Evidence map›Paper›PMID 28804489›Full record

ArticleFrontiers in immunology2017

Normalized Synergy Predicts That CD8 Co-Receptor Contribution to T Cell Receptor (TCR) and pMHC Binding Decreases As TCR Affinity Increases in Human Viral-Specific T Cells.

Chad M Williams, Alexandra A Schonnesen, Shu-Qi Zhang, Ke-Yue Ma, Chenfeng He, Tori Yamamoto, S Gail Eckhardt, Christopher A Klebanoff, Ning Jiang

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
0.9field-weighted citation impact, top 23% 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

14 citing papers in PubMed, 14 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Joining Forces for Cancer Treatment: From "TCR versus CAR" to "TCR and CAR".International journal of molecular sciences · 2022
    Review
  5. Article
  6. Article
  7. Cytotoxic CD8British journal of cancer · 2021
    Review
  8. Review
  9. Article
  10. T Cell Reprogramming Against Cancer.Methods in molecular biology (Clifton, N.J.) · 2020
    Review
  11. Review
  12. Review
  13. A rare population of tumor antigen-specific CD4Journal for immunotherapy of cancer · 2019
    Article
  14. Article
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

9 authors at 4 institutions in 1 country.

Chad M WilliamsDepartment of Biomedical Engineering, University of Texas at Austin, Austin, TX, United States.
Alexandra A SchonnesenDepartment of Biomedical Engineering, University of Texas at Austin, Austin, TX, United States.
Shu-Qi ZhangMcKetta Department of Chemical Engineering, University of Texas at Austin, Austin, TX, United States.
Ke-Yue MaInstitute for Cell and Molecular Biology, University of Texas at Austin, Austin, TX, United States.
Chenfeng HeDepartment of Biomedical Engineering, University of Texas at Austin, Austin, TX, United States.
Tori YamamotoCenter for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD, United States.
S Gail EckhardtLIVESTRONG Cancer Institutes, Dell Medical School, University of Texas at Austin, Austin, TX, United States.
Christopher A KlebanoffCenter for Cell Engineering, Department of Medicine, Memorial Sloan Kettering Cancer Center (MSKCC), New York, NY, United States.
Ning JiangDepartment of Biomedical Engineering, University of Texas at Austin, Austin, TX, United States.
The University of Texas at Austin · USLivestrong Foundation · USParker Institute for Cancer Immunotherapy · USUniversity of Pennsylvania · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Nicholas D Socci · 1985 to 2026
$347.4M
Comprehensive Training Program in Imaging Science and InformaticsT32EB007507 · NIBIB · UNIVERSITY OF TEXAS AT AUSTIN · PI MARKEY, MIA K, RYLANDER, HENRY GRADY · 2009 to 2024
$2.7M
Genomic Approaches to the T Cell Receptor Repertoire during AgingR00AG040149 · NIA · UNIVERSITY OF TEXAS AT AUSTIN · PI JIANG, NING JENNY · 2013 to 2015
$740k
NCI NIH HHS P30 CA008748NIA NIH HHS R00 AG040149NIBIB NIH HHS T32 EB007507
6 · The paper itself

Abstract

The discovery of naturally occurring T cell receptors (TCRs) that confer specific, high-affinity recognition of pathogen and cancer-associated antigens remains a major goal in cellular immunotherapies. The contribution of the CD8 co-receptor to the interaction between the TCR and peptide-bound major histocompatibility complex (pMHC) has previously been correlated with the activation and responsiveness of CD8

Indexed as

CD8 binding independent T cell receptorCD8 cooperationhuman viral-specific polyclonal CTLT cell receptor/pMHC interactiontwo-dimensional affinity and kinetics

Identifiers

PMID28804489
PMCPMC5532383
OpenAlexW2741876477

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.