Toward selective elicitation of T(H)1-controlled vaccination responses: Vaccine applications of bacterial surface layer proteins

被引:28
作者
JahnSchmid, B
Messner, P
Unger, FM
Sleytr, UB
Scheiner, O
Kraft, D
机构
[1] AGR UNIV VIENNA, ZENTRUM ULTRASTRUKTURFORSCH, A-1180 VIENNA, AUSTRIA
[2] AGR UNIV VIENNA, LUDWIG BOLTZMANN INST MOLEK NANOTECHNOL, A-1180 VIENNA, AUSTRIA
[3] UNIV VIENNA, INST ALLGEMEINE & EXPTL PATHOL, A-1090 VIENNA, AUSTRIA
基金
奥地利科学基金会;
关键词
S-layer; vaccine; immunotherapy; tumor-associated antigen; Streptococcus pneumoniae; birch pollen allergen; T-helper subset;
D O I
10.1016/0168-1656(95)00124-7
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Bacterial surface layer proteins have been utilized as combined vaccine carrier/adjuvants and offer a number of advantages in these applications. The crystalline protein arrays contain functional groups in precisely defined orientations for coupling of haptens. Conventional applications of S-layer vaccines do not cause observable trauma or side effects. Depending on the nature of the S-layer preparations, antigenic conjugates will induce immune responses of a predominantly cellular or predominantly humoral nature. Immune responses to S-layer-hapten conjugates are also observed following oral/nasal application. In the present contribution, the status of investigations with S-layer conjugates in three main immunological projects is reviewed. In a project aimed at immunotherapy of cancer, conjugates of S-layer with small, tumor-associated oligosaccharides have been found to elicit hapten-specific DTH responses. An enlarged program of chemical synthesis has now been initiated to prepare a complete set of mucin-derived, tumor-associated oligosaccharides and their chemically modified analogues for elicitation of cell-mediated immune responses to certain tumors in humans. In another application, oligosaccharides derived from capsules of Streptococcus pneumoniae type 8 have been linked to S-layer proteins and have been found to elicit protective antibody responses in animals. Most recently, allergen-S-layer conjugates have been prepared with the intention to suppress the T(H)2-directed, IgE-mediated allergic responses to Bet nu 1, the major allergen of birch pollen. In the former two applications, the S-layer vaccine technology appears to offer the versatility needed to direct vaccination responses toward predominant control by T(H)1 or T(H)2 lymphocytes to meet the different therapeutic or prophylactic requirements in each case. In the third application, work has progressed to a preliminary stage only.
引用
收藏
页码:225 / 231
页数:7
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