CAR-T(CAR-T)细胞疗法在非肿瘤性疾病中的应用
Chimeric antigen receptor T (CAR-T) cell therapy in non-oncological diseases.
CAR-T(CAR-T)细胞在血液系统恶性肿瘤中的应用推动了这种免疫治疗形式的显著进展。
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Targeting the tumor microenvironment in genitourinary cancers: current progress and future directions in prostate cancer.
Targeting the tumor microenvironment in genitourinary cancers: current progress and future directions in prostate cancer.
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持续的研究正在提供强有力的证据,表明像转移性去势抵抗性前列腺癌(mCRPC)这样的“冷”肿瘤现在能够对独特的免疫构建体产生反应。有可能将这些治疗提前到疾病连续过程的更早阶段,甚至作为新辅助疗法。
前列腺癌不再被视为“冷”肿瘤;几种新型免疫平台现在能够克服肿瘤微环境(TME)内的阻碍性细胞和可溶性障碍,从而促进免疫效应细胞的进入。抗肿瘤反应得到常规和分子影像以及血清生物标志物前列腺特异性抗原(PSA)有利变化的支持。涵盖领域:本综述简要概述了当前有前景的多特异性抗体策略,如T细胞衔接器,以及过继性细胞治疗与CAR-T 细胞,这些已成功进入肿瘤微环境并在该疾病中产生先天性和适应性免疫反应。这些结果为在实体瘤中继续推进免疫治疗提供了持续动力,尤其是那些被认为未富含免疫细胞的肿瘤。
INTRODUCTION: Prostate cancer is no longer considered a 'cold' tumor; several novel immune platforms are now capable of overcoming obstructive cellular and soluble impediments within the tumor microenvironment (TME) thus fostering the entry of immune effector cells. Antitumor responses are supported by favorable changes in conventional and molecular imaging and the serum biomarker, prostate-specific antigen (PSA). AREAS COVERED: This review briefly outlines the current promising strategies with multispecific antibodies such as T-cell engagers, and adoptive cellular therapeutics with chimeric antigen receptor T cells that have successfully gained entry into the tumor microenvironment and generated innate and adaptive immune responses in this disease.
These results provide ongoing impetus to pursue immunotherapies in solid tumors, especially those not thought to be enriched with immune cells. EXPERT OPINION: Ongoing research is providing strong evidence that a 'cold' tumor, such as metastatic castration-resistant prostate cancer (mCRPC), can now respond to unique immunologic constructs. It may be possible to bring these treatments earlier in the disease continuum, even as neoadjuvant therapies.
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