Md. Srivastava et al., DELTA(9) TETRAHYDROCANNABINOL AND CANNABIDIOL ALTER CYTOKINE PRODUCTION BY HUMAN IMMUNE CELLS, Immunopharmacology, 40(3), 1998, pp. 179-185
Marijuana, a widely abused drug in the US, and its derivatives (cannab
inoids) have been used in AIDS and cancer patients for treatment of in
tractable nausea and cachexia. Yet, objective investigations of the ef
fect of cannabinoids on the human immune system are few. We investigat
ed the effect of Delta(9) tetrahydrocannabinol (THC) and cannabidiol (
CBD) on cytokine production in vitro by human leukemic T, B, eosinophi
lic and CD8(+) NK cell lines as models. THC decreased constitutive pro
duction of IL-8, MIP-1 alpha, MIP-1 beta, and RANTES and phorbol ester
stimulated production of TNF-alpha, GM-CSF and IFN-gamma by NK cells.
It inhibited MIP-1 beta in HTLV-1 positive B-cells but tripled IL-8;
MIP-1 alpha and MIP-1 beta in B-cells and MIP-1 beta in eosinophilic c
ells but doubled IL-8. Both cannabinoids strongly inhibited IL-10 prod
uction by HUT-78 T-cells. Results indicate that THC and nonpsychotropi
c CBD have complex lineage and derivative specific effects on cytokine
s consistent with previous animal studies. These effects while of pote
ntial benefits in some inflammatory/autoimmune diseases may worsen HIV
infection, tumorigenesis and allergic inflammation in the lung. (C) 1
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