The interaction of cannabinoids and viral infection has been studied in

vitro, in animal models, and in individuals with infections with recreational or medicinal use of cannabinoids. Cannabinoids worsen disease when inflammatory and cell-directed antiviral responses required for viral clearance are reduced, with HSV-2, Kaposi’s sarcoma herpesvirus KSHV, Vesicular stomatitis virus VSV, HCV, Coxpox, HIV, and SIV as examples (reviewed in Reiss, 2010). On the other hand, cannabinoids benefit disease when host inflammatory response is associated with pathology, not recovery, e.g. Theiler’s murine virus TMV (reviewed in Reiss, 2010), Enzalutamide manufacturer BDV (Solbrig and Hermanowicz, 2008 and Solbrig et al., 2010), also HIV and SIV (Molina et al., 2010 and Molina et al., 2011, reviewed in Rom and Persidsky, 2013) Important contributions to understanding

cannabinoid/viral interactions are from the expanding experimental evidence of direct effects of cannabinoids on retroviral replication. Viral replication in immune tissues is reduced in CB2 agonist treated microglia (Rock et al., 2007) or in THC treated animals with SIV where suppression of viral replication is a consequence of suppressed inflammation (Molina et al., 2011). Molecular mechanisms underlying the protective effects of cannabinoids and involving HIV’s replication machinery are decreased HIV-1 LTR activation www.selleckchem.com/products/Bortezomib.html by CB2 ligands in HIV-infected macrophages (Ramirez et al., 2013). Structural mechanisms of viral reduction are alterations of cytoskeletal architecture of resting CD4+ T cells by CB2 R agonism, where reducing F-actin levels inhibit actin reorganization and impair productive infection (Costantino et al., 2012). Important contributions to understanding cannabinoid/viral disease interactions and disease modulation

are emerging from experimental literature on SIV disease. Chronic Δ-9-THC IM treatment of SIVmac251 infected rhesus monkeys decreased serum and CSF viral load and tissue inflammation, reduced morbidity and mortality (Molina et al., 2010). As a result, further investigations are focusing on stress/immune system integration and contributions of genome-wide transcriptional modulation and epigenetic factors to the cannabinoid-associated disease Metalloexopeptidase phenotype. Differential regulation of several genes in the NFkB system, a signaling system linked to virulence factors such as enhanced viral replication, host cell survival, immune response and invasion, has been described (Molina et al., 2011). As in other viral systems, interpretation of cannabinoid treatment effects on BDV is complicated because of the variety of interactions between virus and inflammation. For example, reduced viral load might decrease inflammation or alternatively, reduced viral load could be a consequence of a more robust inflammatory response.