Passive immunization against dental caries and periodontal disease: Development of recombinant and human monoclonal antibodies

被引:46
作者
Abiko, Y [1 ]
机构
[1] Nihon Univ, Sch Dent Matsudo, Dept Biochem, Chiba 2718587, Japan
关键词
Streptococcus mutans; glucosyltransferase; Porphyromonas gingivalis; coaggregation factor; hemagglutinin; ScFv antibody; human-type monoclonal antibody;
D O I
10.1177/10454411000110020101
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Indigenous micro-organisms in the oral cavity can cause two major diseases, dental caries and periodontal diseases. There is neither agreement nor consensus as to the actual mechanisms of pathogenesis of the specific virulence Factors of these micro-organisms. The complexity of the bacterial community in dental plaque has made it difficult for the single bacterial agent of dental caries to be determined. However, there is considerable evidence that Streptococcus mutans is implicated as the primary causative organism of dental caries, and the cell-surface protein antigen (SA I/II) as well as glucosyltransferases (GTFs) produced by S. mutans appear to be major colonization factors. Various forms of periodontal diseases are closely associated with specific subgingival bacteria. Porphyromonas gingivalis has been implicated as an important etiological agent of adult periodontitis. Adherence of bacteria to host tissues is a prerequisite for colonization and one of the important steps in the disease process. Bacterial coaggregation factors and hemagglutinins likely play major roles in colonization in the subgingival area. Emerging evidence suggests that inhibition of these Virulence factors may protect the host against caries and periodontal disease. Active and passive immunization approaches have been developed for immunotherapy of these diseases. Recent advances in mucosal immunology and the introduction of novel strategies for inducing mucosal immune responses now raise the possibility that effective and safe vaccines can be constructed. In this regard, some successful results have been reported in animal experimental models. Nevertheless. since the public at large might be skeptical about the seriousness of oral diseases, immunotherapy must be carried out with absolute safety. For this goal to be achieved, the development of safe antibodies for passive immunization is significant and important, In this review, salient advances in passive immunization against caries acid periodontal diseases are summarized, and the biotechnological approaches for developing recombinant and human-type antibodies are introduced. Furthermore, our own attempts to construct single-chain variable fragments (ScFv) and human-type antibodies capable of neutralizing virulence factors are discussed.
引用
收藏
页码:140 / 158
页数:19
相关论文
共 166 条
[1]   A human monoclonal antibody which inhibits the coaggregation activity of Porphyromonas gingivalis [J].
Abiko, Y ;
Ogura, N ;
Matsuda, U ;
Yanagi, K ;
Takiguchi, H .
INFECTION AND IMMUNITY, 1997, 65 (09) :3966-3969
[2]   CLONING OF THE GENE FOR CELL-SURFACE PROTEIN ANTIGEN-A FROM STREPTOCOCCUS-SOBRINUS (SEROTYPE-D) [J].
ABIKO, Y ;
HAYAKAWA, M ;
AOKI, H ;
SAITO, S ;
TAKIGUCHI, H .
ARCHIVES OF ORAL BIOLOGY, 1989, 34 (07) :571-575
[3]   CLONING OF A BACTEROIDES-GINGIVALIS OUTER-MEMBRANE PROTEIN GENE IN ESCHERICHIA-COLI [J].
ABIKO, Y ;
HAYAKAWA, M ;
AOKI, H ;
KIKUCHI, T ;
SHIMATAKE, H ;
TAKIGUCHI, H .
ARCHIVES OF ORAL BIOLOGY, 1990, 35 (09) :689-695
[4]   THE STIMULATION OF MACROPHAGE PROSTAGLANDIN-E2 AND THROMBOXANE-B2 SECRETION BY STREPTOCOCCUS-MUTANS INSOLUBLE GLUCANS [J].
ABIKO, Y ;
SHIBATA, Y ;
FUKUSHIMA, K ;
MURAI, S ;
TAKIGUCHI, H .
FEBS LETTERS, 1983, 154 (02) :297-300
[5]  
ACKERMANS F, 1991, CLIN EXP IMMUNOL, V85, P265
[6]   ENGINEERING ANTIBODIES FOR THERAPY [J].
ADAIR, JR .
IMMUNOLOGICAL REVIEWS, 1992, 130 :5-40
[7]   The Tla protein of Porphyromonas gingivalis W50: a homolog of the RI protease precursor (PrpRI) is an outer membrane receptor required for growth on low levels of hemin [J].
AduseOpoku, J ;
Slaney, JM ;
Rangarajan, M ;
Muir, J ;
Young, KA ;
Curtis, MA .
JOURNAL OF BACTERIOLOGY, 1997, 179 (15) :4778-4788
[8]   CLONING OF A STREPTOCOCCUS-MUTANS GLUCOSYLTRANSFERASE GENE CODING FOR INSOLUBLE GLUCAN SYNTHESIS [J].
AOKI, H ;
SHIROZA, T ;
HAYAKAWA, M ;
SATO, S ;
KURAMITSU, HK .
INFECTION AND IMMUNITY, 1986, 53 (03) :587-594
[9]   Expression of cholera toxin B subunit oligomers in transgenic potato plants [J].
Arakawa, T ;
Chong, DKX ;
Merritt, JL ;
Langridge, WHR .
TRANSGENIC RESEARCH, 1997, 6 (06) :403-413
[10]   HUMAN MONOCLONAL FAB FRAGMENTS DERIVED FROM A COMBINATORIAL LIBRARY BIND TO RESPIRATORY SYNCYTIAL VIRUS-F GLYCOPROTEIN AND NEUTRALIZE INFECTIVITY [J].
BARBAS, CF ;
CROWE, JE ;
CABABA, D ;
JONES, TM ;
ZEBEDEE, SL ;
MURPHY, BR ;
CHANOCK, RM ;
BURTON, DR .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (21) :10164-10168