Evidence map›Paper›PMID 31278057›Full record

ArticleImmunity2019

T Cell Recruitment to the Intestinal Stem Cell Compartment Drives Immune-Mediated Intestinal Damage after Allogeneic Transplantation.

Ya-Yuan Fu, Anastasiya Egorova, Catherine Sobieski, Jason Kuttiyara, Marco Calafiore, Shuichiro Takashima, Hans Clevers, Alan M Hanash

Open access · bronzeAbstract read
In one paragraph

Article in Immunity, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 72 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
72citing papers in PubMed, 1 pooled it
4.5field-weighted citation impact, top 5% 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

72 citing papers in PubMed, 1 synthesis or guideline pooled it, 104 citations in OpenAlex.

  1. Pooled it
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  9. Loss of GLP-2R signaling in Glp2rMolecular metabolism · 2026
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12 more citing papers are in PubMed but not listed here.

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

8 authors at 2 institutions in 2 countries.

Ya-Yuan FuDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA.
Anastasiya EgorovaDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA.
Catherine SobieskiDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA.
Jason KuttiyaraDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA.
Marco CalafioreDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA.
Shuichiro TakashimaDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA.
Hans CleversHubrecht Institute, Royal Netherlands Academy of Arts and Sciences (KNAW) and University Medical Center Utrecht, 3584 CT Utrecht, the Netherlands.
Alan M HanashDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA; Department of Medicine, Weill Cornell Medical College, New York, NY 10065, USA. Electronic address: hanasha@mskcc.org.
Memorial Sloan Kettering Cancer Center · USRoyal Netherlands Academy of Arts and Sciences · NL

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Elisa de Stanchina · 1985 to 2026
$347.4M
Discriminating EGFR function in T cells and epithelium during immune-mediated tissue damageR01HL146338 · NHLBI · SLOAN-KETTERING INST CAN RESEARCH · PI Alan M Hanash · 2018 to 2026
$4.8M
Regulation of the intestinal stem cell compartment after hematopoietic transplantationR01HL125571 · NHLBI · SLOAN-KETTERING INST CAN RESEARCH · PI Alan M Hanash · 2015 to 2026
$4.4M
IL-22 in epithelial regeneration after allogeneic transplantK08HL115355 · NHLBI · SLOAN-KETTERING INST CAN RESEARCH · PI HANASH, ALAN M · 2012 to 2016
$719k
NCI NIH HHS P30 CA008748NHLBI NIH HHS K08 HL115355NHLBI NIH HHS R01 HL125571NHLBI NIH HHS R01 HL146338
6 · The paper itself

Abstract

The key sites within the gastrointestinal (GI) tract where T cells mediate effector responses and the impact of these responses on intestinal stem cells (ISCs) remain unclear. Using experimental bone marrow transplantation to model immune-mediated GI damage and 3D imaging to analyze T cell localization, we found that the ISC compartment is the primary intestinal site targeted by T cells after transplantation. Recruitment to the crypt base region resulted in direct T cell engagement with the stem cell compartment and loss of crypt base columnar ISCs, which expressed both MHC classes I and II. Vasculature expressing the adhesion molecule MAdCAM-1 clustered near the crypt base, preferentially regulating crypt compartment invasion and ISC reduction without affecting T cell migration to villi. These findings indicate that allogeneic T cells rapidly access the stem cell niche after transplantation, and this targeted recruitment to the stem cell compartment results in ISC loss during immune-mediated GI damage.

Indexed as

Bone Marrow TransplantationAdult Stem CellsAnimalsBlood VesselsCell Adhesion MoleculesCell MovementCytotoxicity, ImmunologicFemaleHumansImaging, Three-DimensionalIntestinal MucosaMiceMice, Inbred BALB CMice, Inbred C57BLMice, TransgenicMiddle AgedCell Adhesion MoleculesMadcam1 protein, mouseMucoproteinsallogeneic bone marrow transplantationbeta7 integrinBMTgraft versus host diseaseGVHDimaging of immunityintestinal stem cellsISCsLPAMMAdCAM-1mucosal immunologyPaneth cellstransplantation

Identifiers

PMID31278057
PMCPMC7239328
OpenAlexW2954200705

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.