Evidence map›Paper›PMID 22941591›Full record

ReviewImmunologic research2013

Antigen and cytokine receptor signals guide the development of the naïve mature B cell repertoire.

Sarah L Rowland, Kathryn Tuttle, Raul M Torres, Roberta Pelanda

Open access · greenAbstract readReview
In one paragraph

Review in Immunologic research, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.8field-weighted citation impact, top 16% 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

19 citing papers in PubMed, 28 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. mTORC1 as a cell-intrinsic rheostat that shapes development, preimmune repertoire, and function of B lymphocytes.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2019
    Article
  8. Review
  9. Article
  10. Immunodeficiency in Bloom's Syndrome.Journal of clinical immunology · 2018
    Article
  11. Article
  12. γδ T Cells Shape Preimmune Peripheral B Cell Populations.Journal of immunology (Baltimore, Md. : 1950) · 2016
    Article
  13. The ageing human B cell repertoire: a failure of selection?Clinical and experimental immunology · 2016
    Review
  14. Review
  15. Human antibody production in transgenic animals.Archivum immunologiae et therapiae experimentalis · 2015
    Review
  16. Antibody repertoire deep sequencing reveals antigen-independent selection in maturing B cells.Proceedings of the National Academy of Sciences of the United States of America · 2014
    Article
  17. Review
  18. Infection-induced changes in hematopoiesis.Journal of immunology (Baltimore, Md. : 1950) · 2014
    Review
  19. 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

4 authors at 2 institutions in 1 country.

Sarah L RowlandIntegrated Department of Immunology, University of Colorado School of Medicine, National Jewish Health, Denver, CO, USA.
Kathryn Tuttle
Raul M Torres
Roberta Pelanda
National Jewish Health · USUniversity of Colorado Denver · US

Funding

THE REGULATION OF V ALPHA 7 EXPRESSING T CELLSP01AI022295 · NIAID · NATIONAL JEWISH HEALTH · PI REFAELI, YOSEF · 1985 to 2011
$11.7M
Chemokine response in B cell development and functionR01AI052157 · NIAID · UNIVERSITY OF COLORADO DENVER · PI TORRES, RAUL MARTIN · 2002 to 2017
$5.4M
Tolerance in Polyclonal and Oligoclonal Immune SystemsR01AI052310 · NIAID · UNIVERSITY OF COLORADO DENVER · PI PELANDA, ROBERTA · 2003 to 2017
$5.0M
Marginal Zone B Cell Response to HIVR21AI078468 · NIAID · UNIVERSITY OF COLORADO DENVER · PI TORRES, RAUL MARTIN · 2008 to 2009
$424k
Tolerance in Polyclonal and Oligoclonal Immune SystemsR56AI052310 · NIAID · NATIONAL JEWISH HEALTH · PI PELANDA, ROBERTA · 2007 to 2007
$363k
NIAID NIH HHS AI022295NIAID NIH HHS AI052157NIAID NIH HHS AI052310NIAID NIH HHS AI078468NIAID NIH HHS P01 AI022295NIAID NIH HHS R01 AI052157NIAID NIH HHS R01 AI052310NIAID NIH HHS R21 AI078468NIAID NIH HHS R56 AI052310
6 · The paper itself

Abstract

Immature B cells are generated daily in the bone marrow tissue. More than half of the newly generated immature B cells are autoreactive and bind a self-antigen, while the others are nonautoreactive. A selection process has evolved on the one hand to thwart development of autoreactive immature B cells and, on the other hand, to promote further differentiation of nonautoreactive immature B cells into transitional and mature B cells. These negative and positive selection events are carefully regulated by signals that emanate from the antigen receptor, whether antigen-mediated or tonic, and are influenced by signals that are generated by receptors that bind cytokines, chemokines, and other factors produced in the bone marrow tissue. These signals, therefore, are the predominant driving forces for the generation of a B cell population that is capable of protecting the body from infections while maintaining self-tolerance. Here, we review recent findings from our group and others that describe how tonic antigen receptor signaling and bone marrow cytokines regulate the selection of immature B cells.

Indexed as

AnimalsB-LymphocytesReceptors, Antigen, B-CellReceptors, CytokineReceptors, Antigen, B-CellReceptors, Cytokine

Identifiers

PMID22941591
PMCPMC3924590
OpenAlexW2065040574

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.