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Proactively Reducing Anti-Drug Antibodies via Immunomodulatory Bioconjugation.

Peng ZhangPriyesh JainCaroline TsaoKan WuShaoyi Jiang
Published in: Angewandte Chemie (International ed. in English) (2019)
Although PEGylation reduces the immunogenicity of protein drugs to some extent, its limitations for highly immunogenic biotherapeutics have been demonstrated. Herein, a proactive strategy to alleviate the development of anti-drug antibodies (ADAs) against protein drugs by immunomodulatory bioconjugation is reported. Rapamycin was conjugated to a PEGylated protein therapeutic via a cleavable disulfide linker. The conjugated rapamycin can be released from the bioconjugate and prevent immune responses once the bioconjugate is uptaken by antigen-presenting cells. The immunomodulatory bioconjugate significantly reduced the titers of ADAs compared with a PEGylated protein. The inhibition of immune responses was specific to the conjugated antigen, avoiding systemic immune suppression and the risk of increased susceptibility to infections. The reported approach breaks the limitations of PEGylation by the proactive prevention of ADAs.
Keyphrases
  • immune response
  • protein protein
  • photodynamic therapy
  • amino acid
  • binding protein
  • induced apoptosis
  • drug induced
  • dendritic cells
  • small molecule
  • toll like receptor
  • signaling pathway
  • cell cycle arrest