NK cell–mediated killing of target cells triggers robust antigen-specific T cell–mediated and humoral responses

Previous work showed that administration of antigen-expressing apoptotic cells in vivo results in antigen-specific CD8+ T-cell responses independent of Toll-like receptor signaling. We report here that natural killer (NK) cells can serve a function directly upstream of this pathway and initiate robu...

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Veröffentlicht in:Blood 2009-06, Vol.113 (26), p.6593-6602
Hauptverfasser: Krebs, Philippe, Barnes, Michael J., Lampe, Kristin, Whitley, Karen, Bahjat, Keith S., Beutler, Bruce, Janssen, Edith, Hoebe, Kasper
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container_end_page 6602
container_issue 26
container_start_page 6593
container_title Blood
container_volume 113
creator Krebs, Philippe
Barnes, Michael J.
Lampe, Kristin
Whitley, Karen
Bahjat, Keith S.
Beutler, Bruce
Janssen, Edith
Hoebe, Kasper
description Previous work showed that administration of antigen-expressing apoptotic cells in vivo results in antigen-specific CD8+ T-cell responses independent of Toll-like receptor signaling. We report here that natural killer (NK) cells can serve a function directly upstream of this pathway and initiate robust adaptive immune responses via killing of antigen-expressing target cells. This pathway is highly sensitive, in that administration of as few as 104 target cells induced detectable antigen-specific CD8+ T-cell responses. Importantly, NK cell–mediated cytotoxicity of target cells could also induce robust antigen-specific CD4+ T-cell responses, which were critical for subsequent CD8+ T-cell priming and IgG responses. Unlike adaptive immune responses induced by gamma-irradiated cells, the NK-cell pathway required myeloid differentiating factor 88 (MyD88) and Toll/interleukin-1 receptor domain–containing adapter-inducinginterferon-β (Trif) signaling. NK cells have previously been shown to detect and kill pathogen-infected host cells, as well as neoplastic cells and tissue allografts. The present data provide further evidence that they also discharge a strong tie with their relatives in the adaptive immune system. We think that the recognition and killing of target cells by NK cells represents an important pathway for the generation of robust CD8+ T and humoral responses that may be exploited for vaccine development.
doi_str_mv 10.1182/blood-2009-01-201467
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source MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Alma/SFX Local Collection
subjects Adaptor Proteins, Vesicular Transport - deficiency
Adaptor Proteins, Vesicular Transport - physiology
Analysis of the immune response. Humoral and cellular immunity
Animals
Antibody Specificity
B-Lymphocytes - immunology
Biological and medical sciences
CD4-Positive T-Lymphocytes - immunology
CD8-Positive T-Lymphocytes - immunology
Cytotoxicity, Immunologic
Fundamental and applied biological sciences. Psychology
Fundamental immunology
H-2 Antigens - immunology
Immunobiology
Immunoglobulin G - biosynthesis
Immunoglobulin G - immunology
Immunologic Memory
Killer Cells, Natural - immunology
Listeria monocytogenes - immunology
Lymphocyte Activation
Mice
Mice, Inbred C3H
Mice, Inbred C57BL
Mice, Knockout
Mice, Mutant Strains
Myeloid Differentiation Factor 88 - deficiency
Myeloid Differentiation Factor 88 - physiology
Organs and cells involved in the immune response
Ovalbumin - immunology
Peptide Fragments - immunology
T-Cell Antigen Receptor Specificity
Vaccination
title NK cell–mediated killing of target cells triggers robust antigen-specific T cell–mediated and humoral responses
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