Recent advances in cancer immunotherapy: Modulation of tumor microenvironment by Toll-like receptor ligands

被引:16
|
作者
Rostamizadeh, Leila [1 ]
Molavi, Ommoleila [2 ,3 ]
Rashid, Mohsen [1 ]
Ramazani, Fatemeh [1 ]
Baradaran, Behzad [4 ]
Lavasanaifar, Afsaneh [5 ]
Lai, Raymond [6 ]
机构
[1] Tabriz Univ Med Sci, Fac Adv Med Sci, Dept Mol Med, Tabriz, Iran
[2] Tabriz Univ Med Sci, Biotechnol Res Ctr, Tabriz, Iran
[3] Tabriz Univ Med Sci, Fac Pharm, Dept Pharmaceut Biotechnol, Tabriz, Iran
[4] Tabriz Univ Med Sci, Immunol Res Ctr, Tabriz, Iran
[5] Univ Alberta, Fac Pharm & Pharmaceut Sci, Edmonton, AB, Canada
[6] Univ Alberta, Fac Med & Dent, Dept Lab Med & Pathol, Edmonton, AB, Canada
关键词
Immunotherapy; Cancer; TLRs; Microenvironment; Agonist; Vaccine; BASAL-CELL CARCINOMA; PHASE-I TRIAL; IMMUNE-RESPONSE MODIFIER; TLR7 AGONIST IMIQUIMOD; MONOPHOSPHORYL-LIPID-A; POLY-L-LYSINE; DENDRITIC CELLS; IMMUNOSUPPRESSIVE CYTOKINES; CPG OLIGODEOXYNUCLEOTIDE; ANTITUMOR EFFICACY;
D O I
10.34172/bi.2022.23896
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Immunotherapy is considered a promising approach for cancer treatment. An important strategy for cancer immunotherapy is the use of cancer vaccines, which have been widely used for cancer treatment. Despite the great potential of cancer vaccines for cancer treatment, their therapeutic effects in clinical settings have been limited. The main reason behind the lack of significant therapeutic outcomes for cancer vaccines is believed to be the immunosuppressive tumor microenvironment (TME). The TME counteracts the therapeutic effects of immunotherapy and provides a favorable environment for tumor growth and progression. Therefore, overcoming the immunosuppressive TME can potentially augment the therapeutic effects of cancer immunotherapy in general and therapeutic cancer vaccines in particular. Among the strategies developed for overcoming immunosuppression in TME, the use of toll-like receptor (TLR) agonists has been suggested as a promising approach to reverse immunosuppression. In this paper, we will review the application of the four most widely studied TLR agonists including agonists of TLR3, 4, 7, and 9 in cancer immunotherapy.
引用
收藏
页码:261 / 290
页数:30
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