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.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Ex Vivo Model to Assess the Exposure of Patients to Plasticizers from Medical Devices during Pre-CAR-T Cells' Apheresis.
Ex Vivo Model to Assess the Exposure of Patients to Plasticizers from Medical Devices during Pre-CAR-T Cells' Apheresis.
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接受 CAR-T 细胞采集前单采的患者主要暴露于 DEHP,由于其内分泌干扰效应,这可能影响他们的健康,但也可能导致 CAR-T 细胞效率/质量下降。
复发/难治性白血病的治疗仍是一个重大问题。在新治疗方法中,使用经过修饰的T淋巴细胞,即CAR-T 细胞(CAR-T 细胞),似乎具有前景。其制备的第一步是白细胞分离术,即从患者体内采集单个核细胞。该医疗操作需要使用大量由增塑聚氯乙烯(PVC)制成的医疗器械(MD)。这些化合物在与患者血液接触期间可从器械中浸出。我们研究的目的是评估在模拟的CAR-T 细胞制备前白细胞分离术过程中,MD中所含增塑剂的迁移情况,并测量患者及其淋巴细胞对这些增塑剂的暴露。
采用气相色谱-质谱联用(GC-MS)测定了用于 pre-CAR-T 细胞采集前 MD 的定性和定量组成。随后,使用乙醇/水模拟液建立离体白细胞采集模型,以评估在 pre-CAR-T 细胞采集模拟临床条件下增塑剂的迁移。释放到模拟液中的增塑剂通过 GC-MS 进行定量。
在单采套件中发现了邻苯二甲酸二乙基己酯(DEHP),其含量范围为25%至59%(g/100 g PVC)。检测到微量己二酸双(2-乙基己基)酯。模拟液中释放的DEHP总量为98.90±11.42 mg,相当于70 kg患者的暴露剂量为1.4 mg/kg。
The treatment of relapsed or refractory leukemia remains a major problem. Among the new therapeutic approaches, the use of modified T lymphocytes, called chimeric antigen receptor T cells (CAR-T cells), seems promising. The first step of their preparation is leukapheresis, which involves the collection of mononuclear cells from the patient. This medical procedure requires numerous medical devices (MDs) made of plasticized polyvinylchloride (PVC). These compounds can leach out of the devices during contact with the patient's blood. The aim of our study was to evaluate the migration of the plasticizers contained in the MD during a simulated pre-CAR-T cell leukapheresis procedure, and to measure the patient's and their lymphocytes' exposure to them.
The qualitative and quantitative composition of the MD used for pre-CAR-T cell apheresis was determined by gas chromatography-mass spectrometry (GC-MS). Then, an ex vivo leukapheresis model using an ethanol/water simulant was performed to evaluate the plasticizers' migration under simulated clinical conditions of pre-CAR-T cells' cytapheresis. The plasticizers released into the simulant were quantified by GC-MS.
Diethylhexylphthalate (DEHP) was found in the apheresis kit, with amounts ranging from 25% to 59% (g/100 g of PVC). Bis(2-ethylhexyl) adipate was detected at trace levels. A total of 98.90 11.42 mg of DEHP was released into the simulant, corresponding to an exposure dose of 1.4 mg/kg for a 70 kg patient.
Patients undergoing a pre-CAR-T cell apheresis are mainly exposed to DEHP, which can impact their health because of its endocrine disruption effect, but could also lead to a decrease in CAR-T cells' efficiency/quality.
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