电荷贴片对肿瘤处置和治疗性抗体生物分布的影响

Jakob C. Stüber, K. Rechberger, S. Miladinović, Thomas Pöschinger, Tamara Zimmermann, Remi Villenave, Miro J. Eigenmann, Thomas E. Kraft, D. Shah, H. Kettenberger, W. Richter
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引用次数: 3

摘要

本研究探讨了抗体表面电荷对包括肿瘤在内的各种组织分布的影响。荷瘤小鼠静脉注射由三种抗体组成的混合物,分别携带负电荷贴片、平衡电荷分布或正贴片(盒式给药)。采用特定的LC-MS/MS方法分析组织水平。此外,抗体混合物给予非荷瘤小鼠。离心取肌肉和皮肤间质液,LC-MS/MS分析。我们探索了体外内皮模型的可行性,以模拟所观察到的分布差异。就肿瘤暴露总量而言,平衡电荷分布是最佳的,而在其他组织中,带负电荷和平衡电荷的抗体给出了类似的结果。相反,正电荷贴片通常导致血清清除率增加,但显著增强肿瘤和器官摄取,导致更高的组织-血清比率。通过对肌肉和皮肤组织液中抗体水平的特异性评估,证实了间质空间中的摄取和可用性,其电荷影响与整个组织中的相似。体外模型能够区分这一系列抗体变体的转运倾向。总之,我们的研究结果表明,抗体表面的电荷贴片对生物分布和肿瘤摄取的不同影响。这些见解可能有助于设计具有适合其用途的生物分布特性的分子,并优化其安全性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Impact of charge patches on tumor disposition and biodistribution of therapeutic antibodies
This study explores the impact of antibody surface charge on tissue distribution into various tissues including tumor. Tumor-bearing mice were dosed intravenously with a mixture comprising three antibodies engineered to carry negative charge patches, a balanced charge distribution, or positive patches, respectively (cassette dosing). Tissue levels were analyzed with a specific LC-MS/MS method. In addition, the antibody mix was administered to non-tumor bearing mice. Muscle and skin interstitial fluid were obtained by centrifugation and analyzed by LC-MS/MS. An in vitro endothelium model was explored for its feasibility to mimic the observed distribution differences. A balanced charge distribution was optimal in terms of total tumor exposure, while in other tissues, negatively charged and balanced charged antibodies gave similar results. In contrast, positive charge patches generally resulted in increased serum clearance but markedly enhanced tumor and organ uptake, leading to higher tissue-to-serum ratios. The uptake and availability in the interstitial space were confirmed by specific assessment of antibody levels in the interstitial fluid of the muscle and skin, with similar charge impact as in total tissue. The in vitro model was able to differentiate the transport propensity of this series of antibody variants. In summary, our results show the differential effects of charge patches on an antibody surface on biodistribution and tumor uptake. These insights may help in the design of molecules with biodistribution properties tailored to their purpose, and an optimized safety profile.
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