Eskandarian Zoya, Hauch Richard, Schuster Sabrina, Winterberg Dorothee, Grabellus Hjördis, Imelmann Carlotta, Heitmann Anna-Lena, Goos Marlene, Rudloff Khadija, Strauss Julia, Wolters-Eisfeld Gerrit, Nollau Peter, Klausz Katja, Schüller Ulrich, Peipp Matthias, Spohn Michael, Horstmann Martin A
Research Institute Children's Cancer Center Hamburg, Hamburg, Germany.
Department of Pediatric Hematology and Oncology, University Medical Center Hamburg, Hamburg, Germany.
Cancer Immunol Res. 2025 Jun 4;13(6):881-896. doi: 10.1158/2326-6066.CIR-24-0746.
Philadelphia-like acute lymphoblastic leukemia (Ph-like ALL) is a molecularly distinct tyrosine kinase-driven cancer that has a high relapse rate and poor response toward combinatorial chemotherapy. Tyrosine kinase inhibitors (TKI) in the clinic improve the survival of patients with Ph-like ALL. Engineered antibody and cell-based immunotherapies can advance treatment for this genetic subtype of ALL. Allogeneic memory-like natural killer (ML-NK) cells have been used to treat leukemia and have shown a low risk of graft-versus-host reaction, which may be combined with leukemia epitope-targeting antibodies. However, mutation or pathway-directed TKI of Ph-like ALL can interfere with memory function and antibody-dependent NK cell-mediated cytotoxicity (ADCC). In this study, we explored the potential of ML-NK cells and Fc-enhanced CD19-ADCC in combination with TKI directed against kinase-driven leukemia models, including patient-derived xenografted Ph-like ALL. We demonstrate that receptor cross-linking in coculture with K562 feeder cells generated a more robust memory-like state of NK cells than coactivation with soluble IL-12, IL-15, and IL-18, as determined by genomic and functional studies. After receptor cross-linking and subsequent ILs preactivation, the optimized ML-NK cells showed enhanced antileukemic effector functions, which could compensate for exhausted B-cell precursor leukemia-infiltrating primary NK cells. TKI differentially affected multiple features of NK cell biology including viability, expansion, metabolism, receptor repertoire, and cytotoxicity. ADCC was maintained upon exposure to specific Abelson (ABL) or Janus kinase (JAK) inhibitors, in contrast to the multitarget TKI dasatinib impeding spleen tyrosine kinase-dependent ADCC. In conclusion, optimized ML-NK cell and CD19 antibody-based immunotherapy combined with carefully selected TKI demonstrates significant in vitro treatment efficacy in kinase-driven leukemia.
费城样急性淋巴细胞白血病(Ph样ALL)是一种分子特征明显的酪氨酸激酶驱动的癌症,具有高复发率且对联合化疗反应不佳。临床中的酪氨酸激酶抑制剂(TKI)可提高Ph样ALL患者的生存率。工程化抗体和基于细胞的免疫疗法可推进对ALL这种基因亚型的治疗。同种异体记忆样自然杀伤(ML-NK)细胞已被用于治疗白血病,且显示出低移植物抗宿主反应风险,其可与靶向白血病表位的抗体联合使用。然而,Ph样ALL的突变或通路导向TKI可干扰记忆功能和抗体依赖性NK细胞介导的细胞毒性(ADCC)。在本研究中,我们探索了ML-NK细胞和Fc增强的CD19-ADCC与针对激酶驱动白血病模型(包括患者来源的异种移植Ph样ALL)的TKI联合使用的潜力。我们证明,通过基因组和功能研究确定,与K562饲养细胞共培养时的受体交联比与可溶性IL-12、IL-15和IL-18共激活产生了更强健的NK细胞记忆样状态。在受体交联及随后白细胞介素预激活后,优化后的ML-NK细胞显示出增强的抗白血病效应功能,可补偿耗竭的B细胞前体白血病浸润的原发性NK细胞。TKI对NK细胞生物学的多个特征有不同影响,包括活力、增殖、代谢、受体库和细胞毒性。与多靶点TKI达沙替尼阻碍脾酪氨酸激酶依赖性ADCC相反,暴露于特异性阿贝尔森(ABL)或Janus激酶(JAK)抑制剂时ADCC得以维持。总之,优化后的基于ML-NK细胞和CD19抗体的免疫疗法与精心选择的TKI联合使用,在激酶驱动的白血病中显示出显著的体外治疗效果。