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Efficacy and Adverse Effects of the Antiviral Compound Plerixafor in Feline Immunodeficiency Virus‐Infected Cats
Background Bicyclam derivatives inhibit feline immunodeficiency virus (FIV) replication through selective blockage of chemokine receptor CXCR4. Hypothesis/Objectives CXCR4 antagonist plerixafor (AMD3100, 1,1′‐bis‐1,4,8,11‐tetraazacyclotetradekan) alone or combination with adefovir (PMEA, 9‐(2‐phosph...
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Published in: | Journal of veterinary internal medicine 2012-05, Vol.26 (3), p.483-490 |
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Main Authors: | , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Request full text |
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Summary: | Background
Bicyclam derivatives inhibit feline immunodeficiency virus (FIV) replication through selective blockage of chemokine receptor CXCR4.
Hypothesis/Objectives
CXCR4 antagonist plerixafor (AMD3100, 1,1′‐bis‐1,4,8,11‐tetraazacyclotetradekan) alone or combination with adefovir (PMEA, 9‐(2‐phosphonylmethoxyethyl)adenine) safe and effective for treating FIV‐infected cats.
Animals
Forty naturally FIV‐infected, privately owned cats.
Materials and Methods
Prospective, placebo‐controlled, double‐blind clinical trial. Cats randomly classified into 4 treatment groups. Received AMD3100, PMEA, AMD3100 in combination with PMEA, or placebo for 6 weeks. Clinical and laboratory parameters, including CD4+ and CD8+ cell counts, FIV proviral and viral load measured by quantitative polymerase chain reaction (qPCR) evaluated. Additionally, FIV isolates from cats treated with AMD3100 tested for drug resistance.
Results
FIV‐infected cats treated with AMD3100 caused significant decrease in proviral load compared to placebo group (2.3 ± 3.8% to 1.9 ± 3.1%, of blood lymphocytes P |
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ISSN: | 0891-6640 1939-1676 |
DOI: | 10.1111/j.1939-1676.2012.00904.x |