TY - JOUR
T1 - Turning adversity into opportunity
T2 - Small extracellular vesicles as nanocarriers for tumor-associated macrophages re-education
AU - Donoso-Meneses, Dario
AU - Figueroa-Valdés, Aliosha I.
AU - Georges, Nicolás
AU - Tobar, Hugo E.
AU - Alcayaga-Miranda, Francisca
N1 - Funding Information:
The authors specially thank Dr Maroun Khoury and Dr Jimena Cuenca (Medicine Faculty, Universidad de Los Andes, Santiago, Chile) for their helpful scientific discussions, and Paulina Lopez Miranda for the English revision of the manuscript. This work was supported by National Agency for Investigation and Development‐ANID, FONDECYT Regular #1190411, and ANID‐Basal funding for Scientific and Technological Center of Excellence, IMPACT #FB210024.
Funding Information:
ANID‐National Agency for Investigation and Development, FONDECYT Regular, Grant/Award Number: 1190411; ANID‐Basal funding for Scientific and Technological Center of Excellence, IMPACT, Grant/Award Number: FB210024 Funding information
Publisher Copyright:
© 2022 The Authors. Bioengineering & Translational Medicine published by Wiley Periodicals LLC on behalf of American Institute of Chemical Engineers.
PY - 2022
Y1 - 2022
N2 - Currently, small extracellular vesicles (sEV) as a nanoscale drug delivery system, are undergoing biotechnological scaling and clinical validation. Nonetheless, preclinical pharmacokinetic studies revealed that sEV are predominantly uptaken by macrophages. Although this “sEV-macrophage” propensity represents a disadvantage in terms of sEV targeting and their bioavailability as nanocarriers, it also represents a strategic advantage for those therapies that involve macrophages. Such is the case of tumor-associated macrophages (TAMs), which can reprogram/repolarize their predominantly immunosuppressive and tumor-supportive phenotype toward an immunostimulatory and anti-tumor phenotype using sEV as nanocarriers of TAMs reprogramming molecules. In this design, sEV represents an advantageous delivery system, providing precision to the therapy by simultaneously matching their tropism to the therapeutic cell target. Here, we review the current knowledge of the role of TAMs in the tumoral microenvironment and the effect generated by the reprogramming of these phagocytic cells fate using sEV. Finally, we discuss how these vesicles can be engineered by different bioengineering techniques to improve their therapeutic cargo loading and preferential uptake by TAMs.
AB - Currently, small extracellular vesicles (sEV) as a nanoscale drug delivery system, are undergoing biotechnological scaling and clinical validation. Nonetheless, preclinical pharmacokinetic studies revealed that sEV are predominantly uptaken by macrophages. Although this “sEV-macrophage” propensity represents a disadvantage in terms of sEV targeting and their bioavailability as nanocarriers, it also represents a strategic advantage for those therapies that involve macrophages. Such is the case of tumor-associated macrophages (TAMs), which can reprogram/repolarize their predominantly immunosuppressive and tumor-supportive phenotype toward an immunostimulatory and anti-tumor phenotype using sEV as nanocarriers of TAMs reprogramming molecules. In this design, sEV represents an advantageous delivery system, providing precision to the therapy by simultaneously matching their tropism to the therapeutic cell target. Here, we review the current knowledge of the role of TAMs in the tumoral microenvironment and the effect generated by the reprogramming of these phagocytic cells fate using sEV. Finally, we discuss how these vesicles can be engineered by different bioengineering techniques to improve their therapeutic cargo loading and preferential uptake by TAMs.
KW - cancer
KW - immunotherapy
KW - macrophages
KW - nanocarrier engineering
KW - small extracellular vesicles
KW - TAMs re-education
UR - http://www.scopus.com/inward/record.url?scp=85131530540&partnerID=8YFLogxK
UR - https://www.mendeley.com/catalogue/c3958e7d-5ef5-3e92-b451-e36d6784eec0/
U2 - 10.1002/btm2.10349
DO - 10.1002/btm2.10349
M3 - Review article
AN - SCOPUS:85131530540
SN - 2380-6761
JO - Bioengineering and Translational Medicine
JF - Bioengineering and Translational Medicine
ER -