Ethanol suppression of the functional state of polymorphonuclear leukocytes obtained from uninfected and simian immunodeficiency virus infected rhesus macaques

Citation
Da. Stoltz et al., Ethanol suppression of the functional state of polymorphonuclear leukocytes obtained from uninfected and simian immunodeficiency virus infected rhesus macaques, ALC CLIN EX, 23(5), 1999, pp. 878-884
Citations number
38
Categorie Soggetti
Clinical Psycology & Psychiatry","Neurosciences & Behavoir
Journal title
ALCOHOLISM-CLINICAL AND EXPERIMENTAL RESEARCH
ISSN journal
01456008 → ACNP
Volume
23
Issue
5
Year of publication
1999
Pages
878 - 884
Database
ISI
SICI code
0145-6008(199905)23:5<878:ESOTFS>2.0.ZU;2-N
Abstract
Background: Human immunodeficiency virus (HIV) infection and alcohol abuse frequently coexist in the host and are known to suppress individually the h ost response to a variety of opportunistic infections. Methods: This study examined the effects of in vitro ethanol exposure on se veral functions of polymorphonuclear leukocytes (PMNs) that were obtained f rom uninfected and simian immunodeficiency virus (SIV)-infected rhesus maca ques, at the asymptomatic and terminal stages of infection. Results: The PMNs obtained from rhesus macaques at both the asymptomatic an d terminal stage of SIV disease had elevated phagocytic activity and increa sed CD11b expression compared with PMNs from uninfected animals. In vitro 1 00 mM ethanol suppressed phagocytosis and CD11b adhesion molecule expressio n by PMNs, regardless of the stage of SIV infection. Treatment of PMNs with granulocyte colony-stimulating factor (G-CSF) attenuated the inhibitory ef fect seen with prior ethanol exposure. Conclusions: These data demonstrate that the functional state of PMNs from uninfected as well as SIV-infected rhesus macaques is impaired by direct ex posure to intoxicating concentrations of ethanol and that this effect can b e attenuated by G-CSF. If alcohol intoxication similarly suppressed PMN fun ction in vivo, it would further increase susceptibility of these hosts to s econdary infections. Furthermore, G-CSF may be useful in overcoming the sup pressive effects of ethanol on PMN function in such patients.