Evidence map›Paper›PMID 36217774›Full record

ReviewImmunological reviews2023

Low-molecular weight inhibitors of the alternative complement pathway.

Anna Schubart, Stefanie Flohr, Tobias Junt, Jörg Eder

Open access · hybridAbstract readReview
In one paragraph

Review in Immunological reviews, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
2.5field-weighted citation impact, top 10% 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

20 citing papers in PubMed, 30 citations in OpenAlex.

  1. Trial
  2. Bioorthogonal tuning of nanosurface opsonisationChemical communications (Cambridge, England) · 2026
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  8. Review
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  11. Role of Complement in Liver Diseases.Seminars in liver disease · 2024
    Review
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  13. Article
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  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

4 authors at 1 institution in 1 country.

Anna SchubartNovartis Institutes for BioMedical Research, Basel, Switzerland.ORCID 0000-0003-4253-0600
Stefanie FlohrNovartis Institutes for BioMedical Research, Basel, Switzerland.ORCID 0000-0003-3317-5811
Tobias JuntNovartis Institutes for BioMedical Research, Basel, Switzerland.ORCID 0000-0003-0260-8346
Jörg EderNovartis Institutes for BioMedical Research, Basel, Switzerland.ORCID 0000-0001-7152-8417
Novartis (Switzerland) · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Dysregulation of the alternative complement pathway predisposes individuals to a number of diseases. It can either be evoked by genetic alterations in or by stabilizing antibodies to important pathway components and typically leads to severe diseases such as paroxysmal nocturnal hemoglobinuria, atypical hemolytic uremic syndrome, C3 glomerulopathy, and age-related macular degeneration. In addition, the alternative pathway may also be involved in many other diseases where its amplifying function for all complement pathways might play a role. To identify specific alternative pathway inhibitors that qualify as therapeutics for these diseases, drug discovery efforts have focused on the two central proteases of the pathway, factor B and factor D. Although drug discovery has been challenging for a number of reasons, potent and selective low-molecular weight (LMW) oral inhibitors have now been discovered for both proteases and several molecules are in clinical development for multiple complement-mediated diseases. While the clinical development of these inhibitors initially focuses on diseases with systemic and/or peripheral tissue complement activation, the availability of LMW inhibitors may also open up the prospect of inhibiting complement in the central nervous system where its activation may also play an important role in several neurodegenerative diseases.

Indexed as

Atypical Hemolytic Uremic SyndromeComplement Pathway, AlternativeComplement ActivationComplement Factor DComplement System ProteinsHumansMolecular WeightComplement Factor DComplement System Proteinsalternative complement pathway; complement factor Bcomplement factor Dcomplement therapeuticsdrug discoverylow-molecular weight inhibitor

Identifiers

PMID36217774
PMCPMC10092480
OpenAlexW4304175728

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.