Evidence map›Paper›PMID 28733484›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2017

Cutting Edge: CD3 ITAM Diversity Is Required for Optimal TCR Signaling and Thymocyte Development.

Matthew L Bettini, Po-Chein Chou, Clifford S Guy, Thomas Lee, Kate M Vignali, Dario A A Vignali

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
1.0field-weighted citation impact, top 26% 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

31 citing papers in PubMed, 53 citations in OpenAlex.

  1. Strategies to eliminate native T cell receptors for adoptive T cell therapies.Molecular therapy : the journal of the American Society of Gene Therapy · 2026
    Review
  2. Article
  3. TCR signal-enhancing mutation alters lipid metabolism of thymocytes and impairs antitumor immunity of mature T cells.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
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  17. CAR-macrophage: Breaking new ground in cellular immunotherapy.Frontiers in cell and developmental biology · 2024
    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

6 authors at 2 institutions in 1 country.

Matthew L BettiniDepartment of Immunology, St. Jude Children's Research Hospital, Memphis, TN 38105; dvignali@pitt.edu matthew.bettini@bcm.edu.ORCID 0000-0001-5596-186X
Po-Chein ChouDepartment of Immunology, St. Jude Children's Research Hospital, Memphis, TN 38105.
Clifford S GuyDepartment of Immunology, St. Jude Children's Research Hospital, Memphis, TN 38105.
Thomas LeeSection of Diabetes and Endocrinology, Department of Pediatrics, Baylor College of Medicine, Texas Children's Hospital, Houston, TX 77030.
Kate M VignaliDepartment of Immunology, St. Jude Children's Research Hospital, Memphis, TN 38105.
Dario A A VignaliDepartment of Immunology, St. Jude Children's Research Hospital, Memphis, TN 38105; dvignali@pitt.edu matthew.bettini@bcm.edu.
St. Jude Children's Research Hospital · USBaylor College of Medicine · US

Funding

Viral Vector Technology (VVTSR)P30CA021765 · NCI · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI CHARLES ROBERTS · 1985 to 2026
$166.9M
VECTOR CORE FACILITYP30CA047904 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI Jessie Nedrow · 1988 to 2026
$158.0M
Molecular Control of TCR Signaling and FunctionR01AI052199 · NIAID · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI VIGNALI, DARIO AA · 2003 to 2015
$3.8M
Structural Analysis of the TCR-CD3 Complex and TCR SignalingR56AI118908 · NIAID · UNIV OF MARYLAND, COLLEGE PARK · PI MARIUZZA, ROY A, ORBAN, JOHN · 2016 to 2016
$700k
Parameters T-Cell Receptor avidity during thymic selection in autoimmune diabetesK22AI104761 · NIAID · BAYLOR COLLEGE OF MEDICINE · PI BETTINI, MATTHEW · 2014 to 2015
$269k
Self-Reactive T Cell Development in Type 1 DiabetesR56DK104903 · NIDDK · BAYLOR COLLEGE OF MEDICINE · PI BETTINI, MATTHEW · 2015 to 2015
$158k
NCI NIH HHS P30 CA021765NCI NIH HHS P30 CA047904NIAID NIH HHS K22 AI104761NIAID NIH HHS R01 AI052199NIAID NIH HHS R56 AI118908NIDDK NIH HHS R56 DK104903
6 · The paper itself

Abstract

For the αβ or γδTCR chains to integrate extracellular stimuli into the appropriate intracellular cellular response, they must use the 10 ITAMs found within the CD3 subunits (CD3γε, CD3δε, and ζζ) of the TCR signaling complex. However, it remains unclear whether each specific ITAM sequence of the individual subunit (γεδζ) is required for thymocyte development or whether any particular CD3 ITAM motif is sufficient. In this article, we show that mice utilizing a single ITAM sequence (γ, ε, δ, ζa, ζb, or ζc) at each of the 10 ITAM locations exhibit a substantial reduction in thymic cellularity and limited CD4

Indexed as

Amino Acid MotifsAnimalsCD3 ComplexCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesCell DifferentiationCells, CulturedHematopoiesisLymphocyte ActivationMiceMice, Inbred C57BLMice, KnockoutMultiprotein ComplexesReceptors, Antigen, T-Cell, alpha-betaReceptors, Antigen, T-Cell, gamma-deltaSignal TransductionCD3 antigen, zeta chainCD3 ComplexMultiprotein ComplexesReceptors, Antigen, T-Cell, alpha-betaReceptors, Antigen, T-Cell, gamma-delta

Identifiers

PMID28733484
PMCPMC5568475
OpenAlexW2737135731

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.