Evidence map›Paper›PMID 20190759›Full record

ArticleNature immunology2010

An Slfn2 mutation causes lymphoid and myeloid immunodeficiency due to loss of immune cell quiescence.

Michael Berger, Philippe Krebs, Karine Crozat, Xiaohong Li, Ben A Croker, Owen M Siggs, Daniel Popkin, Xin Du, Brian R Lawson, Argyrios N Theofilopoulos and 7 more

Abstract read
In one paragraph

Article in Nature immunology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 60 papers.

0numbers the graph read from it
0cells of the map it votes in
60citing papers in PubMed
–field-weighted citation impact
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

60 citing papers in PubMed.

  1. Article
  2. mScience advances · 2026
    Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Review
  8. Unfolded protein responses in T cell immunity.Frontiers in immunology · 2024
    Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. STAT1 maintains naïve CD8Science advances · 2021
    Article
  16. Review
  17. Article
  18. Article
  19. Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

17 authors.

Michael BergerDepartment of Genetics, The Scripps Research Institute, La Jolla, California, USA.
Philippe Krebs
Karine Crozat
Xiaohong Li
Ben A Croker
Owen M Siggs
Daniel Popkin
Xin Du
Brian R Lawson
Argyrios N Theofilopoulos
Yu Xia
Kevin Khovananth
Eva Marie Moresco
Takashi Satoh
Osamu Takeuchi
Shizuo Akira
Bruce Beutler

Funding

Sequencing CoreP01AI070167 · NIAID · UT SOUTHWESTERN MEDICAL CENTER · PI BEUTLER, BRUCE A · 2006 to 2016
$27.2M
Mutagenetic analysis of LPS responsesR37GM067759 · NIGMS · UT SOUTHWESTERN MEDICAL CENTER · PI BEUTLER, BRUCE A · 2007 to 2016
$8.6M
T Cell Homeostasis in Systemic AutoimmunityR01AR031203 · NIAMS · SCRIPPS RESEARCH INSTITUTE, THE · PI THEOFILOPOULOS, ARGYRIOS N · 1986 to 2012
$4.9M
The Role of Transmethylation Reactions in AutoimmunityR01AI076396 · NIAID · SCRIPPS RESEARCH INSTITUTE, THE · PI LAWSON, BRIAN · 2009 to 2012
$1.9M
NIAID NIH HHS P01 AI070167NIAID NIH HHS R01 AI076396NIAMS NIH HHS R01 AR031203NIGMS NIH HHS R37 GM067759
6 · The paper itself

Abstract

Here we describe a previously unknown form of inherited immunodeficiency revealed by an N-ethyl-N-nitrosourea-induced mutation called elektra. Mice homozygous for this mutation showed enhanced susceptibility to bacterial and viral infection and diminished numbers of T cells and inflammatory monocytes that failed to proliferate after infection and died via the intrinsic apoptotic pathway in response to diverse proliferative stimuli. They also had a greater proportion of T cells poised to replicate DNA, and their T cells expressed a subset of activation markers, suggestive of a semi-activated state. We positionally ascribe the elektra phenotype to a mutation in the gene encoding Schlafen-2 (Slfn2). Our findings identify a physiological role for Slfn2 in the defense against pathogens through the regulation of quiescence in T cells and monocytes.

Indexed as

AnimalsApoptosisBase SequenceCell Cycle ProteinsCell SeparationFlow CytometryImmunologic Deficiency SyndromesLeukocytes, MononuclearLymphocyte ActivationMiceMice, TransgenicMutationPhenotypeSignal TransductionT-LymphocytesCell Cycle Proteinsschlafen-2 protein, mouse

Identifiers

PMID20190759
PMCPMC2861894

What OpenQuestion holds

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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.