Evidence map›Paper›PMID 34450180›Full record

ArticleGastroenterology2021

Novel Circulating and Tissue Monocytes as Well as Macrophages in Pancreatitis and Recovery.

Murli Manohar, Elaina K Jones, Samuel J S Rubin, Priyanka B Subrahmanyam, Gayathri Swaminathan, David Mikhail, Lawrence Bai, Gulshan Singh, Yi Wei, Vishal Sharma and 6 more

Open access · greenAbstract readComparative Study
In one paragraph

Article in Gastroenterology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed
10.2field-weighted citation impact, top 1% 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

38 citing papers in PubMed, 64 citations in OpenAlex.

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  13. Mass cytometric analysis of circulating monocyte subsets in a murine model of diabetic gastroparesis.American journal of physiology. Gastrointestinal and liver physiology · 2025
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

16 authors at 3 institutions in 1 country.

Murli ManoharDivision of Gastroenterology and Hepatology, Department of Medicine, Stanford University School of Medicine, Stanford, California; Division of Pediatric Gastroenterology, Department of Pediatrics, Stanford University School of Medicine, Stanford, California. Electronic address: murli27@stanford.edu.
Elaina K JonesDivision of Gastroenterology and Hepatology, Department of Medicine, Stanford University School of Medicine, Stanford, California; Division of Pediatric Gastroenterology, Department of Pediatrics, Stanford University School of Medicine, Stanford, California.
Samuel J S RubinDivision of Gastroenterology and Hepatology, Department of Medicine, Stanford University School of Medicine, Stanford, California.
Priyanka B SubrahmanyamInstitute for Immunity, Transplantation, and Infection, Stanford University School of Medicine, Stanford, California.
Gayathri SwaminathanDivision of Gastroenterology and Hepatology, Department of Medicine, Stanford University School of Medicine, Stanford, California.
David MikhailDivision of Gastroenterology and Hepatology, Department of Medicine, Stanford University School of Medicine, Stanford, California.
Lawrence BaiDivision of Gastroenterology and Hepatology, Department of Medicine, Stanford University School of Medicine, Stanford, California.
Gulshan SinghDivision of Gastroenterology and Hepatology, Department of Medicine, Stanford University School of Medicine, Stanford, California.
Yi WeiDivision of Gastroenterology and Hepatology, Department of Medicine, Stanford University School of Medicine, Stanford, California.
Vishal SharmaDivision of Gastroenterology and Hepatology, Department of Medicine, Stanford University School of Medicine, Stanford, California.
Janet C SiebertCyto Analytics, Denver, Colorado.
Holden T MaeckerInstitute for Immunity, Transplantation, and Infection, Stanford University School of Medicine, Stanford, California.
Sohail Z HusainDivision of Pediatric Gastroenterology, Department of Pediatrics, Stanford University School of Medicine, Stanford, California.
Walter G ParkDivision of Gastroenterology and Hepatology, Department of Medicine, Stanford University School of Medicine, Stanford, California.
Stephen J PandolDepartment of Medicine, Cedars-Sinai Medical Center, Los Angeles, California.
Aida HabtezionDivision of Gastroenterology and Hepatology, Department of Medicine, Stanford University School of Medicine, Stanford, California; Institute for Immunity, Transplantation, and Infection, Stanford University School of Medicine, Stanford, California. Electronic address: aidah@stanford.edu.
Stanford University · USStanford Medicine · USCedars-Sinai Medical Center · US

Funding

MOLECULAR &CELLULAR IMMUNOBIOLOGYT32AI007290 · NIAID · STANFORD UNIVERSITY · PI Sean Curtis Bendall, Olivia M Martinez · 1985 to 2026
$27.0M
Stanford Islet Research CoreP30DK116074 · NIDDK · STANFORD UNIVERSITY · PI Seung K Kim · 2017 to 2026
$19.5M
Role of hemeoxygenase-1 in experimental acute pancreatitisR01DK092421 · NIDDK · STANFORD UNIVERSITY · PI HABTEZION, AIDA · 2011 to 2020
$3.5M
NIAID NIH HHS T32 AI007290NIDDK NIH HHS P30 DK116074NIDDK NIH HHS R01 DK092421
6 · The paper itself

Abstract

BACKGROUND AND

aimsAcute pancreatitis (AP) is an inflammatory disease with mild to severe course that is associated with local and systemic complications and significant mortality. Uncovering inflammatory pathways that lead to progression and recovery will inform ways to monitor and/or develop effective therapies.

methodsWe performed single-cell mass Cytometry by Time Of Flight (CyTOF) analysis to identify pancreatic and systemic inflammatory signals during mild AP (referred to as AP), severe AP (SAP), and recovery using 2 independent experimental models and blood from patients with AP and recurrent AP. Flow cytometric validation of monocytes subsets identified using CyTOF analysis was performed independently.

resultsLy6C

conclusionsWe identified several novel monocyte/macrophage subsets with unique phenotype and functional characteristics that are associated with AP, recovery, and SAP. Our findings highlight differential innate immune responses during AP progression and recovery that can be leveraged for future disease monitoring and targeting.

Indexed as

Immunity, InnateAnimalsBiomarkersCell SeparationDisease Models, AnimalFemaleFlow CytometryHumansImmunophenotypingMacrophagesMiceMice, Inbred BALB CMonocytesPancreasPancreatitisPhenotypeBiomarkersAcute PancreatitisCyTOFMacrophagesMonocytesSevere Acute Pancreatitis

Identifiers

PMID34450180
PMCPMC8796698
OpenAlexW3194808817

What OpenQuestion holds

Textmetadata
LicenceTDM
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.