Evidence map›Paper›PMID 26149491›Full record

ArticleGut2016

Characterisation of liver pathogenesis, human immune responses and drug testing in a humanised mouse model of HCV infection.

Choong Tat Keng, Ching Wooen Sze, Dahai Zheng, Zhiqiang Zheng, Kylie Su Mei Yong, Shu Qi Tan, Jessica Jie Ying Ong, Sue Yee Tan, Eva Loh, Megha Haridas Upadya and 9 more

Open access · hybridAbstract read
In one paragraph

Article in Gut, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
2.2field-weighted citation impact, top 12% 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

26 citing papers in PubMed, 42 citations in OpenAlex.

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  15. Liver fibrosis and CD206JHEP reports : innovation in hepatology · 2020
    Article
  16. CD4Frontiers in immunology · 2020
    Article
  17. Article
  18. Review
  19. Review
  20. Humanized Mice as Unique Tools for Human-Specific Studies.Archivum immunologiae et therapiae experimentalis · 2018
    Review
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 6 institutions in 3 countries.

Choong Tat KengInstitute of Molecular and Cell Biology, Singapore, Singapore.
Ching Wooen SzeDepartment of Microbiology, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore.
Dahai ZhengInstitute of Molecular and Cell Biology, Singapore, Singapore.
Zhiqiang ZhengInstitute of Molecular and Cell Biology, Singapore, Singapore.
Kylie Su Mei YongInstitute of Molecular and Cell Biology, Singapore, Singapore.
Shu Qi TanDepartment of Obstetrics & Gynaecology, KK Women's and Children's Hospital, Singapore, Singapore.
Jessica Jie Ying OngInstitute of Molecular and Cell Biology, Singapore, Singapore.
Sue Yee TanInstitute of Molecular and Cell Biology, Singapore, Singapore.
Eva LohDepartment of Pathology and Laboratory Medicine, KK Women's and Children's Hospital, Singapore, Singapore.
Megha Haridas UpadyaDepartment of Microbiology, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore.
Chik Hong KuickDepartment of Pathology and Laboratory Medicine, KK Women's and Children's Hospital, Singapore, Singapore.
Hak HottaDivision of Microbiology, Kobe University Graduate School of Medicine, Hyogo, Japan.
Seng Gee LimDepartment of Medicine, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore Department of Gastroenterology and Hepatology, National University Health System, Singapore, Singapore.
Thiam Chye TanDepartment of Obstetrics & Gynaecology, KK Women's and Children's Hospital, Singapore, Singapore Duke-NUS Graduate Medical School, Singapore, Singapore.
Kenneth T E ChangDepartment of Pathology and Laboratory Medicine, KK Women's and Children's Hospital, Singapore, Singapore Duke-NUS Graduate Medical School, Singapore, Singapore.
Wanjin HongInstitute of Molecular and Cell Biology, Singapore, Singapore.
Jianzhu ChenInterdisciplinary Research Group in Infectious Diseases, Singapore-Massachusetts Institute of Technology Alliance for Research and Technology, Singapore, Singapore The Koch Institute for Integrative Cancer Research and Department of Biology, Massachusetts Institute of Technology, Cambridge, Massachusetts, USA.
Yee-Joo TanInstitute of Molecular and Cell Biology, Singapore, Singapore Department of Microbiology, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore.
Qingfeng ChenInstitute of Molecular and Cell Biology, Singapore, Singapore Department of Microbiology, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore Interdisciplinary Research Group in Infectious Diseases, Singapore-Massachusetts Institute of Technology Alliance for Research and Technology, Singapore, Singapore.
Institute of Molecular and Cell Biology · SGNational University of Singapore · SGKK Women's and Children's Hospital · SGDuke-NUS Medical School · SGKobe University · JPSingapore-MIT Alliance for Research and Technology · SG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveHCV infection affects millions of people worldwide, and many patients develop chronic infection leading to liver cancers. For decades, the lack of a small animal model that can recapitulate HCV infection, its immunopathogenesis and disease progression has impeded the development of an effective vaccine and therapeutics. We aim to provide a humanised mouse model for the understanding of HCV-specific human immune responses and HCV-associated disease pathologies.

designRecently, we have established human liver cells with a matched human immune system in NOD-scid Il2rg(-/-) (NSG) mice (HIL mice). These mice are infected with HCV by intravenous injection, and the pathologies are investigated.

resultsIn this study, we demonstrate that HIL mouse is capable of supporting HCV infection and can present some of the clinical symptoms found in HCV-infected patients including hepatitis, robust virus-specific human immune cell and cytokine responses as well as liver fibrosis and cirrhosis. Similar to results obtained from the analysis of patient samples, the human immune cells, particularly T cells and macrophages, play critical roles during the HCV-associated liver disease development in the HIL mice. Furthermore, our model is demonstrated to be able to reproduce the therapeutic effects of human interferon alpha 2a antiviral treatment.

conclusionsThe HIL mouse provides a model for the understanding of HCV-specific human immune responses and HCV-associated disease pathologies. It could also serve as a platform for antifibrosis and immune-modulatory drug testing.

Indexed as

Disease Models, AnimalHepatitis C, ChronicMice, Inbred NODAnimalsAntiviral AgentsHumansImmunity, CellularInterferon-alphaInterferon alpha-2MiceRecombinant ProteinsReproducibility of ResultsAntiviral AgentsInterferon-alphaInterferon alpha-2Recombinant ProteinsCYTOKINESFIBROSISHEPATITIS CIMMUNE-MEDIATED LIVER DAMAGEIMMUNOLOGY

Identifiers

PMID26149491
PMCPMC5036242
OpenAlexW2156700662

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.