TY - JOUR
T1 - Extracellular vesicles as next generation immunotherapeutics
AU - Greening, David W.
AU - Xu, Rong
AU - Ale, Anukreity
AU - Hagemeyer, Christoph E.
AU - Chen, Weisan
N1 - Funding Information:
DWG was supported by fellowships from Amelia Hains and Baker Institute and the National Heart Foundation of Australia (DWG: Vanguard #105072), Aust. National Health and Medical Research Council Project (DWG: #1057741), Future Fund (DWG: MRF1201805), Pankind Aust. (DWG), and the Victorian Government's Operational Infrastructure Support Program. RX was supported by a Future Leader Postdoctoral Fellowship from Monash University, and Medicine/Science grants from CASS Foundation and Bethlehem Griffiths Research Foundation. The other authors have no funding sources relevant to the preparation of this text to declare. DG and XU designed, discussed, and evaluated all aspects of this article, with critical input from WC. All authors contributed to researching the data for the article. All authors reviewed/ edited the manuscript before submission.
Funding Information:
DWG was supported by fellowships from Amelia Hains and Baker Institute and the National Heart Foundation of Australia (DWG: Vanguard # 105072 ), Aust. National Health and Medical Research Council Project (DWG: # 1057741 ), Future Fund ( DWG: MRF1201805 ), Pankind Aust. (DWG), and the Victorian Government’s Operational Infrastructure Support Program . RX was supported by a Future Leader Postdoctoral Fellowship from Monash University, and Medicine/Science grants from CASS Foundation and Bethlehem Griffiths Research Foundation . The other authors have no funding sources relevant to the preparation of this text to declare.
Publisher Copyright:
© 2023 Elsevier Ltd
PY - 2023/5
Y1 - 2023/5
N2 - Extracellular vesicles (EVs) function as a mode of intercellular communication and molecular transfer to elicit diverse biological/functional response. Accumulating evidence has highlighted that EVs from immune, tumour, stromal cells and even bacteria and parasites mediate the communication of various immune cell types to dynamically regulate host immune response. EVs have an innate capacity to evade recognition, transport and transfer functional components to target cells, with subsequent removal by the immune system, where the immunological activities of EVs impact immunoregulation including modulation of antigen presentation and cross-dressing, immune activation, immune suppression, and immune surveillance, impacting the tumour immune microenvironment. In this review, we outline the recent progress of EVs in immunorecognition and therapeutic intervention in cancer, including vaccine and targeted drug delivery and summarise their utility towards clinical translation. We highlight the strategies where EVs (natural and engineered) are being employed as a therapeutic approach for immunogenicity, tumoricidal function, and vaccine development, termed immuno-EVs. With seminal studies providing significant progress in the sequential development of engineered EVs as therapeutic anti-tumour platforms, we now require direct assessment to tune and improve the efficacy of resulting immune responses - essential in their translation into the clinic. We believe such a review could strengthen our understanding of the progress in EV immunobiology and facilitate advances in engineering EVs for the development of novel EV-based immunotherapeutics as a platform for cancer treatment.
AB - Extracellular vesicles (EVs) function as a mode of intercellular communication and molecular transfer to elicit diverse biological/functional response. Accumulating evidence has highlighted that EVs from immune, tumour, stromal cells and even bacteria and parasites mediate the communication of various immune cell types to dynamically regulate host immune response. EVs have an innate capacity to evade recognition, transport and transfer functional components to target cells, with subsequent removal by the immune system, where the immunological activities of EVs impact immunoregulation including modulation of antigen presentation and cross-dressing, immune activation, immune suppression, and immune surveillance, impacting the tumour immune microenvironment. In this review, we outline the recent progress of EVs in immunorecognition and therapeutic intervention in cancer, including vaccine and targeted drug delivery and summarise their utility towards clinical translation. We highlight the strategies where EVs (natural and engineered) are being employed as a therapeutic approach for immunogenicity, tumoricidal function, and vaccine development, termed immuno-EVs. With seminal studies providing significant progress in the sequential development of engineered EVs as therapeutic anti-tumour platforms, we now require direct assessment to tune and improve the efficacy of resulting immune responses - essential in their translation into the clinic. We believe such a review could strengthen our understanding of the progress in EV immunobiology and facilitate advances in engineering EVs for the development of novel EV-based immunotherapeutics as a platform for cancer treatment.
KW - Cancer
KW - Extracellular vesicles
KW - Immunity
KW - Immunoregulation
KW - Immunosurveillance
KW - Microenvironment
KW - Nanovesicles
KW - Vaccine
UR - http://www.scopus.com/inward/record.url?scp=85149473671&partnerID=8YFLogxK
U2 - 10.1016/j.semcancer.2023.02.002
DO - 10.1016/j.semcancer.2023.02.002
M3 - Review Article
C2 - 36773820
AN - SCOPUS:85149473671
SN - 1044-579X
VL - 90
SP - 73
EP - 100
JO - Seminars in Cancer Biology
JF - Seminars in Cancer Biology
ER -