Evidence map›Paper›PMID 37790561›Full record

ArticlebioRxiv : the preprint server for biology2023

AML/T cell interactomics uncover correlates of patient outcomes and the key role of ICAM1 in T cell killing of AML.

Ece Canan Sayitoglu, Bogdan A Luca, Allison P Boss, Benjamin Craig Thomas, Robert Arthur Freeborn, Molly J Uyeda, Pauline P Chen, Yusuke Nakauchi, Colin Waichler, Norman Lacayo and 5 more

Open access · greenAbstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed, 0 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

15 authors at 3 institutions in 2 countries.

Ece Canan Sayitoglu
Bogdan A Luca
Allison P Boss
Benjamin Craig Thomas
Robert Arthur Freeborn
Molly J Uyeda
Pauline P Chen
Yusuke Nakauchi
Colin Waichler
Norman Lacayo
Rosa Bacchetta
Ravindra Majeti
Andrew J Gentles
Alma-Martina CepikaORCID 0000-0003-2862-1901
Maria Grazia RoncaroloORCID 0000-0003-1636-1495
Stanford Medicine · USCalifornia Institute for Regenerative Medicine · USStanford University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

T cells are important for the control of acute myeloid leukemia (AML), a common and often deadly malignancy. We observed that some AML patient samples are resistant to killing by human engineered cytotoxic CD4 SIGNIFICANCE: AML is a common leukemia with sub-optimal outcomes. We show that AML transcriptional programs correlate with susceptibility to T cell killing. Killing resistance-associated AML programs are enriched in patients with poor survival. Killing-sensitive, but not resistant AML activate T cells and upregulate GRAPHICAL ABSTRACT:

Identifiers

PMID37790561
PMCPMC10542521
OpenAlexW4386983453

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.