NK cell recognition.
By L. Lanier. Annual Review of Immunology, 2005
3,037 citations recorded by the source corpus.
Subfields: Immunology
View Paper: https://www.semanticscholar.org/paper/f8de0d7528318576c132ee58313dd982646add5d
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In Immunology
Citations in the corpus
- Anti-immunology: evasion of the host immune system by bacterial and viral pathogens. (2006, background): “Among the various classes of leukocytes that can be regulated by viral proteins, particular attention has been paid recently to NK cells, T cells, dendritic cells, and macrophage (Ambagala et al., 2005; Andrews et al., 2005; Lodoen and Lanier, 2005; Pollara et al., 2005).”
- NK cell development, homeostasis and function: parallels with CD8+ T cells (2011, background): “Interestingly, in both mice and humans, activated and memory CD8 + T cells also express inhibitory receptors for MHC class”
- Self-tolerance of natural killer cells (2006, background): “Unlike T and B cells, the specificity of NK cells for target cells is not dominated by a single antigen receptor but, instead, is determined by a range of stimulatory and inhibitory receptors expressed at the surface of each NK cel”
- T cell– and B cell–independent adaptive immunity mediated by natural killer cells (2006, background): “Mouse NK cells express variable combinations of Ly49 receptors, and the absolute number and relative frequency of NK cells expressing each Ly49 receptor combination depends on genetic backgroun”
- Innate Lymphoid Cells: a new paradigm in immunology (2015, background): “In certain tissues, the prompt production of effector cytokines is shared with “innate” T cells, such as mucosa-associated invariant T (MAIT) cells that produce IFN-g, IL-17, and IL-22 (77); invariant NKT (iNKT) cells that produce IFN-g or IL-4 (78); and subsets of gd T cells that produce IFN-g and ”
- Controlling NK Cell Responses: Integration of Signals for Activation and Inhibition (2013, background): “Differential requirements for Vav proteins in DAP10- and ITAM-mediated NK cell cytotoxicity.”
- Cytokine-induced memory-like natural killer cells (2009, background): “Unlike adaptive T and B lymphocytes, NK cells do not somatically rearrange their receptor genes, but rely upon a finite number of germ line-encoded inhibitory and activating NK receptors capable of recognizing MHC class I and class I-like molecules (8, 9).”
- Progressive loss of RORγt expression confers distinct functional fates to natural killer cell receptor-expressing RORγt+ innate lymphocytes (2010, positive): “1) allowing them to eliminate infected, transformed, or stressed cells (Lanier, 2005).”
- Immunobiology of the TAM receptors (2008, background): “1, DX5 and CD69), which recognize ligands on target cell”
- NK cells and cancer immunosurveillance (2008, background): “Altogether, it is now common sense that the activation of NK cells depends on an intricate balance between activating and inhibitory signals (Lanier, 2005): ‘healthy’ cells express NK-inhibiting MHC class I molecules and no or few activating NK ligands leaving NK cells quiescent.”
- Activation, coactivation, and costimulation of resting human natural killer cells (2006, background): “In line with these findings and providing mechanistic insights, a recent study (71) showed that NKG2D–DAP10 recruitment of both a Grb2–Vav complex and the p85 subunit of PI3K is required for NKG2D-mediated cytotoxicity in IL-2-activated NK cells.”
- Recognition of microorganisms and activation of the immune response (2007, background): “They express two types of receptor, activating and inhibitory, and these receptors recognize their cognate, host-encoded ligands on infected (target) cell”
- Functions of natural killer cells (2008, background): “Activating NK cell receptors detect the presence of ligands on cells in 'distress', such as the stress-induced self ligands recognized by NKG2D (human ULBP and MIC molecules, as well as mouse RAE1, H60 and MULT1 molecules”