Journal of Leukocyte Biology
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(Journal of Leukocyte Biology. 2001;69:271-279.)
© 2001 by Society for Leukocyte Biology

Differences in the induction of CD8+ T cell responses by subpopulations of dendritic cells from afferent lymph are related to IL-1{alpha} secretion

Jayne C. Hope, Paul Sopp, Robert A Collins and Chris J. Howard

Institute for Animal Health, Compton, Newbury, Berkshire, United Kingdom

Correspondence: Dr. J. C. Hope, Institute for Animal Health, Compton, Newbury, Berkshire, RG20 7NN, UK. E-mail: Jayne.Hope{at}BBSRC.ac.uk

The major subset of dendritic cells (DC) from bovine afferent lymph expresses the SIRP{alpha} MyD-1 antigen, but not CD11a or the antigen recognized by mAb CC81, and potently stimulates CD4+ and CD8+ T lymphocyte proliferation. The minor subpopulation, that is CD11a+CC81+MyD-1-, effectively stimulates CD4+ but not CD8+ T lymphocyte proliferation. CD11a+CC81+MyD-1- DC did not induce anergy or death or secrete an inhibitory factor. However, supernatant from cultures of CD8+ T cells with CD11a-CC81-MyD-1+ DC significantly enhanced proliferation of CD8+ T cells in response to CD11a+CC81+MyD-1- DC, an effect that was blocked by interleukin (IL)-1{alpha}, but not IL-1ß, specific mAb. The proliferation of CD8+ T cells with CD11a+CC81+MyD-1- DC was also enhanced by adding IL-1{alpha}. IL-1ß slightly enhanced proliferation, whereas IL-2, IL-6, IL-12, and IL-15 had no effect. We conclude that the failure to stimulate CD8+ T cell proliferation results from the lack of IL-1{alpha} synthesis by this population, which may have important consequences in vivo.

Key Words: afferent lymph veiled cells • CD8+ lymphocytes




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