Abstract | Background: Small-molecule CD4-mimetic compounds (CD4mc) inhibit human immunodeficiency virus (HIV-1) entry by blocking binding to the CD4 receptor and by premature triggering of the viral envelope glycoprotein (Env) spike. Methods: The efficacy of a CD4mc in protecting bone marrow-liver-thymus (BLT) humanized mice from vaginal HIV-1 challenge was evaluated. Results: Intravaginal application of the CD4mc JP-III-48, either before or simultaneously with virus challenge, protected BLT humanized mice from HIV-1JR-CSF infection in a dose- dependent manner. Conclusion: The direct antiviral effects of a CD4mc prevent HIV-1 infection in a murine model of sexual transmission.
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Authors | Amy M Princiotto, Vladimir D Vrbanac, Bruno Melillo, Jongwoo Park, Andrew M Tager, Amos B Smith 3rd, Joseph Sodroski, Navid Madani |
Journal | The Journal of infectious diseases
(J Infect Dis)
Vol. 218
Issue 3
Pg. 471-475
(07 02 2018)
ISSN: 1537-6613 [Electronic] United States |
PMID | 29617845
(Publication Type: Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't)
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Chemical References |
- CD4 Antigens
- HIV Fusion Inhibitors
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Topics |
- Administration, Intravaginal
- Animals
- Biomimetics
- Bone Marrow
- CD4 Antigens
(administration & dosage)
- Disease Models, Animal
- Female
- HIV Fusion Inhibitors
(administration & dosage)
- HIV Infections
(prevention & control)
- HIV-1
(drug effects)
- Liver
- Mice, SCID
- Thymus Gland
- Treatment Outcome
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