Evidence map›Paper›PMID 26826598›Full record

ArticleClinical immunology (Orlando, Fla.)2016

Early BAFF receptor blockade mitigates murine Sjögren's syndrome: Concomitant targeting of CXCL13 and the BAFF receptor prevents salivary hypofunction.

Arjun Sharma, Jeremy Kiripolsky, Ekaterina Klimatcheva, Alan Howell, Farzad Fereidouni, Richard Levenson, Thomas L Rothstein, Jill M Kramer

Open access · greenAbstract read
In one paragraph

Article in Clinical immunology (Orlando, Fla.), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
3.1field-weighted citation impact, top 9% 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

23 citing papers in PubMed, 34 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Article
  5. Article
  6. Review
  7. Review
  8. Review
  9. Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Review
  15. Review
  16. Review
  17. Article
  18. Article
  19. Article
  20. Sex differential association of dermatomyositis with Sjögren syndrome.CMAJ : Canadian Medical Association journal = journal de l'Association medicale canadienne · 2017
    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

8 authors at 5 institutions in 1 country.

Arjun Sharma *Department of Oral Biology, School of Dental Medicine, University of Buffalo, The State University of New York, Buffalo, NY USA 14214.
Jeremy Kiripolsky *Department of Oral Biology, School of Dental Medicine, University of Buffalo, The State University of New York, Buffalo, NY USA 14214.
Ekaterina KlimatchevaVaccinex, Inc., Rochester, NY 14620.
Alan HowellVaccinex, Inc., Rochester, NY 14620.
Farzad FereidouniDepartment of Pathology and Laboratory Medicine, UC Davis Medical Center, Sacramento, CA 95817.
Richard LevensonDepartment of Pathology and Laboratory Medicine, UC Davis Medical Center, Sacramento, CA 95817.
Thomas L RothsteinCenter for Oncology and Cell Biology, The Feinstein Institute for Medical Research, Manhasset, NY 11030.
Jill M KramerDepartment of Oral Biology, School of Dental Medicine, University of Buffalo, The State University of New York, Buffalo, NY USA 14214.
University at Buffalo, State University of New York · USUniversity of California Davis Medical Center · USVaccinex (United States) · USFeinstein Institute for Medical Research · USNorthwell Health · US

Funding

PHORBOL ESTER RESPONSIVE B LYMPHOCYTESR01AI029690 · NIAID · WESTERN MICHIGAN UNIV SCHOOL OF MEDICINE · PI ROTHSTEIN, THOMAS L · 1990 to 2019
$6.9M
Advanced Training in Oral BiologyT32DE023526 · NIDCR · STATE UNIVERSITY OF NEW YORK AT BUFFALO · PI Stefan Hans-Klaus Ruhl · 2013 to 2026
$3.7M
Autoantibodies and B Cell Chemotaxis in Sjogren's SyndromeK08DE020882 · NIDCR · STATE UNIVERSITY OF NEW YORK AT BUFFALO · PI KRAMER, JILL MARIE · 2010 to 2014
$697k
NIAID NIH HHS R01 AI029690NIDCR NIH HHS K08 DE020882NIDCR NIH HHS T32 DE023526
6 · The paper itself

Abstract

Sjögren's syndrome (SS) is a debilitating autoimmune disease. Patients with SS may develop xerostomia. This process is progressive, and there are no therapeutics that target disease etiology. We hypothesized BAFF receptor (BAFFR) blockade would mitigate SS disease development, and neutralization of CXCL13 and BAFF signaling would be more efficacious than BAFFR blockade alone. We treated NOD/ShiLtJ SS mice with soluble BAFF receptor (BAFFR-Fc) or anti-CXCL13/BAFFR-Fc in combination, prior to the development of clinical disease. Our results show treatment with BAFFR-Fc reduced peripheral B cell numbers and decreased sialadenitis. In addition, this treatment reduced total serum immunoglobulin as well as IgG and IgM specific anti-nuclear autoantibodies. NOD/ShiLtJ mice treated with BAFFR-Fc and anti-CXCL13 antibody were protected from salivary deficits. Results from this study suggest blockade of CXCL13 and BAFFR together may be an effective therapeutic strategy in preventing salivary hypofunction and reducing autoantibody titers and sialadenitis in patients with SS.

Indexed as

AnimalsAntibodiesB-Cell Activation Factor ReceptorChemokine CXCL13Disease Models, AnimalFemaleMiceMice, Inbred NODSalivaSalivary GlandsSialadenitisSjogren's SyndromeAntibodiesB-Cell Activation Factor ReceptorChemokine CXCL13Cxcl13 protein, mouseTnfrsf13c protein, mouseAutoantibodyBAFF receptorCXCL13Salivary hypofunctionSialadenitisSjögren's syndrome

Identifiers

PMID26826598
PMCPMC4780410
OpenAlexW2292432120

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.