Evidence map›Paper›PMID 39576827›Full record

ArticlePLoS biology2024

CD74 promotes the formation of an immunosuppressive tumor microenvironment in triple-negative breast cancer in mice by inducing the expansion of tolerogenic dendritic cells and regulatory B cells.

Bianca Pellegrino, Keren David, Stav Rabani, Bar Lampert, Thuy Tran, Edward Doherty, Marta Piecychna, Roberto Meza-Romero, Lin Leng, Dov Hershkovitz and 4 more

Abstract read
In one paragraph

Article in PLoS biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing 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

23 citing papers in PubMed.

  1. Article
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  4. Review
  5. CD74Journal of gastrointestinal cancer · 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

14 authors.

Bianca PellegrinoDepartment of Systems Immunology, Weizmann Institute of Science, Rehovot, Israel.
Keren DavidDepartment of Systems Immunology, Weizmann Institute of Science, Rehovot, Israel.
Stav RabaniDepartment of Systems Immunology, Weizmann Institute of Science, Rehovot, Israel.
Bar LampertDepartment of Systems Immunology, Weizmann Institute of Science, Rehovot, Israel.
Thuy TranYale Cancer Center and School of Medicine, New Haven, Connecticut, United States of America.
Edward DohertyYale Cancer Center and School of Medicine, New Haven, Connecticut, United States of America.
Marta PiecychnaYale Cancer Center and School of Medicine, New Haven, Connecticut, United States of America.
Roberto Meza-RomeroNeuroimmunology Research, VA Portland Health Care System, Portland, Oregon, United States of America.
Lin LengYale Cancer Center and School of Medicine, New Haven, Connecticut, United States of America.
Dov HershkovitzInsitute of Pathology, Sourasky Medical Center, Tel Aviv, Israel.
Arthur A VandenbarkNeuroimmunology Research, VA Portland Health Care System, Portland, Oregon, United States of America.
Richard BucalaYale Cancer Center and School of Medicine, New Haven, Connecticut, United States of America.
Shirly Becker-HermanDepartment of Systems Immunology, Weizmann Institute of Science, Rehovot, Israel.
Idit ShacharDepartment of Systems Immunology, Weizmann Institute of Science, Rehovot, Israel.ORCID 0000-0003-0004-6159

Funding

Yale Clinical and Translational Science Award (U Component)UL1TR001863 · NCATS · YALE UNIVERSITY · PI John H. Krystal, LUCILA OHNO-MACHADO · 2016 to 2026
$102.9M
Inflammatory Suppression of Adaptive Immunity by Plasmodium MIFR01AI110452 · NIAID · YALE UNIVERSITY · PI BUCALA, RICHARD J · 2014 to 2023
$4.2M
Defining the Pathogenic Contribution of High Genotypic MIF ExpressionR01AR078334 · NIAMS · YALE UNIVERSITY · PI BUCALA, RICHARD J · 2021 to 2025
$1.8M
Immunoregulation of Myelin-Specific T LymphocytesI01BX000226 · VA · PORTLAND VA MEDICAL CENTER · PI VANDENBARK, ARTHUR A. · 2009 to 2024
–
Preclinical Translational Studies with DRHQI01BX005112 · VA · PORTLAND VA MEDICAL CENTER · PI VANDENBARK, ARTHUR A. · 2020 to 2024
–
BLRD Research Career Scientist Award ApplicationIK6BX004209 · VA · PORTLAND VA MEDICAL CENTER · PI ARTHUR A. VANDENBARK · 2018 to 2026
–
BLRD VA I01 BX000226BLRD VA I01 BX005112BLRD VA IK6 BX004209NCATS NIH HHS UL1 TR001863NIAID NIH HHS R01 AI110452NIAMS NIH HHS R01 AR078334
6 · The paper itself

Abstract

CD74 is a cell-surface receptor for the cytokine macrophage migration inhibitory factor (MIF). MIF binding to CD74 induces a signaling cascade resulting in the release of its cytosolic intracellular domain (CD74-ICD), which regulates transcription in naïve B and chronic lymphocytic leukemia (CLL) cells. In the current study, we investigated the role of CD74 in the regulation of the immunosuppressive tumor microenvironment (TME) in triple-negative breast cancer (TNBC). TNBC is the most aggressive breast cancer subtype and is characterized by massive infiltration of immune cells to the tumor microenvironment, making this tumor a good candidate for immunotherapy. The tumor and immune cells in TNBC express high levels of CD74; however, the function of this receptor in the tumor environment has not been extensively characterized. Regulatory B cells (Bregs) and tolerogenic dendritic cells (tol-DCs) were previously shown to attenuate the antitumor immune response in TNBC. Here, we demonstrate that CD74 enhances tumor growth by inducing the expansion of tumor-infiltrating tol-DCs and Bregs. Utilizing CD74-KO mice, Cre-flox mice lacking CD74 in CD23+ mature B cells, mice lacking CD74 in the CD11c+ population, and a CD74 inhibitor (DRQ), we elucidate the mechanism by which CD74 inhibits antitumor immunity. MIF secreted from the tumor cells activates CD74 expressed on DCs. This activation induces the binding of CD74-ICD to the SP1 promotor, resulting in the up-regulation of SP1 expression. SP1 binds the IL-1β promotor, leading to the down-regulation of its transcription. The reduced levels of IL-1β lead to decreased antitumor activity by allowing expansion of the tol-DC, which induces the expansion of the Breg population, supporting the cross-talk between these 2 populations. Taken together, these results suggest that CD74+ CD11c+ DCs are the dominant cell type involved in the regulation of TNBC progression. These findings indicate that CD74 might serve as a novel therapeutic target in TNBC.

Indexed as

Antigens, Differentiation, B-LymphocyteDendritic CellsHistocompatibility Antigens Class IIMacrophage Migration-Inhibitory FactorsTriple Negative Breast NeoplasmsTumor MicroenvironmentAnimalsCell Line, TumorFemaleHumansImmune ToleranceInterleukin-1betaIntramolecular OxidoreductasesMiceMice, Inbred C57BLMice, KnockoutAntigens, Differentiation, B-LymphocyteHistocompatibility Antigens Class IIInterleukin-1betaIntramolecular Oxidoreductasesinvariant chainMacrophage Migration-Inhibitory FactorsMif protein, mouse

Identifiers

PMID39576827
PMCPMC11623796

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Registered trials

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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.