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Pubmed ID :19858258
Publication Date : //

An albumin-conjugated peptide exhibits potent anti-HIV activity and long in vivo half-life.


The clinical application of conventional peptide drugs often is limited by their short in vivo half-life and potential immunogenicity. Frequent injection presents challenges to the treatment of chronic diseases, such as HIV infection. We chemically modified a peptide HIV fusion inhibitor with 3-maleimidopropionic acid (MPA), which allows rapid and irreversible conjugation with serum albumin at a 1:1 molar ratio. FB006M, with an MPA modification at the 13th amino acid, rapidly formed conjugate with albumin upon intravenous injection, and it exhibited a remarkably extended in vivo half-life. The albumin conjugate of FB006M displayed potent inhibitory activity against a number of laboratory and clinical isolates of HIV-1 in vitro and in vivo. No immunogenicity or antibody formation was detected after repeated dosing. The clinical application of FB006M may decrease the cost of treatment and improve treatment compliance and patient quality of life.

Authors : Xie Dong , Yao Cheng , Wang Li , Min Wenjie , Xu Jiahong , Xiao Jiahai , Huang Mingxian , Chen Bo , Liu Bin , Li Xiaolin , Jiang He ,

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