Shafagati Nazila, Paul Suman, Rozati Sima, Sterling Cole H
The Sidney Kimmel Comprehensive Cancer Center, Johns Hopkins University School of Medicine, Baltimore, MD 21287, USA.
Cancers (Basel). 2024 Oct 15;16(20):3489. doi: 10.3390/cancers16203489.
While antibody-based immunotherapeutic strategies have revolutionized the treatment of B-cell lymphomas, progress in T-cell lymphomas has suffered from suboptimal targets, disease heterogeneity, and limited effective treatment options. Nonetheless, recent advances in our understanding of T-cell biology, the identification of novel targets, and the emergence of new therapies provide hope for the future. In this review, we explore four areas of current and evolving antibody-based strategies for the treatment of peripheral T-cell lymphoma (PTCL): monoclonal antibodies (mAbs), bispecific antibodies (BsAs), chimeric antigen receptor T-cell therapy (CAR-T), and antibody-drug conjugates (ADCs). As part of this discussion, we will also include limitations, lessons learned, and potential future directions.
虽然基于抗体的免疫治疗策略彻底改变了B细胞淋巴瘤的治疗方式,但T细胞淋巴瘤的治疗进展却因靶点不理想、疾病异质性以及有效治疗选择有限而受到阻碍。尽管如此,我们对T细胞生物学理解的最新进展、新靶点的发现以及新疗法的出现为未来带来了希望。在这篇综述中,我们探讨了当前及不断发展的基于抗体的外周T细胞淋巴瘤(PTCL)治疗策略的四个领域:单克隆抗体(mAb)、双特异性抗体(BsA)、嵌合抗原受体T细胞疗法(CAR-T)和抗体药物偶联物(ADC)。作为本次讨论的一部分,我们还将阐述局限性、经验教训以及潜在的未来发展方向。