Evidence map›Paper›PMID 38769158›Full record

ArticleNature biomedical engineering2024

Antibody-displaying extracellular vesicles for targeted cancer therapy.

Oscar P B Wiklander, Doste R Mamand, Dara K Mohammad, Wenyi Zheng, Rim Jawad Wiklander, Taras Sych, Antje M Zickler, Xiuming Liang, Heena Sharma, Andrea Lavado and 12 more

Abstract read
In one paragraph

Article in Nature biomedical engineering, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 88 papers.

0numbers the graph read from it
0cells of the map it votes in
88citing 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

88 citing papers in PubMed.

  1. Review
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  8. Article
  9. Green nanomedicine for cancer therapy.Chinese medical journal · 2026
    Review
  10. Review
  11. Review
  12. Review
  13. Review
  14. Review
  15. Article
  16. Unlocking the potential of extracellular vesicles in cancer diagnosis and therapy: a comprehensive bibliometric study.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
    Article
  17. Review
  18. Endogenous Engineering Reprograms Extracellular Vesicles for Enhanced Therapeutic Function.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Review
  19. Article
  20. Review

28 more citing papers are in PubMed but not listed here.

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

22 authors.

Oscar P B Wiklander *Department of Laboratory Medicine, Unit for Biomolecular and Cellular Medicine, Karolinska Institutet, Stockholm, Sweden. oscar.wiklander@ki.se.ORCID 0000-0003-1176-8114
Doste R Mamand *Department of Laboratory Medicine, Unit for Biomolecular and Cellular Medicine, Karolinska Institutet, Stockholm, Sweden.
Dara K MohammadDepartment of Medicine Huddinge, Karolinska Institute, Stockholm, Sweden.ORCID 0000-0001-9201-0991
Wenyi ZhengDepartment of Laboratory Medicine, Unit for Biomolecular and Cellular Medicine, Karolinska Institutet, Stockholm, Sweden.ORCID 0000-0003-2416-5822
Rim Jawad WiklanderDepartment of Laboratory Medicine, Unit for Biomolecular and Cellular Medicine, Karolinska Institutet, Stockholm, Sweden.
Taras SychScience for Life Laboratory, Department of Women's and Children's Health, Karolinska Institutet, Solna, Sweden.
Antje M ZicklerDepartment of Laboratory Medicine, Unit for Biomolecular and Cellular Medicine, Karolinska Institutet, Stockholm, Sweden.ORCID 0000-0001-5001-6586
Xiuming LiangDepartment of Laboratory Medicine, Unit for Biomolecular and Cellular Medicine, Karolinska Institutet, Stockholm, Sweden.
Heena SharmaEvox Therapeutics Limited, Oxford, UK.
Andrea LavadoEvox Therapeutics Limited, Oxford, UK.
Jeremy BostDepartment of Laboratory Medicine, Unit for Biomolecular and Cellular Medicine, Karolinska Institutet, Stockholm, Sweden.
Samantha RoudiDepartment of Laboratory Medicine, Unit for Biomolecular and Cellular Medicine, Karolinska Institutet, Stockholm, Sweden.
Giulia CorsoDepartment of Laboratory Medicine, Unit for Biomolecular and Cellular Medicine, Karolinska Institutet, Stockholm, Sweden.ORCID 0000-0002-1145-0862
Angus J LennaárdDepartment of Laboratory Medicine, Unit for Biomolecular and Cellular Medicine, Karolinska Institutet, Stockholm, Sweden.
Manuchehr Abedi-ValugerdiDepartment of Laboratory Medicine, Unit for Biomolecular and Cellular Medicine, Karolinska Institutet, Stockholm, Sweden.
Imre MägerDepartment of Physiology, Anatomy and Genetics, University of Oxford, Oxford, UK.ORCID 0000-0003-2242-7227
Evren AliciDepartment of Medicine Huddinge, Karolinska Institute, Stockholm, Sweden.
Erdinc SezginScience for Life Laboratory, Department of Women's and Children's Health, Karolinska Institutet, Solna, Sweden.ORCID 0000-0002-4915-388X
Joel Z NordinDepartment of Laboratory Medicine, Unit for Biomolecular and Cellular Medicine, Karolinska Institutet, Stockholm, Sweden.ORCID 0000-0002-3653-7710
Dhanu GuptaDepartment of Laboratory Medicine, Unit for Biomolecular and Cellular Medicine, Karolinska Institutet, Stockholm, Sweden.
André GörgensDepartment of Laboratory Medicine, Unit for Biomolecular and Cellular Medicine, Karolinska Institutet, Stockholm, Sweden.ORCID 0000-0001-9198-0857
Samir El AndaloussiDepartment of Laboratory Medicine, Unit for Biomolecular and Cellular Medicine, Karolinska Institutet, Stockholm, Sweden. samir.el-andaloussi@ki.se.ORCID 0000-0003-4468-9113

Funding

Stiftelsen för Strategisk Forskning (Swedish Foundation for Strategic Research) SM19-0007Vetenskapsrådet (Swedish Research Council) 2021-02407Vetenskapsrådet (Swedish Research Council) 2022-02449Vetenskapsrådet (Swedish Research Council) 4-258/2021
6 · The paper itself

Abstract

Extracellular vesicles (EVs) function as natural delivery vectors and mediators of biological signals across tissues. Here, by leveraging these functionalities, we show that EVs decorated with an antibody-binding moiety specific for the fragment crystallizable (Fc) domain can be used as a modular delivery system for targeted cancer therapy. The Fc-EVs can be decorated with different types of immunoglobulin G antibody and thus be targeted to virtually any tissue of interest. Following optimization of the engineered EVs by screening Fc-binding and EV-sorting moieties, we show the targeting of EVs to cancer cells displaying the human epidermal receptor 2 or the programmed-death ligand 1, as well as lower tumour burden and extended survival of mice with subcutaneous melanoma tumours when systemically injected with EVs displaying an antibody for the programmed-death ligand 1 and loaded with the chemotherapeutic doxorubicin. EVs with Fc-binding domains may be adapted to display other Fc-fused proteins, bispecific antibodies and antibody-drug conjugates.

Indexed as

Extracellular VesiclesAnimalsCell Line, TumorDoxorubicinDrug Delivery SystemsFemaleHumansImmunoglobulin Fc FragmentsImmunoglobulin GMelanomaMiceNeoplasmsDoxorubicinImmunoglobulin Fc FragmentsImmunoglobulin G

Identifiers

PMID38769158
PMCPMC11584392

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.