Evidence map›Paper›PMID 26676731›Full record

ArticleInternational journal of oncology2016

Evaluation of a novel type of imaging probe based on a recombinant bivalent mini-antibody construct for detection of CD44v6-expressing squamous cell carcinoma.

Anna-Karin Haylock, Diana Spiegelberg, Anja C Mortensen, Ram K Selvaraju, Johan Nilvebrant, Olof Eriksson, Vladimir Tolmachev, Marika V Nestor

Open access · hybridAbstract read
In one paragraph

Article in International journal of oncology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.4field-weighted citation impact, top 19% 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

10 citing papers in PubMed, 17 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.

Anna-Karin HaylockDepartment of Immunology, Genetics and Pathology Uppsala University, Uppsala, Sweden.
Diana SpiegelbergDepartment of Immunology, Genetics and Pathology Uppsala University, Uppsala, Sweden.
Anja C MortensenDepartment of Immunology, Genetics and Pathology Uppsala University, Uppsala, Sweden.
Ram K SelvarajuPreclinical PET Platform, Department of Medicinal Chemistry, Uppsala University, Uppsala, Sweden.
Johan NilvebrantDivision of Protein Technology, School of Biotechnology, Royal Institute of Technology, Stockholm, Sweden.
Olof ErikssonPreclinical PET Platform, Department of Medicinal Chemistry, Uppsala University, Uppsala, Sweden.
Vladimir TolmachevDepartment of Immunology, Genetics and Pathology Uppsala University, Uppsala, Sweden.
Marika V NestorDepartment of Immunology, Genetics and Pathology Uppsala University, Uppsala, Sweden.
Uppsala University · SEKTH Royal Institute of Technology · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We have developed the CD44v6-targeting human bivalent antibody fragment AbD19384, an engineered recombinant human bivalent Fab antibody formed via dimerization of dHLX (synthetic double helix loop helix motif) domains, for potential use in antibody-based molecular imaging of squamous cell carcinoma in the head and neck region. This is a unique construct that has, to the best of our knowledge, never been assessed for molecular imaging in vivo before. The objective of the present study was to evaluate for the first time the in vitro and in vivo binding properties of radio-iodinated AbD19384, and to assess its utility as a targeting agent for molecular imaging of CD44v6-expressing tumors. Antigen specificity and binding properties were assessed in vitro. In vivo specificity and biodistribution of 125I-AbD19384 were next evaluated in tumor-bearing mice using a dual-tumor setup. Finally, AbD19384 was labeled with 124I, and its imaging properties were assessed by small animal PET/CT in tumor bearing mice, and compared with 2-deoxy-2-[18F]fluoro-D-glucose (18F-FDG). In vitro studies demonstrated CD44v6-specific binding with slow off-rate for AbD19384. A favorable biodistribution profile was seen in vivo, with tumor-specific uptake. Small animal PET/CT images of 124I-AbD19384 supported the results through clearly visible high CD44v6-expressing tumors and faintly visible low expressing tumors, with superior imaging properties compared to 18F-FDG. Tumor-to-blood ratios increased with time for the conjugate (assessed up to 72 h p.i.), although 48 h p.i. proved best for imaging. Biodistribution and small-animal PET studies demonstrated that the recombinant Fab-dHLX construct AbD19384 is a promising tracer for imaging of CD44v6 antigen expression in vivo, with the future aim to be used for individualized diagnosis and early detection of squamous cell carcinomas in the head and neck region. Furthermore, this proof-of-concept research established the feasibility of using recombinant Fab-dHLX constructs for in vivo imaging of tumor biomarkers.

Indexed as

AnimalsAntibodies, MonoclonalBiomarkers, TumorCarcinoma, Squamous CellCell Line, TumorFemaleFluorodeoxyglucose F18GlucoseHead and Neck NeoplasmsHumansHyaluronan ReceptorsImmunoglobulin Fab FragmentsMiceMice, Inbred BALB CMice, NudePositron-Emission TomographyAntibodies, MonoclonalBiomarkers, TumorCD44v6 antigenFluorodeoxyglucose F18GlucoseHyaluronan ReceptorsImmunoglobulin Fab FragmentsRadiopharmaceuticalsRecombinant Proteins

Identifiers

PMID26676731
PMCPMC4725455
OpenAlexW2204379188

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.