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Effects of alcohol and nicotine on cytotoxic functions of human lymphocytes

dc.contributor.authorNair, Madhavan P. N.en_US
dc.contributor.authorKronfol, Ziad A.en_US
dc.contributor.authorSchwartz, Stanley A.en_US
dc.date.accessioned2006-04-10T13:49:50Z
dc.date.available2006-04-10T13:49:50Z
dc.date.issued1990-03en_US
dc.identifier.citationNair, Madhavan P. N., Kronfol, Ziad A., Schwartz, Stanley A. (1990/03)."Effects of alcohol and nicotine on cytotoxic functions of human lymphocytes." Clinical Immunology and Immunopathology 54(3): 395-409. <http://hdl.handle.net/2027.42/28716>en_US
dc.identifier.urihttp://www.sciencedirect.com/science/article/B6WCK-4BJW3W4-1MD/2/980580886a3dac459361e9d6c6cf4d92en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/28716
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=1689229&dopt=citationen_US
dc.description.abstractThe in vitro effects of the recreational drugs, ethanol (EtOH) and nicotine, on natural killer (NK) antibody-dependent cellular cytotoxic (ADCC) and lymphokine-activated killer (LAK) cell activities on normal lymphocytes were investigated. Lymphocytes precultured with EtOH at concentrations of 0.4 and 0.6% (v/v) produced significant suppression of NK and ADCC activities. In target-binding assays, EtOH decreased the target-binding capacity of effector cells. EtOH also inhibited the activities of Percoll-separated, NK-enriched large granular lymphocytes. EtOH-induced inhibition of NK activity could be reversed by incubating lymphocytes for 1 hr with interferon. The generation and lytic capacity of LAK cells was also significantly depressed by EtOH when added at the initiation of culture. Nicotine at concentrations of 5 and 10 [mu]g/ml, when added directly to mixtures of effector and target cells, produced significant inhibition of NK activity. Nicotine (2 [mu]g/ml) and EtOH (0.01, 0.1, and 0.2%) at noninhibitory concentrations when added separately, showed significant suppression of NK activity when used in combination. Pretreatment of target cells with either EtOH or nicotine for 4 hr did not affect cytotoxic activity. Inhibition of cytotoxicity was also not due to direct toxicity of effector cells because lymphocytes treated with either EtOH or nicotine showed normal 51Cr release and their viability was comparable to that of untreated control cells. These studies demonstrate that EtOH and nicotine have significant immunomodulatory effects on the cytotoxic activities of human lymphocytes which may be of clinical relevance.en_US
dc.format.extent1148297 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherElsevieren_US
dc.titleEffects of alcohol and nicotine on cytotoxic functions of human lymphocytesen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelMicrobiology and Immunologyen_US
dc.subject.hlbsecondlevelInternal Medicine and Specialtiesen_US
dc.subject.hlbtoplevelScienceen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartment of Epidemiology, The University of Michigan, Ann Arbor, Michigan 48109, USA; Department of Psychiatry, The University of Michigan, Ann Arbor, Michigan 48109, USA; Department of Pediatrics, The University of Michigan, Ann Arbor, Michigan 48109, USA.en_US
dc.contributor.affiliationumDepartment of Epidemiology, The University of Michigan, Ann Arbor, Michigan 48109, USA; Department of Psychiatry, The University of Michigan, Ann Arbor, Michigan 48109, USA; Department of Pediatrics, The University of Michigan, Ann Arbor, Michigan 48109, USA.en_US
dc.contributor.affiliationumDepartment of Epidemiology, The University of Michigan, Ann Arbor, Michigan 48109, USA; Department of Psychiatry, The University of Michigan, Ann Arbor, Michigan 48109, USA; Department of Pediatrics, The University of Michigan, Ann Arbor, Michigan 48109, USA.en_US
dc.identifier.pmid1689229en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/28716/1/0000537.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1016/0090-1229(90)90053-Sen_US
dc.identifier.sourceClinical Immunology and Immunopathologyen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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