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Trial watch: Dendritic cell (DC)-based immunotherapy for cancer

Authors :
Laureano, R.S.
Sprooten, J.
Vanmeerbeerk, I.
Borras, D.M.
Govaerts, J.
Naulaerts, S.
Berneman, Z.N.
Beuselinck, B.
Bol, K.F.
Borst, J.
Coosemans, A.
Datsi, A.
Fučíková, J.
Kinget, L.
Neyns, B.
Schreibelt, G.
Smits, E.
Sorg, R.V.
Spisek, R.
Thielemans, K.
Tuyaerts, S.
Vleeschouwer, S. De
Vries, I.J.M. de
Xiao, Y.
Garg, A.D.
Laureano, R.S.
Sprooten, J.
Vanmeerbeerk, I.
Borras, D.M.
Govaerts, J.
Naulaerts, S.
Berneman, Z.N.
Beuselinck, B.
Bol, K.F.
Borst, J.
Coosemans, A.
Datsi, A.
Fučíková, J.
Kinget, L.
Neyns, B.
Schreibelt, G.
Smits, E.
Sorg, R.V.
Spisek, R.
Thielemans, K.
Tuyaerts, S.
Vleeschouwer, S. De
Vries, I.J.M. de
Xiao, Y.
Garg, A.D.
Source :
Oncoimmunology; 2162-4011; 1; 11; 2096363; ~Oncoimmunology~~~~~2162-4011~1~11~~2096363
Publication Year :
2022

Abstract

Contains fulltext : 283345.pdf (Publisher’s version ) (Open Access)<br />Dendritic cell (DC)-based vaccination for cancer treatment has seen considerable development over recent decades. However, this field is currently in a state of flux toward niche-applications, owing to recent paradigm-shifts in immuno-oncology mobilized by T cell-targeting immunotherapies. DC vaccines are typically generated using autologous (patient-derived) DCs exposed to tumor-associated or -specific antigens (TAAs or TSAs), in the presence of immunostimulatory molecules to induce DC maturation, followed by reinfusion into patients. Accordingly, DC vaccines can induce TAA/TSA-specific CD8(+)/CD4(+) T cell responses. Yet, DC vaccination still shows suboptimal anti-tumor efficacy in the clinic. Extensive efforts are ongoing to improve the immunogenicity and efficacy of DC vaccines, often by employing combinatorial chemo-immunotherapy regimens. In this Trial Watch, we summarize the recent preclinical and clinical developments in this field and discuss the ongoing trends and future perspectives of DC-based immunotherapy for oncological indications.

Details

Database :
OAIster
Journal :
Oncoimmunology; 2162-4011; 1; 11; 2096363; ~Oncoimmunology~~~~~2162-4011~1~11~~2096363
Publication Type :
Electronic Resource
Accession number :
edsoai.on1366814310
Document Type :
Electronic Resource