Evidence map›Paper›PMID 28584005›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2017

Neutrophils Slow Disease Progression in Murine Lupus via Modulation of Autoreactive Germinal Centers.

Anna K Bird, Martin Chang, Jennifer Barnard, Bruce I Goldman, Nida Meednu, Javier Rangel-Moreno, Jennifer H Anolik

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.5field-weighted citation impact, top 19% 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

20 citing papers in PubMed, 29 citations in OpenAlex.

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  8. Inhibition of elastase enhances the adjuvanticity of alum and promotes anti-SARS-CoV-2 systemic and mucosal immunity.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
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  11. Review
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  15. Review
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  17. Article
  18. Review
  19. Autoimmunity in 2017.Clinical reviews in allergy & immunology · 2018
    Review
  20. Androgen-Induced Immunosuppression.Frontiers in immunology · 2018
    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

7 authors at 1 institution in 1 country.

Anna K BirdDepartment of Microbiology and Immunology, University of Rochester Medical Center, Rochester, NY 14642.ORCID 0000-0003-2707-159X
Martin ChangDivision of Allergy, Immunology, and Rheumatology, Department of Medicine, University of Rochester Medical Center, Rochester, NY 14642; and.ORCID 0000-0002-4828-6672
Jennifer BarnardDivision of Allergy, Immunology, and Rheumatology, Department of Medicine, University of Rochester Medical Center, Rochester, NY 14642; and.
Bruce I GoldmanDepartment of Pathology and Laboratory Medicine, University of Rochester Medical Center, Rochester, NY 14642.ORCID 0000-0003-2111-2151
Nida MeednuDivision of Allergy, Immunology, and Rheumatology, Department of Medicine, University of Rochester Medical Center, Rochester, NY 14642; and.ORCID 0000-0002-2868-3339
Javier Rangel-MorenoDivision of Allergy, Immunology, and Rheumatology, Department of Medicine, University of Rochester Medical Center, Rochester, NY 14642; and.ORCID 0000-0002-9738-1182
Jennifer H AnolikDepartment of Microbiology and Immunology, University of Rochester Medical Center, Rochester, NY 14642; jennifer_anolik@urmc.rochester.edu.
University of Rochester Medical Center · US

Funding

Role of B Cells in Synovial Inflammation & LN Remodeling in RA ArthritisP01AI078907 · NIAID · UNIVERSITY OF ROCHESTER · PI ANOLIK, JENNIFER HOWITT · 2010 to 2014
$10.8M
Cellular Dynamics at the Synovium-Bone interface in RAUH2AR067690 · NIAMS · UNIVERSITY OF ROCHESTER · PI ANOLIK, JENNIFER HOWITT · 2014 to 2020
$3.0M
B-Cell Tolerance Mechanisms in Human SLER01AI077674 · NIAID · UNIVERSITY OF ROCHESTER · PI ANOLIK, JENNIFER HOWITT · 2009 to 2013
$2.0M
NIAID NIH HHS P01 AI078907NIAID NIH HHS R01 AI077674NIAMS NIH HHS UH2 AR067690
6 · The paper itself

Abstract

Neutrophils are well characterized as mediators of peripheral tissue damage in lupus, but it remains unclear whether they influence loss of self-tolerance in the adaptive immune compartment. Lupus neutrophils produce elevated levels of factors known to fuel autoantibody production, including IL-6 and B cell survival factors, but also reactive oxygen intermediates, which can suppress lymphocyte proliferation. To assess whether neutrophils directly influence the progression of autoreactivity in secondary lymphoid organs (SLOs), we characterized the localization and cell-cell contacts of splenic neutrophils at several stages in the progression of disease in the NZB/W murine model of lupus. Neutrophils accumulate in SLO over the course of lupus progression, preferentially localizing near T lymphocytes early in disease and B cells with advanced disease. RNA sequencing reveals that the splenic neutrophil transcriptional program changes significantly over the course of disease, with neutrophil expression of anti-inflammatory mediators peaking during early-stage and midstage disease, and evidence of neutrophil activation with advanced disease. To assess whether neutrophils exert predominantly protective or deleterious effects on loss of B cell self-tolerance in vivo, we depleted neutrophils at different stages of disease. Neutrophil depletion early in lupus resulted in a striking acceleration in the onset of renal disease, SLO germinal center formation, and autoreactive plasma cell production. In contrast, neutrophil depletion with more advanced disease did not alter systemic lupus erythematosus progression. These results demonstrate a surprising temporal and context-dependent role for neutrophils in restraining autoreactive B cell activation in lupus.

Indexed as

AutoimmunityDisease ProgressionAnimalsAutoantibodiesB-LymphocytesDisease Models, AnimalGerminal CenterLupus Erythematosus, SystemicLymphocyte ActivationMiceMice, Inbred NZBNeutrophilsSequence Analysis, RNASpleenT-LymphocytesAutoantibodies

Identifiers

PMID28584005
PMCPMC5524201
OpenAlexW2621589320

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.