Evidence map›Paper›PMID 11435470›Full record

ArticleThe Journal of experimental medicine2001

Murine cytomegalovirus is regulated by a discrete subset of natural killer cells reactive with monoclonal antibody to Ly49H.

K A Daniels, G Devora, W C Lai, C L O'Donnell, M Bennett, R M Welsh

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of experimental medicine, 2001. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 188 papers.

0numbers the graph read from it
0cells of the map it votes in
188citing papers in PubMed
9.3field-weighted citation impact, top 1% 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

188 citing papers in PubMed, 420 citations in OpenAlex.

  1. Trial
  2. An autoimmunity-associated allele ofProceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  3. An Autoimmunity-associated allele ofbioRxiv : the preprint server for biology · 2025
    Article
  4. Article
  5. Article
  6. Review
  7. CD94The European respiratory journal · 2024
    Article
  8. Five decades of natural killer cell discovery.The Journal of experimental medicine · 2024
    Review
  9. Article
  10. Review
  11. Review
  12. Review
  13. Review
  14. Article
  15. Article
  16. Article
  17. Review
  18. Article
  19. Review
  20. Article

128 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

6 authors at 2 institutions in 1 country.

K A DanielsDepartment of Pathology, University of Massachusetts Medical School, Worcester, MA 01655, USA.
G Devora
W C Lai
C L O'Donnell
M Bennett
R M Welsh
The University of Texas Southwestern Medical Center · USUniversity of Massachusetts Chan Medical School · US

Funding

IMMUNOBIOLOGY OF HYBRID RESISTANCER01CA036922 · NCI · UT SOUTHWESTERN MEDICAL CENTER · PI BENNETT, MICHAEL · 1985 to 2007
$2.4M
REGULATION OF NATURAL KILLER CELLSR01CA034461 · NCI · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI WELSH, RAYMOND M · 1985 to 2005
$1.3M
NCI NIH HHS CA34461NCI NIH HHS CA36922NCI NIH HHS R01 CA034461NCI NIH HHS R01 CA036922
6 · The paper itself

Abstract

Antiviral roles of natural killer (NK) cell subsets were examined in C57BL/6 mice infected with murine cytomegalovirus (MCMV) and other viruses, including lymphocytic choriomeningitis virus (LCMV), vaccinia virus (VV), and mouse hepatitis virus (MHV). Each virus vigorously induced an NK cell infiltrate into the peritoneal cavity and liver, causing some redistributions of NK cell subsets defined by monoclonal antibody (mAb) directed against Ly49A, C/I, D, and G2. Striking results were seen with a mAb (1F8) reactive with the positively signaling molecule Ly49H, present in MCMV-resistant C57BL/6 mice. mAb 1F8 also stains Ly49 C and I, but exclusion of those reactivities with mAb 5E6, which recognizes Ly49 C and I, indicated that Ly49H(+) cells infiltrated the peritoneal cavity and liver and were particularly effective at synthesizing interferon gamma. Depletion of 1F8(+) but not 5E6(+) cells in vivo by mAb injections enhanced MCMV titers by 20-1,000-fold in the spleen and approximately fivefold in the liver. Titers of LCMV or VV were not enhanced. These anti-MCMV effects were attributed to prototypical NK1.1(+)CD3(-) NK cells and not to NK1.1(+)CD3(+) "NK/T" cells. This is the first evidence that control of a virus infection in vivo is mediated by a distinct NK cell subset.

Indexed as

Antigens, LyAmino Acid SequenceAnimalsAntibodies, MonoclonalCD3 ComplexCross ReactionsFemaleHerpesviridae InfectionsInterferon-gammaKiller Cells, NaturalLectins, C-TypeLymphocyte SubsetsLymphocytic choriomeningitis virusMembrane GlycoproteinsMiceMice, Inbred C57BLAntibodies, MonoclonalAntigens, LyCD3 ComplexInterferon-gammaKlra1 protein, mouseKlra8 protein, mouseLectins, C-TypeMembrane GlycoproteinsNK Cell Lectin-Like Receptor Subfamily AReceptors, NK Cell Lectin-Like

Identifiers

PMID11435470
PMCPMC2193438
OpenAlexW2166807496

What OpenQuestion holds

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LicenceCC BY-NC-SA
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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.