Short peptide sequences containing MHC class I and/or class II epitopes linked to nano-beads induce strong immunity and inhibition of growth of antigen-specific tumour challenge in mice

被引:64
作者
Fifis, T [1 ]
Mottram, P [1 ]
Bogdanoska, V [1 ]
Hanley, J [1 ]
Plebanski, M [1 ]
机构
[1] Austin Hosp, Austin Res Inst, Vaccine Dev & Infect Dis Unit, Heidelberg, Vic 3084, Australia
基金
英国医学研究理事会;
关键词
peptides; tumours; vaccine;
D O I
10.1016/j.vaccine.2004.05.022
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Peptide based vaccines offer practical advantages, but unmodified peptides usually require an adjuvant or delivery vehicle to promote immunogenicity. When peptides containing ovalbumin (OVA) derived CD4 and CD8 T cell epitopes were conjugated to 0.05 mum nano-beads, they gave strong immune responses and inhibition of growth of tumour cells expressing the CD8 T cell epitope with MHC class I. These responses were inducible with both high (50 mug) and low (5 mug) peptide doses after a single immunisation. The helper CD4 T cell epitope was unnecessary for induction of CD8 T cell or tumour challenge responses. However, the CD4 T cell epitope contained a B cell epitope and triggered strong antibody responses. This simple approach offers a convenient experimental tool and a potentially useful clinical method for peptide immunisation. (C) 2004 Elsevier Ltd. All rights reserved.
引用
收藏
页码:258 / 266
页数:9
相关论文
共 38 条
[11]   ROLE OF BONE-MARROW-DERIVED CELLS IN PRESENTING MHC CLASS I-RESTRICTED TUMOR-ANTIGENS [J].
HUANG, AYC ;
GOLUMBEK, P ;
AHMADZADEH, M ;
JAFFEE, E ;
PARDOLL, D ;
LEVITSKY, H .
SCIENCE, 1994, 264 (5161) :961-965
[12]   The central role of CD4+ T cells in the antitumor immune response [J].
Hung, K ;
Hayashi, R ;
Lafond-Walker, A ;
Lowenstein, C ;
Pardoll, D ;
Levitsky, H .
JOURNAL OF EXPERIMENTAL MEDICINE, 1998, 188 (12) :2357-2368
[13]   HELPER ACTIVITY IS REQUIRED FOR THE INVIVO GENERATION OF CYTO-TOXIC LYMPHOCYTES-T [J].
KEENE, JA ;
FORMAN, J .
JOURNAL OF EXPERIMENTAL MEDICINE, 1982, 155 (03) :768-782
[14]   EFFICIENT MAJOR HISTOCOMPATIBILITY COMPLEX CLASS-I PRESENTATION OF EXOGENOUS ANTIGEN UPON PHAGOCYTOSIS BY MACROPHAGES [J].
KOVACSOVICSBANKOWSKI, M ;
CLARK, K ;
BENACERRAF, B ;
ROCK, KL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (11) :4942-4946
[15]  
Marzo AL, 1999, CANCER RES, V59, P1071
[16]   INTRODUCTION OF SOLUBLE-PROTEIN INTO THE CLASS-I PATHWAY OF ANTIGEN PROCESSING AND PRESENTATION [J].
MOORE, MW ;
CARBONE, FR ;
BEVAN, MJ .
CELL, 1988, 54 (06) :777-785
[17]   Intranasal administration of a synthetic peptide vaccine encapsulated in liposome together with an anti-CD40 antibody induces protective immunity against influenza A virus in mice [J].
Ninomiya, A ;
Ogasawara, K ;
Kajino, K ;
Takada, A ;
Kida, H .
VACCINE, 2002, 20 (25-26) :3123-3129
[18]  
O'Hagan D. T., 2001, Current Drug Targets - Infectious Disorders, V1, P273
[19]   Cancer immunotherapy with peptide-based vaccines: What have we achieved? - Where are we going? [J].
Parmiani, G ;
Castelli, C ;
Dalerba, P ;
Mortarini, R ;
Rivoltini, L ;
Marincola, FM ;
Anichini, A .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2002, 94 (11) :805-818
[20]  
Plebanski M, 1998, EUR J IMMUNOL, V28, P4345, DOI 10.1002/(SICI)1521-4141(199812)28:12&lt