Evidence map›Paper›PMID 26104151›Full record

ReviewAnnals of the New York Academy of Sciences2015

Characteristics of natural antibody-secreting cells.

Hannah P Savage, Nicole Baumgarth

Open access · greenAbstract readReview
In one paragraph

Review in Annals of the New York Academy of Sciences, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 49 papers.

0numbers the graph read from it
0cells of the map it votes in
49citing papers in PubMed
4.2field-weighted citation impact, top 5% 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

49 citing papers in PubMed, 73 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Review
  9. Sex Influences Age-Related Changes in Natural Antibodies and CD5Journal of immunology (Baltimore, Md. : 1950) · 2022
    Article
  10. Article
  11. Up-regulation of proBDNF/p75Science advances · 2022
    Article
  12. Review
  13. Review
  14. Higher expression of KCNK10 (TREK-2) KPflugers Archiv : European journal of physiology · 2021
    Article
  15. Review
  16. Review
  17. Evidence of potent humoral immune activity in COVID-19-infected kidney transplant recipients.American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons · 2020
    Article
  18. Review
  19. A Single Human VCell reports · 2020
    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

2 authors at 1 institution in 1 country.

Hannah P SavageGraduate Group in Immunology, Davis, California.
Nicole BaumgarthGraduate Group in Immunology, Davis, California.
University of California, Davis · US

Funding

UC Davis Clinical and Translational Science CenterUL1TR000002 · NCATS · UNIVERSITY OF CALIFORNIA AT DAVIS · PI BERGLUND, LARS F · 2012 to 2015
$12.2M
Virus-induced Cell Fate Decisions in Anti-Viral ImmunityU19AI109962 · NIAID · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI BAUMGARTH, NICOLE · 2014 to 2018
$11.6M
Regulation of Humoral Immunity to Influenza VirusR01AI051354 · NIAID · UNIVERSITY OF CALIFORNIA DAVIS · PI BAUMGARTH, NICOLE · 2002 to 2012
$3.0M
Students Training in Advanced Research (STAR) ProgramT35OD010956 · OD · UNIVERSITY OF CALIFORNIA AT DAVIS · PI DANIKA L BANNASCH · 2012 to 2026
$1.6M
Early Regulation of Immunity in the Respiratory TractR01AI055881 · NIAID · UNIVERSITY OF CALIFORNIA DAVIS · PI BAUMGARTH, NICOLE · 2003 to 2007
$1.5M
Long-lived B cell Immunity in the Respiratory TractR01AI085568 · NIAID · UNIVERSITY OF CALIFORNIA AT DAVIS · PI BAUMGARTH, NICOLE · 2010 to 2013
$1.5M
Year-Long Exposure to Advanced Research (YEAR) Program for Vet StudentsT32OD010931 · OD · UNIVERSITY OF CALIFORNIA AT DAVIS · PI RAYBOULD, HELEN E · 2012 to 2018
$752k
UC Davis Clinical and Translational Science CenterTL1TR000133 · NCATS · UNIVERSITY OF CALIFORNIA AT DAVIS · PI BERGLUND, LARS F · 2012 to 2015
$594k
NCATS NIH HHS TL1 TR000133NCATS NIH HHS UL1 TR000002NIAID NIH HHS AI051354NIAID NIH HHS AI085568NIAID NIH HHS R01 AI051354NIAID NIH HHS R01 AI055881NIAID NIH HHS R01 AI085568NIAID NIH HHS U19 AI109962NIAID NIH HHS U19AI109962NIH HHS 2T32OD010931-09NIH HHS 5T35OD010956-14NIH HHS T32 OD010931NIH HHS T35 OD010956
6 · The paper itself

Abstract

Natural IgM plays a critical role in protection from pathogens and the prevention of autoimmunity. While its importance has been shown in many different settings, its origins are incompletely understood. This review focuses on the properties of the natural IgM antibody-secreting cells (ASCs), which arise mainly from the B-1 cell lineage. B-1 cells are generated in multiple waves during development, mostly in the fetal and early postfetal periods. The developmental time points can affect their repertoire: prenatal B-1 cells express a mainly germ line-encoded repertoire, while postnatally developing B-1 cells can express Ig with a greater degree of variation. Spleen and bone marrow, but not the body cavities, are primary sites of natural IgM secretion. Within these tissues heterogeneous populations of IgM ASCs can be found. While some ASCs express classical markers of B-1 lymphocytes, others express those of terminally differentiated plasma cells. A better understanding of the properties of these different natural IgM ASCs could aid their future therapeutic exploitation.

Indexed as

AnimalsAntibody-Producing CellsB-Lymphocyte SubsetsHumansImmunoglobulin MMicePositive Regulatory Domain I-Binding Factor 1Transcription FactorsImmunoglobulin MPositive Regulatory Domain I-Binding Factor 1Prdm1 protein, mousesecretory IgMTranscription FactorsB-1 cell developmentB-1 cellsBlimp-1natural IgM

Identifiers

PMID26104151
PMCPMC4679694
OpenAlexW1948473898

What OpenQuestion holds

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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.