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- W2017148570 abstract "The IgG-derived immunomodulating peptide tuftsin, Thr-Lys-Pro-Arg, is recognized by specific receptors on phagocytic cells, notably macrophages, and is capable of targeting proteins and peptides to these sites. Aiming to target 3′-azido-3′-deoxythymidine (AZT) to HIV-infected macrophages, a conjugate of AZT with tuftsin was synthesized. The AZT-tuftsin chimera possesses the characteristic capacities of its two components. Thus, like AZT, it inhibits reverse transcriptase activity and HIV-antigen expression, and similarly to tuftsin, it stimulates IL-1 release from mouse macrophages and augments the immunogenic function of the cells. Importantly, the conjugate is not cytotoxic to T-cells. The results suggest that the AZT-tuftsin conjugate might have potential use in AIDS therapy. Copyright © 2004 European Peptide Society and John Wiley & Sons, Ltd." @default.
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- W2017148570 date "2004-01-01" @default.
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- W2017148570 title "Tuftsin-AZT conjugate: potential macrophage targeting for AIDS therapy" @default.
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- W2017148570 doi "https://doi.org/10.1002/psc.587" @default.
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