Evidence map›Paper›PMID 34580321›Full record

ArticleScientific reports2021

Discovery, optimization and biodistribution of an Affibody molecule for imaging of CD69.

Jonas Persson, Emmi Puuvuori, Bo Zhang, Irina Velikyan, Ola Åberg, Malin Müller, Per-Åke Nygren, Stefan Ståhl, Olle Korsgren, Olof Eriksson and 1 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
7.6field-weighted citation impact, top 2% 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

13 citing papers in PubMed, 47 citations in OpenAlex.

  1. Article
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  4. Article
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  8. Article
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  11. Imaging of Activated T Cells.Journal of nuclear medicine : official publication, Society of Nuclear Medicine · 2023
    Review
  12. Novel smallFrontiers in oncology · 2022
    Article
  13. Review
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 at 3 institutions in 1 country.

Jonas Persson *Department of Protein Science, Division of Protein Engineering, KTH Royal Institute of Technology, Roslagstullsbacken 21, 10691, Stockholm, Sweden.
Emmi Puuvuori *Science for Life Laboratory, Department of Medicinal Chemistry, Uppsala University, Dag Hammarskjölds väg 14C, 3tr, 75183, Uppsala, Sweden.
Bo ZhangScience for Life Laboratory, Department of Medicinal Chemistry, Uppsala University, Dag Hammarskjölds väg 14C, 3tr, 75183, Uppsala, Sweden.
Irina VelikyanScience for Life Laboratory, Department of Medicinal Chemistry, Uppsala University, Dag Hammarskjölds väg 14C, 3tr, 75183, Uppsala, Sweden.
Ola ÅbergScience for Life Laboratory, Department of Medicinal Chemistry, Uppsala University, Dag Hammarskjölds väg 14C, 3tr, 75183, Uppsala, Sweden.
Malin MüllerDepartment of Immunology, Genetics and Pathology, Uppsala University, Uppsala, Sweden.
Per-Åke NygrenDepartment of Protein Science, Division of Protein Engineering, KTH Royal Institute of Technology, Roslagstullsbacken 21, 10691, Stockholm, Sweden.
Stefan StåhlDepartment of Protein Science, Division of Protein Engineering, KTH Royal Institute of Technology, Roslagstullsbacken 21, 10691, Stockholm, Sweden.
Olle KorsgrenDepartment of Immunology, Genetics and Pathology, Uppsala University, Uppsala, Sweden.
Olof ErikssonScience for Life Laboratory, Department of Medicinal Chemistry, Uppsala University, Dag Hammarskjölds väg 14C, 3tr, 75183, Uppsala, Sweden. olof.eriksson@ilk.uu.se.
John LöfblomDepartment of Protein Science, Division of Protein Engineering, KTH Royal Institute of Technology, Roslagstullsbacken 21, 10691, Stockholm, Sweden. lofblom@kth.se.
KTH Royal Institute of Technology · SEUppsala University · SEScience for Life Laboratory · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Due to the wide scale of inflammatory processes in different types of disease, more sensitive and specific biomarkers are required to improve prevention and treatment. Cluster of differentiation 69 (CD69) is one of the earliest cell surface proteins expressed by activated leukocytes. Here we characterize and optimize potential new imaging probes, Affibody molecules targeting CD69 for imaging of activated immune cells. Analysis of candidates isolated in a previously performed selection from a Z variant E. coli library to the recombinant extracellular domain of human CD69, identified one cross-reactive Z variant with affinity to murine and human CD69. Affinity maturation was performed by randomization of the primary Z variant, followed by selections from the library. The resulting Z variants were evaluated for affinity towards human and murine CD69 and thermal stability. The in vivo biodistribution was assessed by SPECT/CT in rats following conjugation of the Z variants by a DOTA chelator and radiolabeling with Indium-111. A primary Z variant with a K

Indexed as

AnimalsAntibody AffinityAntigens, CDAntigens, Differentiation, T-LymphocyteCD69 AntigensCross ReactionsHumansImmunoconjugatesIndium RadioisotopesInjections, IntravenousLectins, C-TypeMaleMiceMolecular ImagingProtein StabilityRadiopharmaceuticalsAntigens, CDAntigens, Differentiation, T-LymphocyteCD69 AntigensImmunoconjugatesIndium-111Indium RadioisotopesLectins, C-TypeRadiopharmaceuticalsRecombinant Fusion Proteins

Identifiers

PMID34580321
PMCPMC8476556
OpenAlexW3203524141

What OpenQuestion holds

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Registered trials

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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.