Antibody-displaying extracellular vesicles for targeted cancer therapy

Author:

Wiklander Oscar P. B.ORCID,Mamand Doste R.,Mohammad Dara K.ORCID,Zheng WenyiORCID,Jawad Wiklander Rim,Sych Taras,Zickler Antje M.ORCID,Liang Xiuming,Sharma Heena,Lavado Andrea,Bost Jeremy,Roudi Samantha,Corso GiuliaORCID,Lennaárd Angus J.,Abedi-Valugerdi Manuchehr,Mäger ImreORCID,Alici Evren,Sezgin ErdincORCID,Nordin Joel Z.ORCID,Gupta Dhanu,Görgens AndréORCID,EL Andaloussi SamirORCID

Abstract

AbstractExtracellular 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.

Publisher

Springer Science and Business Media LLC

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