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:Modulating the immune system as a therapeutic target for myelodysplastic syndromes and acute myeloid leukemia.
Modulating the immune system as a therapeutic target for myelodysplastic syndromes and acute myeloid leukemia.
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近年来,通过调节免疫系统来治疗包括髓系恶性肿瘤在内的疾病,已促成大量新型治疗方法的开发。骨髓增生异常综合征或肿瘤(MDS)和急性髓系白血病(AML)是源于造血干细胞和祖细胞(HSPCs)缺陷的血液系统恶性肿瘤。免疫反应失调,尤其是固有免疫和炎症通路的失调,与MDS和AML发病机制中HSPC缺陷的获得高度相关。除了在CAR-T 细胞疗法、疫苗和免疫检查点抑制剂等免疫治疗干预中利用免疫系统外,减轻MDS和AML中固有免疫和炎症反应的失调,仍然是延缓这些髓系恶性肿瘤发生和进展的优先事项。本综述全面总结了利用或调节免疫系统治疗MDS和AML的各种策略的当前进展。
Modulating the immune system to treat diseases, including myeloid malignancies, has resulted in the development of a multitude of novel therapeutics in recent years. Myelodysplastic syndromes or neoplasms (MDS) and acute myeloid leukemia (AML) are hematologic malignancies that arise from defects in hematopoietic stem and progenitor cells (HSPCs). Dysregulated immune responses, especially in innate immune and inflammatory pathways, are highly associated with the acquisition of HSPC defects in MDS and AML pathogenesis.
In addition to utilizing the immune system in immunotherapeutic interventions such as chimeric antigen receptor T cell therapy, vaccines, and immune checkpoint inhibitors, mitigating dysregulation of innate immune and inflammatory responses in MDS and AML remains a priority in slowing the initiation and progression of these myeloid malignancies. This review provides a comprehensive summary of the current progress of diverse strategies to utilize or modulate the immune system in the treatment of MDS and AML.
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