Nature Communications (Dec 2023)

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

  • Di Liu,
  • Yanling Song,
  • Hui Chen,
  • Yuchan You,
  • Luwen Zhu,
  • Jucong Zhang,
  • Xinyi Xu,
  • Jiahao Hu,
  • Xiajie Huang,
  • Xiaochuan Wu,
  • Xiaoling Xu,
  • Saiping Jiang,
  • Yongzhong Du

DOI
https://doi.org/10.1038/s41467-023-43847-2
Journal volume & issue
Vol. 14, no. 1
pp. 1 – 14

Abstract

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Abstract 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.