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Application of PD-1 Blockade in Cancer Immunotherapy.

作者信息

Wu Xiaomo, Gu Zhongkai, Chen Yang, Chen Borui, Chen Wei, Weng Liqiang, Liu Xiaolong

机构信息

Dermatology Institute of Fuzhou, Dermatology Hospital of Fuzhou, Xihong Road 243, Fuzhou 350025, PR China.

Department of Biomedicine, University of Basel, Klingelbergstr. 70, CH-4056 Basel, Switzerland.

出版信息

Comput Struct Biotechnol J. 2019 May 23;17:661-674. doi: 10.1016/j.csbj.2019.03.006. eCollection 2019.


DOI:10.1016/j.csbj.2019.03.006
PMID:31205619
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6558092/
Abstract

The programmed cell death protein 1 (PD-1) pathway has received considerable attention due to its role in eliciting the immune checkpoint response of T cells, resulting in tumor cells capable of evading immune surveillance and being highly refractory to conventional chemotherapy. Application of anti-PD-1/PD-L1 antibodies as checkpoint inhibitors is rapidly becoming a promising therapeutic approach in treating tumors, and some of them have successfully been commercialized in the past few years. However, not all patients show complete responses and adverse events have been noted, suggesting a better understanding of PD-1 pathway mediated immunosuppression is needed to predict patient response and improve treatment efficacy. Here, we review the progresses on the studies of the mechanistic role of PD-1 pathway in the tumor immune evasion, recent clinical development and commercialization of PD-1 pathway inhibitors, the toxicities associated with PD-1 blockade observed in clinical trials as well as how to improve therapeutic efficacy and safety of cancer immunotherapy.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a06a/6558092/ca7ef09cac83/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a06a/6558092/fbe0a2e4dbab/ga1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a06a/6558092/ca7ef09cac83/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a06a/6558092/fbe0a2e4dbab/ga1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a06a/6558092/ca7ef09cac83/gr1.jpg

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本文引用的文献

[1]
Delivery technologies for cancer immunotherapy.

Nat Rev Drug Discov. 2019-3

[2]
Targeting Programmed Cell Death -1 (PD-1) and Ligand (PD-L1): A new era in cancer active immunotherapy.

Pharmacol Ther. 2018-9-28

[3]
Safety and efficacy of durvalumab (MEDI4736) in various solid tumors.

Drug Des Devel Ther. 2018-7-6

[4]
Durvalumab after chemoradiotherapy in stage III non-small cell lung cancer.

J Thorac Dis. 2018-4

[5]
Blocking "don't eat me" signal of CD47-SIRPα in hematological malignancies, an in-depth review.

Blood Rev. 2018-4-14

[6]
Pembrolizumab plus Chemotherapy in Metastatic Non-Small-Cell Lung Cancer.

N Engl J Med. 2018-4-16

[7]
Emerging Concepts for Immune Checkpoint Blockade-Based Combination Therapies.

Cancer Cell. 2018-4-9

[8]
Integrating phosphoproteomics into kinase-targeted cancer therapies in precision medicine.

J Proteomics. 2018-4-3

[9]
The microbiome in cancer immunotherapy: Diagnostic tools and therapeutic strategies.

Science. 2018-3-23

[10]
Cancer immunotherapy using checkpoint blockade.

Science. 2018-3-23

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