Evidence map›Paper›PMID 42643423›Full record

ArticleFrontiers in immunology2026

Point-of-care assessment of complement activation in the ICU: a feasibility study of rapid terminal complement complex detection in critical illness.

Tam Cung, Søren Erik Pischke, Camilla Schjalm, Bettina Mülleder, Loek Willems, Max Sonnleitner, Erik J M Toonen, Tom Eirik Mollnes, Andreas Barratt-Due

Erratum issuedAbstract read
In one paragraph

Article in Frontiers in immunology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors.

Tam CungDepartment of Immunology, Oslo University Hospital and University of Oslo, Oslo, Norway.
Søren Erik PischkeDepartment of Immunology, Oslo University Hospital and University of Oslo, Oslo, Norway.
Camilla SchjalmDepartment of Immunology, Oslo University Hospital and University of Oslo, Oslo, Norway.
Bettina MüllederGENSPEED Biotech GmbH, Rainbach im Mühlkreis, Austria.
Loek WillemsResearch and Development Department, Hycult Biotechnology, Uden, Netherlands.
Max SonnleitnerGENSPEED Biotech GmbH, Rainbach im Mühlkreis, Austria.
Erik J M ToonenResearch and Development Department, Hycult Biotechnology, Uden, Netherlands.
Tom Eirik MollnesDepartment of Immunology, Oslo University Hospital and University of Oslo, Oslo, Norway.
Andreas Barratt-DueDepartment of Immunology, Oslo University Hospital and University of Oslo, Oslo, Norway.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Complement activation is increasingly recognized as a key driver in various critical diseases and a potential therapeutic target. However, conventional enzyme-linked immunosorbent assays (ELISAs) for complement protein detection are laboratory-bound and unsuitable for rapid clinical decision-making in the emergency and intensive care unit setting. We evaluated the feasibility of a point-of-care (POC) multiplex micro-ELISA for complement component C3, activation marker C3d and the soluble terminal complement complex (TCC) in a heterogeneous intensive care unit (ICU) population. Method: Thirty-eight critically ill and three cardiopulmonary bypass patients were prospectively enrolled. Fifteen age- and sex-matched healthy volunteers served as controls. Plasma samples collected at ICU admission and days 2-4 were analyzed using a novel POC multiplex micro-ELISA platform and compared with established in-house and commercial ELISAs using Spearman rank correlation and receiver operating characteristic (ROC) analysis. Additional complement activation markers (C3bc, C3bBbP, C1s/C1-INH, MASP-1/C1-INH and C4d) were assessed to explore specific pathway involvement. Results: TCC levels were significantly elevated in patients (median 3575, IQR 2048-6504 mAU/ml) compared with controls (median 1286, IQR 1032-1903 mAU/ml; Conclusion: Point-of-care TCC quantification is feasible, correlates well with established ELISAs and accurately identifies elevated TCC levels in critically ill patients. Although formal method-comparison analyses were not possible to establish, TCC emerged as the most robust marker of complement activation in this ICU cohort using the evaluated POC prototype. POC testing may facilitate timely identification of complement activation in acute care settings and support integration of complement-directed diagnostics and therapeutics into clinical workflows.

Indexed as

Complement ActivationComplement Membrane Attack ComplexPoint-of-Care SystemsPoint-of-Care TestingAdultAgedBiomarkersComplement C3Critical IllnessEnzyme-Linked Immunosorbent AssayFeasibility StudiesFemaleHumansIntensive Care UnitsMaleMiddle AgedBiomarkersComplement C3Complement Membrane Attack ComplexC3C3dcomplement system activationcritical illnessintensive carepoint-of-care measurementTCCterminal complement complex

Identifiers

PMID42643423
PMCPMC13503546

What OpenQuestion holds

Textmetadata
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.