Rapid and strong human CD8+ T cell responses to vaccination with peptide, IFA, and CpG oligodeoxynucleotide 7909

被引:520
作者
Speiser, DE
Liénard, D
Rufer, N
Rubio-Godoy, V
Rimoldi, D
Lejeune, F
Krieg, AM
Cerottini, JC
Romero, P
机构
[1] CHU Vaudois, Ludwig Inst Canc Res, Div Clin Oncoimmunol, CH-1011 Lausanne, Switzerland
[2] CHU Vaudois, Multidisciplinary Oncol Ctr, CH-1011 Lausanne, Switzerland
[3] Swiss Inst Expt Canc Res, CH-1066 Epalinges, Switzerland
[4] Coley Pharmaceut Grp, Wellesley, MA USA
[5] Univ Lausanne, Lausanne Branch, Ludwig Inst Canc Res, CH-1066 Epalinges, Switzerland
关键词
D O I
10.1172/JCI200523373
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
The induction of potent CD8(+) T cell responses by vaccines to fight microbes or tumors remains a major challenge, as many candidates for human vaccines have proved to be poorly immunogenic. Deoxycytidyl-deoxyguanosin oligodeoxynucleotides (CpG ODNs) trigger Toll-like receptor 9, resulting in dendritic cell maturation that can enhance immunogenicity of peptide-based vaccines in mice. We tested whether a synthetic ODN, CpG 7909, could improve human tumor antigen-specific CD8+ T cell responses. Eight HLA-A2(+) melanoma patients received 4 monthly vaccinations of low-dose CpG 7909 mixed with melanoma antigen A (Melan-A; identical to MART-1) analog peptide and incomplete Freund's adjuvant. All patients exhibited rapid and strong antigen-specific T cell responses: the frequency of Melan-A-specific T cells reached over 3% of circulating CD8(+)T cells. This was one order of magnitude higher than the frequency seen in 8 control patients treated similarly but without CpG and 1-3 orders of magnitude higher than that seen in previous studies with synthetic vaccines. The enhanced T cell populations consisted primarily of effector memory cells, which in part secreted IFN-gamma and expressed granzyme B and perforin ex vivo. In vitro, T cell clones recognized and killed melanoma cells in an antigen-specific manner. Thus, CpG 7909 is an efficient vaccine adjuvant that promotes strong antigen-specific CD8(+) T cell responses in humans.
引用
收藏
页码:739 / 746
页数:8
相关论文
共 51 条
[1]  
ABULAS RM, 2000, J IMMUNOL, V164, P2372
[2]   IFN-α and IFN-β: A link between immune memory and chronic inflammation [J].
Akbar, AN ;
Lord, JM ;
Salmon, M .
IMMUNOLOGY TODAY, 2000, 21 (07) :337-+
[3]   Toll-like receptors: critical proteins linking innate and acquired immunity [J].
Akira, S ;
Takeda, K ;
Kaisho, T .
NATURE IMMUNOLOGY, 2001, 2 (08) :675-680
[4]   Phenotypic analysis of antigen-specific T lymphocytes [J].
Altman, JD ;
Moss, PAH ;
Goulder, PJR ;
Barouch, DH ;
McHeyzerWilliams, MG ;
Bell, JI ;
McMichael, AJ ;
Davis, MM .
SCIENCE, 1996, 274 (5284) :94-96
[5]   Human TLR9 confers responsiveness to bacterial DNA via species-specific CpG motif recognition [J].
Bauer, S ;
Kirschning, CJ ;
Häcker, H ;
Redecke, V ;
Hausmann, S ;
Akira, S ;
Wagner, H ;
Lipford, GB .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (16) :9237-9242
[6]   Therapeutic use of IL-2 to enhance antiviral T-cell responses in vivo [J].
Blattman, JN ;
Grayson, JM ;
Wherry, EJ ;
Kaech, SM ;
Smith, KA ;
Ahmed, R .
NATURE MEDICINE, 2003, 9 (05) :540-547
[7]   Tumour immunology [J].
Boon, T ;
Van den Eynde, B .
CURRENT OPINION IN IMMUNOLOGY, 2003, 15 (02) :129-130
[8]  
Cormier JN, 1997, CANCER J, V3, P37
[9]   Repeated administration of cytosine-phosphorothiolated guanine-containing oligonucleotides together with peptide/protein immunization results in enhanced CTL responses with anti-tumor activity [J].
Davila, E ;
Celis, E .
JOURNAL OF IMMUNOLOGY, 2000, 165 (01) :539-547
[10]   CpG DNA overcomes hyporesponsiveness to hepatitis B vaccine in orangutans [J].
Davis, HL ;
Suparto, I ;
Weeratna, R ;
Jumintarto ;
Iskandriati, D ;
Chamzah, S ;
Ma'ruf, A ;
Nente, C ;
Pawitri, D ;
Krieg, AM ;
Heriyanto ;
Smits, W ;
Sajuthi, D .
VACCINE, 2000, 18 (18) :1920-1924