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Safe use of the CXCR4 inhibitor ALX40-4C in humans
被引:103
作者:

Doranz, BJ
论文数: 0 引用数: 0
h-index: 0
机构: Univ Penn, Dept Microbiol, Philadelphia, PA 19104 USA

Filion, LG
论文数: 0 引用数: 0
h-index: 0
机构: Univ Penn, Dept Microbiol, Philadelphia, PA 19104 USA

Diaz-Mitoma, F
论文数: 0 引用数: 0
h-index: 0
机构: Univ Penn, Dept Microbiol, Philadelphia, PA 19104 USA

Sitar, DS
论文数: 0 引用数: 0
h-index: 0
机构: Univ Penn, Dept Microbiol, Philadelphia, PA 19104 USA

Sahai, J
论文数: 0 引用数: 0
h-index: 0
机构: Univ Penn, Dept Microbiol, Philadelphia, PA 19104 USA

Baribaud, FD
论文数: 0 引用数: 0
h-index: 0
机构: Univ Penn, Dept Microbiol, Philadelphia, PA 19104 USA

Orsini, MJ
论文数: 0 引用数: 0
h-index: 0
机构: Univ Penn, Dept Microbiol, Philadelphia, PA 19104 USA

Benovic, JL
论文数: 0 引用数: 0
h-index: 0
机构: Univ Penn, Dept Microbiol, Philadelphia, PA 19104 USA

Cameron, W
论文数: 0 引用数: 0
h-index: 0
机构: Univ Penn, Dept Microbiol, Philadelphia, PA 19104 USA

Doms, RW
论文数: 0 引用数: 0
h-index: 0
机构: Univ Penn, Dept Microbiol, Philadelphia, PA 19104 USA
机构:
[1] Univ Penn, Dept Microbiol, Philadelphia, PA 19104 USA
[2] Univ Ottawa, Dept Biochem Microbiol & Immunol, Ottawa, ON, Canada
[3] Univ Ottawa, Dept Pediat, Ottawa, ON K1N 6N5, Canada
[4] CHEO Ottawa, Ottawa, ON, Canada
[5] Univ Manitoba, Dept Pharmacol & Therapeut, Winnipeg, MB, Canada
[6] Ottawa Hosp Gen Site, Fac Med, Dept Med, Ottawa, ON, Canada
[7] Thomas Jefferson Univ, Kimmel Canc Inst, Dept Microbiol & Immunol, Philadelphia, PA USA
关键词:
D O I:
10.1089/08892220151126508
中图分类号:
R392 [医学免疫学];
Q939.91 [免疫学];
学科分类号:
100102 ;
摘要:
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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页码:475 / 486
页数:12
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