Evidence map›Paper›PMID 29322086›Full record

ReviewCellular and molecular gastroenterology and hepatology2018

Engineered Livers for Infectious Diseases.

Nil Gural, Liliana Mancio-Silva, Jiang He, Sangeeta N Bhatia

Open access · goldAbstract readReview
In one paragraph

Review in Cellular and molecular gastroenterology and hepatology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
2.9field-weighted citation impact, top 8% 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

27 citing papers in PubMed, 45 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Review
  5. Frontiers in microbiology · 2023
    Review
  6. Review
  7. Article
  8. Advancing Key Gaps in the Knowledge ofFrontiers in cellular and infection microbiology · 2022
    Review
  9. Review
  10. [A review on cell-based models of human liver disease in vitro].Sheng wu yi xue gong cheng xue za zhi = Journal of biomedical engineering = Shengwu yixue gongchengxue zazhi · 2021
    Review
  11. Review
  12. Review
  13. Review
  14. Review
  15. Expansion, in vivo-ex vivo cycling, and genetic manipulation of primary human hepatocytes.Proceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  16. Review
  17. Article
  18. Review
  19. Article
  20. 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

4 authors at 2 institutions in 1 country.

Nil GuralHarvard-MIT Department of Health Sciences and Technology, Institute for Medical Engineering and Science, Massachusetts Institute of Technology, Boston, Massachusetts.
Liliana Mancio-SilvaKoch Institute, Massachusetts Institute of Technology, Cambridge, Massachusetts.
Jiang HeKoch Institute, Massachusetts Institute of Technology, Cambridge, Massachusetts.
Sangeeta N BhatiaKoch Institute, Massachusetts Institute of Technology, Cambridge, Massachusetts.
Massachusetts Institute of Technology · USHoward Hughes Medical Institute · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Engineered liver systems come in a variety of platform models, from 2-dimensional cocultures of primary human hepatocytes and stem cell-derived progeny, to 3-dimensional organoids and humanized mice. Because of the species-specificity of many human hepatropic pathogens, these engineered systems have been essential tools for biologic discovery and therapeutic agent development in the context of liver-dependent infectious diseases. Although improvement of existing models is always beneficial, and the addition of a robust immune component is a particular need, at present, considerable progress has been made using this combination of research platforms. We highlight advances in the study of hepatitis B and C viruses and malaria-causing

Indexed as

2D, 2-dimensional3D3D, 3-dimensionalEBOV, Ebola virusFalciparumHBC, hepatitis C virusHBVHBV, hepatitis B virusHCVHepatotropicHLC, hepatocyte-like cellsiHLC, induced pluripotent stem cell–derived hepatocyte-like cellsin vitroin vivoLASV, Lassa virusLiverLiver ModelsMalariaMPCC, micropatterned coculture systemPathogenPCR, polymerase chain reactionSACC, self-assembling cocultureVivax

Identifiers

PMID29322086
PMCPMC5756057
OpenAlexW2770583059

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.