Evidence map›Paper›PMID 29386231›Full record

ArticleThe Journal of experimental medicine2018

Atypical chemokine receptor 4 shapes activated B cell fate.

Ervin E Kara, Cameron R Bastow, Duncan R McKenzie, Carly E Gregor, Kevin A Fenix, Rachelle Babb, Todd S Norton, Dimitra Zotos, Lauren B Rodda, Jana R Hermes and 11 more

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of experimental medicine, 2018. 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
1.2field-weighted citation impact, top 18% 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

16 citing papers in PubMed, 30 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Atypical chemokine receptors in the immune system.Nature reviews. Immunology · 2024
    Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Scavenging of soluble and immobilized CCL21 by ACKR4 regulates peripheral dendritic cell emigration.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  14. ACKR4 restrains antitumor immunity by regulating CCL21.The Journal of experimental medicine · 2020
    Article
  15. Review
  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

21 authors at 8 institutions in 3 countries.

Ervin E KaraDepartment of Molecular and Cellular Biology, School of Biological Sciences, University of Adelaide, Adelaide, South Australia, Australia.
Cameron R BastowDepartment of Molecular and Cellular Biology, School of Biological Sciences, University of Adelaide, Adelaide, South Australia, Australia.
Duncan R McKenzieDepartment of Molecular and Cellular Biology, School of Biological Sciences, University of Adelaide, Adelaide, South Australia, Australia.
Carly E GregorDepartment of Molecular and Cellular Biology, School of Biological Sciences, University of Adelaide, Adelaide, South Australia, Australia.
Kevin A FenixDepartment of Molecular and Cellular Biology, School of Biological Sciences, University of Adelaide, Adelaide, South Australia, Australia.
Rachelle BabbDepartment of Molecular and Cellular Biology, School of Biological Sciences, University of Adelaide, Adelaide, South Australia, Australia.
Todd S NortonDepartment of Molecular and Cellular Biology, School of Biological Sciences, University of Adelaide, Adelaide, South Australia, Australia.
Dimitra ZotosWalter and Eliza Hall Institute of Medical Research, Parkville, Victoria, Australia.
Lauren B RoddaDepartment of Microbiology and Immunology, University of California, San Francisco, San Francisco, CA.
Jana R HermesImmunology Division, Garvan Institute of Medical Research, Darlinghurst, New South Wales, Australia.
Katherine BourneImmunology Division, Garvan Institute of Medical Research, Darlinghurst, New South Wales, Australia.
Derek S GilchristInstitute of Infection, Immunity and Inflammation, College of Medicine, Veterinary and Life Sciences, University of Glasgow, Glasgow, Scotland, UK.
Robert J NibbsInstitute of Infection, Immunity and Inflammation, College of Medicine, Veterinary and Life Sciences, University of Glasgow, Glasgow, Scotland, UK.
Mohammed AlsharifiDepartment of Molecular and Cellular Biology, School of Biological Sciences, University of Adelaide, Adelaide, South Australia, Australia.
Carola G VinuesaDepartment of Immunology and Infectious Disease, John Curtin School of Medical Research, Australian National University, Canberra, Australian Capital Territory, Australia.
David M TarlintonWalter and Eliza Hall Institute of Medical Research, Parkville, Victoria, Australia.ORCID 0000-0001-9928-686X
Robert BrinkImmunology Division, Garvan Institute of Medical Research, Darlinghurst, New South Wales, Australia.ORCID 0000-0002-9586-3655
Geoffrey R HillImmunology Department, QIMR Berghofer Medical Research Institute, Brisbane, Queensland, Australia.
Jason G CysterDepartment of Microbiology and Immunology, University of California, San Francisco, San Francisco, CA.ORCID 0000-0002-4735-9745
Iain ComerfordDepartment of Molecular and Cellular Biology, School of Biological Sciences, University of Adelaide, Adelaide, South Australia, Australia iain.comerford@adelaide.edu.au.
Shaun R McCollDepartment of Molecular and Cellular Biology, School of Biological Sciences, University of Adelaide, Adelaide, South Australia, Australia shaun.mccoll@adelaide.edu.au.ORCID 0000-0003-0949-4660
The University of Adelaide · AUGarvan Institute of Medical Research · AUUniversity of Glasgow · GBWalter and Eliza Hall Institute of Medical Research · AUAustralian National University · AUHoward Hughes Medical Institute · USQIMR Berghofer Medical Research Institute · AUUniversity of California, San Francisco · US

Funding

MOLECULAR AND CELLULAR IMMUNOLOGYT32AI007334 · NIAID · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI CYSTER, JASON G · 1988 to 2023
$11.0M
Howard Hughes Medical InstituteMedical Research Council MR/L000598/1NIAID NIH HHS T32 AI007334
6 · The paper itself

Abstract

Activated B cells can initially differentiate into three functionally distinct fates-early plasmablasts (PBs), germinal center (GC) B cells, or early memory B cells-by mechanisms that remain poorly understood. Here, we identify atypical chemokine receptor 4 (ACKR4), a decoy receptor that binds and degrades CCR7 ligands CCL19/CCL21, as a regulator of early activated B cell differentiation. By restricting initial access to splenic interfollicular zones (IFZs), ACKR4 limits the early proliferation of activated B cells, reducing the numbers available for subsequent differentiation. Consequently, ACKR4 deficiency enhanced early PB and GC B cell responses in a CCL19/CCL21-dependent and B cell-intrinsic manner. Conversely, aberrant localization of ACKR4-deficient activated B cells to the IFZ was associated with their preferential commitment to the early PB linage. Our results reveal a regulatory mechanism of B cell trafficking via an atypical chemokine receptor that shapes activated B cell fate.

Indexed as

Cell LineageAnimalsAntigensB-LymphocytesCell ProliferationGerminal CenterMice, Inbred C57BLReceptors, CCRSpleenAckr4 protein, mouseAntigensReceptors, CCR

Identifiers

PMID29386231
PMCPMC5839757
OpenAlexW2786342592

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.