4.6 Article

IFN-γ Promotes Generation of IL-10 Secreting CD4+ T Cells that Suppress Generation of CD8 Responses in an Antigen-Experienced Host

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JOURNAL OF IMMUNOLOGY
卷 183, 期 1, 页码 51-58

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AMER ASSOC IMMUNOLOGISTS
DOI: 10.4049/jimmunol.0802047

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资金

  1. National Health and Medical Research Council [351439]
  2. Cancer Council Queensland [Q42]
  3. Australian Cancer Research Foundation
  4. Cancer Research Institute, New York
  5. University of Queensland
  6. Lions Research Foundation
  7. Queensland Government

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Ags characterizing tumors or chronic viral infection are generally presented to the host immune system before specific immunotherapy is initiated, and consequent generation of regulatory CD4(+) T cells can inhibit induction of desired effector CD8 T cell responses. IL-10 produced in response to ongoing Ag exposure inhibits generation of CD8 T cells in an Ag-experienced host. We now show that this IL-10 is produced by Ag experienced CD4(+) glucocorticoid-induced tumor necrosis factor receptor(+) T cells that also secrete IFN-gamma upon antigenic stimulation, that IL-10 secretion by these cells is enhanced through IFN-gamma signaling, and, unexpectedly, that IFN-gamma signaling is required for inhibition of generation of Ag-specific CD8 T cell responses in an Ag-experienced host. Systemic inhibition of both IL-10 and IFN-gamma at the time of immunization may therefore facilitate induction of effective immunotherapeutic responses against tumor specific and viral Ags. The Journal of Immunology, 2009, 183: 51-58.

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