Literature DB >> 11350661

Safe use of the CXCR4 inhibitor ALX40-4C in humans.

B J Doranz1, L G Filion, F Diaz-Mitoma, D S Sitar, J Sahai, F Baribaud, M J Orsini, J L Benovic, W Cameron, R W Doms.   

Abstract

ALX40-4C is a small peptide inhibitor of the chemokine receptor CXCR4 that can inhibit X4 strains of HIV-1. Prior to the discovery of chemokine receptors as the HIV coreceptors, ALX40-4C was used in phase I/II clinical trials to evaluate its therapeutic potential against HIV-1, making ALX40-4C the first anticoreceptor inhibitor to be tested in humans against HIV-1. Patients in the highest dose groups achieved ALX40-4C levels above the effective concentration of the drug for nearly the entire 1-month treatment period. ALX40-4C was well tolerated by 39 of 40 asymptomatic HIV-infected patients, despite the critical role of CXCR4 in normal development and hematopoiesis. No significant or consistent reductions in viral load were observed, but only 12 of the enrolled patients harbored virus types that used CXCR4. We also found that ALX40-4C interacts with the second extracellular loop of CXCR4 and inhibits infection exclusively by blocking direct virus-CXCR4 interactions.

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Year:  2001        PMID: 11350661     DOI: 10.1089/08892220151126508

Source DB:  PubMed          Journal:  AIDS Res Hum Retroviruses        ISSN: 0889-2229            Impact factor:   2.205


  15 in total

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Review 2.  Targeting chemokine receptor CXCR4 for treatment of HIV-1 infection, tumor progression, and metastasis.

Authors:  Won-Tak Choi; Yilei Yang; Yan Xu; Jing An
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3.  A novel approach to block HIV-1 coreceptor CXCR4 in non-toxic manner.

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Review 4.  Biology and clinical relevance of chemokines and chemokine receptors CXCR4 and CCR5 in human diseases.

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Journal:  Exp Biol Med (Maywood)       Date:  2011-05-12

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Authors:  Adam B Edwards; Ryan S Anderton; Neville W Knuckey; Bruno P Meloni
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6.  Antigenically distinct conformations of CXCR4.

Authors:  F Baribaud; T G Edwards; M Sharron; A Brelot; N Heveker; K Price; F Mortari; M Alizon; M Tsang; R W Doms
Journal:  J Virol       Date:  2001-10       Impact factor: 5.103

7.  Novel compounds containing multiple guanide groups that bind the HIV coreceptor CXCR4.

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8.  Computer-based design of novel HIV-1 entry inhibitors: neomycin conjugated to arginine peptides at two specific sites.

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Journal:  J Mol Model       Date:  2008-12-05       Impact factor: 1.810

Review 9.  Protease-resistant peptide design-empowering nature's fragile warriors against HIV.

Authors:  Matthew T Weinstock; J Nicholas Francis; Joseph S Redman; Michael S Kay
Journal:  Biopolymers       Date:  2012       Impact factor: 2.505

Review 10.  Development of Protein-Protein Interaction Inhibitors for the Treatment of Infectious Diseases.

Authors:  Andrew F Voter; James L Keck
Journal:  Adv Protein Chem Struct Biol       Date:  2017-08-24       Impact factor: 3.507

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