Evidence map›Paper›PMID 33115535›Full record

ArticleActa neuropathologica communications2020

Targeted deletions of complement lectin pathway genes improve outcome in traumatic brain injury, with MASP-2 playing a major role.

D Mercurio, M Oggioni, S Fumagalli, N J Lynch, S Roscher, D Minuta, C Perego, S Ippati, R Wallis, W J Schwaeble and 1 more

Open access · goldAbstract read
In one paragraph

Article in Acta neuropathologica communications, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.4field-weighted citation impact, top 14% 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

15 citing papers in PubMed, 24 citations in OpenAlex.

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  10. Review
  11. Article
  12. Tackling Neuroinflammation After Traumatic Brain Injury: Complement Inhibition as a Therapy for Secondary Injury.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2023
    Review
  13. 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

11 authors at 4 institutions in 2 countries.

D MercurioDepartment of Neuroscience, Istituto di Ricerche Farmacologiche Mario Negri IRCCS, via Mario Negri 2, 20156, Milan, Italy.ORCID 0000-0001-5101-7222
M OggioniDepartment of Neuroscience, Istituto di Ricerche Farmacologiche Mario Negri IRCCS, via Mario Negri 2, 20156, Milan, Italy.
S FumagalliDepartment of Neuroscience, Istituto di Ricerche Farmacologiche Mario Negri IRCCS, via Mario Negri 2, 20156, Milan, Italy.
N J LynchDepartment of Neuroscience, Istituto di Ricerche Farmacologiche Mario Negri IRCCS, via Mario Negri 2, 20156, Milan, Italy.
S RoscherDepartment of Respiratory Sciences, University of Leicester, University Road, LE1 9HN, Leicester, UK.
D MinutaDepartment of Neuroscience, Istituto di Ricerche Farmacologiche Mario Negri IRCCS, via Mario Negri 2, 20156, Milan, Italy.
C PeregoDepartment of Neuroscience, Istituto di Ricerche Farmacologiche Mario Negri IRCCS, via Mario Negri 2, 20156, Milan, Italy.
S IppatiDepartment of Neuroscience, Istituto di Ricerche Farmacologiche Mario Negri IRCCS, via Mario Negri 2, 20156, Milan, Italy.
R WallisDepartment of Respiratory Sciences, University of Leicester, University Road, LE1 9HN, Leicester, UK.
W J SchwaebleDepartment of Veterinary Medicine, University of Cambridge, Madingley Road, CB3 0ES, Cambridge, UK.
M-G De SimoniDepartment of Neuroscience, Istituto di Ricerche Farmacologiche Mario Negri IRCCS, via Mario Negri 2, 20156, Milan, Italy. desimoni@marionegri.it.ORCID 0000-0001-6695-5297
Mario Negri Institute for Pharmacological Research · ITUniversity of Leicester · GBUniversity of Cambridge · GBVita-Salute San Raffaele University · IT

Funding

Medical Research Council G0700859Medical Research Council G1000191Medical Research Council (MRC) MR/R002983/1
6 · The paper itself

Abstract

The lectin pathway (LP) of complement activation is believed to contribute to brain inflammation. The study aims to identify the key components of the LP contributing to TBI outcome as possible novel pharmacological targets. We compared the long-term neurological deficits and neuropathology of wild-type mice (WT) to that of mice carrying gene deletions of key LP components after experimental TBI. WT or MASP-2 (Masp2

Indexed as

AnimalsBrainBrain Injuries, TraumaticCollectinsComplement C4bComplement Pathway, Mannose-Binding LectinFicolinsGene DeletionInflammationLectinsMannose-Binding LectinMannose-Binding Protein-Associated Serine ProteasesMiceMice, KnockoutPrognosisRecovery of FunctionColec11 protein, mouseCollectinsComplement C4bFicolinsLectinsMannose-Binding Lectinmannose binding protein AMannose-Binding Protein-Associated Serine ProteasesMASP-1 protein, mouseMASP-2 protein, mouseMbl2 protein, mouseComplement cascadeLectin pathwayMBL-associated serine proteaseNeuroinflammationNeurological deficitsPharmacological targetTraumatic brain injury

Identifiers

PMID33115535
PMCPMC7592565
OpenAlexW3096808898

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.