MENINGOCOCCAL LIPOPOLYSACCHARIDES - VIRULENCE FACTOR AND POTENTIAL VACCINE COMPONENT

被引:94
作者
VERHEUL, AFM
SNIPPE, H
POOLMAN, JT
机构
[1] UNIV UTRECHT, ACAD HOSP, EIJKMAN WINKLER LAB MED MICROBIOL, 3584 CX UTRECHT, NETHERLANDS
[2] NATL INST PUBL HLTH & ENVIRONM PROTECT, BACTERIAL VACCINE DEV & PATHOGENESIS RES UNIT, 3720 BILTHOVEN, NETHERLANDS
关键词
D O I
10.1128/MMBR.57.1.34-49.1993
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Lipopolysaccharides (LPS) are surface components of the outer membrane of Neisseria meningitidis. Today, 12 different types of meningococcal LPS (immunotypes) are known, of which 3 are prevalent in the western world. The differences between these immunotypes are in the oligosaccharide part of the LPS molecule and consist of small differences in the oligosaccharide structure, the amount and location of phosphoethanolamine groups, and the degree of O acetylation of individual monosaccharides. Although the differences between the various immunotypes are small, they have a profound influence on the immunochemical and immunological properties of these molecules. Furthermore, each individual strain synthesizes a number of different LPS molecules. The expression of the various components (protective epitopes) is influenced by growth conditions and growth phase. Meningococci can endogenously sialyate their LPS, which constitutes one of the mechanisms by which N. meningitidis can evade the response of the human host. Meningococcal LPS play a key role in the induction of septic shock and can probably enhance the invasiveness of meningococcal strains and shield protective epitopes. Therefore, incorporation of (detoxified) LPS or oligosaccharide components derived therefrom might be very beneficial for the efficacy of a vaccine against group B meningococci. An overview of the development of vaccines against group B meningococci is given, and the status and potential of meningococcal LPS-derived (synthetic) oligosaccharide-protein conjugate vaccines are discussed.
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页码:34 / 49
页数:16
相关论文
共 154 条
[1]  
ABDILLAHI H, 1987, FEMS MICROBIOL LETT, V48, P361
[2]  
ACHTMAN M, 1991, NEISSERIA 1990
[3]   ENDOTOXIN LIBERATION FROM NEISSERIA MENINGITIDIS ISOLATED FROM CARRIERS AND CLINICAL CASES [J].
ANDERSEN, BM ;
SOLBERG, O ;
BRYN, K ;
FROHOLM, LO ;
GAUSTAD, P ;
HOIBY, EA ;
KRISTIANSEN, BE ;
BOVRE, K .
SCANDINAVIAN JOURNAL OF INFECTIOUS DISEASES, 1987, 19 (04) :409-419
[4]   ENDOTOXIN LIBERATION ASSOCIATED WITH GROWTH, ENCAPSULATION AND VIRULENCE OF NEISSERIA MENINGITIDIS [J].
ANDERSEN, BM ;
SOLBERG, O .
SCANDINAVIAN JOURNAL OF INFECTIOUS DISEASES, 1988, 20 (01) :21-31
[5]   PRIMING AND INDUCTION OF HAEMOPHILUS-INFLUENZAE TYPE B CAPSULAR ANTIBODIES IN EARLY INFANCY BY DPO20, AN OLIGOSACCHARIDE-PROTEIN CONJUGATE VACCINE [J].
ANDERSON, P ;
PICHICHERO, M ;
EDWARDS, K ;
PORCH, CR ;
INSEL, R .
JOURNAL OF PEDIATRICS, 1987, 111 (05) :644-650
[6]  
APICELLA M, 1989, PRINCIPLES PRACTICE, P1600
[7]   MODIFICATION BY SIALIC-ACID OF NEISSERIA-GONORRHOEAE LIPOOLIGOSACCHARIDE EPITOPE EXPRESSION IN HUMAN URETHRAL EXUDATES - AN IMMUNOELECTRON MICROSCOPIC ANALYSIS [J].
APICELLA, MA ;
MANDRELL, RE ;
SHERO, M ;
WILSON, ME ;
GRIFFISS, JM ;
BROOKS, GF ;
LAMMEL, C ;
BREEN, JF ;
RICE, PA .
JOURNAL OF INFECTIOUS DISEASES, 1990, 162 (02) :506-512
[8]  
ARSONS NJ, 1992, FEMS MICROBIOL LETT, V90, P295
[9]   PREVENTION OF MENINGOCOCCAL DISEASE BY GROUP-C POLYSACCHARIDE VACCINE [J].
ARTENSTEIN, MS ;
GOLD, R ;
ZIMMERLY, JG ;
WYLE, FA ;
SCHNEIDER, H ;
HARKINS, C .
NEW ENGLAND JOURNAL OF MEDICINE, 1970, 282 (08) :417-+
[10]  
ASHTON FE, 1985, PATHOGENIC NEISSERIA, P616