Foldvari Zsofia, Brennan Margs S, Titov Aleksei, Jacobsen Sten Eirik W, Olweus Johanna
Department of Cancer Immunology, Oslo University Hospital Radiumhospitalet, Oslo, Norway.
Precision Immunotherapy Alliance, University of Oslo, Oslo, Norway.
Nat Rev Cancer. 2025 Aug 21. doi: 10.1038/s41568-025-00857-0.
Myeloid malignancies are clonal diseases of haematopoietic stem cell or haematopoietic progenitor cell origin, for which allogeneic haematopoietic stem cell transplantation remains the only curative treatment for most patients. However, the severe side effects and high relapse rates underscore the need for novel therapies. The success of adoptive transfer of chimeric antigen receptor (CAR) T cells targeting B cell-specific cell surface molecules in B cell cancers has not been replicated in myeloid malignancies. T cells engineered to express cancer-directed T cell receptors (TCRs) could provide an alternative, enabling targeting also of the intracellular proteome. In this Perspective, we have collated and reviewed available data from clinical trials exploiting TCR-engineered T cells for the treatment of haematological malignancies and discuss specific characteristics that make myeloid malignancies attractive candidates for TCR-based therapies. We also highlight the need to efficiently target the rare and notoriously therapy-resistant leukaemic stem cells, which represent the roots of myeloid malignancies, to achieve cures. This will require identification of novel targets and TCRs, and we discuss different target categories and strategies that can be applied towards this goal. We also highlight the importance of standardized preclinical testing and publicly available data to enable rapid identification and clinical advancement of promising TCRs towards clinical application.
髓系恶性肿瘤是起源于造血干细胞或造血祖细胞的克隆性疾病,对于大多数患者而言,异基因造血干细胞移植仍然是唯一的治愈性治疗方法。然而,严重的副作用和高复发率凸显了新型疗法的必要性。嵌合抗原受体(CAR)T细胞靶向B细胞特异性细胞表面分子用于B细胞癌症的过继性转移取得了成功,但在髓系恶性肿瘤中尚未得到复制。经过工程改造以表达癌症导向性T细胞受体(TCR)的T细胞可能提供一种替代方案,还能够靶向细胞内蛋白质组。在这篇观点文章中,我们整理并回顾了利用TCR工程改造的T细胞治疗血液系统恶性肿瘤的临床试验现有数据,并讨论了使髓系恶性肿瘤成为基于TCR疗法有吸引力候选对象的具体特征。我们还强调了有效靶向罕见且 notoriously 难治的白血病干细胞的必要性,这些干细胞是髓系恶性肿瘤的根源,以实现治愈。这将需要鉴定新型靶点和TCR,我们讨论了可用于实现这一目标的不同靶点类别和策略。我们还强调了标准化临床前测试和公开可用数据对于快速鉴定有前景的TCR并将其推进至临床应用的重要性。 (注:notoriously 这个词在原文语境中不太明确其准确含义,这里保留英文未翻译,因为仅根据现有信息无法准确给出合适的中文表述)