单细胞追踪揭示黑色素瘤 TIL 治疗过程中肿瘤反应性 T 细胞的可塑性
Single-cell tracking reveals tumor-reactive T cell plasticity during melanoma TIL therapy.
TIL(肿瘤浸润淋巴细胞)过继细胞治疗可在转移性黑色素瘤中诱导持久缓解,然而在体外扩增过程中及回输后,调控肿瘤反应性T细胞命运的克隆和转录动态仍知之甚少。
英文原题:Harnessing immunotherapy for brain metastases: insights into tumor-brain microenvironment interactions and emerging treatment modalities.
Harnessing immunotherapy for brain metastases: insights into tumor-brain microenvironment interactions and emerging treatment modalities.
脑转移标志着多种晚期癌症进展中的不利节点,主要原发于肺癌、乳腺癌和黑色素瘤,中位生存时间接近 6 个月。
脑转移标志着多种晚期癌症进展中的不良阶段,原发癌主要来自肺癌、乳腺癌和黑色素瘤;患者中位生存期接近6个月。现有治疗方案效果不理想,但随着对肿瘤微环境认识不断加深,尤其是肿瘤与脑组织相互作用造成的免疫抑制环境,有望推动免疫治疗成为改善脑转移结局的一种前景良好的途径。本综述详细阐述脑转移微环境研究进展,以帮助揭示脑转移的发生和演进全貌。我们总结三种新兴免疫治疗策略:免疫检查点抑制、嵌合抗原受体(CAR)T细胞移植和靶向胶质细胞的免疫增强。我们强调,免疫治疗开发应与对肿瘤微环境的深入理解相结合,并推动创新递送平台发展。此外,还应考虑将免疫治疗与成熟或前沿的物理方法以及局部应用相结合,纳入当前治疗方案。
Brain metastases signify a deleterious milestone in the progression of several advanced cancers, predominantly originating from lung, breast and melanoma malignancies, with a median survival timeframe nearing six months. Existing therapeutic regimens yield suboptimal outcomes; however, burgeoning insights into the tumor microenvironment, particularly the immunosuppressive milieu engendered by tumor-brain interplay, posit immunotherapy as a promising avenue for ameliorating brain metastases. In this review, we meticulously delineate the research advancements concerning the microenvironment of brain metastases, striving to elucidate the panorama of their onset and evolution. We encapsulate three emergent immunotherapeutic strategies, namely immune checkpoint inhibition, chimeric antigen receptor (CAR) T cell transplantation and glial cell-targeted immunoenhancement. We underscore the imperative of aligning immunotherapy development with in-depth understanding of the tumor microenvironment and engendering innovative delivery platforms. Moreover, the integration with established or avant-garde physical methodologies and localized applications warrants consideration in the prevailing therapeutic schema.
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