In:
The Journal of Immunology, The American Association of Immunologists, Vol. 170, No. 10 ( 2003-05-15), p. 5260-5267
Kurzfassung:
LPS hyporesponsiveness is characterized by a diminished production of proinflammatory cytokines which can be caused by pretreatment with either LPS (=LPS desensitization) or the combination of the anti-inflammatory cytokines IL-10 and TGF-β. However, the resulting hyporesponsive states differ regarding their reversibility by the IFN-γ-inducing cytokine IL-12. Therefore, we aimed at studying the reasons for this differential IL-12 responsiveness of IFN-γ-producing cells and its consequences for LPS hyporesponsiveness in more detail. In an in vitro IL-12/IL-18 responsiveness model, we demonstrated that IL-10, if permanently present, does not directly inhibit IL-12/IL-18 responsiveness in T/NK cells but indirectly interferes with IFN-γ production in the presence of monocytes. In contrast, TGF-β acted directly on IFN-γ-producing cells by interfering with IL-12/IL-18 responsiveness. After removal of IL-10 but not of TGF-β, LPS hyporesponsiveness can be reverted by IL-12/IL-18. Consequently, the addition of recombinant TGF-β during LPS desensitization rendered PBMCs hyporesponsive to a reversal by IL-12/IL-18. Our data suggest that the persistence of IL-10 and the presence of TGF-β determine the level of IFN-γ inhibition and may result in different functional phenotypes of LPS desensitization and LPS hyporesponsiveness in vitro and in vivo.
Materialart:
Online-Ressource
ISSN:
0022-1767
,
1550-6606
DOI:
10.4049/jimmunol.170.10.5260
Sprache:
Englisch
Verlag:
The American Association of Immunologists
Publikationsdatum:
2003
ZDB Id:
1475085-5
