Toll-Like Receptor Agonists Are They Good Adjuvants?
被引:134
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作者:
Gnjatic, Sacha
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机构:
Mem Sloan Kettering Canc Ctr, New York Branch, Ludwig Inst Canc Res, New York, NY 10021 USANYU, Sch Med, Langone Med Ctr, Inst Canc, New York, NY 10016 USA
Gnjatic, Sacha
[2
]
Sawhney, Nikhil B.
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机构:
Newark Acad, Livingston, NJ USANYU, Sch Med, Langone Med Ctr, Inst Canc, New York, NY 10016 USA
Sawhney, Nikhil B.
[3
]
Bhardwaj, Nina
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机构:
NYU, Sch Med, Langone Med Ctr, Inst Canc, New York, NY 10016 USANYU, Sch Med, Langone Med Ctr, Inst Canc, New York, NY 10016 USA
Bhardwaj, Nina
[1
]
机构:
[1] NYU, Sch Med, Langone Med Ctr, Inst Canc, New York, NY 10016 USA
[2] Mem Sloan Kettering Canc Ctr, New York Branch, Ludwig Inst Canc Res, New York, NY 10021 USA
toll-like receptors;
cancer vaccines;
dendritic cells;
vaccine adjuvants;
POLYRIBOINOSINIC-POLYRIBOCYTIDYLIC ACID;
PLASMACYTOID DENDRITIC CELLS;
CD8(+) T-CELLS;
POLY-L-LYSINE;
ACTIVE SPECIFIC IMMUNOTHERAPY;
HUMAN-PAPILLOMAVIRUS TYPE-16;
BACILLUS-CALMETTE-GUERIN;
INNATE IMMUNE-RESPONSE;
PHASE-II TRIAL;
NY-ESO-1;
PROTEIN;
D O I:
10.1097/PPO.0b013e3181eaca65
中图分类号:
R73 [肿瘤学];
学科分类号:
100214 ;
摘要:
Therapeutic immunization leading to cancer regression remains a significant challenge. Successful immunization requires activation of adaptive immunity, including tumor specific CD4(+) T cells and CD8(+) T cells. Generally, the activation of T cells is compromised in patients with cancer because of immune suppression, loss of tumor antigen expression, and dysfunction of antigen-presenting cells. Antigen-presenting cells such as dendritic cells (DCs) are key for the induction of adaptive antitumor immune responses. Recently, attention has focused on novel adjuvants that enhance dendritic cell function and their ability to prime T cells. Agonists that target toll-like receptors are being used clinically either alone or in combination with tumor antigens and showing initial success both in terms of enhancing immune responses and eliciting antitumor activity. This review summarizes the application of these adjuvants to treat cancer and the potential for boosting responses in vivo.
机构:
MIT, Koch Inst Integrat Canc Res, 77 Massachusetts Ave, Cambridge, MA 02139 USA
MIT, Dept Chem, Cambridge, MA 02139 USA
MIT, Dept Chem Engn, Cambridge, MA 02139 USA
Ragon Inst MGH MIT & Harvard, Cambridge, MA 02139 USAMIT, Koch Inst Integrat Canc Res, 77 Massachusetts Ave, Cambridge, MA 02139 USA
Bhagchandani, Sachin
Johnson, Jeremiah A.
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机构:
MIT, Koch Inst Integrat Canc Res, 77 Massachusetts Ave, Cambridge, MA 02139 USA
MIT, Dept Chem, Cambridge, MA 02139 USA
Broad Inst MIT & Harvard, Cambridge, MA 02142 USAMIT, Koch Inst Integrat Canc Res, 77 Massachusetts Ave, Cambridge, MA 02139 USA
Johnson, Jeremiah A.
Irvine, Darrell J.
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h-index: 0
机构:
MIT, Koch Inst Integrat Canc Res, 77 Massachusetts Ave, Cambridge, MA 02139 USA
MIT, Dept Biol Engn, 77 Massachusetts Ave, Cambridge, MA 02139 USA
MIT, Dept Mat Sci & Engn, Cambridge, MA 02139 USA
Howard Hughes Med Inst, Chevy Chase, MD 20815 USA
Ragon Inst MGH MIT & Harvard, Cambridge, MA 02139 USAMIT, Koch Inst Integrat Canc Res, 77 Massachusetts Ave, Cambridge, MA 02139 USA
机构:
George Washington Univ, Dept Microbiol Immunol & Trop Med, Washington, DC 20052 USAGeorge Washington Univ, Dept Microbiol Immunol & Trop Med, Washington, DC 20052 USA
Macedo, Amanda B.
Novis, Camille L.
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机构:
Univ Utah, Dept Pathol, Div Microbiol & Immunol, Salt Lake City, UT USAGeorge Washington Univ, Dept Microbiol Immunol & Trop Med, Washington, DC 20052 USA
Novis, Camille L.
Bosque, Alberto
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h-index: 0
机构:
George Washington Univ, Dept Microbiol Immunol & Trop Med, Washington, DC 20052 USAGeorge Washington Univ, Dept Microbiol Immunol & Trop Med, Washington, DC 20052 USA