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Pharmacology

HIV lifecycle and antiretroviral drug classes: mechanisms, toxicity and interactions

Each step of the HIV replication cycle and the drug class that blocks it, from CCR5 antagonists and NRTIs to integrase and capsid inhibitors, with the class and drug-specific toxicities (HLA-B*57:01, tenofovir tubulopathy, OCT2 creatinine rise), barrier to resistance, hepatitis B overlap and the CYP3A4 interactions of pharmacokinetic boosters.

Tier 1Medical sciences concept

Written with AI assistance and fact-checked against the sources below. For exam study, not clinical decisions. How notes are made

3 questions10 flashcards

At a glance

  • HIV is a retrovirus: RNA is reverse-transcribed to DNA, integrated into the host genome, transcribed, then assembled and matured by a protease. Every step is a drug target.
  • Standard ART combines drugs from at least two classes. Preferred initial regimens in Australia are an integrase inhibitor (bictegravir or dolutegravir) with tenofovir plus emtricitabine or lamivudine, or dolutegravir with lamivudine alone when hepatitis B is absent and baseline resistance is excluded.
  • Exams test the mechanism of a toxicity: HLA-B*57:01 with abacavir, proximal tubulopathy with TDF, the OCT2 creatinine rise, unconjugated hyperbilirubinaemia with atazanavir, and boosted regimen interactions.

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Last updated
14 November 2026
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