Evidence map›Paper›PMID 36826509›Full record

ArticleCancer immunology, immunotherapy : CII2023

Murine regulatory T cells utilize granzyme B to promote tumor metastasis.

Ellis Tibbs, Rakhee Rathnam Kalari Kandy, Delong Jiao, Long Wu, Xuefang Cao

Open access · greenAbstract read
In one paragraph

Article in Cancer immunology, immunotherapy : CII, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

14 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
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  3. SRSF3 determines TScience advances · 2026
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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

5 authors at 2 institutions in 1 country.

Ellis TibbsDepartment of Microbiology and Immunology, University of Maryland Baltimore, School of Medicine, Baltimore, MD, 21201, USA.
Rakhee Rathnam Kalari KandyMarlene and Stewart Greenebaum Comprehensive Cancer Center, University of Maryland Baltimore, Baltimore, USA.
Delong JiaoMarlene and Stewart Greenebaum Comprehensive Cancer Center, University of Maryland Baltimore, Baltimore, USA.
Long WuMarlene and Stewart Greenebaum Comprehensive Cancer Center, University of Maryland Baltimore, Baltimore, USA.
Xuefang CaoDepartment of Microbiology and Immunology, University of Maryland Baltimore, School of Medicine, Baltimore, MD, 21201, USA. XuefangCao@som.umaryland.edu.
University of Maryland, Baltimore · USUniversity of Baltimore · US

Funding

UNIVERSITY OF MARYLAND GREENEBAUM CANCER CENTERSUPPORT GRANTP30CA134274 · NCI · UNIVERSITY OF MARYLAND BALTIMORE · PI FEYRUZ VIRGILIA RASSOOL · 2008 to 2026
$51.0M
Signaling Pathways in Innate ImmunityT32AI095190 · NIAID · UNIVERSITY OF MARYLAND BALTIMORE · PI Stefanie N. Vogel · 2012 to 2026
$4.7M
Beta-2 adrenergic signaling in immune homeostasis and reconstitutionR01HL159973 · NHLBI · UNIVERSITY OF MARYLAND BALTIMORE · PI CAO, XUEFANG · 2022 to 2025
$3.0M
CD27/CD70 mediated negative regulation of inflammatory T cell responsesR01HL135325 · NHLBI · UNIVERSITY OF MARYLAND BALTIMORE · PI CAO, XUEFANG · 2018 to 2021
$2.3M
Targeting Granzyme B to Separate GVH from GVL ResponsesR01CA184728 · NCI · UNIVERSITY OF MARYLAND BALTIMORE · PI CAO, XUEFANG · 2015 to 2019
$1.9M
Targeting Beta-Adrenergic Signaling to Control GVH and GVL ResponsesR21CA202358 · NCI · UNIVERSITY OF MARYLAND BALTIMORE · PI CAO, XUEFANG · 2016 to 2017
$435k
NCI NIH HHS P30 CA134274NCI NIH HHS R01 CA184728NCI NIH HHS R01CA184728NCI NIH HHS R21 CA202358NHLBI NIH HHS R01 HL135325NHLBI NIH HHS R01 HL159973NIAID NIH HHS T32 AI095190
6 · The paper itself

Abstract

Regulatory T cells (Tregs) possess a wide range of mechanisms for immune suppression. Among them, Granzyme B (GzmB) and perforin expressed by Tregs were shown to inhibit tumor clearance in previous reports, which contradicted the canonical roles of these cytotoxic molecules expressed by cytotoxic T cells and NK cells in antitumor immune responses. Given the ability of the tumor to manipulate the microenvironment, Treg-derived GzmB function may represent an important approach to aid in tumor growth as well as facilitating tumor metastasis. In this study, we utilized Treg-specific GzmB knockout (Foxp3

Indexed as

T-Lymphocytes, CytotoxicT-Lymphocytes, RegulatoryAnimalsCD8-Positive T-LymphocytesGranzymesLungMiceGranzymesGranzyme B (GzmB)Immune suppressionRegulatory T cells (Tregs)Tumor metastasis

Identifiers

PMID36826509
PMCPMC10690887
OpenAlexW4321748633

What OpenQuestion holds

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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.