Tuftsin-AZT conjugate: potential macrophage targeting for AIDS therapy

被引:21
作者
Fridkin, M [1 ]
Tsubery, H
Tzehoval, E
Vonsover, A
Biondi, L
Filira, F
Rocchi, R
机构
[1] Weizmann Inst Sci, Dept Organ Chem, IL-76100 Rehovot, Israel
[2] Univ Padua, Dept Organ Chem, Padua, Italy
关键词
AZT; tuftsin; HIV; macrophages;
D O I
10.1002/psc.587
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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 (C) 2004 European Peptide Society and John Wiley Sons, Ltd.
引用
收藏
页码:37 / 44
页数:8
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