Evidence map›Paper›PMID 18668213›Full record

ReviewImmunologic research2008

Homeostatic control of B lymphocyte subsets.

Jenni E Crowley, Jean L Scholz, William J Quinn, Jason E Stadanlick, John F Treml, Laura S Treml, Yi Hao, Radhika Goenka, Patrick J O'Neill, Andrew H Matthews and 2 more

Open access · greenAbstract readReview
In one paragraph

Review in Immunologic research, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing 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

17 citing papers in PubMed, 35 citations in OpenAlex.

  1. Review
  2. Impaired B-cell function inFrontiers in immunology · 2024
    Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. B cells and transplantation tolerance.Nature reviews. Nephrology · 2010
    Review
  13. Review
  14. Article
  15. Article
  16. Cracking the BAFF code.Nature reviews. Immunology · 2009
    Review
  17. Cell-autonomous role for NF-kappa B in immature bone marrow B cells.Journal of immunology (Baltimore, Md. : 1950) · 2009
    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

12 authors at 1 institution in 1 country.

Jenni E CrowleyDepartment of Pathology and Laboratory Medicine, University of Pennsylvania School of Medicine, 284 John Morgan Building 36th and Hamilton Walk, Philadelphia, PA, 19104-6082, USA.
Jean L Scholz
William J Quinn
Jason E Stadanlick
John F Treml
Laura S Treml
Yi Hao
Radhika Goenka
Patrick J O'Neill
Andrew H Matthews
Ronald F Parsons
Michael P Cancro
University of Pennsylvania · US

Funding

Immune System Development and RegulationT32AI055428 · NIAID · UNIVERSITY OF PENNSYLVANIA · PI ALLMAN, DAVID M, OLIVER, PAULA MARIA · 2003 to 2025
$4.2M
B LYMPHOCYTE GENERATION AND SELECTION IN AGED MICER01AG016841 · NIA · UNIVERSITY OF PENNSYLVANIA · PI CANCRO, MICHAEL PAUL · 2000 to 2003
$1.1M
NIAID NIH HHS T32 AI055428NIA NIH HHS R01 AG016841
6 · The paper itself

Abstract

Lymphocyte homeostasis poses a multi-faceted biological puzzle, because steady pre-immune populations must be maintained at an acceptable steady state to yield effective protection, despite stringent selective events during their generation. In addition, activated, memory and both short- and long-term effectors must be governed by independent homeostatic mechanisms. Finally, advancing age is accompanied by substantial changes that impact the dynamics and behavior of these pools, leading to cumulative homeostatic perturbations and compensation. Our laboratory has focused on the over-arching role of BLyS family ligands and receptors in these processes. These studies have led to a conceptual framework within which distinct homeostatic niches are specified by BLyS receptor signatures, which define the BLyS family ligands that can afford survival. The cues for establishing these receptor signatures, as well as the downstream survival mechanisms involved, are integrated with cell extrinsic inputs via cross talk among downstream mediators. A refined understanding of these relationships should yield insight into the selection and maintenance of B cell subsets, as well as an appreciation of how homeostatic mechanisms may contribute to immunosenescence.

Indexed as

AnimalsB-Cell Activating FactorB-Cell Activation Factor ReceptorB-Cell Maturation AntigenB-Lymphocyte SubsetsCellular SenescenceHomeostasisReceptors, Antigen, B-CellTransmembrane Activator and CAML Interactor ProteinTumor Necrosis Factor Ligand Superfamily Member 13B-Cell Activating FactorB-Cell Activation Factor ReceptorB-Cell Maturation AntigenReceptors, Antigen, B-CellTransmembrane Activator and CAML Interactor ProteinTumor Necrosis Factor Ligand Superfamily Member 13

Identifiers

PMID18668213
PMCPMC2662706
OpenAlexW2003092997

What OpenQuestion holds

Textmetadata
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.