Evidence map›Paper›PMID 28932227›Full record

ArticleFrontiers in immunology2017

Targeted Delivery of Neutralizing Anti-C5 Antibody to Renal Endothelium Prevents Complement-Dependent Tissue Damage.

Paolo Durigutto, Daniele Sblattero, Stefania Biffi, Luca De Maso, Chiara Garrovo, Gabriele Baj, Federico Colombo, Fabio Fischetti, Antonio F Di Naro, Francesco Tedesco and 1 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.2field-weighted citation impact, top 22% 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

14 citing papers in PubMed, 25 citations in OpenAlex.

  1. Review
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  8. Frontiers in immunology · 2021
    Article
  9. Review
  10. Drug Development in Pemphigoid Diseases.Acta dermato-venereologica · 2020
    Review
  11. Review
  12. Review
  13. Review
  14. Tissue-targeted complement therapeutics.Molecular immunology · 2018
    Review
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

11 authors at 3 institutions in 1 country.

Paolo DuriguttoDepartment of Life Sciences, University of Trieste, Trieste, Italy.
Daniele SblatteroDepartment of Life Sciences, University of Trieste, Trieste, Italy.
Stefania BiffiInstitute for Maternal and Child Health-IRCCS "Burlo Garofolo", Trieste, Italy.
Luca De MasoDepartment of Life Sciences, University of Trieste, Trieste, Italy.
Chiara GarrovoInstitute for Maternal and Child Health-IRCCS "Burlo Garofolo", Trieste, Italy.
Gabriele BajDepartment of Life Sciences, University of Trieste, Trieste, Italy.
Federico ColomboDepartment of Life Sciences, University of Trieste, Trieste, Italy.
Fabio FischettiDipartimento Universitario Clinico di Scienze Mediche, Chirurgiche e della Salute, University of Trieste, Trieste, Italy.
Antonio F Di NaroADIENNE Pharma & Biotech, Lugano, Switzerland.
Francesco TedescoIRCCS Istituto Auxologico Italiano, Milan, Italy.
Paolo MacorDepartment of Life Sciences, University of Trieste, Trieste, Italy.
University of Trieste · ITIRCCS Materno Infantile Burlo Garofolo · ITIRCCS Istituto Auxologico Italiano · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Complement activation is largely implicated in the pathogenesis of several clinical conditions and its therapeutic neutralization has proven effective in preventing tissue and organ damage. A problem that still needs to be solved in the therapeutic control of complement-mediated diseases is how to avoid side effects associated with chronic neutralization of the complement system, in particular, the increased risk of infections. We addressed this issue developing a strategy based on the preferential delivery of a C5 complement inhibitor to the organ involved in the pathologic process. To this end, we generated Ergidina, a neutralizing recombinant anti-C5 human antibody coupled with a cyclic-RGD peptide, with a distinctive homing property for ischemic endothelial cells and effective in controlling tissue damage in a rat model of renal ischemia/reperfusion injury (IRI). As a result of its preferential localization on renal endothelium, the molecule induced complete inhibition of complement activation at tissue level, and local protection from complement-mediated tissue damage without affecting circulating C5. The

Indexed as

complement systemex vivo modelin vivo modelischemia/reperfusion injurytargeted antibody-based therapy

Identifiers

PMID28932227
PMCPMC5592221
OpenAlexW2751063651

What OpenQuestion holds

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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.