Evidence map›Paper›PMID 29127145›Full record

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

TIM-3 Engagement Promotes Effector Memory T Cell Differentiation of Human Antigen-Specific CD8 T Cells by Activating mTORC1.

Nina Chi Sabins, Olesya Chornoguz, Karen Leander, Fred Kaplan, Richard Carter, Michelle Kinder, Kurtis Bachman, Raluca Verona, Shixue Shen, Vipul Bhargava and 1 more

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 27 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed, 1 pooled it
2.1field-weighted citation impact, top 12% 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

27 citing papers in PubMed, 1 synthesis or guideline pooled it, 41 citations in OpenAlex.

  1. Pooled it
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  15. Immune Cell Landscape in Gastric Cancer.BioMed research international · 2021
    Article
  16. TIM-3 and CEACAM1 do not interact in cis and in trans.European journal of immunology · 2020
    Article
  17. Accelerator or Brake: Immune Regulators in Malaria.Frontiers in cellular and infection microbiology · 2020
    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

11 authors at 1 institution in 1 country.

Nina Chi SabinsJanssen Biotherapeutics, Janssen Research and Development, Spring House, PA 19477.
Olesya ChornoguzJanssen Biotherapeutics, Janssen Research and Development, Spring House, PA 19477.
Karen LeanderJanssen Biotherapeutics, Janssen Research and Development, Spring House, PA 19477.
Fred KaplanOncology, Janssen Research and Development, Spring House, PA 19477.
Richard CarterJanssen Biotherapeutics, Janssen Research and Development, Spring House, PA 19477.ORCID 0000-0003-1291-4187
Michelle KinderOncology, Janssen Research and Development, Spring House, PA 19477.
Kurtis BachmanOncology, Janssen Research and Development, Spring House, PA 19477.
Raluca VeronaOncology, Janssen Research and Development, Spring House, PA 19477.ORCID 0000-0003-0044-4341
Shixue ShenOncology, Janssen Research and Development, Spring House, PA 19477.ORCID 0000-0003-1348-7340
Vipul BhargavaComputational and Systems Biology, Janssen Research and Development, Spring House, PA 19477; and.
Sandra Santulli-MarottoAlios BioPharma, Janssen Research and Development, South San Francisco, CA 94080 Ssantull@its.jnj.com.
Janssen (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

T cell expression of TIM-3 following Ag encounter has been associated with a continuum of functional states ranging from effector memory T cells to exhaustion. We have designed an in vitro culture system to specifically address the impact of anti-TIM-3/TIM-3 engagement on human Ag-specific CD8 T cells during a normal response to Ag and found that anti-TIM-3 treatment enhances T cell function. In our in vitro T cell culture system, MART1-specific CD8 T cells were expanded from healthy donors using artificial APCs. To ensure that the T cells were the only source of TIM-3, cells were rechallenged with peptide-loaded artificial APCs in the presence of anti-TIM-3 Ab. In these conditions, anti-TIM-3 treatment promotes generation of effector T cells as shown by acquisition of an activated phenotype, increased cytokine production, enhanced proliferation, and a transcription program associated with T cell differentiation. Activation of mTORC1 has been previously demonstrated to enhance CD8 T cell effector function and differentiation. Anti-TIM-3 drives CD8 T cell differentiation through activation of the mTORC1 as evidenced by increased levels of phosphorylated S6 protein and

Indexed as

Antibodies, MonoclonalAntigensCD8-Positive T-LymphocytesCell DivisionCells, CulturedGene Expression ProfilingGene Expression RegulationHepatitis A Virus Cellular Receptor 2HumansImmunologic MemoryLymphocyte ActivationLymphokinesMART-1 AntigenMechanistic Target of Rapamycin Complex 1PhosphorylationProtein Processing, Post-TranslationalAntibodies, MonoclonalAntigensHAVCR2 protein, humanHepatitis A Virus Cellular Receptor 2LymphokinesMART-1 AntigenMechanistic Target of Rapamycin Complex 1MLANA protein, humanras ProteinsRHEBL1 protein, human

Identifiers

PMID29127145
PMCPMC5713500
OpenAlexW2767645660

What Socratic 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 Socratic graph.