Evidence map›Paper›PMID 10651389›Full record

ReviewDrugs1999

Daclizumab: a review of its use in the prevention of acute rejection in renal transplant recipients.

L R Wiseman, D Faulds

Erratum issuedAbstract readReview
PubMed Publisher
In one paragraph

Review in Drugs, 1999. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
4.6field-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

17 citing papers in PubMed, 71 citations in OpenAlex.

  1. Trial
  2. Article
  3. Review
  4. Therapeutic Antibodies in Medicine.Molecules (Basel, Switzerland) · 2023
    Review
  5. Review
  6. Review
  7. Thrombotic microangiopathy in haematopoietic cell transplantation: an update.Mediterranean journal of hematology and infectious diseases · 2010
    Article
  8. Intravenous daclizumab for recalcitrant ocular inflammatory disease.Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie · 2009
    Article
  9. Review
  10. Structural biology of shared cytokine receptors.Annual review of immunology · 2009
    Review
  11. Review
  12. Review
  13. Article
  14. Review
  15. Small intestinal transplantation.Current gastroenterology reports · 2001
    Review
  16. Advances in interleukin 2 receptor targeted treatment.Annals of the rheumatic diseases · 2000
    Review
  17. Review
4 · The record

Corrections and comments

  • Erratum issued
5 · Who and what money

Authors and funding

2 authors.

L R WisemanAdis International Limited, Mairangi Bay, Auckland, New Zealand. demail@adis.co.nz
D Faulds

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

unlabelledThe humanised monoclonal antibody daclizumab is an immunosuppressive agent that reduces acute rejection in renal transplant recipients. It is specific for the alpha subunit (Tac/CD25) of the interleukin-2 (IL-2) receptor on activated T cells and achieves immunosuppression by competitive antagonism of IL-2-induced T cell proliferation. Daclizumab has advantages over murine antibodies to the IL-2 receptor, including improved effector function, a low potential for immunogenicity and long elimination half-life. When added to standard cyclosporin-based immunosuppressive therapy with or without azathioprine, daclizumab (1 mg/kg prior to surgery and once every 2 weeks thereafter for a total of 5 doses) significantly reduced the 6-month rate of acute rejection compared with placebo in 2 phase III studies. The mean number of rejection episodes was significantly reduced and the time to first acute rejection significantly increased in daclizumab versus placebo recipients. Patient survival at 1 year after transplantation was significantly higher with daclizumab than placebo in 1 study and showed a trend in favour of the drug in the other study. The 1-year graft survival rate tended to be greater in daclizumab than in placebo recipients in both studies, In a phase II study, acute rejection rates in patients treated with both daclizumab and mycophenolate mofetil (plus standard cyclosporin-based immunosuppression) were lower than those achieved with mycophenolate mofetil alone. Preliminary results indicate that daclizumab is also a useful agent in paediatric renal transplant recipients. Further investigation of the efficacy and tolerability of the drug in this patient group is clearly warranted. Daclizumab does not increase the incidence of adverse events when added to standard cyclosporin-based therapy. The incidence of opportunistic infections, lymphoproliferative disorders and malignancies was not increased above that seen with placebo.

conclusionsAlthough the effects of daclizumab on long term graft and patient survival require further investigation, available data indicate that daclizumab is an important advance in renal transplant immunosuppression, reducing acute graft rejection without affecting the tolerability of standard cyclosporin-based immunosuppression.

Indexed as

Acute DiseaseAntibodies, MonoclonalAntibodies, Monoclonal, HumanizedDaclizumabGraft RejectionHumansImmunoglobulin GImmunosuppressive AgentsKidney TransplantationAntibodies, MonoclonalAntibodies, Monoclonal, HumanizedDaclizumabImmunoglobulin GImmunosuppressive Agents

Identifiers

PMID10651389
OpenAlexW1990612749

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.