This project will examine the effect of morphine on parameters of immune function in normal macaques ormacaques chronically infected with Simian Immunodeficiency Virus (SIV), the best model for human infectionwith HIV. Peripheral blood mononuclear cells collected before and after SIV infection oropioid treatmentwill be used to assess Natural Killer cell activity, responses to T and B cell mitogens, and levels ofproinflammatory cytokines. The effect of the drug on immune status and SIV viral load will be madelongitudinally in each animal, as well as among animals in a treatment group and between groups. One thirdof HIV infected individuals in the U.S. are intravenous drug abusers. Morphine is the primary activemetabolite of heroin, and is the classic opioid used in most laboratory studies. Morphine is known to beimmunosuppressive in animal models and has been shown to up-regulate HIV replication in vitro. Yet, theeffect of opioid drugs on progression of retroviral infections in vivo has never been definitively established,nor has the effect of opioids on parameters of immune function been evaluated in retrovirally infectedanimals. Natural Killer cell activity, mitogen responses, and cytokine profiles are the standard functional teststhat have been used in the majority of published studies examining effects of opioids on immune status, andtherefore have been chosen for this project. The proposed studies will provide new data on the effects ofchronic treatment with morphine on immune status in uninfected macaques, as well as testing the effects ofchronic morphine in SIV infected animals, on immune status and disease progression, including neurologicalinvolvement. A novel aspect of the proposed studies is that the effect of morphine will be tested on SIVinfection when the drug is given before or after the virus. Also, few studies in any species have examinedthe effects of chronic opioid treatment on immune functional parameters. The data collected in the proposedwork will be novel, and will help to answer the questions directly as to whether opioids affect progression of aretroviral infection in primates, and whether the drug alters functional immune responses.

Agency
National Institute of Health (NIH)
Institute
National Institute on Drug Abuse (NIDA)
Type
Research Program Projects (P01)
Project #
1P01DA023860-01A1
Application #
7513136
Study Section
Special Emphasis Panel (ZDA1-RXL-E (11))
Project Start
2008-04-01
Project End
2013-03-31
Budget Start
2008-04-01
Budget End
2009-04-30
Support Year
1
Fiscal Year
2008
Total Cost
$50,935
Indirect Cost
Name
Temple University
Department
Type
DUNS #
057123192
City
Philadelphia
State
PA
Country
United States
Zip Code
19122
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Pitcher, Jonathan; Abt, Anna; Myers, Jaclyn et al. (2014) Neuronal ferritin heavy chain and drug abuse affect HIV-associated cognitive dysfunction. J Clin Invest 124:656-69
Bednar, Filip; Song, Changcheng; Bardi, Giuseppe et al. (2014) Cross-desensitization of CCR1, but not CCR2, following activation of the formyl peptide receptor FPR1. J Immunol 192:5305-13
Cornwell, William D; Lewis, Mark G; Fan, Xiaoxuan et al. (2013) Effect of chronic morphine administration on circulating T cell population dynamics in rhesus macaques. J Neuroimmunol 265:43-50
Dave, Rajnish S (2012) Morphine affects HIV-induced inflammatory response without influencing viral replication in human monocyte-derived macrophages. FEMS Immunol Med Microbiol 64:228-36
Rogers, Thomas J (2012) The molecular basis for neuroimmune receptor signaling. J Neuroimmune Pharmacol 7:722-4

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