Evidence map›Paper›PMID 30245803›Full record

ReviewInternational journal of inflammation2018

Potential Pitfalls of the Humanized Mice in Modeling Sepsis.

Krzysztof Laudanski, Michael Stentz, Matthew DiMeglio, William Furey, Toby Steinberg, Arpit Patel

Open access · goldAbstract readReview
In one paragraph

Review in International journal of inflammation, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 1 pooled it
1.1field-weighted citation impact, top 24% 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

12 citing papers in PubMed, 1 synthesis or guideline pooled it, 17 citations in OpenAlex.

  1. Pooled it
  2. Reframing sepsis research through translational integrative models.Journal of translational internal medicine · 2026
    Article
  3. Review
  4. Review
  5. A roadmap for translational cancer glycoimmunology at single cell resolution.Journal of experimental & clinical cancer research : CR · 2022
    Review
  6. Review
  7. Article
  8. International journal of molecular sciences · 2020
    Review
  9. Review
  10. New Insights into the Immune System Using Dirty Mice.Journal of immunology (Baltimore, Md. : 1950) · 2020
    Review
  11. [Development of animal experimental model for bacterial peritonitis].Revista espanola de quimioterapia : publicacion oficial de la Sociedad Espanola de Quimioterapia · 2020
    Article
  12. 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

6 authors at 3 institutions in 1 country.

Krzysztof LaudanskiDepartment of Anesthesiology and Critical Care, University of Pennsylvania, Philadelphia, PA 19104, USA.ORCID 0000-0002-7373-0851
Michael StentzDepartment of Anesthesiology and Intensive Care, Emory University, Atlanta, GA 30322, USA.
Matthew DiMeglioPhiladelphia College of Osteopathic Medicine, Philadelphia, PA 19131, USA.ORCID 0000-0001-9105-5995
William FureyPhiladelphia College of Osteopathic Medicine, Philadelphia, PA 19131, USA.
Toby SteinbergDepartment of Anesthesiology and Critical Care, University of Pennsylvania, Philadelphia, PA 19104, USA.
Arpit PatelDepartment of Anesthesiology and Critical Care, University of Pennsylvania, Philadelphia, PA 19104, USA.
University of Pennsylvania · USPhiladelphia College of Osteopathic Medicine · USEmory University · US

Funding

Epigenetic mediated long-term aberrations in myeloid cells after critical illnessK23GM120630 · NIGMS · UNIVERSITY OF PENNSYLVANIA · PI LAUDANSKI, KRZYSZTOF · 2017 to 2020
$783k
NIGMS NIH HHS K23 GM120630
6 · The paper itself

Abstract

Humanized mice are a state-of-the-art tool used to study several diseases, helping to close the gap between mice and human immunology. This review focuses on the potential obstacles in the analysis of immune system performance between humans and humanized mice in the context of severe acute inflammation as seen in sepsis or other critical care illnesses. The extent to which the reconstituted human immune system in mice adequately compares to the performance of the human immune system in human hosts is still an evolving question. Although certain viral and protozoan infections can be replicated in humanized mice, whether a highly complex and dynamic systemic inflammation like sepsis can be accurately represented by current humanized mouse models in a clinically translatable manner is unclear. Humanized mice are xenotransplant animals in the most general terms. Several organs (e.g., bone marrow mesenchymal cells, endothelium) cannot interact with the grafted human leukocytes effectively due to species specificity. Also the interaction between mice gut flora and the human immune system may be paradoxical. Often, grafting is performed utilizing an identical batch of stem cells in highly inbred animals which fails to account for human heterogeneity. Limiting factors include the substantial cost and restricting supply of animals. Finally, humanized mice offer an opportunity to gain knowledge of human-like conditions, requiring careful data interpretation just as in nonhumanized animals.

Identifiers

PMID30245803
PMCPMC6139216
OpenAlexW2888999967

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.