← 返回前沿论文

CAR T 细胞:改善儿童肿瘤结局所缺失的一环?

英文原题:CAR T cells: the missing piece needed to improve outcomes for children with cancer?

PubMed 2026/01/16(内容时间) J Immunother Cancer Q1 · IF 11.7(JCR 2025)

研究概要

B 细胞急性淋巴细胞白血病 (B-ALL) 是儿童期最常见的癌症。

中文摘要

B细胞急性淋巴细胞白血病(B-ALL)是儿童最常见的癌症。在过去50年间,B-ALL的治疗结局持续改善,最近的进展得益于靶向CD19的嵌合抗原受体修饰T(CAR-T)细胞和双特异性抗体展现出的显著活性。相比之下,其他儿童癌症的治疗进展大多停滞。学术界正投入大量努力,希望将CAR-T细胞疗法从B-ALL扩展到其他儿童血液系统恶性肿瘤、实体瘤和脑肿瘤。靶向GD2神经节苷脂的CAR-T细胞已在神经母细胞瘤和弥漫性中线胶质瘤中显示良好临床活性;靶向Her2用于儿童肉瘤、靶向CD30用于霍奇金淋巴瘤、靶向CD5或CD7用于T细胞淋巴母细胞白血病,以及靶向CD22用于CAR19耐药B-ALL,也均显示令人鼓舞的临床活性。儿童肿瘤的全面表面组分析还发现了其他新的候选CAR靶点,包括广泛表达于儿童实体瘤和脑肿瘤的胎儿癌抗原GPC2和GPC3,以及由PHOX2B等胎儿癌细胞内蛋白产生、与主要组织相容性复合体结合的肽。加入自杀结构域、调控回路、逻辑门和效力增强设计的新一代CAR-T疗法,以及联合免疫治疗,有望在维持安全性的同时进一步增强疗效。目前试验主要将CAR-T细胞用于难治性疾病患者;未来仍需研究,以确定辅助性CAR-T治疗能否结合强度较低的标准方案实现治愈,并减少儿童癌症幸存者的长期毒性。尽管科学和临床研究已取得进展,通过传统生物制药途径开发CAR-T细胞的高成本,仍限制其后期临床开发,因此需要新的商业模式来推动CAR-T细胞在小众市场中的商业化。CAR-T细胞有望改善儿童癌症患者的治疗结局,但若要让患癌儿童真正受益,仍需大量进一步研究和临床开发。

展开英文摘要原文

B cell acute lymphoblastic leukemia (B-ALL) is the most common cancer of childhood. Outcomes for B-ALL have steadily improved over the last five decades, most recently due to impressive activity of chimeric antigen receptor modified T (CAR-T) cells and bispecific antibodies targeting CD19. In contrast, progress against other pediatric cancers has largely stalled. Significant academic effort is underway to expand the reach of CAR T cell therapy in pediatric cancer beyond B-ALL to other hematologic malignancies, solid cancers and brain tumors. Promising clinical activity using CAR-modified T cells has already been demonstrated in neuroblastoma and diffuse midline glioma by targeting the GD2 ganglioside, in pediatric sarcomas by targeting Her2, in Hodgkin's disease by targeting CD30, in T cell lymphoblastic leukemia by targeting CD5 or CD7, and in CAR19 refractory B-ALL by targeting CD22. Comprehensive surfaceome profiling of pediatric tumors is revealing additional novel candidate CAR targets expressed on pediatric cancers, including oncofetal cell surface antigens such as GPC2 and GPC3, which are expressed broadly on pediatric solid and brain tumors, and major histocompatibility complex bound peptides from oncofetal intracellular proteins such as PHOX2B Next-generation CAR T cell therapeutics that incorporate suicide domains, regulatory circuits, logic gating and potency enhancements as well as combination immunotherapies are expected to further augment efficacy while maintaining safety. Current trials are administering CAR T cells in patients with refractory disease, but future studies are warranted to determine whether adjuvant use of CAR T cells could deliver cures with lower intensity standard therapy regimens and thereby reduce long-term toxicities in pediatric cancer survivors. Despite this scientific and clinical progress, the high cost of developing CAR T cells through the traditional biopharma pathway is limiting late-stage clinical development, necessitating the creation of new business models to commercialize CAR T cells for these small markets. CAR T cells hold great promise for improving outcomes for pediatric patients with cancer, but substantial additional research and clinical development is needed if this promise is to be realized for children afflicted with cancer.

论文信息

作者
Mackall C
单位
Center for Cancer Cell Therapy, Stanford Cancer Institute; Parker Institute for Cancer Immunotherapy; Division of Pediatric Hematology/Oncology/Stem Cell Transplantation and Regenerative Medicine, Dept of Pediatrics; Division of Bone Marrow Transplantation and Cell Therapy, Dept of Medicine, Stanford University School of Medicine, Stanford, California, USA cmackall@stanford.edu.United States
文献类型
综述
期刊
Journal for immunotherapy of cancer2026 Jan 16
原文标识
PubMed 41545304 · DOI 10.1136/jitc-2025-013325