Am. J. Respir. Cell Mol. Biol., Vol 13, No. 1, 07 1995, 83-90.
Interleukin-10 decreases tumor necrosis factor alpha and beta in alloreactions induced by human lung dendritic cells and macrophages
LP Nicod, F el Habre, JM Dayer and N Boehringer
Respiratory Division, University Hospital, Geneva, Switzerland.
Human lung dendritic cells (DC) are considerably more potent than alveolar
macrophages (AM) in inducing allogeneic T-cell proliferation. Tumor
necrosis factor (TNF) alpha and beta produced during alloreaction are
likely to be major inflammatory cytokines involved. Their concentrations
were therefore analyzed during the interaction of AM or DC with allogeneic
T cells. TNF alpha and TNF beta levels were respectively three-fold and
sevenfold higher in the presence of DC as compared with AM. Cytokines such
as interleukin-4 (IL-4), interleukin- 10 (IL-10), and transforming growth
factor beta (TGF beta) were compared as to their ability to control
DC-induced T-cell proliferation as well as TNF alpha or TNF beta
production. IL-10 had the unique capacity of reducing both TNF alpha and
TNF beta production by 60 +/- 5% (mean +/- SEM) and 63 +/- 12%,
respectively, while inhibiting T-cell proliferation by only 32 +/- 23%.
IL-4 and TGF beta increased the release of TNF beta by 275 +/- 22% and 95
+/- 32%, respectively, while that of TNF alpha was slightly decreased or
unchanged. An additive effect of IL-10 to cyclosporine was found for all
three parameters studied. Interaction between CD4 or CD8 with DC was
affected similarly by IL-10. Part of this effect could be due to the
downregulation of class I and class II major histocompatibility complex
expression.(ABSTRACT TRUNCATED AT 250 WORDS)
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Copyright © 1995 American Thoracic Society.
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