Evidence map›Paper›PMID 18299564›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2008

Epitope discovery in West Nile virus infection: Identification and immune recognition of viral epitopes.

Curtis P McMurtrey, Alina Lelic, Paolo Piazza, Ayan K Chakrabarti, Eric J Yablonsky, Angela Wahl, Wilfried Bardet, Annette Eckerd, Robert L Cook, Rachael Hess and 5 more

Open access · greenAbstract readComparative Study
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
6.7field-weighted citation impact, top 3% 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

37 citing papers in PubMed, 68 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Immunoproteomics: The Evolution from Classical Methods to Emerging Techniques.Methods in molecular biology (Clifton, N.J.) · 2026
    Review
  4. Cellular Immune Response in Horses After West Nile Neuroinvasive Disease.Animals : an open access journal from MDPI · 2025
    Article
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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

15 authors at 5 institutions in 2 countries.

Curtis P McMurtreyDepartment of Microbiology and Immunology, University of Oklahoma Health Sciences Center, 975 NE 10th Street, Oklahoma City, OK 73104, USA.
Alina Lelic
Paolo Piazza
Ayan K Chakrabarti
Eric J Yablonsky
Angela Wahl
Wilfried Bardet
Annette Eckerd
Robert L Cook
Rachael Hess
Rico Buchli
Mark Loeb
Charles R Rinaldo
Jonathan Bramson
William H Hildebrand
University of Oklahoma Health Sciences Center · USUniversity of Pittsburgh · USMcMaster University · CAPure Protein (United States) · USUniversity of Florida Health · US

Funding

Molecular Basis of Immunity - Kirschtein-NRSAT32AI007633 · NIAID · UNIVERSITY OF OKLAHOMA HLTH SCIENCES CTR · PI CUNNINGHAM, MADELEINE W. · 2001 to 2022
$4.0M
POPULATION GENETICS ANAYLSIS PROGRAM ON WEST NILE VIRUS-266040066N01AI040066 · NIAID · MCMASTER UNIVERSITY · PI LOEB, MARK · 2006 to 2006
–
NIAID NIH HHS HHSN266200400027CNIAID NIH HHS N01 AI040066NIAID NIH HHS T32 AI007633
6 · The paper itself

Abstract

Cytotoxic T lymphocytes (CTL) play an important role in the control and elimination of infection by West Nile virus (WNV), yet the class I human leukocyte antigen (HLA)-presented peptide epitopes that enable CTL recognition of WNV-infected cells remain uncharacterized. The goals of this work were first to discover the peptide epitopes that distinguish the class I HLA of WNV-infected cells and then to test the T cell reactivity of newly discovered WNV epitopes. To discover WNV-immune epitopes, class I HLA was harvested from WNV (NY99 strain)-infected and uninfected HeLa cells. Then peptide epitopes were eluted from affinity-purified HLA, and peptide epitopes from infected and uninfected cells were comparatively mapped by mass spectroscopy. Six virus-derived peptides from five different viral proteins (E, NS2b, NS3, NS4b, and NS5) were discovered as unique to HLA-A*0201 of infected cells, demonstrating that the peptides sampled by class I HLA are distributed widely throughout the WNV proteome. When tested with CTL from infected individuals, one dominant WNV target was apparent, two epitopes were subdominant, and three demonstrated little CTL reactivity. Finally, a sequence comparison of these epitopes with the hundreds of viral isolates shows that HLA-A*0201 presents epitopes derived from conserved regions of the virus. Detection and recovery from WNV infection are therefore functions of the ability of class I HLA molecules to reveal conserved WNV epitopes to an intact cellular immune system that subsequently recognizes infected cells.

Indexed as

AnimalsBase SequenceChlorocebus aethiopsDNA PrimersEpitopes, T-LymphocyteHLA AntigensHumansMass SpectrometryMolecular Sequence DataSequence Analysis, DNASequence HomologyVero CellsWest Nile FeverWest Nile virusDNA PrimersEpitopes, T-LymphocyteHLA Antigens

Identifiers

PMID18299564
PMCPMC2268571
OpenAlexW2046509071

What OpenQuestion holds

Textmetadata
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.