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:The pharmacology of blinatumomab: state of the art on pharmacodynamics, pharmacokinetics, adverse drug reactions and evaluation in clinical trials.
The pharmacology of blinatumomab: state of the art on pharmacodynamics, pharmacokinetics, adverse drug reactions and evaluation in clinical trials.
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已知与目的:双特异性药物(BD)与检查点抑制剂和CAR-T 细胞同属免疫疗法。在肿瘤学领域,BD设计为一端结合肿瘤抗原,另一端结合效应细胞表面抗原。本文综述目前有关首个上市的BiTE形式双特异性抗体blinatumomab(BLINCYTO)用于急性淋巴细胞白血病的信息。方法:在PubMed数据库检索以blinatumomab为关键词发表的英文研究,并审阅选定文献的参考书目以获取相关论文。从ClinicalTrials.gov获取临床试验数据(在研试验、不良事件[AE]),从VigiBase获取全球药物警戒数据。结果与讨论:Blinatumomab是一种融合蛋白,由两个串联排列的单链可变片段组成:第一个结合所有B细胞的表面抗原CD19,第二个靶向T细胞抗原CD3。Blinatumomab结合B细胞和T细胞后,T细胞分泌颗粒酶和穿孔素,诱导B细胞凋亡。T细胞活化还会促使促炎细胞因子分泌,以及T细胞表面活化标志物和黏附分子上调。支持其适应证的主要临床试验显示,blinatumomab可提高总生存期;对血液学缓解且微小残留病灶水平为10^-3的患者,疗效更好。主要AE为细胞因子释放综合征、神经毒性和低丙种球蛋白血症。临床试验中最常见的三个系统器官类别为血液学、胃肠道和全身性疾病。VigiBase数据也显示相同结果,但真实世界神经系统疾病和感染更常见。新意与结论:本文总结有关blinatumomab的现有知识。许多临床试验正在研究改善给药途径并扩大治疗适应证。
WHAT IS KNOWN AND OBJECTIVE: Bispecific drugs (BDs) belong to the family of immunotherapies along with checkpoint inhibitors and CAR-T cells. In the field of oncology, BDs are designed to simultaneously bind a tumour antigen on the one side and an antigen present on the surface of effector cells on the other. This review summarizes the information available to date on the first marketed BiTE-format bispecific antibody, blinatumomab BLINCYTO in acute lymphoblastic leukaemia. METHODS: A literature search was conducted in the PubMed database by including studies published in English using the term blinatumomab. Furthermore, bibliographies of selected references were also evaluated for relevant articles. Clinical trial (CT) data were retrieved from clinicaltrials.gov (ongoing trials, adverse events [AEs]) and global pharmacovigilance data were retrieved from VigiBase . RESULTS AND DISCUSSION: Blinatumomab is a fusion protein which consists of two single-chain variable fragments arranged in tandem: the first binds the CD19 surface antigen of all B cells and the second targets the CD3 antigen of T cells. Binding of blinatumomab to B and T cells induces apoptosis of B cells after secretion of granzymes and perforins by T cells. T-cell activation results in secretion of pro-inflammatory cytokines and upregulation of activation markers and adhesion molecules on the surface of T cells. The major CTs that led to an indication show increased overall survival with blinatumomab with better efficacy in patients in haematological remission with minimal residual disease 10 -3 . The major AEs are cytokine release syndrome, neurotoxicity and hypogammaglobulinemia. The three most frequent system organ classes in CTs are haematological, gastrointestinal and general disorders. These results are also found in VigiBase but neurological disorders and infections appear more frequently in real life. WHAT IS NEW AND CONCLUSION: This review summarizes the current knowledge of blinatumomab in the literature. The subject of many CTs is to improve the route of administration and expand the indications for treatment.
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