效应器
免疫原性
化学
抗体
重组DNA
荧光素酶
中和抗体
分子生物学
报告基因
流式细胞术
受体
配体结合分析
HEK 293细胞
细胞生物学
CTL公司*
内生
细胞培养
生物测定
免疫分析
MTT法
单克隆抗体
高通量筛选
细胞
蛋白质工程
计算生物学
生物
碎片结晶区
作者
Dhanvanthri S. Deevi,Aparna Swarup,Tatyana Yun,Federico Ferrari,Jennifer Nguyen,Chuying Ma,Nazneen Bano,James Schiller,Linlin Luo,Roy Helmy,Faye Vazvaei-Smith,Weifeng Xu
出处
期刊:Bioanalysis
[Future Science Ltd]
日期:2026-09-02
卷期号:18 (12-13): 1065-1074
标识
DOI:10.1080/17576180.2026.2728520
摘要
BACKGROUND: MK-1484 is an engineered, PEGylated interleukin-2 (IL-2) mutein that preferentially binds the βγ subunits of the IL-2 receptor to activate effector T-cells and natural killer (NK) cells. Owing to high sequence homology, anti-drug antibodies (ADAs), including neutralizing antibodies (NAbs), may cross-react with and neutralize endogenous IL-2; MK-1484 is therefore classified as having a high immunogenicity risk, requiring an NAb assay to be ready for early-phase clinical studies. RESEARCH DESIGN AND METHODS: A highly sensitive competitive ligand-binding assay (cLBA) using mixed recombinant β- and γ-IL-2 receptor subunits was considered impractical, so plate- and flow cytometry-based cell-binding assays were attempted using the IL-2-dependent KIT225 cell line. A cell-based functional luciferase reporter assay (KIT225-STAT5-Luc#8) was then developed and qualified. RESULTS: Both cell-binding assays produced only weak signal. The functional reporter assay was successfully developed and qualified as a ready-to-use format for MK-1484 (cut point S/N 0.62; sensitivity 4.0 µg/mL), overcoming cell-line instability, lengthy recovery, and IL-2 starvation by using MK-1484 itself for post-thaw recovery and reducing the workflow from ~6 to 2 days. CONCLUSIONS: The ready-to-use functional NAb assay is fit-for-purpose for early-phase testing when combined with a more sensitive wild-type IL-2 NAb assay as the primary safety screen, and may be adaptable to other IL-2-based biotherapeutics, subject to case-by-case evaluation.
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