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:Microfluidic Chips: Emerging Technologies for Adoptive Cell Immunotherapy.
Microfluidic Chips: Emerging Technologies for Adoptive Cell Immunotherapy.
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过继性细胞治疗(ACT)是一种个性化治疗方法,在临床上治疗血液系统恶性肿瘤已取得巨大成功,并在实体瘤中也展现出潜在应用前景。ACT的流程涉及多个步骤,包括从患者组织中分离所需细胞、通过病毒载体系统进行细胞工程改造,以及经过严格检测以保证产品质量和安全性后回输给患者。ACT是一种正在开发中的创新药物;然而,这种多步骤方法耗时且成本高昂,靶向过继细胞的制备仍然是一个挑战。微流控芯片是一种新型平台,具有在微/纳尺度上操控流体的优势,已被开发用于各种生物学研究应用以及ACT。利用微流控技术在体外分离、筛选和培养细胞具有高通量、低细胞损伤和快速扩增速率等优势,可极大简化ACT制备步骤并降低成本。
此外,可定制的微流控芯片契合ACT的个性化需求。在这篇小型综述中,我们描述了微流控芯片在ACT中用于细胞分选、细胞筛选和细胞培养相较于其他现有方法的优势和应用。
最后,我们讨论了未来微流控相关工作在ACT中的挑战和潜在成果。
Adoptive cell therapy (ACT) is a personalized therapy that has shown great success in treating hematologic malignancies in clinic, and has also demonstrated potential applications for solid tumors. The process of ACT involves multiple steps, including the separation of desired cells from patient tissues, cell engineering by virus vector systems, and infusion back into patients after strict tests to guarantee the quality and safety of the products.
ACT is an innovative medicine in development; however, the multi-step method is time-consuming and costly, and the preparation of the targeted adoptive cells remains a challenge. Microfluidic chips are a novel platform with the advantages of manipulating fluid in micro/nano scales, and have been developed for various biological research applications as well as ACT.
The use of microfluidics to isolate, screen, and incubate cells in vitro has the advantages of high throughput, low cell damage, and fast amplification rates, which can greatly simplify ACT preparation steps and reduce costs.
Moreover, the customizable microfluidic chips fit the personalized demands of ACT. In this mini-review, we describe the advantages and applications of microfluidic chips for cell sorting, cell screening, and cell culture in ACT compared to other existing methods.
Finally, we discuss the challenges and potential outcomes of future microfluidics-related work in ACT.
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