Evidence map›Paper›PMID 12067300›Full record

ArticleClinical and experimental immunology2002

Potential role of phosphodiesterase 7 in human T cell function: comparative effects of two phosphodiesterase inhibitors.

A Nakata, K Ogawa, T Sasaki, N Koyama, K Wada, J Kotera, H Kikkawa, K Omori, O Kaminuma

Open access · greenAbstract readComparative Study
In one paragraph

Article in Clinical and experimental immunology, 2002. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
1.4field-weighted citation impact, top 20% 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

22 citing papers in PubMed, 71 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Review
  5. The Role of PDE8 in T Cell Recruitment and Function in Inflammation.Frontiers in cell and developmental biology · 2021
    Review
  6. New Avenues for Phosphodiesterase Inhibitors in Asthma.Journal of experimental pharmacology · 2021
    Review
  7. Review
  8. Article
  9. The future of bronchodilation: looking for new classes of bronchodilators.European respiratory review : an official journal of the European Respiratory Society · 2019
    Review
  10. Article
  11. Review
  12. Article
  13. Article
  14. Review
  15. Article
  16. Article
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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

9 authors at 1 institution in 1 country.

A NakataDiscovery Research Laboratory, Tanabe Seiyaku Co. Ltd, Saitama, Japan. a-nakata@tanabe.co.jp
K Ogawa
T Sasaki
N Koyama
K Wada
J Kotera
H Kikkawa
K Omori
O Kaminuma
Teikoku Seiyaku (Japan) · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Even though the existence of phosphodiesterase (PDE) 7 in T cells has been proved, the lack of a selective PDE7 inhibitor has confounded an accurate assessment of PDE7 function in such cells. In order to elucidate the role of PDE7 in human T cell function, the effects of two PDE inhibitors on PDE7A activity, cytokine synthesis, proliferation and CD25 expression of human peripheral blood mononuclear cells (PBMC) were determined. Recombinant human PDE7A was obtained and subjected to cyclic AMP-hydrolysis assay. PBMC of Dermatophagoides farinae mite extract (Df)-sensitive donors were stimulated with the relevant antigen or an anti-CD3 monoclonal antibody (MoAb). PBMC produced IL-5 and proliferated in response to stimulation with Df, while stimulation with anti-CD3 MoAb induced CD25 expression and messenger RNA (mRNA) synthesis of IL-2, IL-4 and IL-5 in peripheral T cells. A PDE inhibitor, T-2585, which suppressed PDE4 isoenzyme with high potency (IC50 = 0.00013 microM) and PDE7A with low potency (IC50 = 1.7 microM) inhibited cytokine synthesis, proliferation and CD25 expression in the dose range at which the drug suppressed PDE7A activity. A potent selective inhibitor of PDE4 (IC50 = 0.00031 microM), RP 73401, which did not effectively suppress PDE7A (IC50 > 10 microM), inhibited the Df- and anti-CD3 MoAb-stimulated responses only weakly, even at 10 microM. PDE7 may play a critical role in the regulation of human T cell function, and thereby selective PDE7 inhibitors have the potential to be used to treat immunological and inflammatory disorders.

Indexed as

3',5'-Cyclic-AMP PhosphodiesterasesAnimalsAntigens, DermatophagoidesBenzamidesCell DivisionCells, CulturedChlorocebus aethiopsCOS CellsCyclic Nucleotide Phosphodiesterases, Type 7Cysteine EndopeptidasesGene ExpressionGlycoproteinsHumansInterleukin-2Interleukin-4Interleukin-53',5'-Cyclic-AMP PhosphodiesterasesAntigens, DermatophagoidesBenzamidesCyclic Nucleotide Phosphodiesterases, Type 7Cysteine EndopeptidasesGlycoproteinsInterleukin-2Interleukin-4Interleukin-5IsoenzymesPDE7A protein, humanPhosphodiesterase InhibitorsPhthalazinespiclamilastPyridinesReceptors, Interleukin-2RNA, MessengerT 2585

Identifiers

PMID12067300
PMCPMC1906253
OpenAlexW2092143137

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.