Naatz Lauren C, Dong Shuyun, Evavold Brian, Ye Xiangyang, Chen Mingnan
Department of Molecular Pharmaceutics, University of Utah, Salt Lake City, UT 84112, USA.
Department of Pathology, University of Utah, Salt Lake City, UT 84112, USA.
Acta Pharm Sin B. 2025 Mar;15(3):1230-1241. doi: 10.1016/j.apsb.2024.10.014. Epub 2024 Nov 4.
Bispecific killer cell engagers (BiKEs) are a powerful tool to incite the killing power of natural killer (NK) cells. Here, we posited that the BiKE technology could be utilized to deplete activated immune cells expressing programmed death-1 (PD-1 cells), and hence treat autoimmune diseases since these cells drive the disorders. We designed and generated PD-1 BiKE that targets an activating NK cell receptor, CD16, and PD-1. PD-1 BiKE showed specific binding to PD-1 cells and engaged CD16 simultaneously. PD-1 BiKE enhanced NK cell-mediated apoptosis and depletion of PD-1 Raji cells, but not PD-1 Raji cells. Further, PD-1 BiKE induced apoptosis of primary PD-1 T lymphocytes that are highly relevant to autoimmune disease progression. The BiKE depleted 42% of primary T cells that were stimulated . Importantly, those ablated primary T cells were activated cells. Meanwhile, naive T cells were spared by the BiKE treatment, supporting the crucial selectivity of PD-1 BiKE-directed cell depletion. Lastly, PD-1 BiKE is more effective than a conventional depleting antibody in the depletion of PD-1 cells. The current work supports PD-1 BiKE is a selective, potent, and safe tool to deplete PD-1 cells.
双特异性杀伤细胞衔接器(BiKEs)是激发自然杀伤(NK)细胞杀伤能力的有力工具。在此,我们推测BiKE技术可用于清除表达程序性死亡-1的活化免疫细胞(PD-1细胞),从而治疗自身免疫性疾病,因为这些细胞会引发疾病。我们设计并生成了靶向活化NK细胞受体CD16和PD-1的PD-1 BiKE。PD-1 BiKE显示出与PD-1细胞的特异性结合,并同时结合CD16。PD-1 BiKE增强了NK细胞介导的凋亡以及对PD-1 Raji细胞的清除,但对非PD-1 Raji细胞无此作用。此外,PD-1 BiKE诱导了与自身免疫性疾病进展高度相关的原代PD-1 T淋巴细胞的凋亡。BiKE清除了42%受刺激的原代T细胞。重要的是,那些被清除的原代T细胞是活化细胞。同时,幼稚T细胞在BiKE处理中未受影响,这支持了PD-1 BiKE定向细胞清除的关键选择性。最后,在清除PD-1细胞方面,PD-1 BiKE比传统的清除抗体更有效。目前的研究支持PD-1 BiKE是一种选择性、强效且安全的清除PD-1细胞的工具。