In situ delivery of passive immunity by lactobacilli producing single-chain antibodies

被引:141
作者
Krüger, C
Hu, YZ
Pan, Q
Marcotte, H
Hultberg, A
Delwar, D
van Dalen, PJ
Pouwels, PH
Leer, RJ
Kelly, CG
van Dollenweerd, C
Ma, JK
Hammarström, L [1 ]
机构
[1] Novum, Karolinska Inst, Ctr Oral Biol, SE-14186 Huddinge, Sweden
[2] Huddinge Hosp, Karolinska Inst, Div Clin Immunol, SE-14186 Huddinge, Sweden
[3] TNO Prevent & Hlth, Div Infect Dis & Immunol, NL-2301 CE Leiden, Netherlands
[4] TNO Voeding, Dept Appl Microbiol & Gene Technol, NL-3600 AJ Zeist, Netherlands
[5] Univ London Kings Coll, Guys Hosp, Dept Oral Med & Pathol, London WC2R 2LS, England
关键词
D O I
10.1038/nbt0702-702
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
Lactobacilli have previously been used to deliver vaccine components for active immunization in vivo. Vectors encoding a single-chain Fv (scFv) antibody fragment, which recognizes the streptococcal antigen I/II (SAI/II) adhesion molecule of Streptococcus mutans, were constructed and expressed in Lactobacillus zeae (American Type Culture Collection (ATCC) 393). The scFv antibody fragments secreted into the supernatant or expressed on the surface of the bacteria showed binding activity against SAI/II in enzyme-linked immunosorbent assay (ELISA), and surface scFv-expressing lactobacilli agglutinated SAI/II-expressing S. mutans in vitro without affecting the corresponding SAI/II knockout strain. Lactobacilli expressing the scFv fragment fused to an E-tag were visualized by scanning electron microscopy (SEM) using beads coated with a monoclonal anti-E-tag antibody, and they bound directly to beads coated with SAI/II. After administration of scFv-expressing bacteria to a rat model of dental caries development, S. mutans bacteria counts and caries scores were markedly reduced. As lactobacilli are generally regarded as safe (GRAS) microorganisms, this approach may be of considerable commercial interest for in vivo immunotherapy.
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页码:702 / 706
页数:5
相关论文
共 49 条
[1]  
Ahrné S, 1998, J APPL MICROBIOL, V85, P88
[2]   Therapy of mucosal candidiasis by expression of an anti-idiotype in human commensal bacteria [J].
Beninati, C ;
Oggioni, MR ;
Boccanera, M ;
Spinosa, MR ;
Maggi, T ;
Conti, S ;
Magliani, W ;
De Bernardis, F ;
Teti, G ;
Cassone, A ;
Pozzi, G ;
Polonelli, L .
NATURE BIOTECHNOLOGY, 2000, 18 (10) :1060-1064
[3]   CLONING AND INACTIVATION OF THE GENE RESPONSIBLE FOR A MAJOR SURFACE-ANTIGEN ON STREPTOCOCCUS-MUTANS [J].
BLEIWEIS, AS ;
LEE, SF ;
BRADY, LJ ;
PROGULSKEFOX, A ;
CROWLEY, PJ .
ARCHIVES OF ORAL BIOLOGY, 1990, 35 :S15-S23
[4]   THE EFFECT OF DESALIVATION ON CORONAL AND ROOT SURFACE CARIES IN RATS [J].
BOWEN, WH ;
PEARSON, SK ;
YOUNG, DA .
JOURNAL OF DENTAL RESEARCH, 1988, 67 (01) :21-23
[5]   Oral IgA-IgG treatment of chronic non-specific diarrhoea in infants and children [J].
Casswall, TH ;
Hammarstrom, L ;
Veress, B ;
Nord, CE ;
Bogstedt, A ;
Brockstedt, U ;
Dahlstrom, KA .
ACTA PAEDIATRICA, 1996, 85 (09) :1126-1128
[6]   Gene expression systems for lactic acid bacteria [J].
de Vos, WM .
CURRENT OPINION IN MICROBIOLOGY, 1999, 2 (03) :289-295
[7]   PREVENTION OF NECROTIZING ENTEROCOLITIS IN LOW-BIRTH-WEIGHT INFANTS BY IGA-IGG FEEDING [J].
EIBL, MM ;
WOLF, HM ;
FURNKRANZ, H ;
ROSENKRANZ, A .
NEW ENGLAND JOURNAL OF MEDICINE, 1988, 319 (01) :1-7
[8]   EFFECT OF IMMUNE BOVINE-MILK ON STREPTOCOCCUS-MUTANS IN HUMAN DENTAL PLAQUE [J].
FILLER, SJ ;
GREGORY, RL ;
MICHALEK, SM ;
KATZ, J ;
MCGHEE, JR .
ARCHIVES OF ORAL BIOLOGY, 1991, 36 (01) :41-47
[9]   Transgenic plants as factories for biopharmaceuticals [J].
Giddings, G ;
Allison, G ;
Brooks, D ;
Carter, A .
NATURE BIOTECHNOLOGY, 2000, 18 (11) :1151-1155
[10]   Probiotics in infective diarrhoea and inflammatory bowel diseases [J].
Gionchetti, P ;
Rizzello, F ;
Venturi, A ;
Campieri, M .
JOURNAL OF GASTROENTEROLOGY AND HEPATOLOGY, 2000, 15 (05) :489-493