<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><submitter>van Zyl G</submitter><funding>World Health Organization</funding><funding>NIAID NIH HHS</funding><pubmed_abstract>Although drug resistance could emerge if lenacapavir is initiated during undiagnosed acute infection or if infection occurs during the drug's pharmacokinetic tail, these cases will not compromise the effectiveness of WHO-recommended therapies, as there is no cross-resistance between lenacapavir and other licensed antiretroviral drugs. Lenacapavir pre-exposure prophylaxis (PrEP) is also unlikely to drive population-level lenacapavir resistance given the rarity of breakthrough infections and the reduced replication capacity of most lenacapavir-resistant variants, which most likely reduces their transmission potential. Conversely, the risk of acquiring lenacapavir-resistant HIV-1 while receiving lenacapavir PrEP is likely to remain extremely low, as lenacapavir-associated drug-resistance muta</pubmed_abstract><journal>The lancet. HIV</journal><pagination>S2352-3018(25)00128-6</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12435527</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Lenacapavir-associated drug resistance: implications for scaling up long-acting HIV pre-exposure prophylaxis.</pubmed_title><pmcid>PMC12435527</pmcid><funding_grant_id>001</funding_grant_id><funding_grant_id>R24 AI136618</funding_grant_id><pubmed_authors>Kantor R</pubmed_authors><pubmed_authors>McCluskey SM</pubmed_authors><pubmed_authors>Orrell C</pubmed_authors><pubmed_authors>Vitoria M</pubmed_authors><pubmed_authors>Rodolph M</pubmed_authors><pubmed_authors>van Zyl G</pubmed_authors><pubmed_authors>Shafer RW</pubmed_authors><pubmed_authors>Schapiro JM</pubmed_authors><pubmed_authors>Parikh UM</pubmed_authors><pubmed_authors>Prochazka M</pubmed_authors><pubmed_authors>Schmidt HA</pubmed_authors><pubmed_authors>Jordan MR</pubmed_authors></additional><is_claimable>false</is_claimable><name>Lenacapavir-associated drug resistance: implications for scaling up long-acting HIV pre-exposure prophylaxis.</name><description>Although drug resistance could emerge if lenacapavir is initiated during undiagnosed acute infection or if infection occurs during the drug's pharmacokinetic tail, these cases will not compromise the effectiveness of WHO-recommended therapies, as there is no cross-resistance between lenacapavir and other licensed antiretroviral drugs. Lenacapavir pre-exposure prophylaxis (PrEP) is also unlikely to drive population-level lenacapavir resistance given the rarity of breakthrough infections and the reduced replication capacity of most lenacapavir-resistant variants, which most likely reduces their transmission potential. Conversely, the risk of acquiring lenacapavir-resistant HIV-1 while receiving lenacapavir PrEP is likely to remain extremely low, as lenacapavir-associated drug-resistance muta</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Jun</publication><modification>2026-06-01T15:47:21.133Z</modification><creation>2026-04-08T13:50:56.101Z</creation></dates><accession>S-EPMC12435527</accession><cross_references><pubmed>40543515</pubmed><doi>10.1016/s2352-3018(25)00128-6</doi><doi>10.1016/S2352-3018(25)00128-6</doi></cross_references></HashMap>