Induction of antitumor immunity by vaccination of dendritic cells transfected with MUC1 RNA

被引:144
作者
Koido, S
Kashiwaba, M
Chen, DS
Gendler, S
Kufe, D
Gong, JL
机构
[1] Harvard Univ, Sch Med, Boston, MA 02115 USA
[2] Mayo Clin Scottsdale, Scottsdale, AZ 85259 USA
关键词
D O I
10.4049/jimmunol.165.10.5713
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 (DC) are potent APCs, In this study, murine bone marrow-derived DC were transfected with RNA encoding the MUC1 Ag that is aberrantly overexpressed in human breast and other carcinomas. The MUC1 RNA-transfected DC exhibited cell surface expression of MUC1 and costimulatory molecules, After injection at the base of the tail, the transfected DC were detectable in inguinal lymph nodes by dual immunochemical staining. Vaccination of wild-type mice with MUC1 RNA-transfected DC induced anti-MUC1 immune responses against MUC1-positive MC38/MUC1, but not MUC1-negative, tumor cells. Mice immunized with the transfected DC were protected against challenge with MC38/MUC1 tumor cells, Furthermore, mice with established MC38/MUC1 tumors were eliminated after receiving the vaccination. CTLs isolated from mice immunized with the transfected DC exhibited specific cytolytic activity against MC38/MUC1 tumor cells. In contrast to these findings, there was little if any anti-MUC1 immunity induced with the transfected DC in MUC1 transgenic (MUC1.Tg) mice. However, coadministration of the transfected DC and IL-12 reversed the unresponsiveness to MUC1 Ag in MUC1.Tg mice and induced MUC1-specific immune responses, These findings demonstrate that vaccination of DC transfected with MUC1 RNA and IL-12 reverses tolerance to MUC1 and induces immunity against MUC1-positive tumors.
引用
收藏
页码:5713 / 5719
页数:7
相关论文
共 60 条
[1]   Specificity analysis of sera from breast cancer patients vaccinated with MUC1-KLH plus QS-21 [J].
Adluri, S ;
Gilewski, T ;
Zhang, S ;
Ramnath, V ;
Ragupathi, G ;
Livingston, P .
BRITISH JOURNAL OF CANCER, 1999, 79 (11-12) :1806-1812
[2]   Therapeutic antitumor response after immunization with an admixture of recombinant vaccinia viruses expressing a modified MUC1 gene and the murine T-cell costimulatory molecule B7 [J].
Akagi, J ;
Hodge, JW ;
McLaughlin, JP ;
Gritz, L ;
Mazzara, G ;
Kufe, D ;
Schlom, J ;
Kantor, JA .
JOURNAL OF IMMUNOTHERAPY, 1997, 20 (01) :38-47
[3]   Dendritic cells and the control of immunity [J].
Banchereau, J ;
Steinman, RM .
NATURE, 1998, 392 (6673) :245-252
[4]   SPECIFIC, MAJOR HISTOCOMPATIBILITY COMPLEX - UNRESTRICTED RECOGNITION OF TUMOR-ASSOCIATED MUCINS BY HUMAN CYTO-TOXIC T-CELLS [J].
BARND, DL ;
LAN, MS ;
METZGAR, RS ;
FINN, OJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (18) :7159-7163
[5]  
Bianchi R, 1996, J IMMUNOL, V157, P1589
[6]   Dendritic cells pulsed with RNA are potent antigen-presenting cells in vitro and in vivo [J].
Boczkowski, D ;
Nair, SK ;
Snyder, D ;
Gilboa, E .
JOURNAL OF EXPERIMENTAL MEDICINE, 1996, 184 (02) :465-472
[7]  
Carr-Brendel V, 2000, CANCER RES, V60, P2435
[8]   B70/B7-2 IS IDENTICAL TO CD86 AND IS THE MAJOR FUNCTIONAL LIGAND FOR CD28 EXPRESSED ON HUMAN DENDRITIC CELLS [J].
CAUX, C ;
VANBERVLIET, B ;
MASSACRIER, C ;
AZUMA, M ;
OKUMURA, K ;
LANIER, LL ;
BANCHEREAU, J .
JOURNAL OF EXPERIMENTAL MEDICINE, 1994, 180 (05) :1841-1847
[9]   Peptide-pulsed dendritic cells induce antigen-specific, CTL-mediated protective tumor immunity [J].
Celluzzi, CM ;
Mayordomo, JI ;
Storkus, WJ ;
Lotze, MT ;
Falo, LD .
JOURNAL OF EXPERIMENTAL MEDICINE, 1996, 183 (01) :283-287
[10]   T cell suppression as a mechanism for tolerance to MUC1 antigen in MUC1 transgenic mice [J].
Chen, DS ;
Koido, S ;
Li, YQ ;
Gendler, S ;
Gong, JL .
BREAST CANCER RESEARCH AND TREATMENT, 2000, 60 (02) :107-115