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Author:

Gao, Xinxin (Gao, Xinxin.) | Cao, Kai (Cao, Kai.) | Yang, Jingru (Yang, Jingru.) | Liu, Linhong (Liu, Linhong.) | Gao, Liang (Gao, Liang.) (Scholars:高靓)

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Scopus SCIE

Abstract:

Programmed cell death ligand 1 (PD-L1)/programmed cell death protein 1 (PD-1) checkpoint inhibitor-based immunotherapy has provided a unique and potent weapon against cancer in clinical practice. The likelihood of achieving beneficial effects from PD-L1/PD-1 immune checkpoint blockade (ICB) therapy is clinically assessed by detecting PD-L1 expression through invasive tissue biopsies. However, PD-L1 expression is susceptible to tumor heterogeneity and dynamic response to ICB therapy. Moreover, currently, anti-PD-L1 immunotherapy still faces challenges of the low targeting efficiency of antibody drugs and the risk of immune-associated adverse events. To overcome these issues, advanced nanotechnology has been developed for the purpose of quantitative, non-invasive, and dynamic analyses of PD-L1, and to enhance the efficiency of ICB therapy. In this review, we first introduce the nanoprobe-assisted in vitro/in vivo modalities for the selective and sensitive analysis of PD-L1 during the diagnostic and therapeutic process. On the other hand, the feasibility of fabricating diverse functional nanocarriers as smart delivery systems for precisely targeted delivery of PD-L1 immune checkpoint inhibitors and combined therapies is highlighted. Finally, the current challenges are discussed and future perspectives for PD-L1-targeted cancer theranostics in preclinical research and clinical settings are proposed. Advanced nanotechnology developed for PD-L1 detection and PD-L1/PD-1 immune checkpoint-relevant combined cancer therapies is reviewed.

Keyword:

Author Community:

  • [ 1 ] [Gao, Xinxin]Beijing Univ Technol, Coll Chem & Life Sci, Dept Chem, Beijing 100124, Peoples R China
  • [ 2 ] [Cao, Kai]Beijing Univ Technol, Coll Chem & Life Sci, Dept Chem, Beijing 100124, Peoples R China
  • [ 3 ] [Yang, Jingru]Beijing Univ Technol, Coll Chem & Life Sci, Dept Chem, Beijing 100124, Peoples R China
  • [ 4 ] [Liu, Linhong]Beijing Univ Technol, Coll Chem & Life Sci, Dept Chem, Beijing 100124, Peoples R China
  • [ 5 ] [Gao, Liang]Beijing Univ Technol, Coll Chem & Life Sci, Dept Chem, Beijing 100124, Peoples R China

Reprint Author's Address:

  • 高靓

    [Cao, Kai]Beijing Univ Technol, Coll Chem & Life Sci, Dept Chem, Beijing 100124, Peoples R China;;[Gao, Liang]Beijing Univ Technol, Coll Chem & Life Sci, Dept Chem, Beijing 100124, Peoples R China

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Source :

JOURNAL OF MATERIALS CHEMISTRY B

ISSN: 2050-750X

Year: 2024

Issue: 13

Volume: 12

Page: 3191-3208

7 . 0 0 0

JCR@2022

Cited Count:

WoS CC Cited Count: 1

SCOPUS Cited Count: 1

ESI Highly Cited Papers on the List: 0 Unfold All

WanFang Cited Count:

Chinese Cited Count:

30 Days PV: 11

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