Evidence map›Paper›PMID 16436662›Full record

ArticleThe American journal of pathology2006

A soluble BAFF antagonist, BR3-Fc, decreases peripheral blood B cells and lymphoid tissue marginal zone and follicular B cells in cynomolgus monkeys.

Yulia Vugmeyster, Dhaya Seshasayee, Wesley Chang, Anahid Storn, Kathy Howell, Susan Sa, Tenea Nelson, Flavius Martin, Iqbal Grewal, Ellen Gilkerson and 7 more

Open access · bronzeAbstract read
In one paragraph

Article in The American journal of pathology, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
4.0field-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

25 citing papers in PubMed, 78 citations in OpenAlex.

  1. Review
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  11. B-Cell Depletion Reduces the Maturation of Cerebral Cavernous Malformations in Murine Models.Journal of neuroimmune pharmacology : the official journal of the Society on NeuroImmune Pharmacology · 2016
    Article
  12. Review
  13. Article
  14. Review
  15. Article
  16. Article
  17. Review
  18. Tolerogenic therapies in transplantation.Frontiers in immunology · 2012
    Article
  19. Article
  20. Innate pathways to B-cell activation and tolerance.Annals of the New York Academy of Sciences · 2010
    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

17 authors at 2 institutions in 1 country.

Yulia VugmeysterGenentech, Inc, San Francisco, CA 94080, USA.
Dhaya Seshasayee
Wesley Chang
Anahid Storn
Kathy Howell
Susan Sa
Tenea Nelson
Flavius Martin
Iqbal Grewal
Ellen Gilkerson
Ben Wu
Jeff Thompson
Barbara N Ehrenfels
Song Ren
An Song
Thomas R Gelzleichter
Dimitry M Danilenko
Biogen (United States) · USAcentech (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BAFF (also known as BLyS), a member of the tumor necrosis factor superfamily, plays a critical role in the maturation and development of B cells. BAFF has three receptors on B cells, the most crucial of which is BR3. In this study, we demonstrate the biological outcome of BAFF blockade in cynomolgus monkeys using a soluble fusion protein consisting of human BR3 and human IgG1 Fc. In vitro, BR3-Fc blocked BAFF-mediated survival and proliferation of cynomolgus monkey B cells. Weekly treatment of cynomolgus monkeys with BR3-Fc for 13 to 18 weeks resulted in significant B-cell reduction in the peripheral blood and in lymphoid organs. CD21(high) B cells in lymphoid tissues, a subset analogous to human marginal zone B cells, expressed nearly twofold higher BR3 levels than did CD21(med) B cells. Lymphoid tissue flow cytometric analysis showed that BR3-Fc reduced this CD21(high) B-cell subset to a greater extent than it reduced CD21(med) B cells. Dual-label immunohistochemistry and morphometric image analysis supported these results by demonstrating that BR3-Fc reduced a significant proportion of the B cells within the splenic inner and outer marginal zones. These findings should prove very useful in guiding the desired therapeutic use of BR3-Fc for autoimmune diseases in the clinic.

Indexed as

B-LymphocytesAnimalsB-Cell Activating FactorB-Cell Activation Factor ReceptorCell ProliferationCell SurvivalFemaleFlow CytometryHumansImmunoglobulin Fc FragmentsImmunoglobulin GLymphoid TissueMacaca fascicularisMaleMembrane ProteinsReceptors, Tumor Necrosis FactorB-Cell Activating FactorB-Cell Activation Factor ReceptorImmunoglobulin Fc FragmentsImmunoglobulin GMembrane ProteinsReceptors, Tumor Necrosis FactorRecombinant Fusion ProteinsTNFRSF13C protein, humanTNFSF13B protein, humanTumor Necrosis Factor-alpha

Identifiers

PMID16436662
PMCPMC1606502
OpenAlexW2024742513

What OpenQuestion holds

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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.