Evidence map›Paper›PMID 21220118›Full record

ArticleStructure (London, England : 1993)2011

Molecular insights into γδ T cell costimulation by an anti-JAML antibody.

Petra Verdino, Deborah A Witherden, M Sharon Ferguson, Adam L Corper, André Schiefner, Wendy L Havran, Ian A Wilson

Open access · bronzeAbstract read
In one paragraph

Article in Structure (London, England : 1993), 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.4field-weighted citation impact, top 39% 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

9 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
  2. Article
  3. Junctional Adhesion Molecule-Like Protein (JAML) Is Correlated with Prognosis and Immune Infiltrates in Lung Adenocarcinoma.Medical science monitor : international medical journal of experimental and clinical research · 2022
    Article
  4. The Roles of Junctional Adhesion Molecules (JAMs) in Cell Migration.Frontiers in cell and developmental biology · 2022
    Review
  5. Review
  6. Review
  7. Review
  8. Article
  9. 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

7 authors at 1 institution in 1 country.

Petra VerdinoDepartment of Molecular Biology, The Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, CA 92037, USA.
Deborah A Witherden
M Sharon Ferguson
Adam L Corper
André Schiefner
Wendy L Havran
Ian A Wilson
Scripps Research Institute · US

Funding

Structural Basis of T Cell Receptor RecognitionR37AI042266 · NIAID · SCRIPPS RESEARCH INSTITUTE, THE · PI WILSON, IAN A · 2003 to 2012
$5.8M
JAML: A New Costimulatory Molecule for Gamma Delta T CellsR01AI064811 · NIAID · SCRIPPS RESEARCH INSTITUTE, THE · PI HAVRAN, WENDY L. · 2006 to 2016
$4.8M
STRUCTURAL IMMUNOLOGY OF MOUSE MHC CLASS IR01CA058896 · NCI · SCRIPPS RESEARCH INSTITUTE, THE · PI WILSON, IAN A · 1994 to 2010
$3.9M
Structural basis of TLR and NLR recognition and signalingR01AI042266 · NIAID · SCRIPPS RESEARCH INSTITUTE, THE · PI WILSON, IAN A · 1998 to 2017
$3.7M
NCI NIH HHS CA58896NCI NIH HHS R01 CA058896NIAID NIH HHS AI042266NIAID NIH HHS AI06481NIAID NIH HHS R01 AI042266NIAID NIH HHS R01 AI064811NIAID NIH HHS R37 AI042266
6 · The paper itself

Abstract

γδ T cells bridge innate and adaptive immunity and function in immunosurveillance, immunoregulation, tumor cell recognition, and as first line of defense against microbial infection. Costimulation of epithelial γδ T cell activation by the JAML receptor can be induced by interaction with its endogenous ligand CAR or by binding of the stimulatory antibody HL4E10. We, therefore, determined the crystal structure of the JAML-HL4E10 Fab complex at 2.95 Å resolution. HL4E10 binds the membrane-proximal domain of JAML through hydrophobic interactions that account for nanomolar affinity and long half-life, contrasting with the fast kinetics and micromolar affinity of the hydrophilic CAR interaction with the membrane-distal JAML domain. Thus, despite different binding sites and mechanisms, JAML interaction with these two disparate ligands leads to the same functional outcome, namely JAML triggering and induction of cell signaling. Several characteristics of the HL4E10 antibody might then be harnessed in therapeutic applications, such as promoting healing of acute or chronic wounds.

Indexed as

AnimalsAntibodies, HeterophileAntibodies, MonoclonalBinding Sites, AntibodyCell Adhesion MoleculesCell LineCell ProliferationCoxsackie and Adenovirus Receptor-Like Membrane ProteinCricetinaeCrystallography, X-RayHydrophobic and Hydrophilic InteractionsImmunoglobulin Fab FragmentsLangerhans CellsMicePhosphatidylinositol 3-KinasesProtein BindingAntibodies, HeterophileAntibodies, MonoclonalCell Adhesion MoleculesCLMP protein, mouseCoxsackie and Adenovirus Receptor-Like Membrane ProteinImmunoglobulin Fab FragmentsJAML protein, mousePhosphatidylinositol 3-KinasesReceptors, Antigen, T-Cell, gamma-deltaReceptors, VirusRecombinant Fusion Proteins

Identifiers

PMID21220118
PMCPMC3039130
OpenAlexW2088576518

What OpenQuestion holds

Textmetadata
LicenceTDM
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.