Evidence map›Paper›PMID 33731852›Full record

ArticleLeukemia2021

Interleukin-10 suppression enhances T-cell antitumor immunity and responses to checkpoint blockade in chronic lymphocytic leukemia.

J R Rivas, Y Liu, S S Alhakeem, J M Eckenrode, F Marti, J P Collard, Y Zhang, K A Shaaban, N Muthusamy, G C Hildebrandt and 5 more

Open access · greenAbstract read
In one paragraph

Article in Leukemia, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 49 papers.

0numbers the graph read from it
0cells of the map it votes in
49citing papers in PubMed
6.2field-weighted citation impact, top 3% 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

49 citing papers in PubMed, 62 citations in OpenAlex.

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  9. Immunotherapy in central nervous system tumors.International journal of surgery (London, England) · 2025
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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

15 authors at 2 institutions in 1 country.

J R RivasDepartment of Microbiology, Immunology and Molecular Genetics, University of Kentucky, Lexington, KY, USA.ORCID http://orcid.org/0000-0003-3949-1604
Y LiuDepartment of Pharmaceutical Sciences, University of Kentucky, Lexington, KY, USA.ORCID http://orcid.org/0000-0002-5261-8000
S S AlhakeemDepartment of Microbiology, Immunology and Molecular Genetics, University of Kentucky, Lexington, KY, USA.
J M EckenrodeDepartment of Pharmaceutical Sciences, University of Kentucky, Lexington, KY, USA.
F MartiDepartment of Surgery, University of Kentucky, Lexington, KY, USA.
J P CollardDepartment of Microbiology, Immunology and Molecular Genetics, University of Kentucky, Lexington, KY, USA.ORCID http://orcid.org/0000-0003-4930-7188
Y ZhangDepartment of Pharmaceutical Sciences, University of Kentucky, Lexington, KY, USA.
K A ShaabanDepartment of Pharmaceutical Sciences, University of Kentucky, Lexington, KY, USA.ORCID http://orcid.org/0000-0001-7638-4942
N MuthusamyDepartment of Internal Medicine and Comprehensive Cancer Center, Ohio State University, Columbus, OH, USA.
G C HildebrandtDepartment of Microbiology, Immunology and Molecular Genetics, University of Kentucky, Lexington, KY, USA.ORCID http://orcid.org/0000-0003-0478-3340
R A FleischmanMarkey Cancer Center, University of Kentucky, Lexington, KY, USA.
L ChenMarkey Cancer Center, University of Kentucky, Lexington, KY, USA.
J S ThorsonMarkey Cancer Center, University of Kentucky, Lexington, KY, USA.
M LeggasMarkey Cancer Center, University of Kentucky, Lexington, KY, USA.ORCID http://orcid.org/0000-0003-4314-4533
S BondadaDepartment of Microbiology, Immunology and Molecular Genetics, University of Kentucky, Lexington, KY, USA. bondada@email.uky.edu.ORCID http://orcid.org/0000-0002-1467-9769
University of Kentucky · USThe Ohio State University · US

Funding

University of Kentucky Markey Cancer Center Support Grant ECIA SupplementP30CA177558 · NCI · UNIVERSITY OF KENTUCKY · PI Bernard Mark Evers · 2013 to 2026
$38.3M
Kentucky Center for Clinical and Translational ScienceUL1TR001998 · NCATS · UNIVERSITY OF KENTUCKY · PI HARTMANN, KATHERINE E, KERN, PHILIP A · 2016 to 2025
$34.2M
Understanding the role of anti-apolipoprotein A-I antibodies in atherosclerotic cardiovascular diseaseP20GM130456 · NIGMS · UNIVERSITY OF KENTUCKY · PI M. Ashfaqul Alam · 2020 to 2026
$18.7M
Kentucky Center for Clinical and Translational ScienceUL1TR000117 · NCATS · UNIVERSITY OF KENTUCKY · PI KERN, PHILIP A · 2012 to 2015
$13.3M
Interdisciplinary Research Training in Cancer BiologyT32CA165990 · NCI · UNIVERSITY OF KENTUCKY · PI Bernard Mark Evers, KATHLEEN L. O'CONNOR · 2013 to 2026
$3.2M
(PQ9)A redox-mediated mechanism of chemotherapy-induced cognitive impairmentR01CA217934 · NCI · UNIVERSITY OF KENTUCKY · PI BONDADA, SUBBARAO, BUTTERFIELD, D. ALLAN · 2017 to 2021
$2.7M
Studies to understand and exploit 10-membered enediyne biosynthesisR01CA217255 · NCI · UNIVERSITY OF KENTUCKY · PI PHILLIPS, GEORGE NEAL, THORSON, JON SCOTT · 2017 to 2021
$2.6M
Platform technologies for understanding and exploiting methylationR01GM115261 · NIGMS · UNIVERSITY OF KENTUCKY · PI PHILLIPS, GEORGE NEAL, THORSON, JON SCOTT · 2016 to 2019
$2.2M
Role of Tcl1 and Par-4 in regulation of chronic lymphocytic leukemiaR01CA165469 · NCI · UNIVERSITY OF KENTUCKY · PI BONDADA, SUBBARAO, RANGNEKAR, VIVEK M · 2013 to 2017
$1.9M
NCATS NIH HHS UL1 TR000117NCATS NIH HHS UL1 TR001998NCI NIH HHS F32 CA239480NCI NIH HHS P30 CA177558NCI NIH HHS R01 CA165469NCI NIH HHS R01 CA217255NCI NIH HHS R01 CA217934NCI NIH HHS T32 CA165990NIGMS NIH HHS P20 GM130456NIGMS NIH HHS R01 GM115261
6 · The paper itself

Abstract

T-cell dysfunction is a hallmark of B-cell Chronic Lymphocytic Leukemia (CLL), where CLL cells downregulate T-cell responses through regulatory molecules including programmed death ligand-1 (PD-L1) and Interleukin-10 (IL-10). Immune checkpoint blockade (ICB) aims to restore T-cell function by preventing the ligation of inhibitory receptors like PD-1. However, most CLL patients do not respond well to this therapy. Thus, we investigated whether IL-10 suppression could enhance antitumor T-cell activity and responses to ICB. Since CLL IL-10 expression depends on Sp1, we utilized a novel, better tolerated analogue of the Sp1 inhibitor mithramycin (MTM

Indexed as

AnimalsAntibiotics, AntineoplasticApoptosisB7-H1 AntigenCase-Control StudiesCD8-Positive T-LymphocytesCell ProliferationDisease Models, AnimalGene Expression Regulation, NeoplasticHumansImmune Checkpoint InhibitorsInterleukin-10Leukemia, Lymphocytic, Chronic, B-CellLymphocyte ActivationMiceMice, Inbred NODAntibiotics, AntineoplasticB7-H1 AntigenCD274 protein, humanImmune Checkpoint InhibitorsInterleukin-10Plicamycin

Identifiers

PMID33731852
PMCPMC8446094
OpenAlexW3137521045

What OpenQuestion holds

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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.