Evidence map›Paper›PMID 20345978›Full record

ReviewClinical and experimental immunology2010

Cyclophilin-CD147 interactions: a new target for anti-inflammatory therapeutics.

V Yurchenko, S Constant, E Eisenmesser, M Bukrinsky

Open access · bronzeAbstract readReview
In one paragraph

Review in Clinical and experimental immunology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 134 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
134citing papers in PubMed, 2 pooled it
6.0field-weighted citation impact, top 3% 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

134 citing papers in PubMed, 2 syntheses or guidelines pooled it, 244 citations in OpenAlex.

  1. SARS-CoV-2 cell entry beyond the ACE2 receptor.Molecular biology reports · 2022
    Pooled it
  2. Calprotectin (S100A8/S100A9): a key protein between inflammation and cancer.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2018
    Pooled it
  3. Article
  4. Article
  5. Review
  6. Review
  7. Review
  8. CD147/Basigin: From Integrative Molecular Hub to Translational Therapeutic Target.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Review
  9. Article
  10. Review
  11. Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Review
  18. Article
  19. Article
  20. Review

74 more citing papers are in PubMed but not listed here.

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 4 institutions in 1 country.

V YurchenkoRockefeller University, New York, NY, USA.
S Constant
E Eisenmesser
M Bukrinsky
George Washington University · USRockefeller University · USUniversity of Colorado Denver · USWashington University in St. Louis · US

Funding

Contribution of cyclophilins to leukocyte recruitment in lung inflammationR01AI067254 · NIAID · GEORGE WASHINGTON UNIVERSITY · PI BUKRINSKY, MICHAEL ILYA · 2006 to 2009
$1.3M
Cyclophilin-CD147 interaction in autoimmune arthritisR56AI081152 · NIAID · GEORGE WASHINGTON UNIVERSITY · PI BUKRINSKY, MICHAEL ILYA, CONSTANT, STEPHANIE L · 2009 to 2010
$783k
Leukocyte recruitment by cyclophilin-CD147 interactionR21AI060720 · NIAID · GEORGE WASHINGTON UNIVERSITY · PI BUKRINSKY, MICHAEL ILYA · 2004 to 2005
$421k
NIAID NIH HHS AI067254NIAID NIH HHS AI081152NIAID NIH HHS R01 AI067254NIAID NIH HHS R01 AI081152NIAID NIH HHS R21 AI060720NIAID NIH HHS R56 AI081152
6 · The paper itself

Abstract

CD147 is a widely expressed plasma membrane protein that has been implicated in a variety of physiological and pathological activities. It is best known for its ability to function as extracellular matrix metalloproteinase inducer (hence the other name for this protein, EMMPRIN), but has also been shown to regulate lymphocyte responsiveness, monocarboxylate transporter expression and spermatogenesis. These functions reflect multiple interacting partners of CD147. Among these CD147-interacting proteins cyclophilins represent a particularly interesting class, both in terms of structural considerations and potential medical implications. CD147 has been shown to function as a signalling receptor for extracellular cyclophilins A and B and to mediate chemotactic activity of cyclophilins towards a variety of immune cells. Recent studies using in vitro and in vivo models have demonstrated a role for cyclophilin-CD147 interactions in the regulation of inflammatory responses in a number of diseases, including acute lung inflammation, rheumatoid arthritis and cardiovascular disease. Agents targeting either CD147 or cyclophilin activity showed significant anti-inflammatory effects in experimental models, suggesting CD147-cyclophilin interactions may be a good target for new anti-inflammatory therapeutics. Here, we review the recent literature on different aspects of cyclophilin-CD147 interactions and their role in inflammatory diseases.

Indexed as

Acute Lung InjuryAnimalsAnti-Inflammatory AgentsArthritis, RheumatoidBasiginCardiovascular DiseasesCyclophilin ACyclophilinsDisease Models, AnimalDrug Delivery SystemsFemaleHumansInflammationMaleMonocarboxylic Acid TransportersAnti-Inflammatory AgentsBasiginBSG protein, humanCyclophilin Acyclophilin BCyclophilinsMonocarboxylic Acid Transporters

Identifiers

PMID20345978
PMCPMC2883100
OpenAlexW2112659240

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.