Evidence map›Paper›PMID 20519648›Full record

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

Cutting edge: FcR-like 5 on innate B cells is targeted by a poxvirus MHC class I-like immunoevasin.

Jessica A Campbell, Randall S Davis, Lauren M Lilly, Daved H Fremont, Anthony R French, Leonidas N Carayannopoulos

Abstract 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 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
–field-weighted citation impact
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

16 citing papers in PubMed.

  1. Natural Immunomodulatory Agents as a Complementary Therapy for Poxviruses.Advances in experimental medicine and biology · 2024
    Review
  2. Review
  3. Review
  4. Review
  5. Article
  6. FCRL regulation in innate-like B cells.Annals of the New York Academy of Sciences · 2015
    Review
  7. Article
  8. Article
  9. Emerging roles for the FCRL family members in lymphocyte biology and disease.Current topics in microbiology and immunology · 2014
    Review
  10. Article
  11. FCRL5 exerts binary and compartment-specific influence on innate-like B-cell receptor signaling.Proceedings of the National Academy of Sciences of the United States of America · 2013
    Article
  12. NK cells and poxvirus infection.Frontiers in immunology · 2013
    Article
  13. Article
  14. Article
  15. FcR-like 2 Inhibition of B cell receptor-mediated activation of B cells.Journal of immunology (Baltimore, Md. : 1950) · 2010
    Article
  16. 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

6 authors.

Jessica A CampbellDivision of Pediatric Rheumatology, Department of Pediatrics, Washington University School of Medicine, St Louis, MO 63110, USA.
Randall S Davis
Lauren M Lilly
Daved H Fremont
Anthony R French
Leonidas N Carayannopoulos

Funding

REGULATION OF VIRAL-INDUCED NK CELL PROLIFERATION DURING MURINE CMV INFECTIONR01AI078994 · NIAID · WASHINGTON UNIVERSITY · PI FRENCH, ANTHONY R · 2009 to 2019
$3.8M
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
INNATE IMMUNE RECEPTOR ANTAGONISM BY ORTHOPOXVIRUS PROTEINSR01AI073552 · NIAID · WASHINGTON UNIVERSITY · PI FRENCH, ANTHONY R · 2008 to 2011
$1.5M
Vascular responses in transgenic sickle cell miceK01HL073171 · NHLBI · MOREHOUSE SCHOOL OF MEDICINE · PI GEE, BEATRICE E · 2003 to 2007
$684k
NHLBI NIH HHS K01 HL073171NHLBI NIH HHS T32-HL073171NIAID NIH HHS R01 AI067467NIAID NIH HHS R01 AI073552NIAID NIH HHS R01 AI078994
6 · The paper itself

Abstract

Under selective pressure from host immunity, viruses have retained genes encoding immunoevasins, molecules interfering with host viral recognition and clearance. Due to their binding specificities, immunoevasins can be exploited as affinity labels to identify host-encoded molecules of previously unsuspected importance in defense against the relevant class of virus. We previously described an orthopoxvirus MHC class I-like protein (OMCP) that binds with high affinity to the activating receptor NKG2D on NK and T cell subsets, implicating NKG2D in antiorthopoxvirus immunity. In this study, we report that OMCP also binds in an NKG2D-independent manner to B cells and monocytes/macrophages. We identify murine FcR-like 5 (FCRL5), an orphan immunoregulatory protein highly expressed by innate B lymphocytes, as a specific receptor for OMCP. The three N-terminal Ig domains of FCRL5 are required for OMCP binding. The targeting of FCRL5 by an orthopoxvirus immunoevasin strongly implicates it in contributing to host defense against zoonotic orthopoxviruses.

Indexed as

Immunity, InnateAnimalsB-Lymphocyte SubsetsCell LineCell Line, TumorGene TargetingHistocompatibility Antigens Class IHumansImmune EvasionLigandsMacrophagesMiceMice, Inbred BALB CMice, Inbred C57BLMonocytesNK Cell Lectin-Like Receptor Subfamily KFcRH3 protein, mouseHistocompatibility Antigens Class IKlrk1 protein, mouseLigandsNK Cell Lectin-Like Receptor Subfamily KReceptors, FcViral Proteins

Identifiers

PMID20519648
PMCPMC3321838

What OpenQuestion holds

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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.