TY - JOUR
T1 - Reactive oxygen species-powered cancer immunotherapy
T2 - Current status and challenges
AU - He, Mengying
AU - Wang, Mengyuan
AU - Xu, Tao
AU - Zhang, Mengyao
AU - Dai, Huaxing
AU - Wang, Chao
AU - Ding, Dawei
AU - Zhong, Zhiyuan
N1 - Publisher Copyright:
© 2023 Elsevier B.V.
PY - 2023/4
Y1 - 2023/4
N2 - Reactive oxygen species (ROS) are crucial signaling molecules that can arouse immune system. In recent decades, ROS has emerged as a unique therapeutic strategy for malignant tumors as (i) it can not only directly reduce tumor burden but also trigger immune responses by inducing immunogenic cell death (ICD); and (ii) it can be facilely generated and modulated by radiotherapy, photodynamic therapy, sonodynamic therapy and chemodynamic therapy. The anti-tumor immune responses are, however, mostly downplayed by the immunosuppressive signals and dysfunction of effector immune cells within the tumor microenvironment (TME). The past years have seen fierce developments of various strategies to power ROS-based cancer immunotherapy by e.g. combining with immune checkpoints inhibitors, tumor vaccines, and/or immunoadjuvants, which have shown to potently inhibit primary tumors, metastatic tumors, and tumor relapse with limited immune-related adverse events (irAEs). In this review, we introduce the concept of ROS-powered cancer immunotherapy, highlight the innovative strategies to boost ROS-based cancer immunotherapy, and discuss the challenges in terms of clinical translation and future perspectives.
AB - Reactive oxygen species (ROS) are crucial signaling molecules that can arouse immune system. In recent decades, ROS has emerged as a unique therapeutic strategy for malignant tumors as (i) it can not only directly reduce tumor burden but also trigger immune responses by inducing immunogenic cell death (ICD); and (ii) it can be facilely generated and modulated by radiotherapy, photodynamic therapy, sonodynamic therapy and chemodynamic therapy. The anti-tumor immune responses are, however, mostly downplayed by the immunosuppressive signals and dysfunction of effector immune cells within the tumor microenvironment (TME). The past years have seen fierce developments of various strategies to power ROS-based cancer immunotherapy by e.g. combining with immune checkpoints inhibitors, tumor vaccines, and/or immunoadjuvants, which have shown to potently inhibit primary tumors, metastatic tumors, and tumor relapse with limited immune-related adverse events (irAEs). In this review, we introduce the concept of ROS-powered cancer immunotherapy, highlight the innovative strategies to boost ROS-based cancer immunotherapy, and discuss the challenges in terms of clinical translation and future perspectives.
KW - cancer therapy
KW - cancer vaccines
KW - immune checkpoint inhibitors
KW - immunoadjuvants
KW - immunogenic cell death
KW - Reactive oxygen species
UR - http://www.scopus.com/inward/record.url?scp=85150384854&partnerID=8YFLogxK
U2 - 10.1016/j.jconrel.2023.02.040
DO - 10.1016/j.jconrel.2023.02.040
M3 - Article
C2 - 36868519
AN - SCOPUS:85150384854
SN - 0168-3659
VL - 356
SP - 623
EP - 648
JO - Journal of Controlled Release
JF - Journal of Controlled Release
ER -