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The Journal of Immunology, 1999, 162: 3790-3794.
Copyright © 1999 by The American Association of Immunologists

Naive Human CD4+ T Cells Are a Major Source of Lymphotoxin {alpha}

Y. Ohshima2,*, L-P. Yang2,3,*, M-N. Avice*, M. Kurimoto{dagger}, T. Nakajima, M. Sergerie{ddagger}, C. E. Demeure*, M. Sarfati* and G. Delespesse*

* Centre Hospitalie Université de Montreal Research Centre, University of Montreal, Montreal, Quebec, Canada; {dagger} Fujisaki Institute, Hayashibara Biochemical Laboratories, Okayama, Japan; Department of Bioregulatory Function, University of Tokyo, School of Medicine, Tokyo, Japan; and {ddagger} Department of Obstetrics and Gynecology, University of Montreal, Montreal, Quebec, Canada

It is generally accepted that immunologically naive T cells display a very restricted cytokine production profile consisting mainly of IL-2, which is used as an autocrine growth factor. Here we report that activated naive CD4+ T cells, of neonatal or adult origin, express very high levels of soluble lymphotoxin (LT) {alpha} (LT{alpha}3), as determined by ELISA, RNase protection assay, and intracytoplasmic staining. Besides LT{alpha}3 and IL-2, these cells also produce high levels of TNF-{alpha} together with significant amounts of IFN-{gamma} and IL-13. Naive cells also express LTß mRNA and the membrane form of LT{alpha} (LT{alpha}ß). On average, naive CD4+ T cells secrete four times more LT{alpha}3 than Th1-like cells, twice more than naive CD8+ T cells, and ten times more than B cells. Thus, naive T cells express a large spectrum of cytokines, mainly of the Th1 type, and the very high levels of LT{alpha}3/TNF-{alpha} that they release may play an hitherto unsuspected role in the early stage of T cell-dependent immune responses.




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