TY - JOUR
T1 - Excessive CpG 1668 stimulation triggers IL-10 production by cDC that inhibits IFN-α responses by pDC
AU - Waibler, Zoe
AU - Anzaghe, Martina
AU - Konur, Abdo
AU - Akira, Shizuo
AU - Müller, Werner
AU - Kalinke, Ulrich
PY - 2008
Y1 - 2008
N2 - Upon stimulation with a wide range of concentrations of CpG oligodeoxynucleotide 2216 (CpG 2216), plasmacytoid DC are induced to produce type I IFN (IFN-α/β). In contrast, CpG 1668 shows a bell-shaped dose-response correlation, i.e. only intermediate but not high doses of CpG 1668 induce IFN-α/β. Interestingly, high-dose CpG 1668 completely inhibited IFN-α responses induced by CpG 2216. Experiments using supernatant of high-dose CpG-1668-treated cells indicated that secreted inhibitor(s) mediated the IFN-α shut-off. Among modulating cytokines, IL-10 turned out to be one important negative regulator. In line with this, supernatants of IL-10-deficient DC cultures stimulated with high-dose CpG 1668 did not inhibit IFN-α production. Interestingly, high-dose CpG 1668 also inhibited IFN-α responses induced by the DNA-encoded mouse cytomegalovirus, whereas IFN-α responses induced by negative-strand RNA-encoded vesicular stomatitis virus were only marginally affected. Experiments with DC cultures devoid of TLR9 indicated that TLR9 was critically required to mediate stimulatory and modulatory signals by low and high concentrations of CpG 1668, respectively. Analysis of purified DC subsets showed that conventional DC were the main IL-10 producers, whereas plasmacytoid DC hardly produced any IL-10. © 2008 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.
AB - Upon stimulation with a wide range of concentrations of CpG oligodeoxynucleotide 2216 (CpG 2216), plasmacytoid DC are induced to produce type I IFN (IFN-α/β). In contrast, CpG 1668 shows a bell-shaped dose-response correlation, i.e. only intermediate but not high doses of CpG 1668 induce IFN-α/β. Interestingly, high-dose CpG 1668 completely inhibited IFN-α responses induced by CpG 2216. Experiments using supernatant of high-dose CpG-1668-treated cells indicated that secreted inhibitor(s) mediated the IFN-α shut-off. Among modulating cytokines, IL-10 turned out to be one important negative regulator. In line with this, supernatants of IL-10-deficient DC cultures stimulated with high-dose CpG 1668 did not inhibit IFN-α production. Interestingly, high-dose CpG 1668 also inhibited IFN-α responses induced by the DNA-encoded mouse cytomegalovirus, whereas IFN-α responses induced by negative-strand RNA-encoded vesicular stomatitis virus were only marginally affected. Experiments with DC cultures devoid of TLR9 indicated that TLR9 was critically required to mediate stimulatory and modulatory signals by low and high concentrations of CpG 1668, respectively. Analysis of purified DC subsets showed that conventional DC were the main IL-10 producers, whereas plasmacytoid DC hardly produced any IL-10. © 2008 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.
KW - Autoimmunity
KW - DC
KW - Type I IFN
U2 - 10.1002/eji.200838184
DO - 10.1002/eji.200838184
M3 - Article
C2 - 18991289
SN - 1521-4141
VL - 38
SP - 3127
EP - 3137
JO - European journal of immunology
JF - European journal of immunology
IS - 11
ER -