Evidence map›Paper›PMID 34755134›Full record

ArticleCell reports. Medicine2021

Targeting folate receptor beta on monocytes/macrophages renders rapid inflammation resolution independent of root causes.

Yingjuan J Lu, Leroy W Wheeler, Haiyan Chu, Paul J Kleindl, Michael Pugh, Fei You, Satish Rao, Gabriela Garcia, Henry Y Wu, Andre P da Cunha and 9 more

Open access · goldAbstract read
In one paragraph

Article in Cell reports. Medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.9field-weighted citation impact, top 13% 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

11 citing papers in PubMed, 17 citations in OpenAlex.

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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

19 authors at 3 institutions in 1 country.

Yingjuan J LuNovartis Institutes for Biomedical Research, Cambridge, MA 02139, USA.
Leroy W WheelerNovartis Institutes for Biomedical Research, Cambridge, MA 02139, USA.
Haiyan ChuNovartis Institutes for Biomedical Research, Cambridge, MA 02139, USA.
Paul J KleindlNovartis Institutes for Biomedical Research, Cambridge, MA 02139, USA.
Michael PughNovartis Institutes for Biomedical Research, Cambridge, MA 02139, USA.
Fei YouNovartis Institutes for Biomedical Research, Cambridge, MA 02139, USA.
Satish RaoNovartis Institutes for Biomedical Research, Cambridge, MA 02139, USA.
Gabriela GarciaDivision of Renal Diseases and Hypertension, Department of Medicine, University of Colorado Denver, Aurora, CO 80045, USA.
Henry Y WuDepartment of Ophthalmology, Novartis Institutes for Biomedical Research, Cambridge, MA 02139, USA.
Andre P da CunhaDepartment of Ophthalmology, Novartis Institutes for Biomedical Research, Cambridge, MA 02139, USA.
Richard JohnsonDivision of Renal Diseases and Hypertension, Department of Medicine, University of Colorado Denver, Aurora, CO 80045, USA.
Elaine WestrickNovartis Institutes for Biomedical Research, Cambridge, MA 02139, USA.
Vicky CrossNovartis Institutes for Biomedical Research, Cambridge, MA 02139, USA.
Alex LloydNovartis Institutes for Biomedical Research, Cambridge, MA 02139, USA.
Christina DircksenNovartis Institutes for Biomedical Research, Cambridge, MA 02139, USA.
Patrick J KleinNovartis Institutes for Biomedical Research, Cambridge, MA 02139, USA.
Iontcho R VlahovNovartis Institutes for Biomedical Research, Cambridge, MA 02139, USA.
Philip S LowDepartment of Chemistry, Purdue Institute for Drug Discovery, and Purdue Center for Cancer Research, Purdue University, West Lafayette, IN 47907, USA.
Christopher P LeamonNovartis Institutes for Biomedical Research, Cambridge, MA 02139, USA.
Novartis (United States) · USUniversity of Colorado Denver · USPurdue University West Lafayette · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Provoked by sterile/nonsterile insults, prolonged monocyte mobilization and uncontrolled monocyte/macrophage activation can pose imminent or impending harm to the affected organs. Curiously, folate receptor beta (FRβ), with subnanomolar affinity for the vitamin folic acid (FA), is upregulated during immune activation in hematopoietic cells of the myeloid lineage. This phenomenon has inspired a strong interest in exploring FRβ-directed diagnostics/therapeutics. Previously, we have reported that FA-targeted aminopterin (AMT) therapy can modulate macrophage function and effectively treat animal models of inflammation. Our current investigation of a lead compound (EC2319) leads to discovery of a highly FR-specific mechanism of action independent of the root causes against inflammatory monocytes. We further show that EC2319 suppresses interleukin-6/interleukin-1β release by FRβ

Indexed as

AminopterinAnimalsAntigens, CD19CHO CellsCricetulusCytokine Release SyndromeFemaleFolate Receptor 1Folate Receptor 2Folic AcidFolic Acid AntagonistsHumansInterleukin-1betaInterleukin-6Macrophage ActivationMacrophagesAminopterinAntigens, CD19CD19 molecule, humanFolate Receptor 1Folate Receptor 2Folic AcidFolic Acid AntagonistsFOLR1 protein, humanFOLR2 protein, humanIL1B protein, humanIL6 protein, humanInterleukin-1betaInterleukin-6Receptors, Chimeric Antigenadjuvant arthritisaminopterinautoimmune uveitisautoimmunitycytokine release syndromedihydrofolate reductase inhibitorfolate receptor betaglomerulonephritisinflammationmonocyte/macrophage activation

Identifiers

PMID34755134
PMCPMC8561236
OpenAlexW3206614953

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.