Evidence map›Paper›PMID 30220307›Full record

ReviewMolecular immunology2018

Tissue-targeted complement therapeutics.

Stephen Tomlinson, Joshua M Thurman

Abstract readReview
In one paragraph

Review in Molecular immunology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed, 2 pooled it
–field-weighted citation impact
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

20 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Review
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. A novel injury site-natural antibody targeted complement inhibitor protects against lung transplant injury.American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons · 2021
    Article
  14. Complement and Cancer-A Dysfunctional Relationship?Antibodies (Basel, Switzerland) · 2020
    Review
  15. Drug Development in Pemphigoid Diseases.Acta dermato-venereologica · 2020
    Review
  16. Review
  17. Article
  18. Complement and Complement Targeting Therapies in Glomerular Diseases.International journal of molecular sciences · 2019
    Review
  19. Combining MAP-1:CD35 or MAP-1:CD55 fusion proteins with pattern-recognition molecules as novel targeted modulators of the complement cascade.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2019
    Article
  20. Complement and CD4eLife · 2019
    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

2 authors.

Stephen TomlinsonDepartment of Microbiology and Immunology, Medical University of South Carolina, Charleston, SC, USA.
Joshua M ThurmanDivision of Nephrology and Hypertension, University of Colorado Denver, Aurora, CO, USA. Electronic address: joshua.thurman@ucdenver.edu.

Funding

The Complement System and Ischemic Acute Renal FailureR01DK076690 · NIDDK · UNIVERSITY OF COLORADO DENVER · PI Joshua M Thurman · 2008 to 2026
$6.6M
Graft-targeted anti-complement therapy to reduce cardiac graft injury and allograft vasculopathyU01AI132894 · NIAID · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI ATKINSON, CARL, TOMLINSON, STEPHEN · 2017 to 2021
$1.9M
Antibodies and complement in ischemia reperfusion injury and regenerationR01DK102912 · NIDDK · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI TOMLINSON, STEPHEN · 2015 to 2018
$1.7M
Immunologic Mechanisms of Progressive GlomerulosclerosisR01DK113586 · NIDDK · UNIVERSITY OF COLORADO DENVER · PI THURMAN, JOSHUA M · 2017 to 2020
$1.4M
Complement inhibitors targeted to the ischemic brain for the treatment of strokeR21NS097653 · NINDS · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI TOMLINSON, STEPHEN · 2017 to 2018
$706k
Novel Therapies to Improve Functional Recovery After StrokeI01RX001141 · VA · RALPH H JOHNSON VA MEDICAL CENTER · PI TOMLINSON, STEPHEN · 2014 to 2022
–
NIAID NIH HHS U01 AI132894NIDDK NIH HHS R01 DK076690NIDDK NIH HHS R01 DK102912NIDDK NIH HHS R01 DK113586NINDS NIH HHS R21 NS097653RRD VA I01 RX001141
6 · The paper itself

Abstract

Complement activation contributes to the pathogenesis of numerous inflammatory and autoimmune diseases. Therapeutic complement inhibitors have proven effective in several of these diseases and have now entered clinical use. Complement activation has multiple different biologic effects, however, and the currently available drugs can have undesirable side-effects, such as an increased risk of infection. Several different complement inhibitors have been developed that bind to target molecules, thereby concentrating the drug at a specific anatomic site. This approach appears to be both more effective than untargeted drugs and to have fewer side effects. In this article we review different targeting strategies that have been developed and the evidence supporting the use and benefits of targeted drugs.

Indexed as

Molecular Targeted TherapyComplement ActivationComplement Inactivating AgentsComplement System ProteinsHumansComplement Inactivating AgentsComplement System ProteinsComplementInflammationTargetedTherapeutics

Identifiers

PMID30220307
PMCPMC6146401

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.