Evidence map›Paper›PMID 20631616›Full record

ReviewCurrent opinion in organ transplantation2010

Complement in organ transplantation.

Elham Asgari, Wuding Zhou, Steven Sacks

Registry-linked trialAbstract readReview
In one paragraph

Review in Current opinion in organ transplantation, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03791476 (A Phase I/II,Single Center,Randomized,Double-Blind,Placebo-Controlled Study to Evaluate the Feasibility of Using Human Recombinant C1 Inhibitor), which is not on this map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
4.1field-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.

NCT03791476 phase1unknown statusnot on this mapstarted 2019, after this paper: background citation

A Phase I/II,Single Center,Randomized,Double-Blind,Placebo-Controlled Study to Evaluate the Feasibility of Using Human Recombinant C1 Inhibitor(RUCONEST®) as a Therapeutic Strategy to Reduce the Incidence of Delayed Graft Function in Recipients of Kidneys From Donation After Cardio-Circulatory Death

TypeinterventionalSponsorUniversity of Wisconsin, MadisonRan2019 to 2022Enrolled20ConditionsKidney FailureArmsrhC1INH, Saline Solution
3 · Its place in the literature

Who cites it

27 citing papers in PubMed, 61 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Article
  4. Review
  5. Mouse Sertoli Cells Inhibit Humoral-Based Immunity.International journal of molecular sciences · 2022
    Article
  6. Review
  7. Article
  8. Article
  9. Review
  10. Targeted donor complement blockade after brain death prevents delayed graft function in a nonhuman primate model of kidney transplantation.American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons · 2020
    Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Review
  18. Complement in Action: An Analysis of Patent Trends from 1976 Through 2011.Advances in experimental medicine and biology · 2013
    Article
  19. Progress and Trends in Complement Therapeutics.Advances in experimental medicine and biology · 2013
    Article
  20. A novel role of complement in retinal degeneration.Investigative ophthalmology & visual science · 2012
    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

3 authors at 2 institutions in 1 country.

Elham AsgariMRC Centre for Transplantation, King's College London, Guy's Hospital, Great Maze Pond, London, UK.
Wuding Zhou
Steven Sacks
King's College London · GBGuy's Hospital · GB

Funding

Department of HealthMedical Research Council G0000771Medical Research Council G0000771(53621)Medical Research Council G0600892Medical Research Council G0601202Wellcome Trust
6 · The paper itself

Abstract

purpose of reviewThe aim of this review is to bring to attention the most recent advances made in understanding the role of complement components in both innate and adaptive immune responses in solid organ transplantation with emphasis on the kidney. RECENT

findingsAlongside recent findings related to the role of anaphylatoxins in modulating adaptive immune responses, there has been a genomic study to assess the expression of inflammatory markers in kidney transplantation, showing significant involvement of some complement molecules in predicting graft function. Modulators of complement pathway activity such as decay accelerating factor (CD55) and CD59 have also been shown to have a role in graft rejection. Potential new therapeutic targets related to complement proteins are being investigated. SUMMARY: The mechanism of rejection in solid organ transplantation is influenced by the initial inflammatory response and subsequent adaptive allo-immune response, both of which have been shown to be affected by various complement components. Due to limitations of existing treatments, new approaches are needed to better control these responses to improve graft survival. Built on an expanding knowledge of complement involvement, targeted blocking of the effector complement molecules and modulating the expression of complement inhibitors has suggested potentially useful approaches for reducing the effect of inflammatory damage from cold ischaemia as well as reducing the activation of the adaptive immune system related to complement.

Indexed as

Complement ActivationGraft SurvivalAdaptive ImmunityAnimalsComplement System ProteinsGraft RejectionHumansImmunity, InnateImmunosuppression TherapyInflammation MediatorsKidney TransplantationComplement System ProteinsInflammation Mediators

Identifiers

PMID20631616
PMCPMC3100572
OpenAlexW2033360547

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

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.