Evidence map›Paper›PMID 24821911›Full record

ArticleThe Journal of experimental medicine2014

Pleural innate response activator B cells protect against pneumonia via a GM-CSF-IgM axis.

Georg F Weber, Benjamin G Chousterman, Ingo Hilgendorf, Clinton S Robbins, Igor Theurl, Louisa M S Gerhardt, Yoshiko Iwamoto, Tam D Quach, Muhammad Ali, John W Chen and 4 more

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of experimental medicine, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 104 papers.

0numbers the graph read from it
0cells of the map it votes in
104citing papers in PubMed
5.9field-weighted citation impact, top 3% 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

104 citing papers in PubMed, 151 citations in OpenAlex.

  1. Trial
  2. Article
  3. B1 Cells for Life.Immunological reviews · 2026
    Review
  4. Review
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Science translational medicine · 2025
    Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Review
  16. Pleural macrophages translocate to the lung during infection to promote improved influenza outcomes.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  17. Article
  18. Noncanonical B Cells: Characteristics of Uncharacteristic B Cells.Journal of immunology (Baltimore, Md. : 1950) · 2023
    Review
  19. Diversity of B Cell Populations and Ig Repertoire in Human Lungs.Journal of immunology (Baltimore, Md. : 1950) · 2023
    Article
  20. Review

44 more citing papers are in PubMed but not listed here.

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

14 authors at 4 institutions in 2 countries.

Georg F WeberCenter for Systems Biology, Massachusetts General Hospital, Harvard Medical School, Boston, MA 02114 Department of Visceral, Thoracic and Vascular Surgery, Medizinische Fakultät Carl Gustav Carus, Technische Universität Dresden, 01307 Dresden, Germany fswirski@mgh.harvard.edu georg.weber@uniklinikum-dresden.de.
Benjamin G ChoustermanCenter for Systems Biology, Massachusetts General Hospital, Harvard Medical School, Boston, MA 02114.
Ingo HilgendorfCenter for Systems Biology, Massachusetts General Hospital, Harvard Medical School, Boston, MA 02114.
Clinton S RobbinsCenter for Systems Biology, Massachusetts General Hospital, Harvard Medical School, Boston, MA 02114.
Igor TheurlCenter for Systems Biology, Massachusetts General Hospital, Harvard Medical School, Boston, MA 02114.
Louisa M S GerhardtCenter for Systems Biology, Massachusetts General Hospital, Harvard Medical School, Boston, MA 02114.
Yoshiko IwamotoCenter for Systems Biology, Massachusetts General Hospital, Harvard Medical School, Boston, MA 02114.
Tam D QuachCenter for Oncology and Cell Biology, The Feinstein Institute for Medical Research, Manhasset, NY 11030.
Muhammad AliCenter for Systems Biology, Massachusetts General Hospital, Harvard Medical School, Boston, MA 02114.
John W ChenCenter for Systems Biology, Massachusetts General Hospital, Harvard Medical School, Boston, MA 02114.
Thomas L RothsteinCenter for Oncology and Cell Biology, The Feinstein Institute for Medical Research, Manhasset, NY 11030.
Matthias NahrendorfCenter for Systems Biology, Massachusetts General Hospital, Harvard Medical School, Boston, MA 02114.
Ralph WeisslederCenter for Systems Biology, Massachusetts General Hospital, Harvard Medical School, Boston, MA 02114 Department of Systems Biology, Harvard Medical School, Boston, MA 02115.
Filip K SwirskiCenter for Systems Biology, Massachusetts General Hospital, Harvard Medical School, Boston, MA 02114 fswirski@mgh.harvard.edu georg.weber@uniklinikum-dresden.de.
Center for Systems Biology · USMassachusetts General Hospital · USHarvard University · USFeinstein Institute for Medical Research · US

Funding

PHORBOL ESTER RESPONSIVE B LYMPHOCYTESR01AI029690 · NIAID · WESTERN MICHIGAN UNIV SCHOOL OF MEDICINE · PI ROTHSTEIN, THOMAS L · 1990 to 2019
$6.9M
Monocyte Heterogeneity in Experimental and Human AtherosclerosisR01HL095612 · NHLBI · MASSACHUSETTS GENERAL HOSPITAL · PI SWIRSKI, FILIP K · 2009 to 2016
$3.4M
Imaging of Cardiac Transplant RejectionR01HL095629 · NHLBI · MASSACHUSETTS GENERAL HOSPITAL · PI NAHRENDORF, MATTHIAS · 2009 to 2013
$2.2M
Myeloperoxidase, imaging biomarker and treatment target for multiple sclerosisR01NS070835 · NINDS · MASSACHUSETTS GENERAL HOSPITAL · PI CHEN, JOHN W · 2010 to 2014
$1.9M
Imaging and Treating Inflammation in Stroke by Targeting MyeloperoxidaseR01NS072167 · NINDS · MASSACHUSETTS GENERAL HOSPITAL · PI CHEN, JOHN W · 2010 to 2014
$1.8M
Aberrant Signaling in B-1 CellsR56AI029690 · NIAID · FEINSTEIN INSTITUTE FOR MEDICAL RESEARCH · PI ROTHSTEIN, THOMAS L · 2008 to 2008
$414k
Innate Response Activator B cells in Bacterial Lung InfectionR56AI104695 · NIAID · MASSACHUSETTS GENERAL HOSPITAL · PI SWIRSKI, FILIP K · 2013 to 2013
$403k
ABERRANT SIGNALING IN B1 CELLSR21AI029690 · NIAID · BOSTON MEDICAL CENTER · PI ROTHSTEIN, THOMAS L · 1997 to 1997
–
NHLBI NIH HHS R01 HL095612NHLBI NIH HHS R01HL095612NHLBI NIH HHS R01 HL095629NIAID NIH HHS AI029690NIAID NIH HHS R01 AI029690NIAID NIH HHS R56 AI029690NIAID NIH HHS R56 AI104695NIAID NIH HHS R56AI104695NINDS NIH HHS R01 NS070835NINDS NIH HHS R01 NS072167
6 · The paper itself

Abstract

Pneumonia is a major cause of mortality worldwide and a serious problem in critical care medicine, but the immunophysiological processes that confer either protection or morbidity are not completely understood. We show that in response to lung infection, B1a B cells migrate from the pleural space to the lung parenchyma to secrete polyreactive emergency immunoglobulin M (IgM). The process requires innate response activator (IRA) B cells, a transitional B1a-derived inflammatory subset which controls IgM production via autocrine granulocyte/macrophage colony-stimulating factor (GM-CSF) signaling. The strategic location of these cells, coupled with the capacity to produce GM-CSF-dependent IgM, ensures effective early frontline defense against bacteria invading the lungs. The study describes a previously unrecognized GM-CSF-IgM axis and positions IRA B cells as orchestrators of protective IgM immunity.

Indexed as

AdultAnimalsB-Lymphocyte SubsetsCell MovementCells, CulturedFlow CytometryGranulocyte-Macrophage Colony-Stimulating FactorHumansImmunity, InnateImmunoglobulin MLungMiceMice, Inbred C57BLMice, Inbred StrainsMice, KnockoutMice, TransgenicGranulocyte-Macrophage Colony-Stimulating FactorImmunoglobulin M

Identifiers

PMID24821911
PMCPMC4042649
OpenAlexW2125045881

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.