4.7 Article

Inducible down-regulation of MHC class I results in natural killer cell tolerance

Journal

JOURNAL OF EXPERIMENTAL MEDICINE
Volume 216, Issue 1, Pages 99-116

Publisher

ROCKEFELLER UNIV PRESS
DOI: 10.1084/jem.20181076

Keywords

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Funding

  1. National Institutes of Health [R01AI129545, R01AI131680, F30DK112466]

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Natural killer (NK) cells are innate lymphocytes that are thought to kill cells that down-regulate MHC class I (MHC-I) through missing-self recognition. NK cells from B2m(-/-) mice that lack surface MHC-I, however, are not autoreactive as predicted by the missing-self hypothesis. As a result, it is unclear if MHC-I down-regulation in vivo induces NK cell reactivity or tolerance to missing-self. Here, we generated a floxed B2m mouse to acutely down-regulate MHC-I in vivo in a host that normally expresses MHC-I. Global down-regulation of MHC-I induced NK cell hyporesponsiveness and tolerance to missing-self without overt missing-self reactivity. In contrast, down-regulation of MHC-I on a small fraction of hematopoietic cells triggered missing-self reactivity. Surprisingly, down-regulation of MHC-I only on CD4(+) T cells predominately induced tolerance to missing-self without resetting NK cell responsiveness. In this setting, inflammation triggered substantial missing-self reactivity. These results show that MHC-I down-regulation can induce either NK cell tolerance or killing in vivo and that inflammation promotes missing-self reactivity.

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