Evidence map›Paper›PMID 31922289›Full record

ArticleJournal of leukocyte biology2020

A humanized mouse model to study mast cells mediated cutaneous adverse drug reactions.

Andrea Mencarelli, Merry Gunawan, Kylie Su Mei Yong, Pradeep Bist, Wilson Wei Sheng Tan, Sue Yee Tan, Min Liu, Edwin Kunxiang Huang, Yong Fan, Jerry Kok Yen Chan and 3 more

Open access · hybridAbstract read
In one paragraph

Article in Journal of leukocyte biology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
2.5field-weighted citation impact, top 10% 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

24 citing papers in PubMed, 42 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Review
  11. Review
  12. Article
  13. Review
  14. Article
  15. Review
  16. Review
  17. Review
  18. Review
  19. Review
  20. 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

13 authors at 4 institutions in 4 countries.

Andrea MencarelliProgram in Emerging Infectious Diseases, Duke - National University of Singapore Graduate Medical School, Singapore.
Merry GunawanInstitute of Molecular and Cell Biology, Agency for Science, Technology and Research (A*STAR), Singapore.
Kylie Su Mei YongInstitute of Molecular and Cell Biology, Agency for Science, Technology and Research (A*STAR), Singapore.
Pradeep BistProgram in Emerging Infectious Diseases, Duke - National University of Singapore Graduate Medical School, Singapore.
Wilson Wei Sheng TanInstitute of Molecular and Cell Biology, Agency for Science, Technology and Research (A*STAR), Singapore.
Sue Yee TanInstitute of Molecular and Cell Biology, Agency for Science, Technology and Research (A*STAR), Singapore.
Min LiuInstitute of Molecular and Cell Biology, Agency for Science, Technology and Research (A*STAR), Singapore.
Edwin Kunxiang HuangExperimental Fetal Medicine Group, Yong Loo Lin School of Medicine, National University of Singapore, Singapore.
Yong FanKey Laboratory for Major Obstetric Diseases of Guangdong Province, The Third Affiliated Hospital of Guangzhou Medical University, Guangzhou, China.
Jerry Kok Yen ChanExperimental Fetal Medicine Group, Yong Loo Lin School of Medicine, National University of Singapore, Singapore.
Hae Woong ChoiDepartment of Life Sciences, Korea University, Seoul, South Korea.
Soman N AbrahamProgram in Emerging Infectious Diseases, Duke - National University of Singapore Graduate Medical School, Singapore.
Qingfeng ChenInstitute of Molecular and Cell Biology, Agency for Science, Technology and Research (A*STAR), Singapore.ORCID 0000-0003-0961-1572
Agency for Science, Technology and Research · SGNational University of Singapore · SGKorea University · KRThird Affiliated Hospital of Guangzhou Medical University · CN

Funding

Duke KURe ProgramK12DK100024 · NIDDK · DUKE UNIVERSITY · PI Cindy Amundsen · 2013 to 2026
$8.4M
NIDDK NIH HHS K12 DK100024
6 · The paper itself

Abstract

Recently a G-protein-coupled receptor, MAS Related GPR Family Member X2 (MRGPRX2), was identified as a specific receptor on human mast cells responsible for IgE independent adverse drug reactions (ADR). Although a murine homologue, Mrgprb2, has been identified for this receptor, its affinity for many ADR-causing drugs is poor making it difficult to undertake in vivo studies to examine mechanisms of ADR and to develop therapeutic strategies. Here, we have created humanized mice capable of generating MRGPRX2-expressing human MCs allowing for the study of MRGPRX2 MCs-mediated ADR in vitro as well as in vivo. Humanized mice were generated by hydrodynamic-injection of plasmids expressing human GM-CSF and IL-3 into NOD-scid IL2R-γ

Indexed as

Disease Models, AnimalAnimalsContrast MediaDrug EruptionsGranulocyte-Macrophage Colony-Stimulating FactorHumansInterleukin-3Mast CellsMeglumineMiceMice, Inbred NODMice, SCIDMice, TransgenicNerve Tissue ProteinsOrganometallic CompoundsReceptors, G-Protein-CoupledContrast MediaCSF2 protein, humangadobutrolGranulocyte-Macrophage Colony-Stimulating FactorIL3 protein, humanInterleukin-3MeglumineMRGPRX2 protein, humanNerve Tissue ProteinsOrganometallic CompoundsReceptors, G-Protein-CoupledReceptors, Neuropeptidecontrast agentsmast cellsMRGPRX2 receptornon-immune adverse drug reactionspseudoallergy

Identifiers

PMID31922289
PMCPMC7322799
OpenAlexW2999816963

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.