Evidence map›Paper›PMID 41166286›Full record

ArticleAnalytical chemistry2025

Development of a Novel Homogeneous Liposome-Based One-Step Assay for SARS-CoV-2 Antibody Detection in Human Serum Based on Fluorescent Liposomes and Complement Activity.

Christina Reiner, Kilian Hoecherl, Sebastian Einhauser, Simon Streif, Clemens Spitzenberg, Johannes Konrad, Patrick Neckermann, Miriam Breunig, Diana Pauly, Ralf Wagner and 1 more

Abstract read
In one paragraph

Article in Analytical chemistry, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Article
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.

Christina ReinerInstitute of Analytical Chemistry, Chemo- and Biosensors, University of Regensburg, Universitaetsstr. 31, Regensburg 93053, Germany.ORCID 0009-0006-6683-7091
Kilian HoecherlInstitute of Analytical Chemistry, Chemo- and Biosensors, University of Regensburg, Universitaetsstr. 31, Regensburg 93053, Germany.
Sebastian EinhauserInstitute of Medical Microbiology & Hygiene, Molecular Microbiology (Virology), University of Regensburg, Franz-Joseph-Strauss-Allee 11, Regensburg 93053, Germany.
Simon StreifInstitute of Analytical Chemistry, Chemo- and Biosensors, University of Regensburg, Universitaetsstr. 31, Regensburg 93053, Germany.ORCID 0000-0001-6081-7571
Clemens SpitzenbergInstitute of Analytical Chemistry, Chemo- and Biosensors, University of Regensburg, Universitaetsstr. 31, Regensburg 93053, Germany.
Johannes KonradDepartment of Pharmaceutical Technology, University of Regensburg, Universitaetsstr. 31, Regensburg 93053, Germany.ORCID 0009-0003-2261-1398
Patrick NeckermannInstitute of Medical Microbiology & Hygiene, Molecular Microbiology (Virology), University of Regensburg, Franz-Joseph-Strauss-Allee 11, Regensburg 93053, Germany.
Miriam BreunigDepartment of Pharmaceutical Technology, University of Regensburg, Universitaetsstr. 31, Regensburg 93053, Germany.ORCID 0000-0002-1320-6820
Diana PaulyExperimental Ophthalmology, University of Marburg, Baldingerstr., Marburg 35043, Germany.
Ralf WagnerInstitute of Medical Microbiology & Hygiene, Molecular Microbiology (Virology), University of Regensburg, Franz-Joseph-Strauss-Allee 11, Regensburg 93053, Germany.
Antje J BaeumnerInstitute of Analytical Chemistry, Chemo- and Biosensors, University of Regensburg, Universitaetsstr. 31, Regensburg 93053, Germany.ORCID 0000-0001-7148-3423

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Monitoring antibodies in patient serum enables the diagnosis of infectious and chronic diseases, the assessment of an individual's immune status, and possible protection against infection and could thus be a ubiquitous tool for pandemic preparedness and personalized medicine. Advancing from the traditional enzyme-linked immunosorbent assay (ELISA), a homogeneous assay format was developed that simplifies assay procedures and enables a wash-free one-step performance. SARS-CoV-2 was chosen as the model virus, and its Spike protein-derived receptor binding domain (RBD) was covalently coupled to fluorescent liposomes. The binding of patient antibodies triggered the complement system, led to liposome lysis, and allowed quantitative fluorescent detection. The liposome assay was optimized with respect to liposome lipid composition, RBD coverage and surface chemistry, incubation conditions, and pretreatment of a standardized complement source. A proof-of-principle was demonstrated through artificially supplemented anti-RBD antibodies and full titrations with known positive sera. Testing of 37 SARS-CoV-2 negative sera and 28 sera from individuals with SARS-CoV-2 (breakthrough) infections resulted in a specificity of 95%, sensitivity of 93% and an excellent correlation (

Indexed as

Antibodies, ViralComplement System ProteinsCOVID-19LiposomesSARS-CoV-2Enzyme-Linked Immunosorbent AssayFluorescent DyesHumansSpike Glycoprotein, CoronavirusAntibodies, ViralComplement System ProteinsFluorescent DyesLiposomesSpike Glycoprotein, Coronavirusspike protein, SARS-CoV-2

Identifiers

PMID41166286
PMCPMC12613147

What OpenQuestion holds

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LicenceCC BY
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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.