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Anti-VEGFR2 F(ab') 2 drug conjugate promotes renal accumulation and glomerular repair in diabetic nephropathy.

Di LiuYanling SongHui ChenYuchan YouLuwen ZhuJucong ZhangXinyi XuJiahao HuXiajie HuangXiaochuan WuXiao-Ling XuSaiping JiangYong-Zhong Du
Published in: Nature communications (2023)
Poor renal distribution of antibody-based drugs is the key factor contributing to low treatment efficiency for renal diseases and side effects. Here, we prepare F(ab') 2 fragmented vascular endothelial growth factor receptor 2 antibody (anti-VEGFR2 (F(ab') 2 ) to block VEGFR2 overactivation in diabetic nephropathy (DN). We find that the anti-VEGFR2 F(ab') 2 has a higher accumulation in DN male mice kidneys than the intact VEGFR2 antibody, and simultaneously preserves the binding ability to VEGFR2. Furthermore, we develop an antibody fragment drug conjugate, anti-VEGFR2 F(ab') 2 -SS31, comprising the anti-VEGFR2 F(ab') 2 fragment linked to the mitochondria-targeted antioxidant peptide SS31. We find that introduction of SS31 potentiates the efficacy of anti-VEGFR2 F(ab') 2 . These findings provide proof of concept for the premise that antibody fragment drug conjugate improves renal distribution and merits drug validation in renal disease therapy.
Keyphrases
  • vascular endothelial growth factor
  • diabetic nephropathy
  • endothelial cells
  • cancer therapy
  • oxidative stress
  • stem cells
  • drug induced
  • binding protein
  • endoplasmic reticulum