Evidence map›Paper›PMID 35663952›Full record

ArticleFrontiers in immunology2022

Dynamic Monitoring of Immunoinflammatory Response Identifies Immunoswitching Characteristics of Severe Acute Pancreatitis in Rats.

Qian Zhuang, Liqiang Huang, Yue Zeng, Xu Wu, Gan Qiao, Minghua Liu, Lulu Wang, Yejiang Zhou, Yuxia Xiong

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

7 citing papers in PubMed, 8 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

9 authors at 2 institutions in 1 country.

Qian ZhuangDepartment of Pharmacology, School of Pharmacy, Southwest Medical University, Luzhou, China.
Liqiang HuangDepartment of Pharmacology, School of Pharmacy, Southwest Medical University, Luzhou, China.
Yue ZengDepartment of Pharmacology, School of Pharmacy, Southwest Medical University, Luzhou, China.
Xu WuDepartment of Pharmacology, School of Pharmacy, Southwest Medical University, Luzhou, China.
Gan QiaoDepartment of Pharmacology, School of Pharmacy, Southwest Medical University, Luzhou, China.
Minghua LiuDepartment of Pharmacology, School of Pharmacy, Southwest Medical University, Luzhou, China.
Lulu WangDepartment of Pharmacology, School of Pharmacy, Southwest Medical University, Luzhou, China.
Yejiang ZhouDepartment of Gastrointestinal Surgery, Affiliated Hospital of Southwest Medical University, Luzhou, China.
Yuxia XiongDepartment of Pharmacology, School of Pharmacy, Southwest Medical University, Luzhou, China.
Southwest Medical University · CNAffiliated Hospital of Southwest Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Immune dysfunction is the main characteristic of severe acute pancreatitis (SAP), and the timing of immune regulation has become a major challenge for SAP treatment. Previous reports about the time point at which the immune status of SAP changed from excessive inflammatory response to immunosuppression (hypo-inflammatory response) are conflicting. Purposes: The aims of this study are to explore the immunological dynamic changes in SAP rats from the perspective of intestinal mucosal immune function, and to determine the immunoswitching point from excessive inflammatory response to immunosuppression. Methods: Retrograde injection of sodium taurocholate into the pancreaticobiliary duct was applied to establish a SAP model in rats. The survival rate and the activities of serum amylase and pancreatic lipase in SAP rats were measured at different time points after model construction. The pathological changes in the pancreas and small intestines were analyzed, and the levels of intestinal pro- and anti-inflammatory cytokines and the numbers of intestinal macrophages, dendritic cells, Th1, Th2, and T regulatory cells were assessed. Meanwhile, the SAP rats were challenged with Results: The time periods of 12-24 h and 48-72 h were the two death peaks in SAP rats. The pancreas of SAP rats showed self-limiting pathological changes, and the switching period of intestinal cytokines, and innate and adaptive immunity indexes occurred at 24-48 h. It was further confirmed that 48 h after SAP model construction was the immunoswitching point from excessive inflammatory response to immunosuppression. Conclusion: The SAP rats showed characteristics of intestinal mucosal immune dysfunction after model construction, and the 48th h was identified as the immunoswitching point from excessive inflammatory response to immunosuppression. The results are of great significance for optimizing the timing of SAP immune regulation.

Indexed as

PancreatitisAcute DiseaseAnimalsCytokinesPancreasRatsTaurocholic AcidCytokinesTaurocholic Acidimmunosuppressionimmunoswitchinginflammationintestinal mucosal immune functionsevere acute pancreatitis

Identifiers

PMID35663952
PMCPMC9160235
OpenAlexW4280497478

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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.