Evidence map›Paper›PMID 41830600›Full record

ArticleUnited European gastroenterology journal2026

NLRP3 Inflammasome Activation-Induced Acute Papillitis as a Trigger of Acute Pancreatitis - A Novel Mechanism of Microlithiasis-Induced Acute Pancreatitis.

Simon Sirtl, Mahmood Ahmad, Prince Allawadhi, Thomas Metzler, Oliver Buchstab, Steffen Ormanns, Martina Rudelius, Georg Beyer, Lukasz Krupa, Robert Staron and 11 more

Abstract read
In one paragraph

Article in United European gastroenterology journal, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

21 authors.

Simon SirtlDepartment of Medicine II, University Hospital, LMU, Munich, Germany.ORCID https://orcid.org/0000-0002-6047-334X
Mahmood AhmadDepartment of Medicine II, University Hospital, LMU, Munich, Germany.ORCID https://orcid.org/0000-0002-6642-2324
Prince AllawadhiDepartment of Medicine II, University Hospital, LMU, Munich, Germany.
Thomas MetzlerComparative Experimental Pathology (CEP), Technical University of Munich, Munich, Germany.
Oliver BuchstabFaculty of Medicine, Institute of Pathology, LMU, Munich, Germany.ORCID https://orcid.org/0009-0001-6003-3918
Steffen OrmannsInstitute of General Pathology, Medical University Innsbruck, Innsbruck, Austria.
Martina RudeliusFaculty of Medicine, Institute of Pathology, LMU, Munich, Germany.
Georg BeyerDepartment of Medicine II, University Hospital, LMU, Munich, Germany.
Lukasz KrupaDepartment of Gastroenterology and Hepatology with Internal Disease Unit, Medical Department, University of Rzeszów, Rzeszów, Poland.
Robert StaronDepartment of Gastroenterology and Hepatology with Internal Disease Unit, Medical Department, University of Rzeszów, Rzeszów, Poland.
Christian SchulzDepartment of Medicine II, University Hospital, LMU, Munich, Germany.ORCID https://orcid.org/0000-0003-1841-1337
Lisa FahrDepartment of Medicine II, University Hospital, LMU, Munich, Germany.
Andrea SendelhofertFaculty of Medicine, Institute of Pathology, LMU, Munich, Germany.
Christian SchulzDepartment of Medicine I, University Hospital, LMU, Munich, Germany.
Katja SteigerComparative Experimental Pathology (CEP), Technical University of Munich, Munich, Germany.
Matthias SendlerDepartment of Medicine A, University Medicine Greifswald, Greifswald, Germany.
Markus M LerchLMU University Hospital, Ludwig Maximilian Universität München, Munich, Germany.
Ivonne RegelDepartment of Medicine II, University Hospital, LMU, Munich, Germany.ORCID https://orcid.org/0000-0002-0206-4441
Michal ŻorniakDepartment of Medicine II, University Hospital, LMU, Munich, Germany.
Julia MayerleDepartment of Medicine II, University Hospital, LMU, Munich, Germany.
Ujjwal M MahajanDepartment of Medicine II, University Hospital, LMU, Munich, Germany.

Funding

Deutsche Forschungsgemeinschaft 413635475Deutsche Forschungsgemeinschaft BE-63951EU-IMI2 TransBioLine consortium 821283LMU Munich Advanced Clinical Scientist ProgramLMU Munich Clinician Scientist Program 413635475
6 · The paper itself

Abstract

introductionObstruction of the pancreatic duct by impacted gallstones at the level of the papilla vateri causes acute pancreatitis. How non-obstructing stones such as microlithiasis or sludge cause pancreatitis has not been studied. We aimed to understand the pathomechanism of microlithiasis-induced acute pancreatitis.

methodsIn human papillary biopsies from patients with microlithiasis-induced acute pancreatitis (n = 4), alcohol-induced acute pancreatitis (n = 5), and control subjects without pancreatobiliary disease (n = 4), the inflammatory infiltrate was quantified. Bone marrow-derived macrophages generated from C57BL/6 mice were treated in vitro with cholesterol monohydrate and calcium bilirubinate crystals, and NLRP3 inflammasome-mediated macrophage activation was quantified. Microlithiasis formation in the gallbladder was induced in mice through lithogenic high fat diet and devazepide. Acute pancreatitis was induced by supramaximal caerulein stimulation. Microlithiasis ejection from the gallbladder was achieved through low-dose caerulein i.p. Injections. Pancreatitis severity was compared between caerulein-induced pancreatitis and caerulein-induced pancreatitis after repetitive microlithiasis ejection.

resultsSignificantly higher infiltration of CD45-positive leukocytes and increased NLRP3 expression were observed in papillary biopsies from patients with microlithiasis-induced acute pancreatitis compared with patients with alcohol-induced acute pancreatitis and control subjects. In line with this, significantly higher IL-1ß secretion and caspase-1 activation were observed in vitro in bone marrow-derived macrophages stimulated with cholesterol monohydrate and calcium billirubinate crystals. In vivo microlithiasis formation was achieved in all mice with high fat diet and devazepide. Compared to caerulein-induced pancreatitis, in caerulein + microlithiasis pancreatitis, higher LDH, GPT and ALP levels in serum were observed, but without an impact on pancreatitis severity. However, mice papilla mimicked the phenotype of microlithiasis-induced acute pancreatitis in humans.

conclusionWe propose a novel mechanism in which biliary microlithiasis induces a local inflammatory reaction at the papilla (acute papillitis) via NLRP3 inflammasome activation driven by bone marrow-derived macrophages, without causing pancreatic outflow obstruction.

Indexed as

GallstonesInflammasomesNLR Family, Pyrin Domain-Containing 3 ProteinPancreatitisAcute DiseaseAdultAnimalsBiopsyCaspase 1Disease Models, AnimalFemaleHumansMacrophage ActivationMacrophagesMaleMiceCaspase 1InflammasomesNLR Family, Pyrin Domain-Containing 3 ProteinNLRP3 protein, humanNlrp3 protein, mouseacute pancreatitisbiliary pancreatitisexperimental pancreatitisgallstonemicrolithiasisNLRP3NLRP3 inflammasomesludge

Identifiers

PMID41830600
PMCPMC13098079

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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.