Resumen
To date, the effective management of HIV-1 infection by anti-retroviral drugs has proved remarkably difficult to achieve. This is primarily due to the ease with which HIV-1 becomes resistant to drugs which initially may be very effective at blocking viral replication. In a recent issue of Science, two promising new AIDS treatments were reported. The first described the use of retroviral-type zinc finger structures found in the HIV-1 nucleocapsid protein as targets for antiretroviral drugs(1). The second demonstrated the feasibility of the reverse transcriptase inhibitor (R)-9-(2-phosphonylmethoxypropyl) adenine as a postexposure prophylaxis in blocking HIV-1 infection(2).
Idioma original | English (US) |
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Páginas (desde-hasta) | 343-346 |
Número de páginas | 4 |
Publicación | BioEssays |
Volumen | 18 |
N.º | 5 |
DOI | |
Estado | Published - ene. 1 1996 |
ASJC Scopus subject areas
- Biochemistry, Genetics and Molecular Biology(all)