Currently, several drugs are approved by the US Food and Drug Association or available through expanded access programs for the treatment of HIV-1 patients. They target four distinct steps within the HIV-1 replication cycle, i.e., the entry of the virus particle within the target cell (entry inhibitors [EI] subdivided into fusion inhibitors and CCR5 antagonists), the conversion of viral RNA into DNA (nucleoside and non-nucleoside reverse transcriptase inhibitors [NRTI and NNRTI]), the integration of the viral DNA into the host genome (integrase inhibitors [INI]), and the maturation of the virus particle (protease inhibitors [PI]). At the moment, NRTI remain the backbone components for antiretroviral drug combinations that generally comprise 2 NRTI and 1 NNRTI or 2 NRTI and 1 PI (DHHS 2006).
CITATION STYLE
Van Laethem, K., & Vandamme, A. M. (2009). Clinical implications of reverse transcriptase inhibitor resistance. In Viral Genome Replication (pp. 589–619). Springer US. https://doi.org/10.1007/b135974_26
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