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

The major subset of dendritic cells (DC) from bovine afferent lymph expresses the SIRPα 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...

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Veröffentlicht in:Journal of leukocyte biology Jg. 69; H. 2; S. 271 - 279
Hauptverfasser: Hope, Jayne C., Sopp, Paul, Collins, Robert A, Howard, Chris J.
Format: Journal Article
Sprache:Englisch
Veröffentlicht: United States Society for Leukocyte Biology 01.02.2001
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ISSN:0741-5400, 1938-3673
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Zusammenfassung:The major subset of dendritic cells (DC) from bovine afferent lymph expresses the SIRPα 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)‐1α, but not IL‐1β, specific mAb. The proliferation of CD8+ T cells with CD11a+CC81+MyD‐1− DC was also enhanced by adding IL‐1α. IL‐1β 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‐1α synthesis by this population, which may have important consequences in vivo.
Bibliographie:ObjectType-Article-2
SourceType-Scholarly Journals-1
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ISSN:0741-5400
1938-3673
DOI:10.1189/jlb.69.2.271