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Title: Revealing the Immunogenic Risk of Polymers. Author: Li B, Yuan Z, Hung HC, Ma J, Jain P, Tsao C, Xie J, Zhang P, Lin X, Wu K, Jiang S. Journal: Angew Chem Int Ed Engl; 2018 Oct 15; 57(42):13873-13876. PubMed ID: 30156051. Abstract: Poly(ethylene glycol) (PEG) conjugation has been the gold standard to ameliorate the pharmacokinetic (PK) and immunological profiles of proteins. PEG polymer does become immunogenic once attached to proteins, evoking PEG-specific antibody (Ab) responses. The anti-PEG Abs could cause PEGylated biologic treatments to fail and even result in lethal adverse reactions. Thus the zwitterionic poly(carboxybetaine) (PCB) has been introduced as a PEG substitute for protein modification. Addressed herein is anti-polymer Ab induction by conjugating PEG and PCB polymers to a series of carrier proteins with escalating immunogenicity. Results indicate that titers of PEG-specific Abs were quantitatively correlated to the immunogenicity of carrier proteins, whereas the generation of PCB-specific Abs was minimal and insensitive to increased protein immunogenicity. This work provides insight into the immunological properties of PEG and PCB and has far-reaching implications for the development of polymer-protein conjugates.[Abstract] [Full Text] [Related] [New Search]