Current status of a mucosal vaccine against dental caries

被引:57
作者
Hajishengallis, G
Michalek, SM
机构
[1] Univ Alabama Birmingham, Dept Microbiol, Birmingham, AL 35294 USA
[2] Univ Alabama Birmingham, Dept Oral Biol, Birmingham, AL 35294 USA
来源
ORAL MICROBIOLOGY AND IMMUNOLOGY | 1999年 / 14卷 / 01期
关键词
Streptococcus mutans; Streptococcus sobrinus; vaccine; secretory IgA; dental caries; adhesin; glycosyltransferases; oral bacterial colonization;
D O I
10.1034/j.1399-302X.1999.140101.x
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
The evidence of a specific bacterial cause of dental caries and of the function of the salivary glands as an effector site of the mucosal immune system has provided a scientific basis for the development of a vaccine against this highly prevalent and costly oral disease. Research efforts towards developing an effective and safe caries vaccine have been facilitated by progress in molecular biology, with the cloning and functional characterization of virulence factors from mutans streptococci, the principal causative agent of dental caries, and advancements in mucosal immunology, including the development of sophisticated antigen delivery systems and adjuvants that stimulate the induction of salivary immunoglobulin A antibody responses. Cell-surface fibrillar proteins, which mediate adherence to the salivary pellicle, and glucosyltransferase enzymes, which synthesize adhesive glucans and allow microbial accumulation, are virulence components of mutans streptococci, and primary candidates for a human caries vaccine. Infants, representing the primary target population for a caries vaccine, become mucosally immunocompetent and secrete salivary immunoglobulin A antibodies during the first weeks after birth, whereas mutans streptococci colonize the tooth surfaces at a discrete time period that extends around 26 months of life. Therefore, immunization when infants are about one year old may establish effective immunity against an ensuing colonization attempts by mutans streptococci. The present review critically evaluates recent progress in this field of dental research and attempts to stress the protective potential as well as limitations of caries immunization.
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页码:1 / 20
页数:20
相关论文
共 262 条
[91]   EVIDENCE FOR AN IMMUNOLOGICAL RELATIONSHIP BETWEEN STREPTOCOCCUS-MUTANS AND HUMAN CARDIAC TISSUE [J].
HUGHES, M ;
MACHARDY, SM ;
SHEPPARD, AJ ;
WOODS, NC .
INFECTION AND IMMUNITY, 1980, 27 (02) :576-588
[92]   ORIGIN AND ANTIGEN-DEPENDENT DISTRIBUTION OF IGA-CONTAINING CELLS IN INTESTINE [J].
HUSBAND, AJ ;
GOWANS, JL .
JOURNAL OF EXPERIMENTAL MEDICINE, 1978, 148 (05) :1146-1160
[93]  
IWASE T, 1995, ADV MUCOSAL IMMUNOLO, P1161
[94]  
JACOBSON LO, 1961, P SOC EXP BIOL MED, V108, P487
[95]   Structure, function and immunogenicity of streptococcal antigen I/II polypeptides [J].
Jenkinson, HF ;
Demuth, DR .
MOLECULAR MICROBIOLOGY, 1997, 23 (02) :183-190
[96]   Streptococcal adhesion and colonization [J].
Jenkinson, HF ;
Lamont, RJ .
CRITICAL REVIEWS IN ORAL BIOLOGY & MEDICINE, 1997, 8 (02) :175-200
[97]  
Jespersgaard C, 1998, J DENT RES, V77, P268
[98]  
JESPERSGAARD C, 1997, 97 ASM GEN M
[99]   Coronal caries in the primary and permanent dentition of children and adolescents 1-17 years of age: United States, 1988-1991 [J].
Kaste, LM ;
Selwitz, RH ;
Oldakowski, RJ ;
Brunelle, JA ;
Winn, DM ;
Brown, LJ .
JOURNAL OF DENTAL RESEARCH, 1996, 75 :631-641
[100]   MOLECULAR-BASIS FOR THE ASSOCIATION OF GLUCOSYLTRANSFERASES WITH THE CELL-SURFACE OF ORAL STREPTOCOCCI [J].
KATO, C ;
KURAMITSU, HK .
FEMS MICROBIOLOGY LETTERS, 1991, 79 (2-3) :153-158