodeling, cytokine/chemokine blockade, and combination treatment strategies.
Finally, we highlight the role of biomarker-driven patient stratification and personalized therapeutic strategies, addressing current challenges and future directions in TME-targeted drug development.
Together, these insights underscore the potential of integrating immune modulation and monoclonal antibody-based therapies to improve outcomes for TNBC patients.
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