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Clinical and Diagnostic Laboratory Immunology, May 1998, p. 335-340, Vol. 5, No. 3
1071-412X/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.

Cytokine Gene Expression in Normal Human Lymphocytes in Response to Stimulation

Jiang Fan,dagger Parunag Nishanian,* Elizabeth C. Breen, Matthew McDonald, and John L. Fahey

Center for Interdisciplinary Research in Immunology and Disease at UCLA and Jonsson Comprehensive Cancer Center, UCLA School of Medicine, Los Angeles, California 90095-1747

Received 15 August 1997/Returned for modification 21 October 1997/Accepted 2 February 1998

Sequential gene expression of two type 1 cytokines (interleukin 2 [IL-2] and gamma interferon), one type 2 cytokine (IL-10), two monokines (IL-6 and tumor necrosis factor alpha), and one cytokine receptor (IL-2 receptor [IL-2R]) in normal human peripheral blood mononuclear cells (PBMC) following in vitro stimulation was investigated by reverse transcription-PCR methods. Two stimuli were utilized: phytohemagglutinin (PHA), which acts on the CD2 molecule and T-cell receptors, and anti-CD3 monoclonal antibody, which acts on the CD3 molecule and on T-cell receptors. Increased expression of all studied genes occurred between 1 and 4 hours after stimulation, except for that of the gene encoding IL-10, which was delayed. Expression of all but one of the genes was transient, with a maximal mRNA accumulation at about 8 h on average. IL-2R mRNA expression was an exception, showing a prolonged increase (72 h). The general profiles of expression of the five cytokine genes were similar but not identical, suggesting some shared regulatory mechanisms. When responses to four additional stimuli (pokeweed mitogen, Candida albicans, and IL-2 at high and low doses) were compared, similar profiles of cytokine gene expression were found. Thus, the various stimuli caused induction of all cytokines with quantitative, not qualitative, differences. Altogether, the present data are useful for defining the kinetics of gene expression for key cytokines in response to standard immune-cell stimuli.


* Corresponding author. Mailing address: CIRID at UCLA, UCLA School of Medicine, 10833 Le Conte Ave., Los Angeles, CA 90095-1747. Phone: (310) 825-1997. Fax: (310) 206-1318.

dagger Present address: Medical College of Wisconsin, Department of Pediatrics, Milwaukee, WI 53226.


Clinical and Diagnostic Laboratory Immunology, May 1998, p. 335-340, Vol. 5, No. 3
1071-412X/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.



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