Evidence map›Paper›PMID 24211713›Full record

ArticleClinical immunology (Orlando, Fla.)2013

TSPAN33 is a novel marker of activated and malignant B cells.

Van Phi Luu, Peter Hevezi, Felipe Vences-Catalan, José Luis Maravillas-Montero, Clayton Alexander White, Paolo Casali, Luis Llorente, Juan Jakez-Ocampo, Guadalupe Lima, Natalia Vilches-Cisneros and 3 more

Open access · greenAbstract read
In one paragraph

Article in Clinical immunology (Orlando, Fla.), 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing 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

16 citing papers in PubMed, 29 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Review
  8. Review
  9. Article
  10. Identification of IL-40, a Novel B Cell-Associated Cytokine.Journal of immunology (Baltimore, Md. : 1950) · 2017
    Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. 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

13 authors at 4 institutions in 2 countries.

Van Phi LuuDepartment of Physiology and Biophysics, University of California Irvine, Irvine, CA, USA; Institute for Immunology, University of California Irvine, Irvine, CA, USA.
Peter Hevezi
Felipe Vences-Catalan
José Luis Maravillas-Montero
Clayton Alexander White
Paolo Casali
Luis Llorente
Juan Jakez-Ocampo
Guadalupe Lima
Natalia Vilches-Cisneros
Juan Pablo Flores-Gutiérrez
Leopoldo Santos-Argumedo
Albert Zlotnik
University of California, Irvine · USInstituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán · MXCenter for Research and Advanced Studies of the National Polytechnic Institute · MXUniversidad Autónoma de Nuevo León · MX

Funding

Intrinsic B cell epigenetic regulation of antibody and autoantibody responses by Sirt1R01AI105813 · NIAID · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI CASALI, PAOLO · 2014 to 2023
$4.5M
Characterization of IL36, a novel cytokineR21AI096278 · NIAID · UNIVERSITY OF CALIFORNIA-IRVINE · PI ZLOTNIK, ALBERT · 2011 to 2012
$406k
NIAID NIH HHS R01 AI105813NIAID NIH HHS R21 AI096278PHS HHS R21096278
6 · The paper itself

Abstract

We have identified Tspan33 as a gene encoding a transmembrane protein exhibiting a restricted expression pattern including expression in activated B cells. TSPAN33 is a member of the tetraspanin family. TSPAN33 is not expressed in resting B cells, but is strongly induced in primary human B cells following activation. Human 2E2 cells, a Burkitt's lymphoma-derived B cell model of activation and differentiation, also upregulate TSPAN33 upon activation. TSPAN33 is expressed in several lymphomas including Hodgkin's and Diffuse large B cell lymphoma. TSPAN33 is also expressed in some autoimmune diseases where B cells participate in the pathology, including rheumatoid arthritis patients, systemic lupus erythematosus (SLE), and in spleen B cells from MRL/Fas(lpr/lpr) mice (a mouse model of SLE). We conclude that TSPAN33 may be used as a diagnostic biomarker or as a target for therapeutic antibodies for treatment of certain B cell lymphomas or autoimmune diseases.

Indexed as

AnimalsBiomarkersB-LymphocytesCase-Control StudiesCell LineFemaleGene Expression ProfilingGene Expression RegulationHumansLipopolysaccharidesLupus Erythematosus, SystemicLymphocyte ActivationMaleMiceMice, TransgenicOrgan SpecificityBiomarkersLipopolysaccharidesTetradecanoylphorbol AcetateTetraspaninsTSPAN33 protein, humanB cell maturation antigenB cellsBCMABIGEBiomarkerBLbody index of gene expression (database)Burkitt's lymphomaDiffuse large B cell lymphomaDLBCLHLHodgkin's lymphomaLupus erythematosusLymphomaNHLnon-Hodgkin's lymphomaRArheumatoid arthritisRheumatoid arthritisSLEsystemic lupus erythematosustetraspanin 33Tetraspanin 33TSPAN33

Identifiers

PMID24211713
PMCPMC3956131
OpenAlexW2144078707

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.