| HIV-1 | human immunodeficiency virus type one |
| IN | integrase |
| PR | protease |
| RT | reverse transcriptase |
| WT | wild-type |
| 3′-P | 3′-processing |
| ST | strand transfer |
| PrEP | pre-exposure prophylaxis |
| ART | antiretroviral therapy |
| INSTIs | integrase strand transfer inhibitors |
| NRTIs | nucleoside reverse transcription inhibitors |
| NNRTIs | nonnucleoside RT inhibitors |
| RAL | raltegravir |
| EVG | elvitegravir |
| DTG | dolutegravir |
| BIC | bictegravir |
| PFV | prototype foamy virus |
| SIV | simian immunodeficiency virus |
| HIV-2 | human immunodeficiency virus type two |
| rcm | red-capped mangabey |
| HCV | hepatitis C virus |
| DKAs | 2,4-diketobutanoic acids |
| EFV | efavirenz |
| FTC | emtricitabine |
| TDF | tenofovir disoproxil fumarate |
| RPV | rilpivirine |
| FC | fold change |
| SAR | structure activity relationship |
| CTD | C-terminal domain |
| LATTE | long-acting antiretroviral treatment enabling |
| FLAIR | the first long-acting injectable regimen trial |
| ATLAS | the antiretroviral therapy as long-acting suppression trial |