Evidence map›Paper›PMID 24642562›Full record

ArticlePloS one2014

Increased frequency of Tim-3 expressing T cells is associated with symptomatic West Nile virus infection.

Marion C Lanteri, Michael S Diamond, Jacqueline P Law, Glen M Chew, Shiquan Wu, Heather C Inglis, Derek Wong, Michael P Busch, Philip J Norris, Lishomwa C Ndhlovu

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.2field-weighted citation impact, top 11% 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

12 citing papers in PubMed, 19 citations in OpenAlex.

  1. Cellular Immune Response in Horses After West Nile Neuroinvasive Disease.Animals : an open access journal from MDPI · 2025
    Article
  2. Myeloid-Derived Suppressor Cells Induce Exhaustion-Like CD8International journal of biological sciences · 2024
    Article
  3. Article
  4. Article
  5. Article
  6. Dynamics of Tissue-Specific CD8Journal of virology · 2018
    Article
  7. Review
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  11. Review
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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

10 authors at 4 institutions in 1 country.

Marion C LanteriBlood Systems Research Institute, University of California at San Francisco, San Francisco, California, United States of America.
Michael S DiamondDepartments of Medicine, Molecular Microbiology, and Pathology & Immunology, Washington University School of Medicine, St. Louis, Missouri, United States of America.
Jacqueline P LawBlood Systems Research Institute, University of California at San Francisco, San Francisco, California, United States of America.
Glen M ChewDepartment of Tropical Medicine, John A. Burns School of Medicine, University of Hawaii, Honolulu, Hawaii, United States of America.
Shiquan WuBlood Systems Research Institute, University of California at San Francisco, San Francisco, California, United States of America.
Heather C InglisBlood Systems Research Institute, University of California at San Francisco, San Francisco, California, United States of America.
Derek WongBlood Systems Research Institute, University of California at San Francisco, San Francisco, California, United States of America.
Michael P BuschBlood Systems Research Institute, University of California at San Francisco, San Francisco, California, United States of America; Department of Laboratory Medicine, University of California San Francisco, San Francisco, California, United States of America.
Philip J NorrisBlood Systems Research Institute, University of California at San Francisco, San Francisco, California, United States of America; Department of Laboratory Medicine, University of California San Francisco, San Francisco, California, United States of America; Department of Medicine, University of California San Francisco, San Francisco, California, United States of America.
Lishomwa C NdhlovuDepartment of Tropical Medicine, John A. Burns School of Medicine, University of Hawaii, Honolulu, Hawaii, United States of America.
Blood Systems Research Institute · USUniversity of Hawaiʻi at Mānoa · USUniversity of California, San Francisco · USWashington University in St. Louis · US

Funding

NHLBI NIH HHS RC2HL101PHS HHS R01 C1000214
6 · The paper itself

Abstract

More than a decade after West Nile virus (WNV) entered North America, and despite a significant increase in reported cases during the 2012 and 2013 seasons, no treatment or vaccine for humans is available. Although antiviral T cells contribute to the control of WNV, little is known about their regulation during acute infection. We analyzed the expression of Tim-3 and PD-1, two recently identified T cell negative immune checkpoint receptors, over the course of WNV infection. Symptomatic WNV+ donors exhibited higher frequencies of Tim-3+ cells than asymptomatic subjects within naïve/early differentiated CD28+/-CD57-CD4+ and differentiated CD28-CD57-CD8+ T cells. Our study links Tim-3-expression on T cells during acute WNV infection with the development of symptomatic disease, suggesting Tim-3 and its ligands could be targeted therapeutically to alter anti-WNV immunity and improve disease outcome.

Indexed as

AdolescentAdultAgedAsymptomatic DiseasesCD28 AntigensCD4-Positive T-LymphocytesCD57 AntigensCD8-Positive T-LymphocytesFemaleGene ExpressionHepatitis A Virus Cellular Receptor 2Host-Pathogen InteractionsHumansImmunophenotypingLymphocyte CountMaleCD28 AntigensCD57 AntigensHAVCR2 protein, humanHepatitis A Virus Cellular Receptor 2Membrane ProteinsPDCD1 protein, humanProgrammed Cell Death 1 Receptor

Identifiers

PMID24642562
PMCPMC3958446
OpenAlexW2159606670

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.