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. 2022 Mar 26;12(3):261–290. doi: 10.34172/bi.2022.23896

Table 2. Clinical applications of TLR3 agonists in cancer immunotherapy .

TLR Agonist Combination No. of samples Cancer type Response Ref./The year
3 Poly(A:U) - 40 Breast cancer Enhancing level of 2-5A synthetase and NKC 78 (1985)
3 Poly-ICLC - 28
10
13
ALL, ANLL, Neuroblastoma Increasing the levels of IFN 79 (1985)
3 Poly-ICLC IL2 5
6
5
1
8
Colorectal, melanoma, renal cell, mycosis fungoides, other solid tumors Enhancing lytic NK activity and increaseing the number of CD56+ cells 80 (1992)
3 Poly-ICLC NY-ESO-1 and Montanide 28 Ovarian cancer Increasing antibody, CD4+ and CD8+ T-cells 84 (2012)
3 Poly-ICLC Autologous DC 12 Pancreatic cancer Induction of tumor specific CD8+T cell population 83 (2017)
3 Poly-ICLC - 7
1
Head and neck, squamous cell cancers, melanoma Local and systemic immune responses through augmentation CD4+, CD8+ T cells, PD1, and PD-L1 levels 81 (2018)
3 Poly-ICLC Montanide and NY-ESO-1 4 Melanoma Induction of robust humoral and cellular immune responses specific for NY-ESO-1 85 (2020)
3 or 4 Poly-ICLC or LPS IFA, melanoma peptides and Tet 51 Melanoma Safe and effective vaccine adjuvants associated with IFA 63 (2019)

Abbreviation: ALL: acute lymphoblastic leukemia; ANLL: acute nonlymphocytic leukemia; DC: Dendritic cell; PD-L1: Programmed death-ligand-1; IFA: Incomplete Freund’s adjuvant; Tet: tetanus helper peptide; IFN: Interferon-α; NKC: NK cytotoxicity; Poly(A:U): Polyadenylic:polyuridylic (polyA:U); Poly-ICLC: poly-l-lysine and carboxymethylcellulose; LPS: Lipopolysaccharide; NY-ESO-1:New York esophageal squamous cell carcinoma 1.