Evidence map›Paper›PMID 15728728›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2005

HLA-restricted epitope identification and detection of functional T cell responses by using MHC-peptide and costimulatory microarrays.

Jennifer D Stone, Walter E Demkowicz, Lawrence J Stern

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
3.3field-weighted citation impact, top 7% 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

30 citing papers in PubMed, 76 citations in OpenAlex.

  1. Trial
  2. Article
  3. Review
  4. Article
  5. Development of Peptide Vaccines in Dengue.Current pharmaceutical design · 2018
    Review
  6. Article
  7. Review
  8. Article
  9. Drug-eluting microarrays to identify effective chemotherapeutic combinations targeting patient-derived cancer stem cells.Proceedings of the National Academy of Sciences of the United States of America · 2015
    Article
  10. Article
  11. Article
  12. Life on a microarray: assessing live cell functions in a microarray format.Cellular and molecular life sciences : CMLS · 2012
    Review
  13. Missing: a diagnostic technique to enumerate antigen-specific T cells.Critical reviews in oncology/hematology · 2012
    Review
  14. Article
  15. Article
  16. Article
  17. MHC-based detection of antigen-specific CD8+ T cell responses.Cancer immunology, immunotherapy : CII · 2010
    Review
  18. Article
  19. Review
  20. High throughput T epitope mapping and vaccine development.Journal of biomedicine & biotechnology · 2010
    Review
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

3 authors at 3 institutions in 1 country.

Jennifer D StoneDepartment of Chemistry, Massachusetts Institute of Technology, 77 Massachusetts Avenue, Cambridge, MA 02139, USA.
Walter E Demkowicz
Lawrence J Stern
Albert Einstein College of Medicine · USMassachusetts Institute of Technology · USUniversity of Massachusetts Chan Medical School · US

Funding

Technologies for Human Cellular ImmunologyU19AI057319 · NIAID · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI ROTHMAN, ALAN L · 2003 to 2013
$34.4M
BAA-APPLICATION OF HLA DATA TO DEVELOP &IMPROVE VACCINEN01AI095361 · NIAID · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI STERN, LAWRENCE · 1999 to 2000
$324k
NIAID NIH HHS N01 AI095361NIAID NIH HHS N01 AI 95361NIAID NIH HHS U19 AI057319NIAID NIH HHS U19 AI 57319
6 · The paper itself

Abstract

Identification of T cell epitopes is a vital but often slow and difficult step in studying the immune response to infectious agents and autoantigens. We report a spatially addressable technique for screening large numbers of T cell epitopes for both specific antigen recognition and functional activity induced. This system uses microarrays of immobilized, recombinant MHC-peptide complexes, costimulatory molecules, and cytokine-capture antibodies. The array elements act as synthetic antigen-presenting cells and specifically elicit T cell responses, including adhesion, secretion of cytokines, and modulation of surface markers. The method allows facile identification of pertinent T cell epitopes in a large number of candidates and simultaneous determination of the functional outcome of the interaction. Using this method, we have characterized the activation of human CD4(+) and CD8(+) T cells responding to vaccinia, influenza, HIV-1, and Epstein-Barr viruses.

Indexed as

Epitopes, T-LymphocyteLymphocyte ActivationProtein Array AnalysisAntigen PresentationCytokinesHLA AntigensHumansT-LymphocytesCytokinesEpitopes, T-LymphocyteHLA Antigens

Identifiers

PMID15728728
PMCPMC553304
OpenAlexW2010248348

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.