Effects of Mu-opiate receptor engagement on the persistence of HIV-associated activation and viral reservoirs in individuals receiving medication assisted treatment for opioid use disorder

  • STATUS
    Recruiting
  • participants needed
    70
Updated on 19 February 2024

Summary

Both HIV infection and exposure to opioids, including intravenous heroin in people who inject drugs (PWIDs), are associated with systemic immune activation due to, at least partially, dysbiosis and increased microbial translocation from the gut. Medication-assisted treatment (MAT) approaches based on the administration of Opioid Receptor (MOR) agonists (e.g. methadone) are clinically effective in terms of harm reduction, but may also contribute to sustained immune activation, limiting the positive immunological outcomes of ART in HIV-infected PWIDs. The primary objective of this proposal is to conduct a clinical study to establish whether chronic engagement of mu-opioid receptor (MOR) by full (methadone) or partial (buprenorphine + naloxone) agonists is a major factor in sustaining bacterial translocation and immune activation modulating in ART suppressed individuals with opioid use disorder (OUD) receiving MAT, resulting in A) increased microbial translocation; B) sustained innate and adaptive immune activation and inflammation in blood or GALT; and C) higher levels of HIV persistence on ART (i.e., integrated HIV DNA, cell-associated HIV RNA) when compared to a full MOR antagonist (XR-NTX).

Details
Condition Medical Research
Age 99years or below
Clinical Study IdentifierTBD
Last Modified on19 February 2024

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