Evidence map›Paper›PMID 19800092›Full record

ArticleVirology2009

IL-10 is pathogenic during the development of coxsackievirus B4-induced chronic pancreatitis.

Rui Gu, Anae Shampang, Andrew Reilly, Dusti Fisher, William Glass, Arlene I Ramsingh

Abstract read
In one paragraph

Article in Virology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.2field-weighted citation impact, top 19% 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

8 citing papers in PubMed, 14 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

6 authors at 2 institutions in 1 country.

Rui GuWadsworth Center, New York State Department of Health, 120 New Scotland Avenue, Albany, NY 12208, USA.
Anae Shampang
Andrew Reilly
Dusti Fisher
William Glass
Arlene I Ramsingh
New York State Department of Health · USWadsworth Center · US

Funding

HIV vaccine development using recombinant coxsackievirusesR01AI066938 · NIAID · WADSWORTH CENTER · PI RAMSINGH, ARLENE · 2006 to 2010
$1.4M
NIAID NIH HHS AI 066938NIAID NIH HHS R01 AI066938
6 · The paper itself

Abstract

Using a mouse model of coxsackievirus B4 (CVB4-V)-induced chronic pancreatitis, we investigated whether cytokines are involved in the progression of acute disease to chronic inflammatory disease. We show that IL-10 contributed to the development of chronic pancreatitis since acute disease resolved when IL-10 was absent or when IL-10 signaling was disrupted. We explored the underlying mechanisms by which IL-10 affected disease progression, using a novel approach to assess immunological events occurring in situ. Multiple markers that define functional innate immune responses and functional T cell responses were monitored over the course of CVB4-V infection of wild-type and IL-10 knockout mice, using a multiplex transcriptional profiling approach. We show that high levels of IL-10 early during infection were associated with delayed innate and T cell responses. Furthermore, high IL-10 production correlated with altered kinetics of T regulatory responses indicating a disruption in the balance between effector and regulatory T cell responses.

Indexed as

AnimalsCoxsackievirus InfectionsEnterovirus B, HumanFemaleGene Expression ProfilingInterleukin-10MaleMiceMice, Inbred BALB CMice, KnockoutPancreasPancreatitis, ChronicSignal TransductionT-Lymphocytes, RegulatoryViral LoadVirus ReplicationInterleukin-10

Identifiers

PMID19800092
PMCPMC2783446
OpenAlexW2035833081

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.