The central role played by peptides in the immune response and the design of peptide-based vaccines against infectious diseases and cancer

被引:39
作者
Jackson, DC [1 ]
Purcell, AW
Fitzmaurice, CJ
Zeng, W
Hart, DNJ
机构
[1] Univ Melbourne, Dept Microbiol & Immunol, Cooperat Res Ctr Vaccine Technol, Parkville, Vic 3010, Australia
[2] Mater Med Res Inst, Brisbane, Qld 4101, Australia
关键词
D O I
10.2174/1389450024605436
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Vaccines are one of the most cost effective methods of improving public health thereby increasing the quality of life. Prophylactic and therapeutic treatment by vaccines can prevent infectious diseases and some cancers and could also be used in the treatment of autoimmune disorders. An appreciation of this potential has resulted in a burgeoning literature which not only describes the scientific efforts being made into designing new and improved vaccines out also drives the efforts being made by public health organizations world-wide in delivering vaccines to the community. At the forefront of technologies being applied to the design of vaccines is the use of synthetic peptides; the chemical technologies used to assemble peptides have made great strides over the last decade and assembly of hi-fidelity peptides which can be of high molecular weight, multimeric or even branched is now almost routine. Together with the advances in peptide technology our understanding of the molecular events that are necessary to induce immune responses has also made great strides. The central role that peptides play in immune recognition is now recognised and rules are emerging that are being applied to the construction of peptide-based vaccines that, in the right context, can induce humoral (antibody) and cellular (cytotoxic and helper T cell) immune responses. Synthetic peptides are exquisitely placed to answer questions about immune recognition and along the way to provide us with new and improved vaccines.
引用
收藏
页码:175 / 196
页数:22
相关论文
共 159 条
  • [91] LIU KJ, 1993, J IMMUNOL, V151, P6143
  • [92] CELLS THAT PRESENT BOTH SPECIFIC LIGAND AND COSTIMULATORY ACTIVITY ARE THE MOST EFFICIENT INDUCERS OF CLONAL EXPANSION OF NORMAL CD4 T-CELLS
    LIU, Y
    JANEWAY, CA
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (09) : 3845 - 3849
  • [93] LU YA, 1991, MOL IMMUNOL, V28, P623
  • [94] Killer cell immunoglobulin receptors and T cell receptors bind peptide-major histocompatibility complex class I with distinct thermodynamic and kinetic properties
    Maenaka, K
    Juji, T
    Nakayama, T
    Wyer, JR
    Gao, GF
    Maenaka, T
    Zaccai, NR
    Kikuchi, A
    Yabe, T
    Tokunaga, K
    Tadokoro, K
    Stuart, DI
    Jones, EY
    van der Merwe, PA
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (40) : 28329 - 28334
  • [95] Linear and multiple antigen peptides containing defined T and B epitopes of the Plasmodium yoelii circumsporozoite protein:: antibody-mediated protection and boosting by sporozoite infection
    Marussig, M
    Rénia, L
    Motard, A
    Miltgen, F
    Pétour, P
    Chauhan, V
    Corradin, G
    Mazier, D
    [J]. INTERNATIONAL IMMUNOLOGY, 1997, 9 (12) : 1817 - 1824
  • [96] MATACONIA S, 1989, J EXP MED, V169, P1255
  • [97] Milich D R, 1990, Semin Immunol, V2, P307
  • [98] Polyarginine enters cells more efficiently than other polycationic homopolymers
    Mitchell, DJ
    Kim, DT
    Steinman, L
    Fathman, CG
    Rothbard, JB
    [J]. JOURNAL OF PEPTIDE RESEARCH, 2000, 56 (05): : 318 - 325
  • [99] SELECTIVITY OF MHC-ENCODED PEPTIDE TRANSPORTERS FROM HUMAN, MOUSE AND RAT
    MOMBURG, F
    ROELSE, J
    HOWARD, JC
    BUTCHER, GW
    HAMMERLING, GJ
    NEEFJES, JJ
    [J]. NATURE, 1994, 367 (6464) : 648 - 651
  • [100] SURFACE-PROTEINS INVOLVED IN T-CELL COSTIMULATION
    MONDINO, A
    JENKINS, MK
    [J]. JOURNAL OF LEUKOCYTE BIOLOGY, 1994, 55 (06) : 805 - 815