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Heavy Cannabis Use Associated With Reduction in Activated and Inflammatory Immune Cell Frequencies in Antiretroviral Therapy-Treated Human Immunodeficiency Virus-Infected Individuals.

Authors :
Manuzak, Jennifer A
Gott, Toni M
Kirkwood, Jay S
Coronado, Ernesto
Hensley-McBain, Tiffany
Miller, Charlene
Cheu, Ryan K
Collier, Ann C
Funderburg, Nicholas T
Martin, Jeffery N
Source :
Clinical Infectious Diseases; 6/15/2018, Vol. 66 Issue 12, p1872-1882, 11p
Publication Year :
2018

Abstract

Background. Cannabis is a widely used drug in the United States, and the frequency of cannabis use in the human immunodeficiency virus (HIV)-infected population is disproportionately high. Previous human and macaque studies suggest that cannabis may have an impact on plasma viral load; however, the relationship between cannabis use and HIV-associated systemic inflammation and immune activation has not been well defined. Methods. The impact of cannabis use on peripheral immune cell frequency, activation, and function was assessed in 198 HIV- infected, antiretroviral-treated individuals by flow cytometry. Individuals were categorized into heavy, medium, or occasional cannabis users or noncannabis users based on the amount of the cannabis metabolite 11-nor-carboxy-tetrahydrocannabinol (THC- COOH) detected in plasma by mass spectrometry. Results. Heavy cannabis users had decreased frequencies of human leukocyte antigen (HLA)-DR<superscript>+</superscript>CD38<superscript>+</superscript>CD4<superscript>+</superscript> and CD8<superscript>+</superscript> T-cell frequencies, compared to frequencies of these cells in non-cannabis-using individuals. Heavy cannabis users had decreased frequencies of intermediate and nonclassical monocyte subsets, as well as decreased frequencies of interleukin 23- and tumor necrosis factor-α-producing antigen-presenting cells. Conclusions. While the clinical implications are unclear, our findings suggest that cannabis use is associated with a potentially beneficial reduction in systemic inflammation and immune activation in the context of antiretroviral-treated HIV infection. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
10584838
Volume :
66
Issue :
12
Database :
Complementary Index
Journal :
Clinical Infectious Diseases
Publication Type :
Academic Journal
Accession number :
129945987
Full Text :
https://doi.org/10.1093/cid/cix1116