Evidence map›Paper›PMID 21738769›Full record

ArticlePloS one2011

Analysis of the CD1 antigen presenting system in humanized SCID mice.

Jennifer L Lockridge, Xiuxu Chen, Ying Zhou, Deepika Rajesh, Drew A Roenneburg, Subramanya Hegde, Sarah Gerdts, Tan-Yun Cheng, Regan J Anderson, Gavin F Painter and 3 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
1.5field-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

28 citing papers in PubMed, 35 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. A humanized mouse model forFrontiers in immunology · 2022
    Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Modeling Human Antitumor ResponsesFrontiers in immunology · 2018
    Review
  10. Review
  11. Review
  12. Review
  13. Review
  14. Review
  15. Application of Humanized Mice in Immunological Research.Methods in molecular biology (Clifton, N.J.) · 2016
    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 3 institutions in 1 country.

Jennifer L LockridgeDepartment of Medical Microbiology and Immunology, University of Wisconsin School of Medicine and Public Health, Madison, Wisconsin, United States of America.
Xiuxu Chen
Ying Zhou
Deepika Rajesh
Drew A Roenneburg
Subramanya Hegde
Sarah Gerdts
Tan-Yun Cheng
Regan J Anderson
Gavin F Painter
D Branch Moody
William J Burlingham
Jenny E Gumperz
University of Wisconsin–Madison · USBrigham and Women's Hospital · USWisconsin Division of Public Health · US

Funding

Structural determinants of CD1d-restricted TCR functionR01AI060777 · NIAID · UNIVERSITY OF WISCONSIN-MADISON · PI GUMPERZ, JENNY E. · 2004 to 2008
$1.4M
Functional analysis of human NKT cells and myeloid DCs within murine SCID hostsR21AI076707 · NIAID · UNIVERSITY OF WISCONSIN-MADISON · PI GUMPERZ, JENNY E. · 2009 to 2010
$371k
NIAID NIH HHS R01 AI060777NIAID NIH HHS R01AI060777NIAID NIH HHS R21 AI076707NIAID NIH HHS R21AI076707
6 · The paper itself

Abstract

CD1 molecules are glycoproteins that present lipids and glycolipids for recognition by T cells. CD1-dependent immune activation has been implicated in a wide range of immune responses, however, our understanding of the role of this pathway in human disease remains limited because of species differences between humans and other mammals: whereas humans express five different CD1 gene products (CD1a, CD1b, CD1c, CD1d, and CD1e), muroid rodents express only one CD1 isoform (CD1d). Here we report that immune deficient mice engrafted with human fetal thymus, liver, and CD34(+) hematopoietic stem cells develop a functional human CD1 compartment. CD1a, b, c, and d isoforms were highly expressed by human thymocytes, and CD1a(+) cells with a dendritic morphology were present in the thymic medulla. CD1(+) cells were also detected in spleen, liver, and lungs. APCs from spleen and liver were capable of presenting bacterial glycolipids to human CD1-restricted T cells. ELISpot analyses of splenocytes demonstrated the presence of CD1-reactive IFN-γ producing cells. CD1d tetramer staining directly identified human iNKT cells in spleen and liver samples from engrafted mice, and injection of the glycolipid antigen α-GalCer resulted in rapid elevation of human IFN-γ and IL-4 levels in the blood indicating that the human iNKT cells are biologically active in vivo. Together, these results demonstrate that the human CD1 system is present and functionally competent in this humanized mouse model. Thus, this system provides a new opportunity to study the role of CD1-related immune activation in infections to human-specific pathogens.

Indexed as

AnimalsAntigens, CD1Flow CytometryHumansMiceMice, SCIDAntigens, CD1

Identifiers

PMID21738769
PMCPMC3128084
OpenAlexW1980547668

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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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.