| Literature DB >> 34927922 |
Tian Zhang1, Honggang Xiong2, Xianbin Ma1, Yuan Gao1, Peng Xue1, Yuejun Kang1, Zhi-Jun Sun2, Zhigang Xu1.
Abstract
Tumor-induced immune suppression mediated by myeloid-derived suppressor cells (MDSCs) and insufficient immunogenicity are two major factors for the poor overall response rate to the immune checkpoint blockade (ICB). Here, a tumor microenvironment responsive nanoprodrug (FIT nanoparticles) is presented for co-delivering tadalafil (TAD) and indocyanine green (ICG) photosensitizer to simultaneously targeting intratumor MDSCs and amplifying tumor immunogenicity. The resulting nanoprodrug shows high drug loading (nearly 100%), tumor-specific release, and robust therapeutic efficacy by virtue of promoting immunogenic cell death (ICD) induction and alleviation of MDSCs for augmenting the photothermal immunotherapy. In an in vivo colon tumor model, the released TAD in the tumor can effectively ameliorate MDSCs immunosuppressive activity, while the photosensitizer ICG is capable of inducing ICD to promote sufficient dendritic cells maturation and T cell infiltration. The results reported here may provide a superior candidate of adjuvants for strengthening immune response and ICB efficacy.Entities:
Keywords: myeloid-derived suppressor cells; nano-immunotherapy; phototherapy; stimuli activation; tadalafil
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Year: 2021 PMID: 34927922 DOI: 10.1002/smtd.202100115
Source DB: PubMed Journal: Small Methods ISSN: 2366-9608