Evidence map›Paper›PMID 36269894›Full record

ArticleAnalytical chemistry2022

Multiplex Hybrid Antigen-Capture LC-MRM Quantification in Sera and Nasal Lining Fluid of AZD7442, a SARS-CoV-2-Targeting Antibody Combination.

Ruipeng Mu, Yue Huang, Jerome Bouquet, Jiaqi Yuan, Robert J Kubiak, Eric Ma, Sami Naser, William R Mylott, Omnia A Ismaiel, Aaron M Wheeler and 6 more

Open access · hybridAbstract read
In one paragraph

Article in Analytical chemistry, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.3field-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

11 citing papers in PubMed, 15 citations in OpenAlex.

  1. Trial
  2. Trial
  3. LC-MS/MS method for quantifying the HIV-1 broadly neutralizing antibody PGT 121.414.LS in human serum.Journal of chromatography. B, Analytical technologies in the biomedical and life sciences · 2025
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  7. Article
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  10. Serum AZD7442 (tixagevimab-cilgavimab) concentrations andClinical & translational immunology · 2024
    Article
  11. 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

16 authors at 2 institutions in 2 countries.

Ruipeng MuIntegrated Bioanalysis, Clinical Pharmacology and Safety Sciences, R&D, AstraZeneca, South San Francisco, California 94080, United States.
Yue HuangIntegrated Bioanalysis, Clinical Pharmacology and Safety Sciences, R&D, AstraZeneca, South San Francisco, California 94080, United States.ORCID 0000-0003-2788-0856
Jerome BouquetIntegrated Bioanalysis, Clinical Pharmacology and Safety Sciences, R&D, AstraZeneca, South San Francisco, California 94080, United States.
Jiaqi YuanIntegrated Bioanalysis, Clinical Pharmacology and Safety Sciences, R&D, AstraZeneca, South San Francisco, California 94080, United States.
Robert J KubiakClinical Pharmacology and Quantitative Pharmacology, Clinical Pharmacology and Safety Sciences, R&D, AstraZeneca, Gaithersburg, Maryland 20878, United States.
Eric MaResearch and Development Biologics by LC-MS/MS, PPD Laboratories, Richmond, Virginia 23230, United States.
Sami NaserResearch and Development Biologics by LC-MS/MS, PPD Laboratories, Richmond, Virginia 23230, United States.
William R MylottResearch and Development Biologics by LC-MS/MS, PPD Laboratories, Richmond, Virginia 23230, United States.
Omnia A IsmaielResearch and Development Biologics by LC-MS/MS, PPD Laboratories, Richmond, Virginia 23230, United States.ORCID 0000-0003-3680-621X
Aaron M WheelerResearch and Development Biologics by LC-MS/MS, PPD Laboratories, Richmond, Virginia 23230, United States.
Rebecca BurkartResearch and Development Biologics by LC-MS/MS, PPD Laboratories, Richmond, Virginia 23230, United States.
Diego F CortesResearch and Development Biologics by LC-MS/MS, PPD Laboratories, Richmond, Virginia 23230, United States.
James BrutonResearch and Development Biologics by LC-MS/MS, PPD Laboratories, Richmond, Virginia 23230, United States.
Rosalinda H ArendsClinical Pharmacology and Quantitative Pharmacology, Clinical Pharmacology and Safety Sciences, R&D, AstraZeneca, Gaithersburg, Maryland 20878, United States.
Meina LiangIntegrated Bioanalysis, Clinical Pharmacology and Safety Sciences, R&D, AstraZeneca, South San Francisco, California 94080, United States.
Anton I RosenbaumIntegrated Bioanalysis, Clinical Pharmacology and Safety Sciences, R&D, AstraZeneca, South San Francisco, California 94080, United States.ORCID 0000-0003-1939-951X
AstraZeneca (United States) · USPharmaceutical Product Development (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

AZD7442 (tixagevimab [AZD8895]/cilgavimab [AZD1061]) is a monoclonal antibody (mAb) combination in development for the prevention and treatment of coronavirus disease 2019. Traditionally, bioanalysis of mAbs is performed using ligand binding assays (LBAs), which offer sensitivity, robustness, and ease of implementation. However, LBAs frequently require generation of critical reagents that typically take several months. Instead, we developed a highly sensitive (5 ng/mL limit of quantification) method using a hybrid LBA-liquid chromatography coupled with tandem mass spectrometry (LC-MS/MS) approach for quantification of the two codosed antibodies in serum and nasal lining fluid (NLF), a rare matrix. The method was optimized by careful selection of multiple reaction monitoring, capture reagents, magnetic beads, chromatographic conditions, evaluations of selectivity, and matrix effect. The final assay used viral spike protein receptor-binding domain as capture reagent and signature proteotypic peptides from the complementarity-determining region of each mAb for detection. In contrast to other methods of similar/superior sensitivity, our approach did not require multidimensional separations and can be operated in an analytical flow regime, ensuring high throughput and robustness required for clinical analysis at scale. The sensitivity of this method significantly exceeds typical sensitivity of ∼100 ng/mL for analytical flow 1D LBA-LC-MS/MS methods for large macromolecules, such as antibodies. Furthermore, infection and vaccination status did not impact method performance, ensuring method robustness and applicability to a broad patient population. This report demonstrated the general applicability of the hybrid LBA-LC-MS/MS approach to platform quantification of antibodies with high sensitivity and reproducibility, with specialized extension to matrices of increasing interest, such as NLF.

Indexed as

COVID-19Tandem Mass SpectrometryAntibodies, MonoclonalAntibodies, NeutralizingAntibodies, ViralChromatography, LiquidDrug CombinationsHumansIndicators and ReagentsReproducibility of ResultsSARS-CoV-2Antibodies, MonoclonalAntibodies, NeutralizingAntibodies, Viralcilgavimabcilgavimab and tixagevimab drug combinationDrug CombinationsIndicators and Reagentstixagevimab

Identifiers

PMID36269894
PMCPMC9631352
OpenAlexW4307028303

What OpenQuestion holds

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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.