Toll-Like Receptor-Based Strategies for Cancer Immunotherapy

被引:69
作者
Pahlavanneshan, Saghar [1 ]
Sayadmanesh, Ali [2 ]
Ebrahimiyan, Hamidreza [2 ]
Basiri, Mohsen [2 ]
机构
[1] Shahid Beheshti Univ Med Sci, Funct Neurosurg Res Ctr, Shohada Tajrish Comprehens Neurosurg Ctr Excellen, Tehran, Iran
[2] ACECR, Royan Inst Stem Cell Biol & Technol, Dept Stem Cells & Dev Biol, Cell Sci Res Ctr, Tehran, Iran
关键词
MACROPHAGE-ACTIVATING LIPOPEPTIDE-2; TUMOR-ASSOCIATED MACROPHAGES; ADOPTIVE CELL THERAPY; 9 AGONIST IMO-2055; HUMAN NK CELLS; T-CELLS; IMMUNE-RESPONSES; IN-VIVO; PHASE-I; INTRATUMORAL INJECTION;
D O I
10.1155/2021/9912188
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Toll-like receptors (TLRs) are expressed and play multiple functional roles in a variety of immune cell types involved in tumor immunity. There are plenty of data on the pharmacological targeting of TLR signaling using agonist molecules that boost the antitumor immune response. A recent body of research has also demonstrated promising strategies for improving the cell-based immunotherapy methods by inducing TLR signaling. These strategies include systemic administration of TLR antagonist along with immune cell transfer and also genetic engineering of the immune cells using TLR signaling components to improve the function of genetically engineered immune cells such as chimeric antigen receptor-modified T cells. Here, we explore the current status of the cancer immunotherapy approaches based on manipulation of TLR signaling to provide a perspective of the underlying rationales and potential clinical applications. Altogether, reviewed publications suggest that TLRs make a potential target for the immunotherapy of cancer.
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页数:14
相关论文
共 145 条
[1]   Synthetic agonists of Toll-like receptors 7, 8 and 9 [J].
Agrawal, S. ;
Kandimalla, E. R. .
BIOCHEMICAL SOCIETY TRANSACTIONS, 2007, 35 :1461-1467
[2]   TLR1/2, TLR7, and TLR9 Signals Directly Activate Human Peripheral Blood Naive and Memory B Cell Subsets to Produce Cytokines, Chemokines, and Hematopoietic Growth Factors [J].
Agrawal, Sudhanshu ;
Gupta, Sudhir .
JOURNAL OF CLINICAL IMMUNOLOGY, 2011, 31 (01) :89-98
[3]   Poly(I:C) as cancer vaccine adjuvant: Knocking on the door of medical breakthroughs [J].
Ammi, Rachid ;
De Waele, Jorrit ;
Willemen, Yannick ;
Van Brussel, Ilse ;
Schrijvers, Dorien M. ;
Lion, Eva ;
Smits, Evelien L. J. .
PHARMACOLOGY & THERAPEUTICS, 2015, 146 :120-131
[4]   Harnessing the Complete Repertoire of Conventional Dendritic Cell Functions for Cancer Immunotherapy [J].
Amon, Lukas ;
Hatscher, Lukas ;
Heger, Lukas ;
Dudziak, Diana ;
Lehmann, Christian H. K. .
PHARMACEUTICS, 2020, 12 (07) :1-83
[5]   Macrophage-Based Approaches for Cancer Immunotherapy [J].
Anderson, Nicholas R. ;
Minutolo, Nicholas G. ;
Gill, Saar ;
Klichinsky, Michael .
CANCER RESEARCH, 2021, 81 (05) :1201-1208
[6]   Clinical use of dendritic cells for cancer therapy [J].
Anguille, Sebastien ;
Smits, Evelien L. ;
Lion, Eva ;
van Tendeloo, Viggo F. ;
Berneman, Zwi N. .
LANCET ONCOLOGY, 2014, 15 (07) :E257-E267
[7]   Recent clinical trends in Toll-like receptor targeting therapeutics [J].
Anwar, Muhammad Ayaz ;
Shah, Masaud ;
Kim, Jason ;
Choi, Sangdun .
MEDICINAL RESEARCH REVIEWS, 2019, 39 (03) :1053-1090
[8]   Engagement of Toll-like receptor-2 on cytotoxic T-lymphocytes occurs in vivo and augments antitumor activity [J].
Asprodites, Nicole ;
Zheng, Liqin ;
Geng, Degui ;
Velasco-Gonzalez, Cruz ;
Sanchez-Perez, Luis ;
Davila, Eduardo .
FASEB JOURNAL, 2008, 22 (10) :3628-3637
[9]   Oligodeoxynucleotides ODN 2006 and M362 Exert Potent Adjuvant Effect through TLR-9/-6 Synergy to Exaggerate Mammaglobin-A Peptide Specific Cytotoxic CD8+T Lymphocyte Responses against Breast Cancer Cells [J].
Babaer, Duaa ;
Amara, Suneetha ;
McAdory, Brenda S. ;
Johnson, Owen ;
Myles, Elbert L. ;
Zent, Roy ;
Rathmell, Jeffrey C. ;
Tiriveedhi, Venkataswarup .
CANCERS, 2019, 11 (05)
[10]  
Basiri M., 2021, CELL J