Evidence map›Paper›PMID 32391120›Full record

ArticleOncotarget2020

CrkL is required for donor T cell migration to GvHD target organs.

Nathan H Roy, Mahinbanu Mammadli, Janis K Burkhardt, Mobin Karimi

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.3field-weighted citation impact, top 40% 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

4 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Bifunctional Role of CrkL during Bone Remodeling.International journal of molecular sciences · 2021
    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

4 authors at 3 institutions in 1 country.

Nathan H RoyDepartment of Pathology and Laboratory Medicine, Children's Hospital of Philadelphia Research Institute and Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA 19104, USA.
Mahinbanu MammadliDepartment of Microbiology and Immunology, SUNY Upstate Medical University, Syracuse, NY 13210, USA.
Janis K BurkhardtDepartment of Pathology and Laboratory Medicine, Children's Hospital of Philadelphia Research Institute and Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA 19104, USA.
Mobin KarimiDepartment of Microbiology and Immunology, SUNY Upstate Medical University, Syracuse, NY 13210, USA.
SUNY Upstate Medical University · USChildren's Hospital of Philadelphia · USUniversity of Pennsylvania · US

Funding

IMMUNOBIOLOGY OF NORMAL AND NEOPLASTIC LYMPHOCYTEST32CA009140 · NCI · UNIVERSITY OF PENNSYLVANIA · PI Malay Haldar, WARREN S PEAR · 1985 to 2026
$16.1M
TRAINING PROGRAM/RHEUMATIC DISEASEST32AR007442 · NIAMS · UNIVERSITY OF PENNSYLVANIA · PI BEHRENS, EDWARD M, MERKEL, PETER A · 1986 to 2018
$5.8M
TRANSFUSION MEDICINE RESEARCH TRAINING PROGRAMT32HL007775 · NHLBI · UNIVERSITY OF PENNSYLVANIA · PI SIEGEL, DONALD LAWRENCE · 1993 to 2023
$2.8M
Crosstalk between T cells and inflamed endothelium: regulation by Crk family proteinsR01HL128551 · NHLBI · CHILDREN'S HOSP OF PHILADELPHIA · PI BURKHARDT, JANIS K. · 2015 to 2018
$1.7M
Itk mediated tuning of CD8+ memory T cell developmentR01AI120701 · NIAID · CORNELL UNIVERSITY · PI AUGUST, AVERY · 2016 to 2019
$1.5M
Novel strategies to separate GVHD from GVTK22AI130182 · NIAID · UPSTATE MEDICAL UNIVERSITY · PI KARIMI, MOBIN · 2017 to 2018
$266k
NCI NIH HHS T32 CA009140NHLBI NIH HHS R01 HL128551NHLBI NIH HHS T32 HL007775NIAID NIH HHS K22 AI130182NIAID NIH HHS R01 AI120701NIAMS NIH HHS T32 AR007442NIMHD NIH HHS L32 MD010106
6 · The paper itself

Abstract

The success of cancer therapies based on allogeneic hematopoietic stem cell transplant relies on the ability to separate graft-versus-host disease (GvHD) from graft-versus-tumor (GVT) responses. Controlling donor T cell migration into peripheral tissues is a viable option to limit unwanted tissue damage, but a lack of specific targets limits progress on this front. Here, we show that the adaptor protein CrkL, but not the closely related family members CrkI or CrkII, is a crucial regulator of T cell migration.

Indexed as

CrkLgraft-versus-host diseaseinflammationmigrationT cell

Identifiers

PMID32391120
PMCPMC7197453
OpenAlexW3022984496

What Socratic holds

Textmetadata
LicenceCC BY
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.