决定异体 CAR T 细胞排斥与扩增的细胞和分子机制
Cellular and molecular mechanisms determining allogeneic CAR T cell rejection and expansion.
英文原题:The safety and efficacy of CAR-T cells in the treatment of prostate cancer: review.
The safety and efficacy of CAR-T cells in the treatment of prostate cancer: review.
分数与星级只用于站内排序 —— 不代表疗效、安全性或个人适用性。
为改进免疫疗法的应用,需要更深入地了解前列腺癌微环境。
嵌合抗原受体(CAR)T细胞疗法是癌症治疗领域的新突破。本综述聚焦其在前列腺癌中的疗效和安全性、阻碍临床应用的因素,以及试图克服这些障碍的策略。
检索PubMed和Cochrane图书馆数据库中的相关文献;纳入的研究须以英文全文发表。
多种因素可能限制CAR-T 细胞疗效,包括前列腺癌恶劣的微环境、年龄、合并症和肿瘤分级。治疗不良反应,尤其细胞因子释放综合征,是治疗后主要担忧。另一方面,采用CAR改造γ/δ T细胞和NK细胞,与常规CAR-T 细胞相比已显示出更高疗效和安全性。
为改善免疫治疗应用,需要更深入认识前列腺癌微环境。关于毒性,还需更多研究以寻找特异性最高且高表达的前列腺抗原。此外,发现毒性预测生物标志物并为治疗选择合适患者,可能减少免疫相关副作用并提高缓解率。
A new breakthrough development in cancer treatment is chimeric antigen receptor (CAR)-T cell therapy. In this review, we focussed on its efficacy & safety in prostate cancer, obstacles impeding its clinical use, and some strategies trying to overcome them.
Searching for relevant articles was done using the PubMed and Cochrane Library databases. Studies had to be published in full-text in English in order to be considered.
Many factors can limit optimal CAR-T cell outcomes, including the hostile Prostate microenvironment, age, comorbidities, and tumour grade. The adverse effects of the therapy, particularly the cytokine release syndrome, are a major source of worry after treatment administration. Attempts to alter gamma/delta T-cells and NK cells with CAR, on the other hand, have demonstrated higher effectiveness and safety than conventional CAR-T cells.
To improve the use of immunotherapies, a greater understanding of the prostate cancer microenvironment is required. Concerning toxicity, more research is needed to find the most specific and highly expressed prostate antigens. Furthermore, discovering predictive biomarkers for toxicities, as well as choosing the correct patient for therapy, might decrease immune-related side effects and achieve a greater response.
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