TY - JOUR
T1 - PEGylation technology
T2 - addressing concerns, moving forward
AU - Simberg, Dmitri
AU - Barenholz, Yechezkel
AU - Roffler, Steve R.
AU - Landfester, Katharina
AU - Kabanov, Alexander V.
AU - Moghimi, Seyed M.
N1 - Publisher Copyright:
© 2025 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group.
PY - 2025
Y1 - 2025
N2 - PEGylation technology, that is grafting of poly(ethylene glycol)(PEG) to biologics, vaccines and nanopharmaceuticals, has become a cornerstone of modern medicines with over thirty products used in the clinic. PEGylation of therapeutic proteins, nucleic acids and nanopharmaceuticals improves their stability, pharmacokinetic and biodistribution. While PEGylated medicines are safe in the majority of patients, there are growing concerns about the emergence of anti-PEG antibodies and their impact on the therapeutic efficacy of PEGylated medicines as well as broader immune responses, particularly in complement activation and hypersensitivity reactions. These concerns are beginning to scrutinize the future viability of PEGylation technology in medicine design. Here, we outline these concerns, encourage more efforts into looking for comprehensive scientific evidence on the role of anti-PEG antibodies in hypersensitivity reactions, discuss alternatives to PEG and propose strategies for moving PEGylation technology forward.
AB - PEGylation technology, that is grafting of poly(ethylene glycol)(PEG) to biologics, vaccines and nanopharmaceuticals, has become a cornerstone of modern medicines with over thirty products used in the clinic. PEGylation of therapeutic proteins, nucleic acids and nanopharmaceuticals improves their stability, pharmacokinetic and biodistribution. While PEGylated medicines are safe in the majority of patients, there are growing concerns about the emergence of anti-PEG antibodies and their impact on the therapeutic efficacy of PEGylated medicines as well as broader immune responses, particularly in complement activation and hypersensitivity reactions. These concerns are beginning to scrutinize the future viability of PEGylation technology in medicine design. Here, we outline these concerns, encourage more efforts into looking for comprehensive scientific evidence on the role of anti-PEG antibodies in hypersensitivity reactions, discuss alternatives to PEG and propose strategies for moving PEGylation technology forward.
KW - Anti-poly(ethylene glycol) antibodies
KW - complement system
KW - immunogenicity
KW - nanomedicine
KW - PEGylated therapeutics
UR - http://www.scopus.com/inward/record.url?scp=105003532607&partnerID=8YFLogxK
U2 - 10.1080/10717544.2025.2494775
DO - 10.1080/10717544.2025.2494775
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C2 - 40264371
AN - SCOPUS:105003532607
SN - 1071-7544
VL - 32
JO - Drug Delivery
JF - Drug Delivery
IS - 1
M1 - 2494775
ER -