Adjuvants for Enhancing the Immunogenicity of Whole Tumor Cell Vaccines

被引:85
|
作者
Chiang, Cheryl Lai-Lai [1 ]
Kandalaft, Lana E. [1 ]
Coukos, George [1 ]
机构
[1] Univ Penn, Med Ctr, Ovarian Canc Res Ctr, Philadelphia, PA 19104 USA
关键词
whole tumor cell vaccine; ovarian carcinoma; immunogenicity; adjuvants; cytokines; Toll-like receptor agonists; COLONY-STIMULATING FACTOR; POLYRIBOINOSINIC-POLYRIBOCYTIDYLIC ACID; PHASE-I TRIAL; OVARIAN-CANCER PATIENTS; PULSED DENDRITIC CELLS; MONOPHOSPHORYL-LIPID-A; MACROPHAGE-ACTIVATING LIPOPEPTIDE-2; LYMPHOCYTE-ASSOCIATED ANTIGEN-4; ACTIVE SPECIFIC IMMUNOTHERAPY; ALUMINUM-CONTAINING ADJUVANTS;
D O I
10.3109/08830185.2011.572210
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Whole tumor cell lysates can serve as excellent multivalent vaccines for priming tumor-specific CD8(+) and CD4(+) T cells. Whole cell vaccines can be prepared with hypochlorous acid oxidation, UVB-irradiation and repeat cycles of freeze and thaw. One major obstacle to successful immunotherapy is breaking self-tolerance to tumor antigens. Clinically approved adjuvants, including Montanide (TM) ISA-51 and 720, and keyhole-limpet proteins can be used to enhance tumor cell immunogenicity by stimulating both humoral and cellular anti-tumor responses. Other potential adjuvants, such as Toll-like receptor agonists (e. g., CpG, MPLA and PolyI:C), and cytokines (e.g., granulocyte-macrophage colony stimulating factor), have also been investigated.
引用
收藏
页码:150 / 182
页数:33
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