Evidence map›Paper›PMID 27798616›Full record

ArticleNature immunology2016

Neutrophils license iNKT cells to regulate self-reactive mouse B cell responses.

Thomas Hägglöf, Saikiran K Sedimbi, Jennifer L Yates, Roham Parsa, Briana Hauff Salas, Robert A Harris, Elizabeth A Leadbetter, Mikael C I Karlsson

Abstract read
PubMed Publisher
In one paragraph

Article in Nature immunology, 2016. 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
2.0field-weighted citation impact, top 13% 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, 34 citations in OpenAlex.

  1. Article
  2. Article
  3. B Cell Tolerance and Targeted Therapies in SLE.Journal of clinical medicine · 2023
    Review
  4. T-betCell metabolism · 2022
    Article
  5. Review
  6. Review
  7. Article
  8. Article
  9. Review
  10. Harnessing NKT cells for vaccination.Oxford open immunology · 2021
    Review
  11. Article
  12. Review
  13. Article
  14. Combined proinflammatory cytokine and cognate activation of invariant natural killer T cells enhances anti-DNA antibody responses.Proceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  15. Review
  16. Review
  17. Article
  18. Article
  19. Article
  20. 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

8 authors at 4 institutions in 2 countries.

Thomas HägglöfDepartment of Microbiology, Tumor and Cell Biology, Karolinska Institutet, Solna, Sweden.
Saikiran K SedimbiDepartment of Microbiology, Tumor and Cell Biology, Karolinska Institutet, Solna, Sweden.
Jennifer L YatesTrudeau Institute, Saranac Lake, New York, USA.ORCID http://orcid.org/0000-0001-8841-9401
Roham ParsaDepartment of Clinical Neuroscience, Karolinska Institutet, Centre for Molecular Medicine, Karolinska University Hospital at Solna, Solna, Sweden.ORCID http://orcid.org/0000-0002-0864-6098
Briana Hauff SalasDepartment of Microbiology, Immunology, and Molecular Genetics, University of Texas Health Science Center at San Antonio, San Antonio, Texas, USA.
Robert A HarrisDepartment of Clinical Neuroscience, Karolinska Institutet, Centre for Molecular Medicine, Karolinska University Hospital at Solna, Solna, Sweden.
Elizabeth A LeadbetterTrudeau Institute, Saranac Lake, New York, USA.
Mikael C I KarlssonDepartment of Microbiology, Tumor and Cell Biology, Karolinska Institutet, Solna, Sweden.ORCID http://orcid.org/0000-0001-5582-614X
Karolinska Institutet · SEKarolinska University Hospital · SETrudeau Institute · USThe University of Texas Health Science Center at San Antonio · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The innate responsiveness of the immune system is important not only for quick responses to pathogens but also for the initiation and shaping of the subsequent adaptive immune response. Activation via the cytokine IL-18, a product of inflammasomes, gives rise to a rapid response that includes the production of self-reactive antibodies. As increased concentrations of this cytokine are found in inflammatory diseases, we investigated the origin of the B cell response and its regulation. We identified an accumulation of B cell-helper neutrophils in the spleen that interacted with innate-type invariant natural killer T cells (iNKT cells) to regulate B cell responses. We found that neutrophil-dependent expression of the death-receptor ligand FasL by iNKT cells was needed to restrict autoantibody production. Neutrophils can thus license iNKT cells to regulate potentially harmful autoreactive B cell responses during inflammasome-driven inflammation.

Indexed as

Adaptive ImmunityAnimalsAutoantibodiesB-LymphocytesCells, CulturedFas Ligand ProteinImmunity, InnateInflammasomesInflammationInterleukin-18MiceMice, Inbred C57BLMice, KnockoutNatural Killer T-CellsNeutrophilsAutoantibodiesFas Ligand ProteinInflammasomesInterleukin-18

Identifiers

PMID27798616
OpenAlexW2545875932

What OpenQuestion holds

Textmetadata
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.