Evidence map›Paper›PMID 28257991›Full record

ArticleJournal of controlled release : official journal of the Controlled Release Society2017

Low-dose controlled release of mTOR inhibitors maintains T cell plasticity and promotes central memory T cells.

Joshua M Gammon, Emily A Gosselin, Lisa H Tostanoski, Yu-Chieh Chiu, Xiangbin Zeng, Qin Zeng, Christopher M Jewell

Open access · hybridAbstract read
In one paragraph

Article in Journal of controlled release : official journal of the Controlled Release Society, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
1.3field-weighted citation impact, top 21% 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

22 citing papers in PubMed, 37 citations in OpenAlex.

  1. Article
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  4. Synthetic organic materials for targeting immunotherapies to lymph nodes.Chemistry of materials : a publication of the American Chemical Society · 2024
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  13. Rapamycin Improves the Response of Effector and Memory CD8Frontiers in cellular and infection microbiology · 2021
    Article
  14. Review
  15. Article
  16. Biomaterials as Tools to Decode Immunity.Advanced materials (Deerfield Beach, Fla.) · 2020
    Review
  17. Article
  18. Review
  19. Review
  20. 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 2 institutions in 1 country.

Joshua M GammonFischell Department of Bioengineering, University of Maryland, College Park, MD, United States.
Emily A GosselinFischell Department of Bioengineering, University of Maryland, College Park, MD, United States.
Lisa H TostanoskiFischell Department of Bioengineering, University of Maryland, College Park, MD, United States.
Yu-Chieh ChiuFischell Department of Bioengineering, University of Maryland, College Park, MD, United States.
Xiangbin ZengFischell Department of Bioengineering, University of Maryland, College Park, MD, United States.
Qin ZengFischell Department of Bioengineering, University of Maryland, College Park, MD, United States.
Christopher M JewellFischell Department of Bioengineering, University of Maryland, College Park, MD, United States; Department of Microbiology and Immunology, University of Maryland Medical School, Baltimore, MD, United States; Marlene and Stewart Greenebaum Cancer Center, Baltimore, MD, United States; United States Department of Veterans Affairs, Baltimore, MD, United States. Electronic address: cmjewell@umd.edu.
University of Maryland, College Park · USUnited States Department of Veterans Affairs · US

Funding

Training Grant in Cancer BiologyT32CA154274 · NCI · UNIVERSITY OF MARYLAND BALTIMORE · PI Toni M Antalis, CURT I CIVIN · 2011 to 2026
$6.8M
Damon Runyon Cancer Research Foundation DRR-34-15NCI NIH HHS T32 CA154274
6 · The paper itself

Abstract

An important goal for improving vaccine and immunotherapy technologies is the ability to provide further control over the specific phenotypes of T cells arising from these agents. Along these lines, frequent administration of rapamycin (Rapa), a small molecule inhibitor of the mammalian target of rapamycin (mTOR), exhibits a striking ability to polarize T cells toward central memory phenotypes (T

Indexed as

AnimalsAntigensCell Line, TumorCell PlasticityCell ProliferationCoculture TechniquesCytokinesDelayed-Action PreparationsDendritic CellsMelanoma, ExperimentalMembrane ProteinsMice, Inbred C57BLMice, TransgenicMyelin-Oligodendrocyte GlycoproteinOvalbuminPeptide FragmentsAntigensCytokinesDelayed-Action PreparationsMembrane ProteinsMyelin-Oligodendrocyte GlycoproteinOvalbuminPeptide Fragmentspeptide SVYDFFVWLSirolimusTOR Serine-Threonine KinasesVaccinesImmunologyLymph nodeMicroparticle and nanoparticleRapamycin and mTOR inhibitorT cellVaccine and immunotherapy

Identifiers

PMID28257991
PMCPMC5573661
OpenAlexW2593795304

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.