The source of early IFN-γ that plays a role in Th1 priming

Das, Gobardhan ; Sheridan, Scott ; Janeway, Charles A. (2001) The source of early IFN-γ that plays a role in Th1 priming The Journal of Immunology, 167 (4). pp. 2004-2010. ISSN 0022-1767

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When naive CD4 T cells are primed, they rapidly differentiate into polarized Th1 and/or Th2 phenotypes. A major factor in producing such polarization is the early production of cytokines (IL-12 and IFN-γ in the case of Th1 cells and IL-4 in the case of Th2 cells). One issue that remains unresolved is the source of the early IFN-γ that synergizes with IL-12 to fully polarize CD4 T cells into Th1 cells. We have examined this question by injecting mice with anti-CD3 and examining cells from normal and various MHC-knockout mice. We found that IFN-γ is induced rapidly in a small subset of CD8 T cells. This subset is absent in mice that lack β2-microglobulin, but not in KbDb-double-knockout mice, indicating that these CD8 T cells are dependent on nonclassical MHC class Ib molecules. The early burst of IFN-γ polarizes CD4 T cells toward Th1 cells, in part by stimulating the release of IL-12 from APC. We also use TAP- and CD1-knockout mice to show that such cells are not CD1-restricted NK T cells, nor are they dependent on TAP-1 transport for surface expression of the relevant MHC class Ib molecule. Therefore, they arise on MHC class Ib molecules that do not depend on TAP-1 transporters.

Item Type:Article
Source:Copyright of this article belongs to American Association of Immunologists.
ID Code:113626
Deposited On:07 Jun 2018 05:10
Last Modified:07 Jun 2018 05:10

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