A clinical grade cocktail of cytokines and PGE2 results in uniform maturation of human monocyte-derived dendritic cells:: implications for immunotherapy

被引:163
作者
Lee, AW
Truong, T
Bickham, K
Fonteneau, JF
Larsson, M
Da Silva, I
Somersan, S
Thomas, EK
Bhardwaj, N
机构
[1] Rockefeller Univ, Cellular Physiol & Immunol Lab, New York, NY 10021 USA
[2] Immunex Corp, Seattle, WA USA
关键词
dendritic cells; T cell activation; vaccination; immunotherapy;
D O I
10.1016/S0264-410X(02)00382-1
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Dendritic cells (DCs) can induce tumor- or pathogen-specific T cell responses in humans. We comprehensively compared the clinically available DC maturation stimuli for their ability to promote uniformly mature DCs that elicit higher levels of T cell responses. We compared the standard maturation stimulus, autologous monocyte-conditioned medium (MCM), with a synthetic double stranded RNA (poly l:Q, soluble CD40 ligand trimer, and a defined cocktail of cytokines (TNF-alpha, IL-1beta, IL-6) and PGE(2) to promote mature phenotype and function in human monocyte-derived DCs. The cocktail was the most efficient despite the lack of induction of IL-12p70. While these results support the use of the MCM-mimic cocktail in clinical DC immunotherapy trials, the roles of it's individual constituents remain to be completely defined. (C) 2002 Published by Elsevier Science Ltd.
引用
收藏
页码:A8 / A22
页数:15
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