A new dendritic cell vaccine generated with interleukin-3 and interferon-β induces CD8+ T cell responses against NA17-A2 tumor peptide in melanoma patients

被引:52
作者
Trakatelli, M
Toungouz, M
Blocklet, D
Dodoo, Y
Gordower, L
Laporte, M
Vereecken, P
Sales, F
Mortier, L
Mazouz, N
Lambermont, M
Goldman, S
Coulie, P
Goldman, M
Velu, T
机构
[1] Univ Libre Bruxelles, Erasme Hosp, Dept Med Oncol, B-1070 Brussels, Belgium
[2] Erasme Univ Hosp, Dept Dermatol, Brussels, Belgium
[3] Erasme Univ Hosp, Cellular & Mol Therapy Unit, Brussels, Belgium
[4] Erasme Univ Hosp, Dept Nucl Med, Brussels, Belgium
[5] Univ Louvain, Inst Cellular Pathol, Brussels, Belgium
[6] Bordet Inst, Brussels, Belgium
[7] Huriez Hosp, Dept Dermatol, Lille, France
[8] Inst Med Immunol, Gosselies, Belgium
关键词
D O I
10.1007/s00262-005-0056-z
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Dendritic cells derived from monocytes cultured in the presence of type I interferon were found to induce efficient T cell responses against tumor antigens in vitro. We vaccinated eight stage III or IV melanoma patients with dendritic cells generated with interferon-beta and interleukin-3, activated by poly I: C, and pulsed with the tumor-specific antigen NA17.A2. This dendritic cell vaccine was well-tolerated with only minor and transient flu-like symptoms and inflammatory reactions at the injection sites. In most patients, isotopic imaging documented dendritic cells (DC) migration from the intradermal injection site to the draining lymph nodes. Finally, mixed lymphocyte-peptide culture under limiting dilution conditions followed by tetramer labeling indicated that three out of eight patients mounted a CD8 T cell response against the NA17.A2 antigenic peptide. We conclude that DC generated in type I-IFN represent an interesting alternative to DC generated in IL-4 and GM-CSF for cancer immunotherapy.
引用
收藏
页码:469 / 474
页数:6
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