Evidence map›Paper›PMID 18759922›Full record

ReviewImmunological reviews2008

Regulation of NK cell responsiveness to achieve self-tolerance and maximal responses to diseased target cells.

Nathalie T Joncker, David H Raulet

Open access · greenAbstract readReview
In one paragraph

Review in Immunological reviews, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 79 papers.

0numbers the graph read from it
0cells of the map it votes in
79citing papers in PubMed
5.4field-weighted citation impact, top 4% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

79 citing papers in PubMed, 133 citations in OpenAlex.

  1. Review
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  13. Deciphering Natural Killer Cell Homeostasis.Frontiers in immunology · 2020
    Review
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19 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors at 1 institution in 1 country.

Nathalie T JonckerDepartment of Molecular and Cell Biology, University of California Berkeley, Berkeley, CA 94720-3200, USA.
David H Raulet
University of California, Berkeley · US

Funding

EXPRESSION OF CLASS I-SPECIFIC RECEPTORS IN NK CELLSR01AI039642 · NIAID · UNIVERSITY OF CALIFORNIA BERKELEY · PI RAULET, DAVID H · 1996 to 2014
$4.9M
Role of NKG2D in immune responses to turmorsR01CA093678 · NCI · UNIVERSITY OF CALIFORNIA BERKELEY · PI RAULET, DAVID H · 2003 to 2019
$4.2M
Role of MHC molecules in NK recognitionR01AI035021 · NIAID · UNIVERSITY OF CALIFORNIA BERKELEY · PI RAULET, DAVID H · 1994 to 2008
$1.9M
NCI NIH HHS R01 CA093678NIAID NIH HHS R01 AI035021NIAID NIH HHS R01 AI039642
6 · The paper itself

Abstract

Inhibitory receptors specific for major histocompatibility complex (MHC) class I molecules govern the capacity of natural killer (NK) cells to attack class I-deficient cells ('missing-self recognition'). These receptors are expressed stochastically, such that the panel of expressed receptors varies between NK cells. This review addresses how the activity of NK cells is coordinated in the face of this variation to achieve a repertoire that is self-tolerant and optimally reactive with diseased cells. Recent studies show that NK cells arise in normal animals or humans that lack any known inhibitory receptors specific for self-MHC class I. These NK cells exhibit self-tolerance and exhibit functional hyporesponsiveness to stimulation through various activating receptors. Evidence suggests that hyporesponsiveness is induced because these NK cells cannot engage inhibitory MHC class I molecules and are therefore persistently over-stimulated by normal cells in the environment. Finally, we discuss evidence that hyporesponsiveness is a quantitative trait that varies depending on the balance of signals encountered by developing NK cells. Thus, a tuning process determines the functional set-point of NK cells, providing a basis for discriminating self from missing-self, and at the same time endowing each NK cell with the highest inherent responsiveness compatible with self-tolerance.

Indexed as

Cytotoxicity, ImmunologicSelf ToleranceAnimalsAntigens, CDAntigens, SurfaceCell Adhesion MoleculesHistocompatibility Antigens Class IHumansKiller Cells, NaturalLectins, C-TypeLymphocyte ActivationMiceMice, TransgenicNK Cell Lectin-Like Receptor Subfamily BReceptors, ImmunologicReceptors, KIRAntigens, CDAntigens, SurfaceCd244a protein, mouseCD66 antigensCell Adhesion MoleculesHistocompatibility Antigens Class IKLRB1 protein, humanKLRG1 protein, humanLectins, C-TypeNK Cell Lectin-Like Receptor Subfamily BReceptors, ImmunologicReceptors, KIRSignaling Lymphocytic Activation Molecule FamilyTrans-Activators

Identifiers

PMID18759922
PMCPMC3017429
OpenAlexW1991650736

What OpenQuestion holds

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Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.