Evidence map›Paper›PMID 20519654›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2010

Cutting edge: FcR-like 6 is an MHC class II receptor.

Daniel M Schreeder, John P Cannon, Jiongru Wu, Ran Li, Mikhail A Shakhmatov, Randall S Davis

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
2.1field-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

39 citing papers in PubMed, 69 citations in OpenAlex.

  1. Article
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  6. Article
  7. Evidence for Extensive Duplication and Subfunctionalization ofInternational journal of molecular sciences · 2023
    Article
  8. Review
  9. Review
  10. Review
  11. Article
  12. Review
  13. Article
  14. Article
  15. Review
  16. Article
  17. The dormant cancer cell life cycle.Nature reviews. Cancer · 2020
    Review
  18. Review
  19. Regulation of NK-Cell Function by HLA Class II.Frontiers in cellular and infection microbiology · 2020
    Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 3 institutions in 2 countries.

Daniel M SchreederDepartment of Microbiology, University of Alabama at Birmingham, Birmingham, AL 35294, USA.
John P Cannon
Jiongru Wu
Ran Li
Mikhail A Shakhmatov
Randall S Davis
University of Alabama at Birmingham · USCzech Academy of Sciences, Institute of Microbiology · CZFlorida College · US

Funding

MEDICAL SCIENTIST TRAINING PROGRAMT32GM008361 · NIGMS · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI YACOUBIAN, TALENE ALENE · 1992 to 2024
$16.8M
IMMUNOLOGIC DISEASES AND BASIC IMMUNOLOGYT32AI007051 · NIAID · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI Laurie Ellen Harrington · 1985 to 2026
$13.1M
Functional Role of Fc Receptor Homologs on B Lineage CellsR01AI067467 · NIAID · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI DAVIS, RANDALL S · 2007 to 2011
$1.6M
Biological definition of Fc receptor homologsK08AI055638 · NIAID · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI DAVIS, RANDALL S · 2003 to 2005
$363k
Biological Definition of FCRL Molecules in MalignancyR21CA131656 · NCI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI DAVIS, RANDALL S · 2008 to 2009
$359k
NCI NIH HHS CA131656NCI NIH HHS R21 CA131656NIAID NIH HHS AI007051NIAID NIH HHS AI055638NIAID NIH HHS AI067467NIAID NIH HHS K08 AI055638NIAID NIH HHS R01 AI067467NIAID NIH HHS T32 AI007051NIGMS NIH HHS T32 GM008361
6 · The paper itself

Abstract

Receptors for the Fc portion of Ig have been extensively characterized and are known to regulate humoral responses, but members of the closely related FcR-like (FCRL) family have not been found to bind Ig, and to date, no ligand has been identified for any FCRL. Using a cell-based GFP reporter system and a recombinant Fc chimeric protein, we show that human FCRL6, a receptor selectively expressed by cytotoxic T and NK cells, directly binds HLA-DR, an MHC class II molecule. Given the similarity among constant regions of Ig and MHC molecules, these findings suggest that representatives of the FcR and FCRL multigene families may have independently evolved to engage two ancestral elements fundamental to adaptive immunity. This discovery may offer new insight into the interaction between cytotoxic lymphocytes and APCs and may have important implications for better understanding HLA disease susceptibility and pathogenesis.

Indexed as

AdultAnimalsAntibodies, BlockingAntigen-Presenting CellsCell LineCell Line, TumorCoculture TechniquesHLA-DR AntigensHumansKiller Cells, NaturalLigandsMiceMice, Inbred BALB CMultigene FamilyProtein BindingReceptors, Cell SurfaceAntibodies, BlockingFCRL6 protein, humanHLA-DR AntigensLigandsReceptors, Cell SurfaceReceptors, FcRecombinant Fusion Proteins

Identifiers

PMID20519654
PMCPMC4876727
OpenAlexW2162286370

What OpenQuestion holds

Textmetadata
LicenceTDM
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.