Evidence map›Paper›PMID 24853370›Full record

ArticleClinical and experimental immunology2014

A novel method for direct measurement of complement convertases activity in human serum.

A M Blom, E B Volokhina, V Fransson, P Strömberg, L Berghard, M Viktorelius, T E Mollnes, M López-Trascasa, L P van den Heuvel, T H Goodship and 2 more

Abstract read
In one paragraph

Article in Clinical and experimental immunology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
–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

30 citing papers in PubMed.

  1. Article
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  5. Review
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  8. Clinical Isolates ofFrontiers in immunology · 2022
    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

12 authors.

A M BlomDepartment of Laboratory Medicine Malmö, Lund University, Malmö, Sweden.
E B Volokhina
V Fransson
P Strömberg
L Berghard
M Viktorelius
T E Mollnes
M López-Trascasa
L P van den Heuvel
T H Goodship
K J Marchbank
M Okroj

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Complement convertases are enzymatic complexes that play a central role in sustaining and amplification of the complement cascade. Impairment of complement function leads directly or indirectly to pathological conditions, including higher infection rate, kidney diseases, autoimmune- or neurodegenerative diseases and ischaemia-reperfusion injury. An assay for direct measurement of activity of the convertases in patient sera is not available. Existing assays testing convertase function are based on purified complement components and, thus, convertase formation occurs under non-physiological conditions. We designed a new assay, in which C5 blocking compounds enabled separation of the complement cascade into two phases: the first ending at the stage of C5 convertases and the second ending with membrane attack complex formation. The use of rabbit erythrocytes or antibody-sensitized sheep erythrocytes as the platforms for convertase formation enabled easy readout based on measurement of haemolysis. Thus, properties of patient sera could be studied directly regarding convertase activity and membrane attack complex formation. Another advantage of this assay was the possibility to screen for host factors such as C3 nephritic factor and other anti-complement autoantibodies, or gain-of-function mutations, which prolong the half-life of complement convertases. Herein, we present proof of concept, detailed description and validation of this novel assay.

Indexed as

AnimalsAutoantibodiesComplement C3-C5 ConvertasesComplement C3 Nephritic FactorComplement Pathway, AlternativeComplement System ProteinsErythrocytesGuinea PigsHalf-LifeHumansImmunoassayRabbitsSheepAutoantibodiesComplement C3-C5 ConvertasesComplement C3 Nephritic FactorComplement System Proteinscomplement systemconvertaseeculizumabOmCI

Identifiers

PMID24853370
PMCPMC4360204

What OpenQuestion holds

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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.