Gandhi Manav, Sharma Bhirisha, Nair Sujit, Vaidya Ashok D B
Department of Physiology and Biophysics, University of Illinois at Chicago, Chicago, IL, USA.
University of Mumbai, Santa Cruz (East), Mumbai, 400055, India.
Pharm Res. 2024 Sep;41(9):1757-1773. doi: 10.1007/s11095-024-03761-8. Epub 2024 Aug 26.
Myelodysplastic syndromes (MDS) are due to defective hematopoiesis in bone marrow characterized by cytopenia and dysplasia of blood cells, with a varying degree of risk of acute myeloid leukemia (AML). Currently, the only potentially curative strategy is hematopoietic stem cell transplantation (HSCT). Many patients are ineligible for HSCT, due to late diagnosis, presence of co-morbidities, old age and complications likely due to graft-versus-host disease (GvHD). As a consequence, patients with MDS are often treated conservatively with blood transfusions, chemotherapy, immunotherapy etc. based on the grade and manifestations of MDS. The development of chimeric antigen receptor (CAR)-T cell therapy has revolutionized immunotherapy for hematological malignancies, as evidenced by a large body of literature. However, resistance and toxicity associated with it are also a challenge. Hence, there is an urgent need to develop new strategies for immunological and hematopoetic management of MDS. Herein, we discuss current limitations of CAR T-cell therapy and summarize novel approaches to mitigate this. Further, we discuss the in vivo activation of tumor-specific T cells, immune check inhibitors (ICI) and other approaches to normalize the bone marrow milieu for the management of MDS.
骨髓增生异常综合征(MDS)是由于骨髓造血功能缺陷所致,其特征为血细胞减少和发育异常,伴有不同程度的急性髓系白血病(AML)风险。目前,唯一可能治愈的策略是造血干细胞移植(HSCT)。由于诊断较晚、存在合并症、年龄较大以及可能因移植物抗宿主病(GvHD)引发的并发症,许多患者不符合HSCT的条件。因此,MDS患者通常根据MDS的分级和表现,采用输血、化疗、免疫治疗等保守方法进行治疗。嵌合抗原受体(CAR)-T细胞疗法的发展彻底改变了血液系统恶性肿瘤的免疫治疗,大量文献证明了这一点。然而,与之相关的耐药性和毒性也是一项挑战。因此,迫切需要开发新的策略来对MDS进行免疫和造血管理。在此,我们讨论CAR T细胞疗法目前的局限性,并总结减轻这些局限性的新方法。此外,我们还讨论肿瘤特异性T细胞的体内激活、免疫检查点抑制剂(ICI)以及其他使骨髓微环境正常化以管理MDS的方法。