Evidence map›Paper›PMID 27500835›Full record

ArticleJournal of visualized experiments : JoVE2016

Retroviral Transduction of Bone Marrow Progenitor Cells to Generate T-cell Receptor Retrogenic Mice.

Thomas Lee, Ivan Shevchenko, Maran L Sprouse, Maria Bettini, Matthew L Bettini

Open access · bronzeAbstract readVideo-Audio Media
In one paragraph

Article in Journal of visualized experiments : JoVE, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.4field-weighted citation impact, top 16% 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

10 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
  2. Article
  3. A Novel Animal Model of Emphysema Induced by Anti-Elastin Autoimmunity.Journal of immunology (Baltimore, Md. : 1950) · 2019
    Article
  4. Generation of T Cell Receptor Retrogenic Mice.Current protocols in immunology · 2019
    Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. 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

5 authors at 1 institution in 1 country.

Thomas LeeDepartment of Pediatrics, Baylor College of Medicine.
Ivan ShevchenkoDepartment of Pediatrics, Baylor College of Medicine.
Maran L SprouseDepartment of Pediatrics, Baylor College of Medicine.
Maria BettiniDepartment of Pediatrics, Baylor College of Medicine.
Matthew L BettiniDepartment of Pediatrics, Baylor College of Medicine; Matthew.Bettini@bcm.edu.
Baylor College of Medicine · US

Funding

Diabetes Endocrinology Research CenterP30DK079638 · NIDDK · BAYLOR COLLEGE OF MEDICINE · PI CHAN, LAWRENCE · 2008 to 2012
$6.4M
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
NIAID NIH HHS K22 AI104761NIDDK NIH HHS P30 DK079638NIDDK NIH HHS R56 DK104903
6 · The paper itself

Abstract

T cell receptor (TCR) signaling is essential in the development and differentiation of T cells in the thymus and periphery, respectively. The vast array of TCRs proves studying a specific antigenic response difficult. Therefore, TCR transgenic mice were made to study positive and negative selection in the thymus as well as peripheral T cell activation, proliferation and tolerance. However, relatively few TCR transgenic mice have been generated specific to any given antigen. Thus, studies involving TCRs of varying affinities for the same antigenic peptide have been lacking. The generation of a new TCR transgenic line can take six or more months. Additionally, any specific backcrosses can take an additional six months. In order to allow faster generation and screening of multiple TCRs, a protocol for retroviral transduction of bone marrow was established with stoichiometric expression of the TCRα and TCRβ chains and the generation of retrogenic mice. Each retrogenic mouse is essentially a founder, virtually negating a founder effect, while the length of time to generate a TCR retrogenic is cut from six months to approximately six weeks. Here we present a rapid and flexible alternative to TCR transgenic mice that can be expressed on any chosen background with any particular TCR.

Indexed as

Mice, TransgenicRetroviridaeAnimalsBone MarrowMiceReceptors, Antigen, T-CellStem CellsThymus GlandT-LymphocytesTransduction, GeneticReceptors, Antigen, T-Cell

Identifiers

PMID27500835
PMCPMC4993443
OpenAlexW2464019133

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.