Evidence map›Paper›PMID 35947526›Full record

ArticleeLife2022

Soluble MAC is primarily released from MAC-resistant bacteria that potently convert complement component C5.

Dennis J Doorduijn, Marie V Lukassen, Marije F L van 't Wout, Vojtech Franc, Maartje Ruyken, Bart W Bardoel, Albert J R Heck, Suzan H M Rooijakkers

Open access · goldAbstract read
In one paragraph

Article in eLife, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.4field-weighted citation impact, top 20% 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

13 citing papers in PubMed, 18 citations in OpenAlex.

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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

8 authors at 2 institutions in 1 country.

Dennis J DoorduijnDepartment of Medical Microbiology, University Medical Center Utrecht, Utrecht, Netherlands.ORCID 0000-0002-1679-5739
Marie V LukassenBiomolecular Mass Spectrometry and Proteomics, Bijvoet Center for Biomolecular Research and Utrecht Institute for Pharmaceutical Sciences, University of Utrecht, Utrecht, Netherlands.ORCID 0000-0003-3237-2696
Marije F L van 't WoutDepartment of Medical Microbiology, University Medical Center Utrecht, Utrecht, Netherlands.
Vojtech FrancBiomolecular Mass Spectrometry and Proteomics, Bijvoet Center for Biomolecular Research and Utrecht Institute for Pharmaceutical Sciences, University of Utrecht, Utrecht, Netherlands.
Maartje RuykenDepartment of Medical Microbiology, University Medical Center Utrecht, Utrecht, Netherlands.
Bart W BardoelDepartment of Medical Microbiology, University Medical Center Utrecht, Utrecht, Netherlands.ORCID 0000-0001-6450-277X
Albert J R HeckBiomolecular Mass Spectrometry and Proteomics, Bijvoet Center for Biomolecular Research and Utrecht Institute for Pharmaceutical Sciences, University of Utrecht, Utrecht, Netherlands.ORCID 0000-0002-2405-4404
Suzan H M RooijakkersDepartment of Medical Microbiology, University Medical Center Utrecht, Utrecht, Netherlands.ORCID 0000-0003-4102-0377
University Medical Center Utrecht · NLUtrecht University · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The membrane attack complex (MAC or C5b-9) is an important effector of the immune system to kill invading microbes. MAC formation is initiated when complement enzymes on the bacterial surface convert complement component C5 into C5b. Although the MAC is a membrane-inserted complex, soluble forms of MAC (sMAC), or terminal complement complex (TCC), are often detected in sera of patients suffering from infections. Consequently, sMAC has been proposed as a biomarker, but it remains unclear when and how it is formed during infections. Here, we studied mechanisms of MAC formation on different Gram-negative and Gram-positive bacteria and found that sMAC is primarily formed in human serum by bacteria resistant to MAC-dependent killing. Surprisingly, C5 was converted into C5b more potently by MAC-resistant compared to MAC-sensitive

Indexed as

Complement C5Escherichia coli InfectionsComplement ActivationComplement Membrane Attack ComplexEscherichia coliGram-Positive BacteriaHumansVitronectinComplement C5Complement Membrane Attack ComplexVitronectinC5complementE. coliEscherichia coliimmunologyinflammationmembrane attack complexStaphylococcusterminal complement complex

Identifiers

PMID35947526
PMCPMC9402229
OpenAlexW4293105758

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.