Immunotherapeutic applications of CpG oligodeoxynucleotide TLR9 agonists

被引:552
作者
Vollmer, Joerg [2 ]
Krieg, Arthur M. [1 ]
机构
[1] Pfizer Inc, Res Technol Ctr, Cambridge, MA 02139 USA
[2] Pfizer Co, Coley Pharmaceut GmbH, D-40225 Dusseldorf, Germany
关键词
Toll-like receptor; Oligonucleotide; Innate immunity; Vaccine; TOLL-LIKE RECEPTOR-9; B SURFACE-ANTIGEN; SYSTEMIC-LUPUS-ERYTHEMATOSUS; T-CELL RESPONSES; PLASMACYTOID DENDRITIC CELLS; NF-KAPPA-B; INTERFERON-ALPHA INDUCTION; INDUCED IMMUNE ACTIVATION; SIMPLEX-VIRUS TYPE-2; NON-HODGKIN-LYMPHOMA;
D O I
10.1016/j.addr.2008.12.008
中图分类号
R9 [药学];
学科分类号
100702 [药剂学];
摘要
Toll-like receptor 9 (TLR9) agonists have demonstrated substantial potential as vaccine adjuvants, and as mono- or combination therapies for the treatment of cancer and infectious and allergic diseases. Commonly referred to as CpG oligodeoxynucleotides (ODN), TLR9 agonists directly induce the activation and maturation of plasmacytoid dendritic cells and enhance differentiation of B cells into antibody-secreting plasma cells. Preclinical and early clinical data support the use of TLR9 agonists as vaccine adjuvants, where they can enhance both the humoral and cellular responses to diverse antigens. In mouse tumor models TLR9 agonists have shown activity not only as monotherapy, but also in combination with multiple other therapies including vaccines, antibodies, cellular therapies, other immunotherapies, antiangiogenic agents, radiotherapy, cryotherapy, and some chemotherapies. Phase I and If clinical trials have indicated that these agents have antitumor activity as single agents and enhance the development of antitumor T-cell responses when used as therapeutic vaccine adjuvants. CpG ODN have shown benefit in multiple rodent and primate models of asthma and other allergic diseases, with encouraging results in some early human clinical trials. Although their potential clinical contributions are enormous, the safety and efficacy of these TLR9 agonists in humans remain to be determined. (c) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:195 / 204
页数:10
相关论文
共 199 条
[1]
Ahmad-Nejad P, 2002, EUR J IMMUNOL, V32, P1958, DOI 10.1002/1521-4141(200207)32:7<1958::AID-IMMU1958>3.0.CO
[2]
2-U
[3]
ALIGNANI D, 2005, J LEUKOC BIOL
[4]
Circulating plasma levels of nucleosomes in patients with systemic lupus erythematosus - Correlation with serum antinucleosome antibody titers and absence of clear association with disease activity [J].
Amoura, Z ;
Piette, JC ;
Chabre, H ;
Cacoub, P ;
Papo, T ;
Wechsler, B ;
Bach, JF ;
Koutouzov, S .
ARTHRITIS AND RHEUMATISM, 1997, 40 (12) :2217-2225
[5]
New generation vaccine induces effective melanoma-specific CD8+ T cells in the circulation but not in the tumor site [J].
Appay, Victor ;
Jandus, Camilla ;
Voelter, Verena ;
Reynard, Severine ;
Coupland, Sarah E. ;
Rimoldi, Donata ;
Lienard, Danielle ;
Guillaume, Philippe ;
Krieg, Arthur M. ;
Cerottini, Jean-Charles ;
Romero, Pedro ;
Leyvraz, Serge ;
Rufer, Nathalie ;
Speiser, Daniel E. .
JOURNAL OF IMMUNOLOGY, 2006, 177 (03) :1670-1678
[6]
Local delivery of CpG oligodeoxynucleotides induces rapid changes in the genital mucosa and inhibits replication, but not entry, of herpes simplex virus type 2 [J].
Ashkar, AA ;
Bauer, S ;
Mitchell, WJ ;
Vieira, J ;
Rosenthal, KL .
JOURNAL OF VIROLOGY, 2003, 77 (16) :8948-8956
[7]
Sequence requirements for oligodeoxyribonucleotide inhibitory activity [J].
Ashman, RF ;
Goeken, JA ;
Drahos, J ;
Lenert, P .
INTERNATIONAL IMMUNOLOGY, 2005, 17 (04) :411-420
[8]
Ballas ZK, 1996, J IMMUNOL, V157, P1840
[9]
Combination of a CpG-oligodeoxynucleotide and a topoisomerase I inhibitor in the therapy of human tumour xenografts [J].
Balsari, A ;
Tortoreto, M ;
Besusso, D ;
Petrangolini, G ;
Sfondrini, L ;
Maggi, R ;
Ménard, S ;
Pratesi, G .
EUROPEAN JOURNAL OF CANCER, 2004, 40 (08) :1275-1281
[10]
Nucleic acids of mammalian origin can act as endogenous ligands for toll-like receptors and may promote systemic lupus erythematosus [J].
Barrat, FJ ;
Meeker, T ;
Gregorio, J ;
Chan, JH ;
Uematsu, S ;
Akira, S ;
Chang, B ;
Duramad, O ;
Coffman, RL .
JOURNAL OF EXPERIMENTAL MEDICINE, 2005, 202 (08) :1131-1139