Juwita Werner, Alex G. Lee, Chujing Zhang, Sydney Abelson, Sherin Xirenayi, Jose Rivera, Khadija Yousuf, Hanna Shin, Bonell Patiño-Escobar, Stefanie Bachl, Kamal Mandal, Abhilash Barpanda, Emilio Ramos, Adila Izgutdina, Sibapriya Chaudhuri, William C. Temple, Shubhmita Bhatnagar, Jackson K. Dardis, Julia Meyer, Carolina Morales, Soheil Meshinchi, Mignon L. Loh, Benjamin Braun, Sarah K. Tasian, Arun P. Wiita, Elliot Stieglitz
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引用次数: 0
摘要
青少年髓单细胞白血病(JMML)是一种主要影响婴儿和幼儿的骨髓增生性疾病。造血干细胞移植(HSCT)是标准的治疗方法,但HSCT后复发很常见,这突出了对创新治疗方法的需求。虽然嵌合抗原受体(CAR) T细胞过继免疫疗法改善了晚期淋巴细胞恶性肿瘤患者的预后,但尚未对JMML进行全面评估。在本研究中,我们使用大细胞和单细胞RNA测序、质谱分析和流式细胞术来鉴定JMML患者细胞表面上CLL-1(由CLEC12A编码)的过表达。我们开发了使用CLL-1 CAR - T细胞(CLL1CART)进行临床前测试的免疫疗法,并报告了体外和体内抗白血病活性。值得注意的是,CLL1CART减少了白血病干细胞的数量和体内连续移植的可移植性。这些临床前数据支持cll -1靶向免疫疗法在复发/难治性JMML患儿中的开发和临床研究。
Cellular immunotherapy targeting CLL-1 for juvenile myelomonocytic leukemia
Juvenile myelomonocytic leukemia (JMML) is a myeloproliferative disorder that predominantly affects infants and young children. Hematopoietic stem cell transplantation (HSCT) is standard of care, but post-HSCT relapse is common, highlighting the need for innovative therapies. While adoptive immunotherapy with chimeric antigen receptor (CAR) T cells has improved outcomes for patients with advanced lymphoid malignancies, it has not been comprehensively evaluated in JMML. In the present study, we use bulk and single-cell RNA sequencing, mass spectrometry, and flow cytometry to identify overexpression of CLL-1 (encoded by CLEC12A) on the cell surface of cells from patients with JMML. We develop immunotherapy with CLL-1 CAR T cells (CLL1CART) for preclinical testing and report in vitro and in vivo anti-leukemia activity. Notably, CLL1CART reduce the number of leukemic stem cells and serial transplantability in vivo. These preclinical data support the development and clinical investigation of CLL-1-targeting immunotherapy in children with relapsed/refractory JMML.
期刊介绍:
Nature Communications, an open-access journal, publishes high-quality research spanning all areas of the natural sciences. Papers featured in the journal showcase significant advances relevant to specialists in each respective field. With a 2-year impact factor of 16.6 (2022) and a median time of 8 days from submission to the first editorial decision, Nature Communications is committed to rapid dissemination of research findings. As a multidisciplinary journal, it welcomes contributions from biological, health, physical, chemical, Earth, social, mathematical, applied, and engineering sciences, aiming to highlight important breakthroughs within each domain.